Nancy J. Cox
Genetics · 2000–2021
A researcher in the Science corpus: 16 papers; trusts 7 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 250 citations into it; #5,892 of 6,854 by trust here, #188 by citations
- Molecular Biology — 182 citations into it; #10,491 of 17,773 by trust here, #1,534 by citations
Whom Nancy J. Cox trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Robert Tibshirani
- J. K. Pritchard
- Sean Davis
- Rafael A. Irizarry
- Mathew Garnett
- Trevor J. Hastie
- Laurent Gautier
- Paul Geeleher
- N. Risch
- Maqc Consortium
Who trusts Nancy J. Cox overall
Papers from Nancy J. Cox's perspective
Ordered by how strongly the researchers Nancy J. Cox trusts endorse each paper. Same corpus, a different order for every researcher.
- The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity (Nature)
- Systematic identification of genomic markers of drug sensitivity in cancer cells (Nature)
- Diagnosis of multiple cancer types by shrunken centroids of gene expression
- Exploration, normalization, and summaries of high density oligonucleotide array probe level data. (Biostatistics)
- A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
- The Structure of Haplotype Blocks in the Human Genome (Science)
- Next-generation genotype imputation service and methods (Nature Genetics)
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Nature)
- Mutations in the epidermal growth factor receptor and in KRAS are predictive and prognostic indicators in patients with non-small-cell lung cancer treated with chemotherapy alone and in combination… (Journal of Clinical Oncology)
- A general test of association for quantitative traits in nuclear families. (American Journal of Human Genetics)
Their papers
- A gene-based association method for mapping traits using reference transcriptome data (2015) — 1,739 citations
- Clinical drug response can be predicted using baseline gene expression levels and in vitro drug sensitivity in cell lines (2014) — 773 citations
- The Genotype-Tissue Expression (GTEx) project (2013) — 8,629 citations
- The GTEx Consortium atlas of genetic regulatory effects across human tissues (2019) — 4,770 citations
- Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS (2010) — 1,330 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- The allelic architecture of human disease genes: common disease-common variant...or not? (2002) — 743 citations
- Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus (2000) — 1,471 citations
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record (2017) — 336 citations
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations
- pRRophetic: An R Package for Prediction of Clinical Chemotherapeutic Response from Tumor Gene Expression Levels (2014) — 1,996 citations
- Human polymorphism at microRNAs and microRNA target sites. (2013) — 605 citations
- Finding the missing heritability of complex diseases (2009) — 8,360 citations
- Finding the missing heritability of complex (2009) — 88 citations