FRANCESC SOLE

All Stories

1. 
   A Murine Model of Glioblastoma Initiating Cells and Human Brain Organoid Xenograft for Photodynamic Therapy Testing

   Article • International Journal of Molecular Sciences, September 2025, MDPI AG

   FRANCESC SOLE

2. 
   Prenatal and Perinatal Factors Associated with Infant Acute Lymphoblastic Leukaemia: A Scoping Review

   Article • Cancers, January 2025, MDPI AG

   FRANCESC SOLE

3. 
   Beyond myeloid neoplasms germline guidelines: Validation of the thresholds criteria in the search of germline predisposition variants

   Article • eJHaem, October 2024, Wiley

   FRANCESC SOLE

4. 
   Persistence of Chronic Lymphocytic Leukemia Stem-like Populations under Simultaneous In Vitro Treatment with Curcumin, Fludarabine, and Ibrutinib: Implications for Therapy Resistance

   Article • International Journal of Molecular Sciences, February 2024, MDPI AG

   FRANCESC SOLE

5. 
   A framework for the clinical implementation of optical genome mapping in hematologic malignancies

   Article • American Journal of Hematology, January 2024, Wiley

   FRANCESC SOLE

6. 
   Two-Time Multiplexed Targeted Next-Generation Sequencing Might Help the Implementation of Germline Screening Tools for Myelodysplastic Syndromes/Hematologic Neoplasms

   Article • Biomedicines, December 2023, MDPI AG

   FRANCESC SOLE

7. 
   Mutational Profile Enables the Identification of a High-Risk Subgroup in Myelodysplastic Syndromes with Isolated Trisomy 8

   Article • Cancers, July 2023, MDPI AG

   FRANCESC SOLE

8. 
   Real-World Validation of Molecular International Prognostic Scoring System for Myelodysplastic Syndromes

   Article • Journal of Clinical Oncology, May 2023, American Society of Clinical Oncology (ASCO)

   FRANCESC SOLE

9. 
   Abstract LB130: Single-cell multiomics analysis of myelodysplastic syndrome predicts clinical response to DNA methylation inhibitor therapy

   Article • Cancer Research, April 2023, American Association for Cancer Research (AACR)

   FRANCESC SOLE

10. 
    Supplementary Data from Targeting the EIF2AK1 Signaling Pathway Rescues Red Blood Cell Production in <i>SF3B1</i>-Mutant Myelodysplastic Syndromes With Ringed Sideroblasts

    Article • April 2023, American Association for Cancer Research (AACR)

    FRANCESC SOLE

11. 
    Abstract 6168: Implementation and adoption of a web tool to support precision diagnostic and treatment decisions for patient with myelodysplastic syndromes

    Article • Cancer Research, April 2023, American Association for Cancer Research (AACR)

    FRANCESC SOLE

12. 
    Data from Targeting the EIF2AK1 Signaling Pathway Rescues Red Blood Cell Production in <i>SF3B1</i>-Mutant Myelodysplastic Syndromes With Ringed Sideroblasts

    Article • April 2023, American Association for Cancer Research (AACR)

    FRANCESC SOLE

13. 
    Supplementary Data from Targeting the EIF2AK1 Signaling Pathway Rescues Red Blood Cell Production in <i>SF3B1</i>-Mutant Myelodysplastic Syndromes With Ringed Sideroblasts

    Article • April 2023, American Association for Cancer Research (AACR)

    FRANCESC SOLE

14. 
    Supplementary Data from Targeting the EIF2AK1 Signaling Pathway Rescues Red Blood Cell Production in <i>SF3B1</i>-Mutant Myelodysplastic Syndromes With Ringed Sideroblasts

    Article • April 2023, American Association for Cancer Research (AACR)

    FRANCESC SOLE

15. 
    European standard clinical practice – Key issues for the medical care of individuals with familial leukemia

    Article • European Journal of Medical Genetics, April 2023, Elsevier

    FRANCESC SOLE

16. 
    The Secondary Myelodysplastic Neoplasms (MDS) Jigsaw

    Article • Cancers, February 2023, MDPI AG

    FRANCESC SOLE

17. 
    A sex-informed approach to improve the personalised decision making process in myelodysplastic syndromes: a multicentre, observational cohort study

    Article • The Lancet Haematology, February 2023, Elsevier

    FRANCESC SOLE

18. 
    Mutational Profile Enables the Identification of a High Risk Subgroup in Myelodysplastic Syndromes With Isolated Trisomy 8

    Article • February 2023, Research Square

    FRANCESC SOLE

19. 
    Are the current guidelines for identification of myelodysplastic syndrome with germline predisposition strong enough?

    Article • British Journal of Haematology, January 2023, Wiley

    FRANCESC SOLE

20. 
    MUTATIONAL PROFILE ENABLES THE IDENTIFICATION OF A HIGH RISK SUBGROUP IN MYELODYSPLASTIC SYNDROMES WITH ISOLATED TRISOMY 8

    Article • January 2023, Cold Spring Harbor Laboratory Press

    FRANCESC SOLE

21. 
    3032 – SIMULTANEOUS SINGLE-CELL DNA METHYLATION AND TRANSCRIPTOMIC ANALYSIS DISCLOSE CLONAL PHYLO-EPIGENETIC EVOLUTION IN MYELODYSPLASTIC SYNDROME

    Article • Experimental Hematology, January 2023, Elsevier

    FRANCESC SOLE

22. 
    Genomic profiling for clinical decision making in myeloid neoplasms and acute leukemia

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

23. 
    Bone Marrow WT1 mRNA Upregulation in Acute Myeloid Leukemia (AML) in Complete Molecular Remission (mCR): Understanding the Limitations and Advantages of WT1 As a Measurable Residual Disease (MRD) Target

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

24. 
    Characterization of Transcriptional Alterations Leading to Aberrant Myeloid Differentiation in Myelodysplastic Syndromes

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

25. 
    Clinical Implications of p53 Dysfunction in Patients with Myelodysplastic Syndromes

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

26. 
    ERCC6L2 in Early-Onset Adult Myelodysplastic Syndrome without Pre-Existing Disorder

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

27. 
    Incidence, Clinical Associations, and Co-Mutation Patterns of UBA1 Mutations in MDS

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

28. 
    Pilot Inter-Laboratory Comparison Study of Optical Genome Mapping Analysis for Cytogenomic Characterization of Hematological Malignancies: A Spanish Multicentric Study

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

29. 
    Real-World Validation of Molecular International Prognostic Scoring System (IPSS-M) for Myelodysplastic Syndromes

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

30. 
    Subclonal KIT D816V Mutations Are Prevalent in Chronic Myelomonocytic Leukemia and Correlate with Distinct Phenotypic Features

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

31. 
    TP53 Allelic State in Myelodysplastic Syndromes with 5q Deletion

    Article • Blood, November 2022, American Society of Hematology

    FRANCESC SOLE

32. 
    Myelodysplastic Syndromes with Isolated del(5q): Value of Molecular Alterations for Diagnostic and Prognostic Assessment

    Article • Cancers, November 2022, MDPI AG

    FRANCESC SOLE

33. 
    Targeting the EIF2AK1 Signaling Pathway Rescues Red Blood Cell Production in SF3B1-Mutant Myelodysplastic Syndromes With Ringed Sideroblasts

    Article • Blood Cancer Discovery, August 2022, American Association for Cancer Research (AACR)

    FRANCESC SOLE

34. 
    CD34+CD19−CD22+ B-cell progenitors may underlie phenotypic escape in patients treated with CD19-directed therapies

    Article • Blood, July 2022, American Society of Hematology

    FRANCESC SOLE

35. 
    Pathophysiologic and clinical implications of molecular profiles resultant from deletion 5q

    Article • EBioMedicine, June 2022, Elsevier

    FRANCESC SOLE

36. 
    Guiding the global evolution of cytogenetic testing for hematologic malignancies

    Article • Blood, April 2022, American Society of Hematology

    FRANCESC SOLE

37. 
    Clinical relevance of clonal hematopoiesis in persons aged ≥80 years

    Article • Blood, November 2021, American Society of Hematology

    FRANCESC SOLE

38. 
    Deficiency of RPS14 Beyond the Haploinsufficient Loss in Del(5q)

    Article • Blood, November 2021, American Society of Hematology

    FRANCESC SOLE

39. 
    Germline and Somatic Variants Co-Ocurrence Profile in Early Onset Adult Myelodysplastic Syndromes without a Preexisting Disorder

    Article • Blood, November 2021, American Society of Hematology

    FRANCESC SOLE

40. 
    Prevalence and characteristics of clonal hematopoiesis in heart failure

    Article • Revista Española de Cardiología (English Edition), November 2021, Elsevier

    FRANCESC SOLE

41. 
    Prevalencia y características de la hematopoyesis clonal en insuficiencia cardiaca

    Article • Revista Española de Cardiología, November 2021, Elsevier

    FRANCESC SOLE

42. 
    Divergent leukaemia subclones as cellular models for testing vulnerabilities associated with gains in chromosomes 7, 8 or 18

    Article • Scientific Reports, October 2021, Springer Science + Business Media

    FRANCESC SOLE

43. 
    Adverse prognostic impact of complex karyotype (≥3 cytogenetic alterations) in adult T-cell acute lymphoblastic leukemia (T-ALL)

    Article • Leukemia Research, October 2021, Elsevier

    FRANCESC SOLE

44. 
    Beyond morphology: to be or not to be an MDS

    Article • British Journal of Haematology, June 2021, Wiley

    FRANCESC SOLE

45. 
    Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

    Article • Nature Reports Stem Cells, May 2021, Springer Science + Business Media

    FRANCESC SOLE

46. 
    Genetic Aspects of Myelodysplastic/Myeloproliferative Neoplasms

    Article • Cancers, April 2021, MDPI AG

    FRANCESC SOLE

47. 
    A Single-Run Next-Generation Sequencing (NGS) Assay for the Simultaneous Detection of Both Gene Mutations and Large Chromosomal Abnormalities in Patients with Myelodysplastic Syndromes (MDS) and Related Myeloid Neoplasms

    Article • Cancers, April 2021, MDPI AG

    FRANCESC SOLE

48. 
    Classification and Personalized Prognostic Assessment on the Basis of Clinical and Genomic Features in Myelodysplastic Syndromes

    Article • Journal of Clinical Oncology, April 2021, American Society of Clinical Oncology (ASCO)

    FRANCESC SOLE

49. 
    Analysis of Intratumoral Heterogeneity in Myelodysplastic Syndromes with Isolated del(5q) Using a Single Cell Approach

    Article • Cancers, February 2021, MDPI AG

    FRANCESC SOLE

50. 
    Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

    Article • Nature Reports Stem Cells, February 2021, Springer Science + Business Media

    FRANCESC SOLE

51. 
    Genetic characterization of acute myeloid leukemia patients with mutations in IDH1/2 genes

    Article • Leukemia Research, February 2021, Elsevier

    FRANCESC SOLE

52. 
    Aneuploidy in Cancer: Lessons from Acute Lymphoblastic Leukemia

    Article • Trends in Cancer, January 2021, Elsevier

    FRANCESC SOLE

53. 
    Acute Myeloid Leukemia with Isocitrate Dehydrogenases (IDH) 1 and 2 Mutations. a Real-World Study from the European IDH Research Group

    Article • Blood, November 2020, American Society of Hematology

    FRANCESC SOLE

54. 
    Analysis of distinct SF3B1 hotspot mutations in relation to clinical phenotypes and response to therapy in myeloid neoplasia

    Article • Leukemia & Lymphoma, November 2020, Taylor & Francis

    FRANCESC SOLE

55. 
    Molecular landscape and clonal architecture of adult myelodysplastic/myeloproliferative neoplasms

    Article • Blood, October 2020, American Society of Hematology

    FRANCESC SOLE

56. 
    Cytogenetics in the genomic era

    Article • Best Practice & Research Clinical Haematology, September 2020, Elsevier

    FRANCESC SOLE

57. 
    ALL-257: Unraveling IKZF1 Deletion Therapeutic Vulnerabilities in Adult B-Cell Precursor Acute Lymphoblastic Leukemia

    Article • Clinical Lymphoma Myeloma & Leukemia, September 2020, Elsevier

    FRANCESC SOLE

58. 
    Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

    Article • Nature Reports Stem Cells, August 2020, Springer Science + Business Media

    FRANCESC SOLE

59. 
    SF3B1: the lord of the rings in MDS

    Article • Blood, July 2020, American Society of Hematology

    FRANCESC SOLE

60. 
    Therapy-related myelodysplastic syndromes deserve specific diagnostic sub-classification and risk-stratification—an approach to classification of patients with t-MDS

    Article • Leukemia, June 2020, Springer Science + Business Media

    FRANCESC SOLE

61. 
    Distinct mutational pattern of myelodysplastic syndromes with and without 5q– treated with lenalidomide

    Article • British Journal of Haematology, March 2020, Wiley

    FRANCESC SOLE

62. 
    Impact of somatic mutations in myelodysplastic patients with isolated partial or total loss of chromosome 7

    Article • Leukemia, February 2020, Springer Science + Business Media

    FRANCESC SOLE

63. 
    Rare germline variant contributions to myeloid malignancy susceptibility

    Article • Leukemia, January 2020, Springer Science + Business Media

    FRANCESC SOLE

64. 
    Non-del(5q) myelodysplastic syndromes–associated loci detected by SNP-array genome-wide association meta-analysis

    Article • Blood Advances, November 2019, American Society of Hematology

    FRANCESC SOLE

65. 
    Can Monosomy 7 be Targeted By Next Generation Cereblon-Modulating Agents?

    Article • Blood, November 2019, American Society of Hematology

    FRANCESC SOLE

66. 
    Germinal Predisposition in Myelodysplastic Syndromes in Young Adults without a Preexisting Disorder or Organ Dysfunction: Identification of Deleterious Variants in Microsatellite Instability Genes

    Article • Blood, November 2019, American Society of Hematology

    FRANCESC SOLE

67. 
    Hotspot U2AF1 Mutations Determine Missplicing Selectivity: Novel Mechanisms Altering Splicing Factors

    Article • Blood, November 2019, American Society of Hematology

    FRANCESC SOLE

68. 
    Integrated Transcriptomic and Proteomic Analyses of Inflammasome in Myelodysplastic Syndromes and Chronic Myelomonocytic Leukemia

    Article • Blood, November 2019, American Society of Hematology

    FRANCESC SOLE

69. 
    MPO as a Novel Susceptibility Gene in Myeloid Malignancies

    Article • Blood, November 2019, American Society of Hematology

    FRANCESC SOLE

70. 
    Molecular Dissection of Del(5q): Distinction between Primary and Secondary Del(5q) and Pathogenetic Implications

    Article • Blood, November 2019, American Society of Hematology

    FRANCESC SOLE

71. 
    TP53 State Dictates Genome Stability, Clinical Presentation and Outcomes in Myelodysplastic Syndromes

    Article • Blood, November 2019, American Society of Hematology

    FRANCESC SOLE

72. 
    TP53 Status As Well As Cytogenetic Complexity Significantly Impact on Prognosis in Myelodysplastic Syndromes with Complex (≥3 anomalies) Aberrant Karyotypes

    Article • Blood, November 2019, American Society of Hematology

    FRANCESC SOLE

73. 
    Spanish Guidelines for the use of targeted deep sequencing in myelodysplastic syndromes and chronic myelomonocytic leukaemia

    Article • British Journal of Haematology, October 2019, Wiley

    FRANCESC SOLE, Dr Marta Fernandez-Mercado

74. 
    Report of the SMZL meeting in Badalona, Barcelona, Spain

    Article • Leukemia & Lymphoma, October 2019, Taylor & Francis

    Dr Estella Matutes, FRANCESC SOLE

75. 
    Molecular profiling refines minimal residual disease‐based prognostic assessment in adults with Philadelphia chromosome‐negative B‐cell precursor acute lymphoblastic leukemia

    Article • Genes Chromosomes and Cancer, August 2019, Wiley

    FRANCESC SOLE

76. 
    Diagnostic and prognostic contribution of targeted NGS in patients with triple‐negative myeloproliferative neoplasms

    Article • American Journal of Hematology, August 2019, Wiley

    FRANCESC SOLE

77. 
    Comprehensive analysis of isolated der(1;7)(q10;p10) in a large international homogenous cohort of patients with myelodysplastic syndromes

    Article • Genes Chromosomes and Cancer, April 2019, Wiley

    FRANCESC SOLE

78. 
    The poor prognosis of low hypodiploidy in adults with B‐cell precursor acute lymphoblastic leukaemia is restricted to older adults and elderly patients

    Article • British Journal of Haematology, March 2019, Wiley

    FRANCESC SOLE

79. 
    Opposing Pathogenesis of Germline SAMD9/SAMD9L Variants in Adult Myelodysplastic Syndrome (MDS)

    Article • Blood, November 2018, American Society of Hematology

    FRANCESC SOLE

80. 
    Germline and Acquired Genetic Variants in Myelodysplastic Syndromes in Young Adults without a Preexisting Disorder or Organ Dysfunction

    Article • Blood, November 2018, American Society of Hematology

    FRANCESC SOLE

81. 
    Molecular Spectrum of CSF3R variants Correlate with Specific Myeloid Malignancies and Secondary Mutations

    Article • Blood, November 2018, American Society of Hematology

    FRANCESC SOLE

82. 
    SNP-Array Genome Wide Association Study Meta-Analysis Identifies Innate Immune Susceptibility Loci Associated with Non-Del(5q) Myelodysplastic Syndromes Predisposition

    Article • Blood, November 2018, American Society of Hematology

    FRANCESC SOLE

83. 
    Therapy-Related MDS Can be Separated into Different Risk-Groups According to Tools for Classification and Prognostication of Primary MDS

    Article • Blood, November 2018, American Society of Hematology

    FRANCESC SOLE

84. 
    Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes

    Article • Blood, November 2018, American Society of Hematology

    FRANCESC SOLE

85. 
    Translational Research Opportunities Regarding Homologous Recombination in Ovarian Cancer

    Article • International Journal of Molecular Sciences, October 2018, MDPI AG

    FRANCESC SOLE

86. 
    Differing clinical features between Japanese and Caucasian patients with myelodysplastic syndromes: Analysis from the International Working Group for Prognosis of MDS

    Article • Leukemia Research, October 2018, Elsevier

    FRANCESC SOLE

87. 
    Clonal architecture in patients with myelodysplastic syndromes and double or minor complex abnormalities: Detailed analysis of clonal composition, involved abnormalities, and prognostic significance

    Article • Genes Chromosomes and Cancer, September 2018, Wiley

    MD PhD ELISA E LUÑO , FRANCESC SOLE

88. 
    Serotonin receptor type 1B constitutes a therapeutic target for MDS and CMML

    Article • Scientific Reports, September 2018, Springer Science + Business Media

    FRANCESC SOLE

89. 
    Frequency and clinical impact of CDKN2A/ARF/CDKN2B gene deletions as assessed by in-depth genetic analyses in adult T cell acute lymphoblastic leukemia

    Article • Journal of Hematology & Oncology, July 2018, Springer Science + Business Media

    FRANCESC SOLE

90. 
    Transcriptomic rationale for synthetic lethality-targeting ERCC1 and CDKN1A in chronic myelomonocytic leukaemia

    Article • British Journal of Haematology, May 2018, Wiley

    FRANCESC SOLE

91. 
    Targeted deep sequencing of CD34+ cells from peripheral blood can reproduce bone marrow molecular profile in myelodysplastic syndromes

    Article • American Journal of Hematology, April 2018, Wiley

    FRANCESC SOLE

92. 
    Clinical and biological significance of isolated Y chromosome loss in myelodysplastic syndromes and chronic myelomonocytic leukemia. A report from the Spanish MDS Group

    Article • Leukemia Research, December 2017, Elsevier

    MD PhD ELISA E LUÑO , FRANCESC SOLE

93. 
    DNA methylation profile in chronic myelomonocytic leukemia associates with distinct clinical, biological and genetic features

    Article • Epigenetics, November 2017, Taylor & Francis

    FRANCESC SOLE

94. 
    Copy number profiling of adult relapsed B-cell precursor acute lymphoblastic leukemia reveals potential leukemia progression mechanisms

    Article • Genes Chromosomes and Cancer, August 2017, Wiley

    Professor Josep-Maria Ribera, FRANCESC SOLE

95. 
    Inspecting Targeted Deep Sequencing of Whole Genome Amplified DNA Versus Fresh DNA for Somatic Mutation Detection: A Genetic Study in Myelodysplastic Syndrome Patients

    Article • Biopreservation and Biobanking, August 2017, Mary Ann Liebert Inc

    FRANCESC SOLE

96. 
    Monosomal karyotype in chronic lymphocytic leukemia: Association with clinical and biological features and potential prognostic significance

    Article • American Journal of Hematology, June 2017, Wiley

    MD PhD ELISA E LUÑO , FRANCESC SOLE

97. 
    A Single Next-Generation Sequencing (NGS) Assay for the Detection of Point Mutations and Large Chromosomal Abnormalities in MDS Patients

    Article • Leukemia Research, April 2017, Elsevier

    FRANCESC SOLE

98. 
    Ancestral Events Including Germline and Somatic Mutations Determine Subclonal Events and Affect Phenotype of Progression in MDS

    Article • Leukemia Research, April 2017, Elsevier

    FRANCESC SOLE

99. 
    Chromosomal Aberrations in Therapy-Related Myelodysplastic Syndromes – Relations to Primary Disease, Therapy and Prognostic Significance

    Article • Leukemia Research, April 2017, Elsevier

    FRANCESC SOLE

100. 
     DNA Methylation Profiling in Patients with CMML Differs Between Normal and Altered Karyotype

     Article • Leukemia Research, April 2017, Elsevier

     FRANCESC SOLE

101. 
     DNA Repair Genes Transcriptome in Chronic Myelomonocytic Leukemia

     Article • Leukemia Research, April 2017, Elsevier

     FRANCESC SOLE

102. 
     Mutational Signature and Clonal Architecture of Low Risk Myelodysplastic Syndromes with Del(5Q)

     Article • Leukemia Research, April 2017, Elsevier

     FRANCESC SOLE

103. 
     Spanish Guidelines for the use of Targeted Deep Sequencing in MDS and CMML

     Article • Leukemia Research, April 2017, Elsevier

     FRANCESC SOLE

104. 
     Targeted Deep Sequencing of Peripheral CD34+ Cells can Reproduce Bone Marrow Molecular Profile in MDS Patients

     Article • Leukemia Research, April 2017, Elsevier

     FRANCESC SOLE

105. 
     Computational drug treatment simulations on projections of dysregulated protein networks derived from the myelodysplastic mutanome match clinical response in patients

     Article • Leukemia Research, January 2017, Elsevier

     FRANCESC SOLE

106. 
     In MDS Targeted Deep Sequencing of CD34+ Blood Cells but Not Peripheral Blood Mononuclear Cells Give Results Which Are Representative for Bone Marrow

     Article • Blood, December 2016, American Society of Hematology

     FRANCESC SOLE

107. 
     Application of Trusight Myeloid Panel on Whole Genome Amplified DNA in Myelodysplastic Syndrome Patients

     Article • Blood, December 2016, American Society of Hematology

     FRANCESC SOLE

108. 
     Comparison of the Molecular Spectrum of Lenalidomide-Treated Myelodysplastic Syndrome with and without Del(5q)

     Article • Blood, December 2016, American Society of Hematology

     FRANCESC SOLE

109. 
     Frequency and Prognostic Significance of Cytogenetic Abnormalities in 1269 Patients with Therapy-Related Myelodysplastic Syndrome - a Study of the International Working Group (IWG-PM) for Myelodysplastic Syndromes (MDS)

     Article • Blood, December 2016, American Society of Hematology

     FRANCESC SOLE

110. 
     Genomic Characterization of Paired Diagnosis and Relapse Samples from Adult Patients with B-Cell Precursor Acute Lymphoblastic Leukemia

     Article • Blood, December 2016, American Society of Hematology

     FRANCESC SOLE

111. 
     Landscape of Subclonal Mutations in Myelodysplastic Syndromes (MDS) Allows for a Novel Hierarchy of Clonal Advantage By Combining Germline and Somatic Mutations

     Article • Blood, December 2016, American Society of Hematology

     FRANCESC SOLE

112. 
     Molecular and Clinical Characterization of Patients with Myeloid Neoplasms Carrying the 12p Deletion

     Article • Blood, December 2016, American Society of Hematology

     FRANCESC SOLE

113. 
     Immunophenotypic, cytogenetic, and mutational characterization of cell lines derived from myelodysplastic syndrome patients after progression to acute myeloid leukemia

     Article • Genes Chromosomes and Cancer, November 2016, Wiley

     FRANCESC SOLE

114. 
     Cytopenia levels for aiding establishment of the diagnosis of myelodysplastic syndromes

     Article • Blood, October 2016, American Society of Hematology

     FRANCESC SOLE

115. 
     Molecular predictors of response in patients with myeloid neoplasms treated with lenalidomide

     Article • Leukemia, August 2016, Springer Science + Business Media

     FRANCESC SOLE

116. 
     Time-dependent changes in mortality and transformation risk in MDS

     Article • Blood, August 2016, American Society of Hematology

     FRANCESC SOLE

117. 
     Targeted deep sequencing improves outcome stratification in chronic myelomonocytic leukemia with low risk cytogenetic features

     Article • Oncotarget, July 2016, Impact Journals, LLC

     FRANCESC SOLE

118. 
     Abstract 2570: Identification of genetic polymorphisms associated with myelodysplastic syndromes by genome-wide association study

     Article • Cancer Research, July 2016, American Association for Cancer Research (AACR)

     FRANCESC SOLE

119. 
     Feasibility of the AML profiler (Skyline™ Array) for patient risk stratification in a multicentre trial: a preliminary comparison with the conventional approach

     Article • Hematological Oncology, May 2016, Wiley

     Josep Nomdedeu, FRANCESC SOLE

120. 
     Prognostic impact of chromosomal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemia patients. A study by the spanish group of myelodysplastic syndromes

     Article • Genes Chromosomes and Cancer, December 2015, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

121. 
     Impact of SNP array karyotyping on the diagnosis and the outcome of chronic myelomonocytic leukemia with low risk cytogenetic features or no metaphases

     Article • American Journal of Hematology, December 2015, Wiley

     FRANCESC SOLE

122. 
     Molecular Genetic Profiling in Chronic Myelomonocytic Leukemia with Low Risk Cytogenetic Features

     Article • Blood, December 2015, American Society of Hematology

     FRANCESC SOLE

123. 
     Downregulation of BAP1 in Chronic Myelomonocytic Leukemia: Correlated with a Post-Translational Reduction of BRCA1 Levels and Independent of Promoter Methylation

     Article • Blood, December 2015, American Society of Hematology

     FRANCESC SOLE

124. 
     Predicting MDS Response to Drug Therapies Based on a New Method of Interpreting the MDS Mutanome

     Article • Blood, December 2015, American Society of Hematology

     FRANCESC SOLE

125. 
     Prognostic Impact of Rare Single Abnormalities in Myelodysplastic Syndromes

     Article • Blood, December 2015, American Society of Hematology

     FRANCESC SOLE

126. 
     Refining the Breakpoints of Three New Translocations Identified in Myelodysplastic Syndromes

     Article • Acta Haematologica, October 2015, Karger Publishers

     FRANCESC SOLE

127. 
     TP53 and MDM2 single nucleotide polymorphisms influence survival in non-del(5q) myelodysplastic syndromes

     Article • Oncotarget, September 2015, Impact Journals, LLC

     FRANCESC SOLE

128. 
     Frequency of del(12p) is commonly underestimated in myelodysplastic syndromes: Results from a German diagnostic study in comparison with an international control group

     Article • Genes Chromosomes and Cancer, September 2015, Wiley

     FRANCESC SOLE

129. 
     TP53 and MDM2 single nucleotide polymorphisms influence survival in myelodysplastic syndromes

     Article • Clinical Lymphoma Myeloma & Leukemia, September 2015, Elsevier

     FRANCESC SOLE

130. 
     Prognostic significance of copy number alterations in adolescent and adult patients with precursor B acute lymphoblastic leukemia enrolled in PETHEMA protocols

     Article • Cancer, July 2015, Wiley

     Professor Josep-Maria Ribera, Josep Nomdedeu, FRANCESC SOLE

131. 
     Trisomy 8, a Cytogenetic Abnormality in Myelodysplastic Syndromes, Is Constitutional or Not?

     Article • PLOS One, June 2015, PLOS

     MD PhD ELISA E LUÑO , FRANCESC SOLE

132. 
     Copy Number Alterations in patients with mature B (Burkitt-type) acute lymphoblastic leukaemia treated with specific immunochemotherapy

     Article • Clinical Lymphoma Myeloma & Leukemia, June 2015, Elsevier

     FRANCESC SOLE

133. 
     Fluorescencein situhybridization ofTP53for the detection of chromosome 17 abnormalities in myelodysplastic syndromes

     Article • Leukemia & Lymphoma, May 2015, Taylor & Francis

     MD PhD ELISA E LUÑO , FRANCESC SOLE

134. 
     The relationship of TP53 R72P polymorphism to disease outcome and TP53 mutation in myelodysplastic syndromes

     Article • Blood Cancer Journal, March 2015, Springer Science + Business Media

     FRANCESC SOLE

135. 
     Validation of WHO classification-based Prognostic Scoring System (WPSS) for myelodysplastic syndromes and comparison with the revised International Prognostic Scoring System (IPSS-R). A study of the International Working Group for Prognosis in Myelodys...

     Article • Leukemia, February 2015, Springer Science + Business Media

     FRANCESC SOLE

136. 
     Correlation of myelodysplastic syndromes with i(17)(q10) andTP53andSETBP1mutations

     Article • British Journal of Haematology, February 2015, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

137. 
     Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2): Clinical and biological features and comparison with other acute myeloid leukemias with cytogenetic aberrations involving long arm of chromosome 3

     Article • Hematology, February 2015, Taylor & Francis

     MD PhD ELISA E LUÑO , FRANCESC SOLE

138. 
     20th International Chromosome Conference (ICCXX)

     Article • Chromosome Research, January 2015, Springer Science + Business Media

     Professor Karol Marhold, FRANCESC SOLE

139. 
     Genomic Microarray Alterations Add Prognostic Power to the IPSS-R in MDS with Normal Karyotype

     Article • Blood, December 2014, American Society of Hematology

     FRANCESC SOLE

140. 
     Whole-Exome Sequencing in Myelodysplastic Syndromes with 5q Deletion

     Article • Blood, December 2014, American Society of Hematology

     FRANCESC SOLE

141. 
     Genetic Markers Add Significant Prognostic Information to Age and WBC Count in High-Risk, Ph-Negative, B-Precursor Adult Acute Lymphoblastic Leukemia (ALL): Study of 96 Patients Treated According to Risk-Adapted Protocols from the Pethema Group

     Article • Blood, December 2014, American Society of Hematology

     FRANCESC SOLE

142. 
     Utility of SNP Arrays in Chronic Myelomonocytic Leukemia with Low Risk Cytogenetic Features or No Metaphases

     Article • Blood, December 2014, American Society of Hematology

     FRANCESC SOLE

143. 
     Validation of cytogenetic risk groups according to International Prognostic Scoring Systems by peripheral blood CD34+FISH: results from a German diagnostic study in comparison with an international control group

     Article • Haematologica, October 2014, Ferrata Storti Foundation (Haematologica)

     FRANCESC SOLE

144. 
     Combined analysis of copy number alterations by single-nucleotide polymorphism array and MYC status in non-metastatic breast cancer patients: comparison according to the circulating tumor cell status

     Article • Tumor Biology, October 2014, Springer Science + Business Media

     FRANCESC SOLE

145. 
     Role of Casein Kinase 1A1 in the Biology and Targeted Therapy of del(5q) MDS

     Article • Cancer Cell, October 2014, Elsevier

     FRANCESC SOLE

146. 
     TERT gene amplification is associated with poor outcome in acral lentiginous melanoma

     Article • Journal of the American Academy of Dermatology, October 2014, Elsevier

     FRANCESC SOLE

147. 
     Paraffin Treasures: Do They Last Forever?

     Article • Biopreservation and Biobanking, August 2014, Mary Ann Liebert Inc

     FRANCESC SOLE

148. 
     EMT and EGFR in CTCs cytokeratin negative non-metastatic breast cancer

     Article • Oncotarget, July 2014, Impact Journals, LLC

     FRANCESC SOLE

149. 
     Guidance for laboratories performing molecular pathology for cancer patients

     Article • Journal of Clinical Pathology, July 2014, BMJ

     FRANCESC SOLE

150. 
     Fluorescencein situhybridization analysis does not increase detection rate for trisomy 8 in chronic myelomonocytic leukemia

     Article • Leukemia & Lymphoma, June 2014, Taylor & Francis

     FRANCESC SOLE

151. 
     Translocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin

     Article • Cancer Genetics, June 2014, Elsevier

     FRANCESC SOLE

152. 
     Errors in the interpretation of copy number variations due to the use of public databases as a reference

     Article • Cancer Genetics, April 2014, Elsevier

     FRANCESC SOLE

153. 
     Intervention to improve social and family support for caregivers of dependent patients: ICIAS study protocol

     Article • BMC Family Practice, March 2014, Springer Science + Business Media

     FRANCESC SOLE

154. 
     TERT and AURKA Gene Copy Number Gains Enhance the Detection of Acral Lentiginous Melanomas by Fluorescence in Situ Hybridization

     Article • Journal of Molecular Diagnostics, March 2014, Elsevier

     Susana Puig, FRANCESC SOLE

155. 
     Distinction between Asymptomatic Monoclonal B-cell Lymphocytosis with Cyclin D1 Overexpression and Mantle Cell Lymphoma: From Molecular Profiling to Flow Cytometry

     Article • Clinical Cancer Research, December 2013, American Association for Cancer Research (AACR)

     MD PhD ELISA E LUÑO , FRANCESC SOLE

156. 
     Whole-exome sequencing in splenic marginal zone lymphoma reveals mutations in genes involved in marginal zone differentiation

     Article • Leukemia, December 2013, Springer Science + Business Media

     Dr Francesco Bertoni, FRANCESC SOLE

157. 
     Analysis Of Transfusion Dependence Development and Disease Evolution In Patients With MDS and Del(5q) and Without Transfusion Needs At Diagnosis

     Article • Blood, November 2013, American Society of Hematology

     FRANCESC SOLE

158. 
     Prognostic Significance Of Copy Number Alterations In B-Lineage Adult Acute Lymphoblastic Leukemia Patients Enrolled In Risk-Adapted Protocols From The Pethema Group

     Article • Blood, November 2013, American Society of Hematology

     FRANCESC SOLE

159. 
     Time Changes In Predictive Power Of MDS Prognostic Scores – Effects On Revised Scores Such As The IPSS-R, Impact Of Age

     Article • Blood, November 2013, American Society of Hematology

     FRANCESC SOLE

160. 
     Whole-Exome Sequencing In Myelodysplastic Syndromes With 5q- and Normal Karyotype

     Article • Blood, November 2013, American Society of Hematology

     FRANCESC SOLE

161. 
     Single nucleotide polymorphism array karyotyping: A diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing

     Article • Genes Chromosomes and Cancer, October 2013, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

162. 
     The pursuit of knowledge transfer activities: An efficiency analysis of Spanish universities

     Article • Journal of Business Research, October 2013, Elsevier

     Dr Jasmina Berbegal-Mirabent, FRANCESC SOLE

163. 
     5q− syndrome and multiple myeloma diagnosed simultaneously and successful treated with lenalidomide

     Article • Leukemia Research, October 2013, Elsevier

     FRANCESC SOLE

164. 
     Acquisition of cytogenetic abnormalities in patients with IPSS defined lower‐risk myelodysplastic syndrome is associated with poor prognosis and transformation to acute myelogenous leukemia

     Article • American Journal of Hematology, July 2013, Wiley

     FRANCESC SOLE

165. 
     Biallelic losses of 13q do not confer a poorer outcome in chronic lymphocytic leukaemia: analysis of 627 patients with isolated 13q deletion

     Article • British Journal of Haematology, July 2013, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

166. 
     Roles‐purpose‐and‐culture misalignments: a setback to bottom‐up SME clusters

     Article • Journal of Knowledge Management, July 2013, Emerald

     FRANCESC SOLE

167. 
     CD133 expression in circulating tumor cells from breast cancer patients: Potential role in resistance to chemotherapy

     Article • International Journal of Cancer, July 2013, Wiley

     FRANCESC SOLE

168. 
     Characterization and prognostic implication of 17 chromosome abnormalities in myelodysplastic syndrome

     Article • Leukemia Research, July 2013, Elsevier

     MD PhD ELISA E LUÑO , FRANCESC SOLE

169. 
     Corrigendum to “Incidence and survival of chronic myelomonocytic leukemia in Girona (Spain): A population-based study, 1993–2007” [Leukemia Res. 36 (2012) 1262–1266]

     Article • Leukemia Research, July 2013, Elsevier

     FRANCESC SOLE

170. 
     Remisión espontánea de una aplasia de médula ósea asociada a una trisomía del cromosoma 8, con posterior evolución a leucemia monoblástica aguda y reaparición de la alteración clonal

     Article • Medicina Clínica, July 2013, Elsevier

     FRANCESC SOLE

171. 
     Monosomal karyotype in MDS: explaining the poor prognosis?

     Article • Leukemia, June 2013, Nature

     MD PhD ELISA E LUÑO , FRANCESC SOLE

172. 
     Reciprocal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemias: Review of 5,654 patients with an evaluable karyotype

     Article • Genes Chromosomes and Cancer, May 2013, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

173. 
     P-068 Trisomy 8 in de novo MDS, constitutional or not constitutional?

     Article • Leukemia Research, May 2013, Elsevier

     MD PhD ELISA E LUÑO , FRANCESC SOLE

174. 
     P-069 Contribution of SNP-arrays and mutational studies to diagnosis and prognosis of CMML with low-risk cytogenetic features or no metaphases

     Article • Leukemia Research, May 2013, Elsevier

     FRANCESC SOLE

175. 
     P-017 Genetic alterations of the epigenetic pathways on MDS patients with a 5q deletion drive specific methylation signatures

     Article • Leukemia Research, May 2013, Elsevier

     FRANCESC SOLE

176. 
     P-113 Revised International Prognostic Scoring System (IPSS-R) for primary treated myelodysplastic syndromes (MDS) patients: A report from the IWG-PM

     Article • Leukemia Research, May 2013, Elsevier

     FRANCESC SOLE

177. 
     Response to lenalidomide in myelodysplastic syndromes with del(5q): influence of cytogenetics and mutations

     Article • British Journal of Haematology, April 2013, Wiley

     FRANCESC SOLE

178. 
     Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: Does −7/7q− detection by FISH have prognostic value?

     Article • Leukemia Research, April 2013, Elsevier

     MD PhD ELISA E LUÑO , FRANCESC SOLE

179. 
     Complex, Not Monosomal, Karyotype Is the Cytogenetic Marker of Poorest Prognosis in Patients With Primary Myelodysplastic Syndrome

     Article • Journal of Clinical Oncology, March 2013, American Society of Clinical Oncology (ASCO)

     MD PhD ELISA E LUÑO , FRANCESC SOLE

180. 
     Identification of Temporal and Region-Specific Myocardial Gene Expression Patterns in Response to Infarction in Swine

     Article • PLOS One, January 2013, PLOS

     FRANCESC SOLE

181. 
     Study of Regulatory T-Cells in Patients with Gastric Malt Lymphoma: Influence on Treatment Response and Outcome

     Article • PLOS One, December 2012, PLOS

     FRANCESC SOLE

182. 
     Association of MDM2 Gene Polymorphisms SNP285 and 309 with Myelodysplastic Syndromes (MDS) Susceptibility and Outcome.

     Article • Blood, November 2012, American Society of Hematology

     FRANCESC SOLE

183. 
     Age, Performance Status and Plasma Interleukin-10 Levels At Diagnosis: A Triad for Improving Survival Prediction of Patients with Myelodysplastic Syndromes Already Stratified by IPSS-R. Spanish MDS Group (GESMD)

     Article • Blood, November 2012, American Society of Hematology

     FRANCESC SOLE

184. 
     Feasibility of the AMLprofiler™ (Skyline array) in Patient Risk-Stratification in a Multicenter Trial. Comparison with the Standard Approach

     Article • Blood, November 2012, American Society of Hematology

     FRANCESC SOLE

185. 
     Mutational Status of Splenic Marginal Zone Lymphoma Revealed by Whole Exome Sequencing.

     Article • Blood, November 2012, American Society of Hematology

     FRANCESC SOLE

186. 
     Genomic arrays in chronic lymphocytic leukemia routine clinical practice: are we ready to substitute conventional cytogenetics and fluorescencein situhybridization techniques?

     Article • Leukemia & Lymphoma, October 2012, Taylor & Francis

     FRANCESC SOLE

187. 
     C0149 Long-term treatment of venous thromboembolism, with moderate-intensity vitamin-k antagonists (VKA) (INR range between 1.8 - 2.5), improve patient comfort and decreases treatment costs, without increasing adverse effects: A matched paired study

     Article • Thrombosis Research, October 2012, Elsevier

     FRANCESC SOLE

188. 
     Incidence and survival of chronic myelomonocytic leukemia in Girona (Spain): A population-based study, 1993–2007

     Article • Leukemia Research, October 2012, Elsevier

     FRANCESC SOLE

189. 
     Revised International Prognostic Scoring System for Myelodysplastic Syndromes

     Article • Blood, September 2012, American Society of Hematology

     FRANCESC SOLE

190. 
     Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes

     Article • British Journal of Haematology, September 2012, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

191. 
     Applying a systems thinking framework to assess knowledge assets dynamics for business performance improvement

     Article • Expert Systems with Applications, July 2012, Elsevier

     Dr Daniela Carlucci, FRANCESC SOLE

192. 
     Will a peripheral blood (PB) sample yield the same diagnostic and prognostic cytogenetic data as the concomitant bone marrow (BM) in myelodysplasia?

     Article • Leukemia Research, July 2012, Elsevier

     FRANCESC SOLE

193. 
     Biomarkers characterization of circulating tumour cells in breast cancer patients

     Article • May 2012, Springer Science + Business Media

     FRANCESC SOLE

194. 
     Are ER+PR+ and ER+PR− breast tumors genetically different? A CGH array study

     Article • Cancer Genetics, April 2012, Elsevier

     FRANCESC SOLE

195. 
     New Comprehensive Cytogenetic Scoring System for Primary Myelodysplastic Syndromes (MDS) and Oligoblastic Acute Myeloid Leukemia After MDS Derived From an International Database Merge

     Article • Journal of Clinical Oncology, March 2012, American Society of Clinical Oncology (ASCO)

     MD PhD ELISA E LUÑO , FRANCESC SOLE

196. 
     Update on developments in the diagnosis and prognostic evaluation of patients with myelodysplastic syndromes (MDS): Consensus statements and report from an expert workshop

     Article • Leukemia Research, March 2012, Elsevier

     FRANCESC SOLE

197. 
     ALK status in a primary lung tumour and metachronous metastases

     Article • Histopathology, January 2012, Wiley

     FRANCESC SOLE

198. 
     Molecular Biology of Myelodysplastic Syndromes

     Article • January 2012, Springer Science + Business Media

     FRANCESC SOLE

199. 
     Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?

     Article • Blood Cells Molecules and Diseases, December 2011, Elsevier

     FRANCESC SOLE

200. 
     Prognostic Impact of Monosomal Karyotype in Patients with Myelodysplastic Syndrome and Abnormal Karyotype. A Report From the Spanish Group of MDS (GESMD)

     Article • Blood, November 2011, American Society of Hematology

     FRANCESC SOLE

201. 
     Circulating cancer cells in division in an early breast cancer patient

     Article • Annals of Oncology, September 2011, Elsevier

     FRANCESC SOLE

202. 
     Deletion of TET2 gene in an acute myeloid leukemia case with a t(4;15)(q24;q26) characterized by glass needle based chromosome microdissection and oligonucleotide array

     Article • Leukemia Research, September 2011, Elsevier

     FRANCESC SOLE

203. 
     Increased MLL gene rearrangements in amniocytes from fetuses of mothers who smoke

     Article • Leukemia Research, August 2011, Elsevier

     FRANCESC SOLE

204. 
     Absence of TCR loci chromosomal translocations in cutaneous T-cell lymphomas

     Article • Cancer Genetics, July 2011, Elsevier

     FRANCESC SOLE

205. 
     De la citogenética convencional al análisis por micromatrices. Cincuenta años del cromosoma Filadelfia

     Article • Medicina Clínica, July 2011, Elsevier

     FRANCESC SOLE

206. 
     Better prognosis for patients with del(7q) than for patients with monosomy 7 in myelodysplastic syndrome

     Article • Cancer, June 2011, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

207. 
     A multicolor fluorescence in situ hybridization assay: A monitoring tool in the surveillance of patients with a history of non-muscle-invasive urothelial cell carcinoma

     Article • Cancer Cytopathology, June 2011, Wiley

     FRANCESC SOLE

208. 
     Clinical impact of the clone size in MDS cases with monosomy 7 or 7q deletion, trisomy 8, 20q deletion and loss of Y chromosome

     Article • Leukemia Research, June 2011, Elsevier

     MD PhD ELISA E LUÑO , FRANCESC SOLE

209. 
     Linfocitosis B policlonal persistente: estudio de 35 casos

     Article • Medicina Clínica, May 2011, Elsevier

     FRANCESC SOLE

210. 
     Molecular diagnosis of dermatofibrosarcoma protuberans: A comparison between reverse transcriptase-polymerase chain reaction and fluorescence in situ hybridization methodologies

     Article • Genes Chromosomes and Cancer, April 2011, Wiley

     FRANCESC SOLE

211. 
     Absence of mutations of the histone methyltransferase gene EZH2 in splenic b-cell marginal zone lymphoma

     Article • Leukemia Research, March 2011, Elsevier

     FRANCESC SOLE

212. 
     Cryptic IGH/BCL2 rearrangements with variant FISH patterns in follicular lymphoma

     Article • Leukemia Research, February 2011, Elsevier

     FRANCESC SOLE

213. 
     Identification of t(17;22)(q22;q13) (COL1A1/PDGFB) in dermatofibrosarcoma protuberans by fluorescence in situ hybridization in paraffin-embedded tissue microarrays

     Article • Human Pathology, February 2011, Elsevier

     FRANCESC SOLE

214. 
     Which services support research activities at universities?

     Article • Service Industries Journal, January 2011, Taylor & Francis

     Dr Jasmina Berbegal-Mirabent, FRANCESC SOLE

215. 
     Increased ALK Gene Copy Number and Amplification are Frequent in Non-small Cell Lung Cancer

     Article • Journal of Thoracic Oncology, January 2011, Elsevier

     FRANCESC SOLE

216. 
     Primary Cutaneous CD30+ Anaplastic Large-Cell Lymphomas Show a Heterogeneous Genomic Profile: An Oligonucleotide ArrayCGH Approach

     Article • Journal of Investigative Dermatology, January 2011, Elsevier

     FRANCESC SOLE

217. 
     Cytogenetic risk stratification in chronic myelomonocytic leukemia

     Article • Haematologica, November 2010, Ferrata Storti Foundation (Haematologica)

     MD PhD ELISA E LUÑO , FRANCESC SOLE

218. 
     Prognostic Impact of Monosomy 7 as a Single Anomaly In Primary MDS – Reclassification From Poor to Intermediate Prognosis

     Article • Blood, November 2010, American Society of Hematology

     FRANCESC SOLE

219. 
     Unrelated Clones In Myelodysplastic Syndromes and Acute Myeloid Leukemia - Characterization and Prognostic Relevance

     Article • Blood, November 2010, American Society of Hematology

     FRANCESC SOLE

220. 
     Kinetics of Regulatory T-Cells Are Highly Influenced by Treatment In Patients with Gastric MALT Lymphoma

     Article • Blood, November 2010, American Society of Hematology

     FRANCESC SOLE

221. 
     Loss of the Y Chromosome in MDS - Age-Related Phenomenon or Clonal Abnormality?

     Article • Blood, November 2010, American Society of Hematology

     FRANCESC SOLE

222. 
     Will a Peripheral Blood (PB) Sample Yield the Same Diagnostic and Prognostic Cytogenetic Data as the Concomitant Bone Marrow (BM) In Myelodysplasia? An International Study Comparing Cytogenetics and Interphase FISH Using Parallel PB and BM Samples

     Article • Blood, November 2010, American Society of Hematology

     FRANCESC SOLE

223. 
     Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q

     Article • Leukemia, September 2010, Nature

     MD PhD ELISA E LUÑO , FRANCESC SOLE

224. 
     Does monosomy 5 really exist in myelodysplastic syndromes and acute myeloid leukemia?

     Article • Leukemia Research, September 2010, Elsevier

     FRANCESC SOLE

225. 
     CKS1B amplification is a frequent event in cutaneous squamous cell carcinoma with aggressive clinical behaviour

     Article • Genes Chromosomes and Cancer, August 2010, Wiley

     FRANCESC SOLE

226. 
     Multiple genetic copy number alterations in oral squamous cell carcinoma: study of MYC , TP53 , CCDN1, EGFR and ERBB2 status in primary and metastatic tumours

     Article • British Journal of Dermatology, July 2010, Oxford University Press (OUP)

     FRANCESC SOLE

227. 
     TET2 gene is not deleted in chronic myelomonocytic leukemia: a FISH retrospective study

     Article • Haematologica, June 2010, Ferrata Storti Foundation (Haematologica)

     FRANCESC SOLE

228. 
     ALK chromosomal alterations in colon cancer patients.

     Article • Journal of Clinical Oncology, May 2010, American Society of Clinical Oncology (ASCO)

     FRANCESC SOLE

229. 
     Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group

     Article • Blood, May 2010, American Society of Hematology

     MD PhD ELISA E LUÑO , FRANCESC SOLE

230. 
     The capital gap for small technology companies: public venture capital to the rescue?

     Article • Small Business Economics, April 2010, Springer Science + Business Media

     FRANCESC SOLE

231. 
     Oligonucleotide Array-CGH Identifies Genomic Subgroups and Prognostic Markers for Tumor Stage Mycosis Fungoides

     Article • Journal of Investigative Dermatology, April 2010, Elsevier

     FRANCESC SOLE

232. 
     Loss of poly(ADP-ribose) polymerase-2 leads to rapid development of spontaneous T-cell lymphomas in p53-deficient mice

     Article • Oncogene, February 2010, Springer Science + Business Media

     FRANCESC SOLE

233. 
     Genomic and Gene Expression Profiling Defines Indolent Forms of Mantle Cell Lymphoma

     Article • Cancer Research, February 2010, American Association for Cancer Research (AACR)

     FRANCESC SOLE

234. 
     Epidermal growth factor receptor gene numerical aberrations are frequent events in actinic keratoses and invasive cutaneous squamous cell carcinomas

     Article • Experimental Dermatology, February 2010, Wiley

     FRANCESC SOLE

235. 
     Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma

     Article • Genes Chromosomes and Cancer, January 2010, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

236. 
     Cytogenetic Risk Features in MDS-Update and Present State.

     Article • Blood, November 2009, American Society of Hematology

     FRANCESC SOLE

237. 
     Prognostic Value of Monosomal Karyotype in Patients with Primary Acute Myeloid Leukemia On Behalf of Spanish CETLAM Group.

     Article • Blood, November 2009, American Society of Hematology

     FRANCESC SOLE

238. 
     MYCgene numerical aberrations in actinic keratosis and cutaneous squamous cell carcinoma

     Article • British Journal of Dermatology, November 2009, Oxford University Press (OUP)

     FRANCESC SOLE

239. 
     SOX11 expression is highly specific for mantle cell lymphoma and identifies the cyclin D1-negative subtype

     Article • Haematologica, October 2009, Ferrata Storti Foundation (Haematologica)

     FRANCESC SOLE

240. 
     3q26 (hTERC) gain studied by fluorescence in situ hybridization as a persistence-progression indicator in low-grade squamous intraepithelial lesion cases

     Article • Human Pathology, October 2009, Elsevier

     FRANCESC SOLE

241. 
     MicroRNA Expression, Chromosomal Alterations, and Immunoglobulin Variable Heavy Chain Hypermutations in Mantle Cell Lymphomas

     Article • Cancer Research, August 2009, American Association for Cancer Research (AACR)

     FRANCESC SOLE

242. 
     Cytogenetic characterization of NCI-H69 and NCI-H69AR small cell lung cancer cell lines by spectral karyotyping

     Article • Cancer Genetics and Cytogenetics, June 2009, Elsevier

     FRANCESC SOLE

243. 
     P029 Prognostic relevance of specific chromosomal abnormalities in chronic myelomonocytic leukemia

     Article • Leukemia Research, May 2009, Elsevier

     MD PhD ELISA E LUÑO , FRANCESC SOLE

244. 
     C005 Prognostic impact of the proportion of aberrant metaphases in patients with a primary myelodysplastic syndrome

     Article • Leukemia Research, May 2009, Elsevier

     MD PhD ELISA E LUÑO , FRANCESC SOLE

245. 
     P030 Prognostic impact on survival of an unsuccessful conventional cytogenetic study in patients with myelodysplastic syndromes (MDS)

     Article • Leukemia Research, May 2009, Elsevier

     MD PhD ELISA E LUÑO , FRANCESC SOLE

246. 
     12 Updated cytogenetic risk features in MDS – present state

     Article • Leukemia Research, May 2009, Elsevier

     FRANCESC SOLE

247. 
     Spiculated red cells in erythroleukemia

     Article • European Journal Of Haematology, April 2009, Wiley

     FRANCESC SOLE

248. 
     FISH and immunohistochemical status of the hepatocyte growth factor receptor (c-Met) in 184 invasive breast tumors

     Article • April 2009, Springer Science + Business Media

     FRANCESC SOLE

249. 
     HPV Determination in the Control After LEEP Due to CIN II-III: Prospective Study and Predictive Model

     Article • International Journal of Gynecological Pathology, March 2009, Wolters Kluwer Health

     FRANCESC SOLE

250. 
     Some remarks on a current study involving preservice elementary teachers and some basic astronomical phenomena

     Article • Proceedings of the International Astronomical Union, January 2009, Cambridge University Press

     FRANCESC SOLE

251. 
     Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques

     Article • Genes Chromosomes and Cancer, December 2008, Wiley

     FRANCESC SOLE

252. 
     New Prognostic Data on Rare Cytogenetic Abnormalities in MDS: A Collaborative Study of the International Working Group on MDS Cytogenetics

     Article • Blood, November 2008, American Society of Hematology

     FRANCESC SOLE

253. 
     Blast cells with nuclear extrusions in the form of micronuclei are associated with MYC amplification in acute myeloid leukemia

     Article • Cancer Genetics and Cytogenetics, August 2008, Elsevier

     FRANCESC SOLE

254. 
     Gene expression profiling distinguishes JAK2V617F-negative from JAK2V617F-positive patients in essential thrombocythemia

     Article • Leukemia, May 2008, Springer Science + Business Media

     FRANCESC SOLE

255. 
     New chromosomal alterations in a series of 23 splenic marginal zone lymphoma patients revealed by Spectral Karyotyping (SKY)

     Article • Leukemia Research, May 2008, Elsevier

     MD PhD ELISA E LUÑO , FRANCESC SOLE

256. 
     FISH is better than BIOMED-2 PCR to detect IgH/BCL2 translocation in follicular lymphoma at diagnosis using paraffin-embedded tissue sections

     Article • Leukemia Research, May 2008, Elsevier

     FRANCESC SOLE

257. 
     Estudio de las lesiones citogenéticas en el carcinoma escamoso cutáneo mediante la técnica de arrays de hibridación genómica comparada

     Article • Actas Dermo-Sifiliográficas, April 2008, Elsevier

     FRANCESC SOLE

258. 
     Complex chromosome 8;21 translocation with associated hyperdiploidy in acute myeloid leukemia (FAB-M2)

     Article • Pediatric Blood & Cancer, March 2008, Wiley

     FRANCESC SOLE

259. 
     Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-

     Article • Haematologica, January 2008, Ferrata Storti Foundation (Haematologica)

     MD PhD ELISA E LUÑO , FRANCESC SOLE

260. 
     Gene expression analysis provides a potential rationale for revising the histological grading of follicular lymphomas

     Article • Haematologica, January 2008, Ferrata Storti Foundation (Haematologica)

     FRANCESC SOLE

261. 
     Splenic marginal zone lymphoma proposals for a revision of diagnostic, staging and therapeutic criteria

     Article • Leukemia, December 2007, Springer Science + Business Media

     FRANCESC SOLE

262. 
     Gain of multiple copies of the CBFB gene: a new genetic aberration in a case of granulocytic sarcoma

     Article • Cancer Genetics and Cytogenetics, November 2007, Elsevier

     FRANCESC SOLE

263. 
     Could ATRA/Idarubicin treatment of acute promyelocytic leukemia induce the appearance of new clonal cytogenetic abnormalities in patients in complete remission?

     Article • Leukemia Research, September 2007, Elsevier

     FRANCESC SOLE

264. 
     A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation

     Article • Leukemia, May 2007, Springer Science + Business Media

     FRANCESC SOLE

265. 
     A higher JAK2 V617F-mutated clone is observed in platelets than in granulocytes from essential thrombocythemia patients, but not in patients with polycythemia vera and primary myelofibrosis

     Article • Leukemia, March 2007, Springer Science + Business Media

     FRANCESC SOLE

266. 
     Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes

     Article • Pathologie Biologie, February 2007, Elsevier

     FRANCESC SOLE

267. 
     Small supernumerary marker chromosome causing partial trisomy 6p in a child with craniosynostosis

     Article • American Journal of Medical Genetics Part A, January 2007, Wiley

     FRANCESC SOLE

268. 
     Does Polysomy of Chromosome 17 Have a Role in ERBB2 and Topoisomerase IIα Expression?

     Article • Tumor Biology, January 2007, Springer Science + Business Media

     FRANCESC SOLE

269. 
     Duplication dup(1)(q41q44) defined by fluorescence in situ hybridization: delineation of the ‘trisomy 1q42→qter syndrome’

     Article • Cytogenetic and Genome Research, January 2007, Karger Publishers

     FRANCESC SOLE

270. 
     Primitive neuroectodermal tumor of the central nervous system with glial differentiation: a FISH study of an adult case

     Article • Clinical Neuropathology, January 2007, Dustri-Verlgag Dr. Karl Feistle

     FRANCESC SOLE

271. 
     Detection of the JAK2 V617F Mutation by Real Time PCR in Granulocytes and Platelets of ET Patients.

     Article • Blood, November 2006, American Society of Hematology

     FRANCESC SOLE

272. 
     Elderly Patients with De Novo Acute Myeloid Leukemia (AML): Prognostic Factors in 132 Cases.

     Article • Blood, November 2006, American Society of Hematology

     FRANCESC SOLE

273. 
     Gastrointestinal Involvement in Mantle Cell Lymphoma: A Prospective Clinic, Endoscopic, and Pathologic Study

     Article • The American Journal of Surgical Pathology, October 2006, Wolters Kluwer Health

     FRANCESC SOLE

274. 
     JAK2 V617F mutation analysis in different myeloid lineages (granulocytes, platelets, CFU-MK, BFU-E and CFU-GM) in essential thrombocythemia patients

     Article • Leukemia, August 2006, Springer Science + Business Media

     FRANCESC SOLE

275. 
     Aberrant nuclear BCL10 expression and lack of t(11;18)(q21;q21) in primary cutaneous marginal zone B-cell lymphoma

     Article • Human Pathology, July 2006, Elsevier

     FRANCESC SOLE

276. 
     Detection of abnormalities of PRV-1, TPO, and c-MPL genes detected by fluorescence in situ hybridization in essential thrombocythemia

     Article • Cancer Genetics and Cytogenetics, May 2006, Elsevier

     FRANCESC SOLE

277. 
     The MYC oncogene in breast cancer progression: from benign epithelium to invasive carcinoma

     Article • Cancer Genetics and Cytogenetics, March 2006, Elsevier

     FRANCESC SOLE

278. 
     JAK2 V617F mutation, PRV-1 overexpression and endogenous erythroid colony formation show different coexpression patterns among Ph-negative chronic myeloproliferative disorders

     Article • Leukemia, February 2006, Springer Science + Business Media

     FRANCESC SOLE

279. 
     MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

     Article • Human Molecular Genetics, February 2006, Oxford University Press (OUP)

     FRANCESC SOLE

280. 
     Study of chromosomal abnormalities in 11 cases of cervical dysplasia using comparative genomic hybridization on cotton-lint cervical samples

     Article • Cancer Genetics and Cytogenetics, January 2006, Elsevier

     FRANCESC SOLE

281. 
     Comparative genomic hybridization analysis of cutaneous large B-cell lymphomas

     Article • Experimental Dermatology, December 2005, Wiley

     FRANCESC SOLE

282. 
     Identification of Male Cardiomyocytes of Extracardiac Origin in the Hearts of Women with Male Progeny: Male Fetal Cell Microchimerism of the Heart

     Article • The Journal of Heart and Lung Transplantation, December 2005, Elsevier

     FRANCESC SOLE

283. 
     Insertion (8;11) in a renal oncocytoma with multifocal transformation to chromophobe renal cell carcinoma

     Article • Cancer Genetics and Cytogenetics, December 2005, Elsevier

     FRANCESC SOLE

284. 
     Characterization of New Aberrations in 25 Splenic Marginal Zone B-Cell Lymphomas (SMZBCL) Using Spectral Karyotyping Technique (SKY).

     Article • Blood, November 2005, American Society of Hematology

     FRANCESC SOLE

285. 
     Gastrointestinal Involvement in Mantle Cell Lymphoma (MCL). A Prospective Clinical, Endoscopical, Pathological and Molecular Study.

     Article • Blood, November 2005, American Society of Hematology

     FRANCESC SOLE

286. 
     Clonal proliferation of cyclin D1–positive mantle lymphocytes in an asymptomatic patient: an early-stage event in the development or an indolent form of a mantle cell lymphoma?

     Article • Human Pathology, November 2005, Elsevier

     FRANCESC SOLE

287. 
     Absence of CHEK2 mutations in Spanish families with hereditary breast cancer

     Article • Cancer Genetics and Cytogenetics, August 2005, Elsevier

     FRANCESC SOLE

288. 
     CD5 negative and CD5 positive splenic marginal B-cell lymphomas have differential cytogenetic patterns

     Article • Leukemia Research, August 2005, Elsevier

     FRANCESC SOLE

289. 
     Correlation between histologic findings and cytogenetic abnormalities in bladder carcinoma: A FISH study

     Article • Urology, May 2005, Elsevier

     FRANCESC SOLE

290. 
     Polysomy of chromosome 17 in breast cancer tumors showing an overexpression of ERBB2: a study of 175 cases using fluorescence in situhybridization and immunohistochemistry

     Article • January 2005, Springer Science + Business Media

     FRANCESC SOLE

291. 
     Characterization of HER1 (c-erbB1) Status in Locally Advanced Breast Cancer Using Fluorescence in situ Hybridization and Immunohistochemistry

     Article • Tumor Biology, January 2005, Springer Science + Business Media

     FRANCESC SOLE

292. 
     Collaborative Network Space: Infrastructure and Learning Application

     Article • January 2005, Institute of Electrical & Electronics Engineers (IEEE)

     FRANCESC SOLE

293. 
     Cytogenetic and FISH Study of 92 Patients with Splenic Marginal Zone B-Cell Lymphoma (SMZBCL).

     Article • Blood, November 2004, American Society of Hematology

     FRANCESC SOLE

294. 
     Lymphomatoid Papulosis Associated with Mycosis Fungoides: Clinicopathological and Molecular Studies of 12 Cases

     Article • Acta Dermato Venereologica, November 2004, Acta Dermato-Venereologica

     FRANCESC SOLE

295. 
     Activation of mitochondrial apoptotic pathway in mantle cell lymphoma: high sensitivity to mitoxantrone in cases with functional DNA-damage response genes

     Article • Oncogene, October 2004, Springer Science + Business Media

     FRANCESC SOLE

296. 
     Intratumoral heterogeneity of HER2/neu and topoisomerase IIα in breast cancer: a case with clonal monosomy 17

     Article • Cancer Genetics and Cytogenetics, October 2004, Elsevier

     FRANCESC SOLE

297. 
     Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia

     Article • Cancer Genetics and Cytogenetics, August 2004, Elsevier

     FRANCESC SOLE

298. 
     Is fluorescence in situ hybridization a useful method in diagnosis of polycythemia vera patients?

     Article • Cancer Genetics and Cytogenetics, June 2004, Elsevier

     FRANCESC SOLE

299. 
     Heterogeneity of structural abnormalities in the 7q31.3∼q34 region in myeloid malignancies

     Article • Cancer Genetics and Cytogenetics, April 2004, Elsevier

     FRANCESC SOLE

300. 
     Type IMOZ/CBP (MYST3/CREBBP)is the most common chimeric transcript in acute myeloid leukemia with t(8;16)(p11;p13) translocation

     Article • Genes Chromosomes and Cancer, March 2004, Wiley

     FRANCESC SOLE

301. 
     Endogenous erythroid and megakaryocytic circulating progenitors, HUMARA clonality assay, and PRV-1 expression are useful tools for diagnosis of polycythemia vera and essential thrombocythemia

     Article • Blood, March 2004, American Society of Hematology

     FRANCESC SOLE

302. 
     Cytogenetic and fluorescence in situ hybridization studies in 60 patients with multiple myeloma and plasma cell leukemia

     Article • Cancer Genetics and Cytogenetics, January 2004, Elsevier

     FRANCESC SOLE

303. 
     Comparative Analysis of TCR-γ Gene Rearrangements by Genescan and Polyacrylamide Gel-electrophoresis in Cutaneous T-cell Lymphoma

     Article • Acta Dermato Venereologica, December 2003, Acta Dermato-Venereologica

     FRANCESC SOLE

304. 
     Two cases of tetrasomy 9p syndrome with tissue limited mosaicism

     Article • American Journal of Medical Genetics Part A, September 2003, Wiley

     FRANCESC SOLE

305. 
     Cytogenetic findings in familial B-cell chronic lymphocytic leukemia

     Article • Cancer Genetics and Cytogenetics, June 2003, Elsevier

     FRANCESC SOLE

306. 
     Genomic rearrangements involving rDNA and centromeric heterochromatin in vulvar epidermoid carcinoma cell line A-431

     Article • Cancer Genetics and Cytogenetics, May 2003, Elsevier

     FRANCESC SOLE

307. 
     Additional i(1)(q10) in a primitive neuroectodermal tumor type Merkel cell carcinoma as a primary cytogenetic change

     Article • Cancer Genetics and Cytogenetics, April 2003, Elsevier

     FRANCESC SOLE

308. 
     3572 Fetal cell microchimerism in the heart of women with dilated cardiomyopathy

     Article • European Heart Journal, March 2003, Elsevier

     FRANCESC SOLE

309. 
     Chimeric BCR/ABL gene detected by fluorescence in situ hybridization in three new cases of Philadelphia chromosome-negative chronic myelocytic leukemia

     Article • Cancer Genetics and Cytogenetics, March 2003, Elsevier

     FRANCESC SOLE

310. 
     De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19

     Article • Genes Chromosomes and Cancer, January 2003, Wiley

     FRANCESC SOLE

311. 
     RxFISH karyotype andMYCamplification in the HT-29 colon adenocarcinoma cell line

     Article • Genes Chromosomes and Cancer, January 2003, Wiley

     FRANCESC SOLE

312. 
     Molecular heterogeneity in MCL defined by the use of specific VH genes and the frequency of somatic mutations

     Article • Blood, January 2003, American Society of Hematology

     FRANCESC SOLE

313. 
     HLA-G positive trophoblastic cells in transcervical samples and their isolation and analysis by laser microdissection and QF-PCR

     Article • Prenatal Diagnosis, January 2003, Wiley

     FRANCESC SOLE

314. 
     Genomic Abnormalities Acquired in the Blastic Transformation of Splenic Marginal Zone B-cell Lymphoma

     Article • Leukemia & Lymphoma, January 2003, Taylor & Francis

     FRANCESC SOLE

315. 
     Medical Malpractice Liability in Spain: Cases, Trends and Developments

     Article • European Journal of Health Law, January 2003, Brill

     FRANCESC SOLE

316. 
     Analysis of T-Cell Receptor γ Gene Rearrangements by PCR-Genescan and PCR-Polyacrylamide Gel Electrophoresis in Early-Stage Mycosis fungoides/Large-Plaque Parapsoriasis

     Article • Dermatology, January 2003, Karger Publishers

     FRANCESC SOLE

317. 
     Host cell-derived cardiomyocytes in sex-mismatch cardiac allografts

     Article • Cardiovascular Research, December 2002, European Society of Cardiology

     FRANCESC SOLE

318. 
     Clinical Utility of a Multiprobe FISH Assay in Voided Urine Specimens for the Detection of Bladder Cancer and its Recurrences, Compared with Urinary Cytology

     Article • European Urology, December 2002, Elsevier

     FRANCESC SOLE

319. 
     Genetic characterization of the paraimmunoblastic variant of small lymphocytic lymphoma/chronic lymphocytic leukemia: A case report and review of the literature

     Article • Human Pathology, November 2002, Elsevier

     FRANCESC SOLE

320. 
     Genetic Imbalances in Progressed B-Cell Chronic Lymphocytic Leukemia and Transformed Large-Cell Lymphoma (Richter's Syndrome)

     Article • American Journal Of Pathology, September 2002, Elsevier

     FRANCESC SOLE

321. 
     Cultures of myeloid progenitor cells in pediatric essential thrombocythemia

     Article • Leukemia, August 2002, Springer Science + Business Media

     FRANCESC SOLE

322. 
     Report of 46,XX/46,XY/47,XXY/48,XXYY mosaicism in an adult phenotypic male

     Article • American Journal of Medical Genetics, May 2002, Wiley

     FRANCESC SOLE

323. 
     Monosomy 15 in chronic myelomonocytic leukemia

     Article • Cancer Genetics and Cytogenetics, April 2002, Elsevier

     FRANCESC SOLE

324. 
     Analysis of the IgVH somatic mutations in splenic marginal zone lymphoma defines a group of unmutated cases with frequent 7q deletion and adverse clinical course

     Article • Blood, February 2002, American Society of Hematology

     FRANCESC SOLE

325. 
     Pentasomy 21 with two isochromosomes 21 in a case of acute myeloid leukemia without maturation

     Article • Cancer Genetics and Cytogenetics, January 2002, Elsevier

     FRANCESC SOLE

326. 
     A new case of acute nonlymphocytic leukemia (French–American–British subtype M1) with double minutes and c-MYC amplification

     Article • Cancer Genetics and Cytogenetics, January 2002, Elsevier

     FRANCESC SOLE

327. 
     Contribution of cytogenetics and in situ hybridization to the study of monoclonal gammopathies of undetermined significance

     Article • Cancer Genetics and Cytogenetics, January 2002, Elsevier

     FRANCESC SOLE

328. 
     Translocation (5;17)(q13;q21) in a case with precursor T-lymphoblastic lymphoma/leukemia

     Article • Cancer Genetics and Cytogenetics, January 2002, Elsevier

     FRANCESC SOLE

329. 
     Loss of a novel tumor suppressor gene locus at chromosome 8p is associated with leukemic mantle cell lymphoma

     Article • Blood, December 2001, American Society of Hematology

     FRANCESC SOLE

330. 
     Cyclin D3 is a target gene of t(6;14)(p21.1;q32.3) of mature B-cell malignancies

     Article • Blood, November 2001, American Society of Hematology

     Prof. Emanuele Zucca, FRANCESC SOLE

331. 
     A female infant with a 46,XX/48,XY,+8,+10 karyotype in prenatal diagnosis: a ‘vanishing twin’ phenomenon?

     Article • Prenatal Diagnosis, October 2001, Wiley

     FRANCESC SOLE

332. 
     Progression to Large B-Cell Lymphoma in Splenic Marginal Zone Lymphoma

     Article • The American Journal of Surgical Pathology, October 2001, Wolters Kluwer Health

     FRANCESC SOLE

333. 
     Detection of translocations affecting the BCL6 locus in B cell non-Hodgkin’s lymphoma by interphase fluorescence in situ hybridization

     Article • Leukemia, September 2001, Nature

     Dr ALESSANDRO Gozzetti, FRANCESC SOLE

334. 
     Acute myeloid leukemia with 17p abnormality in untreated essential thrombocythemia

     Article • Leukemia, July 2001, Springer Science + Business Media

     FRANCESC SOLE

335. 
     New t(11;12)(q12;q11) characterized by RxFISH in a patient with T-cell large granular lymphocyte leukemia

     Article • Cancer Genetics and Cytogenetics, February 2001, Elsevier

     FRANCESC SOLE

336. 
     Cytogenetic and Fluorescence In Situ Hybridization Studies in Four Cases of Plasma Cell Leukemia

     Article • Cancer Genetics and Cytogenetics, September 2000, Elsevier

     FRANCESC SOLE

337. 
     Dicentric (17;18) in a Case of Atypical B-Cell Chronic Lymphocytic Leukemia

     Article • Cancer Genetics and Cytogenetics, September 2000, Elsevier

     FRANCESC SOLE

338. 
     Translocation t(6;14)(p12;q32): a novel cytogenetic abnormality in splenic lymphoma with villous lymphocytes

     Article • British Journal of Haematology, July 2000, Wiley

     FRANCESC SOLE

339. 
     Isochromosome +i(3)(q10) in a new case of persistent polyclonal B-cell lymphocytosis (PPBL)

     Article • European Journal Of Haematology, May 2000, Wiley

     FRANCESC SOLE

340. 
     Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes

     Article • British Journal of Haematology, February 2000, Wiley

     MD PhD ELISA E LUÑO , FRANCESC SOLE

341. 
     A New Case of Turner Syndrome Associated with Multiple Myeloma

     Article • Cancer Genetics and Cytogenetics, February 2000, Elsevier

     FRANCESC SOLE

342. 
     Simultaneous occurrence of the 5q- syndrome and multiple myeloma

     Article • International Journal of Laboratory Hematology, February 2000, Wiley

     FRANCESC SOLE

343. 
     Translocation (11;14)(q13;q32) and Preferential Involvement of Chromosomes 1, 2, 9, 13, and 17 in Mantle Cell Lymphoma

     Article • Cancer Genetics and Cytogenetics, May 1999, Elsevier

     FRANCESC SOLE

344. 
     Cytogenetic Findings in Five Patients with Hairy Cell Leukemia

     Article • Cancer Genetics and Cytogenetics, April 1999, Elsevier

     FRANCESC SOLE

345. 
     Major vascular complications in essential thrombocythemia: a study of the predictive factors in a series of 148 patients

     Article • Leukemia, February 1999, Springer Science + Business Media

     FRANCESC SOLE

346. 
     Cytogenetic Abnormalities in Three Patients with B-Cell Prolymphocytic Leukemia

     Article • Cancer Genetics and Cytogenetics, May 1998, Elsevier

     FRANCESC SOLE

347. 
     Two New Cases of Near-Tetraploidy in Adult Acute Myeloid Leukemia

     Article • Cancer Genetics and Cytogenetics, April 1998, Elsevier

     FRANCESC SOLE

348. 
     Frequent involvement of chromosomes 1, 3, 7 and 8 in splenic marginal zone B‐cell lymphoma

     Article • British Journal of Haematology, August 1997, Wiley

     FRANCESC SOLE

349. 
     A new case of trisomy 21 in a patient with an acute nonlymphocytic leukemia (M5b)

     Article • Cancer Genetics and Cytogenetics, June 1997, Elsevier

     FRANCESC SOLE

350. 
     Coexistence of tetrasomy 8 and trisomy 8 in a case with myeloid metaplasia with myelofibrosis

     Article • Cancer Genetics and Cytogenetics, April 1997, Elsevier

     FRANCESC SOLE

351. 
     116 Cytogenetic studies in 429 myelodysplastic syndromes:Prognostic value

     Article • Leukemia Research, April 1997, Elsevier

     FRANCESC SOLE

352. 
     26 Cytoplasmic abnormalities of erythroblasts in a patient with refractory anaemia with ring sideroblasts

     Article • Leukemia Research, April 1997, Elsevier

     FRANCESC SOLE

353. 
     129 Deletion sq- in a patient with a secondary myelodysplastic syndromes post multiple myeloma

     Article • Leukemia Research, April 1997, Elsevier

     FRANCESC SOLE

354. 
     Cytogenetic analysis of 280 patients with multiple myeloma and related disorders: Primary breakpoints and clinical correlations

     Article • Genes Chromosomes and Cancer, February 1997, Wiley

     FRANCESC SOLE

355. 
     Cytogenetic studies in seventy-six cases of B-chronic lymphoproliferative disorders

     Article • Cancer Genetics and Cytogenetics, February 1997, Elsevier

     FRANCESC SOLE

356. 
     Trisomy 12 is a rare cytogenetic finding in typical chronic lymphocytic leukemia

     Article • Leukemia Research, May 1996, Elsevier

     FRANCESC SOLE

357. 
     Cytogenetic abnormalities in 13 patients with multiple myeloma

     Article • Cancer Genetics and Cytogenetics, February 1996, Elsevier

     FRANCESC SOLE

358. 
     Mortality in Testicular Cancer: 10 Years’ Experience at a Single Centre

     Article • Urologia Internationalis, January 1996, Karger Publishers

     FRANCESC SOLE

359. 
     A new case of trisomy 5 as sole cytogenetic anomaly in acute myeloid leukemia

     Article • Cancer Genetics and Cytogenetics, October 1995, Elsevier

     FRANCESC SOLE

360. 
     Trisomy 13 in a patient with a myelodysplastic syndrome

     Article • Cancer Genetics and Cytogenetics, June 1995, Elsevier

     FRANCESC SOLE

361. 
     Refractory anemia with excess of blasts and isochromosome 12p in a patient with primary mediastinal germ-cell tumor

     Article • Cancer Genetics and Cytogenetics, October 1994, Elsevier

     FRANCESC SOLE

362. 
     Burkitt's type translocation in multiple myeloma

     Article • Leukemia Research, September 1994, Elsevier

     FRANCESC SOLE

363. 
     Chromosomal and in vitro culture studies in a case of primary plasma cell leukemia

     Article • Cancer Genetics and Cytogenetics, August 1994, Elsevier

     FRANCESC SOLE

364. 
     Congenital dyserythropoietic anemia type II: Morphological characterization of the erythroid colonies (BFU-E) from the bone marrow and peripheral blood of two patients

     Article • Annals of Hematology, August 1994, Springer Science + Business Media

     FRANCESC SOLE

365. 
     A new case of t(14;19) (q32;q13) in a patient with follicular lymphoma in leukemic phase

     Article • Cancer Genetics and Cytogenetics, July 1994, Elsevier

     FRANCESC SOLE

366. 
     Cytogenetic studies in five patients with Sézary syndrome

     Article • Cancer Genetics and Cytogenetics, July 1994, Elsevier

     FRANCESC SOLE

367. 
     Granular lymphocyte proliferative disorders: A multicenter study of 20 cases

     Article • Annals of Hematology, June 1994, Springer Science + Business Media

     FRANCESC SOLE

368. 
     Trisomy 4 in a patient with acute myelomonocytic leukemia (M4)

     Article • Cancer Genetics and Cytogenetics, October 1993, Elsevier

     FRANCESC SOLE

369. 
     A case of monosomy 20 in an adult acute lymphoblastic leukemia

     Article • Cancer Genetics and Cytogenetics, September 1993, Elsevier

     FRANCESC SOLE

370. 
     Chronic neutrophilic leukemia associated with monoclonal gammopathy of undetermined significance

     Article • Annals of Hematology, September 1993, Springer Science + Business Media

     FRANCESC SOLE

371. 
     Isochromosome 17q as a sole anomaly: A distinct myelodysplastic syndrome entity?

     Article • Leukemia Research, August 1993, Elsevier

     FRANCESC SOLE

372. 
     A new chromosomal anomaly associated with mature B-cell chronic lymphoproliferative disorders: del(7)(q32)

     Article • Cancer Genetics and Cytogenetics, February 1993, Elsevier

     FRANCESC SOLE

373. 
     Microwaves improve chromosome G-banding in fresh blood and bone marrow.

     Article • Journal of Clinical Pathology, December 1992, BMJ

     FRANCESC SOLE

374. 
     Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes

     Article • Cancer Genetics and Cytogenetics, November 1992, Elsevier

     FRANCESC SOLE

375. 
     t(6;9)(p22;q34) associated with acute myeloblastic leukemia (M1)

     Article • Cancer Genetics and Cytogenetics, October 1992, Elsevier

     FRANCESC SOLE

376. 
     Cytogenetic studies in acute nonlymphocytic leukemia

     Article • Cancer Genetics and Cytogenetics, June 1992, Elsevier

     FRANCESC SOLE

377. 
     New chromosomal abnormality

     Article • Cancer Genetics and Cytogenetics, June 1992, Elsevier

     FRANCESC SOLE

378. 
     t(3;14)(q26;q11) associated with megakaryoblastic transformation of chronic myeloid leukemia

     Article • Cancer Genetics and Cytogenetics, August 1991, Elsevier

     FRANCESC SOLE

379. 
     Isochromosome 14q in myeloid dysplastic disorder

     Article • Cancer Genetics and Cytogenetics, July 1991, Elsevier

     FRANCESC SOLE

380. 
     G-banding improvement for the MAC method

     Article • Cancer Genetics and Cytogenetics, January 1991, Elsevier

     FRANCESC SOLE

381. 
     Acute lymphoblastic leukemia with t(4;11) in a patient previously exposed to a carcinogen

     Article • Cancer Genetics and Cytogenetics, October 1990, Elsevier

     FRANCESC SOLE

382. 
     Cytogenetic study of a patient with the Sézary syndrome

     Article • Cancer Genetics and Cytogenetics, February 1990, Elsevier

     FRANCESC SOLE

383. 
     Translocation (2;7)(p13;q36) in a case of acute nonlymphocytic leukemia evolving from a myelodysplastic syndrome

     Article • Cancer Genetics and Cytogenetics, October 1988, Elsevier

     FRANCESC SOLE