Author

Madiha Shadab

Observed names: M. D. Shadab, Shadab, Madiha

Institution: Mirpur University of Science and Technology

Observed institutions: UCL Queen Square Institute of Neurology, University College London, Sri Siddhartha Medical College, Mirpur University of Science and Technology

ORCID: 0009-0009-6043-6811

Observed ORCID: 0009-0009-6043-6811

OpenAlex ID: A5074290306

Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades

2024 · Madiha Shadab, Ansar Ahmed Abbasi, et al. · Journal of Cellular and Molecular Medicine · 9

Factors Influencing Delayed Presentation of Congenitally Hearing Impaired Children in Rural India

2011 · Geetha Chary, M. K. Manjunath, et al. · Indian Journal of Otolaryngology and Head & Neck Surgery · 5

Recurrent and Novel Pathogenic Variants in Genes Involved with Hearing Loss in the Pakistani Population

2025 · Madiha Shadab, Afif Ben-Mahmoud, et al. · Molecular Diagnosis & Therapy · 2

Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics

2026 · Asuman Koparir, Paulina Bahena Carbajal, et al. · Molecular Medicine · 1

Expanding the mutational spectrum of congenital microcephaly in Pakistani families

2026 · Sundas Farooq, Maria Asif, et al. · Frontiers in Genetics · 1

Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics

2026 · Koparir, Asuman, Carbajal, Paulina Bahena, et al. · Figshare

Additional file 1 of Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics

2026 · Koparir, Asuman, Carbajal, Paulina Bahena, et al. · Figshare

Works count: 7

Citation count: 18

H-index: 2

I10-index: