Gene-gene Interaction Analyses for Atrial Fibrillation
暂无分享,去创建一个
K. Lunetta | M. Waldenberger | O. Franco | A. Hofman | A. Uitterlinden | M. Chung | M. Rienstra | D. Chasman | V. Gudnason | P. Macfarlane | L. Chen | C. Albert | E. Benjamin | P. Ellinor | H. Völzke | T. Meitinger | K. Lohman | Yongmei Liu | B. Psaty | D. Arking | B. Stricker | S. Kathiresan | J. Rotter | W. März | T. Harris | E. Soliman | J. Jukema | P. Natarajan | J. Barnard | L. Launer | D. V. Van Wagoner | S. Heckbert | T. Bartz | S. Weiss | Jingzhong Ding | L. Rose | P. van der Harst | T. Kacprowski | M. Kleber | A. Hendricks | M. Mueller-Nurasyid | M. Dörr | J. Kors | S. Lubitz | S. Trompet | G. Delgado | N. Verweij | I. Ford | Honghuang Lin | Jonathan D. Smith | B. Geelhoed | Zhijun Xie | S. Kääb | Á. Alonso | D. Klarin | Moritz F. Sinner | J. Heeringa | M. Niemeijer | Traci M. Bartz | A. Smith | P. van der harst | A. Smith | L. Rose | A. Uitterlinden | Martina Mueller-Nurasyid | A. Hofman | B. Psaty | Honghuang Lin | Á. Alonso
[1] M. Banach,et al. Differences in biochemical and genetic biomarkers in patients with heart failure of various etiologies. , 2016, International journal of cardiology.
[2] R. Płoski,et al. The 4q25, 1q21, and 16q22 polymorphisms and recurrence of atrial fibrillation after pulmonary vein isolation , 2016, Archives of medical science : AMS.
[3] Gabor T. Marth,et al. A global reference for human genetic variation , 2015, Nature.
[4] R. Elston,et al. Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation , 2015, PLoS genetics.
[5] K. Lunetta,et al. Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation , 2014, Circulation.
[6] K. Lunetta,et al. Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. , 2014, Journal of the American College of Cardiology.
[7] C. Murray,et al. Worldwide Epidemiology of Atrial Fibrillation: A Global Burden of Disease 2010 Study , 2014, Circulation.
[8] K. Lunetta,et al. Meta-analysis identifies six new susceptibility loci for atrial fibrillation , 2012, Nature Genetics.
[9] Jianmin Wu,et al. PINA v2.0: mining interactome modules , 2011, Nucleic Acids Res..
[10] Michael J Pencina,et al. Association between familial atrial fibrillation and risk of new-onset atrial fibrillation. , 2010, JAMA.
[11] Yun Li,et al. METAL: fast and efficient meta-analysis of genomewide association scans , 2010, Bioinform..
[12] Thomas Meitinger,et al. Common Variants in KCNN3 are Associated with Lone Atrial Fibrillation , 2010, Nature Genetics.
[13] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[14] M. Banach,et al. Genetic determinants of cardiovascular disease: the renin-angiotensin-aldosterone system, paraoxonases, endothelin-1, nitric oxide synthase and adrenergic receptors. , 2009, In vivo.
[15] G. Lip,et al. Lone atrial fibrillation: what do we know? , 2009, Heart.
[16] Eric Boerwinkle,et al. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry , 2009, Nature Genetics.
[17] B. Maher. Personal genomes: The case of the missing heritability , 2008, Nature.
[18] M. LeBlanc,et al. Increasing the power of identifying gene × gene interactions in genome‐wide association studies , 2008, Genetic epidemiology.
[19] Eric E. Smith,et al. Variants conferring risk of atrial fibrillation on chromosome 4q25 , 2007, Nature.
[20] Laurent Briollais,et al. SNP-SNP interactions in breast cancer susceptibility , 2006, BMC Cancer.
[21] K. Stefánsson,et al. Familial aggregation of atrial fibrillation in Iceland. , 2006, European heart journal.
[22] J. Ruskin,et al. Familial aggregation in lone atrial fibrillation , 2005, Human Genetics.
[23] Ralph B D'Agostino,et al. Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring. , 2004, JAMA.
[24] C. Carlson,et al. Mapping complex disease loci in whole-genome association studies , 2004, Nature.
[25] Douglas L Packer,et al. Familial atrial fibrillation is a genetically heterogeneous disorder. , 2003, Journal of the American College of Cardiology.
[26] P. Bork,et al. Functional organization of the yeast proteome by systematic analysis of protein complexes , 2002, Nature.
[27] J. H. Moore,et al. Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. , 2001, American journal of human genetics.
[28] J M Gauthier,et al. Protein--protein interaction maps: a lead towards cellular functions. , 2001, Trends in genetics : TIG.
[29] C. Sing,et al. A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation. , 2001, Genome research.
[30] P. Vernant,et al. [Familial auricular fibrillation]. , 1976, La Nouvelle presse medicale.
[31] B. Maher,et al. The case of the missing heritability , 2008 .
[32] Taesung Park,et al. Odds ratio based multifactor-dimensionality reduction method for detecting gene – gene interactions , 2006 .
[33] M. Vidal,et al. Protein interaction maps for model organisms , 2001, Nature Reviews Molecular Cell Biology.