Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS

Meta-analysis of association between obsessive-compulsive disorder and the 3′ region of neuronal glutamate transporter geneSLC1A1

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Common genetic background in anorexia nervosa and obsessive compulsive disorder: Preliminary results from an association study

(2013) Sergi Mas et al.   JOURNAL OF PSYCHIATRIC RESEARCH

Population-Based, Multigenerational Family Clustering Study of Obsessive-compulsive Disorder

(2013) David Mataix-Cols et al.   JAMA Psychiatry

Common Genetic Variants and Gene-Expression Changes Associated with Bipolar Disorder Are Over-Represented in Brain Signaling Pathway Genes

(2012) Inti Pedroso et al.   BIOLOGICAL PSYCHIATRY

Genome-wide association study of obsessive-compulsive disorder

(2012) S E Stewart et al.   MOLECULAR PSYCHIATRY

Selective control of inhibitory synapse development by Slitrk3-PTPδ trans-synaptic interaction

(2012) Hideto Takahashi et al.   NATURE NEUROSCIENCE

Comprehensive family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder

(2011) Jack Samuels et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Exome sequencing of a pedigree with tourette syndrome or chronic tic disorder

(2011) Senthil K. Sundaram et al.   ANNALS OF NEUROLOGY

Forgetting what you have checked: A link between working memory impairment and checking behaviors in obsessive-compulsive disorder

(2011) N. Jaafari et al.   EUROPEAN PSYCHIATRY

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

(2011) M Rietschel et al.   MOLECULAR PSYCHIATRY

Genome-wide association study identifies five new schizophrenia loci

(2011)   NATURE GENETICS

Postsynaptic TrkC and Presynaptic PTPσ Function as a Bidirectional Excitatory Synaptic Organizing Complex

(2011) Hideto Takahashi et al.   NEURON

Comparative interactomics with Funcoup 2.0

(2011) A. Alexeyenko et al.   NUCLEIC ACIDS RESEARCH

Glutamate abnormalities in obsessive compulsive disorder: Neurobiology, pathophysiology, and treatment

(2011) Christopher Pittenger et al.   PHARMACOLOGY & THERAPEUTICS

The role of glutamate signaling in the pathogenesis and treatment of obsessive–compulsive disorder

(2011) Ke Wu et al.   PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR

On Genome-wide Association Studies for Family-Based Designs: An Integrative Analysis Approach Combining Ascertained Family Samples with Unselected Controls

(2010) Jessica Lasky-Su et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

(2010) William McLaren et al.   BIOINFORMATICS

METAL: fast and efficient meta-analysis of genomewide association scans

(2010) C. J. Willer et al.   BIOINFORMATICS

Trans-synaptic Adhesions between Netrin-G Ligand-3 (NGL-3) and Receptor Tyrosine Phosphatases LAR, Protein-tyrosine Phosphatase δ (PTPδ), and PTPσ via Specific Domains Regulate Excitatory Synapse Formation

(2010) Seok-Kyu Kwon et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa

(2010) K Wang et al.   MOLECULAR PSYCHIATRY

A map of human genome variation from population-scale sequencing

(2010) Richard M. Durbin et al.   NATURE

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

(2010) Taye H Hamza et al.   NATURE GENETICS

Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive–like behaviors in mice

(2010) Sergey V Shmelkov et al.   NATURE MEDICINE

A family-based association study of the glutamate transporter geneSLC1A1in obsessive-compulsive disorder in 378 families

(2009) Y.Y. Shugart et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

A Haplotype Containing Quantitative Trait Loci for SLC1A1 Gene Expression and Its Association With Obsessive-Compulsive Disorder

(2009) Jens R. Wendland et al.   ARCHIVES OF GENERAL PSYCHIATRY

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

(2009) J Elia et al.   MOLECULAR PSYCHIATRY

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

(2009) Kai Wang et al.   NATURE

Trans-synaptic adhesion between NGL-3 and LAR regulates the formation of excitatory synapses

(2009) Jooyeon Woo et al.   NATURE NEUROSCIENCE

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

(2008) A. D. Johnson et al.   BIOINFORMATICS

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

(2008) Barbara Schormair et al.   NATURE GENETICS

Identification of loci associated with schizophrenia by genome-wide association and follow-up

(2008) Michael C O'Donovan et al.   NATURE GENETICS