Amita Moirangthem

22PUBLICATIONS
27CO-AUTHORS
AutoimmunityNeonatologyGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)
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Publications (22)

|Sep 03, 2026
Exome Sequencing Uncovers Phenotypic and Genotypic Heterogeneity in 196 Indian Families Evaluated for Autoinflammatory Disorders.

|Jul 23, 2026
Genotypic and Phenotypic Profile of Hereditary Spastic Paraplegia in Children: A Single-Centre Study from Northern India.

|Jun 15, 2026
Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic Disorders.

|Feb 11, 2026
Childhood-onset ataxia with dystonia: expanding the spectrum of VWA3B-related disorders.

Naik Adarsha, Pradip Paria, Amita Moirangthem

|Feb 05, 2026
Bleeding from umbilicus in a neonate: exploring aetiologies of a common presentation.

Arohi Gupta, Anita Singh, Abhishek Paul

|Dec 22, 2025
A Case Report of PLXNA1-Related Dworschak-Punetha Neurodevelopmental Disorder With Pachygyria and Polymicrogyria.

Niladri Das, Rajesh Kumar Maurya, Shubha R Phadke

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Frequent Collaborators

13 joint publications

Shubha R Phadke

3 joint publications

Deepti Saxena

3 joint publications

Haseena Sait

2 joint publications

Katta Mohan Girisha