Publications

	Core Programs

	CHG Resources

	Publications

	Amyotrophic Lateral Sclerosis (ALS) Chiari Malformations and Syringomyelia Early Onset Cardiovascular Disease Essential Tremer Facioscapulohumeral Muscular Dystrophy Focal Segmental Glomerulosclerosis (FSGS) Glaucoma Limb-Girdle Muscular Dystrophy Multiple Sclerosis (MS) Myopia Neural Tube Defects (NTD) Parkinson Disease

As CHG researchers work to define the genetic causes of human disease, they publish their findings in leading academic journals and share their knowledge with colleagues at meetings and conferences.

Center for Human Genetics faculty members are also developing new methods for understanding the genetic basis of human disease.

Methodological Development

Supporting Publications Data