Resultados de procura - Finny G. Kuruvilla
- Mostrando 1 - 7 Resultados de 7
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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs por Joshua M. Korn, Finny G. Kuruvilla, Steven A. McCarroll, Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick Collins, Katayoon Darvishi, Charles Lee, Marcia M. Nizzari, Stacey B. Gabriel, Shaun Purcell, Mark J. Daly, David Altshuler
Publicado 2008Artigo -
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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease por Manuel A. Rivas, Mélissa Beaudoin, Agnès Gardet, Christine Stevens, Yashoda Sharma, Hu Zhang, Gabrielle Boucher, Stephan Ripke, David Ellinghaus, Noël P. Burtt, Tim Fennell, Andrew Kirby, Anna Latiano, Philippe Goyette, Todd J. Green, Jonas Halfvarson, Talin Haritunians, Joshua M. Korn, Finny G. Kuruvilla, Caroline Lagacé, Benjamin M. Neale, Ken Sin Lo, L. Philip Schumm, Leif Törkvist, Marla C. Dubinsky, Steven R. Brant, Mark S. Silverberg, Richard H. Duerr, David Altshuler, Stacey Gabriel, Guillaume Lettre, André Franke, Mauro D’Amato, Dermot McGovern, Judy H. Cho, John D. Rioux, Ramnik J. Xavier, Mark J. Daly
Publicado 2011Artigo -
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder por Shaun Purcell, Naomi R. Wray, Jennifer Stone, Peter M. Visscher, Michael O’Donovan, Patrick F. Sullivan, Pamela Sklar, Douglas M. Ruderfer, Andrew McQuillin, Derek W. Morris, Colm O’Dushlaine, Aiden Corvin, Peter Holmans, Stuart MacGregor, Hugh Gurling, Douglas Blackwood, Nick Craddock, Michael Gill, Christina M. Hultman, George Kirov, Paul Lichtenstein, Walter Muir, Michael J. Owen, Carlos N. Pato, Edward M. Scolnick, David St Clair, Nigel Williams, Lyudmila Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Mariofanna Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, Emma M. Quinn, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, Caroline Crombie, Gillian Fraser, Soh Leh Kuan, Nicholas Walker, Kevin A. McGhee, Ben Pickard, P. Malloy, Alan Maclean, M. Van Beck, Michele T. Pato, Helena Medeiros, Frank A. Middleton, Célia Barreto Carvalho, Christopher P. Morley, Ayman H. Fanous, David V. Conti, James A. Knowles, Carlos Paz Ferreira, A. Macedo, M.H. Azevedo, Andrew Kirby, Manuel A. R. Ferreira, Mark Daly, Kimberly Chambert, Finny G. Kuruvilla, Stacey B. Gabriel, Kristin Ardlie, Jennifer L. Moran
Publicado 2009Artigo -
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Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes por Eleftheria Zeggini, Laura J. Scott, Richa Saxena, Benjamin F. Voight, Jonathan Marchini, Tianle Hu, Paul IW de Bakker, Gonçalo R. Abecasis, Peter Almgren, Gary L. Andersen, Kristin Ardlie, Kristina Bengtsson Boström, Richard N. Bergman, Lori L. Bonnycastle, Knut Borch‐Johnsen, Noël P. Burtt, Hong Chen, Peter S. Chines, Mark J. Daly, Parimal Deodhar, Chia-Jen Ding, Alex S. F. Doney, William L. Duren, Katherine S. Elliott, Michael R. Erdos, Timothy M. Frayling, Rachel M. Freathy, Lauren Gianniny, Harald Grallert, Niels Grarup, Christopher J. Groves, Candace Guiducci, Torben Hansen, Christian Herder, G. A. Hitman, Thomas E. Hughes, Bo Isomaa, Anne Jackson, Torben Jørgensen, Augustine Kong, Kari Kubalanza, Finny G. Kuruvilla, Johanna Kuusisto, Claudia Langenberg, Hana Lango Allen, Torsten Lauritzen, Yun Li, Cecilia M. Lindgren, Valeriya Lyssenko, Amanda F. Marvelle, Christa Meisinger, Kristian Midthjell, Karen L. Mohlke, Mario A. Morken, Andrew D. Morris, Narisu Narisu, Peter M. Nilsson, Katharine R. Owen, Colin N. A. Palmer, Felicity Payne, John R. B. Perry, Elin Pettersen, Carl G. P. Platou, Inga Prokopenko, Lu Qi, Qin Li, Nigel W. Rayner, Matthew G. Rees, Jeffrey J. Roix, Anelli Sandbæk, Beverley M. Shields, Marketa Sjögren, Valgerður Steinthórsdóttir, Heather M. Stringham, Amy J. Swift, Gudmar Thorleifsson, Unnur Þorsteinsdóttir, Nicholas J. Timpson, Jaakko Tuomilehto, Seppo Lehto, Mark Walker, Richard M. Watanabe, Michael N. Weedon, Cristen J. Willer, Thomas Illig, Kristian Hveem, Frank B. Hu, Markku Laakso, Kāri Stefánsson, Oluf Pedersen, Nicholas J. Wareham, Inês Barroso, Andrew T. Hattersley, Francis S. Collins, Leif Groop, Mark I. McCarthy, Michael Boehnke, David Altshuler
Publicado 2008Revisão -
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A genome-wide linkage and association scan reveals novel loci for autism por Lauren A. Weiss, Dan E. Arking, Mark J. Daly, Aravinda Chakravarti, Camille W. Brune, Kristen M. West, Ashley O’Connor, Gina M. Hilton, R Tomlinson, Andrew B. West, Edwin H. Cook, Todd Green, Shun-Chiao Chang, Stacey B. Gabriel, Casey Gates, Ellen Hanson, Andrew Kirby, Joshua M. Korn, Finny G. Kuruvilla, Steven McCarroll, Eric M. Morrow, Benjamin M. Neale, Shaun Purcell, Roksana Sasanfar, Carrie Sougnez, Christine Stevens, David Altshuler, James F. Gusella, Susan L. Santangelo, Pamela Sklar, Rudolph E. Tanzi, Richard Anney, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Catalina Betancur, Sven Bölte, Patrick Bolton, Jessica Brian, Susan E. Bryson, Joseph D. Buxbaum, Ines Cabrito, Guiqing Cai, Rita M. Cantor, Hilary Coon, Judith Conroy, Catarina Correia, Christina Corsello, Emily L. Crawford, Michael L. Cuccaro, Géraldine Dawson, Maretha Jonge, Bernie Devlin, Eftichia Duketis, Sean Ennis, Annette Estes, Penny Farrar, Éric Fombonne, Christine M. Freitag, Louise Gallagher, Daniel H. Geschwind, John R. Gilbert, Michael Gill, Christopher Gillberg, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Jonathan L. Haines, Joachim Hallmayer, Vanessa Hus, Sabine M. Klauck, Olena Korvatska, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett L. Leventha, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Elena Maestrini, Tiago R. Magalhães, William J. Mahoney, Carine Mantoulan, Helen McConachie, Christopher J. McDougle, William M. McMahon, Christian R. Marshall, Judith Miller, Nancy J. Minshew, Anthony P. Monaco, Jeff Munson, John I. Nürnberger, Guiomar Oliveira, Alistair T. Pagnamenta, Katerina Papanikolaou, Jeremy Parr, Andrew D. Paterson
Publicado 2009Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Gene
Genetics
Genotype
Single-nucleotide polymorphism
Genetic association
Computational biology
Genome-wide association study
Medicine
Cell biology
Genome
Genotyping
Internal medicine
Psychiatry
Activator (genetics)
Astrophysics
Autism
Biochemistry
Bipolar disorder
Case-control study
Chromosome
Citric acid cycle
Cognition
Copy-number variation
Diabetes mellitus
Disease
Effector
Endocrinology
Genetic linkage
Glycolysis