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Refinado por: assunto: Polymorphism, Single Nucleotide remover
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Polygenic Type 2 Diabetes Prediction at the Limit of Common Variant Detection
Polygenic Type 2 Diabetes Prediction at the Limit of Common Variant Detection
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Polygenic Type 2 Diabetes Prediction at the Limit of Common Variant Detection

VASSY, Jason L ; HIVERT, Marie-France ; MEIGS, James B ; PORNEALA, Bianca ; DAURIZ, Marco ; FLOREZ, Jose C ; DUPUIS, Josée ; SISCOVICK, David S ; FORNAGE, Myriam ; RASMUSSEN-TORVIK, Laura J ; BOUCHARD, Claude

Diabetes (New York, N.Y.), 2014-06, Vol.63 (6), p.2172-2182 [Periódico revisado por pares]

Alexandria, VA: American Diabetes Association

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2
Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs
Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs
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Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

Castellani, Christina A ; Longchamps, Ryan J ; Sumpter, Jason A ; Newcomb, Charles E ; Lane, John A ; Grove, Megan L ; Bressler, Jan ; Brody, Jennifer A ; Floyd, James S ; Bartz, Traci M ; Taylor, Kent D ; Wang, Penglong ; Tin, Adrienne ; Coresh, Josef ; Pankow, James S ; Fornage, Myriam ; Guallar, Eliseo ; O'Rourke, Brian ; Pankratz, Nathan ; Liu, Chunyu ; Levy, Daniel ; Sotoodehnia, Nona ; Boerwinkle, Eric ; Arking, Dan E

Genome medicine, 2020-09, Vol.12 (1), p.84-84, Article 84 [Periódico revisado por pares]

England: BioMed Central Ltd

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3
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease
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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

French, Curtis R ; Seshadri, Sudha ; Destefano, Anita L ; Fornage, Myriam ; Arnold, Corey R ; Gage, Philip J ; Skarie, Jonathan M ; Dobyns, William B ; Millen, Kathleen J ; Liu, Ting ; Dietz, William ; Kume, Tsutomu ; Hofker, Marten ; Emery, Derek J ; Childs, Sarah J ; Waskiewicz, Andrew J ; Lehmann, Ordan J

The Journal of clinical investigation, 2014-11, Vol.124 (11), p.4877-4881 [Periódico revisado por pares]

United States: American Society for Clinical Investigation

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4
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium
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Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium

Guan, Weihua ; Steffen, Brian T ; Lemaitre, Rozenn N ; Wu, Jason H Y ; Tanaka, Toshiko ; Manichaikul, Ani ; Foy, Millennia ; Rich, Stephen S ; Wang, Lu ; Nettleton, Jennifer A ; Tang, Weihong ; Gu, Xiangjun ; Bandinelli, Stafania ; King, Irena B ; McKnight, Barbara ; Psaty, Bruce M ; Siscovick, David ; Djousse, Luc ; Chen, Yii-Der Ida ; Ferrucci, Luigi ; Fornage, Myriam ; Mozafarrian, Dariush ; Tsai, Michael Y ; Steffen, Lyn M

Circulation. Cardiovascular genetics, 2014-06, Vol.7 (3), p.321-331 [Periódico revisado por pares]

United States

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5
Genome-Wide Association Study of Intracranial Aneurysms Confirms Role of Anril and SOX17 in Disease Risk
Genome-Wide Association Study of Intracranial Aneurysms Confirms Role of Anril and SOX17 in Disease Risk
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Genome-Wide Association Study of Intracranial Aneurysms Confirms Role of Anril and SOX17 in Disease Risk

FOROUD, Tatiana ; KOLLER, Daniel L ; MOOMAW, Charles J ; HORNUNG, Richard ; HUSTON, John ; MEISSNER, Irene ; BAILEY-WILSON, Joan E ; LANGEFELD, Carl ; ROULEAU, Guy ; CONNOLLY, E. Sander ; WORRALL, Bradford B ; KLEINDORFER, Dawn ; DONGBING LAI ; FLAHERTY, Matthew L ; MARTINI, Sharyl ; MACKEY, Jason ; DE LOS RIOS LA ROSA, Felipe ; BROWN, Robert D ; BRODERICK, Joseph P ; SAUERBECK, Laura ; ANDERSON, Craig ; KO, Nerissa ; DEKA, Ranjan ; MOSLEY, Thomas H ; FORNAGE, Myriam ; WOO, Daniel

Stroke (1970), 2012-11, Vol.43 (11), p.2846-2852 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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6
Whole exome sequence-based association analyses of plasma amyloid-β in African and European Americans; the Atherosclerosis Risk in Communities-Neurocognitive Study
Whole exome sequence-based association analyses of plasma amyloid-β in African and European Americans; the Atherosclerosis Risk in Communities-Neurocognitive Study
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Whole exome sequence-based association analyses of plasma amyloid-β in African and European Americans; the Atherosclerosis Risk in Communities-Neurocognitive Study

Simino, Jeannette ; Wang, Zhiying ; Bressler, Jan ; Chouraki, Vincent ; Yang, Qiong ; Younkin, Steven G ; Seshadri, Sudha ; Fornage, Myriam ; Boerwinkle, Eric ; Mosley, Jr, Thomas H Sleegers, Kristel

PloS one, 2017-07, Vol.12 (7), p.e0180046 [Periódico revisado por pares]

United States: Public Library of Science

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7
Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment
Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment
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Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment

Granot-Hershkovitz, Einat ; Spitzer, Brian ; Yang, Yunju ; Tarraf, Wassim ; Yu, Bing ; Boerwinkle, Eric ; Fornage, Myriam ; Mosley, Thomas H ; DeCarli, Charles ; Kristal, Bruce S ; González, Hector M ; Sofer, Tamar

Translational psychiatry, 2023-04, Vol.13 (1), p.140-140, Article 140 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics
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Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics

Hodonsky, Chani J ; Baldassari, Antoine R ; Bien, Stephanie A ; Raffield, Laura M ; Highland, Heather M ; Sitlani, Colleen M ; Wojcik, Genevieve L ; Tao, Ran ; Graff, Marielisa ; Tang, Weihong ; Thyagarajan, Bharat ; Buyske, Steve ; Fornage, Myriam ; Hindorff, Lucia A ; Li, Yun ; Lin, Danyu ; Reiner, Alex P ; North, Kari E ; Loos, Ruth J F ; Kooperberg, Charles ; Avery, Christy L

BMC genomics, 2020-03, Vol.21 (1), p.228-228, Article 228 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Associations of plasma clusterin and Alzheimer's disease-related MRI markers in adults at mid-life: The CARDIA Brain MRI sub-study
Associations of plasma clusterin and Alzheimer's disease-related MRI markers in adults at mid-life: The CARDIA Brain MRI sub-study
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Associations of plasma clusterin and Alzheimer's disease-related MRI markers in adults at mid-life: The CARDIA Brain MRI sub-study

Haight, Thaddeus ; Bryan, R Nick ; Meirelles, Osorio ; Tracy, Russell ; Fornage, Myriam ; Richard, Melissa ; Nasrallah, Ilya ; Yaffe, Kristine ; Jacobs, Jr, David R ; Lewis, Cora ; Schreiner, Pamela ; Sidney, Stephen ; Davatzikos, Christos ; Launer, Lenore J Rosenberg, Paul B.

PloS one, 2018-01, Vol.13 (1), p.e0190478-e0190478 [Periódico revisado por pares]

United States: Public Library of Science

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10
A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains
A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains
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A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains

Avery, Christy L ; He, Qianchuan ; North, Kari E ; Ambite, Jose L ; Boerwinkle, Eric ; Fornage, Myriam ; Hindorff, Lucia A ; Kooperberg, Charles ; Meigs, James B ; Pankow, James S ; Pendergrass, Sarah A ; Psaty, Bruce M ; Ritchie, Marylyn D ; Rotter, Jerome I ; Taylor, Kent D ; Wilkens, Lynne R ; Heiss, Gerardo ; Lin, Dan Yu Gibson, Greg

PLoS genetics, 2011-10, Vol.7 (10), p.e1002322-e1002322 [Periódico revisado por pares]

United States: Public Library of Science

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