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Molecular Biology Reports|July 27, 2014
Development of ARMS-PCR assay for genotyping of Pro12Ala SNP of PPARG gene: a cost effective way for case-control studies of type 2 diabetes in developing countriesMehboob Islam, Fazli Rabbi Awan, Shahid Mahmood Baig
JPMA. the Journal of the Pakistan Medical Association|April 1, 2015
Serum adiponectin levels in diabetes, obesity and gender in Punjabi subjects from Faisalabad, PakistanSyeda Sadia Najam, Fazli Rabbi Awan, Shahid Mahmood Baig
Pakistan Journal of Medical Sciences|September 16, 2024
A novel mutation in SETX and ATM causes ataxia in consanguineous Pakistani familiesRabia Akram, Shahid Mahmood Baig, Haseeb Anwar, et al.
Journal of Diabetes and Metabolic Disorders|May 14, 2015
A case control association study of COMT gene polymorphism (I/D) with type 2 diabetes and its related factors in Pakistani Punjabi populationMaryam Zain, Fazli Rabbi Awan, Sidra Amir, et al.
European Journal of Dermatology : EJD|April 26, 2012
A novel mutation in lysophosphatidic acid receptor 6 gene in autosomal recessive hypotrichosis and evidence for a founder effectAysha Azhar, Muhammad Tariq, Shahid Mahmood Baig, et al.
Molecular Vision|April 3, 2010
A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani familyIram Anjum, Hans Eiberg, Shahid Mahmood Baig, et al.
Scientific Reports|October 16, 2012
A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hairMuhammad Tariq, Aysha Azhar, Shahid Mahmood Baig, et al.
Pakistan Journal of Medical Sciences|January 17, 2022
Whole exome sequencing identifies a novel mutation in ASPM and ultra-rare mutation in CDK5RAP2 causing Primary microcephaly in consanguineous Pakistani familiesEhtisham Ul Haq Makhdoom, Haseeb Anwar, Shahid Mahmood Baig, et al.
Biomed Research International|March 14, 2022
Identification of Pathogenic Mutations in Primary Microcephaly- (MCPH-) Related Three Genes CENPJ, CASK, and MCPH1 in Consanguineous Pakistani FamiliesNiaz Muhammad Khan, Muhammad Shareef Masoud, Shahid Mahmood Baig, et al.
BMC Medical Genetics|July 20, 2020
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani familiesYingjie Zhou, Muhammad Tariq, Sijie He, et al.
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