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Matthew W. State · Study

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Matthew W. State

14 works· latest 2018· 5 institutionscluster: provisionalORCID 0000-0003-1624-8302

h-index14

i1014

Citations2,954

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Most cited in this library

Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome2005 · 940 citations
L-Histidine Decarboxylase and Tourette's Syndrome2010 · 364 citations
Histidine Decarboxylase Deficiency Causes Tourette Syndrome: Parallel Findings in Humans and Mice2014 · 255 citations
Genome-wide association study of Tourette's syndrome2012 · 211 citations
Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism2011 · 208 citations

Works

14 shown

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

Cell Reports·2018·87 authors·Open access

126citations

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

Neuron·2017·87 authors·Open access

187citations

Mental disorders of known aetiology and precision medicine in psychiatry: a promising but neglected alliance

Psychological Medicine·2016·6 authors·Open access

29citations

The inheritance of Tourette Disorder: A review

Journal of Obsessive-Compulsive and Related Disorders·2014·5 authors·Open access

88citations

Psychiatric Disorders: Diagnosis to Therapy

Cell·2014·2 authors·review·Open access

190citations

Histidine Decarboxylase Deficiency Causes Tourette Syndrome: Parallel Findings in Humans and Mice

Neuron·2014·23 authors·Open access

255citations

Genome-wide association study of Tourette's syndrome

Molecular Psychiatry·2012·93 authors·Open access

211citations

Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism

Biological Psychiatry·2011·23 authors·Open access

208citations

Recent advances in Tourette syndrome

Current Opinion in Neurology·2011·3 authors·review·Open access

91citations

L-Histidine Decarboxylase and Tourette's Syndrome

New England Journal of Medicine·2010·28 authors·Open access

364citations

Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome

The Journal of Comparative Neurology·2008·7 authors·Open access

95citations

Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome

Science·2005·23 authors

940citations

Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype

Proceedings of the National Academy of Sciences·2003·17 authors·Open access

81citations

Cerebrospinal fluid levels of oxytocin in Prader–Willi syndrome: a preliminary report

Biological Psychiatry·1998·8 authors·Open access

89citations