Kim Ng, MD
Assistant Professor of Clinical Pediatrics (Human Genetics)
Attending Physician, Biochemical Genetics (Metabolism), Division of Genetics, Children's Hospital of Philadelphia
Department: Pediatrics
Contact information
Children's Hospital of Philadelphia
Division of Human Genetics
3401 Civic Center Blvd
HUB - 12th Floor
Philadelphia, PA 19104
Division of Human Genetics
3401 Civic Center Blvd
HUB - 12th Floor
Philadelphia, PA 19104
Education:
BSc (Biomedical Science)
Monash University, 2009.
MD (Medicine)
Duke-NUS Graduate Medical School, Singapore, 2014.
Permanent linkBSc (Biomedical Science)
Monash University, 2009.
MD (Medicine)
Duke-NUS Graduate Medical School, Singapore, 2014.
Selected Publications
Kim Ng, James Collins, Filippo Vairo, Kacie Riley, Yong-Hui Jiang: Defect In Chromatin Modifications in Autism Spectrum Disorder (ASD) and Neurodevelopmental Disorders- Report of 3 novel and de novo pathogenic mutations of chromatin-modifying enzyme MSL2 and review of the literature. Poster presented at Cold Spring Harbor Asia Conference, Cold Spring Harbor, NY 2018.Leonard AS, Hyder SN, Kolls BJ, Arehart E, Ng KC, Veerapandiyan A, Mikati MA.: Seizure predisposition after perinatal hypoxia: effects of subsequent age and of an epilepsy predisposing gene mutation. Epilepsia 54(10): 1789-800, Oct 2013.
Kim Ng, Eric Arehart, Marie McDonald, Dwight Koerbel, Mohamad Mikati: Co-existence of Coenzyme Q10 Deficiency and a MCM4 Mutation. Poster presented at the International Congress of Pediatrics 2013 and Duke University Department of Pediatrics Research Retreat 2013.
Kim Ng, Soren Leonard, Eric Arehart, Mohamad A. Mikati: Kv1.1 mutation results in long-term enhancement of post perinatal hypoxia predisposition to seizures without affecting the severity of acute hypoxic seizures. Poster presented at the International Congress of Pediatrics 2013.
Kim Ng, Soren Leonard, Eric Arehart, Mohamad A. Mikati: Single gene mutation can influence long-term outcome after mild perinatal hypoxia by resulting spontaneous recurrent seizures without affecting the severity of acute hypoxic seizures. Poster presented at the Child Neurology Society 2013.
Kim Ng, Eric Arehart, Marie McDonald, Mohamad Mikati: ARHGEF6 Gene Mutation Can be Associated with Lennox-Gastaut Syndrome? Poster presented at the International Congress of Pediatrics 2013.