Muzammil Ahmad Khan

9PUBLICATIONS
17CO-AUTHORS
Medical infection agents (incl. prions)Gene mappingSport and exercise psychologyDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)
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Publications (9)

|Sep 04, 2026
Potentially Deleterious Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in the Human MCPH1 Gene: Systematic In Silico Predictions and Implications for Structure and Function.

|Feb 13, 2026
A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.

Sana Fatima, Dong Sun, Jianguo Han

|Apr 28, 2023
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly.

Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal

|Jul 30, 2022
The molecular genetics of human appendicular skeleton.

Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal

|Apr 23, 2022
In Silico Analysis of the L-2-Hydroxyglutarate Dehydrogenase Gene Mutations and Their Biological Impact on Disease Etiology.

Muhammad Muzammal, Alessandro Di Cerbo, Eman M Almusalami

|Apr 23, 2022
In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in Human SLITRK1 Gene.

Muhammad Zeeshan Ali, Arshad Farid, Safeer Ahmad

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Frequent Collaborators

2 joint publications

Arshad Farid

2 joint publications

Mohammed Al Mohaini

2 joint publications

Maitham A Al Hawaj

2 joint publications

Yousef N Alhashem