Stephen W. Scherer
Genetics · 2001–2019
A researcher in the Science corpus: 26 papers; trusts 3 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 424 citations into it; #4,971 of 6,854 by trust here, #117 by citations
- Molecular Biology — 323 citations into it; #13,610 of 17,773 by trust here, #1,162 by citations
- Plant Science — 124 citations into it
Whom Stephen W. Scherer trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Stephen W. Scherer overall
Papers from Stephen W. Scherer's perspective
Ordered by how strongly the researchers Stephen W. Scherer trusts endorse each paper. Same corpus, a different order for every researcher.
- Detection of large-scale variation in the human genome (Nature Genetics)
- Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
- Global variation in copy number in the human genome (Nature)
- The Influence of CCL3L1 Gene-Containing Segmental Duplications on HIV-1/AIDS Susceptibility (Science)
- The Human Gene Mutation Database: 2008 update
- Copy Number Variation in Human Health, Disease, and Evolution (Annual review of genomics and human genetics (Print))
- A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. (American Journal of Human Genetics)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (Neuron)
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. (American Journal of Human Genetics)
- ClinGen--the Clinical Genome Resource. (New England Journal of Medicine)
Their papers
- The Diploid Genome Sequence of an Individual Human (2007) — 1,867 citations
- Experimental annotation of the human genome using microarray technology (2001) — 469 citations
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- The human splicing code reveals new insights into the genetic determinants of disease (2014) — 1,219 citations
- The Database of Genomic Variants: a curated collection of structural variation in the human genome (2013) — 1,239 citations
- Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. (2010) — 2,697 citations
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
- Copy-number variations associated with neuropsychiatric conditions (2008) — 658 citations
- Subgroup-specific structural variation across 1,000 medulloblastoma genomes (2012) — 871 citations
- Mutations in SUFU predispose to medulloblastoma (2002) — 830 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
- A copy number variation map of the human genome (2015) — 834 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
- Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (2011) — 431 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
- Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) — 710 citations
- This Provisional PDF corresponds to the article as it appeared upon acceptance. Copyedited and fully formatted PDF and full text (HTML) versions will be made available soon. Towards a comprehensive structural variation map of an individual human genome (2010) — 354 citations
- Origins and functional impact of copy number variation in the human genome (2009) — 1,997 citations