Bari Ballew, Ph.D., joined the Clinical Genetics Branch (CGB) in March, 2012 as a postdoctoral CRTA fellow. She obtained her Ph.D. in biology from the University of California, San Diego in 2012. Her Ph.D. dissertation focused on the regulation of DNA end-processing at telomeres and at DNA double strand breaks. Dr. Ballew completed her undergraduate training at Johns Hopkins University, where she was awarded a Howard Hughes Undergraduate Research Fellowship prior to earning her Bachelor of Science degree in molecular and cellular biology. Dr. Ballew works primarily on the telomere molecular epidemiology program with mentor Sharon A. Savage, M.D., Chief of CGB. Her current research focuses on studies of the genetic contribution of aberrant telomere biology on human disease. She is conducting studies on disease susceptibility in patients with dyskeratosis congenita, an inherited cancer predisposition syndrome, which is caused by germline mutations in telomere biology genes, and new cancer gene discovery in DCEG’s Whole Exome Sequencing initiative.
Nicholas Khan joined the Clinical Genetics Branch (CGB) as a postbaccalaureate fellow in November 2013. Mr. Khan received his B.A. in public health studies from the Johns Hopkins University and is earning an M.S.P.H. in health policy from the Johns Hopkins Bloomberg School of Public Health. His work prior to joining CGB includes experience with both laboratory and public health research and covers a range of topics including childhood obesity and intimate-partner violence. In DCEG, Mr. Khan works under the mentorship of Jennifer T. Loud, R.N., C.R.N.P., D.N.P., Assistant Branch Chief of CGB, and Douglas Stewart, M.D., investigator, CGB, on several projects, including the association of phenotype and DICER1 mutations in a prospective cohort.
Payal Khincha, M.B.B.S., has joined the Clinical Genetics Branch (CGB) as a clinical fellow. Dr. Khincha first came to CGB as a special volunteer and clinical collaborator in July 2012 for the research component of a clinical fellowship in pediatric hematology-oncology at the Children’s National Medical Center (CNMC), Washington, D.C., which she recently completed. She received her M.B.B.S. degree in 2005 from Kempegowda Institute of Medical Sciences, Bangalore, India, and completed her residency training in pediatrics in 2010 at Maimonides Medical Center, Brooklyn, New York and CNMC, Washington D.C. Dr. Khincha began her clinical pediatric hematology-oncology fellowship at CNMC in 2011, and as part of her research component at CGB, focused on the clinical management, diagnosis, and genotype-phenotype relationships of dyskeratosis congenita (DC), a cancer-prone inherited bone marrow failure syndrome and telomere biology disorder. As a clinical fellow in CGB, Dr. Khincha works with Sharon A. Savage, M.D., Chief of CGB, on DC and telomere biology studies, and with Dr. Savage and Phuong Mai, M.D., on the Li-Fraumeni Syndrome study.
Jenni Young, M.A., M.S., LGMFT, joined the Clinical Genetics Branch (CGB) of NCI as a predoctoral fellow in September, 2014. She is a first year family science doctoral student at the University of Maryland, College Park. She earned a B.A. in psychology and Mandarin Chinese from the University of Wisconsin, Madison, and an M.A. in Chinese language and culture from The Ohio State University. Ms. Young graduated from the University of Maryland’s Couple and Family Therapy M.S. Program in May and is a licensed Couple and Family Therapist in the state of Maryland. In CGB, she works with Mark H. Greene, M.D., senior investigator, and Jennifer T. Loud, R.N., C.R.N.P., D.N.P., Assistant Branch Chief, doing psychosocial and qualitative research on Li-Fraumeni syndrome families.