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The Annals of Applied Statistics|October 10, 2017
ALLELE-SPECIFIC COPY NUMBER ESTIMATION BY WHOLE EXOME SEQUENCINGHao Chen, Yuchao Jiang, Kara N Maxwell, et al.The British Journal of Dermatology|February 16, 2016
CDKN2A mutations with p14 loss predisposing to multiple nerve sheath tumours, melanoma, dysplastic naevi and internal malignancies: a case series and review of the literatureM R Sargen, S L Merrill, E Y Chu, et al.BMC Family Practice|September 7, 2019
Impact of rural address and distance from clinic on depression outcomes within a primary care medical home practiceHailon Wong, Kyle Moore, Kurt B Angstman, et al.The Journal of the American Osteopathic Association|June 1, 1989
Comparison of two office tests for determining blood theophylline levelsM Garrison, J A Brose, M M Russell, et al.Applied Biosafety : Journal of the American Biological Safety Association|December 30, 2024
Approaches for the Inactivation of Yersinia pestisAmanda Brady, Maggie Tomaszewski, Taylor M Garrison, et al.Annals of Surgical Oncology|March 21, 2013
Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testingLauren Fishbein, Shana Merrill, Douglas L Fraker, et al.Journal of the National Cancer Institute|August 21, 2003
Pheochromocytoma: the expanding genetic differential diagnosisJennifer Bryant, Jennifer Farmer, Lisa J Kessler, et al.Journal of the National Comprehensive Cancer Network : JNCCN|April 4, 2023
Nationwide Trends and Determinants of Germline BRCA1/2 Testing in Patients With Breast and Ovarian CancerKelsey S Lau-Min, Anne Marie McCarthy, Katherine L Nathanson, et al.Statistical Applications in Genetics and Molecular Biology|December 4, 2018
A practical approach to adjusting for population stratification in genome-wide association studies: principal components and propensity scores (PCAPS)Huaqing Zhao, Nandita Mitra, Peter A Kanetsky, et al.Pageof 70