Andrew D. Skol, Ph.D.
Affiliations: | 2006 | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
Biostatistics BiologyGoogle:
"Andrew Skol"Parents
Sign in to add mentor| Michael L. Boehnke | grad student | 2006 | University of Michigan | |
| (Efficient methods for gene mapping of complex diseases.) | ||||
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Publications
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| Lin WY, Fordham SE, Hungate E, et al. (2021) Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Nature Communications. 12: 6233 |
| Oliva M, Muñoz-Aguirre M, Kim-Hellmuth S, et al. (2020) The impact of sex on gene expression across human tissues. Science (New York, N.Y.). 369 |
| Crona DJ, Skol AD, Leppänen VM, et al. (2018) Genetic variants of VEGFA and FLT4 are determinants of survival in renal cell carcinoma patients treated with sorafenib. Cancer Research |
| Clay-Gilmour AI, Hahn T, Preus LM, et al. (2017) Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. Blood Advances. 1: 1717-1728 |
| Hungate EA, Applebaum MA, Skol AD, et al. (2017) Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma. Journal of the National Cancer Institute. 109 |
| Hulur I, Skol AD, Gamazon ER, et al. (2017) Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma. Plos One. 12: e0185730 |
| Skol AD, Sasaki MM, Onel K. (2016) The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance. Breast Cancer Research : Bcr. 18: 99 |
| Hungate EA, Vora SR, Gamazon ER, et al. (2016) A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology. Nature Communications. 7: 10635 |
| Pinto N, Volchenboum SL, Skol AD, et al. (2015) Establishing a translational genomics infrastructure in pediatric cancer: the GREAT KIDS experience. Personalized Medicine. 12: 221-229 |
| Sasaki MM, Skol AD, Bao R, et al. (2015) Integrated Genomic Analysis Suggests MLL3 Is a Novel Candidate Susceptibility Gene for Familial Nasopharyngeal Carcinoma. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology |