Naveed Wasif
10PUBLICATIONS
33CO-AUTHORS
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Publications (10)
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|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 06, 2025
A Novel Biallelic Variant in IHH Causing Acrocapitofemoral Dysplasia in a Pakistani Family.Tayyaba Saeed, Nousheen Bibi, Ashfaq Ahmad
|Sep 18, 2023
Molecular insight into CREBBP and TANGO2 variants causing intellectual disability.Syeda Iqra Hussain, Nazif Muhammad, Niamatullah Khan
|May 23, 2023
A novel frameshift variant in UBA2 causing split-hand/foot malformations in a Pakistani family.Asia Parveen, Muhammad Tariq, Sher Alam Khan
|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
|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
Sulman Basit
2 joint publications
Asia Parveen
2 joint publications
Muhammad Usman Mirza
2 joint publications
Saadullah Khan
2 joint publications
Sher Alam Khan
1 joint publications
Michiel Vanmeert
1 joint publications
Matheus Froeyen
1 joint publications
Wasim Ahmed
1 joint publications
Hyung-Goo Kim
1 joint publications
Syed Shoaib Ahmed
