Chris C. A. Spencer

Genetics · 2007–2019

A researcher in the Science corpus: 18 papers; trusts 2 researchers and is trusted by 1 researcher here, as inferred from the citation graph.

Subfields

Genetics — 270 citations into it; #5,745 of 6,854 by trust here, #78 by citations

Whom Chris C. A. Spencer trusts overall

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

Who trusts Chris C. A. Spencer overall

Papers from Chris C. A. Spencer's perspective

Ordered by how strongly the researchers Chris C. A. Spencer trusts endorse each paper. Same corpus, a different order for every researcher.

A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Nature Genetics)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. (American Journal of Human Genetics)
Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
The genetics and immunopathogenesis of inflammatory bowel disease (Nature reviews. Immunology)
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (Nature Genetics)

Their papers

A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
FINEMAP: efficient variable selection using summary data from genome-wide association studies (2015) — 774 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
Designing Genome-Wide Association Studies: Sample Size, Power, Imputation, and the Choice of Genotyping Chip (2009) — 632 citations
Multiple Sclerosis Genomic Map implicates peripheral immune cells & microglia in susceptibility (2019) — 1,186 citations
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) — 996 citations
Class II HLA interactions modulate genetic risk for multiple sclerosis (2015) — 366 citations
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) — 595 citations
Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) — 7,422 citations
Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) — 740 citations
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis (2013) — 1,073 citations
Identification of fifteen new psoriasis susceptibility loci highlights the role of innate immunity (2012) — 721 citations
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility (2011) — 898 citations
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) — 2,780 citations
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 (2010) — 1,032 citations
Identification of loci associated with schizophrenia by genome-wide association and follow-up (2008) — 1,107 citations
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) — 9,550 citations