All Stories

  1. A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease
  2. Mechanisms of CFTR Functional Variants That Impair Regulated Bicarbonate Permeation and Increase Risk for Pancreatitis but Not for Cystic Fibrosis
  3. Parental attitudes toward newborn screening for Duchenne/Becker muscular dystrophy and spinal muscular atrophy
  4. Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice
  5. Connecting the Dots: Potential of Data Integration to Identify Regulatory SNPs in Late-Onset Alzheimer's Disease GWAS Findings
  6. Genetic variants within the MHC region are associated with immune responsiveness to childhood vaccinations
  7. P3–012: Genetic determinants of progression of Alzheimer's disease
  8. P3–007: An examination of regulatory function for GWAS‐confirmed and suggestive loci of late‐onset Alzheimer's disease
  9. Physical and Mental Quality of Life in Chronic Pancreatitis
  10. Genome-Wide Association Study of Antiphospholipid Antibodies
  11. Vitamin D Insufficiency and Severe Asthma Exacerbations in Puerto Rican Children
  12. African ancestry and lung function in Puerto Rican children
  13. African Ancestry, SES, FEV1 And Asthma Exacerbations In Puerto Rican Children
  14. Association of CLU and PICALM variants with Alzheimer's disease
  15. A Bayesian Method for Evaluating and Discovering Disease Loci Associations
  16. Prostaglandin E2 and IL-23 plus IL-1β Differentially Regulate the Th1/Th17 Immune Response of Human CD161+CD4+ Memory T Cells
  17. P1‐236: Genome‐Wide Association Study for Alzheimer's Disease with Psychotic Symptoms
  18. Learning genetic epistasis using Bayesian network scoring criteria
  19. Combined Bicarbonate Conductance-Impairing Variants in CFTR and SPINK1 Variants Are Associated With Chronic Pancreatitis in Patients Without Cystic Fibrosis
  20. Identifying genetic interactions in genome‐wide data using Bayesian networks
  21. A Novel Locus for Familial Migraine on Xp22
  22. Pooling-Based Genome-Wide Association Study Implicates Gamma-Glutamyltransferase 1 (GGT1) Gene in Pancreatic Carcinogenesis
  23. M1871 Use of Mathematical and Statistical Model Predictions to Identify a Novel Pancreas-Specific Class of CFTR Variants Linked to SPINK1 Mutations and Idiopathic Chronic Pancreatitis
  24. 475o Resistin, a Potent Adipokine, is Associated With Acute Pancreatitis: Assessment of Functional Genetic Polymorphisms and Serum Levels
  25. “Predicting” parental longevity from offspring endophenotypes: Data from the Long Life Family Study (LLFS)
  26. Integrative Systems Biology
  27. Increasing Incidence of Acute Pancreatitis at an American Pediatric Tertiary Care Center
  28. Physical Activity Levels in American-Indian Adults
  29. Integrative Systems Biology: Implications for the Understanding of Human Disease
  30. Multicenter Approach to Recurrent Acute and Chronic Pancreatitis in the United States: The North American Pancreatitis Study 2 (NAPS2)
  31. Genetic Variation in C-Reactive Protein (CRP) Gene May Be Associated with Risk of Systemic Lupus Erythematosus and CRP Concentrations
  32. Genetic Variants in Major Histocompatibility Complex-Linked Genes Associate With Pediatric Liver Transplant Rejection
  33. Pathways to Injury in Chronic Pancreatitis: Decoding the Role of the High-Risk SPINK1 N34S Haplotype Using Meta-Analysis
  34. S2091 Does the Pain-Protective GTP Cyclohydrolase Haplotype Significantly Alter the Severity of Pain in Humans with Chronic Pancreatitis?
  35. S2090 SPINK1 N34s Is Not Associated with the Sentinel Acute Pancreatitis Episode But Predisposes Patients to Recurrent Attacks
  36. Does the Pain-Protective GTP Cyclohydrolase Haplotype Significantly Alter the Pattern or Severity of Pain in Humans with Chronic Pancreatitis?
  37. The Serotonin Transporter: Sequence Variation in Macaca fascicularis and its Relationship to Dominance
  38. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
  39. Association of the peroxisome proliferator–activated receptor γ gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado
  40. The PPARγ Pro12Ala Polymorphism Is Not Associated with Body Mass Index or Waist Circumference among Hispanics from Colorado
  41. X-linked infantile spinal muscular atrophy: Clinical definition and molecular mapping
  42. Whole Genome Association Identifies Novel Susceptibility Genes for Crohn's Disease and Implicates a Crucial Role for Autophagy
  43. The MCP-1 ᐠ2518 A/G Polymorphism Is Not a Susceptibility Factor for Chronic Pancreatitis
  44. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment
  45. Keratin 8 Mutations Are Not Associated with Familial, Sporadic and Alcoholic Pancreatitis in a Population from the United States
  46. Phenotype-Stratified Genetic Linkage Study Demonstrates that IBD2 Is an Extensive Ulcerative Colitis Locus
  47. Evaluating Disorders with a Complex Genetics Basis. The Future Roles of Meta-analysis and Systems Biology
  48. The C161→T polymorphism in peroxisome proliferator–activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator–activated rece...
  49. Challenges of Examining Complex Genetic Disorders like GERD
  50. Is the Monocyte Chemotactic Protein-1 −2518 G Allele a Risk Factor for Severe Acute Pancreatitis?
  51. The IBD International Genetics Consortium Provides Further Evidence for Linkage to IBD4 and Shows Gene-Environment Interaction
  52. KERATIN 8 MUTATIONS ARE NOT ASSOCIATED WITH HEREDITARY OR ALCOHOLIC CHRONIC PANCREATITIS IN THE UNITED STATES.
  53. THE MCP-1 -2518 G ALLELE ACTS AS A POTENT DISEASE SEVERITY MODIFIER IN ACUTE PANCREATITIS.
  54. A Genome Scan in 260 Inflammatory Bowel Disease-Affected Relative Pairs
  55. Genetic analysis of the glutathione s-transferase genes MGST1, GSTM3, GSTT1, and GSTM1 in patients with hereditary pancreatitis
  56. Genetic and Environmental Influences on Thyroid Hormone Variation in Mexican Americans
  57. Transforming growth factor-β1, interleukin-10 and interferon-γ cytokine polymorphisms in patients with hereditary, familial and sporadic chronic pancreatitis
  58. A Genome Scan in 260 Inflammatory Bowel Disease-Affected Relative Pairs
  59. African American Hypertensive Nephropathy Maps to a New Locus on Chromosome 9q31-q32
  60. Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13
  61. Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor α (TNF-α) promoter region or the TNF receptor 1 (TNFR1) gene
  62. Stability of exploratory multivariate data modeling in longitudinal data
  63. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families
  64. Investigation of oxidized LDL-receptor 1 (OLR1) as the candidate gene for Alzheimer's disease on chromosome 12
  65. Perinuclear neutrophil antibodies are not markers for genetic susceptibility or indicators of genetic heterogeneity in familial ulcerative colitis
  66. Genetics of Gastroesophageal Reflux Disease: A Review
  67. The IBD4 locus shows linkage heterogeneity between Crohn's disease and ulcerative colitis
  68. Transmission/disequilibrium test analysis of a genome scan dataset detects a novel, significant inflammatory bowel disease linkage to chromosome 3p
  69. Autosomal dominant infant GERD: Exclusion of a 13q14 locus in 6 well-characterized families suggests genetic heterogeneity
  70. SPINK 1 mutations modify phenotypic expression in hereditary pancreatitis (HP) caused by cationic trypsinogen (PRSS1) mutations R122H and N291
  71. Reply
  72. High-Density Genome Scan in Crohn Disease Shows Confirmed Linkage to Chromosome 14q11-12
  73. A genome scan at 751 microsatellite loci reveals linkage between Crohn's disease and chromosome 14q11–12, the IBD4 locus
  74. A simple allele sharing statistic for multiple locus systems
  75. Linkage and Association between Inflammatory Bowel Disease and a Locus on Chromosome 12
  76. Recombination hotspots in the HLA region of chromosome 6