Debbie Nickerson
Affiliations: | University of Washington, Seattle, Seattle, WA |
Area:
Genetics, Bioinformatics Biology, Evolution and Development BiologyGoogle:
"Debbie Nickerson"Children
Sign in to add trainee| Cindy Desmarais | grad student | 2010 | University of Washington |
| Jennifer Elizabeth Below | post-doc | University of Washington |
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Publications
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| Olson NC, Raffield LM, Moxley AH, et al. (2021) Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Blacks. Circulation. Genomic and Precision Medicine. CIRCGEN121003421 |
| Karas S, Etheridge AS, Nickerson DA, et al. (2021) Integration of DNA sequencing with population pharmacokinetics to improve the prediction of irinotecan exposure in cancer patients. British Journal of Cancer |
| Mikhaylova AV, McHugh CP, Polfus LM, et al. (2021) Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. American Journal of Human Genetics |
| Miller DE, Sulovari A, Wang T, et al. (2021) Targeted long-read sequencing identifies missing disease-causing variation. American Journal of Human Genetics |
| Bharadwaj T, Schrauwen I, Rehman S, et al. (2021) ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment. European Journal of Human Genetics : Ejhg |
| Hu Y, Stilp AM, McHugh CP, et al. (2021) Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics |
| Van De Weghe JC, Giordano JL, Mathijssen IB, et al. (2021) TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes. Hgg Advances. 2 |
| Hildebrandt CC, Patel N, Graham JM, et al. (2021) Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. American Journal of Medical Genetics. Part A |
| Taliun D, Harris DN, Kessler MD, et al. (2021) Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 590: 290-299 |
| Meitlis I, Allenspach EJ, Bauman BM, et al. (2020) Multiplexed Functional Assessment of Genetic Variants in CARD11. American Journal of Human Genetics |