David B. Goldstein
Genetics · 2002–2019
A researcher in the Science corpus: 24 papers; trusts 6 researchers and is trusted by 15 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 264 citations into it; #1,058 of 6,854 by trust here, #132 by citations
- Molecular Biology — 169 citations into it
Whom David B. Goldstein trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts David B. Goldstein overall
- Samuel P. Dickson
- Eric E. Schadt
- Elizabeth T. Cirulli
- Kai Wang
- Evan A. Boyle
- David Houle
- Isabelle M Guyon
- Albert-László Barabási
- Teri Manolio
- Ian D. Krantz
Papers from David B. Goldstein's perspective
Ordered by how strongly the researchers David B. Goldstein trusts endorse each paper. Same corpus, a different order for every researcher.
- Copy Number Variation in Human Health, Disease, and Evolution (Annual review of genomics and human genetics (Print))
- The Human Gene Mutation Database: 2008 update
- On the allelic spectrum of human disease. (Trends in Genetics)
- Common genetic variation and human traits. (New England Journal of Medicine)
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
- A method and server for predicting damaging missense mutations
- Controlling the false discovery rate: a practical and powerful approach to multiple testing
- Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. (Human Molecular Genetics)
- Distribution and intensity of constraint in mammalian genomic sequence. (Genome Research)
- Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1 (Nature Genetics)
Their papers
- Genome-wide association studies for complex traits: consensus, uncertainty and challenges (2008) — 3,055 citations
- Large recurrent microdeletions associated with schizophrenia (2008) — 1,814 citations
- Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes (2013) — 881 citations
- Rare Variants Create Synthetic Genome-Wide Associations (2010) — 920 citations
- Genome-wide transcript profiles in aging and calorically restricted Drosophila melanogaster. (2002) — 597 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- Diagnostic Utility of Exome Sequencing for Kidney Disease (2018) — 666 citations
- Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways (2015) — 948 citations
- The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity (2015) — 131 citations
- Correction: Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes (2013) — 86 citations
- Mutations in the Profilin 1 Gene Cause Familial Amyotrophic Lateral Sclerosis (2012) — 618 citations
- HLA-A★3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans (2011) — 839 citations
- Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus. (2010) — 743 citations
- Uncovering the roles of rare variants in common disease through whole-genome sequencing (2010) — 1,175 citations
- Finding the missing heritability of complex diseases (2009) — 8,360 citations
- A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci (2009) — 803 citations
- Common genetic variation and human traits. (2009) — 966 citations
- Next generation disparities in human genomics: concerns and remedies. (2009) — 360 citations
- Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance (2009) — 3,837 citations
- Common variants conferring risk of schizophrenia (2009) — 1,753 citations