Amita Moirangthem

21PUBLICATIONS
22CO-AUTHORS
NeonatologyEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesAnthropological genetics
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Publications (21)

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

|Jul 12, 2026
Correction to: Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic Disorders.

|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

|Jan 08, 2026
Clinical and Genetic Characterization of Patients with ADNP Related Helsmoortel-Van der Aa Syndrome.

Pragya Kafley, Deepti Saxena, Amita Moirangthem

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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

Niladri Das