James S. Sutcliffe

发表

A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis

Wei Chen, Rui Chen, Qiang Wei, 2015, Bioinform..

Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes

Alex Rodriguez, Ian T. Foster, Ravi K. Madduri, 2015, Bioinform..

Pro 32 Pro 33 Mutations in the Integrin b 3 PSI Domain Result in a IIb b 3 Priming and Enhanced Adhesion : Reversal of the Hypercoagulability Phenotype by the Src Inhibitor SKI-606 s

James S. Sutcliffe, Chang Y. Chung, Emily L. Crawford, 2014 .

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Robert T. Schultz, Margaret A. Pericak-Vance, Takeshi Sakurai, 2009, Nature.

A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

Eric M. Morrow, Shrikant M. Mane, Edwin H. Cook, 2015, Biological Psychiatry.

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

Daniele Merico, Joseph Piven, Veronica J. Vieland, 2014, Human Genetics.

Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls

Kathryn Roeder, Stephan Ripke, Shannon Gross, 2013, PLoS genetics.

Classroom-based teaching decisions

James S. Sutcliffe, J. Sutcliffe, R. Whitfield, 2018, Teacher Decision-Making in the Classroom.

SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research

Anibal Gutierrez, Robert T. Schultz, Nicholas Carriero, 2018, Neuron.

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

Kathryn Roeder, Murim Choi, Eric M. Morrow, 2011, Neuron.

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

Nancy J. Cox, Eric Courchesne, Edwin H. Cook, 2009, Molecular Psychiatry.

Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders

Kathryn Roeder, Stephan Ripke, Shannon Gross, 2013, Neuron.

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

John A. Sweeney, Geraldine Dawson, Daniel H. Geschwind, 2009, PLoS genetics.

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

Ping Fang, Johanna M. Rommens, James S. Sutcliffe, 1997, Nature Genetics.

Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome

David E. Housman, James S. Sutcliffe, David L. Nelson, 1993, Nature Genetics.

Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

Kathryn Roeder, Xin He, Richard A. Gibbs, 2013, PLoS genetics.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

The impact of genotype calling errors on family-based studies

Wei Chen, Qi Yan, Edwin H. Cook, 2016, Scientific Reports.

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

Bekim Sadikovic, Roger E. Stevenson, Daniel H. Geschwind, 2012, Proceedings of the National Academy of Sciences.

Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell

Kevin A. Pelphrey, Ellen M. Wijsman, Zachary Warren, 2012 .

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

Alistair T. Pagnamenta, Veronica J. Vieland, Anthony P. Monaco, 2011, Journal of Neurodevelopmental Disorders.

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

Robert T. Schultz, Takeshi Sakurai, Joseph Piven, 2009, Nature.

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.