Daniel Chasman
Genetics · 2001–2021
A researcher in the Science corpus: 32 papers; trusts 7 researchers and is trusted by 10 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 535 citations into it; #1,492 of 6,854 by trust here, #189 by citations
- Computational Biology & Bioinformatics — 58 citations into it
- Evaluation & Benchmarks — 10 citations into it
Whom Daniel Chasman trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Christopher Sander
- Burkhard Rost
- Alexey G. Murzin
- Reinhard Schneider
- Steven E. Brenner
- Tim J. P. Hubbard
Who trusts Daniel Chasman overall
- V. Ramensky
- H. Tabor
- Shamil R. Sunyaev
- Yana Bromberg
- Peer Bork
- Pauline Crystal Ng
- N. Risch
- Christopher T. Saunders
- Richard M. Myers
- Burkhard Rost
Papers from Daniel Chasman's perspective
Ordered by how strongly the researchers Daniel Chasman trusts endorse each paper. Same corpus, a different order for every researcher.
- SCOP: a structural classification of proteins database for the investigation of sequences and structures.
- Regression Shrinkage and Selection via the Lasso
- Conservation and prediction of solvent accessibility in protein families
- PANTHER: a library of protein families and subfamilies indexed by function. (Genome Research)
- Database of homology‐derived protein structures and the structural meaning of sequence alignment
- Genetic studies of the lac repressor. XIV. Analysis of 4000 altered Escherichia coli lac repressors reveals essential and non-essential residues, as well as "spacers" which do not require a specific…
- A variational Bayes algorithm for fast and accurate multiple locus genome-wide association analysis
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- An efficient multi-locus mixed model approach for genome-wide association studies in structured populations (Nature Genetics)
- DrugBank: a comprehensive resource for in silico drug discovery and exploration
Their papers
- Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation. (2001) — 420 citations
- Understanding multicellular function and disease with human tissue-specific networks (2015) — 816 citations
- Multiple Novel Loci are Associated with Indices of Renal Function and Chronic Kidney Disease (2009) — 639 citations
- Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores (2015) — 1,263 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
- Multiple New Loci Associated with Kidney Function and Chronic Kidney Disease: The CKDGen consortium (2010) — 799 citations
- HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials (2015) — 671 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- Recovery of trait heritability from whole genome sequence data (2019) — 222 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) — 744 citations
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations
- Analysis of shared heritability in common disorders of the brain (2018) — 1,836 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Multi-Ethnic Genome-wide Association Study for Atrial Fibrillation (2018) — 699 citations
- Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease (2018) — 80 citations