Works by Steinthorsdottir, Valgerdur
Results: 42
Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality.
- Published in:
- Human Genetics, 2021, v. 140, n. 3, p. 529, doi. 10.1007/s00439-020-02223-6
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- Article
Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans.
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- Frontiers in Endocrinology, 2023, v. 14, p. 1, doi. 10.3389/fendo.2023.1081741
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- Article
Parental origin of sequence variants associated with complex diseases.
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- Nature, 2009, v. 462, n. 7275, p. 868, doi. 10.1038/nature08625
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- Article
Genetics of gene expression and its effect on disease.
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- Nature, 2008, v. 452, n. 7186, p. 423, doi. 10.1038/nature06758
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- Article
Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling.
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- Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-024-55761-2
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- Article
Sequence variants associated with BMI affect disease risk through BMI itself.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-53568-9
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- Article
FTO genotype is associated with phenotypic variability of body mass index.
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- Nature, 2012, v. 490, n. 7419, p. 267, doi. 10.1038/nature11401
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- Article
InterPregGen: genetic studies of pre-eclampsia in three continents.
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- Norsk Epidemiologi, 2014, v. 24, n. 1/2, p. 141, doi. 10.5324/nje.v24i1-2.1815
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- Article
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.
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- European Heart Journal, 2020, v. 41, n. 28, p. 2618, doi. 10.1093/eurheartj/ehaa531
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- Article
The epidemiology of pituitary adenomas in Iceland, 1955-2012: a nationwide population-based study.
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- European Journal of Endocrinology, 2015, v. 173, n. 5, p. 655, doi. 10.1530/EJE-15-0189
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- Article
Paternity Change and the Recurrence Risk in Familial Hypertensive Disorder in Pregnancy.
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- Hypertension in Pregnancy, 2004, v. 23, n. 2, p. 219, doi. 10.1081/PRG-120037889
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- Article
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.
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- Nature Communications, 2017, v. 8, n. 5, p. 15539, doi. 10.1038/ncomms15539
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- Article
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.
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- Nature Communications, 2016, v. 7, n. 7, p. 12350, doi. 10.1038/ncomms12350
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- Article
Neuregulin 1 and schizophrenia.
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- Annals of Medicine, 2004, v. 36, n. 1, p. 62, doi. 10.1080/07853890310017585
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- Article
Evaluating differences in linkage disequilibrium between populations.
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- Annals of Human Genetics, 2010, v. 74, n. 3, p. 233, doi. 10.1111/j.1469-1809.2010.00571.x
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- Article
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05428-6
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- Article
Genetic Architecture of Vitamin B<sub>12</sub> and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets.
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- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003530
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- Article
Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases.
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- PLoS Genetics, 2012, v. 8, n. 5, p. 1, doi. 10.1371/journal.pgen.1002741
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- Article
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
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- 2023
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- Correction Notice
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38951-2
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- Publication type:
- Article
Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.
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- Nature Genetics, 2014, v. 46, n. 3, p. 294, doi. 10.1038/ng.2882
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- Article
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.
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- Nature Genetics, 2012, v. 44, n. 9, p. 981, doi. 10.1038/ng.2383
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- Article
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
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- 2011
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- Correction Notice
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.
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- 2011
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- Correction Notice
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
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- Nature Genetics, 2010, v. 42, n. 11, p. 949, doi. 10.1038/ng.685
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- Article
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
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- Nature Genetics, 2010, v. 42, n. 11, p. 937, doi. 10.1038/ng.686
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- Article
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.
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- Nature Genetics, 2010, v. 42, n. 7, p. 579, doi. 10.1038/ng.609
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- Article
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
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- 2010
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- Correction Notice
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
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- Nature Genetics, 2010, v. 42, n. 2, p. 105, doi. 10.1038/ng.520
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- Article
Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.
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- Nature Genetics, 2009, v. 41, n. 6, p. 734, doi. 10.1038/ng.383
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- Article
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.
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- Nature Genetics, 2009, v. 41, n. 3, p. 342, doi. 10.1038/ng.323
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- Article
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.
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- Nature Genetics, 2009, v. 41, n. 1, p. 18, doi. 10.1038/ng.274
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- Article
Many sequence variants affecting diversity of adult human height.
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- Nature Genetics, 2008, v. 40, n. 5, p. 609, doi. 10.1038/ng.122
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- Article
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.
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- Nature Genetics, 2008, v. 40, n. 2, p. 217, doi. 10.1038/ng.72
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- Article
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.
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- Nature Genetics, 2007, v. 39, n. 8, p. 977, doi. 10.1038/ng2062
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- Article
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.
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- Nature Genetics, 2007, v. 39, n. 6, p. 770, doi. 10.1038/ng2043
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- Article
A common inversion under selection in Europeans.
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- Nature Genetics, 2005, v. 37, n. 2, p. 129, doi. 10.1038/ng1508
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- Article
Sequence variants associating with urinary biomarkers.
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- Human Molecular Genetics, 2019, v. 28, n. 7, p. 1199, doi. 10.1093/hmg/ddy409
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- Article
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.
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- PLoS Genetics, 2015, v. 11, n. 9, p. 1, doi. 10.1371/journal.pgen.1005379
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- Article
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-19733-6
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- Article
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
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- 2017
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- Publication type:
- journal article
Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant at CCND2 Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion.
- Published in:
- Diabetes, 2015, v. 64, n. 6, p. 2279, doi. 10.2337/db14-1456
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- Article