Risultati della ricerca - Camille W. Brune

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  1. 1
    Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism

    Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism di Suma Jacob, Camille W. Brune, C. S. Carter, Bennett Leventhal, Catherine Lord, Edwin H. Cook

    Pubblicazione 2007
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  2. 2
    A pharmacogenetic study of escitalopram in autism spectrum disorders

    A pharmacogenetic study of escitalopram in autism spectrum disorders di Thomas Owley, Camille W. Brune, Jeff Salt, Laura Walton, Stephen J. Guter, Nelson Ayuyao, Robert D. Gibbons, Bennett Leventhal, Edwin H. Cook

    Pubblicazione 2009
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  3. 3
    Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

    Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism di Ryan Delahanty, Jing‐Qiong Kang, Camille W. Brune, Emily O. Kistner, Eric Courchesne, Nancy J. Cox, Edwin H. Cook, Robert L. Macdonald, James S. Sutcliffe

    Pubblicazione 2009
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  4. 4
    A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

    A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism di Revati Kumar, Jyotsna Sudi, TD Babatz, Camille W. Brune, Donald P. Oswald, Michael T. Yen, Norma J. Nowak, Edwin H. Cook, Susan L. Christian, William B. Dobyns

    Pubblicazione 2009
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  5. 5
    A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

    A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism di Dan E. Arking, David J. Cutler, Camille W. Brune, Tanya M. Teslovich, Kristen M. West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin, Edwin H. Cook, Aravinda Chakravarti

    Pubblicazione 2008
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  6. 6
    Recurrent 16p11.2 microdeletions in autism

    Recurrent 16p11.2 microdeletions in autism di Revati Kumar, Samer Karamohamed, Jyotsna Sudi, Donald F. Conrad, Camille W. Brune, Judith A. Badner, T. Conrad Gilliam, Norma J. Nowak, Edwin H. Cook, William B. Dobyns, Susan L. Christian

    Pubblicazione 2007
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  7. 7
    Association and Mutation Analyses of 16p11.2 Autism Candidate Genes

    Association and Mutation Analyses of 16p11.2 Autism Candidate Genes di Ravinesh A. Kumar, Christian R. Marshall, Judith A. Badner, Timothy D. Babatz, Zohar Mukamel, Kimberly A. Aldinger, Jyotsna Sudi, Camille W. Brune, Gerald Goh, Samer Karamohamed, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, William B. Dobyns, Stephen W. Scherer, Susan L. Christian

    Pubblicazione 2009
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  8. 8
    Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

    Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder di Susan L. Christian, Camille W. Brune, Jyotsna Sudi, Ravinesh A. Kumar, Shaung Liu, Samer Karamohamed, Judith A. Badner, Seiichi Matsui, Jeffrey M. Conroy, Devin McQuaid, James Gergel, Eli Hatchwell, T. Conrad Gilliam, Elliot S. Gershon, Norma J. Nowak, William B. Dobyns, Edwin H. Cook

    Pubblicazione 2008
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  9. 9
    Common genetic variants on 5p14.1 associate with autism spectrum disorders

    Common genetic variants on 5p14.1 associate with autism spectrum disorders di Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bućan, Joseph Glessner, Brett S. Abrahams, Daria Salyakina, Marcin Imieliński, Jonathan P. Bradfield, Patrick Sleiman, Chong Ae Kim, Cuiping Hou, Edward C. Frackelton, Rosetta Chiavacci, Nagahide Takahashi, Takeshi Sakurai, Eric Rappaport, Clara Lajonchere, Jeffrey Munson, Annette Estes, Olena Korvatska, Joseph Piven, Lisa I. Sonnenblick, Ana I. Alvarez Retuerto, Edward I. Herman, Hongmei Dong, Ted Hutman, Marian Sigman, Sally Ozonoff, Ami Klin, Thomas Owley, John A. Sweeney, Camille W. Brune, Rita M. Cantor, Raphael Bernier, John R. Gilbert, Michael L. Cuccaro, William M. McMahon, Judith Miller, Matthew W. State, Thomas H. Wassink, Hilary Coon, Susan E. Levy, Robert T. Schultz, John I. Nürnberger, Jonathan L. Haines, James S. Sutcliffe, Edwin H. Cook, Nancy J. Minshew, Joseph D. Buxbaum, Géraldine Dawson, Struan F.A. Grant, Daniel H. Geschwind, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Hákon Hákonarson

    Pubblicazione 2009
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  10. 10
    Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

    Autism genome-wide copy number variation reveals ubiquitin and neuronal genes di Joseph Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imieliński, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James H. Flory, F. George Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana M. Michaels, Alexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Géraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nürnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F.A. Grant, Maja Bućan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Hákon Hákonarson

    Pubblicazione 2009
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  11. 11
    A genome-wide linkage and association scan reveals novel loci for autism

    A genome-wide linkage and association scan reveals novel loci for autism di 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

    Pubblicazione 2009
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