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Connection

Nancy Jean Cox to Genomics

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This is a "connection" page, showing publications Nancy Jean Cox has written about Genomics.
Nancy Jean Cox
Connection Strength
1.180
Genomics
  1. Human genetics: an expression of interest. Nature. 2004 Aug 12; 430(7001):733-4.
    View in: PubMed
    Score: 0.141
  2. Advancing genomics to improve health equity. Nat Genet. 2024 May; 56(5):752-757.
    View in: PubMed
    Score: 0.138
  3. A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data. Nat Neurosci. 2019 05; 22(5):691-699.
    View in: PubMed
    Score: 0.097
  4. UK Biobank shares the promise of big data. Nature. 2018 10; 562(7726):194-195.
    View in: PubMed
    Score: 0.094
  5. An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies. Genome Med. 2018 01 29; 10(1):7.
    View in: PubMed
    Score: 0.090
  6. Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record. PLoS One. 2017; 12(7):e0175508.
    View in: PubMed
    Score: 0.086
  7. Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research. Cell. 2017 03 23; 169(1):6-12.
    View in: PubMed
    Score: 0.084
  8. A genome-wide integrative study of microRNAs in human liver. BMC Genomics. 2013 Jun 13; 14:395.
    View in: PubMed
    Score: 0.065
  9. Clinical translation of cell-based pharmacogenomic discovery. Clin Pharmacol Ther. 2012 Oct; 92(4):425-7.
    View in: PubMed
    Score: 0.061
  10. On sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacy. Am J Hum Genet. 2012 Apr 06; 90(4):591-8.
    View in: PubMed
    Score: 0.060
  11. Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases. Stat Appl Genet Mol Biol. 2010; 9:Article18.
    View in: PubMed
    Score: 0.052
  12. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2. Diabetologia. 2007 Jul; 50(7):1418-22.
    View in: PubMed
    Score: 0.043
  13. Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood. Am J Hum Genet. 2025 Feb 06; 112(2):276-290.
    View in: PubMed
    Score: 0.036
  14. FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Nucleic Acids Res. 2023 01 06; 51(D1):D1300-D1311.
    View in: PubMed
    Score: 0.032
  15. A brief history of human disease genetics. Nature. 2020 01; 577(7789):179-189.
    View in: PubMed
    Score: 0.026
  16. Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity. BMC Genomics. 2014 Apr 16; 15:292.
    View in: PubMed
    Score: 0.017
  17. Chemotherapy-induced peripheral neurotoxicity and ototoxicity: new paradigms for translational genomics. J Natl Cancer Inst. 2014 Mar 12; 106(5).
    View in: PubMed
    Score: 0.017
  18. Quantitative allelic test--a fast test for very large association studies. Genet Epidemiol. 2013 Dec; 37(8):831-9.
    View in: PubMed
    Score: 0.017
  19. Genetic Analysis in Translational Medicine: The 2010 GOLDEN HELIX Symposium. Hum Mutat. 2011 Jun; 32(6):698-703.
    View in: PubMed
    Score: 0.014
  20. Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium. Hum Hered. 2008; 66(1):35-49.
    View in: PubMed
    Score: 0.010
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.