Parag Tamhankar

5PUBLICATIONS
32CO-AUTHORS
Cell and nuclear divisionMedical mycologyNeurogeneticsNeurology and neuromuscular diseases
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Publications (5)

|Jun 18, 2026
Report of a Homozygous Nonsense Variant in the WDR91 Gene Associated With Severe Communicating Hydrocephalus, Dandy Walker Malformation, and Cerebellar Hypoplasia.

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

|May 22, 2026
Mendelian susceptibility to mycobacterial disease: Clinical, immunological, and genetic study in India.

|Dec 10, 2024
A Homozygous Nonsense Variant in the BICC1 Gene Associated With Fetal Cystic Kidney Disease and Lower Limb Post-Axial Polydactyly.

Vasundhara Parag Tamhankar, Malathy Prasad, Shalin Vaniawala

|Oct 17, 2021
Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes.

Lucia Laugwitz, Annette Seibt, Diran Herebian

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Frequent Collaborators

1 joint publications

Inusha Panigrahi

1 joint publications

Ahmet Okay Caglayan

1 joint publications

Anita Rauch

1 joint publications

Tawfiq Froukh