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1
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
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Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Lee, James J ; Wedow, Robbee ; Okbay, Aysu ; Kong, Edward ; Maghzian, Omeed ; Zacher, Meghan ; Nguyen-Viet, Tuan Anh ; Bowers, Peter ; Sidorenko, Julia ; Karlsson Linnér, Richard ; Fontana, Mark Alan ; Kundu, Tushar ; Lee, Chanwook ; Li, Hui ; Li, Ruoxi ; Royer, Rebecca ; Timshel, Pascal N ; Walters, Raymond K ; Willoughby, Emily A ; Yengo, Loïc ; Alver, Maris ; Bao, Yanchun ; Clark, David W ; Day, Felix R ; Furlotte, Nicholas A ; Joshi, Peter K ; Kemper, Kathryn E ; Kleinman, Aaron ; Langenberg, Claudia ; Mägi, Reedik ; Trampush, Joey W ; Verma, Shefali Setia ; Wu, Yang ; Lam, Max ; Zhao, Jing Hua ; Zheng, Zhili ; Boardman, Jason D ; Campbell, Harry ; Freese, Jeremy ; Harris, Kathleen Mullan ; Hayward, Caroline ; Herd, Pamela ; Kumari, Meena ; Lencz, Todd ; Luan, Jian'an ; Malhotra, Anil K ; Metspalu, Andres ; Milani, Lili ; Ong, Ken K ; Perry, John R B ; Porteous, David J ; Ritchie, Marylyn D ; Smart, Melissa C ; Smith, Blair H ; Tung, Joyce Y ; Wareham, Nicholas J ; Wilson, James F ; Beauchamp, Jonathan P ; Conley, Dalton C ; Esko, Tõnu ; Lehrer, Steven F ; Magnusson, Patrik K E ; Oskarsson, Sven ; Pers, Tune H ; Robinson, Matthew R ; Thom, Kevin ; Watson, Chelsea ; Chabris, Christopher F ; Meyer, Michelle N ; Laibson, David I ; Yang, Jian ; Johannesson, Magnus ; Koellinger, Philipp D ; Turley, Patrick ; Visscher, Peter M ; Benjamin, Daniel J ; Cesarini, David

Nature genetics, 2018-08, Vol.50 (8), p.1112-1121 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
An atlas of genetic influences on osteoporosis in humans and mice
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Artigo
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An atlas of genetic influences on osteoporosis in humans and mice

Morris, John A ; Kemp, John P ; Youlten, Scott E ; Laurent, Laetitia ; Logan, John G ; Chai, Ryan C ; Vulpescu, Nicholas A ; Forgetta, Vincenzo ; Kleinman, Aaron ; Mohanty, Sindhu T ; Sergio, C Marcelo ; Quinn, Julian ; Nguyen-Yamamoto, Loan ; Luco, Aimee-Lee ; Vijay, Jinchu ; Simon, Marie-Michelle ; Pramatarova, Albena ; Medina-Gomez, Carolina ; Trajanoska, Katerina ; Ghirardello, Elena J ; Butterfield, Natalie C ; Curry, Katharine F ; Leitch, Victoria D ; Sparkes, Penny C ; Adoum, Anne-Tounsia ; Mannan, Naila S ; Komla-Ebri, Davide S K ; Pollard, Andrea S ; Dewhurst, Hannah F ; Hassall, Thomas A D ; Beltejar, Michael-John G ; Adams, Douglas J ; Vaillancourt, Suzanne M ; Kaptoge, Stephen ; Baldock, Paul ; Cooper, Cyrus ; Reeve, Jonathan ; Ntzani, Evangelia E ; Evangelou, Evangelos ; Ohlsson, Claes ; Karasik, David ; Rivadeneira, Fernando ; Kiel, Douglas P ; Tobias, Jonathan H ; Gregson, Celia L ; Harvey, Nicholas C ; Grundberg, Elin ; Goltzman, David ; Adams, David J ; Lelliott, Christopher J ; Hinds, David A ; Ackert-Bicknell, Cheryl L ; Hsu, Yi-Hsiang ; Maurano, Matthew T ; Croucher, Peter I ; Williams, Graham R ; Bassett, J H Duncan ; Evans, David M ; Richards, J Brent

Nature genetics, 2019-02, Vol.51 (2), p.258-266 [Periódico revisado por pares]

United States: Nature Publishing Group

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3
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
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Artigo
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

Karlsson Linnér, Richard ; Biroli, Pietro ; Kong, Edward ; Meddens, S Fleur W ; Wedow, Robbee ; Fontana, Mark Alan ; Lebreton, Maël ; Tino, Stephen P ; Abdellaoui, Abdel ; Hammerschlag, Anke R ; Nivard, Michel G ; Okbay, Aysu ; Rietveld, Cornelius A ; Timshel, Pascal N ; Trzaskowski, Maciej ; Vlaming, Ronald de ; Zünd, Christian L ; Bao, Yanchun ; Buzdugan, Laura ; Caplin, Ann H ; Chen, Chia-Yen ; Eibich, Peter ; Fontanillas, Pierre ; Gonzalez, Juan R ; Joshi, Peter K ; Karhunen, Ville ; Kleinman, Aaron ; Levin, Remy Z ; Lill, Christina M ; Meddens, Gerardus A ; Muntané, Gerard ; Sanchez-Roige, Sandra ; Rooij, Frank J van ; Taskesen, Erdogan ; Wu, Yang ; Zhang, Futao ; Auton, Adam ; Boardman, Jason D ; Clark, David W ; Conlin, Andrew ; Dolan, Conor C ; Fischbacher, Urs ; Groenen, Patrick J F ; Harris, Kathleen Mullan ; Hasler, Gregor ; Hofman, Albert ; Ikram, Mohammad A ; Jain, Sonia ; Karlsson, Robert ; Kessler, Ronald C ; Kooyman, Maarten ; MacKillop, James ; Männikkö, Minna ; Morcillo-Suarez, Carlos ; McQueen, Matthew B ; Schmidt, Klaus M ; Smart, Melissa C ; Sutter, Matthias ; Thurik, A Roy ; Uitterlinden, André G ; White, Jon ; Wit, Harriet de ; Yang, Jian ; Bertram, Lars ; Boomsma, Dorret I ; Esko, Tõnu ; Fehr, Ernst ; Hinds, David A ; Johannesson, Magnus ; Kumari, Meena ; Laibson, David ; Magnusson, Patrik K E ; Meyer, Michelle N ; Navarro, Arcadi ; Palmer, Abraham A ; Pers, Tune H ; Posthuma, Danielle ; Schunk, Daniel ; Stein, Murray B ; Svento, Rauli ; Tiemeier, Henning ; Timmers, Paul R H J ; Turley, Patrick ; Ursano, Robert J ; Wagner, Gert G ; Wilson, James F ; Gratten, Jacob ; Lee, James J ; Cesarini, David ; Benjamin, Daniel J ; Koellinger, Philipp D ; Beauchamp, Jonathan P

Nature genetics, 2019-02, Vol.51 (2), p.245-257 [Periódico revisado por pares]

United States: Nature Publishing Group

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4
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
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Artigo
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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Mahajan, Anubha ; Petty, Lauren E ; Chiou, Joshua ; Miguel-Escalada, Irene ; Nakatochi, Masahiro ; Huerta-Chagoya, Alicia ; Bielak, Lawrence F ; Hai, Yang ; Kals, Mart ; Grarup, Niels ; Wuttke, Matthias ; Nousome, Darryl ; Long, Jirong ; Ahmad, Meraj ; Jensen, Richard A ; An, Ping ; Cade, Brian E ; Abaitua, Fernando ; Akiyama, Masato ; Bertoni, Alain ; Bian, Zheng ; Brummett, Chad M ; Chee, Miao-Li ; Das, Swapan K ; Du, Shufa ; Duan, Qing ; Eckardt, Kai-Uwe ; Fischer, Krista ; Floyd, James S ; Genter, Pauline ; González-Villalpando, Maria Elena ; Gordon-Larsen, Penny ; Gorkin, David ; Herder, Christian ; Hung, Yi-Jen ; Hwu, Chii-Min ; Ikram, Mohammad Arfan ; Ingelsson, Martin ; Islam, Md Tariqul ; Isono, Masato ; Kamatani, Yoichiro ; Katsuya, Tomohiro ; Khor, Chiea-Chuen ; Kohara, Katsuhiko ; Kriebel, Jennifer ; Kuusisto, Johanna ; Läll, Kristi ; Leong, Aaron ; Luan, Jian'an ; Lv, Jun ; Lyssenko, Valeriya ; Meitinger, Thomas ; Morris, Andrew D ; Nadkarni, Girish N ; Nayak, Uma ; Ntalla, Ioanna ; Peters, Annette ; Preissl, Sebastian ; Rasmussen-Torvik, Laura J ; Roden, Michael ; Sabanayagam, Charumathi ; Schönherr, Sebastian ; Shahriar, Mohammad ; Shi, Jinxiu ; Stančáková, Alena ; Strauch, Konstantin ; Thorleifsson, Gudmar ; Thorsteinsdottir, Unnur ; Tsai, Fuu-Jen ; Tusie-Luna, Teresa ; Udler, Miriam S ; Valladares-Salgado, Adan ; Yajnik, Chittaranjan S ; Yoon, Kyungheon ; Igase, Michiya ; Hanis, Craig L ; Ingelsson, Erik ; Zeggini, Eleftheria ; Rich, Stephen S ; Kooperberg, Charles ; Engert, James C ; Wilson, James G ; Kardia, Sharon L R ; Groop, Leif ; Bharadwaj, Dwaipayan ; Sale, Michèle M ; Cruz, Miguel ; Tai, E-Shyong ; Kato, Norihiro ; Laakso, Markku ; Köttgen, Anna ; Loos, Ruth J F ; Saleheen, Danish ; Hansen, Torben ; Kadowaki, Takashi ; Walters, Robin G ; Stefansson, Kari ; Meigs, James B ; Gloyn, Anna L ; Chambers, John C

Nature genetics, 2022-05, Vol.54 (5), p.560-572 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk
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Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk

Castel, Stephane E ; Cervera, Alejandra ; Mohammadi, Pejman ; Aguet, François ; Reverter, Ferran ; Wolman, Aaron ; Guigo, Roderic ; Iossifov, Ivan ; Vasileva, Ana ; Lappalainen, Tuuli

Nature genetics, 2018-09, Vol.50 (9), p.1327-1334 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
Signatures of negative selection in the genetic architecture of human complex traits
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Artigo
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Signatures of negative selection in the genetic architecture of human complex traits

Zeng, Jian ; de Vlaming, Ronald ; Wu, Yang ; Robinson, Matthew R ; Lloyd-Jones, Luke R ; Yengo, Loic ; Yap, Chloe X ; Xue, Angli ; Sidorenko, Julia ; McRae, Allan F ; Powell, Joseph E ; Montgomery, Grant W ; Metspalu, Andres ; Esko, Tonu ; Gibson, Greg ; Wray, Naomi R ; Visscher, Peter M ; Yang, Jian

Nature genetics, 2018-05, Vol.50 (5), p.746-753 [Periódico revisado por pares]

United States: Nature Publishing Group

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7
Fine-mapping from summary data with the "Sum of Single Effects" model
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Artigo
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Fine-mapping from summary data with the "Sum of Single Effects" model

Zou, Yuxin ; Carbonetto, Peter ; Wang, Gao ; Stephens, Matthew Epstein, Michael P.

PLoS genetics, 2022-07, Vol.18 (7), p.e1010299-e1010299 [Periódico revisado por pares]

United States: Public Library of Science

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8
Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits
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Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits

Evans, Luke M ; Tahmasbi, Rasool ; Vrieze, Scott I ; Abecasis, Gonçalo R ; Das, Sayantan ; Gazal, Steven ; Bjelland, Douglas W ; de Candia, Teresa R ; Goddard, Michael E ; Neale, Benjamin M ; Yang, Jian ; Visscher, Peter M ; Keller, Matthew C

Nature genetics, 2018-05, Vol.50 (5), p.737-745 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
CHiCAGO: robust detection of DNA looping interactions in Capture Hi-C data
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CHiCAGO: robust detection of DNA looping interactions in Capture Hi-C data

Cairns, Jonathan ; Freire-Pritchett, Paula ; Wingett, Steven W ; Várnai, Csilla ; Dimond, Andrew ; Plagnol, Vincent ; Zerbino, Daniel ; Schoenfelder, Stefan ; Javierre, Biola-Maria ; Osborne, Cameron ; Fraser, Peter ; Spivakov, Mikhail

Genome Biology, 2016-06, Vol.17 (1), p.127-127, Article 127 [Periódico revisado por pares]

England: BioMed Central Ltd

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10
High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction
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High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction

McClay, Joseph L ; Shabalin, Andrey A ; Dozmorov, Mikhail G ; Adkins, Daniel E ; Kumar, Gaurav ; Nerella, Srilaxmi ; Clark, Shaunna L ; Bergen, Sarah E ; Hultman, Christina M ; Magnusson, Patrik K E ; Sullivan, Patrick F ; Aberg, Karolina A ; van den Oord, Edwin J C G

Genome Biology, 2015-12, Vol.16 (1), p.291-291, Article 291 [Periódico revisado por pares]

England: BioMed Central Ltd

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