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1
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

Holmans, Peter ; Moskvina, Valentina ; Jones, Lesley ; Sharma, Manu ; Vedernikov, Alexey ; Buchel, Finja ; Saad, Mohamad ; Sadd, Mohamad ; Bras, Jose M ; Bettella, Francesco ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Mittag, Florian ; Gibbs, J Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nicholas W ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Morris, Huw R ; Williams, Nigel M

Human molecular genetics, 2013-03, Vol.22 (5), p.1039-1049 [Periódico revisado por pares]

England: Oxford University Press

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2
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
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Artigo
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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

Holmans, P. ; Moskvina, V. ; Jones, L. ; Sharma, M. ; Vedernikov, A. ; Buchel, F. ; Saad, M. ; Bras, J. M. ; Bettella, F. ; Nicolaou, N. ; Simon-Sanchez, J. ; Mittag, F. ; Gibbs, J. R. ; Schulte, C. ; Durr, A. ; Guerreiro, R. ; Hernandez, D. ; Brice, A. ; Stefansson, H. ; Majamaa, K. ; Gasser, T. ; Heutink, P. ; Wood, N. W. ; Martinez, M. ; Singleton, A. B. ; Nalls, M. A. ; Hardy, J. ; Morris, H. R. ; Williams, N. M.

Human molecular genetics, 2014-01, Vol.23 (2), p.562-562 [Periódico revisado por pares]

Oxford University Press

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3
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
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Artigo
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Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

Wood, Andrew R ; Hernandez, Dena G ; Nalls, Michael A ; Yaghootkar, Hanieh ; Gibbs, J. Raphael ; Harries, Lorna W ; Chong, Sean ; Moore, Matthew ; Weedon, Michael N ; Guralnik, Jack M ; Bandinelli, Stefania ; Murray, Anna ; Ferrucci, Luigi ; Singleton, Andrew B ; Melzer, David ; Frayling, Timothy M

Human molecular genetics, 2011-10, Vol.20 (20), p.4082-4092 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
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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5
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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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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6
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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7
Distinct DNA methylation changes highly correlated with chronological age in the human brain
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Distinct DNA methylation changes highly correlated with chronological age in the human brain

HERNANDEZ, Dena G ; NALLS, Michael A ; SINGLETON, Andrew B ; RAPHAEL GIBBS, J ; AREPALLI, Sampath ; VAN DER BRUG, Marcel ; CHONG, Sean ; MOORE, Matthew ; LONGO, Dan L ; COOKSON, Mark R ; TRAYNOR, Bryan J

Human molecular genetics, 2011-03, Vol.20 (6), p.1164-1172 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies
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Artigo
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Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

Bras, Jose ; Guerreiro, Rita ; Darwent, Lee ; Parkkinen, Laura ; Ansorge, Olaf ; Escott-Price, Valentina ; Hernandez, Dena G ; Nalls, Michael A ; Clark, Lorraine N ; Honig, Lawrence S ; Marder, Karen ; Van Der Flier, Wiesje M ; Lemstra, Afina ; Scheltens, Philip ; Rogaeva, Ekaterina ; St George-Hyslop, Peter ; Londos, Elisabet ; Zetterberg, Henrik ; Ortega-Cubero, Sara ; Pastor, Pau ; Ferman, Tanis J ; Graff-Radford, Neill R ; Ross, Owen A ; Barber, Imelda ; Braae, Anne ; Brown, Kristelle ; Morgan, Kevin ; Maetzler, Walter ; Berg, Daniela ; Troakes, Claire ; Al-Sarraj, Safa ; Lashley, Tammaryn ; Compta, Yaroslau ; Revesz, Tamas ; Lees, Andrew ; Cairns, Nigel ; Halliday, Glenda M ; Mann, David ; Pickering-Brown, Stuart ; Dickson, Dennis W ; Singleton, Andrew ; Hardy, John

Human molecular genetics, 2014-12, Vol.23 (23), p.6139-6146 [Periódico revisado por pares]

England: Oxford University Press

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9
Genetic variation associated with circulating monocyte count in the eMERGE Network
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Artigo
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Genetic variation associated with circulating monocyte count in the eMERGE Network

Crosslin, David R ; McDavid, Andrew ; Weston, Noah ; Zheng, Xiuwen ; Hart, Eugene ; de Andrade, Mariza ; Kullo, Iftikhar J ; McCarty, Catherine A ; Doheny, Kimberly F ; Pugh, Elizabeth ; Kho, Abel ; Hayes, M Geoffrey ; Ritchie, Marylyn D ; Saip, Alexander ; Crawford, Dana C ; Crane, Paul K ; Newton, Katherine ; Carrell, David S ; Gallego, Carlos J ; Nalls, Michael A ; Li, Rongling ; Mirel, Daniel B ; Crenshaw, Andrew ; Couper, David J ; Tanaka, Toshiko ; van Rooij, Frank J A ; Chen, Ming-Huei ; Smith, Albert V ; Zakai, Neil A ; Yango, Qiong ; Garcia, Melissa ; Liu, Yongmei ; Lumley, Thomas ; Folsom, Aaron R ; Reiner, Alex P ; Felix, Janine F ; Dehghan, Abbas ; Wilson, James G ; Bis, Joshua C ; Fox, Caroline S ; Glazer, Nicole L ; Cupples, L Adrienne ; Coresh, Josef ; Eiriksdottir, Gudny ; Gudnason, Vilmundur ; Bandinelli, Stefania ; Frayling, Timothy M ; Chakravarti, Aravinda ; van Duijn, Cornelia M ; Melzer, David ; Levy, Daniel ; Boerwinkle, Eric ; Singleton, Andrew B ; Hernandez, Dena G ; Longo, Dan L ; Witteman, Jacqueline C M ; Psaty, Bruce M ; Ferrucci, Luigi ; Harris, Tamara B ; O'Donnell, Christopher J ; Ganesh, Santhi K ; Larson, Eric B ; Carlson, Chris S ; Jarvik, Gail P

Human molecular genetics, 2013-05, Vol.22 (10), p.2119-2127 [Periódico revisado por pares]

England: Oxford University Press

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10
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
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Artigo
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Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network

Chen, Zhao ; Tang, Hua ; Qayyum, Rehan ; Schick, Ursula M ; Nalls, Michael A ; Handsaker, Robert ; Li, Jin ; Lu, Yingchang ; Yanek, Lisa R ; Keating, Brendan ; Meng, Yan ; van Rooij, Frank JA ; Okada, Yukinori ; Kubo, Michiaki ; Rasmussen-Torvik, Laura ; Keller, Margaux F ; Lange, Leslie ; Evans, Michele ; Bottinger, Erwin P ; Linderman, Michael D ; Ruderfer, Douglas M ; Hakonarson, Hakon ; Papanicolaou, George ; Zonderman, Alan B ; Gottesman, Omri ; Project, CHARGE Consortium BioBank Japan ; Thomson, Cynthia ; Ziv, Elad ; Singleton, Andrew B ; Loos, Ruth JF ; Sleiman, Patrick MA ; Ganesh, Santhi ; McCarroll, Steven ; Becker, Diane M ; Wilson, James G ; Lettre, Guillaume ; Reiner, Alexander P

Human Molecular Genetics, 2013-06, Vol.22 (12), p.2529-2538

eScholarship, University of California

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