James T. McCracken

发表

Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q

Y Wang, A J Fyer, J A Knowles, 2006, Molecular Psychiatry.

A family‐based association study of the glutamate transporter gene SLC1A1 in obsessive–compulsive disorder in 378 families

A. Fyer, Benjamin D. Greenberg, G. Nestadt, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

Richard A Marini, Deana D. Li, B. O’Roak, 2022, Nature Genetics.

Obsessive–compulsive disorder: subclassification based on co-morbidity

S. Rauch, D. Murphy, B. Greenberg, 2008, Psychological Medicine.

Transmission disequilibrium testing of dopamine-related candidate gene polymorphisms in ADHD: confirmation of association of ADHD with DRD4 and DRD5

V. Kustanovich, S. Nelson, J. McGough, 2004, Molecular Psychiatry.

Gender differences in genetic linkage and association on 11p15 in obsessive–compulsive disorder families

Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD

B. Greenberg, A. Fyer, J. Knowles, 2017, European Neuropsychopharmacology.

S-adenosyl-L-methionine (SAM) in adults with ADHD, RS: preliminary results from an open trial.

J. McCracken, G. Hanna, W. Shekim, 1990, Psychopharmacology bulletin.

Genome-Wide Association Study in Obsessive-Compulsive Disorder: Results from the OCGAS

S. E. Stewart, D. Murphy, B. Greenberg, 2014, Molecular Psychiatry.

Genome-wide association study identiﬁes new locus associated with OCD

Laurent F. Thomas, Jason A. Elias, Zachary F. Gerring, 2022 .