User profiles for Jeremiah M Scharf
Jeremiah M. ScharfCenter for Genomic Medicine, Departments of Neurology & Psychiatry, MGH Verified email at broadinstitute.org Cited by 19429 |
[HTML][HTML] Analysis of protein-coding genetic variation in 60,706 humans
Large-scale reference data sets of human genetic variation are critical for the medical and
functional interpretation of DNA sequence changes. Here we describe the aggregation and …
functional interpretation of DNA sequence changes. Here we describe the aggregation and …
Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome
…, R Kurlan, MM Robertson, L Osiecki, JM Scharf… - JAMA …, 2015 - jamanetwork.com
Importance Tourette syndrome (TS) is characterized by high rates of psychiatric comorbidity;
however, few studies have fully characterized these comorbidities. Furthermore, most …
however, few studies have fully characterized these comorbidities. Furthermore, most …
Genome-wide association study of obsessive-compulsive disorder
Obsessive-compulsive disorder (OCD) is a common, debilitating neuropsychiatric illness
with complex genetic etiology. The International OCD Foundation Genetics Collaborative (…
with complex genetic etiology. The International OCD Foundation Genetics Collaborative (…
Gilles de la Tourette syndrome
Gilles de la Tourette syndrome (GTS) is a childhood-onset neurodevelopmental disorder that
is characterized by several motor and phonic tics. Tics usually develop before 10 years of …
is characterized by several motor and phonic tics. Tics usually develop before 10 years of …
Population prevalence of Tourette syndrome: A systematic review and meta‐analysis
The aim of this study was to refine the population prevalence estimate of Tourette Syndrome
(TS) in children and to investigate potential sources of heterogeneity in previously …
(TS) in children and to investigate potential sources of heterogeneity in previously …
[HTML][HTML] Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
The direct estimation of heritability from genome-wide common variant data as implemented
in the program Genome-wide Complex Trait Analysis (GCTA) has provided a means to …
in the program Genome-wide Complex Trait Analysis (GCTA) has provided a means to …
Interrogating the genetic determinants of Tourette's syndrome and other tic disorders through genome-wide association studies
…, G Coppola, CA Mathews, JM Scharf… - American Journal of …, 2019 - Am Psychiatric Assoc
Objective: Tourette’s syndrome is polygenic and highly heritable. Genome-wide association
study (GWAS) approaches are useful for interrogating the genetic architecture and …
study (GWAS) approaches are useful for interrogating the genetic architecture and …
Genome-wide association study of Tourette's syndrome
Tourette's syndrome (TS) is a developmental disorder that has one of the highest familial
recurrence rates among neuropsychiatric diseases with complex inheritance. However, the …
recurrence rates among neuropsychiatric diseases with complex inheritance. However, the …
Association of the SLC1A1 glutamate transporter gene and obsessive‐compulsive disorder
…, J Platko, JW Smoller, JM Scharf… - American Journal of …, 2007 - Wiley Online Library
Context: Obsessive‐Compulsive Disorder (OCD) is a debilitating illness with putative
glutamatergic abnormalities. Two separate proximal haplotypes in the glutamate transporter gene, …
glutamatergic abnormalities. Two separate proximal haplotypes in the glutamate transporter gene, …
The genetics of Tourette syndrome: a review
JA O'Rourke, JM Scharf, D Yu, DL Pauls - Journal of psychosomatic …, 2009 - Elsevier
OBJECTIVES: This article summarizes and evaluates recent advances in the genetics of
Gilles de la Tourette syndrome (GTS). METHODS: This is a review of recent literature focusing …
Gilles de la Tourette syndrome (GTS). METHODS: This is a review of recent literature focusing …