I am Dr. Neha Pichad, a pediatrician with specialized
training in Clinical Genetics, with a strong academic and clinical interest in
pediatric genetic disorders, rare diseases, metabolic disorders, and pediatric
critical care. I have been actively involved in the evaluation and management
of children with complex and rare disorders, along with academic teaching and
research activities. My research experience includes work on lysosomal storage
disorders, particularly Niemann–Pick disease and mucopolysaccharidoses, as well
as preparation and peer review of scientific manuscripts. With my combined
experience in clinical pediatrics, genetics, research, and medical education, I
hope to contribute to the journal through critical and constructive manuscript
review, promotion of scientific rigor, and support for clinically relevant
pediatric research.

Introduction
AFFILIATION
RESEARCH IDS
RESEARCH INTERESTS
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BOOKS PUBLISHED
BOOK CHAPTERS PUBLISHED
ACADEMIC PROFILE
EMPLOYMENT DETAILS
PAPERS PRESENTED IN CONFERENCES
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HONOURS AWARDS AND DISTINCTIONS
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EVENTS ORGANIZED