Muhammad Naeem
Muhammad Naeem
Tenured Professor, Biotechnology Deptt, Quaid-i-Azam University
Verified email at - Homepage
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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
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
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
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
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
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), 1-7, 2013
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
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), 1-6, 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), 1-5, 2009
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
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
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), 1-8, 2012
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
The British journal of dermatology 177 (5), e191-e192, 2017
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
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
Serotype diversity of astroviruses in Rawalpindi, Pakistan during 2009–2010
MM Alam, A Khurshid, MS Rana, S Shaukat, S Sharif, M Angez, M Naeem, ...
Plos one 8 (4), e61667, 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: Continuing professional development …, 2007
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
UGT1A1 Gene Mutations in Pakistani Children Suffering from Inherited Nonhemolytic Unconjugated Hyperbilirubinemias
S Khan, M Irfan, G Sher, B Zubaida, MA Alvi, M Yasinzai, M Naeem
Annals of Human Genetics 77 (6), 482-487, 2013
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
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