Unnur Thorsteinsdottir


Ontology type: schema:Person     


Person Info

NAME

Unnur

SURNAME

Thorsteinsdottir

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 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 A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin in COMMUNICATIONS BIOLOGY
  • 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 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
  • 2018-11 Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps in NATURE GENETICS
  • 2018-09 Biobank-driven genomic discovery yields new insight into atrial fibrillation biology in NATURE GENETICS
  • 2018-09 Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition in NATURE GENETICS
  • 2018-09 Relatedness disequilibrium regression estimates heritability without environmental bias in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-04 Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition in NATURE GENETICS
  • 2018-04 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-04 Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis in NATURE GENETICS
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity 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 Large meta-analysis of genome-wide association studies identifies five loci for lean body mass in NATURE COMMUNICATIONS
  • 2017-12 Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass in NATURE COMMUNICATIONS
  • 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
  • 2017-09-21 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 Identification of sequence variants influencing immunoglobulin levels in NATURE GENETICS
  • 2017-07 Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci 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
  • 2017-04-25 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
  • 2017-02-14 A genome-wide association study yields five novel thyroid cancer risk loci in NATURE COMMUNICATIONS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-12 A sequence variant associating with educational attainment also affects childhood cognition in SCIENTIFIC REPORTS
  • 2016-12 Genome-wide analysis identifies 12 loci influencing human reproductive behavior in NATURE GENETICS
  • 2016-11-23 A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape in NATURE COMMUNICATIONS
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