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Camille W. Brune

Research Profile

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Bacterial Artificial Chromosomes

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Publications

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Suma Jacob; Bennett L Leventhal; Catherine Lord; Judith A Badner; Camille W. Brune; Edwin H Cook; Eric Courchesne; Katherine Ernstrom; Soo-Jeong Kim
Family-based association testing of glutamate transporter genes in autism.
Thomas Owley; Camille W. Brune; Jeff Salt; Laura Walton; Steve Guter; Nelson Ayuyao; Robert D Gibbons; Bennett L Leventhal; Edwin H Cook
A pharmacogenetic study of escitalopram in autism spectrum disorders.
Ravinesh A Kumar; Jyotsna Sudi; Timothy D Babatz; Camille W. Brune; Donald Oswald; Mayon Yen; Norma J Nowak; Edwin H Cook; Susan L Christian; William B Dobyns
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.

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All Publications

2011: Suma Jacob; Bennett L Leventhal; Catherine Lord; Judith A Badner; Camille W. Brune; Edwin H Cook; Eric Courchesne; Katherine Ernstrom; Soo-Jeong Kim
Family-based association testing of glutamate transporter genes in autism.
Psychiatric genetics 2011;21(4):212-3.
2010: Thomas Owley; Camille W. Brune; Jeff Salt; Laura Walton; Steve Guter; Nelson Ayuyao; Robert D Gibbons; Bennett L Leventhal; Edwin H Cook
A pharmacogenetic study of escitalopram in autism spectrum disorders.
Autism research : official journal of the International Society for Autism Research 2010;3(1):1-7.
2010: Ravinesh A Kumar; Jyotsna Sudi; Timothy D Babatz; Camille W. Brune; Donald Oswald; Mayon Yen; Norma J Nowak; Edwin H Cook; Susan L Christian; William B Dobyns
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.
Journal of medical genetics 2010;47(2):81-90.
2009: Joseph T Glessner; Kai Wang; Guiqing Cai; Olena Korvatska; Cecilia E Kim; Shawn Wood; Haitao Zhang; Annette Estes; Camille W. Brune; Jonathan P Bradfield; Marcin Imielinski; Edward C Frackelton; Jennifer Reichert; Emily L Crawford; Jeffrey Munson; Patrick M A Sleiman; Rosetta Chiavacci; Kiran Annaiah; Kelly Thomas; Cuiping Hou; Wendy Glaberson; James Flory; Frederick 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 Davis; Judith Miller; David J Posey; Shana Michaels; Alexander Kolevzon; Jeremy Silverman; Raphael Bernier; Susan E Levy; Robert T Schultz; Geraldine Dawson; Thomas Owley; William M McMahon; Thomas H Wassink; John A Sweeney; John I Nurnberger; Hilary Coon; James S Sutcliffe; Nancy J Minshew; Struan F A Grant; Maja Bucan; Edwin H Cook; Joseph Buxbaum; Bernie Devlin; Gerard D Schellenberg; Hakon Hakonarson
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Nature 2009;459(7246):569-73.
2009: Kai Wang; Haitao Zhang; Deqiong Ma; Maja Bucan; Joseph T Glessner; Brett S. Abrahams; Daria Salyakina; Marcin Imielinski; Jonathan P Bradfield; Patrick M A Sleiman; Cecilia E Kim; Cuiping Hou; Edward Frackelton; Rosetta Chiavacci; Nagahide Takahashi; Takeshi Sakurai; Eric Rappaport; Clara M 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 Gilbert; Michael Cuccaro; William M McMahon; Judith Miller; Sate Matthew; Thomas H Wassink; Hilary Coon; Susan E Levy; Robert T Schultz; John I Nurnberger; Jonathan L Haines; James S Sutcliffe; Edwin H Cook; Nancy J Minshew; Joseph Buxbaum; Geraldine Dawson; Struan F A Grant; Daniel Geschwind; Margaret Pericak-Vance; Gerard D Schellenberg; Hakon Hakonarson
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature 2009;459(7246):528-33.
2009: 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 Geschwind; William B Dobyns; Stephen W Scherer; Susan L Christian
Association and mutation analyses of 16p11.2 autism candidate genes.
PloS one 2009;4(2):e4582.
2008: Soo-Jeong Kim; Camille W. Brune; Emily O Kistner; Susan L Christian; Eric Courchesne; Nancy J Cox; Edwin H Cook
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(7):1116-25.
2008: Susan L Christian; Camille W. Brune; Jyotsna Sudi; Ravinesh A Kumar; Shaung Liu; Samer Karamohamed; Judith A Badner; Seiichi Matsui; Jeffrey Conroy; Devin McQuaid; James Gergel; Eli Hatchwell; T Conrad Gilliam; Elliot S Gershon; Norma J Nowak; William B Dobyns; Edwin H Cook
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
Biological psychiatry 2008;63(12):1111-7.
2008: Camille W. Brune; Soo-Jeong Kim; Gregory L Hanna; Eric Courchesne; Catherine Lord; Bennett L Leventhal; Edwin H Cook
Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample.
Autism research : official journal of the International Society for Autism Research 2008;1(2):108-13.
2008: Camille W. Brune; Elena Korvatska; Kristina Allen-Brady; Edwin H Cook; Geraldine Dawson; Bernie Devlin; Annette Estes; Meghann Hennelly; Susan L Hyman; William M McMahon; Jeffrey Munson; Patricia M Rodier; Gerard D Schellenberg; Stodgell Christopher; Hilary Coon
Heterogeneous association between engrailed-2 and autism in the CPEA network.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(2):187-93.
2008: Ravinesh 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
Recurrent 16p11.2 microdeletions in autism.
Human molecular genetics 2008;17(4):628-38.
2008: Dan E Arking; David J Cutler; Camille W. Brune; Tanya M Teslovich; Kristen West; Morna Ikeda; Alexis Rea; Moltu Guy; Shin Lin; Edwin H Cook; Aravinda Chakravarti
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
American journal of human genetics 2008;82(1):160-4.
2007: Suma Jacob; Camille W. Brune; Carol Sue Carter Porges; Bennett L Leventhal; Catherine Lord; Edwin H Cook
Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism.
Neuroscience letters 2007;417(1):6-9.
2006: Camille W. Brune; Soo-Jeong Kim; Jeff Salt; Bennett L Leventhal; Catherine Lord; Edwin H Cook
5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism.
The American journal of psychiatry 2006;163(12):2148-56.