A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
Arking, Dan E., Cutler, David J., Brune, Camille W., Teslovich, Tanya M., West, Kristen, Ikeda, Morna, Rea, Alexis, Guy, Moltu, Lin, Shin, Cook, Edwin H., Chakravarti, Aravinda
Published in American journal of human genetics (01.01.2008)
Published in American journal of human genetics (01.01.2008)
Get full text
Journal Article
Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder
Christian, Susan L, Brune, Camille W, Sudi, Jyotsna, Kumar, Ravinesh A, Liu, Shaung, Karamohamed, Samer, Badner, Judith A, Matsui, Seiichi, Conroy, Jeffrey, McQuaid, Devin, Gergel, James, Hatchwell, Eli, Gilliam, T. Conrad, Gershon, Elliot S, Nowak, Norma J, Dobyns, William B, Cook, Edwin H
Published in Biological psychiatry (1969) (15.06.2008)
Published in Biological psychiatry (1969) (15.06.2008)
Get full text
Journal Article
Association and mutation analyses of 16p11.2 autism candidate genes
Kumar, Ravinesh A, Marshall, Christian R, Badner, Judith A, Babatz, Timothy D, Mukamel, Zohar, Aldinger, Kimberly A, Sudi, Jyotsna, Brune, Camille W, Goh, Gerald, Karamohamed, Samer, Sutcliffe, James S, Cook, Edwin H, Geschwind, Daniel H, Dobyns, William B, Scherer, Stephen W, Christian, Susan L
Published in PloS one (26.02.2009)
Published in PloS one (26.02.2009)
Get full text
Journal Article
5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism
Brune, Camille W., Kim, Soo-Jeong, Salt, Jeff, Leventhal, Bennett L., Lord, Catherine, Cook, Edwin H.
Published in The American journal of psychiatry (01.12.2006)
Published in The American journal of psychiatry (01.12.2006)
Get full text
Journal Article
Social Cognition and Social Responsiveness in 10-month-old Infants
Brune, Camille W., Woodward, Amanda L.
Published in Journal of cognition and development (13.04.2007)
Published in Journal of cognition and development (13.04.2007)
Get full text
Journal Article
Parent-of-origin effects of the serotonin transporter gene associated with autism
Kistner-Griffin, Emily, Brune, Camille W., Davis, Lea K., Sutcliffe, James S., Cox, Nancy J., Cook Jr, Edwin H.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2011)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2011)
Get full text
Journal Article
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism
Kumar, Ravinesh A, Sudi, Jyotsna, Babatz, Timothy D, Brune, Camille W, Oswald, Donald, Yen, Mayon, Nowak, Norma J, Cook, Edwin H, Christian, Susan L, Dobyns, William B
Published in Journal of medical genetics (01.02.2010)
Published in Journal of medical genetics (01.02.2010)
Get full text
Journal Article
A pharmacogenetic study of escitalopram in autism spectrum disorders
Owley, Thomas, Brune, Camille W, Salt, Jeff, Walton, Laura, Guter, Steve, Ayuyao, Nelson, Gibbons, Robert D, Leventhal, Bennett L, Cook, Edwin H
Published in Autism research (01.02.2010)
Published in Autism research (01.02.2010)
Get more information
Journal Article
Family-based association testing of glutamate transporter genes in autism
Jacob, Suma, Brune, Camille W, Badner, Judith A, Ernstrom, Katherine, Courchesne, Eric, Lord, Catherine, Leventhal, Bennett L, Cook, Edwin H, Kim, Soo-Jeong
Published in Psychiatric genetics (01.08.2011)
Published in Psychiatric genetics (01.08.2011)
Get more information
Journal Article
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism
Kim, Soo-Jeong, Brune, Camille W., Kistner, Emily O., Christian, Susan L., Courchesne, Eric H., Cox, Nancy J., Cook, Edwin H.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.10.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.10.2008)
Get full text
Journal Article
Heterogeneous association between engrailed-2 and autism in the CPEA network
Brune, Camille W., Korvatska, Elena, Allen-Brady, Kristina, Cook Jr, Edwin H., Dawson, Geraldine, Devlin, Bernie, Estes, Annette, Hennelly, Meghann, Hyman, Susan L., McMahon, William M., Munson, Jeffrey, Rodier, Patricia M., Schellenberg, Gerard D., Stodgell, Christopher J., Coon, Hilary
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.03.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.03.2008)
Get full text
Journal Article
Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism
Delahanty, R J, Kang, J Q, Brune, C W, Kistner, E O, Courchesne, E, Cox, N J, Cook, E H, Macdonald, R L, Sutcliffe, J S
Published in Molecular psychiatry (01.01.2011)
Published in Molecular psychiatry (01.01.2011)
Get full text
Journal Article
A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism. Commentary
STEPHAN, Dietrich A, ARKING, Dan E, COOK, Edwin H, CHAKRAVARTI, Aravinda, CUTLER, David J, BRUNE, Camille W, TESLOVICH, Tanya M, WEST, Kristen, IKEDA, Morna, REA, Alexis, GUY, Moltu, LIN, Shin
Published in American journal of human genetics (2008)
Get full text
Published in American journal of human genetics (2008)
Journal Article