Diana Zélénika
Active 1998–2016
- Also published as
- Diana Zelenika
- 65
- Papers
- 32,004
- Citations
- 64
- h-index
- 65
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.2%
- Inserm0.8%
- Massachusetts General Hospital0.7%
- Broad Institute0.6%
- Brigham and Women's Hospital0.6%
- University College London0.6%
- Other95.5%
Fields
- Biochemistry, Genetics and Molecular Biology40.8%
- Medicine39.7%
- Neuroscience9.6%
- Immunology and Microbiology5.1%
- Nursing0.7%
- Psychology0.7%
- Other3.4%
Topics
- Genetic Associations and Epidemiology6.1%
- Alzheimer's disease research and treatments6%
- Neuroinflammation and Neurodegeneration Mechanisms2.8%
- Bioinformatics and Genomic Networks2.2%
- Epigenetics and DNA Methylation1.8%
- Dementia and Cognitive Impairment Research1.5%
- Other79.6%
Coauthors
- Mark Lathrop22
- Simon Heath12
- Jean‐Charles Lambert9
- Benjamin Grenier‐Boley7
- Vincent Chouraki7
- Anne Boland6
- Denise Harold6
- M. Arfan Ikram6
- Marta Gut6
- Valérie Gaborieau6
- Albert V. Smith5
- Céline Bellenguez5
- Elizabeth Adams5
- Gary W. Beecham5
- Herman Waldmann5
- Nathalie Fiévet5
- Pilar Galán5
- Rebecca Sims5
- Stephen Cobbold5
- Yoichiro Kamatani5
- Adam C. Naj4
- Amy Gerrish4
- Anita L. DeStefano4
- Carla A. Ibrahim‐Verbaas4
All papers
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Authors: European Alzheimer's Disease Initiative (EADI), Jean‐Charles Lambert, Genetic and Environmental Risk in Alzheimer's Disease (GERAD), Carla A. Ibrahim‐Verbaas, Denise Harold, Adam C. Naj, Rebecca Sims, Céline Bellenguez, Gyungah Jun, Anita L. DeStefano, Joshua C Bis, Gary W. Beecham, Benjamin Grenier‐Boley, Giancarlo Russo, Tricia A. Thornton‐Wells, Nicola Jones, Albert V. Smith, Vincent Chouraki, Charlene Thomas, M. Arfan Ikram, Diana Zélénika, Badri N. Vardarajan, Yoichiro Kamatani, Chiao‐Feng Lin, Amy Gerrish, Helena Schmidt, Brian W. Kunkle, Melanie Dunstan, Agustı́n Ruiz, Marie‐Thérèse Bihoreau, Seung‐Hoan Choi, Christiane Reitz, Florence Pasquier, Paul Hollingworth, Alfredo Ramı́rez, Olivier Hanon, Annette L. Fitzpatrick, Joseph D. Buxbaum, Dominique Campion, Paul K. Crane, Clinton T. Baldwin, Tim Becker, Vilmundur Guðnason, Carlos Cruchaga, David Craig, Najaf Amin, Claudine Berr, Oscar L Lopez, Philip L. De Jager, Vincent Deramecourt, Janet Johnston, Denis A. Evans, Simon Lovestone, Luc Letenneur, Francisco Jesús Morón, David C. Rubinsztein, Gudny Eiriksdottir, Kristel Sleegers, Alison Goate, Nathalie Fiévet, Matthew J. Huentelman, Michael Gill, Kristelle Brown, M. Ilyas Kamboh, Lina Keller, Pascale Barberger‐Gateau, Bernadette McGuinness, Eric B. Larson, Robert C. Green, Amanda Myers, Carole Dufouil, Stephen Todd, David Wallon, Seth Love, Ekaterina Rogaeva, John Gallacher, Peter St George‐Hyslop, Jordi Clarimón, Alberto Lleó, Anthony Bayer, Debby W. Tsuang, Lei Yu, Magda Tsolaki, Paola Bossù, Gianfranco Spalletta, Petroula Proitsi, John Collinge, Sandro Sorbi, Florentino Sánchez-García, Nick C. Fox, John Hardy, María Cándida Déniz Naranjo, Paolo Bosco, Robert Clarke, Carol Brayne, Daniela Galimberti, Michelangelo Mancuso, Fiona E. Matthews, Susanne Moebus, Patrizia Mecocci and 84 more - Nature Genetics 2013 cited by 4,659
- Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Authors: the European Alzheimer's Disease Initiative Investigators, Jean‐Charles Lambert, Simon Heath, Gaël Even, Dominique Campion, Kristel Sleegers, Mikko Hiltunen, Onofre Combarros, Diana Zélénika, María J. Bullido, Béatrice Tavernier, Luc Letenneur, Karolien Bettens, Claudine Berr, Florence Pasquier, Nathalie Fiévet, Pascale Barberger‐Gateau, Sebastiaan Engelborghs, Peter Paul De Deyn, Ignacio Mateo, A. Franck, Seppo Helisalmi, Elisa Porcellini, Olivier Hanon, Marian M. de Pancorbo, Corinne Lendon, Carole Dufouil, Céline Jaillard, Thierry Léveillard, Victoria Álvarez, 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 Dartigues, Christophe Tzourio, Marta Gut, Christine Van Broeckhoven, Annick Alpérovitch, Mark Lathrop, Philippe Amouyel - Nature Genetics 2009 cited by 2,271
- Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Authors: Dan E. Arking, Vasyl Pihur, Aravinda Chakravarti, Gina M. Hilton, Gina Hilton, Aravinda Chakravarti, Murielle Bochud, Patricia B. Munroe, Sue Shaw-Hawkins, Toby Johnson, Mark J. Caulfield, Sue Shaw‐Hawkins, Patricia B. Munroe, Kenneth Rice, Ramachandran S. Vasan, Ramachandran S. Vasan, Martin G. Larson, Daniel Levy, Martin G. Larson, Thomas J. Wang, Daniel Levy, Albert V. Smith, Thor Aspelund, Daniel I. Chasman, Paul M. Ridker, Paul M. Ridker, Maria Soler Artigas, Daniel I. Chasman, Albert V. Smith, Vilmundur Guðnason, Thor Aspelund, Albert V. Smith, Vilmundur Guðnason, Thor Aspelund, Albert Hofman, María Soler Artigas, Nick Shrine, Louise V. Wain, Martin D. Tobin, André G. Uitterlinden, Najaf Amin, Yurii S. Aulchenko, Cornelia M. van Duijn, M. Arfan Ikram, Eric J.G. Sijbrands, John C. Chambers, Cornelia M. van Duijn, Peter Würtz, Ayşe Demirkan, Albert Hofman, Aaron Isaacs, Gonçalo R. Abecasis, Germaine C. Verwoert, André G. Uitterlinden, Eric J.G. Sijbrands, Joshua C. Bis, Bruce M. Psaty, Lenore Launer, Germaine C. Verwoert, Tamara B. Harris, M. Arfan Ikram, Jian’an Luan, Germaine C. Verwoert, André G. Uitterlinden, Simon Heath, Daniel Levy, Péter Vollenweider, Peter Würtz, Elin Org, Gudrun Veldre, John C. Chambers, Paul Elliott, Weihua Zhang, Gonçalo R. Abecasis, Jennifer L. Bragg‐Gresham, Uwe Völker, Alexander Teumer, Joshua C. Bis, Nicole L. Glazer, Bruce M. Psaty, Tamara B. Harris, Melissa N. Garcia, Lenore J. Launer, Nicole Soranzo, Jing Zhao, Ruth J. F. Loos, Nicholas J. Wareham, Mark Lathrop, Diana Zélénika, Simon Heath, Siim Sõber, Maris Laan, Gudrun Veldre, Elin Org, Halit Ongen, Anuj Goel, Afshin Parsa, Nanette Steinle, Alan R. Shuldiner, Yuri Milaneschi and 246 more - Nature 2011 cited by 2,083
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Authors: Jeffrey C. Barrett, Sarah Hansoul, Dan L. Nicolae, Judy H. Cho, Richard H. Duerr, John D. Rioux, Steven R. Brant, Mark S. Silverberg, Kent D. Taylor, M. Michael Barmada, Alain Bitton, Themistocles Dassopoulos, Lisa W. Datta, Todd J. Green, Anne M. Griffiths, Emily O. Kistner, Michael T. Murtha, Miguel Regueiro, Jerome I. Rotter, L. Philip Schumm, A. Hillary Steinhart, Stephan R. Targan, Ramnik J. Xavier, Cécile Libioulle, Cynthia Sandor, Mark Lathrop, Jacques Bélaïche, Olivier Dewit, Marta Gut, Simon Heath, Debby Laukens, Myriam Mni, Paul Rutgeerts, A. Van Gossum, Diana Zélénika, Denis Franchimont, Jean‐Pierre Hugot, Martine De Vos, Séverine Vermeire, Édouard Louis, Lon R. Cardon, Carl A. Anderson, Hazel E. Drummond, Elaine R. Nimmo, Tariq Ahmad, Natalie J. Prescott, Clive M. Onnie, Sheila Fisher, Jonathan Marchini, Jilur Ghori, Suzannah Bumpstead, Rhian Gwilliam, Mark Tremelling, Panos Deloukas, John Mansfield, Derek P. Jewell, Jack Satsangi, Christopher G. Mathew, Miles Parkes, Michel Georges, Mark J. Daly - Nature Genetics 2008 cited by 2,628
- Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
Authors: Claire S. Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kévin Mouzat, Dalila Pinto, Jennifer Howe, Nathalie Lemière, Christelle M. Durand, Jessica Guibert, Elodie Ey, Roberto Toro, Hugo Peyre, Alexandre Mathieu, Frédérique Amsellem, Maria Råstam, I. Carina Gillberg, Gudrun Rappold, Richard Holt, Anthony P. Monaco, Elena Maestrini, Pilar Galán, Delphine Héron, Aurélia Jacquette, Alexandra Afenjar, Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiésa, François Rivier, Dominique Bonneau, Béatrice Regnault, Diana Zélénika, Marc Délepine, Mark Lathrop, Damien Sanlaville, Caroline Schluth‐Bolard, Patrick Edery, Laurence Perrin, Anne Claude Tabet, Michael J. Schmeißer, Tobias M. Boeckers, Mary Coleman, Daisuke Sato, Péter Szatmári, Stephen W. Scherer, Guy A. Rouleau, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron - PLoS Genetics 2014 cited by 664
- Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
Authors: Tasha E. Fingerlin, Elissa Murphy, Weimin Zhang, Anna L. Peljto, Kevin M. Brown, Mark P. Steele, James E. Loyd, Gregory P. Cosgrove, David A. Lynch, Steve D. Groshong, Harold R. Collard, Paul J. Wolters, Williamson Z. Bradford, Karl Kossen, Scott D. Seiwert, Roland M. du Bois, Christine Kim Garcia, Megan Devine, Gunnar Gudmundsson, Helgi J. Ísaksson, Naftali Kaminski, Yingze Zhang, Kevin F. Gibson, Lisa Lancaster, Joy D Cogan, Wendi R. Mason, Toby M. Maher, Philip L. Molyneaux, Athol U. Wells, Miriam F. Moffatt, Moisés Selman, Annie Pardo, Dong Soon Kim, James D. Crapo, Barry J. Make, Elizabeth A. Regan, Dinesha Walek, Jerry Daniel, Yoichiro Kamatani, Diana Zélénika, Keith P. Smith, David McKean, Brent S. Pedersen, Janet Talbert, Raven N Kidd, Cheryl Markin, Kenneth B. Beckman, Mark Lathrop, Marvin I. Schwarz, David A. Schwartz - Nature Genetics 2013 cited by 825
- Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology
Authors: Julien Chapuis, Franck Hansmannel, Marc Gistelinck, A Mounier, Caroline Van Cauwenberghe, Kristof Van Kolen, Frank Geller, Yoann Sottejeau, Denise Harold, Pierre Dourlen, Benjamin Grenier‐Boley, Y Kamatani, B. Delepine, Florie Demiautte, Diana Zélénika, Nadège Zommer, Malika Hamdane, Céline Bellenguez, Dartigues Jf, J J Hauw, Florent Letronne, A-M Ayral, Kristel Sleegers, Ann Schellens, Lies Vanden Broeck, Sebastiaan Engelborghs, Peter Paul De Deyn, Rik Vandenberghe, Michael O‘Donovan, Michael J. Owen, Jacques Epelbaum, Marc Mercken, Eric Karran, Marcus Bantscheff, Gerard Drewes, Gérard Joberty, Dominique Campion, J-N Octave, Claudine Berr, Mark Lathrop, Patrick Callaerts, David M. A. Mann, Julie Williams, Luc Buée, Ilse Dewachter, Christine Van Broeckhoven, Philippe Amouyel, Dieder Moechars, Bart Dermaut, J-C Lambert - Molecular Psychiatry 2013 cited by 440
- A novel Alzheimer disease locus located near the gene encoding tau protein
Authors: Gyungah Jun, Carla A. Ibrahim‐Verbaas, Maria Vronskaya, J-C Lambert, Jaeyoon Chung, Adam C. Naj, Brian W. Kunkle, Li‐Shun Wang, Joshua C. Bis, Céline Bellenguez, Denise Harold, Kathryn L. Lunetta, Anita L. DeStefano, Benjamin Grenier‐Boley, Rebecca Sims, Gary W. Beecham, Albert V. Smith, Vincent Chouraki, Kara L. Hamilton‐Nelson, M. Arfan Ikram, Nathalie Fiévet, Nicola Denning, Eden R. Martin, Helena Schmidt, Y Kamatani, Melanie Dunstan, Otto Valladares, Agustín Ruiz Laza, Diana Zélénika, Alfredo Ramı́rez, Tatiana Foroud, S-H Choi, Anne Boland, Tim Becker, Walter A. Kukull, Sven J. van der Lee, Florence Pasquier, Carlos Cruchaga, Duane Beekly, Annette L. Fitzpatrick, Olivier Hanon, Michael Gill, Robert C. Barber, Vilmundur Guðnason, Dominique Campion, Seth Love, David A. Bennett, Najaf Amin, Claudine Berr, Magda Tsolaki, Joseph D. Buxbaum, Oscar L. López, Vincent Deramecourt, Nick C. Fox, Laura B. Cantwell, Lluís Tárraga, Carole Dufouil, John Hardy, Paul K. Crane, Gudny Eiriksdottir, Didier Hannequin, Robert Clarke, Denis A. Evans, Thomas H. Mosley, Luc Letenneur, Carol Brayne, Wolfgang Maier, Philip L. De Jager, Valur Emilsson, Dartigues Jf, Harald Hampel, M. Ilyas Kamboh, Renée F.A.G. de Bruijn, Christophe Tzourio, Pau Pástor, Eric B. Larson, Jerome I. Rotter, Michael O‘Donovan, Thomas J. Montine, Michael A. Nalls, Simon Mead, Eric M. Reiman, Pálmi V. Jónsson, Clive Holmes, Peter St George‐Hyslop, Merçé Boada, Peter Passmore, Jens R. Wendland, R. Schmidt, Kevin Morgan, Ashley R. Winslow, John Powell, M Carasquillo, Steven G. Younkin, Jóhanna Jakobsdóttir, John Kauwe, K C Wilhelmsen, Dan Rujescu, Markus M. Nöthen, Albert Hofman and 329 more - Molecular Psychiatry 2015 cited by 309
- Newly identified loci that influence lipid concentrations and risk of coronary artery disease
Authors: Cristen J. Willer, Serena Sanna, Anne Jackson, Angelo Scuteri, Lori L. Bonnycastle, Robert Clarke, Simon Heath, Nicholas J. Timpson, Samer S. Najjar, Heather M. Stringham, James Strait, William L. Duren, Andrea Maschio, Fabio Busonero, Antonella Mulas, Giuseppe Albai, Amy J. Swift, Mario A. Morken, Narisu Narisu, Derrick Bennett, Sarah Parish, Haiqing Shen, Pilar Galán, Pierre Meneton, Serge Herçberg, Diana Zélénika, Wei‐Min Chen, Yun Li, Laura J. Scott, Paul Scheet, Jouko Sundvall, Richard M. Watanabe, Ramaiah Nagaraja, Shah Ebrahim, Debbie A. Lawlor, Yoav Ben‐Shlomo, George Davey-Smith, Alan R. Shuldiner, Rory Collins, Richard N. Bergman, Manuela Uda, Jaakko Tuomilehto, Antonio Cao, Francis S. Collins, Edward G. Lakatta, G.M. Lathrop, Michael Boehnke, David Schlessinger, Karen L. Mohlke, Gonçalo R. Abecasis - Nature Genetics 2008 cited by 1,600
- Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
Authors: Karine Poirier, Nicolas Lebrun, Loïc Broix, Guoling Tian, Yoann Saillour, Cécile Boscheron, Elena Parrini, Stéphanie Valence, Benjamin Saint Pierre, Madison Oger, Didier Lacombe, David Geneviève, Elena Fontana, Francesca Darra, Claude Cancès, Magalie Barth, Dominique Bonneau, Bernardo Dalla Bernadina, Sylvie Nguyen, Cyril Gitiaux, Philippe Parent, Vincent des Portes, Jean Michel Pedespan, Victoire Legrez, Laetitia Castelnau-Ptakine, Patrick Nitschké, Thierry Hieu, Cécile Masson, Diana Zélénika, Annie Andrieux, Fiona Francis, Renzo Guerrini, Nicholas J. Cowan, Nadia Bahi‐Buisson, Jamel Chelly - Nature Genetics 2013 cited by 498
- A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
Authors: Stephan Menzel, Chad Garner, Marta Gut, Fumihiko Matsuda, Masao Yamaguchi, Simon Heath, Mario Foglio, Diana Zélénika, Anne Boland, Helen Rooks, Steve Best, Tim D. Spector, Martin Farrall, Mark Lathrop, Swee Lay Thein - Nature Genetics 2007 cited by 530
- A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma
Authors: Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub, Mahaut de Lichy, Karine Bille, Philippe Dessen, Benoit d’Hayer, Hamida Mohamdi, Audrey Remenieras, E. Maubec, Arnaud de la Fouchardière, Vincent Molinié, P. Vabres, Stéphane Dalle, Nicolas Poulalhon, Tanguy Martin‐Denavit, L. Thomas, Pascale Andry-Benzaquen, N. Dupin, F. Boitier, Annick Rossi, Jean‐Luc Perrot, B. Labeille, Caroline Robert, Bernard Escudier, Olivier Caron, Laurence Brugières, Simon Saule, Betty Gardie, Sophie Gad, Stéphane Richard, Jérôme Couturier, Bin Tean Teh, Paola Ghiorzo, Lorenza Pastorino, Susana Puig, Célia Bádenas, Håkan Olsson, Christian Ingvar, Etienne Rouleau, Rosette Lidereau, Philippe Bahadoran, Philippe Vielh, Eve Corda, Hélène Blanché, Diana Zélénika, Pilar Galán, The French Familial Melanoma Study Group, F. Aubin, Bertrand Bachollet, Céline Becuwe, Pascaline Berthet, Yves Jean Bignon, Valérie Bonadona, Jean‐Louis Bonafé, Marie‐Noëlle Bonnet‐Dupeyron, F. Cambazard, J. Chevrant‐Breton, Isabelle Coupier, S. Dalac, Liliane Demange, M. D’Incan, Catherine Dugast, Laurence Faivre, Lynda Vincent-Fétita, Marion Gauthier-Villars, Brigitte Gilbert, Florent Grange, Jean‐Jacques Grob, Philippe Humbert, Nicolas Janin, Pascal Joly, Delphine Kérob, Christine Lasset, Dominique Leroux, J. Levang, Jean‐Marc Limacher, C. Bulaï Livideanu, Michel Longy, Alain Lortholary, Dominique Stoppa-Lyonnet, Sandrine Mansard, L Mansuy, Karine Marrou, Christine Matéus, Christine Maugard, Nicolás Meyer, Catherine Noguès, P Souteyrand, Laurence Venat‐Bouvet, Hélène Zattara, Valérie Chaudru, Gilbert Lenoir, Mark Lathrop, Irwin Davidson, Marie-Françoise Avril, Florence Démenais, Robert Ballotti, Brigitte Bressac–de Paillerets - Nature 2011 cited by 522
- Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease
Authors: Rachel Soemedi, Ian Wilson, Jamie Bentham, Rebecca Darlay, Ana Töpf, Diana Zélénika, Catherine Cosgrove, Kerry Setchfield, Chris Thornborough, Javier T Granados-Riveron, Gillian M. Blue, Jeroen Breckpot, Stephen Hellens, Simon Zwolinkski, Elise Glen, Chrysovalanto Mamasoula, Thahira Rahman, Darroch Hall, Anita Rauch, Koenraad Devriendt, Marc Gewillig, John O’ Sullivan, David S. Winlaw, Frances Bu’Lock, J. David Brook, Shoumo Bhattacharya, Mark Lathrop, Mauro Santibanez‐Koref, Heather J. Cordell, Judith A. Goodship, Bernard Keavney - The American Journal of Human Genetics 2012 cited by 338
- CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs
Authors: Anne‐Christine Merveille, Erica E. Davis, Anita Becker-Heck, Marie Legendre, Israel Amirav, Géraldine Bataille, John W. Belmont, Nicole Beydon, Frédéric Billen, Annick Clément, Cécile Clercx, A. Coste, Rachelle H. Crosbie, J. de Blic, Stephane Deleuze, Philippe Duquesnoy, Denise Escalier, Estelle Escudier, Manfred Fliegauf, Judith Horvath, Kent L. Hill, Mark Jorissen, J. Just, Andreas Kispert, Mark Lathrop, Niki T. Loges, June K. Marthin, Yukihide Momozawa, Guy Montantin, Kim G. Nielsen, Heike Olbrich, Jean‐François Papon, I Rayet, Gilles Roger, Miriam Schmidts, Henrique Tenreiro, Jeffrey A. Towbin, Diana Zélénika, Hanswalter Zentgraf, Michel Georges, Anne‐Sophie Lequarré, Nicholas Katsanis, Heymut Omran, Serge Amselem - Nature Genetics 2010 cited by 345
- Common variants at 30 loci contribute to polygenic dyslipidemia
Authors: Sekar Kathiresan, Cristen J. Willer, Gina M. Peloso, Serkalem Demissie, Kiran Musunuru, Eric E. Schadt, Lee M. Kaplan, Derrick Bennett, Yun Li, Toshiko Tanaka, Benjamin F. Voight, Lori L. Bonnycastle, Anne Jackson, Gabriel Crawford, Aarti Surti, Candace Guiducci, Noël P. Burtt, Sarah Parish, Robert Clarke, Diana Zélénika, Kari Kubalanza, Mario A. Morken, Laura J. Scott, Heather M. Stringham, Pilar Galán, Amy J. Swift, Johanna Kuusisto, Richard N. Bergman, Jouko Sundvall, Markku Laakso, Luigi Ferrucci, Paul Scheet, Serena Sanna, Manuela Uda, Qiong Yang, Kathryn L. Lunetta, Josée Dupuis, Paul I. W. de Bakker, Christopher J. O’Donnell, John C. Chambers, Jaspal S. Kooner, Serge Herçberg, Pierre Meneton, Edward G. Lakatta, Angelo Scuteri, David Schlessinger, Jaakko Tuomilehto, Francis S. Collins, Leif Groop, David Altshuler, Rory Collins, G.M. Lathrop, Olle Melander, Veikko Salomaa, Leena Peltonen, Marju Orho‐Melander, José M. Ordovás, Michael Boehnke, Gonçalo R. Abecasis, Karen L. Mohlke, L. Adrienne Cupples - Nature Genetics 2008 cited by 1,375
- A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Authors: Rayjean J. Hung, James McKay, Valérie Gaborieau, Paolo Boffetta, Mia Hashibe, Давид Заридзе, Anush Mukeria, Neonilia Szeszenia‐Dabrowska, Jolanta Lissowska, Péter Rudnai, Eleonóra Fabiánová, Dana Mateș, Vladimír Bencko, Lenka Foretová, Vladimír Janout, Chu Chen, Gary E. Goodman, John K. Field, Triantafillos Liloglou, George Xinarianos, Adrian Cassidy, John McLaughlin, Geoffrey Liu, Steven A. Narod, Hans E. Krokan, Frank Skorpen, Maiken Bratt Elvestad, Kristian Hveem, Lars J. Vatten, Jakob Linseisen, Françoise Clavel‐Chapelon, Paolo Vineis, H. Bas Bueno‐de‐Mesquita, Eiliv Lund, Carmen Martı́nez, Sheila Bingham, Torgny Rasmuson, Pierre Hainaut, Elio Ríboli, Wolfgang Ahrens, Simone Benhamou, Παγώνα Λάγιου, Dimitrios Trichopoulos, Ivana Holcátová, Franco Merletti, Kristina Kjærheim, Antonio Agudo, Gary J. Macfarlane, Renato Talamini, Lorenzo Simonato, Ray Lowry, David I. Conway, Ariana Znaor, Claire M. Healy, Diana Zélénika, Anne Boland, Marc Délepine, Mario Foglio, Doris Lechner, Fumihiko Matsuda, Hélène Blanché, Marta Gut, Simon Heath, Mark Lathrop, Paul Brennan - Nature 2008 cited by 1,291
- Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Authors: Claire S. Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Råstam, Henrik Anckarsäter, Gudrun Nygren, I. Carina Gillberg, Jonas Melke, Roberto Toro, Béatrice Regnault, Fabien Fauchereau, Oriane Mercati, Nathalie Lemière, David Skuse, Martin Poot, Richard Holt, Anthony P. Monaco, Irma Järvelä, Katri Kantojärvi, Raija Vanhala, Sarah Curran, David Collier, Patrick Bolton, Andreas G. Chiocchetti, Sabine M. Klauck, Fritz Poustka, Christine M. Freitag, Regina Waltes, Marnie Kopp, Eftichia Duketis, Elena Bacchelli, Fiorella Minopoli, Liliana Ruta, Agatino Battaglia, Luigi Mazzone, Elena Maestrini, Ana Filipa Sequeira, Bárbara Oliveira, Astrid M. Vicente, Guiomar Oliveira, Dalila Pinto, Stephen W. Scherer, Diana Zélénika, Marc Délepine, Mark Lathrop, Dominique Bonneau, Vincent Guinchat, Françoise Devillard, Brigitte Assouline, Marie–Christine Mouren, Marion Leboyer, Christopher Gillberg, Tobias M. Boeckers, Thomas Bourgeron - PLoS Genetics 2012 cited by 443
- Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Authors: Heather J. Cordell, Jamie Bentham, Ana Töpf, Diana Zélénika, Simon Heath, Chrysovalanto Mamasoula, Catherine Cosgrove, Gillian M. Blue, Javier T Granados-Riveron, Kerry Setchfield, Chris Thornborough, Jeroen Breckpot, Rachel Soemedi, Ruairidh Martin, Thahira Rahman, Darroch Hall, Klaartje van Engelen, Antoon F.M. Moorman, A. H. Zwinderman, Phil Barnett, Tamara T. Koopmann, Michiel Adriaens, András Varró, Alfred L. George, C. Dos Remedios, Nanette H. Bishopric, Connie R. Bezzina, John O’Sullivan, Marc Gewillig, Frances Bu’Lock, David S. Winlaw, Shoumo Bhattacharya, Koenraad Devriendt, J. David Brook, Barbara J.M. Mulder, Seema Mital, Alex V. Postma, G.M. Lathrop, Martin Farrall, Judith A. Goodship, Bernard Keavney - Nature Genetics 2013 cited by 165
- Serial translocation by means of circular intermediates underlies colour sidedness in cattle
Authors: Keith Durkin, Wouter Coppieters, Cord Drögemüller, Naïma Ahariz, Nadine Cambisano, Tom Druet, Corinne Fasquelle, Aynalem Haile, Petr Hořín, Lusheng Huang, Yohichiro Kamatani, Latifa Karim, Mark Lathrop, Simon Moser, Kor Oldenbroek, Stefan Rieder, Arnaud Sartelet, Johann Sölkner, H. Stålhammar, Diana Zélénika, Zhiyan Zhang, Tosso Leeb, Michel Georges, Carole Charlier - Nature 2012 cited by 200
- Effect of 17q21 Variants and Smoking Exposure in Early-Onset Asthma
Authors: Emmanuelle Bouzigon, Eve Corda, Hugues Aschard, Marie‐Hélène Dizier, Anne Boland, Jean Bousquet, Nicolas Chateigner, F. Gormand, J. Just, Nicole Le Moual, P. Scheinmann, Valérie Siroux, D. Vervloët, Diana Zélénika, Isabelle Pin, F. Kauffmann, Mark Lathrop, Florence Démenais - New England Journal of Medicine 2008 cited by 405
- Convergent genetic and expression data implicate immunity in Alzheimer's disease
Authors: Lesley Jones, Jean‐Charles Lambert, Weixin Wang, Seung‐Hoan Choi, Denise Harold, Alexey Vedernikov, Valentina Escott‐Price, Timothy Stone, Alexander Richards, Céline Bellenguez, Carla A. Ibrahim‐Verbaas, Adam C. Naj, Rebecca Sims, Amy Gerrish, Gyungah Jun, Anita L. DeStefano, Joshua C. Bis, Gary W. Beecham, Benjamin Grenier‐Boley, Giancarlo Russo, Tricia A. Thornton‐Wells, Nicola Jones, Albert V. Smith, Vincent Chouraki, Charlene Thomas, M. Arfan Ikram, Diana Zélénika, Badri N. Vardarajan, Yoichiro Kamatani, Chiao‐Feng Lin, Helena Schmidt, Brian W. Kunkle, Melanie Dunstan, Agustı́n Ruiz, Marie‐Thérèse Bihoreau, Christiane Reitz, Florence Pasquier, Paul Hollingworth, Olivier Hanon, Annette L. Fitzpatrick, Joseph D. Buxbaum, Dominique Campion, Paul K. Crane, Tim Becker, Vilmundur Guðnason, Carlos Cruchaga, David W. Craig, Najaf Amin, Claudine Berr, Oscar L. López, Philip L. De Jager, Vincent Deramecourt, Janet Johnston, Denis A. Evans, Simon Lovestone, Luc Letteneur, Johanes Kornhuber, Lluís Tárraga, David C. Rubinsztein, Gudny Eiriksdottir, Kristel Sleegers, Alison Goate, Nathalie Fiévet, Matthew J. Huentelman, Michael Gill, Valur Emilsson, Kristelle Brown, M. Ilyas Kamboh, Lina Keller, Pascale Barberger‐Gateau, Bernadette McGuinness, Eric B. Larson, Amanda Myers, Carole Dufouil, Stephen Todd, David Wallon, Seth Love, Patrick G. Kehoe, Ekaterina Rogaeva, John Gallacher, Peter St George‐Hyslop, Jordi Clarimón, Alberti Lleὀ, Anthony Bayer, Debby W. Tsuang, Lei Yu, Magda Tsolaki, Paola Bossù, Gianfranco Spalletta, Petra Proitsi, John Collinge, Sandro Sorbi, Florentino Sánchez-García, Nick C. Fox, John Hardy, María Cándida Déniz Naranjo, Cristina Razquín, Paola Bosco, Robert Clarke, Carol Brayne and 87 more - Alzheimer s & Dementia 2014 cited by 207
- Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease
Authors: J-C Lambert, Benjamin Grenier‐Boley, Denise Harold, Diana Zélénika, Vincent Chouraki, Y Kamatani, Kristel Sleegers, M. Arfan Ikram, Mikko Hiltunen, Christiane Reitz, Ignacio Mateo, Thomas Feulner, María J. Bullido, Daniela Galimberti, Letizia Concari, Victoria Álvarez, Rebecca Sims, Amy Gerrish, Jade Chapman, C Deniz-Naranjo, Vincenzo Solfrizzi, Sandro Sorbi, Beatrice Arosio, Gianfranco Spalletta, Gabriele Siciliano, Jacques Epelbaum, Didier Hannequin, Dartigues Jf, Christophe Tzourio, Claudine Berr, Elisabeth M. C. Schrijvers, Robert S. Rogers, Giuseppe Tosto, Florence Pasquier, Karolien Bettens, Caroline Van Cauwenberghe, Laura Fratiglioni, Caroline Graff, Marc Délepine, Raffaele Ferri, Chandra A. Reynolds, Lars Lannfelt, Martin Ingelsson, Jonathan A. Prince, Caterina Chillotti, Alberto Pilotto, Davide Seripa, Anne Boland, Michelangelo Mancuso, Paola Bossù, Giorgio Annoni, Benedetta Nacmias, Paolo Bosco, Francesco Panza, Florentino Sánchez-García, Maria Del Zompo, Eliécer Coto, Michael J. Owen, Michael O‘Donovan, Fernando Valdivieso, P Caffara, Elio Scarpini, Onofre Combarros, Luc Buée, Dominique Campion, Hilkka Soininen, Monique M.B. Breteler, Markus J. Riemenschneider, Christine Van Broeckhoven, Annick Alpérovitch, M Lathrop, David‐Alexandre Trégouët, Julie Williams, Philippe Amouyel - Molecular Psychiatry 2012 cited by 146
- Genome-wide association study identifies three loci associated with melanoma risk
Authors: D. Timothy Bishop, Florence Démenais, Mark M. Iles, Mark Harland, John Taylor, Eve Corda, Juliette A. Randerson‐Moor, Joanne F. Aitken, Marie‐Françoise Avril, Esther Azizi, Egbert Bakker, Giovanna Bianchi‐Scarrà, Brigitte Bressac–de Paillerets, Donato Calista, Lisa Cannon‐Albright, Thomas F. C. Chin‐A‐Woeng, Tadeusz Dębniak, Gilli Galore-Haskel, Paola Ghiorzo, Marta Gut, Johan Hansson, Marko Hočevar, Veronica Höiom, John L. Hopper, Christian Ingvar, Peter A. Kanetsky, Richard Kefford, Maria Teresa Landi, Julie Lang, Jan Lubiński, Rona M. MacKie, Josep Malvehy, Graham J. Mann, Nicholas G. Martin, Grant W. Montgomery, Frans A. van Nieuwpoort, Srdjan Novaković, Håkan Olsson, Susana Puig, Marjan M. Weiss, Wilbert van Workum, Diana Zélénika, Kevin M Brown, Alisa M. Goldstein, Elizabeth M. Gillanders, Anne Boland, Pilar Galán, David E. Elder, Nelleke A. Gruis, Nicholas K. Hayward, G.M. Lathrop, Jennifer H. Barrett, Julia Newton‐Bishop - Nature Genetics 2009 cited by 464
- Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection
Authors: Stéphanie Debette, the CADISP group, Yoichiro Kamatani, Tiina M. Metso, Manja Kloß, Ganesh Chauhan, Stefan T. Engelter, Alessandro Pezzini, Vincent Thijs, Hugh S. Markus, Martin Dichgans, Christiane Wolf, Ralf Dittrich, Emmanuel Touzé, Andrew M. Southerland, Yves Samson, Shérine Abboud, Yannick Béjot, Valeria Caso, Anna Bersano, Andreas Gschwendtner, Maria Sessa, John Cole, Chantal Lamy, Elisabeth Medeiros, Simone Beretta, Leo H. Bonati, Armin Grau, Patrik Michel, Jennifer J. Majersik, Pankaj Sharma, Ludmila А. Kalashnikova, Maria Nazarova, Л А Добрынина, Eva Bartels, B. Guillon, Evita G. van den Herik, Israel Fernández‐Cadenas, Katarina Jood, Michael A. Nalls, Frank‐Erik de Leeuw, Christina Jern, Yu‐Ching Cheng, Inge Werner, Antti J. Metso, Christoph Lichy, Philippe Lyrer, Tobias Brandt, Giorgio B. Boncoraglio, Heinz‐Erich Wichmann, Christian Gieger, Andrew D. Johnson, Thomas Böttcher, Maurizio Castellano, Dominique Arveiler, M. Arfan Ikram, Monique M.B. Breteler, Alessandro Padovani, James F. Meschia, Gregor Kuhlenbäumer, Arndt Rolfs, Bradford B. Worrall, Ringelstein Erich-Bernd, Diana Zélénika, Turgut Tatlisumak, Mark Lathrop, Didier Leys, Philippe Amouyel, Jean Dallongeville - Nature Genetics 2014 cited by 233
