A homozygous nonsense variant in DYM underlies Dyggve–Melchior–Clausen syndrome associated with ectodermal features - Abdullah; Pashmina Wiqar Shah; Shoaib Nawaz; Shabir Hussain; Asmat Ullah; Sulman Basit; Wasim Ahmad (Molecular Biology Reports, 2020)

CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly - Sulman Basit; Khalid M. Al-Harbi; Sabri A. M. Alhijji; Alia M. Albalawi; Essa Alharby; Amr Eldardear; Mohammed I. Samman (Human Genetics, 2016)

A novel WDR62 mutation causes primary microcephaly in a Pakistani family - Mazhar Mustafa Memon; Syed Irfan Raza; Sulman Basit; Rizwana Kousar; Wasim Ahmad; Muhammad Ansar (Molecular Biology Reports, 2013)

Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3–q21.2 and screening of the candidate genes - Umm-e-Kalsoom; Sulman Basit; Syed Kamran-ul-Hassan Naqvi; Muhammad Ansar; Wasim Ahmad (Human Genetics, 2012)

Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families - Naveed Wasif; Syed Kamran ul-Hassan Naqvi; Sulman Basit; Nadir Ali; Muhammad Ansar; Wasim Ahmad (Human Genetics, 2011)

DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2 - Sulman Basit; Kwanghyuk Lee; Rabia Habib; Leon Chen; Umm-e-Kalsoom; Regie Lyn P. Santos-Cortez; Zahid Azeem; Paula Andrade; Muhammad Ansar; Wasim Ahmad; Suzanne M. Leal (Human Genetics, 2011)

Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes - Sulman Basit; Ghazanfar Ali; Naveed Wasif; Muhammad Ansar; Wasim Ahmad (Human Genetics, 2010)