E. Scolnick

Genetics · 2008–2022

A researcher in the Science corpus: 13 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 213 citations into it
• Molecular Biology — 157 citations into it

Whom E. Scolnick trusts

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

1. Michael Olivier (in Genetics)

Papers from E. Scolnick's perspective

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

1. A gene atlas of the mouse and human protein-encoding transcriptomes. (Proceedings of the National Academy of Sciences of the United States of America)
2. Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (Science)
3. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
4. A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
5. MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
6. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Nature Genetics)
7. Newly identified loci that influence lipid concentrations and risk of coronary artery disease (Nature Genetics)
8. Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes. (American Journal of Human Genetics)
9. 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
10. Literature mining for the biologist: from information retrieval to biological discovery (Nature reviews genetics)

Their papers

• De novo mutations in schizophrenia implicate synaptic networks (2014) — 1,622 citations
• A polygenic burden of rare disruptive mutations in schizophrenia (2014) — 1,469 citations
• Rare chromosomal deletions and duplications increase risk of schizophrenia (2008) — 1,525 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
• Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022) — 659 citations
• Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
• Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 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
• Validating therapeutic targets through human genetics (2013) — 688 citations
• Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions (2009) — 468 citations
• Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder (2008) — 1,273 citations
• Whole-genome association study of bipolar disorder (2008) — 739 citations