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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
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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2
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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3
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 [Periódico revisado por pares]

United States: Public Library of Science

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4
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
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Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

Chauhan, Ganesh ; Arnold, Corey R ; Chu, Audrey Y ; Reyahi, Azadeh ; Bis, Joshua C ; Havulinna, Aki S ; Trompet, Stella ; Manichaikul, Ani ; Teumer, Alexander ; Gustafsson, Stefan ; Bartz, Traci M ; Bellenguez, Céline ; Vidal, Jean Sebastien ; Kjartansson, Olafur ; Satizabal, Claudia L ; Xue, Flora ; Liu, Yongmei ; Bevan, Steve ; Hopewell, Jemma C ; Heckbert, Susan R ; Rice, Kenneth ; Smith, Nicholas L ; Levi, Christopher ; Sharma, Pankaj ; Sudlow, Cathie LM ; Cole, John W ; Schmidt, Reinhold ; Meschia, James ; Thijs, Vincent ; Melander, Olle ; Grewal, Raji P ; Sacco, Ralph L ; Rundek, Tatjana ; Rothwell, Peter M ; Jern, Christina ; Johnson, Julie A ; Benavente, Oscar R ; Lee, Jin-Moo ; Wong, Quenna ; Aparicio, Hugo J ; Engelter, Stefan T ; Kloss, Manja ; Pezzini, Alessandro ; Buring, Julie E ; Ridker, Paul M ; Berr, Claudine ; Dartigues, Jean-François ; Hamsten, Anders ; Traylor, Matthew ; Pedersen, Nancy L ; Lannfelt, Lars ; Morris, Andrew P ; Jimenez-Conde, Jordi ; Montaner, Joan ; Slowik, Agnieszka ; Woo, Daniel ; Hofman, Albert ; Koudstaal, Peter J ; Portegies, Marileen L P ; Uitterlinden, André G ; Ford, Ian ; Jukema, J Wouter ; Stott, David J ; Allen, Norrina B ; Johnson, Andrew D ; De Jager, Philip L ; White, Charles C ; Markus, Marcello Ricardo Paulista ; Schminke, Ulf ; Boncoraglio, Giorgio B ; Clarke, Robert ; Kamatani, Yoichiro ; Dallongeville, Jean ; Rotter, Jerome I ; Nalls, Michael A ; Griswold, Michael E ; Knopman, David S ; Windham, B Gwen ; Beiser, Alexa ; Vartiainen, Erkki ; French, Curtis R ; Pastinen, Tomi ; Gudnason, Vilmundur ; Kurth, Tobias ; Harris, Tamara B ; Rich, Stephen S ; deStefano, Anita L ; Rosand, Jonathan ; Mosley, Thomas H ; Ingelsson, Erik ; van Duijn, Cornelia M ; Tzourio, Christophe ; Rexrode, Kathryn M ; Lehmann, Ordan J ; Launer, Lenore J ; Carlsson, Peter ; Chasman, Daniel I ; Childs, Sarah J ; Seshadri, Sudha ; Debette, Stéphanie

Lancet neurology, 2016-06, Vol.15 (7), p.695-707 [Periódico revisado por pares]

England: Elsevier Ltd

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5
Frontotemporal dementia and its subtypes: a genome-wide association study
Frontotemporal dementia and its subtypes: a genome-wide association study
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Frontotemporal dementia and its subtypes: a genome-wide association study

Hernandez, Dena G, MSc ; Nalls, Michael A, PhD ; Kwok, John B J, PhD ; Dobson-Stone, Carol, PhD ; Brooks, William S, MBBS ; Schofield, Peter R, Prof ; Halliday, Glenda M, Prof ; Hodges, John R, Prof ; Piguet, Olivier, PhD ; Bartley, Lauren, MSc ; Thompson, Elizabeth, MD ; Haan, Eric, Prof ; Ruiz, Agustín, MD ; Boada, Mercè, MD ; Borroni, Barbara, MD ; Cruchaga, Carlos, PhD ; Benussi, Luisa, PhD ; Galimberti, Daniela, PhD ; Fenoglio, Chiara, PhD ; Serpente, Maria, PhD ; Scarpini, Elio, MD ; Lleó, Alberto, MD ; Waldö, Maria Landqvist, MD ; Nilsson, Karin, PhD ; Hsiung, Ging-Yuek R, MD ; Mann, David M A, Prof ; Morris, Christopher M, PhD ; Attems, Johannes, Prof ; Griffiths, Timothy D, Prof ; McKeith, Ian G, Prof ; Thomas, Alan J, Prof ; Huey, Edward D, MD ; Jaros, Evelyn, PhD ; Pastor, Pau, MD ; Razquin, Cristina, PhD ; Ortega-Cubero, Sara, MD ; Alonso, Elena, BSc ; Perneczky, Robert, MD ; Alexopoulos, Panagiotis, MD ; Kurz, Alexander, MD ; Rubino, Elisa, MD ; Pinessi, Lorenzo, Prof ; St George-Hyslop, Peter, MD ; Rowe, James B, PhD ; Schlachetzki, Johannes C M, MD ; Uphill, James, BSc ; Mead, Simon, Prof ; Danek, Adrian, MD ; Van Deerlin, Vivianna M, PhD ; van der Zee, Julie, PhD ; Deschamps, William, MSc ; Van Broeckhoven, Christine, Prof ; Cappa, Stefano F, Prof ; Le Ber, Isabelle, MD ; Vercelletto, Martine, MD ; Brice, Alexis, MD ; Nacmias, Benedetta, PhD ; Piaceri, Irene, PhD ; Nielsen, Jørgen E, MD ; Hjermind, Lena E, MD ; Riemenschneider, Matthias, Prof ; Gasparoni, Gilles, PhD ; Gu, Wei, PhD ; Rossor, Martin N, Prof ; Fox, Nick C, Prof ; Morris, Huw R, Prof ; Rizzu, Patrizia, PhD ; Heutink, Peter, Prof ; Snowden, Julie S, Prof ; Rollinson, Sara, PhD ; Richardson, Anna, MB ; Bruni, Amalia C, MD ; Maletta, Raffaele, MD ; Frangipane, Francesca, MD ; Bernardi, Livia, PhD ; Anfossi, Maria, PhD ; Gallo, Maura, PhD ; Conidi, Maria Elena, PhD ; Smirne, Nicoletta, BSc ; Baker, Matt, BSc ; Dickson, Dennis W, Prof ; Petersen, Ronald C, Prof ; Boeve, Bradley F, Prof ; Seeley, William W, MD ; Miller, Bruce L, Prof ; Karydas, Anna M, BA ; Rosen, Howard, Prof ; van Swieten, John C, Prof ; Scheltens, Philip, Prof ; Capozzo, Rosa, MD ; Franceschi, Massimo, MD ; Postiglione, Alfredo, Prof ; Chiang, Huei-Hsin, PhD ; Graff, Caroline, Prof ; Rollin, Adeline, MD ; Deramecourt, Vincent, MD ; Lebert, Florence, MD ; Kapogiannis, Dimitrios, MD ; Pickering-Brown, Stuart, Prof ; Hardy, John, Prof

Lancet neurology, 2014-07, Vol.13 (7), p.686-699 [Periódico revisado por pares]

England: Elsevier Ltd

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6
Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry
Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry
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Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry

N'Diaye, Amidou ; Chen, Gary K ; Palmer, Cameron D ; Ge, Bing ; Tayo, Bamidele ; Mathias, Rasika A ; Ding, Jingzhong ; Nalls, Michael A ; Adeyemo, Adebowale ; Adoue, Véronique ; Ambrosone, Christine B ; Atwood, Larry ; Bandera, Elisa V ; Becker, Lewis C ; Berndt, Sonja I ; Bernstein, Leslie ; Blot, William J ; Boerwinkle, Eric ; Britton, Angela ; Casey, Graham ; Chanock, Stephen J ; Demerath, Ellen ; Deming, Sandra L ; Diver, W Ryan ; Fox, Caroline ; Harris, Tamara B ; Hernandez, Dena G ; Hu, Jennifer J ; Ingles, Sue A ; John, Esther M ; Johnson, Craig ; Keating, Brendan ; Kittles, Rick A ; Kolonel, Laurence N ; Kritchevsky, Stephen B ; Le Marchand, Loic ; Lohman, Kurt ; Liu, Jiankang ; Millikan, Robert C ; Murphy, Adam ; Musani, Solomon ; Neslund-Dudas, Christine ; North, Kari E ; Nyante, Sarah ; Ogunniyi, Adesola ; Ostrander, Elaine A ; Papanicolaou, George ; Patel, Sanjay ; Pettaway, Curtis A ; Press, Michael F ; Redline, Susan ; Rodriguez-Gil, Jorge L ; Rotimi, Charles ; Rybicki, Benjamin A ; Salako, Babatunde ; Schreiner, Pamela J ; Signorello, Lisa B ; Singleton, Andrew B ; Stanford, Janet L ; Stram, Alex H ; Stram, Daniel O ; Strom, Sara S ; Suktitipat, Bhoom ; Thun, Michael J ; Witte, John S ; Yanek, Lisa R ; Ziegler, Regina G ; Zheng, Wei ; Zhu, Xiaofeng ; Zmuda, Joseph M ; Zonderman, Alan B ; Evans, Michele K ; Liu, Yongmei ; Becker, Diane M ; Cooper, Richard S ; Pastinen, Tomi ; Henderson, Brian E ; Hirschhorn, Joel N ; Lettre, Guillaume ; Haiman, Christopher A Visscher, Peter M.

PLoS genetics, 2011-10, Vol.7 (10), p.e1002298 [Periódico revisado por pares]

United States: Public Library of Science

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7
Genome-wide association study of retinopathy in individuals without diabetes
Genome-wide association study of retinopathy in individuals without diabetes
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Genome-wide association study of retinopathy in individuals without diabetes

Jensen, Richard A ; Sim, Xueling ; Li, Xiaohui ; Cotch, Mary Frances ; Ikram, M Kamran ; Holliday, Elizabeth G ; Eiriksdottir, Gudny ; Harris, Tamara B ; Jonasson, Fridbert ; Klein, Barbara E K ; Launer, Lenore J ; Smith, Albert Vernon ; Boerwinkle, Eric ; Cheung, Ning ; Hewitt, Alex W ; Liew, Gerald ; Mitchell, Paul ; Wang, Jie Jin ; Attia, John ; Scott, Rodney ; Glazer, Nicole L ; Lumley, Thomas ; McKnight, Barbara ; Psaty, Bruce M ; Taylor, Kent ; Hofman, Albert ; de Jong, Paulus T V M ; Rivadeneira, Fernando ; Uitterlinden, Andre G ; Tay, Wan-Ting ; Teo, Yik Ying ; Seielstad, Mark ; Liu, Jianjun ; Cheng, Ching-Yu ; Saw, Seang-Mei ; Aung, Tin ; Ganesh, Santhi K ; O'Donnell, Christopher J ; Nalls, Mike A ; Wiggins, Kerri L ; Kuo, Jane Z ; van Duijn, Cornelia M ; Gudnason, Vilmundur ; Klein, Ronald ; Siscovick, David S ; Rotter, Jerome I ; Tai, E Shong ; Vingerling, Johannes ; Wong, Tien Y Mittal, Balraj

PloS one, 2013-02, Vol.8 (2), p.e54232-e54232 [Periódico revisado por pares]

United States: Public Library of Science

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8
Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort
Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort
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Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort

Heckerman, David ; Traynor, Bryan J ; Picca, Anna ; Calvani, Riccardo ; Marzetti, Emanuele ; Hernandez, Dena ; Nalls, Michael ; Arepali, Sampath ; Ferrucci, Luigi ; Landi, Francesco

Scientific reports, 2017-11, Vol.7 (1), p.15879-9, Article 15879 [Periódico revisado por pares]

England: Nature Publishing Group

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