معرفی
Neil Hanchard, M.D., Ph.D., is an Assistant Professor in the Department of Molecular and Human Genetics at Baylor College of Medicine. He also holds a position at the USDA/ARS Children's Nutrition Research Center. His work bridges clinical genetics and population genomics.
- MBBS from University of the West Indies (1999)
- PhD in Human Genetics from University of Oxford (2004)
- Pediatrics Residency at Mayo Clinic (2009)
- Clinical Genetics Fellowship at Baylor College of Medicine (2011)
His research focuses on using genomics to unravel complex pediatric diseases, particularly severe childhood malnutrition, sickle cell disease, and HIV-TB comorbidities in sub-Saharan Africa. His work integrates genome-wide SNP genotyping, metabolomics, and DNA methylation analyses to identify genetic pathways influencing disease outcomes.
Recent publications highlight his expertise in African population genomics, epigenetic mechanisms in malnutrition, and genetic studies of hemoglobinopathies. Collaborations span institutions in Malawi, Jamaica, Uganda, and Botswana through networks like CAfGEN and AfroSickleNet.
Scientific Awards
- Fellow, American College of Medical Genetics and Genomics
He contributes to clinical research through the Undiagnosed Disease Network and maintains active memberships in the American Society of Human Genetics and American Medical Association, focusing on translational genomics and global health equity.
