vplagnol's association [64 articles] Export

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	Disruption of the neurexin 1 gene is associated with schizophrenia. [My Copy] Human molecular genetics, Vol. 18, No. 5. (1 March 2009), pp. 988-996. by Dan Rujescu, Andres Ingason, Sven Cichon, et al.Olli P. Pietiläinen, Michael R. Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon, Robin Murray, Mirella Ruggeri, Sarah Tosato, Chiara Bonetto, Stacy Steinberg, Engilbert Sigurdsson, Thordur Sigmundsson, Hannes Petursson, Arnaldur Gylfason, Pall I. Olason, Gudmundur Hardarsson, Gudrun A. Jonsdottir, Omar Gustafsson, Ragnheidur Fossdal, Ina Giegling, Hans-Jürgen J. Möller, Annette M. Hartmann, Per Hoffmann, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lonnqvist, Jaana Suvisaari, Annamari Tuulio-Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris Veltman, Jacobine E. Buizer-Voskamp, GROUP Investigators, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kari Stefansson, Leena Peltonen, David St Clair, Hreinn Stefansson, David A. Collier posted to schizophrenia nrxn1 association by vplagnol on 2009-10-30 16:33:26 as along with 1 person Terkko
	Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. [My Copy] Nature, Vol. 393, No. 6686. (18 June 1998), pp. 702-705. by M. Hutton, C. L. Lendon, P. Rizzu, et al.M. Baker, S. Froelich, H. Houlden, S. Pickering-Brown, S. Chakraverty, A. Isaacs, A. Grover, J. Hackett, J. Adamson, S. Lincoln, D. Dickson, P. Davies, R. C. Petersen, M. Stevens, E. de Graaff, E. Wauters, J. van Baren, M. Hillebrand, M. Joosse, J. M. Kwon, P. Nowotny, L. K. Che, J. Norton, J. C. Morris, L. A. Reed, J. Trojanowski, H. Basun, L. Lannfelt, M. Neystat, S. Fahn, F. Dark, T. Tannenberg, P. R. Dodd, N. Hayward, J. B. Kwok, P. R. Schofield, A. Andreadis, J. Snowden, D. Craufurd, D. Neary, F. Owen, B. A. Oostra, J. Hardy, A. Goate, J. van Swieten, D. Mann, T. Lynch, P. Heutink posted to tau_gene parkinson linkage association by vplagnol on 2009-10-30 15:21:30 as along with 2 people marlenlunow daforerog
	Microduplications of 16p11.2 are associated with schizophrenia [My Copy] Nature Genetics, Vol. 41, No. 11. (25 October 2009), pp. 1223-1227. by Shane E. McCarthy, Vladimir Makarov, George Kirov, et al.Anjene M. Addington, Jon McClellan, Seungtai Yoon, Diana O. Perkins, Diane E. Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A. Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H. Zackai, Paige Kaplan, Jaya Ganesh, Ian D. Krantz, Nancy B. Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B. Lakshmi, Anthony Leotta, Jude Kendall, Yoon-ha Lee, Vladimir Vacic, Sydney Gary, Lilia M. Iakoucheva, Timothy J. Crow, Susan L. Christian, Jeffrey A. Lieberman, T. Scott Stroup, Terho Lehtimaki, Kaija Puura, Chad Haldeman-Englert, Justin Pearl, Meredith Goodell, Virginia L. Willour, Pamela DeRosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J. McMahon, Anil K. Malhotra, James B. Potash, Thomas G. Schulze, Markus M. Nothen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara M. Lajonchere, James S. Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R. Mendell, Nick Craddock, Michael J. Owen, Michael C. O'Donovan, Tamim H. Shaikh, Ezra Susser, Lynn E. DeLisi, Patrick F. Sullivan, Curtis K. Deutsch, Judith Rapoport, Deborah L. Levy, Mary-Claire King, Jonathan Sebat posted to schizophrenia cnv association by vplagnol on 2009-10-27 11:48:46 as along with 2 people dchughes daforerog
	Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer [My Copy] Nature Genetics, Vol. 41, No. 9. (02 August 2009), pp. 986-990. by Laufey Amundadottir, Peter Kraft, Rachael Z. Stolzenberg-Solomon, et al.Charles S. Fuchs, Gloria M. Petersen, Alan A. Arslan, H. Bas Bueno-de-Mesquita, Myron Gross, Kathy Helzlsouer, Eric J. Jacobs, Andrea LaCroix, Wei Zheng, Demetrius Albanes, William Bamlet, Christine D. Berg, Franco Berrino, Sheila Bingham, Julie E. Buring, Paige M. Bracci, Federico Canzian, Francoise Clavel-Chapelon, Sandra Clipp, Michelle Cotterchio, Mariza de Andrade, Eric J. Duell, John W. Fox Jr, Steven Gallinger, J. Michael Gaziano, Edward L. Giovannucci, Michael Goggins, Carlos A. Gonzalez, Goran Hallmans, Susan E. Hankinson, Manal Hassan, Elizabeth A. Holly, David J. Hunter, Amy Hutchinson, Rebecca Jackson, Kevin B. Jacobs, Mazda Jenab, Rudolf Kaaks, Alison P. Klein, Charles Kooperberg, Robert C. Kurtz, Donghui Li, Shannon M. Lynch, Margaret Mandelson, Robert R. McWilliams, Julie B. Mendelsohn, Dominique S. Michaud, Sara H. Olson, Kim Overvad, Alpa V. Patel, Petra H. M. Peeters, Aleksandar Rajkovic, Elio Riboli, Harvey A. Risch, Xiao-Ou Shu, Gilles Thomas, Geoffrey S. Tobias, Dimitrios Trichopoulos, Stephen K. Van Den Eeden, Jarmo Virtamo, Jean Wactawski-Wende, Brian M. Wolpin, Herbert Yu, Kai Yu, Anne Zeleniuch-Jacquotte, Stephen J. Chanock, Patricia Hartge, Robert N. Hoover posted to cancer association by vplagnol on 2009-10-21 13:37:31 as along with 1 person fedecan
	Possible interaction between HLA-DRbeta1 and thyroglobulin variants in Graves' disease. [My Copy] Thyroid : official journal of the American Thyroid Association, Vol. 16, No. 4. (April 2006), pp. 351-355. by Susan E. Hodge, Yoshiyuki Ban, Lisa J. Strug, et al.David A. Greenberg, Terry F. Davies, Erlinda S. Concepcion, Ronald Villanueva, Yaron Tomer posted to hla graves association by vplagnol on 2009-10-20 23:08:58 as
	A variant associated with nicotine dependence, lung cancer and peripheral arterial disease. [My Copy] Nature, Vol. 452, No. 7187. (3 April 2008), pp. 638-642. by Thorgeir E. Thorgeirsson, Frank Geller, Patrick Sulem, et al.Thorunn Rafnar, Anna Wiste, Kristinn P. Magnusson, Andrei Manolescu, Gudmar Thorleifsson, Hreinn Stefansson, Andres Ingason, Simon N. Stacey, Jon T. Bergthorsson, Steinunn Thorlacius, Julius Gudmundsson, Thorlakur Jonsson, Margret Jakobsdottir, Jona Saemundsdottir, Olof Olafsdottir, Larus J. Gudmundsson, Gyda Bjornsdottir, Kristleifur Kristjansson, Halla Skuladottir, Helgi J. Isaksson, Tomas Gudbjartsson, Gregory T. Jones, Thomas Mueller, Anders Gottsäter, Andrea Flex, Katja K. Aben, Femmie de Vegt, Peter F. Mulders, Dolores Isla, Maria J. Vidal, Laura Asin, Berta Saez, Laura Murillo, Thorsteinn Blondal, Halldor Kolbeinsson, Jon G. Stefansson, Ingunn Hansdottir, Valgerdur Runarsdottir, Roberto Pola, Bengt Lindblad, Andre M. van Rij, Benjamin Dieplinger, Meinhard Haltmayer, Jose I. Mayordomo, Lambertus A. Kiemeney, Stefan E. Matthiasson, Hogni Oskarsson, Thorarinn Tyrfingsson, Daniel F. Gudbjartsson, Jeffrey R. Gulcher, Steinn Jonsson, Unnur Thorsteinsdottir, Augustine Kong, Kari Stefansson posted to lungcancer association addiction by vplagnol on 2009-10-19 21:45:12 as along with 5 people jo_davies operon caseybrown MPEYTO guhjy
	Identification of loci associated with schizophrenia by genome-wide association and follow-up [My Copy] Nature Genetics, Vol. 40, No. 9. (30 July 2008), pp. 1053-1055. by Michael C. O'Donovan, Nicholas Craddock, Nadine Norton, et al.Hywel Williams, Timothy Peirce, Valentina Moskvina, Ivan Nikolov, Marian Hamshere, Liam Carroll, Lyudmila Georgieva, Sarah Dwyer, Peter Holmans, Jonathan L. Marchini, Chris C. A. Spencer, Bryan Howie, Hin-Tak Leung, Annette M. Hartmann, Hans-Jurgen Moller, Derek W. Morris, YongYong Shi, GuoYin Feng, Per Hoffmann, Peter Propping, Catalina Vasilescu, Wolfgang Maier, Marcella Rietschel, Stanley Zammit, Johannes Schumacher, Emma M. Quinn, Thomas G. Schulze, Nigel M. Williams, Ina Giegling, Nakao Iwata, Masashi Ikeda, Ariel Darvasi, Sagiv Shifman, Lin He, Jubao Duan, Alan R. Sanders, Douglas F. Levinson, Pablo V. Gejman, Sven Cichon, Markus M. Nothen, Michael Gill, Aiden Corvin, Dan Rujescu, George Kirov, Michael J. Owen posted to bd association by vplagnol on 2009-10-19 21:40:55 as along with 1 person psique
	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. [My Copy] Nature genetics, Vol. 41, No. 10. (06 October 2009), pp. 1094-1099. by Jean-Charles C. Lambert, Simon Heath, Gael Even, et al.Dominique Campion, Kristel Sleegers, Mikko Hiltunen, Onofre Combarros, Diana Zelenika, Maria J. Bullido, Béatrice Tavernier, Luc Letenneur, Karolien Bettens, Claudine Berr, Florence Pasquier, Nathalie Fiévet, Pascale Barberger-Gateau, Sebastiaan Engelborghs, Peter De Deyn, Ignacio Mateo, Ana Franck, Seppo Helisalmi, Elisa Porcellini, Olivier Hanon, European Alzheimer's Disease Initiative Investigators, Marian M. de Pancorbo, Corinne Lendon, Carole Dufouil, Céline Jaillard, Thierry Leveillard, Victoria Alvarez, Paolo Bosco, Michelangelo Mancuso, Francesco Panza, Benedetta Nacmias, Paola Bossù, Paola Piccardi, Giorgio Annoni, Davide Seripa, Daniela Galimberti, Didier Hannequin, Federico Licastro, Hilkka Soininen, Karen Ritchie, Hélène Blanché, Jean-François F. Dartigues, Christophe Tzourio, Ivo Gut, Christine Van Broeckhoven, Annick Alpérovitch, Mark Lathrop, Philippe Amouyel posted to association alzheimer by vplagnol on 2009-10-19 21:35:12 as along with 2 people giovanni daforerog
	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease [My Copy] Nature Genetics, Vol. 41, No. 10. (06 September 2009), pp. 1088-1093. by Denise Harold, Richard Abraham, Paul Hollingworth, et al.Rebecca Sims, Amy Gerrish, Marian L. Hamshere, Jaspreet S. Pahwa, Valentina Moskvina, Kimberley Dowzell, Amy Williams, Nicola Jones, Charlene Thomas, Alexandra Stretton, Angharad R. Morgan, Simon Lovestone, John Powell, Petroula Proitsi, Michelle K. Lupton, Carol Brayne, David C. Rubinsztein, Michael Gill, Brian Lawlor, Aoibhinn Lynch, Kevin Morgan, Kristelle S. Brown, Peter A. Passmore, David Craig, Bernadette McGuinness, Stephen Todd, Clive Holmes, David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, John Hardy, Simon Mead, Nick Fox, Martin Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Britta Schurmann, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frolich, Harald Hampel, Michael Hull, Dan Rujescu, Alison M. Goate, John S. K. Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin Mayo, Kristel Sleegers, Karolien Bettens, Sebastiaan Engelborghs, Peter P. De Deyn, Christine Van Broeckhoven, Gill Livingston, Nicholas J. Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panagiotis Deloukas, Ammar Al-Chalabi, Christopher E. Shaw, Magda Tsolaki, Andrew B. Singleton, Rita Guerreiro, Thomas W. Muhleisen, Markus M. Nothen, Susanne Moebus, Karl-Heinz Jockel, Norman Klopp, H-Erich Wichmann, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, Peter A. Holmans, Michael O'Donovan, Michael J. Owen, Julie Williams posted to association alzheimer by vplagnol on 2009-10-19 21:34:45 as along with 3 people psique giovanni daforerog
	Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes [My Copy] Science, Vol. 324, No. 5925. (17 April 2009), pp. 387-389. by Sergey Nejentsev, Neil Walker, David Riches, Michael Egholm, John A. Todd posted to ifih1 association by vplagnol on 2009-09-23 18:34:44 as along with 8 people and 2 groups liqbbi n00c jandot APRegier myzhang pkonings absterga jbhiatt Journal picks Marcotte_Lab
	Accounting for uncertainty when assessing association between copy number and disease: a latent class model. [My Copy] BMC bioinformatics, Vol. 10 (06 June 2009), 172. by Juan R. González, Isaac Subirana, Geòrgia Escaramís, et al.Solymar Peraza, Alejandro Cáceres, Xavier Estivill, Lluís Armengol posted to cnvbook cnv association by vplagnol on 2009-08-27 22:43:46 as along with 2 people sameersoi rdiaz
	Methods and strategies for analyzing copy number variation using DNA microarrays. [My Copy] Nature genetics, Vol. 39, No. 7 Suppl. (July 2007) by Nigel P. Carter posted to cnv association by vplagnol on 2009-08-18 08:34:24 as along with 5 people and 1 group jo_davies guhjy jfr mrkrause rdiaz Bioinformatics
	On the adjustment for covariates in genetic association analysis: a novel, simple principle to infer direct causal effects. [My Copy] Genetic epidemiology, Vol. 33, No. 5. (July 2009), pp. 394-405. by Stijn Vansteelandt, Sylvie Goetgeluk, Sharon Lutz, et al.Irwin Waldman, Helen Lyon, Eric E. Schadt, Scott T. Weiss, Christoph Lange posted to association statistics by vplagnol on 2009-07-07 15:21:06 as along with 2 people guhjy pkonings
	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease [My Copy] Nat Genet, Vol. 40, No. 8. (29 August 2008), pp. 955-962. by Jeffrey C. Barrett, Sarah Hansoul, Dan L. Nicolae, et al.Judy H. Cho, Richard H. Duerr, John D. Rioux, Steven R. Brant, Mark S. Silverberg, Kent D. Taylor, Michael M. Barmada, Alain Bitton, Themistocles Dassopoulos, Lisa W. Datta, Todd Green, Anne M. Griffiths, Emily O. Kistner, Michael T. Murtha, Miguel D. Regueiro, Jerome I. Rotter, L. Philip Schumm, A. Hillary Steinhart, Stephan R. Targan, Ramnik J. Xavier, Cecile Libioulle, Cynthia Sandor, Mark Lathrop, Jacques Belaiche, Olivier Dewit, Ivo Gut, Simon Heath, Debby Laukens, Myriam Mni, Paul Rutgeerts, Andre Van Gossum, Diana Zelenika, Denis Franchimont, Jean-Pierre Hugot, Martine de Vos, Severine Vermeire, Edouard Louis, Lon R. Cardon, Carl A. Anderson, Hazel Drummond, Elaine Nimmo, Tariq Ahmad, Natalie J. Prescott, Clive M. Onnie, Sheila A. Fisher, Jonathan Marchini, Jilur Ghori, Suzannah Bumpstead, Rhian Gwilliam, Mark Tremelling, Panos Deloukas, John Mansfield, Derek Jewell, Jack Satsangi, Christopher G. Mathew, Miles Parkes, Michel Georges, Mark J. Daly posted to association cd by vplagnol on 2009-06-22 15:17:23 as along with 3 people pkonings kimorley gruberjd
	Genome-wide association study of blood pressure and hypertension. [My Copy] Nature genetics (10 May 2009) by Daniel Levy, Georg B B. Ehret, Kenneth Rice, et al.Germaine C C. Verwoert, Lenore J J. Launer, Abbas Dehghan, Nicole L L. Glazer, Alanna C C. Morrison, Andrew D D. Johnson, Thor Aspelund, Yurii Aulchenko, Thomas Lumley, Anna Köttgen, Ramachandran S S. Vasan, Fernando Rivadeneira, Gudny Eiriksdottir, Xiuqing Guo, Dan E E. Arking, Gary F F. Mitchell, Francesco U S U. Mattace-Raso, Albert V V. Smith, Kent Taylor, Robert B B. Scharpf, Shih-Jen J. Hwang, Eric J G J. Sijbrands, Joshua Bis, Tamara B B. Harris, Santhi K K. Ganesh, Christopher J J. O'Donnell, Albert Hofman, Jerome I I. Rotter, Josef Coresh, Emelia J J. Benjamin, André G G. Uitterlinden, Gerardo Heiss, Caroline S S. Fox, Jacqueline C M C. Witteman, Eric Boerwinkle, Thomas J J. Wang, Vilmundur Gudnason, Martin G G. Larson, Aravinda Chakravarti, Bruce M M. Psaty, Cornelia M M. van Duijn posted to association hypertension by vplagnol on 2009-06-17 13:30:15 as along with 1 person guhjy
	Genome-wide association study identifies eight loci associated with blood pressure. [My Copy] Nature genetics (10 May 2009) by Christopher Newton-Cheh, Toby Johnson, Vesela Gateva, et al.Martin D D. Tobin, Murielle Bochud, Lachlan Coin, Samer S S. Najjar, Jing Hua H. Zhao, Simon C C. Heath, Susana Eyheramendy, Konstantinos Papadakis, Benjamin F F. Voight, Laura J J. Scott, Feng Zhang, Martin Farrall, Toshiko Tanaka, Chris Wallace, John C C. Chambers, Kay-Tee T. Khaw, Peter Nilsson, Pim van der Harst, Silvia Polidoro, Diederick E E. Grobbee, N Charlotte C. Onland-Moret, Michiel L L. Bots, Louise V V. Wain, Katherine S S. Elliott, Alexander Teumer, Jian'an Luan, Gavin Lucas, Johanna Kuusisto, Paul R R. Burton, David Hadley, Wendy L L. McArdle, , Morris Brown, Anna Dominiczak, Stephen J J. Newhouse, Nilesh J J. Samani, John Webster, Eleftheria Zeggini, Jacques S S. Beckmann, Sven Bergmann, Noha Lim, Kijoung Song, Peter Vollenweider, Gerard Waeber, Dawn M M. Waterworth, Xin Yuan, Leif Groop, Marju Orho-Melander, Alessandra Allione, Alessandra Di Gregorio, Simonetta Guarrera, Salvatore Panico, Fulvio Ricceri, Valeria Romanazzi, Carlotta Sacerdote, Paolo Vineis, Inês Barroso, Manjinder S S. Sandhu, Robert N N. Luben, Gabriel J J. Crawford, Pekka Jousilahti, Markus Perola, Michael Boehnke, Lori L L. Bonnycastle, Francis S S. Collins, Anne U U. Jackson, Karen L L. Mohlke, Heather M M. Stringham, Timo T T. Valle, Cristen J J. Willer, Richard N N. Bergman, Mario A A. Morken, Angela Döring, Christian Gieger, Thomas Illig, Thomas Meitinger, Elin Org, Arne Pfeufer, H Erich E. Wichmann, Sekar Kathiresan, Jaume Marrugat, Christopher J J. O'Donnell, Stephen M M. Schwartz, David S S. Siscovick, Isaac Subirana, Nelson B B. Freimer, Anna-Liisa L. Hartikainen, Mark I I. McCarthy, Paul F F. O'Reilly, Leena Peltonen, Anneli Pouta, Paul E E. de Jong, Harold Snieder, Wiek H H. van Gilst, Robert Clarke, Anuj Goel, Anders Hamsten, John F F. Peden, Udo Seedorf, Ann-Christine C. Syvänen, Giovanni Tognoni, Edward G G. Lakatta, Serena Sanna, Paul Scheet, David Schlessinger, Angelo Scuteri, Marcus Dörr, Florian Ernst, Stephan B B. Felix, Georg Homuth, Roberto Lorbeer, Thorsten Reffelmann, Rainer Rettig, Uwe Völker, Pilar Galan, Ivo G G. Gut, Serge Hercberg, G Mark M. Lathrop, Diana Zelenika, Panos Deloukas, Nicole Soranzo, Frances M M. Williams, Guangju Zhai, Veikko Salomaa, Markku Laakso, Roberto Elosua, Nita G G. Forouhi, Henry Völzke, Cuno S S. Uiterwaal, Yvonne T T. van der Schouw, Mattijs E E. Numans, Giuseppe Matullo, Gerjan Navis, Göran Berglund, Sheila A A. Bingham, Jaspal S S. Kooner, John M M. Connell, Stefania Bandinelli, Luigi Ferrucci, Hugh Watkins, Tim D D. Spector, Jaakko Tuomilehto, David Altshuler, David P P. Strachan, Maris Laan, Pierre Meneton, Nicholas J J. Wareham, Manuela Uda, Marjo-Riitta R. Jarvelin, Vincent Mooser, Olle Melander, Ruth Jf J. Loos, Paul Elliott, Gonçalo R R. Abecasis, Mark Caulfield, Patricia B B. Munroe posted to association hypertension by vplagnol on 2009-06-17 13:29:57 as along with 4 people reyez pengchy Terkko guhjy
	Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes [My Copy] Nat Genet, Vol. 41, No. 6. (10 June 2009), pp. 703-707. by Jeffrey C. Barrett, David G. Clayton, Patrick Concannon, et al.Beena Akolkar, Jason D. Cooper, Henry A. Erlich, Cécile Julier, Grant Morahan, Jørn Nerup, Concepcion Nierras, Vincent Plagnol, Flemming Pociot, Helen Schuilenburg, Deborah J. Smyth, Helen Stevens, John A. Todd, Neil M. Walker, Stephen S. Rich posted to association t1d by vplagnol on 2009-05-12 14:45:50 as along with 2 people chriswallace PabloMarin
	Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility. [My Copy] The Journal of clinical endocrinology and metabolism, Vol. 92, No. 8. (August 2007), pp. 3338-3341. by A. Sutherland, J. Davies, C. J. Owen, et al.S. Vaikkakara, C. Walker, T. D. Cheetham, R. A. James, P. Perros, P. T. Donaldson, H. J. Cordell, R. Quinton, S. H. Pearce posted to association graves ifih1 by vplagnol on 2009-05-12 13:48:12 as
	Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease. [My Copy] The Journal of clinical endocrinology and metabolism, Vol. 91, No. 3. (March 2006), pp. 1056-1061. by M. J. Simmonds, J. M. Heward, J. Carr-Smith, H. Foxall, J. A. Franklyn, S. C. Gough posted to association fcrl3 graves by vplagnol on 2009-05-12 13:44:06 as
	Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease. [My Copy] Human molecular genetics, Vol. 18, No. 9. (1 May 2009), pp. 1704-1713. by O. J. Brand, J. C. Barrett, M. J. Simmonds, et al.P. R. Newby, C. J. Mccabe, C. K. Bruce, B. Kysela, J. D. Carr-Smith, T. Brix, P. J. Hunt, W. M. Wiersinga, L. Hegedüs, J. Connell, J. A. Wass, J. A. Franklyn, A. P. Weetman, J. M. Heward, S. C. Gough posted to association graves by vplagnol on 2009-05-12 13:39:04 as
	Association tests and software for copy number variant data. [My Copy] Human genomics, Vol. 3, No. 2. (1 January 2009), pp. 191-194. by Vincent Plagnol posted to association cnv by vplagnol on 2009-04-26 08:36:40 as along with 3 people guhjy daforerog jdbowes
	Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci [My Copy] Nature Genetics, Vol. 40, No. 12. (02 November 2008), pp. 1399-1401. by Jason D. Cooper, Deborah J. Smyth, Adam M. Smiles, et al.Vincent Plagnol, Neil M. Walker, James E. Allen, Kate Downes, Jeffrey C. Barrett, Barry C. Healy, Josyf C. Mychaleckyj, James H. Warram, John A. Todd posted to association gwas t1d by vplagnol on 2009-04-26 08:34:41 as
	Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis [My Copy] Nature Genetics, Vol. 39, No. 9. (29 July 2007), pp. 1108-1113. by Frida Lundmark, Kristina Duvefelt, Ellen Iacobaeus, et al.Ingrid Kockum, Erik Wallström, Mohsen Khademi, Annette Oturai, Lars P. Ryder, Janna Saarela, Hanne F. Harbo, Elisabeth G. Celius, Hugh Salter, Tomas Olsson, Jan Hillert posted to association il7r ms by vplagnol on 2009-04-06 23:39:24 as
	Meta-analysis of genome scans and replication identify CD6, ICSBP1, and TNFRSF1A as novel multiple sclerosis susceptibility loci [My Copy] In Future of Neuroscience Conference: 'New Genetics: The Future of Neurology (May 2009) by Philip De Jager posted to association ms by vplagnol on 2009-04-06 23:36:53 as
	Shared and Distinct Genetic Variants in Type 1 Diabetes and Celiac Disease [My Copy] New England Journal of Medicine, Vol. 359 (10 December 2008), pp. 2837-2838. by Deborah J. Smyth, Vincent Plagnol, Neil M. Walker, et al.Jason D. Cooper, Kate Downes, Jennie H. Yang, Joanna M. Howson, Helen Stevens, Ross Mcmanus, Cisca Wijmenga, Graham A. Heap, Patrick C. Dubois, David G. Clayton, Karen A. Hunt, David A. van Heel, John A. Todd posted to association celiac t1d by vplagnol on 2009-03-16 17:22:40 as along with 5 people and 4 groups jbhiatt booker HEIRS jdbowes ccots HEIRS Inflammatory Bowel Disease, Colititis, and IBS HEIRS Genetics HEIRS - Environmental Illness Research HEIRS Diabetes, Insulin Resistance and Metabolic Syndrome Research
	Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13. [My Copy] Biostatistics (Oxford, England) (27 November 2008) by Vincent Plagnol, Deborah J J. Smyth, John A A. Todd, David G G. Clayton posted to association geneexpression rps26 t1d by vplagnol on 2008-12-01 08:35:58 as
	STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus. [My Copy] The New England journal of medicine, Vol. 357, No. 10. (6 September 2007), pp. 977-986. by E. F. Remmers, R. M. Plenge, A. T. Lee, et al.R. R. Graham, G. Hom, T. W. Behrens, P. I. de Bakker, J. M. Le, H. S. Lee, F. Batliwalla, W. Li, S. L. Masters, M. G. Booty, J. P. Carulli, L. Padyukov, L. Alfredsson, L. Klareskog, W. V. Chen, C. I. Amos, L. A. Criswell, M. F. Seldin, D. L. Kastner, P. K. Gregersen posted to association ra sle stat4 by vplagnol on 2008-11-18 14:41:56 as along with 1 person Amazoness
	Genetic mapping in human disease. [My Copy] Science (New York, N.Y.), Vol. 322, No. 5903. (7 November 2008), pp. 881-888. by David Altshuler, Mark J. Daly, Eric S. Lander posted to association by vplagnol on 2008-11-14 07:53:59 as along with 19 people and 1 group psique mingzhi buyske Zephyrus ilyashl rdiaz zufar jfr maren guhjy daforerog gbloeb jbhiatt eetadic cheyloveday songpku renatomilani lp2 pkonings Roswell Cancer Crosstalk
	Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci [My Copy] Nature Genetics, Vol. 40, No. 2. (20 January 2008), pp. 204-210. by John B. Harley, Marta E. Alarcón-Riquelme, Lindsey A. Criswell, et al.Chaim O. Jacob, Robert P. Kimberly, Kathy L. Moser, Betty P. Tsao, Timothy J. Vyse, Carl D. Langefeld posted to association sle by vplagnol on 2008-11-04 17:58:18 as
	RA/T1D paper [My Copy] Genes and Immunity (2008) by Erik Fung, Deborah Smyth, John A. Todd posted to association autoimmunity ra t1d by vplagnol on 2008-10-24 10:42:56 as
	Tests for Linear Trends in Proportions and Frequencies [My Copy] Biometrics, Vol. 11, No. 3. (1955), pp. 375-386. by P. Armitage posted to statistics cnvbook association by vplagnol on 2008-10-12 08:54:26 as along with 1 person lamvuxuan
	A robust statistical method for case-control association testing with copy number variation. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1245-1252. by Chris Barnes, Vincent Plagnol, Tomas Fitzgerald, et al.Richard Redon, Jonathan Marchini, David Clayton, Matthew E. Hurles posted to association cnv statistics by vplagnol on 2008-10-12 08:45:26 as along with 15 people and 1 group daed zufar daforerog pengchy ptrobajo waszak caseybrown Zephyrus dakelley buyske misonneh djkt rdiaz Stew guhjy Roswell Cancer Crosstalk
	PLINK: a tool set for whole-genome association and population-based linkage analyses. [My Copy] American journal of human genetics, Vol. 81, No. 3. (September 2007), pp. 559-575. by Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, et al.Lori Thomas, Manuel A. Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I. de Bakker, Mark J. Daly, Pak C. Sham posted to association cnv by vplagnol on 2008-10-11 17:32:22 as along with 10 people and 3 groups shikin natstreet xingxu maren daforerog ekostem misonneh Zephyrus stajich psique Roswell Cancer Crosstalk Mycology parkinson's disease references
	Copy-number variation and association studies of human disease. [My Copy] Nature genetics, Vol. 39, No. 7 Suppl. (July 2007) by Steven A. McCarroll, David M. Altshuler posted to association cnv by vplagnol on 2008-09-16 14:46:37 as along with 9 people and 1 group psique daforerog waszak jo_davies guhjy mrkrause balicea rdiaz jasonflannick Bioinformatics
	On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test. [My Copy] Genetic epidemiology, Vol. 32, No. 3. (April 2008), pp. 273-284. by I. Ionita-Laza, G. H. Perry, B. A. Raby, et al.B. Klanderman, C. Lee, N. M. Laird, S. T. Weiss, C. Lange posted to cnvbook cnv association by vplagnol on 2008-09-16 14:04:40 as along with 3 people rdiaz maren guhjy
	Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1253-1260. by Joshua M. Korn, Finny G. Kuruvilla, Steven A. McCarroll, et al.Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick J. Collins, Katayoon Darvishi, Charles Lee, Marcia M. Nizzari, Stacey B. Gabriel, Shaun Purcell, Mark J. Daly, David Altshuler posted to cnvbook cnv association by vplagnol on 2008-09-16 13:32:19 as along with 13 people sameersoi fenghezi psique buyske maren guhjy pdexheimer pengchy caseybrown dakelley djkt daed rdiaz
	Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease [My Copy] Nat Genet, Vol. 40, No. 9. (2008), pp. 1107-1112. by Steven A. Mccarroll, Alan Huett, Petric Kuballa, et al.Shannon D. Chilewski, Aimee Landry, Philippe Goyette, Michael C. Zody, Jennifer L. Hall, Steven R. Brant, Judy H. Cho, Richard H. Duerr, Mark S. Silverberg, Kent D. Taylor, John D. Rioux, David Altshuler, Mark J. Daly, Ramnik J. Xavier posted to association cnv ibd by vplagnol on 2008-08-27 19:50:29 as along with 2 people gruberjd caseybrown
	Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms. [My Copy] Human heredity, Vol. 54, No. 1. (2002), pp. 22-33. by D. Gordon, S. J. Finch, M. Nothnagel, J. Ott posted to association genotyping by vplagnol on 2008-07-23 16:36:10 as
	Psoriasis is associated with increased beta-defensin genomic copy number. [My Copy] Nature genetics, Vol. 40, No. 1. (2 January 2008), pp. 23-25. by Edward J. J. Hollox, Ulrike Huffmeier, Patrick L. J. M. L. Zeeuwen, et al.Raquel Palla, Jesús Lascorz, Diana Rodijk-Olthuis, Peter C. M. C. van de Kerkhof, Heiko Traupe, Gys de Jongh, Martin, André Reis, John A. L. A. Armour, Joost Schalkwijk posted to association cnv psoriasis by vplagnol on 2008-06-10 11:55:49 as along with 5 people leemachado daed jo_davies bootsy caseybrown
	Genome-wide association studies for complex traits: consensus, uncertainty and challenges [My Copy] Nature Reviews Genetics, Vol. 9, No. 5. (01 May 2008), pp. 356-369. by Mark I. Mccarthy, Gonçalo R. Abecasis, Lon R. Cardon, et al.David B. Goldstein, Julian Little, John P. A. Ioannidis, Joel N. Hirschhorn posted to association by vplagnol on 2008-06-05 14:49:34 as along with 19 people and 1 group roys PabloMarin akundaje ilyashl sameersoi rdiaz qfwills Zephyrus daforerog cheyloveday klo misonneh psique guhjy xingxu echinotrix aconesa ptrobajo srp33 Roswell Cancer Crosstalk
	PTPN22 Trp620 explains the association of chromosome 1p13 with type 1 diabetes and shows a statistical interaction with HLA class II genotypes. [My Copy] Diabetes, Vol. 57, No. 6. (June 2008), pp. 1730-1737. by D. J. Smyth, J. D. Cooper, J. M. Howson, et al.N. M. Walker, V. Plagnol, H. Stevens, D. G. Clayton, J. A. Todd posted to association hla ptpn22 by vplagnol on 2008-06-03 07:14:19 as
	A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 [My Copy] Nature Genetics, Vol. 39, No. 7. (10 June 2007), pp. 827-829. by David A. van Heel, Lude Franke, Karen A. Hunt, et al.Rhian Gwilliam, Alexandra Zhernakova, Mike Inouye, Martin C. Wapenaar, Martin C. N. M. Barnardo, Graeme Bethel, Geoffrey K. T. Holmes, Con Feighery, Derek Jewell, Dermot Kelleher, Parveen Kumar, Simon Travis, Julian R. F. Walters, David S. Sanders, Peter Howdle, Jill Swift, Raymond J. Playford, William M. Mclaren, Luisa M. Mearin, Chris J. Mulder, Ross Mcmanus, Ralph Mcginnis, Lon R. Cardon, Panos Deloukas, Cisca Wijmenga posted to association celiac il2 by vplagnol on 2008-06-03 06:38:21 as
	Guilt beyond a reasonable doubt [My Copy] Nature Genetics, Vol. 39, No. 7., pp. 813-815. by David Altshuler, Mark Daly posted to association by vplagnol on 2008-01-13 16:07:09 as along with 6 people felsani jessopher hpiwowar jasonbobe mimulus_99 jasonflannick
	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls [My Copy] Nature, Vol. 447, No. 7145. (07 June 2007), pp. 661-678. by WTCCC posted to association statgen_mphil wtccc by vplagnol on 2008-01-13 11:55:49 as along with 35 people and 3 groups joseph_x_zhou rdiaz psique zufar mattwa daforerog ilyashl ekostem cchurc1 gruberjd Hans45 lkolodziej xingxu raistrick guhjy jfr yas hpiwowar larios jandot frohike qmwwallace joepickrell massivemayhem Garamonfok PredictER hms jo_davies caseybrown mcgannd raiyar ramensky wenhui balicea mfm11 Bioinformatics T_lab parkinson's disease references
	Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes [My Copy] Nature Genetics, Vol. 39, No. 9. (05 August 2007), pp. 1074-1082. by Christopher E. Lowe, Jason D. Cooper, Todd Brusko, et al.Neil M. Walker, Deborah J. Smyth, Rebecca Bailey, Kirsi Bourget, Vincent Plagnol, Sarah Field, Mark Atkinson, David G. Clayton, Linda S. Wicker, John A. Todd posted to association il2ra t1d by vplagnol on 2007-12-11 22:53:39 as
	Testing the gene or testing a variant? The case of TCF7L2. [My Copy] Diabetes, Vol. 56, No. 10. (October 2007), pp. 2417-2419. by M. O. Goodarzi, J. I. Rotter posted to association t2d by vplagnol on 2007-10-30 10:46:07 as
	Association of apolipoprotein E genotypes with lipid levels and coronary risk. [My Copy] JAMA : the journal of the American Medical Association, Vol. 298, No. 11. (19 September 2007), pp. 1300-1311. by A. M. Bennet, E. Di Angelantonio, Z. Ye, et al.F. Wensley, A. Dahlin, A. Ahlbom, B. Keavney, R. Collins, B. Wiman, U. de Faire, J. Danesh posted to apoe association chd by vplagnol on 2007-10-16 12:42:51 as along with 1 person daforerog
	Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma [My Copy] Nature, Vol. 448 (04 July 2007), pp. 470-473. by Miriam F. Moffatt, Michael Kabesch, Liming Liang, et al.Anna L. Dixon, David Strachan, Simon Heath, Martin Depner, Andrea von Berg, Albrecht Bufe, Ernst Rietschel, Andrea Heinzmann, Burkard Simma, Thomas Frischer, Saffron A. G. Willis-Owen, Kenny C. C. Wong, Thomas Illig, Christian Vogelberg, Stephan K. Weiland, Erika von Mutius, Gonçalo R. Abecasis, Martin Farrall, Ivo G. Gut, Mark G. Lathrop, William O. C. Cookson posted to association asthma geneexpression by vplagnol on 2007-09-10 14:10:50 as along with 3 people and 1 group gruberjd dpollard jo_davies EisenLab
	Copy number polymorphism in FCGR3 predisposes to glomerulonephritis in rats and humans [My Copy] Nature, Vol. 439, No. 7078. (16 February 2006), pp. 851-855. by Timothy J. Aitman, Rong Dong, Timothy J. Vyse, et al.Penny J. Norsworthy, Michelle D. Johnson, Jennifer Smith, Jonathan Mangion, Cheri Roberton-Lowe, Amy J. Marshall, Enrico Petretto, Matthew D. Hodges, Gurjeet Bhangal, Sheetal G. Patel, Kelly Sheehan-Rooney, Mark Duda, Paul R. Cook, David J. Evans, Jan Domin, Jonathan Flint, Joseph J. Boyle, Charles D. Pusey, Terence H. Cook posted to association cnv fcgr3b by vplagnol on 2007-09-09 11:49:57 as along with 7 people and 2 groups leemachado cscweb daed ccots cmm breden guhjy FAB-lab SFUAntibodyResearch
	FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity. [My Copy] Nature genetics, Vol. 39, No. 6. (21 May 2007), pp. 721-723. by Manuela Fanciulli, Penny J. Norsworthy, Enrico Petretto, et al.Rong Dong, Lorraine Harper, Lavanya Kamesh, Joanne M. Heward, Stephen C. L. Gough, Adam de Smith, Alexandra I. F. Blakemore, Philippe Froguel, Catherine J. Owen, Simon H. S. Pearce, Luis Teixeira, Loic Guillevin, Deborah, Charles D. Pusey, Terence H. Cook, Timothy J. Vyse, Timothy J. Aitman posted to association cnv fcgr3b by vplagnol on 2007-09-09 11:32:09 as along with 3 people leemachado yanicem daed

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association	64
t1d	39
geneexpression	38
autoantibody	27
cnv	27
statistics	22
facs	18
x-chromosome-inactivation	14
ase	11
bacteria	11
facscalibration	11
cnvbook	10
popgen	10
ucl	10
autoimmunity	9
hla	9
ld	9
clustering	8
ibd	8
rnaseq	8
statgen_mphil	8
genotyping	7
gut	7
wtcccplus_paper	7
bcells	6
il2ra	6
mass_spectrometry	6
sle	6
alzheimer	5
ifih1	5
linkage	5
ms	5
ptpn22	5
ra	5
ctla4	4
dasl	4
facsnormpaper	4
graves	4
arabidopsis	3
autophagy	3
bayes	3
cd6	3
celiac	3
epidemiology	3
fcgr3b	3
gwas	3
ia2	3
nod2	3
pca_antibodies	3
pernicious_anemia	3
schizophrenia	3
vitamind	3
abo	2
asthma	2
ccl2	2
ccr2	2
cd	2
fcgr	2
fcrl3	2
genomics	2
hgp	2
hts	2
hypertension	2
iga	2
il2	2
ips	2
mcp1	2
methylation	2
neanderthal	2
neurological_disease	2
nod	2
normalisation	2
nrxn1	2
psoriasis	2
rps26	2
structure	2
t2d	2
tpo	2
treg	2
addiction	1
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als	1
apoe	1
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bd	1
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cd226	1
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chipseq	1
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disc1	1
duchenne	1
em	1
epigenetics	1
eqtl	1
eqtls	1
fdr	1
gad	1
gender_bias	1
gene_expression	1
glm	1
icam	1
il10	1
il7r	1
immunity	1
imputation	1
indels	1
ins	1
insulin	1
inversion	1
lcls	1
luminex	1
lungcancer	1
lupus	1
mcmc	1
microarray	1
mmc	1
mouse	1
mrp814	1
nanostring	1
parkinson	1
review	1
rma	1
scoretest	1
stat4	1
tau_gene	1
trios	1
tuberculosis	1
variability	1
wtccc	1

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