Congratulations to Adi V. Gundlapalli, MD, PhD, MS (Epidemiology) for receiving the 2017 Leadership in Inclusive Excellence Award in Research from the Office of Health Equity and Inclusion (OHEI) at...
Next-generation sequencing technologies have afforded unprecedented characterization of low-frequency and rare genetic variation. Due to low power for single-variant testing, aggregative methods are commonly used to combine observed rare variation...
A population-based genealogical resource with linked medical data was used to define the observed familial clustering of Chiari malformation Type I (CM-I).
There are few published familial relative risks (RR) for lethal prostate cancer. This study estimates RRs for lethal prostate cancer based on comprehensive family history data, with the goal of...
