David L. Pauls

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.

AKAPs integrate genetic findings for autism spectrum disorders

B. Franke, J. Glennon, D. Pauls, 2013, Translational Psychiatry.

Autism and the serotonin transporter: the long and short of it

G. Dawson, N. Minshew, E. Cook, 2005, 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.

Linkage genome scan for loci predisposing to panic disorder or agoraphobia.

S. Woods, G. Page, J. Gelernter, 2001, American journal of medical genetics.

A chromosome 14 risk locus for simple phobia: results from a genomewide linkage scan

S. Woods, G. Page, J. Gelernter, 2003, Molecular Psychiatry.

A genetic family-based association study of OLIG2 in obsessive-compulsive disorder.

R. Delorme, M. Leboyer, S. Rauch, 2007, Archives of general psychiatry.

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

K. Kidd, P. Paschou, J. Kidd, 2004, American journal of human genetics.

Obsessive–compulsive disorder: subclassification based on co-morbidity

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

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.

Genome-wide association study identiﬁes new locus associated with OCD

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

Psychiatric disorders in relatives of probands with opiate addiction.

M. Weissman, K. Merikangas, D. Pauls, 1991, Archives of general psychiatry.

Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia

Melissa J. Green, R. Ophoff, E. Gamazon, 2013, Molecular Psychiatry.