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James S. Sutcliffe | Researchclopedia

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James S. Sutcliffe

King's College London ORCID

183

Works

49,330

Citations

76

h-index

134

i10-index

Research Topics

Autism Spectrum Disorder Research Genetics and Neurodevelopmental Disorders Genomic variations and chromosomal abnormalities

Affiliations

Tufts Medical Center2003–2003

National Institutes of Health1996–1996

Allen Institute for Brain Science2012–2012

Howard Hughes Medical Institute1991–1998

University of Wisconsin–Madison2015–2015

Top Works

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Annemieke J.M.H. Verkerk,Maura Pieretti,et al.

19913,494 citations

Genetic Syndromes and Imprinting

Genomics and Rare Diseases

Synaptic, transcriptional and chromatin genes disrupted in autism

The DDD Study,Silvia De Rubeis,et al.

20142,894 citations

Strong Association of De Novo Copy Number Mutations with Autism

Jonathan Sebat,B. Lakshmi,et al.

20072,826 citations

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Ying‐Hui Fu,Derek P.A. Kuhl,et al.

19912,092 citations

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Benjamin M. Neale,Yan Kou,et al.

20121,788 citations

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Stephan Sanders,Xin He,et al.

20151,527 citations

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Joseph Glessner,Kai Wang,et al.

20091,435 citations

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Péter Szatmári,Ping G. Tepper,et al.

20071,388 citations

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Stephan Sanders,A. Gulhan Ercan‐Sencicek,et al.

20111,287 citations