W. Marston Linehan
Molecular Biology · 2001–2020
A researcher in the Science corpus: 21 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 273 citations into it
- Cancer Research — 179 citations into it
Whom W. Marston Linehan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts W. Marston Linehan overall
Papers from W. Marston Linehan's perspective
Ordered by how strongly the researchers W. Marston Linehan trusts endorse each paper. Same corpus, a different order for every researcher.
- C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. (Cell)
- Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer (Nature Genetics)
- BLAT--the BLAST-like alignment tool. (Genome Research)
- HIF prolyl‐hydroxylase 2 is the key oxygen sensor setting low steady‐state levels of HIF‐1α in normoxia (EMBO Journal)
- Basic local alignment search tool.
- Leukemic IDH1 and IDH2 mutations result in a hypermethylation phenotype, disrupt TET2 function, and impair hematopoietic differentiation (Cancer Cell)
- HIF-1 mediates adaptation to hypoxia by actively downregulating mitochondrial oxygen consumption. (Cell Metabolism)
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
- Hysterectomy Rates in the United States 1990–1997 (Obstetrics and Gynecology)
- Denaturing high‐performance liquid chromatography: A review (Human Mutation)
Their papers
- Reductive carboxylation supports growth in tumor cells with defective mitochondria (2011) — 1,311 citations
- Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients (2018) — 792 citations
- Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome. (2002) — 900 citations
- Serum proteomic patterns for detection of prostate cancer. (2002) — 759 citations
- Comprehensive Characterization of Cancer Driver Genes and Mutations (2018) — 2,007 citations
- Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America. (2003) — 606 citations
- Post-analysis follow-up and validation of microarray experiments (2002) — 476 citations
- Comprehensive Molecular Characterization of Papillary Renal Cell Carcinoma (2015) — 1,150 citations
- MRI-Targeted, Systematic, and Combined Biopsy for Prostate Cancer Diagnosis. (2020) — 757 citations
- Integrated Proteogenomic Characterization of Clear Cell Renal Cell Carcinoma (2019) — 634 citations
- Pathogenic germline variants in 10,389 adult cancers (2018) — 734 citations
- Oncogenic Signaling Pathways in The Cancer Genome Atlas (2018) — 2,663 citations
- The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma (2018) — 731 citations
- Ionic immune suppression within the tumour microenvironment limits T cell effector function (2016) — 607 citations
- The molecular taxonomy of primary prostate cancer (2015) — 2,751 citations
- Comparison of MR/Ultrasound Fusion–Guided Biopsy With Ultrasound-Guided Biopsy for the Diagnosis of Prostate Cancer (2015) — 1,517 citations
- The somatic genomic landscape of chromophobe renal cell carcinoma (2014) — 802 citations
- The genetic basis of kidney cancer: a metabolic disease (2010) — 720 citations
- HIF overexpression correlates with biallelic loss of fumarate hydratase in renal cancer: novel role of fumarate in regulation of HIF stability. (2005) — 965 citations
- von Hippel-Lindau disease. (2003) — 2,062 citations