Afif Ben-Mahmoud
5PUBLICATIONS
61CO-AUTHORS
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Publications (5)
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|May 16, 2025
Recurrent and Novel Pathogenic Variants in Genes Involved with Hearing Loss in the Pakistani Population.Madiha Shadab, Afif Ben-Mahmoud, Luis Nicolás Martínez Völter
|Apr 16, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.Eric N Anderson, Stephan Drukewitz, Sukhleen Kour
|Apr 14, 2025
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3).Seda Susgun, Afif Ben-Mahmoud, Franz Rüschendorf
|Mar 27, 2024
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades.Madiha Shadab, Ansar Ahmed Abbasi, Ahsan Ejaz
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Frequent Collaborators
5 joint publications
Hyung-Goo Kim
3 joint publications
Vijay Gupta
2 joint publications
Madiha Shadab
2 joint publications
Ansar Ahmed Abbasi
2 joint publications
Ahsan Ejaz
2 joint publications
Barbara Vona
1 joint publications
Seda Susgun
1 joint publications
Franz Rüschendorf
1 joint publications
Bonsu Ku
1 joint publications
Syeda Iqra Hussain
