| A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type M Naeem, M Wajid, K Lee, SM Leal, W Ahmad Journal of medical genetics 43 (3), 274-279, 2006 | 66 | 2006 |
| Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia M Naeem, D Muhammad, W Ahmad British Journal of Dermatology 153 (1), 46-50, 2005 | 42 | 2005 |
| Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease M Naeem, S Hussain, N Akhtar American journal of nephrology 34 (3), 241-248, 2011 | 36 | 2011 |
| Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12–q21. 2 M Naeem, M Jelani, K Lee, G Ali, MS Chishti, A Wali, A Gul, P John, ... British Journal of Dermatology 155 (6), 1184-1190, 2006 | 33 | 2006 |
| Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family OU Rahman, N Khawar, MA Khan, J Ahmed, K Khattak, JY Al-Aama, ... Diagnostic Pathology 8, 1-7, 2013 | 28 | 2013 |
| A novel missense mutation in the CLPP gene causing Perrault syndrome type 3 in a Turkish family F Dursun, HSA Mohamoud, N Karim, M Naeem, M Jelani, ... Journal of clinical research in pediatric endocrinology 8 (4), 472, 2016 | 27 | 2016 |
| Molecular analysis of lipoid proteinosis: identification of a novel nonsense mutation in the ECM1 gene in a Pakistani family M Nasir, A Latif, M Ajmal, R Qamar, M Naeem, A Hameed Diagnostic Pathology 6, 1-6, 2011 | 25 | 2011 |
| A mutation in CTSK gene in an autosomal recessive pycnodysostosis family of Pakistani origin M Naeem, S Sheikh, W Ahmad BMC medical genetics 10, 1-5, 2009 | 25 | 2009 |
| Human parechovirus genotypes-10,-13 and-15 in Pakistani children with acute dehydrating gastroenteritis MM Alam, A Khurshid, S Shaukat, MS Rana, S Sharif, M Angez, N Nisar, ... PLoS One 8 (11), e78377, 2013 | 24 | 2013 |
| Identification of human parechovirus genotype, HPeV-12, in a paralytic child with diarrhea MM Alam, A Khurshid, S Shaukat, S Sharif, MS Rana, M Angez, M Naeem, ... Journal of clinical virology 55 (4), 339-342, 2012 | 22 | 2012 |
| A novel CHSY1 gene mutation underlies Temtamy preaxial brachydactyly syndrome in a Pakistani family G Sher, M Naeem European Journal of Medical Genetics 57 (1), 21-24, 2014 | 19 | 2014 |
| Whole‐exome sequencing identified a novel frameshift mutation in SDR9C7 underlying autosomal recessive congenital ichthyosis in a Pakistani family N Karim, G Murtaza, M Naeem British Journal of Dermatology 177 (5), e191-e192, 2017 | 16 | 2017 |
| Genome-wide association mapping for high temperature tolerance in wheat through 90k SNP array using physiological and yield traits HGMD Ahmed, M Naeem, Y Zeng, MAR Rashid, A Ullah, A Saeed, ... Plos one 17 (1), e0262569, 2022 | 15 | 2022 |
| Study of the effect of antiviral therapy on homocysteinemia in hepatitis C virus-infected patients M Mustafa, S Hussain, S Qureshi, SA Malik, AR Kazmi, M Naeem BMC gastroenterology 12, 1-8, 2012 | 15 | 2012 |
| Molecular genetic analysis of consanguineous Pakistani families with autosomal recessive hypohidrotic ectodermal dysplasia N Bibi, S Ahmad, W Ahmad, M Naeem Australasian journal of dermatology 52 (1), 37-42, 2011 | 13 | 2011 |
| INDUCING EFFECT OF CHITOSAN ON THE PHYSIOLOGICAL AND BIOCHEMICAL INDICES OF EGGPLANT (SOLANUM MELONGENA L.) GENOTYPES UNDER HEAT AND HIGH IRRADIANCE. A Liaqat, MZ Ihsan, MS Rizwan, A Mehmood, M Ijaz, M Alam, M Abdullah, ... Applied Ecology & Environmental Research 17 (5), 2019 | 9 | 2019 |
| Novel TGM1 mutation in a Pakistani family affected with severe lamellar ichthyosis M Rasheed, N Karim, FA Shah, M Naeem Pediatrics & Neonatology 59 (6), 628-629, 2018 | 8 | 2018 |
| Autosomal recessive isolated familial acanthosis nigricans in a Pakistani family due to a homozygous mutation in the insulin receptor gene S Ahmad, H Mahmoudi, M Naeem, RC Betz British Journal of Dermatology 169 (2), 476-478, 2013 | 8 | 2013 |
| Pure hair–nail ectodermal dysplasia maps to chromosome 12p11. 1–q21. 1 in a consanguineous Pakistani family M Naeem, P John, G Ali, W Ahmad Clinical and experimental dermatology 32 (5), 502-505, 2007 | 8 | 2007 |
| Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani family T Khan, M Khan, A Yousaf, S Khan, M Naeem, A Shah, G Murtaza, A Ali, ... Journal of Human Genetics 63 (10), 1071-1076, 2018 | 7 | 2018 |
Ali GhazanfarUniversity of Azad Jammu and Kashmir, Quaid-i-Azam University, King Saud University Saudi ArabiaVerified email at ajku.edu.pk
