Publications by authors named "Nazif Muhammad"

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The Genetic Basis of Neurological Disorders: Missense and Nonsense Variants in Three Pakistani Families With Syndromic Intellectual Disability.
Kenza Javed, Nazif Muhammad, Syeda Iqra Hussain, Fozia Fozia, Muhammad Irfan Ullah, Muhammad Daud Khan, Noor Muhammad

Ann Hum Genet· December 2025

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Truncated Variants in FAM20A and WDR72 Genes Underlie Autosomal Recessive Amelogenesis Imperfecta in Four Pakistani Families.
Sadaqat Ullah, Sher Alam Khan, Samin Jan, Salah Ud Din, Nazif Muhammad, Muhammad Tariq, Noor Muhammad

Biochem Genet· March 2025

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Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families.
Syeda Iqra Hussain, Nazif Muhammad, Shahbaz Ali Shah, Adil U Rehman, Sher Alam Khan, Yar Muhammad Khan, Noor Muhammad

BMC Med Genomics· July 2024

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Molecular insight into CREBBP and TANGO2 variants causing intellectual disability.
Syeda Iqra Hussain, Nazif Muhammad, Niamatullah Khan, Mobeen Khan, Fardous Fardous, Muhammad Yasin, Noor Muhammad

J Gene Med· January 2024

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Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability.
Syeda Iqra Hussain, Nazif Muhammad, Salah Ud Din Shah, Fardous Fardous, Sher Alam Khan, Noor Muhammad, Muhammad Usman Mirza

BMC Neurol· October 2023

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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, Sher A Khan, Nazif Muhammad, Noor Muhammad

Int J Dermatol· May 2023

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Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.
Hamed Nawaz, Mujahid, Sher Alam Khan, Farhana Bibi, Ahmed Waqas, Nazif Muhammad, Noor Muhammad, Muhammad Umair

Genes (Basel)· May 2023

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Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms.
Nazif Muhammad, Syeda Iqra Hussain, Zia Ur Rehman, Sher Alam Khan, Samin Jan, Muhammad Muzammal, Muhammad Usman Mirza, Noor Muhammad

Front Neurol· May 2023

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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, Mahmoud Izadi, Kevin Huang, Nazif Muhammad, Noor Muhammad

Hum Mutat· October 2022

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Glycine Improved Cryopreserved Spermatozoa Quality in Achai Bull.
Muhammad Sohail Nazif, Zia Ur Rehman, Humayun Khan, Farhan Anwar Khan, Tarique Hussain, Safdar Muhammad

Biomed Res Int· August 2022

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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, Hina Bashir, Niamat Khan, Noor Muhammad

BMC Med Genet· May 2020

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Association of sequence variants in frizzled-6 with autosomal recessive nail dysplasia (NDNC-10) in Pashtun families.
Saadullah Khan, Anwar Kamal Khan, Malaika Hamid, Muhammad Nazif, Muhammad Abbas, Noor Muhammad

J Pak Med Assoc· January 2020

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