Author

Zainab Akhtar

Institutions: Quaid-i-Azam University, Fondation Asile des Aveugles, University of Lausanne

Observed institutions: Quaid-i-Azam University, Fondation Asile des Aveugles, University of Lausanne

OpenAlex ID: A5115621036

Phenotypic and Genetic Heterogeneity of a Pakistani Cohort of 15 Consanguineous Families Segregating Variants in Leber Congenital Amaurosis-Associated Genes

2024 · Zainab Akhtar, Sumaira Altaf, et al. · Genes · 2

Mutations in retinal cyclic nucleotide-gated channels identified in familial cases of inherited retinal dystrophies from Pakistan

2025 · Zainab Akhtar, Kiran Afshan, et al. · Molecular vision · 1

Haploinsufficiency, de novo and biallelic missense variants in CSMD2 are associated with neurodevelopmental disorders

2026 · Clara Pailler-Pradeau, Marianne Victoria Lemée, et al. · medRxiv

Molecular epidemiology of ABCA4 -related retinopathies in Pakistan: report of disease-causing variants in 10 families and review of the literature

2025 · Zainab Akhtar, Sumaira Altaf, et al. · Molecular vision

Works count: 4

Citation count: 3

H-index: 1

I10-index: