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Common variants at 12q14 and 12q24 are associated with hippocampal volume
Common variants at 12q14 and 12q24 are associated with hippocampal volume
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Common variants at 12q14 and 12q24 are associated with hippocampal volume

Bis, Joshua C ; DeCarli, Charles ; Smith, Albert Vernon ; van der Lijn, Fedde ; Crivello, Fabrice ; Fornage, Myriam ; Debette, Stephanie ; Shulman, Joshua M ; Schmidt, Helena ; Srikanth, Velandai ; Schuur, Maaike ; Yu, Lei ; Choi, Seung-Hoan ; Sigurdsson, Sigurdur ; Verhaaren, Benjamin F J ; DeStefano, Anita L ; Lambert, Jean-Charles ; Jack, Jr, Clifford R ; Struchalin, Maksim ; Stankovich, Jim ; Ibrahim-Verbaas, Carla A ; Fleischman, Debra ; Zijdenbos, Alex ; den Heijer, Tom ; Mazoyer, Bernard ; Coker, Laura H ; Enzinger, Christian ; Danoy, Patrick ; Amin, Najaf ; Arfanakis, Konstantinos ; van Buchem, Mark A ; de Bruijn, Renée F A G ; Beiser, Alexa ; Dufouil, Carole ; Huang, Juebin ; Cavalieri, Margherita ; Thomson, Russell ; Niessen, Wiro J ; Chibnik, Lori B ; Gislason, Gauti K ; Hofman, Albert ; Pikula, Aleksandra ; Amouyel, Philippe ; Freeman, Kevin B ; Phan, Thanh G ; Oostra, Ben A ; Stein, Jason L ; Medland, Sarah E ; Vasquez, Alejandro Arias ; Hibar, Derrek P ; Wright, Margaret J ; Franke, Barbara ; Martin, Nicholas G ; Thompson, Paul M ; Nalls, Michael A ; Uitterlinden, Andre G ; Au, Rhoda ; Elbaz, Alexis ; Beare, Richard J ; van Swieten, John C ; Lopez, Oscar L ; Harris, Tamara B ; Chouraki, Vincent ; Breteler, Monique M B ; De Jager, Philip L ; Becker, James T ; Vernooij, Meike W ; Knopman, David ; Fazekas, Franz ; Wolf, Philip A ; van der Lugt, Aad ; Gudnason, Vilmundur ; Longstreth, Jr, W T ; Brown, Matthew A ; Bennett, David A ; van Duijn, Cornelia M ; Mosley, Thomas H ; Schmidt, Reinhold ; Tzourio, Christophe ; Launer, Lenore J ; Ikram, M Arfan ; Seshadri, Sudha

Nature genetics, 2012-05, Vol.44 (5), p.545-551 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
Common variants at 12ql4 and 12q24 are associated with hippocampal volume
Common variants at 12ql4 and 12q24 are associated with hippocampal volume
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Common variants at 12ql4 and 12q24 are associated with hippocampal volume

BIS, Joshua C ; DECARLI, Charles ; SCHUUR, Maaike ; LEI YU ; CHOI, Seung-Hoan ; SIGURDSSON, Sigurdur ; VERHAAREN, Benjamin F. J ; DESTEFANO, Anita L ; LAMBERT, Jean-Charles ; JACK, Clifford R ; STRUCHALIN, Maksim ; STANKOVICH, Jim ; SMITH, Albert Vernon ; IBRAHIM-VERBAAS, Carla A ; FLEISCHMAN, Debra ; ZIJDENBOS, Alex ; HEIJER, Tom Den ; MAZOYER, Bernard ; COKER, Laura H ; ENZINGER, Christian ; DANOY, Patrick ; AMIN, Najaf ; ARFANAKIS, Konstantinos ; DER LIJN, Fedde Van ; BUCHEM, Mark A.van ; DE BRUIJN, Renée F.a G ; BEISER, Alexa ; DUFOUIL, Carole ; JUEBIN HUANG ; CAVALIERI, Margherita ; THOMSON, Russell ; NIESSEN, Wiro J ; CHIBNIK, Lori B ; GISLASON, Gauti K ; CRIVELLO, Fabrice ; HOFMAN, Albert ; PIKULA, Aleksandra ; AMOUYEL, Philippe ; FREEMAN, Kevin B ; PHAN, Thanh G ; OOSTRA, Ben A ; STEIN, Jason L ; MEDLAND, Sarah E ; ARIAS VASQUEZ, Alejandro ; HIBAR, Derrek P ; FORNAGE, Myriam ; WRIGHT, Margaret J ; FRANKE, Barbara ; MARTIN, Nicholas G ; THOMPSON, Paul M ; NALLS, Michael A ; UITTERLINDEN, Andre G ; AU, Rhoda ; ELBAZ, Alexis ; BEARE, Richard J ; SWIETEN, John C.van ; DEBETTE, Stephanie ; SHULMAN, Joshua M ; SCHMIDT, Helena ; SRIKANTH, Velandai

Nature genetics, 2012, Vol.44 (5), p.545-551 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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3
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke
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Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

HOLLIDAY, Elizabeth G ; MAGUIRE, Jane M ; MALIK, Rainer ; MCEVOY, Mark ; BIROS, Erik ; LEWIS, Martin D ; LINCZ, Lisa F ; PEEL, Roseanne ; OLDMEADOW, Christopher ; SMITH, Wayne ; MOSCATO, Pablo ; BARLERA, Simona ; EVANS, Tiffany-Jane ; BEVAN, Steve ; BIS, Joshua C ; BOERWINKLE, Eric ; BONCORAGLIO, Giorgio B ; BROTT, Thomas G ; BROWN, Robert D ; CHENG, Yu-Ching ; COLE, John W ; COTLARCIUC, Ioana ; DEVAN, William J ; KOBLAR, Simon A ; FORNAGE, Myriam ; FURIE, Karen L ; GRETARSDOTTIR, Sólveig ; GSCHWENDTNER, Andreas ; IKRAM, M. Arfan ; LONGSTRETH, W. T ; MESCHIA, James F ; MITCHELL, Braxton D ; MOSLEY, Thomas H ; NAILS, Michael A ; JANNES, Jim ; PARATI, Eugenio A ; PSATY, Bruce M ; SHARMA, Pankaj ; STEFANSSON, Kari ; THORLEIFSSON, Gudmar ; THORSTEINSDOTTIR, Unnur ; TRAYLOR, Matthew ; VERHAAREN, Benjamin F. J ; WIGGINS, Kerri L ; WORRALL, Bradford B ; STURM, Jonathan W ; SUDLOW, Cathie ; ROTHWELL, Peter M ; FARRALL, Martin ; DICHGANS, Martin ; ROSAND, Jonathan ; MARKUS, Hugh S ; SCOTT, Rodney J ; LEVI, Christopher ; ATTIA, John ; HANKEY, Graeme J ; BAKER, Ross ; GOLLEDGE, Jonathan ; PARSONS, Mark W

Nature genetics, 2012-10, Vol.44 (10), p.1147-1151 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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4
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection
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Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection

Debette, Stéphanie ; Kamatani, Yoichiro ; Metso, Tiina M ; Kloss, Manja ; Chauhan, Ganesh ; Engelter, Stefan T ; Pezzini, Alessandro ; Thijs, Vincent ; Markus, Hugh S ; Dichgans, Martin ; Wolf, Christiane ; Dittrich, Ralf ; Touzé, Emmanuel ; Southerland, Andrew M ; Samson, Yves ; Abboud, Shérine ; Béjot, Yannick ; Caso, Valeria ; Bersano, Anna ; Gschwendtner, Andreas ; Sessa, Maria ; Cole, John ; Lamy, Chantal ; Medeiros, Elisabeth ; Beretta, Simone ; Bonati, Leo H ; Grau, Armin J ; Michel, Patrik ; Majersik, Jennifer J ; Sharma, Pankaj ; Kalashnikova, Ludmila ; Nazarova, Maria ; Dobrynina, Larisa ; Bartels, Eva ; Guillon, Benoit ; van den Herik, Evita G ; Fernandez-Cadenas, Israel ; Jood, Katarina ; Nalls, Michael A ; De Leeuw, Frank-Erik ; Jern, Christina ; Cheng, Yu-Ching ; Werner, Inge ; Metso, Antti J ; Lichy, Christoph ; Lyrer, Philippe A ; Brandt, Tobias ; Boncoraglio, Giorgio B ; Wichmann, Heinz-Erich ; Gieger, Christian ; Johnson, Andrew D ; Böttcher, Thomas ; Castellano, Maurizio ; Arveiler, Dominique ; Ikram, M Arfan ; Breteler, Monique M B ; Padovani, Alessandro ; Meschia, James F ; Kuhlenbäumer, Gregor ; Rolfs, Arndt ; Worrall, Bradford B ; Ringelstein, Erich-Bernd ; Zelenika, Diana ; Tatlisumak, Turgut ; Lathrop, Mark ; Leys, Didier ; Amouyel, Philippe ; Dallongeville, Jean

Nature genetics, 2015-01, Vol.47 (1), p.78-83 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
Defining the role of common variation in the genomic and biological architecture of adult human height
Defining the role of common variation in the genomic and biological architecture of adult human height
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Defining the role of common variation in the genomic and biological architecture of adult human height

Wood, Andrew R ; Esko, Tonu ; Yang, Jian ; Vedantam, Sailaja ; Pers, Tune H ; Gustafsson, Stefan ; Chu, Audrey Y ; Estrada, Karol ; Luan, Jian'an ; Kutalik, Zoltán ; Amin, Najaf ; Buchkovich, Martin L ; Croteau-Chonka, Damien C ; Day, Felix R ; Duan, Yanan ; Fall, Tove ; Fehrmann, Rudolf ; Ferreira, Teresa ; Jackson, Anne U ; Karjalainen, Juha ; Lo, Ken Sin ; Locke, Adam E ; Mägi, Reedik ; Mihailov, Evelin ; Porcu, Eleonora ; Randall, Joshua C ; Scherag, André ; Vinkhuyzen, Anna AE ; Westra, Harm-Jan ; Winkler, Thomas W ; Workalemahu, Tsegaselassie ; Zhao, Jing Hua ; Absher, Devin ; Albrecht, Eva ; Anderson, Denise ; Baron, Jeffrey ; Beekman, Marian ; Demirkan, Ayse ; Ehret, Georg B ; Feenstra, Bjarke ; Feitosa, Mary F ; Fischer, Krista ; Fraser, Ross M ; Goel, Anuj ; Gong, Jian ; Justice, Anne E ; Kanoni, Stavroula ; Kleber, Marcus E ; Kristiansson, Kati ; Lim, Unhee ; Lotay, Vaneet ; Lui, Julian C ; Mangino, Massimo ; Leach, Irene Mateo ; Medina-Gomez, Carolina ; Nalls, Michael A ; Nyholt, Dale R ; Palmer, Cameron D ; Pasko, Dorota ; Pechlivanis, Sonali ; Prokopenko, Inga ; Ried, Janina S ; Ripke, Stephan ; Shungin, Dmitry ; Stancáková, Alena ; Strawbridge, Rona J ; Sung, Yun Ju ; Tanaka, Toshiko ; Teumer, Alexander ; Trompet, Stella ; van der Laan, Sander W ; van Setten, Jessica ; Van Vliet-Ostaptchouk, Jana V ; Wang, Zhaoming ; Yengo, Loïc ; Zhang, Weihua ; Afzal, Uzma ; Ärnlöv, Johan ; Arscott, Gillian M ; Bandinelli, Stefania ; Barrett, Amy ; Bellis, Claire ; Bennett, Amanda J ; Berne, Christian ; Blüher, Matthias ; Bolton, Jennifer L ; Böttcher, Yvonne ; Boyd, Heather A ; Bruinenberg, Marcel ; Buckley, Brendan M ; Buyske, Steven ; Caspersen, Ida H ; Chines, Peter S ; Clarke, Robert ; Claudi-Boehm, Simone ; Cooper, Matthew ; Daw, E Warwick ; De Jong, Pim A ; Deelen, Joris ; Delgado, Graciela

Nature Genetics, 2014-11, Vol.46 (11), p.1173-1186

eScholarship, University of California

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6
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis
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Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

EMOND, Mary J ; LOUIE, Tin ; BARNES, Kathleen C ; GIBSON, Ronald L ; BAMSHAD, Michael J ; EMERSON, Julia ; WEI ZHAO ; MATHIAS, Rasika A ; KNOWLES, Michael R ; WRIGHT, Fred A ; RIEDER, Mark J ; TABOR, Holly K ; NICKERSON, Deborah A

Nature genetics, 2012-08, Vol.44 (8), p.886-889 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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7
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
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Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Albrecht, Eva ; Krumsiek, Jan ; Pistis, Giorgio ; Ruggiero, Daniela ; O'Seaghdha, Conall M ; Haller, Toomas ; Johnson, Andrew D ; Struchalin, Maksim ; Brown, Morris J ; Gaffo, Angelo L ; Pirastu, Nicola ; Hayward, Caroline ; Demirkan, Ayse ; Feitosa, Mary F ; Liu, Xuan ; Malerba, Giovanni ; van der Harst, Pim ; Kleber, Marcus E ; Murgia, Federico ; Wild, Sarah H ; Bakker, Stephan J L ; Peden, John F ; Dehghan, Abbas ; Lagou, Vasiliki ; Lehtimäki, Terho ; Woodward, Owen M ; Tin, Adrienne ; Putku, Margus ; Gislason, Gauti Kjartan ; Harris, Tamara B ; Schallert, Michael ; Montgomery, Grant W ; Nakamura, Yusuke ; Munroe, Patricia B ; Samani, Nilesh J ; Jacobs, Jr, David R ; D'Adamo, Pio ; Rotter, Jerome I ; Waeber, Gerard ; Devuyst, Olivier ; Hastie, Nicholas ; Khaw, Kay Tee ; Wareham, Nicholas J ; Isaacs, Aaron ; Holliday, Elizabeth G ; Viigimaa, Margus ; Metter, Jeffrey E ; Trabetti, Elisabetta ; Lattka, Eva ; Strauch, Konstantin ; Theis, Fabian ; Bruinenberg, Marcel ; Stolk, Ronald P ; Lucae, Susanne ; Smit, Johannes H ; Kirin, Mirna ; Mateo Leach, Irene ; van Gilst, Wiek H ; Goel, Anuj ; Hofman, Albert ; Rivadeneira, Fernando ; Imboden, Medea ; von Eckardstein, Arnold ; Cucca, Francesco ; Nauck, Matthias ; Schurmann, Claudia ; Budde, Kathrin ; Farrington, Susan M ; Prokopenko, Inga ; Spector, Tim D ; Sala, Cinzia ; Ridker, Paul M ; Kähönen, Mika ; Hengstenberg, Christian ; Nelson, Christopher P ; Meschia, James F ; Nalls, Michael A ; Laan, Maris ; Kloiber, Stefan ; Tore, Silvia ; Probst-Hensch, Nicole M ; Schmidt, Reinhold ; Fornage, Myriam ; Gasparini, Paolo ; Siscovick, David S ; Polašek, Ozren ; Rudan, Igor ; Metspalu, Andres ; van Duijn, Cornelia M ; Gambaro, Giovanni ; Wolffenbuttel, Bruce H R ; März, Winfried ; Gyllensten, Ulf ; Wright, Alan F ; Navis, Gerjan ; Watkins, Hugh ; Schipf, Sabine ; Dunlop, Malcolm G ; Kao, W H Linda ; Caulfield, Mark

Nature genetics, 2013-02, Vol.45 (2), p.145-154 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Warren, Helen R ; Evangelou, Evangelos ; Cabrera, Claudia P ; Gao, He ; Ren, Meixia ; Mifsud, Borbala ; Ntalla, Ioanna ; Surendran, Praveen ; Liu, Chunyu ; Cook, James P ; Kraja, Aldi T ; Drenos, Fotios ; Loh, Marie ; Verweij, Niek ; Marten, Jonathan ; Karaman, Ibrahim ; Lepe, Marcelo P Segura ; O'Reilly, Paul F ; Knight, Joanne ; Snieder, Harold ; Kato, Norihiro ; He, Jiang ; Tai, E Shyong ; Said, M Abdullah ; Porteous, David ; Alver, Maris ; Poulter, Neil ; Farrall, Martin ; Gansevoort, Ron T ; Padmanabhan, Sandosh ; Mägi, Reedik ; Stanton, Alice ; Connell, John ; Bakker, Stephan J L ; Metspalu, Andres ; Shields, Denis C ; Thom, Simon ; Brown, Morris ; Sever, Peter ; Esko, Tõnu ; Hayward, Caroline ; van der Harst, Pim ; Saleheen, Danish ; Chowdhury, Rajiv ; Chambers, John C ; Chasman, Daniel I ; Chakravarti, Aravinda ; Newton-Cheh, Christopher ; Lindgren, Cecilia M ; Levy, Daniel ; Kooner, Jaspal S ; Keavney, Bernard ; Tomaszewski, Maciej ; Samani, Nilesh J ; Howson, Joanna M M ; Tobin, Martin D ; Munroe, Patricia B ; Ehret, Georg B ; Wain, Louise V

Nature genetics, 2017-03, Vol.49 (3), p.403-415 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
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Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

International Stroke Genetics Consortium (ISGC) ; Wellcome Trust Case Control Consortium 2 (WTCCC2) ; Bellenguez, Céline ; Bevan, Steve ; Gschwendtner, Andreas ; Spencer, Chris CA ; Burgess, Annette I ; Pirinen, Matti ; Jackson, Caroline A ; Traylor, Matthew ; Strange, Amy ; Su, Zhan ; Band, Gavin ; Syme, Paul D ; Malik, Rainer ; Pera, Joanna ; Norrving, Bo ; Lemmens, Robin ; Freeman, Colin ; Schanz, Renata ; James, Tom ; Poole, Deborah ; Murphy, Lee ; Segal, Helen ; Cortellini, Lynelle ; Cheng, Yu-Ching ; Woo, Daniel ; Nalls, Michael A ; Müller-Myhsok, Bertram ; Meisinger, Christa ; Seedorf, Udo ; Ross-Adams, Helen ; Boonen, Steven ; Wloch-Kopec, Dorota ; Valant, Valerie ; Slark, Julia ; Furie, Karen ; Delavaran, Hossein ; Langford, Cordelia ; Deloukas, Panos ; Edkins, Sarah ; Hunt, Sarah ; Gray, Emma ; Dronov, Serge ; Peltonen, Leena ; Gretarsdottir, Solveig ; Thorleifsson, Gudmar ; Thorsteinsdottir, Unnur ; Stefansson, Kari ; Boncoraglio, Giorgio B ; Parati, Eugenio A ; Attia, John ; Holliday, Elizabeth ; Levi, Chris ; Franzosi, Maria-Grazia ; Goel, Anuj ; Helgadottir, Anna ; Blackwell, Jenefer M ; Bramon, Elvira ; Brown, Matthew A ; Casas, Juan P ; Corvin, Aiden ; Duncanson, Audrey ; Jankowski, Janusz ; Mathew, Christopher G ; Palmer, Colin NA ; Plomin, Robert ; Rautanen, Anna ; Sawcer, Stephen J ; Trembath, Richard C ; Viswanathan, Ananth C ; Wood, Nicholas W ; Worrall, Bradford B ; Kittner, Steven J ; Mitchell, Braxton D ; Kissela, Brett ; Meschia, James F ; Thijs, Vincent ; Lindgren, Arne ; Macleod, Mary Joan ; Slowik, Agnieszka ; Walters, Matthew ; Rosand, Jonathan ; Sharma, Pankaj ; Farrall, Martin ; Sudlow, Cathie LM ; Rothwell, Peter M ; Dichgans, Martin ; Donnelly, Peter ; Markus, Hugh S

Nature genetics, 2012, Vol.44 (3), p.328-333 [Periódico revisado por pares]

Nature Research

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10
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
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Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Bellenguez, Céline ; Bevan, Steve ; Gschwendtner, Andreas ; Spencer, Chris C A ; Burgess, Annette I ; Pirinen, Matti ; Jackson, Caroline A ; Traylor, Matthew ; Strange, Amy ; Su, Zhan ; Band, Gavin ; Syme, Paul D ; Malik, Rainer ; Pera, Joanna ; Norrving, Bo ; Lemmens, Robin ; Freeman, Colin ; Schanz, Renata ; James, Tom ; Poole, Deborah ; Murphy, Lee ; Segal, Helen ; Cortellini, Lynelle ; Cheng, Yu-Ching ; Woo, Daniel ; Nalls, Michael A ; Müller-Myhsok, Bertram ; Meisinger, Christa ; Seedorf, Udo ; Ross-Adams, Helen ; Boonen, Steven ; Wloch-Kopec, Dorota ; Valant, Valerie ; Slark, Julia ; Furie, Karen ; Delavaran, Hossein ; Langford, Cordelia ; Deloukas, Panos ; Edkins, Sarah ; Hunt, Sarah ; Gray, Emma ; Dronov, Serge ; Peltonen, Leena ; Gretarsdottir, Solveig ; Thorleifsson, Gudmar ; Thorsteinsdottir, Unnur ; Stefansson, Kari ; Boncoraglio, Giorgio B ; Parati, Eugenio A ; Attia, John ; Holliday, Elizabeth ; Levi, Chris ; Franzosi, Maria-Grazia ; Goel, Anuj ; Helgadottir, Anna ; Blackwell, Jenefer M ; Bramon, Elvira ; Brown, Matthew A ; Casas, Juan P ; Corvin, Aiden ; Duncanson, Audrey ; Jankowski, Janusz ; Mathew, Christopher G ; Palmer, Colin N A ; Plomin, Robert ; Rautanen, Anna ; Sawcer, Stephen J ; Trembath, Richard C ; Viswanathan, Ananth C ; Wood, Nicholas W ; Worrall, Bradford B ; Kittner, Steven J ; Mitchell, Braxton D ; Kissela, Brett ; Meschia, James F ; Thijs, Vincent ; Lindgren, Arne ; Macleod, Mary Joan ; Slowik, Agnieszka ; Walters, Matthew ; Rosand, Jonathan ; Sharma, Pankaj ; Farrall, Martin ; Sudlow, Cathie L M ; Rothwell, Peter M ; Dichgans, Martin ; Donnelly, Peter ; Markus, Hugh S

Nature genetics, 2012-03, Vol.44 (3), p.328-333 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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