Edwin H. Cook Jr.
Genetics · 2000–2019
A researcher in the Science corpus: 18 papers; trusts 3 researchers and is trusted by 8 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 262 citations into it; #1,972 of 6,854 by trust here, #123 by citations
- Cognitive Neuroscience — 117 citations into it; #5,624 of 10,852 by trust here, #217 by citations
- Plant Science — 39 citations into it
Whom Edwin H. Cook Jr. trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Edwin H. Cook Jr. overall
Papers from Edwin H. Cook Jr.'s perspective
Ordered by how strongly the researchers Edwin H. Cook Jr. trusts endorse each paper. Same corpus, a different order for every researcher.
- Detection of large-scale variation in the human genome (Nature Genetics)
- Large-Scale Copy Number Polymorphism in the Human Genome (Science)
- Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (Science)
- Global variation in copy number in the human genome (Nature)
- Disruption of two novel genes by a translocation co-segregating with schizophrenia. (Human Molecular Genetics)
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
- Association between microdeletion and microduplication at 16p11.2 and autism. (New England Journal of Medicine)
- Large recurrent microdeletions associated with schizophrenia (Nature)
- Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. (New England Journal of Medicine)
- A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. (American Journal of Human Genetics)
Their papers
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- A framework for the interpretation of de novo mutation in human disease (2014) — 1,035 citations
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011) — 1,286 citations
- Copy-number variations associated with neuropsychiatric conditions (2008) — 658 citations
- A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. (2008) — 608 citations
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
- Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder (2017) — 752 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
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders (2014) — 930 citations
- Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) — 1,772 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes (2009) — 1,451 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
- Recurrent 16p11.2 microdeletions in autism. (2007) — 716 citations
- The screening and diagnosis of autistic spectrum disorders. (2004) — 601 citations
- The Autism Diagnostic Observation Schedule—Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism (2000) — 7,851 citations