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 mentorMichael L. Boehnke | grad student | 2006 | University of Michigan | |
(Efficient methods for gene mapping of complex diseases.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
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 |