Ingileif Jonsdottir


Ontology type: schema:Person     


Person Info

NAME

Ingileif

SURNAME

Jonsdottir

Publications in SciGraph latest 50 shown

  • 2019-02 A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis in NATURE GENETICS
  • 2018-12 DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis in NATURE COMMUNICATIONS
  • 2018-12 A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide analysis yields new loci associating with aortic valve stenosis in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide association meta-analysis yields 20 loci associated with gallstone disease in NATURE COMMUNICATIONS
  • 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 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 Insights into imprinting from parent-of-origin phased methylomes and transcriptomes in NATURE GENETICS
  • 2018-09 Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis in NATURE GENETICS
  • 2018-08 Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis 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 COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA in BMC MEDICAL GENETICS
  • 2017-11 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits in NATURE GENETICS
  • 2017-11 Graphtyper enables population-scale genotyping using pangenome graphs in NATURE GENETICS
  • 2017-08 Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis in NATURE GENETICS
  • 2017-08 Identification of sequence variants influencing immunoglobulin levels in NATURE GENETICS
  • 2017-06-06 Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis in NATURE COMMUNICATIONS
  • 2017-05 Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis in NATURE GENETICS
  • 2017-03 Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets in NATURE GENETICS
  • 2017-02-22 Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation in NATURE COMMUNICATIONS
  • 2016-09-13 Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis in NATURE COMMUNICATIONS
  • 2016-08-09 A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis 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
  • 2016-03 HLA class II sequence variants influence tuberculosis risk in populations of European ancestry in NATURE GENETICS
  • 2016-02-03 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase in NATURE COMMUNICATIONS
  • 2014-05 Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31 in NATURE GENETICS
  • 2013-11 A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration in NATURE GENETICS
  • 2013-08 Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization in NATURE GENETICS
  • 2011-11 Identification of low-frequency variants associated with gout and serum uric acid levels in NATURE GENETICS
  • 2011-09 Competition for FcRn-mediated transport gives rise to short half-life of human IgG3 and offers therapeutic potential in NATURE COMMUNICATIONS
  • 2010-08 A sequence variant on 17q21 is associated with age at onset and severity of asthma in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-03 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction in NATURE GENETICS
  • 2009-01 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity in NATURE GENETICS
  • 1985-07 Specificities and binding properties of 2 monoclonal antibodies against carcinoma cells of the human urinary bladder in BRITISH JOURNAL OF CANCER
  • 1984-09 Monoclonal antibodies to antigens associated with transitional cell carcinoma of the human urinary bladder in CANCER IMMUNOLOGY, IMMUNOTHERAPY
  • 1981-11 Electrophoretic mobility of mouse T-cell hybrids in BRITISH JOURNAL OF CANCER
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