Aaqib Zaffar Banday

39PUBLICATIONS
42CO-AUTHORS
AutoimmunityEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Gene mappingCardiology (incl. cardiovascular diseases)
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Publications (39)

|May 22, 2026
Partial STX11 deficiency due to a hypomorphic variant-self-limiting inflammatory disease preceding HLH onset.

|May 18, 2026
Nuances of Genetic Diagnosis, Variant Interpretation, and Targeted Molecular Testing in Limited-Resource Settings: Lessons From Inherited Glycerol-3-Phosphate Dehydrogenase 1 Deficiency.

|Mar 17, 2026
Founder Effect of the c.500G>A Variant in South Asian Patients With Inherited GPD1 Deficiency: Report on 16 Patients and Variant Review.

Ishaq Malik, Aaqib Zaffar Banday, Abdus Sami Bhat

|Jan 23, 2026
Congenital diarrhea/enteropathy due to a novel biallelic PERCC1 variant - a case-based review and variant analysis.

Aaqib Zaffar Banday, Ishaq Malik, Anit Kaur

|Jul 16, 2025
The c.64 + 2 T > A Founder Variant Hits Home: Report on 14 Patients Expands the Phenotypic Landscape of Inherited ARPC1B Deficiency - a Comparative Analysis.

Dharmagat Bhattarai, Aaqib Zaffar Banday, Pratap Kumar Patra

|Jun 28, 2025
Genotype-phenotype correlations in specific granule deficiency: loss of DNA-binding ability and impaired nuclear localization cause severe manifestations due to the c.655_665del CEBPE variant.

Tomoya Tamaru, Rina Katayama, Juna Momokino

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Frequent Collaborators

11 joint publications

Pratap Kumar Patra

8 joint publications

Dharmagat Bhattarai

6 joint publications

Ankur Kumar Jindal

6 joint publications

Vignesh Pandiarajan