Sher Alam Khan
6PUBLICATIONS
35CO-AUTHORS
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Publications (6)
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|May 27, 2023
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.Hamed Nawaz, Mujahid, Sher Alam Khan
|Feb 15, 2023
Biallelic mutations in FLG, TGM1, and STS genes segregated with different types of ichthyoses in eight families of Pakistani origin.Niamatullah Khan, Khadim Shah, Fozia Fozia
|Dec 23, 2022
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (ARMC3).Adil U Rehman, Malaika Hamid, Sher Alam Khan
|Jul 11, 2022
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function.Sheng-Jia Lin, Barbara Vona, Hillary M Porter
|Nov 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.Julia Doll, Barbara Vona, Linda Schnapp
|May 09, 2020
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family.Sher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad
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Frequent Collaborators
2 joint publications
Barbara Vona
2 joint publications
Saadullah Khan
2 joint publications
Naveed Wasif
2 joint publications
Franz Rüschendorf
1 joint publications
Sheng-Jia Lin
1 joint publications
Hillary M Porter
1 joint publications
Muhammad Umair
1 joint publications
Kevin Huang
1 joint publications
Yves Lacassie
1 joint publications
Jill A Rosenfeld
