Syed Kamran Ul Hassan Naqvi
Syed Kamran Ul Hassan Naqvi
COMSATS University Islamabad, Pakistan
Verified email at
Cited by
Cited by
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)
Z Azeem, M Jelani, G Naz, M Tariq, N Wasif, S Kamran-ul-Hassan Naqvi, ...
Human genetics 123 (5), 515-519, 2008
MiR-421, miR-155 and miR-650: emerging trends of regulation of cancer and apoptosis
AA Farooqi, MZ Qureshi, E Coskunpinar, SKH Naqvi, I Yaylim, M Ismail
Asian Pacific Journal of Cancer Prevention 15 (5), 1909-1912, 2014
A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family
S Basit, SKH Naqvi, N Wasif, G Ali, M Ansar, W Ahmad
BMC medical genetics 9 (1), 1-6, 2008
Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
N Wasif, S Basit, N Ali, M Ansar, W Ahmad
Human genetics 129 (4), 419-424, 2011
Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13. 3–q21. 2 and screening of the candidate genes
S Basit, S Kamran-ul-Hassan Naqvi, M Ansar, W Ahmad
Human genetics 131 (3), 415-422, 2012
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan
S Khan, R Habib, H Mir, G Naz, M Ayub, S Shafique, T Yamin, N Ali, ...
Clinical and Experimental Dermatology: Experimental dermatology 36 (6), 652-654, 2011
A novel splice-acceptor site mutation in CDH3 gene in a consanguineous family exhibiting hypotrichosis with juvenile macular dystrophy
S Kamran-ul-Hassan Naqvi, Z Azeem, G Ali, W Ahmad
Archives of dermatological research 302 (9), 701-703, 2010
A novel deletion mutation in proteoglycan-4 underlies camptodactyly-arthropathy-coxa-vara-pericarditis syndrome in a consanguineous pakistani family
S Basit, Z Iqbal, M Umicevic-Mirkov, SKUH Naqvi, M Coenen, M Ansar, ...
Archives of medical research 42 (2), 110-114, 2011
Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia
Z Azeem, SKUH Naqvi, M Ansar, A Wali, AK Naveed, G Ali, MJ Hassan, ...
Archives of dermatological research 301 (8), 625-629, 2009
Anticancer activity of essential oils: targeting of protein networks in cancer cells
A Aras, MJ Iqbal, SKH Naqvi, YC Gercek, K Boztas, ML Gasparri, ...
Asian Pacific Journal of Cancer Prevention 15 (19), 8047-8050, 2014
Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11. 23–22.3
G Naz, G Ali, S Kamran-ul-Hassan Naqvi, Z Azeem, W Ahmad
Human genetics 127 (4), 395-401, 2010
Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
Z Azeem, N Wasif, S Basit, S Razak, RA Waheed, A Islam, M Ayub, ...
The Journal of dermatology 38 (8), 755-760, 2011
A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2)
S Kamran‐ul‐Hassan Naqvi, SI Raza, AK Naveed, P John, W Ahmad
British Journal of Dermatology 160 (1), 194-196, 2009
Two novel mutations in the gene EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia
SK Naqvi, N Wasif, H Javaid, W Ahmad
Orthodontics & craniofacial research 14 (3), 156-159, 2011
TRAIL mediated signaling in pancreatic cancer
DR Nogueira, I Yaylim, Q Aamir, OT Kahraman, S Fayyaz, SKH Naqvi, ...
Asian Pacific Journal of Cancer Prevention 15 (15), 5977-5982, 2014
A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36. 31–p36. 13
M Ansar, K Lee, SKH Naqvi, PB Andrade, S Basit, RLP Santos-Cortez, ...
Journal of human genetics 56 (12), 866-868, 2011
Natural agents-mediated targeting of histone deacetylases
AA Farooqi, SKH Naqvi, AA Perk, O Yanar, S Tabassum, MS Ahmad, ...
Archivum Immunologiae et Therapiae Experimentalis 66 (1), 31-44, 2018
Tudor tells about new twists in the story tale of SMURFs
MZ Qureshi, S Jabeen, G Butt, A Aslam, SK Naqvi, R Attar, S Tabassum, ...
Cellular and Molecular Biology 62 (5), 38-43, 2016
Genetic analysis of Xp22. 3 micro-deletions in seventeen families segregating isolated form of X-linked ichthyosis
RH Ali, S Mahmood, SI Raza, A Aziz, SKH Naqvi, N Wasif, M Ansar, ...
Journal of Dermatological Science 80 (3), 214-217, 2015
Journal of Rashid Latif Medical College
SKUH Naqvi
Journal of Rashid Latif Medical College 1, 12-14, 2012
The system can't perform the operation now. Try again later.
Articles 1–20