Assistant Professor of Pediatrics, Boston Children's Hospital
Neurology
Dr. Ganeshwaran H. Mochida, MD
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Ganeshwaran H. Mochida practices Neurology. He graduated from Keio Gujuku University School of Medicine. Ganeshwaran H. Mochida, MD has written publications. He has 30 publications published with PubMed. The lastest publication is: 'Another case of internal carotid artery dissection after mandibular osteotomy.'
Publications
- Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number.
- Neuropsychological function in a child with 18p deletion syndrome: a case report.
- METTL23, a transcriptional partner of GABPA, is essential for human cognition.
- Studying rare genetic disorders in child neurology - the need for an international network of collaboration.
- Mutations in QARS, Encoding Glutaminyl-tRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures.
- Posterior Fossa in Primary Microcephaly: Relationships between Forebrain and Mid-Hindbrain Size in 110 Patients.
- CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development.
- Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly.
- A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.
- Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.
- Developmental and degenerative features in a complicated spastic paraplegia.
- A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly.
- Genetics and biology of microcephaly and lissencephaly.
- A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasia.
- An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation.
- Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion.
- Genetic basis of developmental malformations of the cerebral cortex.
- [Molecular genetics of lissencephaly and microcephaly].
- Protein-truncating mutations in ASPM cause variable reduction in brain size.
- ASPM is a major determinant of cerebral cortical size.
- Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females.
- Molecular genetics of human microcephaly.
- A two-year-old female with methylmalonic acidemia and progressive low density lesions in the basal ganglia on CT scans.
- Another case of internal carotid artery dissection after mandibular osteotomy.
- ASPM mutations identified in patients with primary microcephaly and seizures.
- The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein.
- Cortical malformation and pediatric epilepsy: a molecular genetic approach.
- Broader geographical spectrum of Cohen syndrome due to COH1 mutations.
- A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21.
Conditions Treated
- Headache
- Lyme Disease
Doctors Specialties
- Pediatric Neurology
- Neurology
Accepted Insurances
Education
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Massachusetts General Hospital -
Keio Gujuku University School of Medicine
Hospital
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Boston Children's Hospital -
Brigham and Women's Hospital -
Massachusetts General Hospital
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