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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
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
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, 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
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
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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
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
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
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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
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
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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7
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
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 [Periódico revisado por pares]

England: Oxford University Press

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8
Distinct DNA methylation changes highly correlated with chronological age in the human brain
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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9
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies
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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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10
Genetic variation associated with circulating monocyte count in the eMERGE Network
Genetic variation associated with circulating monocyte count in the eMERGE Network
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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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