Dr. Ross is the Nathan Cummings Professor of Neurology and Neuroscience and Director of the Center for Neurognetics in the Brain and Mind Research Institute at Weill Cornell Medicine. She received her MD and PhD from Cornell University Medical College her Neurology residency at Massachusetts General Hospital and molecular genetic fellowships at MGH and Rockefeller University. She built her laboratory at University of Minnesota before returning to Weill Cornell Medicine as a tenured Professor.  She is a physician scientist who leads the Laboratory of Neurogenetics and Development. Common threads in her work have been discovery of gene mutations causing neurological disorders as a window on the drivers of brain development and function.  The Center for Neurogenetics at WCM that she directs has both basic science and clinical arms, and operates a patient DNA and cell biobank. Dr. Ross has devoted much of her career to medical and neuroscience education. While at the University of Minnesota, she directed the NIH funded MD-PhD training program. At Weill Cornell Medicine she is Chair of the Neuroscience Graduate Program and is the founding Chair of the Master of Science in Genetic Counseling program.

Dr. Rahman is Division Chief of Genetics in the Department of Pediatrics at Weill Cornell Medicine. He has practiced as an ABMGG-certified clinical geneticist for 17 years working with various genetic counselors in  pediatric, adult, prenatal, and cancer settings. He has served in various education roles including lecturer and facilitator for genetics to first-year medical students, nursing students, pharmacy students, pediatric residents, and fellows. He has taught genetic counseling students in a clinical setting for several years and in a classroom setting from 2019 to the present. He has previously served as the associate program director for pediatrics, as vice-chair of faculty development, and as division chief and department director for medical genetics in two institutions. He is also a faculty member of the ACGME-accredited medical genetics residency at UNMC. 

Dr. Walsh is a pediatric oncologist and clinical geneticist. His work focuses on identifying patients at risk for cancer and utilizing this information for screening, risk reduction and therapeutic purposes. To identify at risk individuals my research agenda entails defining and expanding our understanding of known cancer predisposition syndromes, discovering new cancer predisposition genes as well as helping define means to annotate molecular variations based on scientific rigor. He has been fortunate to train under Victor McKusick, MD, Ada Hamosh, MD, MPH (founders of MIM & OMIM), and James Downing, MD (Pediatric Cancer Genome Project). As a result, he has obtained a unique understanding and skill set related to classical Mendelian genetics and modern genomics relating to tumor- matched normal sequencing. He is now part of an expert Clinical Cancer Genetics team led by Kenneth Offit, MD, MPH and Pediatrics Department directed by Andrew Kung, MD, PhD at Memorial Sloan Kettering (MSK) with a track record in gene discovery, phenotypic description and translational genomic care. Given his training and practice environment, he has a unique opportunity to practice genetics and oncology and aggregate data from these purviews of care. 

Maullika is the Program Administrator for the MSGC program. She received her Bachelor's degree from University at Buffalo and her Master's in Public Health degree from Mount Sinai.