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Chitra Prasad

Affiliation : Western University · London Health Sciences Centre

• 2Publications (affiliation in Canada)
• 181Total publications
• 4282Citations
• 35h-index

ORCIDOpenAlex

Research profile

Chitra Prasad has 2 indexed publications (2017–2024). Their work appears mainly in “Brain Communications” and “Nature Genetics”. Their most cited article, “Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly” (2017), has been cited 220 times. Their work is co-authored with at least 8 researchers.

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Research areas

• Metabolism and Genetic Disorders
• Genomics and Rare Diseases
• Lysosomal Storage Disorders Research
• Genetics and Neurodevelopmental Disorders
• Epilepsy research and treatment

Publications (2)

• Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment
  2024 · Brain Communications · cited 4 times
• Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
  2017 · Nature Genetics · cited 220 times

Publication venues

• Brain Communications × 1
• Nature Genetics × 1

Publications per year

• 20241
• 20171

Collaborations

Partner institutions : University of Toronto · Hospital for Sick Children · McGill University · Centre Hospitalier Universitaire Sainte-Justine · Université de Montréal

Co-authors

• Jessica Jakobczyk
• Emmanuelle Lemyre
• Pekka Kannus
• Maxime Bouchard
• Asuri Narayan Prasad
• Oraly Sanchez-Ferras
• Tony Rupar
• David A. Chitayat

Bibliographic data from OpenAlex (open database).