Matthew W. State

Cognitive Neuroscience · 2005–2020

A researcher in the Science corpus: 16 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Cognitive Neuroscience — 188 citations into it
• Clinical Psychology — 43 citations into it

Whom Matthew W. State trusts

Their strongest outbound trust, strongest first, inferred from their citations.

1. E. Goldson (in Cognitive Neuroscience)

Papers from Matthew W. State's perspective

Ordered by how strongly the researchers Matthew W. State trusts endorse each paper. Same corpus, a different order for every researcher.

1. Global variation in copy number in the human genome (Nature)
2. Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
3. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders (Nature Genetics)
4. Association between microdeletion and microduplication at 16p11.2 and autism. (New England Journal of Medicine)
5. DAVID: Database for Annotation, Visualization, and Integrated Discovery (Genome Biology)
6. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders (American Journal of Human Genetics)
7. Advances in autism genetics: on the threshold of a new neurobiology (Nature reviews genetics)
8. Principal components analysis corrects for stratification in genome-wide association studies
9. Educating Children with Autism
10. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. (American Journal of Human Genetics)

Their papers

• Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome (2005) — 972 citations
• Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011) — 1,286 citations
• Rare independent mutations in renal salt handling genes contribute to blood pressure variation (2008) — 846 citations
• Functional and Evolutionary Insights Into Human Brain Development Through Global Transcriptome Analysis (2009) — 606 citations
• Integrative functional genomic analysis of human brain development and neuropsychiatric risks (2018) — 740 citations
• Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
• Autism spectrum disorder (2020) — 1,164 citations
• Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (2015) — 1,391 citations
• Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
• The contribution of de novo coding mutations to autism spectrum disorder (2014) — 2,476 citations
• Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder. (2014) — 681 citations
• Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism (2013) — 905 citations
• Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO (2013) — 832 citations
• De novo mutations revealed by whole-exome sequencing are strongly associated with autism (2012) — 2,079 citations
• Common genetic variants on 5p14.1 associate with autism spectrum disorders (2009) — 1,008 citations
• Mapping autism risk loci using genetic linkage and chromosomal rearrangements (2007) — 1,398 citations