Huda Zoghbi

Specialty: Neurology (Neurogenetics)

Location: Houston, Lebanon

Tier: TITAN

H-Index: 140

Years Active: 0

Hospital Affiliations

• Baylor College of Medicine - Professor of Molecular and Human Genetics
• Texas Children's Hospital - Director, Jan and Dan Duncan Neurological Research Institute
• Howard Hughes Medical Institute - Investigator

Key Publications

1. "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2" - Nature Genetics (1999) [4992 citations]
2. "Towards a proteome-scale map of the human protein–protein interaction network" - Nature (2005) [3001 citations]
3. "MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription" - Science (2008) [1822 citations]
4. "Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation." - PubMed (1992) [1713 citations]
5. "Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1" - Nature Genetics (1993) [1652 citations]
6. "Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel" - Nature Genetics (1997) [1582 citations]
7. "Trinucleotide Repeat Disorders" - Annual Review of Neuroscience (2007) [1376 citations]
8. "Glutamine Repeats and Neurodegeneration" - Annual Review of Neuroscience (2000) [1313 citations]
9. "The Story of Rett Syndrome: From Clinic to Neurobiology" - Neuron (2007) [1261 citations]
10. "Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes" - Nature (2010) [1173 citations]

Knowledge Graph Relationships

Huda Zoghbi is a Neurology specialist affiliated with Baylor College of Medicine, Texas Children's Hospital, Howard Hughes Medical Institute. Authored 10 scholarly articles.