Muhammad Jafar Hussain Hafiz

6PUBLICATIONS
20CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Genetic immunologyGene mappingDevelopmental genetics (incl. sex determination)
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Publications (6)

|Mar 04, 2026
Assessment of In-Frame Indel Variants in an Unsolved Cohort of Inherited Retinal Diseases Using Machine Learning.

David E Rauch, Meng Wang, Muhammad Jafar Hussain Hafiz

|Jul 31, 2025
Biallelic loss-of-function variants in C19orf44 lead to retinal degeneration.

Hafiz Muhammad Jafar Hussain, Wang Meng, Yumei Li

|Jan 08, 2025
Phenotypic and Genetic Heterogeneity of a Pakistani Cohort of 15 Consanguineous Families Segregating Variants in Leber Congenital Amaurosis-Associated Genes.

Zainab Akhtar, Sumaira Altaf, Yumei Li

|Feb 25, 2023
Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases.

Hafiz Muhammad Jafar Hussain, Meng Wang, Austin Huang

|Sep 29, 2020
Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family.

Muhammad Ismail Khan, Muhammad Latif, Maria Saif

|Aug 26, 2020
Whole-exome sequencing identifies a novel mutation in spermine synthase gene (SMS) associated with Snyder-Robinson Syndrome.

Talal J Qazi, Qiao Wu, Ailikemu Aierken

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Frequent Collaborators

4 joint publications

Rui Chen

3 joint publications

Meng Wang

2 joint publications

Sabika Firasat

1 joint publications

Talal J Qazi