G. Kryukov

Genetics · 2003–2020

A researcher in the Science corpus: 16 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 109 citations into it

Whom G. Kryukov trusts overall

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

1. Jonathan C. Cohen
2. J. K. Pritchard
3. V. Ramensky
4. D. Charlesworth
5. Shamil R. Sunyaev
6. Ivan A. Adzhubei
7. Joel Hirschhorn

Who trusts G. Kryukov overall

1. Seunggeun Lee
2. Michael Bamshad
3. C. Wood
4. Benjamin M. Neale
5. D. Hatfield
6. Michael C. Wu
7. Dean P. Jones
8. M. Rayman
9. B. E. Madsen
10. Xiaoming Liu

Papers from G. Kryukov's perspective

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

1. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
2. Aligning multiple genomic sequences with the threaded blockset aligner. (Genome Research)
3. Solution Hybrid Selection with Ultra-long Oligonucleotides for Massively Parallel Targeted Sequencing (Nature Biotechnology)
4. Balancing Selection and Its Effects on Sequences in Nearby Genome Regions (PLoS Genetics)
5. Genetic Mapping in Human Disease (Science)
6. The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity (Nature)
7. Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data
8. Genome-wide association studies for common diseases and complex traits (Nature reviews genetics)
9. Distinct sets of genetic alterations in melanoma. (New England Journal of Medicine)
10. The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling

Their papers

• The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity (2012) — 7,455 citations
• Highly recurrent TERT promoter mutations in human melanoma (2013) — 1,816 citations
• The Mutational Landscape of Head and Neck Squamous Cell Carcinoma (2011) — 2,541 citations
• Mutational heterogeneity in cancer and the search for new cancer genes (2013) — 1,147 citations
• An APOBEC Cytidine Deaminase Mutagenesis Pattern is Widespread in Human Cancers (2013) — 1,129 citations
• The genetic landscape of clinical resistance to RAF inhibition in metastatic melanoma. (2014) — 705 citations
• A Landscape of Driver Mutations in Melanoma (2012) — 2,528 citations
• Punctuated Evolution of Prostate Cancer Genomes (2013) — 1,269 citations
• An interactive resource to identify cancer genetic and lineage dependencies targeted by small molecules (2013) — 761 citations
• Defining a Cancer Dependency Map (2017) — 2,742 citations
• Next-generation characterization of the Cancer Cell Line Encyclopedia (2019) — 2,830 citations
• Quantitative Proteomics of the Cancer Cell Line Encyclopedia (2020) — 836 citations
• Pooled association tests for rare variants in exon-resequencing studies. (2010) — 651 citations
• Pooled Association Tests for Rare Variants in Exon-Resequencing Studies (2010) — 246 citations
• Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. (2007) — 634 citations
• Characterization of Mammalian Selenoproteomes (2003) — 2,243 citations