Irfanullah, Zeb A, Shinwari N, Shah K, Gilani SZT, Khan S, Lee KW, Raza SI, Hussain S, Liaqat K, Ahmad W. Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type Maroteaux. Int J Biochem Cell Biol. 2018 Sep;102:76-86. doi: 10.1016/j.biocel.2018.07.004. Epub 2018 Jul 18. PMID: 30016695.

ufail Akbar Mughal, Muhammad Asim, Syed Haseeb ul Hassan Gillani, Nimra Obaid Chughtai, Syeda Afifa Batool, Amir Hussain, Kulsoom Shujaat, Syed Zohaib Tayyab Gilani; A Novel Missense Variant in the CHST3 Underlies Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations. Mol Syndromol 2024; https://doi.org/10.1159/000538039

2. Characterization of STKLD1 Gene Underlying Inherited Pre-axial Polydactyly Type- I (PPD-1) in Consanguineous Families of Azad Kashmir

3. Genetic Characterization of Polydactyly in Consanguineous Families of Azad Jammu and Kashmir

4.Molecular and in silicoanalysis of Albinism in consanguineous families of Bagh Azad Kashmir

2.National conference on ISESCO Women in Science: Contribution of Pakistani Women in Scientificand Social Development

3.Seminar on Role of Biotechnology in Health Sciences and Agriculture

4. Seminar on Freelancing and Entrepreneurship: Introduction in Academia

5. Seminar on "The Skill and Scholarship Hunt: Thriving in the modern era"

6. Seminar on "Recent advancements in diagnosis and treatment of Cancer"