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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
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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6
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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7
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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8
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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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 reveals genetic risk underlying Parkinson's disease
Genome-wide association study reveals genetic risk underlying Parkinson's disease
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Genome-wide association study reveals genetic risk underlying Parkinson's disease

Singleton, Andrew B ; Gasser, Thomas ; Simón-Sánchez, Javier ; Schulte, Claudia ; Bras, Jose M ; Sharma, Manu ; Gibbs, J Raphael ; Berg, Daniela ; Paisan-Ruiz, Coro ; Lichtner, Peter ; Scholz, Sonja W ; Hernandez, Dena G ; Krüger, Rejko ; Federoff, Monica ; Klein, Christine ; Goate, Alison ; Perlmutter, Joel ; Bonin, Michael ; Nalls, Michael A ; Illig, Thomas ; Gieger, Christian ; Houlden, Henry ; Steffens, Michael ; Okun, Michael S ; Racette, Brad A ; Cookson, Mark R ; Foote, Kelly D ; Fernandez, Hubert H ; Traynor, Bryan J ; Schreiber, Stefan ; Arepalli, Sampath ; Zonozi, Ryan ; Gwinn, Katrina ; van der Brug, Marcel ; Lopez, Grisel ; Chanock, Stephen J ; Schatzkin, Arthur ; Park, Yikyung ; Hollenbeck, Albert ; Gao, Jianjun ; Huang, Xuemei ; Wood, Nick W ; Lorenz, Delia ; Deuschl, Günther ; Chen, Honglei ; Riess, Olaf ; Hardy, John A

Nature genetics, 2009-12, Vol.41 (12), p.1308-1312 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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