2017 - Rhoda and Bernard Sarnat International Prize in Mental Health, National Academy of Medicine
2013 - Member of the National Academy of Medicine (NAM)
Matthew W. State mainly investigates Genetics, Autism, Autism spectrum disorder, Exome sequencing and Copy-number variation. Matthew W. State mostly deals with Heritability of autism in his studies of Autism. His Autism spectrum disorder study integrates concerns from other disciplines, such as Loss function and Gene knockdown.
The study incorporates disciplines such as Pachygyria and Locus heterogeneity in addition to Exome sequencing. The various areas that he examines in his Copy-number variation study include Spectrum disorder, Allele frequency and Developmental disorder. The concepts of his Exome study are interwoven with issues in SYNGAP1 and Genetic heterogeneity.
Genetics, Autism, Autism spectrum disorder, Gene and Copy-number variation are his primary areas of study. Many of his studies on Genetics involve topics that are commonly interrelated, such as Tourette syndrome. His Autism research is multidisciplinary, incorporating elements of Genetic heterogeneity, Neuroscience, Intellectual disability and Proband.
His work in Autism spectrum disorder covers topics such as Schizophrenia which are related to areas like Major depressive disorder and Genotyping. His Copy-number variation research integrates issues from Bioinformatics and Medical genetics. His Heritability of autism study which covers Allele that intersects with Genetic association.
Matthew W. State mostly deals with Autism spectrum disorder, Gene, Genetics, Genome and Autism. His studies in Autism spectrum disorder integrate themes in fields like Gene Discovery, Genotyping, Computational biology and Genomics. His biological study deals with issues like Bioinformatics, which deal with fields such as 22q11 Deletion Syndrome, Genetic high risk, Macaque, Neocortex and Gene expression profiling.
His study in Copy-number variation, Exome sequencing, Missense mutation, Mutation and Exome is carried out as part of his studies in Genetics. The concepts of his Genome study are interwoven with issues in Schizophrenia, Prefrontal cortex and Transcriptome. Matthew W. State has included themes like Psychological intervention, Genome-wide association study, Physical medicine and rehabilitation, Phenotype and Xenopus in his Autism study.
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The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov;Brian J. O'Roak;Stephan J. Sanders;Stephan J. Sanders;Michael Ronemus.
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Stephan J. Sanders;Michael T. Murtha;Abha R. Gupta;John D. Murdoch.
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan J. Sanders;A. Gulhan Ercan-Sencicek;Vanessa Hus;Rui Luo.
Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome
Jesse F. Abelson;Kenneth Y. Kwan;Brian J. O'Roak;Danielle Y. Baek.
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang;Haitao Zhang;Deqiong Ma;Maja Bucan.
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J. Sanders;Xin He;A. Jeremy Willsey;A. Gulhan Ercan-Sencicek.
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
Weizhen Ji;Jia Nee Foo;Brian J O'Roak;Hongyu Zhao.
Nature Genetics (2008)
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