Ali Muhammad Waryah

8PUBLICATIONS
14CO-AUTHORS
Gene mappingComparative language studiesVision scienceEpigenetics (incl. genome methylation and epigenomics)Haematological tumours
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Publications (8)

|Jan 02, 2026
Caste-based genetic diagnosis: evidence from a pathogenic SLC26A4 variant implicated in hereditary hearing loss.

Munir Ahmad Bhinder, Haleema Sadia, Bisma Rauff

|Jul 11, 2023
Association of MSX1 Gene Variants with Nonsyndromic Cleft Lip and/or Palate in the Pakistani Population.

Anny Memon, Feriha Fatima Khidri, Yar Muhammad Waryah

|Feb 25, 2023
Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees.

Ali Raza Rao, Aamir Nazir, Samina Imtiaz

|Apr 23, 2022
Delineating the Molecular and Phenotypic Spectrum of the CNGA3-Related Cone Photoreceptor Disorder in Pakistani Families.

Sairah Yousaf, Nabeela Tariq, Zureesha Sajid

|Oct 13, 2021
Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract.

Priya Jarwar, Shakeel Ahmed Sheikh, Yar Muhammad Waryah

|Apr 03, 2021
Genetic Causes of Oculocutaneous Albinism in Pakistani Population.

Zureesha Sajid, Sairah Yousaf, Yar M Waryah

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Frequent Collaborators

4 joint publications

Zubair M Ahmed

2 joint publications

Zureesha Sajid

2 joint publications

Munir Ahmad Bhinder

1 joint publications

Ansar A Abbasi