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  1. No Access

    Article

    The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

    Recently, two common sequence variants on 9p21, tagged by rs10757278-G and rs10811661-T, were reported to be associated with coronary artery disease (CAD)1,2,3,4 and type 2 diabetes (T2D)5,6,7, respectively. We p...

    Anna Helgadottir, Gudmar Thorleifsson, Kristinn P Magnusson in Nature Genetics (2008)

  2. Article

    Open Access

    Genetic and functional association of FAM5C with myocardial infarction

    We previously identified a 40 Mb region of linkage on chromosome 1q in our early onset coronary artery disease (CAD) genome-wide linkage scan (GENECARD) with modest evidence for linkage (n = 420, LOD 0.95). Wh...

    Jessica J Connelly, Svati H Shah, Jennifer F Doss, Shera Gadson in BMC Medical Genetics (2008)

  3. No Access

    Article

    Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

    Daniel Gudbjartsson and colleagues report results of a genome-wide association study for loci influencing eosinophil counts. Follow-up studies showed that a subset of the variants identified in this screen wer...

    Daniel F Gudbjartsson, Unnur S Bjornsdottir, Eva Halapi in Nature Genetics (2009)

  4. No Access

    Article

    Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis

    Leukotrienes are arachidonic acid derivatives long known for their inflammatory properties and their involvement with a number of human diseases, most particularly asthma. Recently, leukotriene-based inflammat...

    David R. Crosslin, Svati H. Shah, Sarah C. Nelson, Carol S. Haynes in Human Genetics (2009)

  5. No Access

    Article

    Genetics of cardiac repolarization

    Prolongation of the electrocardiographic QT interval, a measure of cardiac repolarization, is associated with arrhythmogenic disorders and is a risk factor for sudden cardiac death. Two genome-wide association...

    Svati H Shah, Geoffrey S Pitt in Nature Genetics (2009)

  6. No Access

    Article

    Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

    Solveig Gretarsdottir, Kari Stefansson and colleagues report a genome-wide association study for abdominal aortic aneurysm. They identified a variant located within the DAB2IP gene on 9q33 associated with risk of...

    Solveig Gretarsdottir, Annette F Baas, Gudmar Thorleifsson, Hilma Holm in Nature Genetics (2010)

  7. No Access

    Article

    Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease

    Tenascin-C (TNC) is an extracellular matrix protein implicated in biological processes important for atherosclerotic plaque development and progression, including smooth muscle cell migration and proliferation. P...

    Mollie A. Minear, David R. Crosslin, Beth S. Sutton, Jessica J. Connelly in Human Genetics (2011)

  8. No Access

    Article

    Large-scale association analysis identifies new risk loci for coronary artery disease

    Panos Deloukas, Nilesh Samani and colleagues report a large-scale association analysis using the Metabochip array in 63,746 coronary artery disease cases and 130,681 controls. They identify 15 susceptibility l...

    Panos Deloukas, Stavroula Kanoni, Christina Willenborg, Martin Farrall in Nature Genetics (2013)

  9. No Access

    Article

    Gene–smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort

    We performed a gene–smoking interaction analysis using families from an early-onset coronary artery disease cohort (GENECARD). This analysis was focused on validating and expanding results from previous studie...

    Cavin Ward-Caviness, Carol Haynes, Colette Blach, Elaine Dowdy in Human Genetics (2013)

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    Article

    Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

    Patrick Ellinor and colleagues report meta-analyses of common and rare variant association studies for atrial fibrillation across multiple populations. They identify 12 new loci, some of which implicate genes ...

    Ingrid E Christophersen, Michiel Rienstra, Carolina Roselli, **aoyan Yin in Nature Genetics (2017)

  11. Article

    Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

    Nat. Genet.; 10.1038/ng.3843; corrected online 11 May 2017 In the version of this article initially published online, the authors were incorrectly defined as members of the AFGen consortium in the author list....

    Ingrid E Christophersen, Michiel Rienstra, Carolina Roselli, **aoyan Yin in Nature Genetics (2017)

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    Article

    Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    Genome-wide association studies (GWAS) have identified >250 loci for body mass index (BMI), implicating pathways related to neuronal biology. Most GWAS loci represent clusters of common, noncoding variants fro...

    Valérie Turcot, Yingchang Lu, Heather M. Highland, Claudia Schurmann in Nature Genetics (2018)

  13. Article

    Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    In the version of this article originally published, one of the two authors with the name Wei Zhao was omitted from the author list and the affiliations for both authors were assigned to the single Wei Zhao in...

    Valérie Turcot, Yingchang Lu, Heather M. Highland, Claudia Schurmann in Nature Genetics (2018)

  14. Article

    Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    In the published version of this paper, the name of author Emanuele Di Angelantonio was misspelled. This error has now been corrected in the HTML and PDF versions of the article.

    Valérie Turcot, Yingchang Lu, Heather M. Highland, Claudia Schurmann in Nature Genetics (2018)

  15. Article

    Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    An amendment to this paper has been published and can be accessed via a link at the top of the paper.

    Valérie Turcot, Yingchang Lu, Heather M. Highland, Claudia Schurmann in Nature Genetics (2019)

  16. Article

    Open Access

    The association of accelerated epigenetic age with all-cause mortality in cardiac catheterization patients as mediated by vascular and cardiometabolic outcomes

    Epigenetic age is a DNA methylation-based biomarker of aging that is accurate across the lifespan and a range of cell types. The difference between epigenetic age and chronological age, termed age acceleration...

    Rong Jiang, Elizabeth R. Hauser, Lydia Coulter Kwee, Svati H. Shah in Clinical Epigenetics (2022)

  17. Article

    Open Access

    Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

    Restless legs syndrome (RLS) affects up to 10% of older adults. Their healthcare is impeded by delayed diagnosis and insufficient treatment. To advance disease prediction and find new entry points for therapy,...

    Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen in Nature Genetics (2024)