We are honored to have the following health professionals and researchers be part of our Medical and Scientific Advisory group, helping guide the research roadmap for our Foundation.
Professor of Human Genetics, Cincinnati Children’s Hospital Medical Center
Director, Tuberous Sclerosis Clinic, Cincinnati Children’s Hospital Medical Center
Professor, University of Cincinnati Department of Pediatrics
Assistant Professor, University of Cincinnati Department of Psychiatry and Behavioral Neuroscience
Clinician, Cincinnati Children’s Hospital Medical Center
Associate Professor. Department of Physiology and Functional Genomics, University of Florida College of Medicine
Director, Centre de Medicina Genòmica, Parc Taulí
Associate Professor, Pediatrics and Medical Genetics, University of Washington School of Medicine
Principal Investigator, Center for Integrative Brain Research, Seattle Children’s Research Institute
Division Head, Genetics, Genomics and Metabolism; Valerie and George D. Kennedy Research Professorship in Human Molecular Genetics, Ann & Robert H. Lurie Children’s Hospital of Chicago
Professor of Pediatrics (Genetics, Genomics and Metabolism), Northwestern University Feinberg School of Medicine
Clinical geneticist
Erasmus Medical Center
Genetic Counselor II, Genetics, Genomics and Metabolism
Ann & Robert H. Lurie Children’s Hospital of Chicago
Assistant Professor, UC Department of Otolaryngology, Head and Neck Surgery, Cincinnati Children’s Hospital Medical Center
Medical geneticist. First to document Smith-Kingsmore syndrome in Smith, L. D., Saunders, C. J., Dinwiddie, D. L., et al. Exome sequencing reveals de novo germline mutation of mammalian target of rapamycin (MTOR) in a patient with megalencephaly and intractable seizures. Genomes Exomes 2: 63-72, 2013.
Professor in Clinical Genetics and Genomic Education (St George’s, University of London), consultant in Clinical Genetics (St George’s University Hospitals NHS Foundation Trust)
~ Bernard Williams