Daniel F Gudbjartsson


Ontology type: schema:Person     


Person Info

NAME

Daniel F

SURNAME

Gudbjartsson

Publications in SciGraph latest 50 shown

  • 2019-12 Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma in NATURE COMMUNICATIONS
  • 2019-02 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use in NATURE GENETICS
  • 2019-02 A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis in NATURE GENETICS
  • 2018-12 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide association meta-analysis yields 20 loci associated with gallstone disease in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide analysis yields new loci associating with aortic valve stenosis in NATURE COMMUNICATIONS
  • 2018-12 Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes in NATURE COMMUNICATIONS
  • 2018-12 A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease in NATURE COMMUNICATIONS
  • 2018-12 A rare missense variant in NR1H4 associates with lower cholesterol levels in COMMUNICATIONS BIOLOGY
  • 2018-12 Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 in GENOME BIOLOGY
  • 2018-12 Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis in NATURE GENETICS
  • 2018-12 Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits in NATURE COMMUNICATIONS
  • 2018-12 PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity in NATURE COMMUNICATIONS
  • 2018-12 A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin in COMMUNICATIONS BIOLOGY
  • 2018-12 MAP1B mutations cause intellectual disability and extensive white matter deficit in NATURE COMMUNICATIONS
  • 2018-12 Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma in NATURE COMMUNICATIONS
  • 2018-12 Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation in COMMUNICATIONS BIOLOGY
  • 2018-11-05 Multiple transmissions of de novo mutations in families in NATURE GENETICS
  • 2018-11 Author Correction: The rate of meiotic gene conversion varies by sex and age in NATURE GENETICS
  • 2018-11 Insights into imprinting from parent-of-origin phased methylomes and transcriptomes in NATURE GENETICS
  • 2018-09 Biobank-driven genomic discovery yields new insight into atrial fibrillation biology in NATURE GENETICS
  • 2018-09 Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence in MOLECULAR PSYCHIATRY
  • 2018-09 Relatedness disequilibrium regression estimates heritability without environmental bias in NATURE GENETICS
  • 2018-01 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks in NATURE GENETICS
  • 2017-12 Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations in NPJ GENOMIC MEDICINE
  • 2017-12 Sequence variant at 4q25 near PITX2 associates with appendicitis in SCIENTIFIC REPORTS
  • 2017-12 Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters in BMC MEDICAL GENETICS
  • 2017-12 COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA in BMC MEDICAL GENETICS
  • 2017-11 Graphtyper enables population-scale genotyping using pangenome graphs in NATURE GENETICS
  • 2017-09-21 Whole genome characterization of sequence diversity of 15,220 Icelanders in SCIENTIFIC DATA
  • 2017-09 Parental influence on human germline de novo mutations in 1,548 trios from Iceland in NATURE
  • 2017-09 Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability in NATURE GENETICS
  • 2017-08 Truncating mutations in RBM12 are associated with psychosis in NATURE GENETICS
  • 2017-08 Identification of sequence variants influencing immunoglobulin levels in NATURE GENETICS
  • 2017-06-13 Reproductive fitness and genetic risk of psychiatric disorders in the general population in NATURE COMMUNICATIONS
  • 2017-06-06 Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis in NATURE COMMUNICATIONS
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2017-05 Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis in NATURE GENETICS
  • 2017-05 Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility in NATURE GENETICS
  • 2017-04-25 15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia in TRANSLATIONAL PSYCHIATRY
  • 2017-04 Diversity in non-repetitive human sequences not found in the reference genome in NATURE GENETICS
  • 2017-02-22 Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation in NATURE COMMUNICATIONS
  • 2016-12 Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality in NATURE GENETICS
  • 2016-12 A sequence variant associating with educational attainment also affects childhood cognition in SCIENTIFIC REPORTS
  • 2016-11-16 Epigenetic and genetic components of height regulation in NATURE COMMUNICATIONS
  • 2016-11 The rate of meiotic gene conversion varies by sex and age in NATURE GENETICS
  • 2016-08-09 A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis in NATURE COMMUNICATIONS
  • 2016-07-25 Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis in NATURE COMMUNICATIONS
  • 2016-07-01 Genome-wide association study identifies multiple susceptibility loci for multiple myeloma in NATURE COMMUNICATIONS
  • 2016-06 Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease in NATURE GENETICS
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