D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics and Molecular Biology D-index 65 Citations 27,948 105 World Ranking 1859 National Ranking 952

Research.com Recognitions

Awards & Achievements

2017 - Rhoda and Bernard Sarnat International Prize in Mental Health, National Academy of Medicine

2013 - Member of the National Academy of Medicine (NAM)

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

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.

His most cited work include:

  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (1570 citations)
  • Synaptic, transcriptional and chromatin genes disrupted in autism (1544 citations)
  • De novo mutations revealed by whole-exome sequencing are strongly associated with autism (1516 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Genetics (55.44%)
  • Autism (36.79%)
  • Autism spectrum disorder (24.35%)

What were the highlights of his more recent work (between 2016-2021)?

  • Autism spectrum disorder (24.35%)
  • Gene (22.28%)
  • Genetics (55.44%)

In recent papers he was focusing on the following fields of study:

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.

Between 2016 and 2021, his most popular works were:

  • Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (373 citations)
  • Integrative functional genomic analysis of human brain development and neuropsychiatric risks (241 citations)
  • An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. (125 citations)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

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.
Nature (2014)

2075 Citations

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.
Nature (2012)

1907 Citations

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)

1708 Citations

Synaptic, transcriptional and chromatin genes disrupted in autism

Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney.
Nature (2014)

1623 Citations

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)

1454 Citations

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.
Neuron (2011)

1241 Citations

Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome

Jesse F. Abelson;Kenneth Y. Kwan;Brian J. O'Roak;Danielle Y. Baek.
Science (2005)

1117 Citations

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

Kai Wang;Haitao Zhang;Deqiong Ma;Maja Bucan.
Nature (2009)

977 Citations

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.
Neuron (2015)

921 Citations

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)

837 Citations

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