Shamil R. Sunyaev
Molecular Biology · 1999–2018
A researcher in the Science corpus: 27 papers; trusts 21 researchers and is trusted by 52 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 346 citations into it; #1,074 of 17,773 by trust here, #179 by citations
- Genetics — 269 citations into it; #220 of 6,854 by trust here, #75 by citations
- Computational Biology & Bioinformatics — 30 citations into it; #325 of 660 by trust here, #120 by citations
- Pathology and Forensic Medicine — 21 citations into it
Whom Shamil R. Sunyaev trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Stephen F. Altschul
- V. Ramensky
- William R. Pearson
- Steven Henikoff
- Julie Dawn Thompson
- Ziheng Yang
- Daniel Chasman
- Jorja G. Henikoff
- Pauline Crystal Ng
- Peer Bork
Who trusts Shamil R. Sunyaev overall
- Yana Bromberg
- Pauline Crystal Ng
- Ivan A. Adzhubei
- Jimin Pei
- Emidio Capriotti
- V. Ramensky
- William S. J. Valdar
- Burkhard Rost
- Haiming Tang
- Steven Henikoff
Papers from Shamil R. Sunyaev's perspective
Ordered by how strongly the researchers Shamil R. Sunyaev trusts endorse each paper. Same corpus, a different order for every researcher.
- Basic local alignment search tool.
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
- Human non-synonymous SNPs: server and survey. (Nucleic Acids Research)
- Statistics of Local Complexity in Amino Acid Sequences and Sequence Databases
- The Protein Data Bank.
- NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins (Nucleic Acids Res.)
- Position-based sequence weights.
- Comparison of methods for searching protein sequence databases
- Repbase update: a database and an electronic journal of repetitive elements. (Trends in Genetics)
Their papers
- A method and server for predicting damaging missense mutations (2010) — 13,139 citations
- The accessible chromatin landscape of the human genome (2012) — 2,728 citations
- Prediction of deleterious human alleles. (2001) — 1,095 citations
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- Human non-synonymous SNPs: server and survey. (2002) — 2,455 citations
- Integrative analysis of 111 reference human epigenomes (2015) — 6,046 citations
- Systematic Localization of Common Disease-Associated Variation in Regulatory DNA (2012) — 3,679 citations
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
- Genomic variation landscape of the human gut microbiome (2012) — 855 citations
- Predicting Functional Effect of Human Missense Mutations Using PolyPhen-2 (2013) — 3,725 citations
- Mutational heterogeneity in cancer and the search for new cancer genes (2013) — 1,147 citations
- Assessing the Evolutionary Impact of Amino Acid Mutations in the Human Genome (2008) — 675 citations
- The mystery of missing heritability: Genetic interactions create phantom heritability (2012) — 1,592 citations
- Charting the proteomes of organisms with unsequenced genomes by MALDI-quadrupole time-of-flight mass spectrometry and BLAST homology searching. (2001) — 583 citations
- Searching for missing heritability: Designing rare variant association studies (2014) — 633 citations
- Extremely low-coverage sequencing and imputation increases power for genome-wide association studies (2012) — 257 citations
- Impact of selection, mutation rate and genetic drift on human genetic variation. (2003) — 36 citations
- Signals of polygenic adaptation on height have been overestimated due to uncorrected population structure in genome-wide association studies (2018) — 30 citations
- Estimating the Selective Effects of Heterozygous Protein Truncating Variants from Human Exome Data (2017) — 161 citations
- Quantifying unobserved protein-coding variants in human populations provides a roadmap for large-scale sequencing projects (2016) — 22 citations