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1
ABCA7 p.G215S as potential protective factor for Alzheimer’s disease
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Artigo
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ABCA7 p.G215S as potential protective factor for Alzheimer’s disease

Sassi, C ; Nalls, M.A ; Ridge, P.G ; Gibbs, R ; Ding, J ; Lupton, M.K ; Troakes, C ; Lunnon, K ; Al-Sarraj, S ; Brown, K.S ; Medway, C ; Clement, N ; Lord, J ; Turton, J ; Bras, J ; Almeida, M.R ; Holstege, H ; Louwersheimer, E ; van der Flier, W ; Scheltens, P ; Van Swieten, J.C ; Santana, I ; Oliveira, C ; Morgan, K ; Powell, J.F ; Kauwe, J.S ; Cruchaga, C ; Goate, A.M ; Singleton, A.B ; Guerreiro, R ; Hardy, J

Neurobiology of aging, 2016-10, Vol.46, p.235.e1-235.e9 [Periódico revisado por pares]

United States: Elsevier Inc

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2
Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X
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Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X

Cheng, Ching-Yu ; Kao, W H Linda ; Patterson, Nick ; Tandon, Arti ; Haiman, Christopher A ; Harris, Tamara B ; Xing, Chao ; John, Esther M ; Ambrosone, Christine B ; Brancati, Frederick L ; Coresh, Josef ; Press, Michael F ; Parekh, Rulan S ; Klag, Michael J ; Meoni, Lucy A ; Hsueh, Wen-Chi ; Fejerman, Laura ; Pawlikowska, Ludmila ; Freedman, Matthew L ; Jandorf, Lina H ; Bandera, Elisa V ; Ciupak, Gregory L ; Nalls, Michael A ; Akylbekova, Ermeg L ; Orwoll, Eric S ; Leak, Tennille S ; Miljkovic, Iva ; Li, Rongling ; Ursin, Giske ; Bernstein, Leslie ; Ardlie, Kristin ; Taylor, Herman A ; Boerwinckle, Eric ; Zmuda, Joseph M ; Henderson, Brian E ; Wilson, James G ; Reich, David McCarthy, Mark I.

PLoS genetics, 2009-05, Vol.5 (5), p.e1000490-e1000490 [Periódico revisado por pares]

United States: Public Library of Science

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3
Admixture Mapping of White Cell Count: Genetic Locus Responsible for Lower White Blood Cell Count in the Health ABC and Jackson Heart Studies
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Artigo
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Admixture Mapping of White Cell Count: Genetic Locus Responsible for Lower White Blood Cell Count in the Health ABC and Jackson Heart Studies

Nalls, Michael A. ; Wilson, James G. ; Patterson, Nick J. ; Tandon, Arti ; Zmuda, Joseph M. ; Huntsman, Scott ; Garcia, Melissa ; Hu, Donglei ; Li, Rongling ; Beamer, Brock A. ; Patel, Kushang V. ; Akylbekova, Ermeg L. ; Files, Joe C. ; Hardy, Cheryl L. ; Buxbaum, Sarah G. ; Taylor, Herman A. ; Reich, David ; Harris, Tamara B. ; Ziv, Elad

American journal of human genetics, 2008-01, Vol.82 (1), p.81-87 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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4
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
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Artigo
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Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk

Moskvina, Valentina ; Harold, Denise ; Russo, GianCarlo ; Vedernikov, Alexey ; Sharma, Manu ; Saad, Mohamad ; Holmans, Peter ; Bras, Jose M ; Bettella, Francesco ; Keller, Margaux F ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Gibbs, J. Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nick ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Owen, Michael J ; O’Donovan, Michael C ; Williams, Julie ; Morris, Huw R ; Williams, Nigel M

JAMA neurology, 2013-10, Vol.70 (10), p.1268-1276 [Periódico revisado por pares]

United States: American Medical Association

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5
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
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Artigo
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Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

FOX, Ervin R ; HUNTER YOUNG, J ; RAMACHANDRAN, VasanS ; POLAK, JosefF ; FABSITZ, Richard R ; DRIES, Daniel L ; FARLOW, Deborah N ; REDLINE, Susan ; ADEYEMO, Adebowale ; HIRSCHORN, Joel N ; SUN, Yan V ; WYATT, Sharon B ; YALI LI ; PENMAN, Alan D ; PALMAS, Walter ; ROTTER, Jerome I ; TOWNSEND, Raymond R ; DOUMATEY, Ayo P ; TAYO, Bamidele O ; MOSLEY, Thomas H ; LYON, Helen N ; KANG, Sun J ; ROTIMI, Charles N ; DREISBACH, Albert W ; COOPER, Richard S ; FRANCESCHINI, Nora ; CURB, J. David ; MARTIN, Lisa W ; EATON, Charles B ; KARDIA, Sharon L. R ; TAYLOR, Herman A ; CAULFIELD, Mark J ; EHRET, Georg B ; JOHNSON, Toby ; KEATING, Brendan J ; CHAKRAVARTI, Aravinda ; XIAOFENG ZHU ; LEVY, Daniel ; MUSANI, Solomon K ; KIANG LIU ; MORRISON, Alanna C ; GANESH, Santhi ; KUTLAR, Abdullah

Human molecular genetics, 2011-06, Vol.20 (11), p.2273-2284 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
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Artigo
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Laaksovirta, Hannu, MD ; Peuralinna, Terhi, MSc ; Schymick, Jennifer C, PhD ; Scholz, Sonja W, MD ; Lai, Shaoi-Lin, MD ; Myllykangas, Liisa, MD ; Sulkava, Raimo, MD ; Jansson, Lilja ; Hernandez, Dena G, MSc ; Gibbs, J Raphael, BS ; Nalls, Michael A, PhD ; Heckerman, David, MD ; Tienari, Pentti J, MD ; Traynor, Bryan J, Dr

Lancet neurology, 2010-10, Vol.9 (10), p.978-985 [Periódico revisado por pares]

England: Elsevier Ltd

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7
Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage
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Artigo
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Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage

ANDERSON, Christopher D ; BIFFI, Alessandro ; VISWANATHAN, Anand ; WORRALL, Bradford B ; BROTT, Thomas G ; GOLDSTEIN, Joshua N ; BROWN, Devin ; BRODERICK, Joseph P ; NORRVING, Bo ; GREENBERG, Steven M ; SILLIMAN, Scott L ; HANSEN, Björn M ; NALLS, Michael A ; TIRSCHWELL, David L ; LINDGREN, Arne ; SLOWIK, Agnieszka ; SCHMIDT, Reinhold ; SELIM, Magdy ; ROQUER, Jaume ; MONTANER, Joan ; SINGLETON, Andrew B ; KIDWELL, Chelsea S ; WOO, Daniel ; DEVAN, William J ; FURIE, Karen L ; MESCHIA, James F ; ROSAND, Jonathan ; SCHWAB, Kristin ; AYRES, Alison M ; VALANT, Valerie ; ROSS, Owen A ; ROST, Natalia S ; SAXENA, Richa

Stroke (1970), 2013-03, Vol.44 (3), p.612-619 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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8
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease
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Artigo
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Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

Simón-Sánchez, Javier ; Kilarski, Laura L ; Nalls, Michael A ; Martinez, Maria ; Schulte, Claudia ; Holmans, Peter ; Gasser, Thomas ; Hardy, John ; Singleton, Andrew B ; Wood, Nicholas W ; Brice, Alexis ; Heutink, Peter ; Williams, Nigel ; Morris, Huw R Lewin, Alfred

PloS one, 2012-03, Vol.7 (3), p.e28787-e28787 [Periódico revisado por pares]

United States: Public Library of Science

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9
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
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Artigo
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Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium

Jensen, Majken K ; Jensen, Richard A ; Mukamal, Kenneth J ; Guo, Xiuqing ; Yao, Jie ; Sun, Qi ; Cornelis, Marilyn ; Liu, Yongmei ; Chen, Ming-Huei ; Kizer, Jorge R ; Djoussé, Luc ; Siscovick, David S ; Psaty, Bruce M ; Zmuda, Joseph M ; Rotter, Jerome I ; Garcia, Melissa ; Harris, Tamara ; Chen, Ida ; Goodarzi, Mark O ; Nalls, Michael A ; Keller, Margaux ; Arnold, Alice M ; Newman, Anne B ; Hoogeveen, Ron C ; Rexrode, Kathryn M ; Rimm, Eric B ; Hu, Frank B ; Ramachandran, Vasan S ; Katz, Ronit ; Pankow, James S ; Ix, Joachim H

Human Molecular Genetics, 2017-06, Vol.26 (11), p.2156-2163

eScholarship, University of California

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10
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
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Artigo
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Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium

Jensen, Majken K ; Jensen, Richard A ; Mukamal, Kenneth J ; Guo, Xiuqing ; Yao, Jie ; Sun, Qi ; Cornelis, Marilyn ; Liu, Yongmei ; Chen, Ming-Huei ; Kizer, Jorge R ; Djoussé, Luc ; Siscovick, David S ; Psaty, Bruce M ; Zmuda, Joseph M ; Rotter, Jerome I ; Garcia, Melissa ; Harris, Tamara ; Chen, Ida ; Goodarzi, Mark O ; Nalls, Michael A ; Keller, Margaux ; Arnold, Alice M ; Newman, Anne B ; Hoogeveen, Ron C ; Rexrode, Kathryn M ; Rimm, Eric B ; Hu, Frank B ; Ramachandran, Vasan S ; Katz, Ronit ; Pankow, James S ; Ix, Joachim H

Human molecular genetics, 2017-06, Vol.26 (11), p.2156-2163 [Periódico revisado por pares]

England: Oxford University Press

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