Stacey Gabriel

Molecular Biology · 2002–2022

A researcher in the Science corpus: 116 papers; trusts 6 researchers and is trusted by 18 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 1,469 citations into it; #6,706 of 17,773 by trust here, #10 by citations
• Genetics — 1,143 citations into it; #1,429 of 6,854 by trust here, #3 by citations

Whom Stacey Gabriel trusts overall

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

1. Jay Shendure

Who trusts Stacey Gabriel overall

1. M. Thomson
2. Jeffrey D. Wall
3. Michael Olivier
4. J. K. Pritchard
5. Xiaoyi Gao
6. Nick Patterson
7. Seunggeun Lee
8. C. Pareek
9. C. Carlson
10. Jonathan Marchini

Papers from Stacey Gabriel's perspective

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

1. ARID1A mutations in endometriosis-associated ovarian carcinomas. (New England Journal of Medicine)
2. Tumour evolution inferred by single-cell sequencing (Nature)
3. Malignant astrocytic glioma: genetics, biology, and paths to treatment. (Genes & Development)
4. Supervised risk predictor of breast cancer based on intrinsic subtypes.
5. SOAP: short oligonucleotide alignment program (Bioinform.)
6. BreakDancer: An algorithm for high resolution mapping of genomic structural variation (Nature Methods)
7. A framework for variation discovery and genotyping using next-generation DNA sequencing data
8. RECURRENT MUTATIONS IN THE U2AF1 SPLICING FACTOR IN MYELODYSPLASTIC SYNDROMES (Nature Genetics)
9. Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
10. GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers (Genome Biology)

Their papers

• A framework for variation discovery and genotyping using next-generation DNA sequencing data (2011) — 11,249 citations
• The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (2010) — 25,882 citations
• A global reference for human genetic variation (2015) — 16,925 citations
• The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity (2012) — 7,455 citations
• A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
• Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 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
• Solution Hybrid Selection with Ultra-long Oligonucleotides for Massively Parallel Targeted Sequencing (2009) — 1,475 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
• Analysis of 6,515 exomes reveals a recent origin of most human protein-coding variants (2012) — 970 citations
• The Structure of Haplotype Blocks in the Human Genome (2002) — 5,956 citations
• The mutational constraint spectrum quantified from variation in 141,456 humans (2020) — 8,441 citations
• Comprehensive Molecular Characterization of Human Colon and Rectal Cancer (2012) — 7,754 citations
• Characterizing the cancer genome in lung adenocarcinoma (2007) — 1,146 citations
• Pangenomics enables genotyping known structural variants in 5,202 diverse genomes (2021) — 309 citations
• Melanoma genome sequencing reveals frequent PREX2 mutations (2012) — 752 citations
• A framework for the interpretation of de novo mutation in human disease (2014) — 1,035 citations