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Jeremiah M. Scharf

Massachusetts Institute of Technology · US
Area of research
Clinical Psychology · Cognitive Neuroscience
Research interest
Research focused on Tourette syndrome and Genetics, with related work in Genome-wide association study, Variation (astronomy), Coding (social sciences). Notable publications include 'Analysis of protein-coding genetic variation in 60,706 humans', 'Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome', and 'Genome-wide association study of obsessive-compulsive disorder'.
h-index
citations
13,243
works
15
NIH funding
primary concept
email

Recent publications

Mapping the genetic landscape across 14 psychiatric disorders
Nature 2025cited by 43position: middledoi
Contextualizing genetic risk score for disease screening and rare variant discovery
Nature Communications 2021cited by 31position: middledoi
Genome-wide Association Study identifies two novel loci for Gilles de la Tourette Syndrome
medRxiv 2021cited by 5position: middledoi
Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
bioRxiv (Cold Spring Harbor Laboratory) 2019cited by 56position: middledoi
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis
Cell Reports 2018cited by 131position: middledoi
Gilles de la Tourette syndrome
Nature Reviews Disease Primers 2017cited by 347position: middledoi
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
Neuron 2017cited by 196position: middledoi
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
Neuron 2017cited by 181position: middledoi
Analysis of protein-coding genetic variation in 60,706 humans
Nature 2016cited by 10,290position: middledoi
Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome
JAMA Psychiatry 2015cited by 758position: middledoi
Analysis of protein-coding genetic variation in 60,706 humans
bioRxiv (Cold Spring Harbor Laboratory) 2015cited by 143position: middledoi
Population prevalence of Tourette syndrome: A systematic review and meta‐analysis
Movement Disorders 2014cited by 370position: firstdoi
CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1
PLoS ONE 2013cited by 86position: middledoi
Genome-wide association study of obsessive-compulsive disorder
Molecular Psychiatry 2012cited by 391position: middledoi
Genome-wide association study of Tourette's syndrome
Molecular Psychiatry 2012cited by 215position: firstdoi

Grants

No grants ingested yet.

Frequent collaborators

Mary M. Robertson · University of Cape Town2 papers (2015–2017) · 1 papers (2017–2017)Veit Roessner · University of New Mexico1 papers (2017–2017)Marwan Hariz · National Institute of Neurological Disorders and Stroke1 papers (2017–2017)Eric R. Gamazon · New York University1 papers (2021–2021)Dan Zhou · Pingxiang University1 papers (2021–2021)Laura L. Miller · University of Iowa1 papers (2014–2014)Paul Sandor · Hospital for Sick Children1 papers (2015–2015)William M. McMahon · University of Utah1 papers (2015–2015)Edwin H. Cook · University of Illinois Chicago1 papers (2021–2021)Gholson J. Lyon · Rockefeller University1 papers (2015–2015) · 1 papers (2015–2015)Yves Dion · McGill University Health Centre1 papers (2015–2015)Paul C. Lee · Northwell Health1 papers (2015–2015) · 1 papers (2014–2014)Rudi Črnčec · UNSW Sydney1 papers (2017–2017) · 1 papers (2014–2014)James F. Leckman · Johns Hopkins Medicine1 papers (2017–2017)David L. Pauls · Johns Hopkins Medicine1 papers (2015–2015)Peristera Paschou · Hospital for Sick Children1 papers (2017–2017)