Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Finny G Kuruvilla"'
Autor:
Charleston W K Chiang, Zofia K Z Gajdos, Joshua M Korn, Finny G Kuruvilla, Johannah L Butler, Rachel Hackett, Candace Guiducci, Thutrang T Nguyen, Rainford Wilks, Terrence Forrester, Christopher A Haiman, Katherine D Henderson, Loic Le Marchand, Brian E Henderson, Mark R Palmert, Colin A McKenzie, Helen N Lyon, Richard S Cooper, Xiaofeng Zhu, Joel N Hirschhorn
Publikováno v:
PLoS Genetics, Vol 6, Iss 3, p e1000866 (2010)
As we move forward from the current generation of genome-wide association (GWA) studies, additional cohorts of different ancestries will be studied to increase power, fine map association signals, and generalize association results to additional popu
Externí odkaz:
https://doaj.org/article/dd8333722d85479091e08623ee749a13
Autor:
Bo Isomaa, Anne U. Jackson, Richard N. Bergman, A Sandbaek, Yun Li, Oluf Pedersen, Thomas Edward Hughes, Mike Erdos, Christine Meisinger, Kari Kubalanza, Felicity Payne, Mark Walker, E Pettersen, William L. Duren, Kristin Ardlie, Palmer Cna., Michael Boehnke, Peter M. Nilsson, Graham A. Hitman, Rachel M. Freathy, Matthew G. Rees, Johanna Kuusisto, Finny G Kuruvilla, Kari Stefansson, P Deodhar, Knut Borch-Johnsen, Perry Jrb., Inês Barroso, Hana Lango, Richa Saxena, Augustine Kong, Gonçalo R. Abecasis, Katherine S. Elliott, Jonathan Marchini, Richard M. Watanabe, Christopher J. Groves, Niels Grarup, Unnur Thorsteinsdottir, Doney Asf., Kristina Bengtsson Boström, Peter Almgren, Cristen J. Willer, Torben Jørgensen, Lauren Gianniny, Beverley M. Shields, Christian Herder, Mario A. Morken, Lu Qi, Valgerdur Steinthorsdottir, Cecilia M. Lindgren, Nigel W. Rayner, Benjamin F. Voight, H Chen, J J Roix, Karen L. Mohlke, Heather M. Stringham, Andrew D. Morris, Mark I. McCarthy, Gudmar Thorleifsson, Frank B. Hu, Narisu Narisu, Mark J. Daly, Amanda F. Marvelle, Markku Laakso, Leif Groop, Laura J. Scott, Ding C-J., L Qin, Lori L. Bonnycastle, Thomas Illig, Noël P. Burtt, Michael N. Weedon, Valeriya Lyssenko, Amy J. Swift, Timothy M. Frayling, Nicholas J. Wareham, de Bakker Piw., Tiinamaija Tuomi, Kristian Hveem, Candace Guiducci, T Hu, Andrew T. Hattersley, David Altshuler, Harald Grallert, Peter S. Chines, Inga Prokopenko, Torsten Lauritzen, Katharine R. Owen, Eleftheria Zeggini, Carl Platou, Marketa Sjögren, Jaakko Tuomilehto, Nicholas J. Timpson, Francis S. Collins, Kristian Midthjell, Gregers S. Andersen, Claudia Langenberg, Torben Hansen
Publikováno v:
Zeggini, E, Scott, L J, Saxena, R, Voight, B F, Marchini, J L, Hu, T, de Bakker, P I W, Abecasis, G R, Almgren, P, Ardlie, K, Boström, K B, Bergman, R N, Bonnycastle, L L, Borch-Johnsen, K, Burtt, N P, Chen, H, Chines, P S, Daly, M J, Deodhar, P, Ding, C-J, Doney, A S F, Duren, W L, Elliott, K S, Erdos, M R, Frayling, T M, Freathy, R M, Gianniny, L, Grallert, H, Grarup, N, Groves, C J, Guiducci, C, Hansen, T, Herder, C, Hitman, G A, Hughes, T E, Isomaa, B, Jackson, A U, Jørgensen, T, Kong, A, Kubalanza, K, Kuruvilla, F G, Kuusisto, J, Langenberg, C, Lango, H, Lauritzen, T, Li, Y, Lindgren, C M, Lyssenko, V, Marvelle, A F, Wellcome Trust Case Control Consortium & Pedersen, O 2008, ' Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes ', Nature Genetics, vol. 40, no. 5, pp. 638-45 . https://doi.org/10.1038/ng.120
Udgivelsesdato: 2008-May Genome-wide association (GWA) studies have identified multiple loci at which common variants modestly but reproducibly influence risk of type 2 diabetes (T2D). Established associations to common and rare variants explain only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00392d7da17ace671783f6901fb9bf96
https://doi.org/10.1038/ng.120
https://doi.org/10.1038/ng.120
Autor:
Mélissa Beaudoin, Stephan Ripke, Jonas Halfvarson, Leif Törkvist, Dermot P.B. McGovern, Caroline Lagacé, Todd Green, David Ellinghaus, Mauro D'Amato, Andrew Kirby, Manuel A. Rivas, Steven R. Brant, Ramnik J. Xavier, Stacey Gabriel, Guillaume Lettre, Joshua M. Korn, Philippe Goyette, Finny G Kuruvilla, Clarence K. Zhang, Noël P. Burtt, Agnes Gardet, Richard H. Duerr, Timothy Fennell, Yashoda Sharma, Benjamin M. Neale, Andre Franke, Ken Sin Lo, David Altshuler, Gabrielle Boucher, Talin Haritunians, Marla Dubinsky, Phil Schumm, John D. Rioux, Mark J. Daly, Judy H. Cho, Mark S. Silverberg, Anna Latiano, Christine Stevens
Publikováno v:
Nature Genetics, 43(11), 1066-U50
Nature Genetics, 43, 1066-73
Nature Genetics, 43, 11, pp. 1066-73
Nature genetics, 43(11), 1066-1073. Nature Publishing Group
Nature genetics
Nature Genetics, 43, 1066-73
Nature Genetics, 43, 11, pp. 1066-73
Nature genetics, 43(11), 1066-1073. Nature Publishing Group
Nature genetics
Item does not contain fulltext More than 1,000 susceptibility loci have been identified through genome-wide association studies (GWAS) of common variants; however, the specific genes and full allelic spectrum of causal variants underlying these findi
Autor:
Pamela Sklar, Paul Lichtenstein, Carlos Ferreira, Derek W. Morris, Douglas M. Ruderfer, Nigel Williams, Lyudmila Georgieva, Alan W Maclean, Emma M. Quinn, Srinivasa Thirumalai, Jacob Lawrence, Peter M. Visscher, Andrew McQuillin, António Macedo, Christina M. Hultman, Elaine Kenny, Kevin A. McGhee, George Kirov, Emma Flordal Thelander, Ayman H. Fanous, Walter J. Muir, Stacey Gabriel, Michael Conlon O'Donovan, Finny G Kuruvilla, Aiden Corvin, Edward M. Scolnick, Colm O'Dushlaine, Khalid Choudhury, Patrick Sullivan, Frank A. Middleton, Kimberly Chambert, Nicholas Walker, Christopher P. Morley, Patrick F. Sullivan, Michael Gill, Célia Barreto Carvalho, Manuel A. R. Ferreira, Susmita Datta, Robert Krasucki, M. Helena Azevedo, Soh Leh Kuan, Jennifer L. Moran, Stuart MacGregor, Draga Toncheva, P. Malloy, Douglas Blackwood, Shaun Purcell, Jonathan Pimm, Michael John Owen, Peter Holmans, David V. Conti, Gillian Fraser, Vinay Puri, Naomi R. Wray, Andrew Kirby, Margaret Van Beck, Digby Quested, Kristin G. Ardlie, Ben S. Pickard, Caroline Crombie, Vihra Milanova, Carlos N. Pato, Nicholas John Craddock, Jennifer Stone, Nadine Norton, Mark J. Daly, James A. Knowles, Hugh Gurling, David St Clair, Hywel Williams, Michele T. Pato, Helena Medeiros, Nicholas Bass, Ivan Nikolov
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Schizophrenia is a severe mental disorder with a lifetime risk of about 1%, characterized by hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80%. We performed a genome-wide association study of 3,322 European in
Autor:
John E. Blume, James Nemesh, Andrew Kirby, Julian Maller, Rui Mei, Steven A. McCarroll, Earl Hubbell, Joshua M. Korn, Steve Lincoln, Paul I.W. de Bakker, Stacey Gabriel, Marcia M. Nizzari, Amanda F. Elliott, Rich Rava, Patrick J Collins, Melissa Parkin, Finny G Kuruvilla, Mark J. Daly, Michael H. Shapero, Teresa Webster, Simon Cawley, Keith W. Jones, Robert E. Handsaker, Alec Wysoker, James Veitch, David Altshuler
Publikováno v:
Nature Genetics. 40:1166-1174
Dissecting the genetic basis of disease risk requires measuring all forms of genetic variation, including SNPs and copy number variants (CNVs), and is enabled by accurate maps of their locations, frequencies and population-genetic properties. We desi
Publikováno v:
Proceedings of the National Academy of Sciences. 98:7283-7288
The target of rapamycin (Tor) proteins sense nutrients and control transcription and translation relevant to cell growth. Treating cells with the immunosuppressant rapamycin leads to the intracellular formation of an Fpr1p-rapamycin-Tor ternary compl
Autor:
Finny G. Kuruvilla, Alykhan F. Shamji, Stuart L. Schreiber, James S. Hardwick, Jeffrey K. Tong
Publikováno v:
Proceedings of the National Academy of Sciences. 96:14866-14870
The immunosuppressant rapamycin inhibits Tor1p and Tor2p (target of rapamycin proteins), ultimately resulting in cellular responses characteristic of nutrient deprivation through a mechanism involving translational arrest. We measured the immediate t
Publikováno v:
Chemistry & Biology. 6(5):R129-R136
Early efforts to place the first cloned mammalian PIK-related kinase, FRAP, into a conventional membrane to nuclear pathway met with little success. More recent data suggest that members of the family of PIK-related kinases act as intracellular senso
Autor:
Zak Kohane, Jeremy Goldberg, Carine Mantoulan, Shaun Purcell, Jessica Brian, Magdalena Laskawiec, Christopher A. Walsh, Irma Moilanen, Ridha Joober, Peter Szatmari, Olena Korvatska, Kerim Munir, James F. Gusella, Rudolph E. Tanzi, David L. Pauls, Generoso G. Gascon, Christine Stevens, Linda Lotspeich, John I. Nurnberger, Ramzi Nazir, Jonathan Green, Brian L. Yaspan, Marion Leboyer, Ann P. Thompson, Shun-Chiao Chang, Carolyn Bridgemohan, Louise Gallagher, Jeff Munson, Michael Gill, Guiqing Cai, Fritz Poustka, Regina Regan, Aislyn Cangialose, Gerard D. Schellenberg, Christopher J. McDougle, Christina Corsello, Wendy Roberts, Thomas H. Wassink, Majid Ghadami, Ellen M. Hanson, Benjamin M. Neale, Stacey Gabriel, Lonnie Zwaigenbaum, John Tsiantis, Hanna Ebeling, Sabine M. Klauck, Elaine LeClair, Bernie Devlin, Steven A. McCarroll, Ashley O'Connor, Andrew Pickles, Emily L. Crawford, Katja Jussila, Helen McConachie, Christopher Gillberg, Brenda E. Barry, Lou Kunkel, Seung Yun Yoo, Jennifer N. Partlow, Stephanie Brewster O'Neil, Ingrid A. Holm, Judith Miller, Guy A. Rouleau, Val C. Sheffield, Catherine Lord, Judith S. Palfrey, Ellen M. Wijsman, Astrid M. Vicente, Azam Hosseinipour, Ronald E. Becker, James S. Sutcliffe, Fred R. Volkmar, Marja Leena Mattila, Katerina Papanikolaou, Jennifer Reichert, Edwin H. Cook, Pamela Sklar, Elena Maestrini, Hilary Coon, Sek Won Kong, Stephen A. Haddad, Todd Green, Gillian Baird, Andrew Kirby, Patrick Bolton, Robert Sean Hill, Eric M. Morrow, Tom Berney, Jonathan L. Haines, Maryam Valujerdi, Casey Gates, David J. Posey, Karola Rehnström, Alistair T. Pagnamenta, Christine M. Freitag, Eric Fombonne, Janice Ware, Christian R. Marshall, Janine A. Lamb, Lauren A. Weiss, Agatino Battaglia, Nancy J. Minshew, Roksana Sasanfar, Elizabeth Baroni, Maretha de Jonge, Lennart von Wendt, Gina Hilton, Dalila Pinto, Nahit Motavalli Mukaddes, Ala Tolouei, Catalina Betancur, Michael Rutter, Tram Tran, Eftichia Duketis, Laurent Mottron, Margaret A. Pericak-Vance, Kristen West, Joachim Hallmayer, Kirsty Wing, Kerstin Wittemeyer, Rachel J. Hundley, Herman van Engeland, Judith Conroy, Mark J. Daly, Asif Hashmi, Michael L. Cuccaro, Geraldine Dawson, Sanna Kuusikko, Richard Anney, Anthony P. Monaco, Brian Winkloski, Samira Al-Saad, Dan E. Arking, Veronica J. Vieland, Stephen W. Scherer, Soher Balkhy, Kara Andresen, Rebecca L. Tomlinson, Joseph D. Buxbaum, Aravinda Chakravarti, Xiao-Qing Liu, Lindsay Jackson, Jaakko Ignatius, Catarina Correia, Leonard Rappaport, Heather Peters, Julie Gauthier, John R. Gilbert, Jeremy R. Parr, Carrie Sougnez, Katherine E. Tansey, Bennett L. Leventha, Annemarie Poustka, Daniel H. Geschwind, Annette Estes, Leena Peltonen, Maryam Rostami, Jeff Salt, David Altshuler, Simon Wallace, Susan E. Bryson, William M. Mahoney, Katy Renshaw, Robert M. Joseph, Lisa H. Albers, Inês Cabrito, Sean Ennis, Vanessa Hus, Guiomar Oliveira, Ann Le Couteur, Joseph Piven, Sandra L. Friedman, Penny Farrar, Joshua M. Korn, Sven Bölte, Camille W. Brune, Esau Simmons, Susan L. Santangelo, Andrew D. Paterson, Rita M. Cantor, Andrew B. West, Finny G Kuruvilla, Tiago R. Magalhaes, Andrew Green, Alison Schonwald, Stephen J. Guter, Anthony J. Bailey, Bernadette Rogé, William M. McMahon
Publikováno v:
Nature
Nature, 2009, 461 (7265), pp.802-808. ⟨10.1038/nature08490⟩
Nature, Nature Publishing Group, 2009, 461 (7265), pp.802-808. ⟨10.1038/nature08490⟩
Nature, 2009, 461 (7265), pp.802-808. ⟨10.1038/nature08490⟩
Nature, Nature Publishing Group, 2009, 461 (7265), pp.802-808. ⟨10.1038/nature08490⟩
Member of the Autism Genome Project Consortium: Astrid M. Vicente Although autism is a highly heritable neurodevelopmental disorder, attempts to identify specific susceptibility genes have thus far met with limited success. Genome-wide association st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::399dbcded0de45863411f1e50a5de20f
https://www.hal.inserm.fr/inserm-03135302
https://www.hal.inserm.fr/inserm-03135302
Autor:
James Nemesh, Patrick J Collins, Earl Hubbell, Simon Cawley, Charles Lee, Mark J. Daly, Finny G Kuruvilla, Steven A. McCarroll, Stacey Gabriel, Shaun Purcell, Jim Veitch, Marcia M. Nizzari, Alec Wysoker, Joshua M. Korn, David Altshuler, Katayoon Darvishi
Accurate and complete measurement of single nucleotide (SNP) and copy number (CNV) variants, both common and rare, will be required to understand the role of genetic variation in disease. We present Birdsuite, a four-stage analytical framework instan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9142e5ae25a5092620a422b578a5578
https://europepmc.org/articles/PMC2756534/
https://europepmc.org/articles/PMC2756534/