Gad Getz
Molecular Biology · 2000–2020
A researcher in the Science corpus: 105 papers; trusts 11 researchers and is trusted by 30 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 1,728 citations into it; #2,147 of 17,773 by trust here, #16 by citations
- Genetics — 813 citations into it
- Cancer Research — 793 citations into it; #261 of 1,780 by trust here, #1 by citations
- Oncology — 446 citations into it
- Artificial Intelligence — 69 citations into it
- Statistics and Probability — 29 citations into it
- Evaluation & Benchmarks — 27 citations into it
Whom Gad Getz trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Gad Getz overall
- Jan Ihmels
- Adrian E. Raftery
- Sara Cordeiro Madeira
- Ruxandra I. Dima
- Amos Tanay
- Sven Bergmann
- Roy Varshavsky
- Yuval Kluger
- Ali Anaissi
- Leping Li
Papers from Gad Getz's perspective
Ordered by how strongly the researchers Gad Getz trusts endorse each paper. Same corpus, a different order for every researcher.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Malignant astrocytic glioma: genetics, biology, and paths to treatment. (Genes & Development)
- ARID1A mutations in endometriosis-associated ovarian carcinomas. (New England Journal of Medicine)
- GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers (Genome Biology)
- RECURRENT MUTATIONS IN THE U2AF1 SPLICING FACTOR IN MYELODYSPLASTIC SYNDROMES (Nature Genetics)
- Molecular portraits of human breast tumours (Nature)
- Supervised risk predictor of breast cancer based on intrinsic subtypes.
- Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. (Journal of the National Cancer Institute)
- Small molecule-mediated disruption of Wnt-dependent signaling in tissue regeneration and cancer (Nature Chemical Biology)
- Loss of IGF2 Imprinting: A Potential Marker of Colorectal Cancer Risk (Science)
Their papers
- Integrative Genomics Viewer (2011) — 14,177 citations
- MicroRNA expression profiles classify human cancers (2005) — 9,882 citations
- The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity (2012) — 7,455 citations
- Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma (2007) — 1,099 citations
- GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers (2011) — 3,145 citations
- Discovery and saturation analysis of cancer genes across 21 tumor types (2014) — 2,932 citations
- An integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR and NF1 (2010) — 7,152 citations
- High-resolution mapping of copy-number alterations with massively parallel sequencing (2008) — 550 citations
- Somatic mutations affect key pathways in lung adenocarcinoma (2008) — 2,751 citations
- Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer (2012) — 1,524 citations
- Comprehensive molecular portraits of human breast tumors (2012) — 7,518 citations
- The Mutational Landscape of Head and Neck Squamous Cell Carcinoma (2011) — 2,541 citations
- Comprehensive Molecular Characterization of Human Colon and Rectal Cancer (2012) — 7,754 citations
- Mutational heterogeneity in cancer and the search for new cancer genes (2013) — 1,147 citations
- Toil enables reproducible, open source, big biomedical data analyses (2017) — 1,154 citations
- Characterizing the cancer genome in lung adenocarcinoma (2007) — 1,146 citations
- The Genotype-Tissue Expression (GTEx) project (2013) — 8,629 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
- Melanoma genome sequencing reveals frequent PREX2 mutations (2012) — 752 citations