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Inusha Panigrahi

30PUBLICATIONS
33CO-AUTHORS
Medical mycologyEpigenetics (incl. genome methylation and epigenomics)Infant and child healthGenome structure and regulationDevelopmental genetics (incl. sex determination)
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Journal

Publications (30)

Sort by Publication Date:
|Jun 17, 2026
Novel Homozygous Exonic Deletion of the TMEM17 Gene Associated With Meckel-Gruber Syndrome Phenotype.

|Jun 17, 2026
Uniparental Disomy: A Scoping Review of Diagnostic Challenges, Clinical Spectrum, and Counselling Implications.

|Sep 22, 2025
Clinical and Genetic Landscape of Children With Congenital Muscular Dystrophies From North India.

Anirban Basu, Renu Suthar, Abhishek Pandey

|Nov 06, 2024
<i>TWIST1</i> Gene Variants Cause Craniosynostosis with Limb Abnormalities in Asian Patients.

Shalini Dhiman, Inusha Panigrahi, Maryada Sharma

|Sep 12, 2024
Intellectual Disability and Blended Phenotypes: Insights from a Centre in North India.

Inusha Panigrahi, Sudha Rao, Shalu Verma Kumar

|Apr 09, 2024
Novel Compound Heterozygous Mutations of LIG4 Gene in an Indian <i>LIG4</i> Syndrome Patient with Severe Microcephaly: Case Report, <i>In-silico</i> Analysis and Systematic Review.

Amit Singh, Sabyasachi Senapati, Inusha Panigrahi

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Frequent Collaborators

7 joint publications

Chakshu Chaudhry

6 joint publications

Anupriya Kaur

4 joint publications

Preeti Khetarpal

3 joint publications

Harvinder Kaur

3 joint publications

Amit Singh

3 joint publications

Devi Dayal

2 joint publications

Ankita Tyagi

2 joint publications

Navdeep Dhoat

2 joint publications

Sabyasachi Senapati

2 joint publications

Divya Kumari

Frequent Collaborators

7 joint publications

Chakshu Chaudhry

6 joint publications

Anupriya Kaur

4 joint publications

Preeti Khetarpal

3 joint publications

Harvinder Kaur