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11 |
Material Type: Artigo
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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular riskWarren, 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 VNature genetics, 2017-03, Vol.49 (3), p.403-415 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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12 |
Material Type: Artigo
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Common variants in WFS1 confer risk of type 2 diabetesSandhu, Manjinder S ; Barroso, Inês ; Weedon, Michael N ; Fawcett, Katherine A ; Wasson, Jon ; Debenham, Sally L ; Daly, Allan ; Lango, Hana ; Frayling, Timothy M ; Neumann, Rosalind J ; Sherva, Richard ; Blech, Ilana ; Pharoah, Paul D ; Palmer, Colin N A ; Kimber, Charlotte ; Tavendale, Roger ; Morris, Andrew D ; McCarthy, Mark I ; Walker, Mark ; Hitman, Graham ; Glaser, Benjamin ; Permutt, M Alan ; Hattersley, Andrew T ; Wareham, Nicholas JNature genetics, 2007-08, Vol.39 (8), p.951-953 [Periódico revisado por pares]London: Nature Publishing GroupTexto completo disponível |
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13 |
Material Type: Artigo
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertensionWarren, Helen ; Cook, James P ; Manning, Alisa K ; Grarup, Niels ; Witkowska, Kate ; Tukiainen, Taru ; Ferreira, Teresa ; Harakalova, Magdalena ; Mihailov, Evelin ; Kraja, Aldi T ; Rasheed, Asif ; Samuel, Maria ; Jackson, Anne U ; Swift, Amy J ; Fava, Cristiano ; Matchan, Angela ; Stirrups, Kathleen E ; Bork-Jensen, Jette ; Gjesing, Anette P ; Kontto, Jukka ; Shaw-Hawkins, Susan ; Rayner, N William ; Neville, Matt J ; Yiorkas, Andrianos M ; Kajantie, Eero ; Zhang, Weihua ; Malerba, Giovanni ; Verweij, Niek ; Moayyeri, Alireza ; Caslake, Muriel ; de Craen, Anton Jm ; Luan, Jian'an ; Farmaki, Aliki-Eleni ; Renström, Frida ; Huffman, Jennifer E ; Hassinen, Maija ; Burgess, Stephen ; Felix, Janine F ; Uria-Nickelsen, Maria ; Highland, Heather M ; Marouli, Eirini ; Lindström, Jaana ; Rudan, Igor ; Rolandsson, Olov ; Franks, Paul W ; Spector, Timothy D ; Jousilahti, Pekka ; Männistö, Satu ; Starr, John M ; Langenberg, Claudia ; Brown, Morris J ; Connell, John M ; Jukema, J Wouter ; Sattar, Naveed ; Ford, Ian ; Esko, Tõnu ; Mägi, Reedik ; van der Harst, Pim ; Gambaro, Giovanni ; Lind, Lars ; de Bakker, Paul Iw ; Numans, Mattijs E ; Brandslund, Ivan ; Christensen, Cramer ; Petersen, Eva Rb ; Chambers, John C ; Kooner, Jaspal S ; Jarvelin, Marjo-Riitta ; Thuesen, Betina ; Karpe, Fredrik ; Tuomilehto, Jaakko ; Doney, Alex Sf ; Morris, Andrew D ; Palotie, Aarno ; Alam, Dewan S ; Chowdhury, Rajiv ; McCarthy, Mark I ; Amouyel, Philippe ; Arveiler, Dominique ; Blankenberg, Stefan ; Kee, Frank ; Veronesi, Giovanni ; Deloukas, Panos ; Elliott, Paul ; Kathiresan, Sekar ; Melander, Olle ; Scotland, Generation ; Hansen, Torben ; Pedersen, Oluf ; Boehnke, Michael ; Frossard, Philippe ; Newton-Cheh, Christopher ; Nordestgaard, Børge Grønne ; Caulfield, Mark J ; Samani, Nilesh J ; Saleheen, Danish ; Asselbergs, Folkert W ; Wain, Louise V ; Butterworth, Adam S ; Howson, Joanna MmNature genetics, 2016-10, Vol.48 (10), p.1151-1161 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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14 |
Material Type: Artigo
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Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility lociKooner, Jaspal S ; Chambers, John C ; Saleheen, Danish ; Sim, Xueling ; Sehmi, Joban ; Zhang, Weihua ; Frossard, Philippe ; Been, Latonya F ; Chia, Kee-Seng ; Dimas, Antigone S ; Hassanali, Neelam ; Jafar, Tazeen ; Jowett, Jeremy B M ; Li, Xinzhing ; Radha, Venkatesan ; Rees, Simon D ; Takeuchi, Fumihiko ; Young, Robin ; Aung, Tin ; Basit, Abdul ; Chidambaram, Manickam ; Das, Debashish ; Grunberg, Elin ; Hedman, Åsa K ; Hydrie, Zafar I ; Islam, Muhammed ; Khor, Chiea-Chuen ; Kowlessur, Sudhir ; Kristensen, Malene M ; Liju, Samuel ; Lim, Wei-Yen ; Matthews, David R ; Liu, Jianjun ; Morris, Andrew P ; Nica, Alexandra C ; Pinidiyapathirage, Janani M ; Prokopenko, Inga ; Rasheed, Asif ; Samuel, Maria ; Shah, Nabi ; Shera, A Samad ; Small, Kerrin S ; Suo, Chen ; Wickremasinghe, Ananda R ; Wong, Tien Yin ; Yang, Mingyu ; Zhang, Fan ; Abecasis, Goncalo R ; Barnett, Anthony H ; Caulfield, Mark ; Deloukas, Panos ; Frayling, Timothy M ; Froguel, Philippe ; Kato, Norihiro ; Katulanda, Prasad ; Kelly, M Ann ; Liang, Junbin ; Mohan, Viswanathan ; Sanghera, Dharambir K ; Scott, James ; Seielstad, Mark ; Zimmet, Paul Z ; Elliott, Paul ; Teo, Yik Ying ; McCarthy, Mark I ; Danesh, John ; Tai, E ShyongNature genetics, 2011-10, Vol.43 (10), p.984-989 [Periódico revisado por pares]New York, NY: Nature Publishing GroupTexto completo disponível |
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15 |
Material Type: Artigo
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Neutral tumor evolution?Tarabichi, Maxime ; Martincorena, Iñigo ; Gerstung, Moritz ; Leroi, Armand M ; Markowetz, Florian ; Spellman, Paul T ; Morris, Quaid D ; Lingjærde, Ole Christian ; Wedge, David C ; Van Loo, PeterNature genetics, 2018-12, Vol.50 (12), p.1630-1633 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseBurn, John ; Barker, William A ; Markham, Alex F ; Curtis, Ann ; Chinnery, Patrick F ; Coulthard, Alan ; Fey, Constanze ; Jackson, Andrew P ; Jackson, Margaret J ; Bates, David ; Curtis, Andrew R.J ; McHale, Duncan P ; Bindoff, Laurence A ; Ince, Paul G ; Hay, David ; Morris, Christopher MNature genetics, 2001-08, Vol.28 (4), p.350-354 [Periódico revisado por pares]London: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2Horstmann, Rolf D ; Hill, Adrian V S ; Thye, Thorsten ; Vannberg, Fredrik O ; Wong, Sunny H ; Owusu-Dabo, Ellis ; Osei, Ivy ; Gyapong, John ; Sirugo, Giorgio ; Sisay-Joof, Fatou ; Enimil, Anthony ; Chinbuah, Margaret A ; Floyd, Sian ; Warndorff, David K ; Sichali, Lifted ; Malema, Simon ; Crampin, Amelia C ; Ngwira, Bagrey ; Teo, Yik Y ; Small, Kerrin ; Rockett, Kirk ; Kwiatkowski, Dominic ; Fine, Paul E ; Hill, Philip C ; Newport, Melanie ; Lienhardt, Christian ; Adegbola, Richard A ; Corrah, Tumani ; Ziegler, Andreas ; Morris, Andrew P ; Meyer, Christian GNature genetics, 2010-09, Vol.42 (9), p.739-741 [Periódico revisado por pares]New York, NY: Nature Publishing GroupTexto completo disponível |
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18 |
Material Type: Artigo
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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selectionPardiñas, Antonio F ; Holmans, Peter ; Pocklington, Andrew J ; Escott-Price, Valentina ; Ripke, Stephan ; Carrera, Noa ; Legge, Sophie E ; Bishop, Sophie ; Cameron, Darren ; Hamshere, Marian L ; Han, Jun ; Hubbard, Leon ; Lynham, Amy ; Mantripragada, Kiran ; Rees, Elliott ; MacCabe, James H ; McCarroll, Steven A ; Baune, Bernhard T ; Breen, Gerome ; Byrne, Enda M ; Dannlowski, Udo ; Eley, Thalia C ; Hayward, Caroline ; Martin, Nicholas G ; McIntosh, Andrew M ; Plomin, Robert ; Porteous, David J ; Wray, Naomi R ; Caballero, Armando ; Geschwind, Daniel H ; Huckins, Laura M ; Ruderfer, Douglas M ; Santiago, Enrique ; Sklar, Pamela ; Stahl, Eli A ; Won, Hyejung ; Agerbo, Esben ; Als, Thomas D ; Andreassen, Ole A ; Bækvad-Hansen, Marie ; Mortensen, Preben Bo ; Pedersen, Carsten Bøcker ; Børglum, Anders D ; Bybjerg-Grauholm, Jonas ; Djurovic, Srdjan ; Durmishi, Naser ; Pedersen, Marianne Giørtz ; Golimbet, Vera ; Grove, Jakob ; Hougaard, David M ; Mattheisen, Manuel ; Molden, Espen ; Mors, Ole ; Nordentoft, Merete ; Pejovic-Milovancevic, Milica ; Sigurdsson, Engilbert ; Silagadze, Teimuraz ; Hansen, Christine Søholm ; Stefansson, Kari ; Stefansson, Hreinn ; Steinberg, Stacy ; Tosato, Sarah ; Werge, Thomas ; Collier, David A ; Rujescu, Dan ; Kirov, George ; Owen, Michael J ; O'Donovan, Michael C ; Walters, James T RNature genetics, 2018-03, Vol.50 (3), p.381-389 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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19 |
Material Type: Artigo
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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsyMüller, Ulrich ; Schellenberg, Gerard D ; Höglinger, Günter U ; Melhem, Nadine M ; Dickson, Dennis W ; Sleiman, Patrick M A ; Wang, Li-San ; Klei, Lambertus ; Rademakers, Rosa ; de Silva, Rohan ; Litvan, Irene ; Riley, David E ; van Swieten, John C ; Heutink, Peter ; Wszolek, Zbigniew K ; Uitti, Ryan J ; Vandrovcova, Jana ; Hurtig, Howard I ; Gross, Rachel G ; Maetzler, Walter ; Goldwurm, Stefano ; Tolosa, Eduardo ; Borroni, Barbara ; Pastor, Pau ; Cantwell, Laura B ; Han, Mi Ryung ; Dillman, Allissa ; van der Brug, Marcel P ; Gibbs, J Raphael ; Cookson, Mark R ; Hernandez, Dena G ; Singleton, Andrew B ; Farrer, Matthew J ; Yu, Chang-En ; Golbe, Lawrence I ; Revesz, Tamas ; Hardy, John ; Lees, Andrew J ; Devlin, Bernie ; Hakonarson, HakonNature genetics, 2011-07, Vol.43 (7), p.699-705 [Periódico revisado por pares]New York, NY: Nature Publishing GroupTexto completo disponível |
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20 |
Material Type: Artigo
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An atlas of genetic influences on osteoporosis in humans and miceMorris, 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 BrentNature genetics, 2019-02, Vol.51 (2), p.258-266 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |