Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder

Large duplications at reciprocal translocation breakpoints that might be the counterpart of large deletions and could arise from stalled replication bubbles

(2011) K. D. Howarth et al.   GENOME RESEARCH

Additional support for the association of SLITRK1 var321 and Tourette syndrome

(2010) B J O'Roak et al.   MOLECULAR PSYCHIATRY

The Genetics of Child Psychiatric Disorders: Focus on Autism and Tourette Syndrome

(2010) Matthew W. State   NEURON

L-Histidine Decarboxylase and Tourette's Syndrome

(2010) A. Gulhan Ercan-Sencicek et al.   NEW ENGLAND JOURNAL OF MEDICINE

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Tourette Syndrome in Children: An Updated Review

(2010) Jung-Chieh Du et al.   Pediatrics and Neonatology

Autistic features with speech delay in a girl with an ∼1.5-Mb deletion in 6q16.1, includingGPR63andFUT9

(2009)   CLINICAL GENETICS

Lipid G Protein-coupled Receptor Ligand Identification Using β-Arrestin PathHunter™ Assay

(2009) Hong Yin et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The international prevalence, epidemiology, and clinical phenomenology of Tourette syndrome: A cross-cultural perspective

(2009) Mary May Robertson et al.   JOURNAL OF PSYCHOSOMATIC RESEARCH

Mechanisms of change in gene copy number

(2009) P. J. Hastings et al.   NATURE REVIEWS GENETICS

Predictors of Early Adult Outcomes in Pediatric-Onset Obsessive-Compulsive Disorder

(2009) M. H. Bloch et al.   PEDIATRICS

The genetics of obsessive compulsive disorder: A review of the evidence

(2008) David L. Pauls   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Father-to-Son Transmission of 6;17 Translocation in Tourette’s Syndrome

(2008) SANDRA DEHNING et al.   AMERICAN JOURNAL OF PSYCHIATRY

Familial deletion within NLGN4 associated with autism and Tourette syndrome

(2008) Amy Lawson-Yuen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure

(2008) Mahmoud Reza Mansouri et al.   HUMAN MOLECULAR GENETICS