David Alexander Van Heel


Ontology type: schema:Person     


Person Info

NAME

David Alexander

SURNAME

Van Heel

Publications in SciGraph latest 50 shown

  • 2022-08-09 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals in NATURE COMMUNICATIONS
  • 2022-08-03 A first update on mapping the human genetic architecture of COVID-19 in NATURE
  • 2021-12-10 Fine-scale population structure and demographic history of British Pakistanis in NATURE COMMUNICATIONS
  • 2021-12-09 The power of genetic diversity in genome-wide association studies of lipids in NATURE
  • 2021-11-03 MC3R links nutritional state to childhood growth and the timing of puberty in NATURE
  • 2021-07-08 Mapping the human genetic architecture of COVID-19 in NATURE
  • 2021-02-03 Author Correction: Evaluating drug targets through human loss-of-function genetic variation in NATURE
  • 2020-12-11 Genetic mechanisms of critical illness in COVID-19 in NATURE
  • 2020-05-27 Evaluating drug targets through human loss-of-function genetic variation in NATURE
  • 2019-10-31 Associations of autozygosity with a broad range of human phenotypes in NATURE COMMUNICATIONS
  • 2018-04-12 Identification of rare sequence variation underlying heritable pulmonary arterial hypertension in NATURE COMMUNICATIONS
  • 2018-02-19 Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference in NATURE COMMUNICATIONS
  • 2017-08-21 Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes in NATURE COMMUNICATIONS
  • 2015-08-10 Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases in NATURE GENETICS
  • 2015-04-20 Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease in NATURE GENETICS
  • 2014-09-14 HLA-DQA1–HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants in NATURE GENETICS
  • 2013-08-06 Genetic insights into common pathways and complex relationships among immune-mediated diseases in NATURE REVIEWS GENETICS
  • 2013-05-22 Negligible impact of rare autoimmune-locus coding-region variants on missing heritability in NATURE
  • 2013-04-21 Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis in NATURE GENETICS
  • 2011-12-27 Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry in NATURE GENETICS
  • 2011-11-06 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease in NATURE GENETICS
  • 2010-02-28 Multiple common variants for celiac disease influencing immune gene expression in NATURE GENETICS
  • 2009-10-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium in NATURE GENETICS
  • 2009-02-17 Sex Differences in HLA DQ in Celiac Disease in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2008-06 New susceptibility genes for ulcerative colitis in NATURE GENETICS
  • 2008-04-17 Association study of IL2/IL21 and FcgRIIa: significant association with the IL2/IL21 region in Scandinavian coeliac disease families in GENES & IMMUNITY
  • 2008-03-02 Newly identified genetic risk variants for celiac disease related to the immune response in NATURE GENETICS
  • 2007-06-10 A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 in NATURE GENETICS
  • 2005-01-12 A common CTLA4 haplotype associated with coeliac disease in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2001-12-01 Identification of novel polymorphisms in the β7 integrin gene: family-based association studies in inflammatory bowel disease in GENES & IMMUNITY
  • 2001-08-30 Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3) in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2000-08 A revised sequence of the human β7 integrin gene (ITGB7) promoter region obtained by inverse PCR in IMMUNOGENETICS
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