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Refinado por: assunto: Genotype remover
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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

Gibbs, J Raphael ; van der Brug, Marcel P ; Hernandez, Dena G ; Traynor, Bryan J ; Nalls, Michael A ; Lai, Shiao-Lin ; Arepalli, Sampath ; Dillman, Allissa ; Rafferty, Ian P ; Troncoso, Juan ; Johnson, Robert ; Zielke, H Ronald ; Ferrucci, Luigi ; Longo, Dan L ; Cookson, Mark R ; Singleton, Andrew B Flint, Jonathan

PLoS genetics, 2010-05, Vol.6 (5), p.e1000952-e1000952 [Periódico revisado por pares]

United States: Public Library of Science

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2
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
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Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

Wood, Andrew R ; Perry, John R B ; Tanaka, Toshiko ; Hernandez, Dena G ; Zheng, Hou-Feng ; Melzer, David ; Gibbs, J Raphael ; Nalls, Michael A ; Weedon, Michael N ; Spector, Tim D ; Richards, J Brent ; Bandinelli, Stefania ; Ferrucci, Luigi ; Singleton, Andrew B ; Frayling, Timothy M Arking, Dan E.

PloS one, 2013-05, Vol.8 (5), p.e64343-e64343 [Periódico revisado por pares]

United States: Public Library of Science

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3
Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration
Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration
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Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration

Spencer, Kylee L ; Olson, Lana M ; Schnetz-Boutaud, Nathalie ; Gallins, Paul ; Agarwal, Anita ; Iannaccone, Alessandro ; Kritchevsky, Stephen B ; Garcia, Melissa ; Nalls, Michael A ; Newman, Anne B ; Scott, William K ; Pericak-Vance, Margaret A ; Haines, Jonathan L Toland, Amanda

PloS one, 2011-03, Vol.6 (3), p.e17784-e17784 [Periódico revisado por pares]

United States: Public Library of Science

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4
Genetic variability in CLU and its association with Alzheimer's disease
Genetic variability in CLU and its association with Alzheimer's disease
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Genetic variability in CLU and its association with Alzheimer's disease

Guerreiro, Rita J ; Beck, John ; Gibbs, J Raphael ; Santana, Isabel ; Rossor, Martin N ; Schott, Jonathan M ; Nalls, Michael A ; Ribeiro, Helena ; Santiago, Beatriz ; Fox, Nick C ; Oliveira, Catarina ; Collinge, John ; Mead, Simon ; Singleton, Andrew ; Hardy, John Weedon, Michael Nicholas

PloS one, 2010-03, Vol.5 (3), p.e9510-e9510 [Periódico revisado por pares]

United States: Public Library of Science

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5
Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics
Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics
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Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics

Biffi, Alessandro ; Anderson, Christopher D. ; Nalls, Michael A. ; Rahman, Rosanna ; Sonni, Akshata ; Cortellini, Lynelle ; Rost, Natalia S. ; Matarin, Mar ; Hernandez, Dena G. ; Plourde, Anna ; de Bakker, Paul I.W. ; Ross, Owen A. ; Greenberg, Steven M. ; Furie, Karen L. ; Meschia, James F. ; Singleton, Andrew B. ; Saxena, Richa ; Rosand, Jonathan

American journal of human genetics, 2010-06, Vol.86 (6), p.904-917 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

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6
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

Johnson, Janel O ; Pioro, Erik P ; Boehringer, Ashley ; Chia, Ruth ; Feit, Howard ; Renton, Alan E ; Pliner, Hannah A ; Abramzon, Yevgeniya ; Marangi, Giuseppe ; Winborn, Brett J ; Gibbs, J Raphael ; Nalls, Michael A ; Morgan, Sarah ; Shoai, Maryam ; Hardy, John ; Pittman, Alan ; Orrell, Richard W ; Malaspina, Andrea ; Sidle, Katie C ; Fratta, Pietro ; Harms, Matthew B ; Baloh, Robert H ; Pestronk, Alan ; Weihl, Conrad C ; Rogaeva, Ekaterina ; Zinman, Lorne ; Drory, Vivian E ; Borghero, Giuseppe ; Mora, Gabriele ; Calvo, Andrea ; Rothstein, Jeffrey D ; Drepper, Carsten ; Sendtner, Michael ; Singleton, Andrew B ; Taylor, J Paul ; Cookson, Mark R ; Restagno, Gabriella ; Sabatelli, Mario ; Bowser, Robert ; Chiò, Adriano ; Traynor, Bryan J

Nature neuroscience, 2014-05, Vol.17 (5), p.664-666 [Periódico revisado por pares]

United States: Nature Publishing Group

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7
A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies
A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies
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A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

Nalls, Michael A ; Duran, Raquel ; Lopez, Grisel ; Kurzawa-Akanbi, Marzena ; McKeith, Ian G ; Chinnery, Patrick F ; Morris, Christopher M ; Theuns, Jessie ; Crosiers, David ; Cras, Patrick ; Engelborghs, Sebastiaan ; De Deyn, Peter Paul ; Van Broeckhoven, Christine ; Mann, David M. A ; Snowden, Julie ; Pickering-Brown, Stuart ; Halliwell, Nicola ; Davidson, Yvonne ; Gibbons, Linda ; Harris, Jenny ; Sheerin, Una-Marie ; Bras, Jose ; Hardy, John ; Clark, Lorraine ; Marder, Karen ; Honig, Lawrence S ; Berg, Daniela ; Maetzler, Walter ; Brockmann, Kathrin ; Gasser, Thomas ; Novellino, Fabiana ; Quattrone, Aldo ; Annesi, Grazia ; De Marco, Elvira Valeria ; Rogaeva, Ekaterina ; Masellis, Mario ; Black, Sandra E ; Bilbao, Juan M ; Foroud, Tatiana ; Ghetti, Bernardino ; Nichols, William C ; Pankratz, Nathan ; Halliday, Glenda ; Lesage, Suzanne ; Klebe, Stephan ; Durr, Alexandra ; Duyckaerts, Charles ; Brice, Alexis ; Giasson, Benoit I ; Trojanowski, John Q ; Hurtig, Howard I ; Tayebi, Nahid ; Landazabal, Claudia ; Knight, Melanie A ; Keller, Margaux ; Singleton, Andrew B ; Wolfsberg, Tyra G ; Sidransky, Ellen

JAMA neurology, 2013-06, Vol.70 (6), p.727-735 [Periódico revisado por pares]

United States: American Medical Association

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8
A Genome-wide Association Study of Myasthenia Gravis
A Genome-wide Association Study of Myasthenia Gravis
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A Genome-wide Association Study of Myasthenia Gravis

Renton, Alan E ; Pliner, Hannah A ; Provenzano, Carlo ; Evoli, Amelia ; Ricciardi, Roberta ; Nalls, Michael A ; Marangi, Giuseppe ; Abramzon, Yevgeniya ; Arepalli, Sampath ; Chong, Sean ; Hernandez, Dena G ; Johnson, Janel O ; Bartoccioni, Emanuela ; Scuderi, Flavia ; Maestri, Michelangelo ; Gibbs, J. Raphael ; Errichiello, Edoardo ; Chiò, Adriano ; Restagno, Gabriella ; Sabatelli, Mario ; Macek, Mark ; Scholz, Sonja W ; Corse, Andrea ; Chaudhry, Vinay ; Benatar, Michael ; Barohn, Richard J ; McVey, April ; Pasnoor, Mamatha ; Dimachkie, Mazen M ; Rowin, Julie ; Kissel, John ; Freimer, Miriam ; Kaminski, Henry J ; Sanders, Donald B ; Lipscomb, Bernadette ; Massey, Janice M ; Chopra, Manisha ; Howard, James F ; Koopman, Wilma J ; Nicolle, Michael W ; Pascuzzi, Robert M ; Pestronk, Alan ; Wulf, Charlie ; Florence, Julaine ; Blackmore, Derrick ; Soloway, Aimee ; Siddiqi, Zaeem ; Muppidi, Srikanth ; Wolfe, Gil ; Richman, David ; Mezei, Michelle M ; Jiwa, Theresa ; Oger, Joel ; Drachman, Daniel B ; Traynor, Bryan J

JAMA neurology, 2015-04, Vol.72 (4), p.396-404 [Periódico revisado por pares]

United States: American Medical Association

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9
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
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Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene

Reich, David ; Nalls, Michael A ; Kao, W H Linda ; Akylbekova, Ermeg L ; Tandon, Arti ; Patterson, Nick ; Mullikin, James ; Hsueh, Wen-Chi ; Cheng, Ching-Yu ; Coresh, Josef ; Boerwinkle, Eric ; Li, Man ; Waliszewska, Alicja ; Neubauer, Julie ; Li, Rongling ; Leak, Tennille S ; Ekunwe, Lynette ; Files, Joe C ; Hardy, Cheryl L ; Zmuda, Joseph M ; Taylor, Herman A ; Ziv, Elad ; Harris, Tamara B ; Wilson, James G Visscher, Peter M.

PLoS genetics, 2009-01, Vol.5 (1), p.e1000360-e1000360 [Periódico revisado por pares]

United States: Public Library of Science

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10
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
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Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

Corneveaux, Jason J. ; Myers, Amanda J. ; Allen, April N. ; Pruzin, Jeremy J. ; Ramirez, Manuel ; Engel, Anzhelika ; Nalls, Michael A. ; Chen, Kewei ; Lee, Wendy ; Chewning, Kendria ; Villa, Stephen E. ; Meechoovet, Hunsar B. ; Gerber, Jill D. ; Frost, Danielle ; Benson, Hollie L. ; O'Reilly, Sean ; Chibnik, Lori B. ; Shulman, Joshua M. ; Singleton, Andrew B. ; Craig, David W. ; Van Keuren-Jensen, Kendall R. ; Dunckley, Travis ; Bennett, David A. ; De Jager, Philip L. ; Heward, Christopher ; Hardy, John ; Reiman, Eric M. ; Huentelman, Matthew J.

Human molecular genetics, 2010-08, Vol.19 (16), p.3295-3301 [Periódico revisado por pares]

Oxford: Oxford University Press

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