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Pharmacogenetics and Genomics|September 25, 2013
GABRG2, rs211037 is associated with epilepsy susceptibility, but not with antiepileptic drug resistance and febrile seizuresShabeesh Balan, Sanish Sathyan, Saradalekshmi K Radha, et al.Plos One|March 4, 2014
Genetic association analysis of ATP binding cassette protein family reveals a novel association of ABCB1 genetic variants with epilepsy risk, but not with drug-resistanceShabeesh Balan, Sumitha Prameela Bharathan, Neetha Nanoth Vellichiramal, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 5, 2022
SNPs at SMG7 Associated with Time from Biochemical Recurrence to Prostate Cancer DeathXiaoyu Song, Meng Ru, Zoe Steinsnyder, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 14, 2016
Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex TestingJudith Balmaña, Laura Digiovanni, Pragna Gaddam, et al.Journal of Community Genetics|July 18, 2020
Utilization of clinical genetic counseling among childhood and young adult cancer survivors in a registry trialNassim Anderson, Arash Delavar, Danielle Novetsky Friedman, et al.Cancers|November 27, 2025
Whole-Exome Sequencing-Based Linkage Analysis of Multiple Myeloma (MM) and Monoclonal Gammopathy of Undetermined Significance (MGUS) PedigreesAlyssa I Clay-Gilmour, Nicola J Camp, Xiaomu Wei, et al.Blood Advances|June 13, 2025
BRCA1/2 impact on the development of implant-associated lymphoma in women with breast cancer and textured implantsPaola Ghione, Diana Mandelker, Maria E Arcila, et al.European Journal of Human Genetics : EJHG|February 6, 2019
Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genesMykyta Artomov, Vijai Joseph, Grace Tiao, et al.Human Genetics|April 30, 2018
High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputationTodd Lencz, Jin Yu, Cameron Palmer, et al.Blood Advances|April 4, 2019
Germline deletion of <i>ETV6</i> in familial acute lymphoblastic leukemiaEvadnie Rampersaud, David S Ziegler, Ilaria Iacobucci, et al.Pageof 6