نتائج البحث - Claudine Laurent

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  1. 1
    Pre‐, peri‐ and neonatal risk factors for autism

    Pre‐, peri‐ and neonatal risk factors for autism حسب Vincent Guinchat, Poul Thorsen, Claudine Laurent, Christine Cans, Nicolas Bodeau, David Cohen

    منشور في 2011
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  2. 2
    Genetic Association Studies of Suicidal Behavior: A Review of the Past 10 Years, Progress, Limitations, and Future Directions

    Genetic Association Studies of Suicidal Behavior: A Review of the Past 10 Years, Progress, Limitations, and Future Directions حسب Bojan Mirkovic, Claudine Laurent, Marc-Antoine Podlipski, Thierry Frébourg, Doron Cohen, Priscille Gérardin

    منشور في 2016
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  3. 3
    Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?

    Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk? حسب Claire Amiet, Isabelle Gourfinkel‐An, Claudine Laurent, Nicolas Bodeau, Bérengère Génin, Eric Leguern, Sylvie Tordjman, David Cohen

    منشور في 2013
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  4. 4
    Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders

    Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders حسب Caroline Nava, Boris Keren, Cyril Mignot, Agnès Rastetter, Sandra Chantot‐Bastaraud, Anne Faudet, Eric Fonteneau, Claire Amiet, Claudine Laurent, Aurélia Jacquette, Sandra Whalen, Alexandra Afenjar, Didier Périsse, Diane Doummar, Nathalie Dorison, Marion Leboyer, Jean‐Pierre Siffroi, David Cohen, Alexis Brice, Delphine Héron, Christel Depienne

    منشور في 2013
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  5. 5
    Multicenter Linkage Study of Schizophrenia Candidate Regions on Chromosomes 5q, 6q, 10p, and 13q: Schizophrenia Linkage Collaborative Group III

    Multicenter Linkage Study of Schizophrenia Candidate Regions on Chromosomes 5q, 6q, 10p, and 13q: Schizophrenia Linkage Collaborative Group III حسب Douglas F. Levinson, Peter Holmans, Richard E. Straub, Michael J. Owen, Dieter B. Wildenauer, Pablo V. Gejman, Ann E. Pulver, Claudine Laurent, Kenneth S. Kendler, Dermot Walsh, Nadine Norton, Nigel Williams, Sibylle G. Schwab, Bernard Lerer, Bryan Mowry, Alan R. Sanders, Stylianos E. Antonarakis, Jean-Louis Blouin, Jean‐François Deleuze, Jacques Mallet

    منشور في 2000
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  6. 6
    Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE

    Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE حسب Caroline Nava, Foudil Lamari, Delphine Héron, Cyril Mignot, Agnès Rastetter, Boris Keren, David Cohen, Anne Faudet, Delphine Bouteiller, Martine Gilleron, Aurélia Jacquette, Sandra Whalen, Alexandra Afenjar, Didier Périsse, Claudine Laurent, Céline Dupuits, Cécile Gautier, Marion Gérard, Guillaume Huguet, S Caillet, Bruno Leheup, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron, Alexis Brice, Christel Depienne

    منشور في 2012
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  7. 7
    Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms

    Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms حسب Peter Holmans, Brien P. Riley, Ann E. Pulver, Michael J. Owen, Dieter B. Wildenauer, Pablo V. Gejman, Bryan Mowry, Claudine Laurent, Kenneth S. Kendler, Gerald Nestadt, Nigel Williams, Sibylle G. Schwab, A R Sanders, Deborah A. Nertney, Jacques Mallet, Brandon Wormley, Virginia K. Lasseter, Michael O’Donovan, Jubao Duan, Margot Albus, Madeline Alexander, Stephanie Godard, R. Ribble, K.-Y. Liang, Nadine Norton, Wolfgang Maier, George N. Papadimitriou, Dermot Walsh, Melanie Jay, F. Anthony O’Neill, F. B. Lerer, Dimitris Dikeos, R R Crowe, Jeremy M. Silverman, Douglas F. Levinson

    منشور في 2009
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  8. 8
    Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees

    Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees حسب Douglas F. Levinson, Jianxin Shi, Kai Wang, Sang‐Yun Oh, Brien P. Riley, Ann E. Pulver, Dieter B. Wildenauer, Claudine Laurent, Bryan Mowry, Pablo V. Gejman, Michael J. Owen, Kenneth S. Kendler, Gerald Nestadt, Sibylle G. Schwab, Jacques Mallet, Deborah A. Nertney, Alan R. Sanders, Nigel Williams, Brandon Wormley, Virginia K. Lasseter, Margot Albus, Stéphanie Bauché, Madeline Alexander, Jubao Duan, Michael O’Donovan, Dermot Walsh, F. Anthony O’Neill, George N. Papadimitriou, Dimitris Dikeos, Wolfgang Maier, Bernard Lerer, Dominique Campion, David Cohen, Maurice Jay, Ayman H. Fanous, Peter Eichhammer, Jeremy M. Silverman, Nadine Norton, Nancy Zhang, Hákon Hákonarson, Cynthia Gao, Ami Citri, Thomas Hansen, Stephan Ripke, Frank Dudbridge, Peter Holmans

    منشور في 2012
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  9. 9
    Follow‐up of a report of a potential linkage for schizophrenia on chromosome 22q12‐q13.1: Part 2

    Follow‐up of a report of a potential linkage for schizophrenia on chromosome 22q12‐q13.1: Part 2 حسب Ann E. Pulver, Maria Karayiorgou, Virginia K. Lasseter, Paula Wolyniec, Laura Kasch, Stylianos E. Antonarakis, David E. Housman, Haig H. Kazazian, Deborah A. Meyers, Gerald Nestadt, Jürg Ott, Kung‐Yee Liang, Malgorzata Lamacz, Marion Thomas, Barton Childs, Scott R. Diehl, Shengbiao Wang, Bernadette Murphy, Cuie Sun, F. Anthony O’Neill, Li Nie, Pak C. Sham, John Burke, Betty W. Duke, Fiona Duke, Barbara R. Kipps, Joseph Bray, Wanda Hunt, Rosmarie Shinkwin, Maurin Ni Nuallain, Ying Su, Charles J. MacLean, Dermot Walsh, Kenneth S. Kendler, Michael Gill, Homero Vallada, R. Mant, Philip Asherson, David Collier, E. Parfitt, E. E. Roberts, Shin Nanko, Cathy Walsh, Johanna Daniels, Robin Murray, Peter McGuffin, Mike Owen, Claudine Laurent, Jean‐Baptiste Dumas, Thierry d’Amato, Maurice Jay, María Martínez, Dominique Campion, Jacques Mallet

    منشور في 1994
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  10. 10
    Meta-analysis of 32 genome-wide linkage studies of schizophrenia

    Meta-analysis of 32 genome-wide linkage studies of schizophrenia حسب Mandy Ng, Douglas F. Levinson, Stephen V. Faraone, Brian K. Suarez, Lynn E. DeLisi, Tadao Arinami, Brien P. Riley, Tiina Paunio, Ann E. Pulver, Irmansyah, Peter Holmans, Michael Escamilla, Dieter B. Wildenauer, Nigel Williams, Claudine Laurent, Bryan Mowry, Linda M. Brzustowicz, Michel Maziade, Pamela Sklar, D. Garver, Gonçalo R. Abecasis, Bernard Lerer, M. Daniele Fallin, Hugh Gurling, Pablo V. Gejman, Eva Lindholm, Hans W. Moises, William Byerley, Ellen M. Wijsman, Paola Forabosco, Ming T. Tsuang, Hai‐Gwo Hwu, Yozo Okazaki, Kenneth S. Kendler, Brandon Wormley, Ayman H. Fanous, Dermot Walsh, F. Anthony O’Neill, L. Peltonen, Gerald Nestadt, Virginia K. Lasseter, Kung‐Yee Liang, G. Papadimitriou, Dimitris Dikeos, Sibylle G. Schwab, Michael J. Owen, Michael O’Donovan, Nadine Norton, Elizabeth Hare, Henriette Raventós, Humberto Nicolini, Margot Albus, W. Maier, Vishwajit L. Nimgaonkar, Lars Terenius, Jacques Mallet, Melanie Jay, Stephanie Godard, Deborah A. Nertney, Madeline Alexander, R R Crowe, Jeremy M. Silverman, Anne S. Bassett, M-A Roy, Chantal Mérette, Carlos N. Pato, Michele T. Pato, Johannes L. Roos, Yoav Kohn, Daniela Amann‐Zalcenstein, G. Kalsi, Andrew McQuillin, David Curtis, Jon Brynjolfson, Thordur Sigmundsson, Hannes Pétursson, Alan R. Sanders, Jubao Duan, Elena Jazin, Marina Myles‐Worsley, Maria Karayiorgou, Cathryn M. Lewis

    منشور في 2008
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  11. 11
    Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

    Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions حسب Eduardo A. Maury, Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris, Prashanth Rajarajan, Erin Flaherty, Schahram Akbarian, Andrew Chess, Steven A. McCarroll, Po‐Ru Loh, Jennifer E. Phillips‐Cremins, Kristen Brennand, Evan Z. Macosko, James Walters, Michael O’Donovan, Patrick F. Sullivan, Jonathan Sebat, Eunjung A. Lee, Christopher A. Walsh, Christian R. Marshall, Daniele Merico, Bhooma Thiruvahindrapuram, Zhouzhi Wang, Stephen W. Scherer, Daniel P. Howrigan, Stephan Ripke, Brendan Bulik‐Sullivan, Kai-How Farh, Menachem Fromer, Jacqueline I. Goldstein, Hailiang Huang, Phil Lee, Mark J. Daly, Benjamin M. Neale, Richard A. Belliveau, Sarah E. Bergen, Elizabeth Bevilacqua, Kimberley D. Chambert, Colm Ó'Dúshláine, Edward M. Scolnick, Jordan W. Smoller, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Wenting Wu, Douglas S. Greer, Danny Antaki, Aniket Shetty, Madhusudan Gujral, William M. Brandler, Dheeraj Malhotra, Karin V. Fuentes Fajarado, Michelle S. Maile, Peter Holmans, Noa Carrera, Nick Craddock, Valentina Escott‐Price, Lyudmila Georgieva, Marian L. Hamshere, David Kavanagh, Sophie E. Legge, Andrew Pocklington, Alexander Richards, Douglas M. Ruderfer, Nigel Williams, George Kirov, Michael J. Owen, Dalila Pinto, Guiqing Cai, Kenneth L. Davis, Elodie Drapeau, Joseph I. Friedman, Vahram Haroutunian, Elena Parkhomenko, Abraham Reichenberg, Jeremy M. Silverman, Joseph D. Buxbaum, Enrico Domenici, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Ole A. Andreassen, Erik G. Jönsson, Erik Söderman, Margot Albus, Madeline Alexander, Claudine Laurent, Douglas F. Levinson, Farooq Amin, Joshua Atkins, Murray J. Cairns, Rodney J. Scott, Paul A. Tooney, Jing Qin Wu, Silviu‐Alin Bacanu, Tim B. Bigdeli, Mark A. Reimers

    منشور في 2023
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