All Stories

  1. A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women’s experiences and negotiations of living with an underdeveloped uterus and vagina

    Article • Disability and Rehabilitation, March 2023, Taylor & Francis

    Dr Morten Herlin

  2. Compromised PAR1 activation - a cause for bleeding in X-men?

    Article • Thrombosis and Haemostasis, January 2023, Thieme Publishing Group

    Dr Morten Herlin

  3. Proteogenomic analysis of acute myeloid leukemia associates relapsed disease with reprogrammed energy metabolism both in adults and children

    Article • Leukemia, December 2022, Springer Science + Business Media

    Dr Morten Herlin

  4. Description of a novel subtype of acute myeloid leukemia defined by recurrent CBFB insertions

    Article • Blood, September 2022, American Society of Hematology

    Dr Morten Herlin

  5. Novel homozygous CD46 variant with C‐isoform expression affects C3b inactivation in atypical hemolytic uremic syndrome

    Article • European Journal of Immunology, August 2022, Wiley

    Dr Morten Herlin

  6. Autosomal dominant sleep-related hypermotor epilepsy caused by a previously unreported CHRNA4 variant

    Article • European Journal of Medical Genetics, March 2022, Elsevier

    Dr Morten Herlin

  7. Transcriptomic analysis reveals proinflammatory signatures associated with acute myeloid leukemia progression

    Article • Blood Advances, January 2022, American Society of Hematology

    Dr Morten Herlin

  8. What Is Abnormal in Normal Karyotype Acute Myeloid Leukemia in Children? Analysis of the Mutational Landscape and Prognosis of the TARGET-AML Cohort

    Article • Genes, May 2021, MDPI AG

    Dr Morten Herlin

  9. Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets

    Article • Blood Advances, February 2021, American Society of Hematology

    Dr Morten Herlin

  10. Genomic and Transcriptomic Characterization of Adult and Pediatric Relapsed Acute Myeloid Leukemia Reveals Novel Therapeutic Targets

    Article • Blood, November 2020, American Society of Hematology

    Dr Morten Herlin

  11. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update

    Article • Orphanet Journal of Rare Diseases, August 2020, Springer Science + Business Media

    Dr Morten Herlin

  12. Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome. A case report

    Article • Human Reproduction, August 2019, Oxford University Press (OUP)

    Dr Morten Herlin

  13. Treatment of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser syndrome in Denmark: a nationwide comparative study of anatomical outcome and complications

    Article • Fertility and Sterility, September 2018, Elsevier

    Dr Morten Herlin

  14. Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literature

    Article • Journal of Medical Case Reports, December 2016, Springer Science + Business Media

    Dr Morten Herlin

  15. Prevalence and patient characteristics of Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide registry-based study

    Article • Human Reproduction, September 2016, Oxford University Press (OUP)

    Dr Morten Herlin

  16. Accelerometer-assessed daily physical activity in relation to pain cognition in juvenile idiopathic arthritis

    Article • Scandinavian Journal of Rheumatology, June 2016, Taylor & Francis

    Dr Morten Herlin

  17. Familial occurrence of Mayer-Rokitansky-Küster-Hauser syndrome: A case report and review of the literature

    Article • American Journal of Medical Genetics Part A, June 2014, Wiley

    Dr Morten Herlin