|Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum|
S Mahmood, W Ahmad, MJ Hassan
Orphanet journal of rare diseases 6 (1), 1-15, 2011
|CtIP Mutations Cause Seckel and Jawad Syndromes|
P Qvist, P Huertas, S Jimeno, M Nyegaard, MJ Hassan, SP Jackson, ...
PLoS genetics 7 (10), e1002310, 2011
|Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39|
JM Schultz, SN Khan, ZM Ahmed, S Riazuddin, AM Waryah, D Chhatre, ...
The American Journal of Human Genetics 85 (1), 25-39, 2009
|Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene|
A Gul, MJ Hassan, S Mahmood, W Chen, S Rahmani, MI Naseer, ...
Neurogenetics 7 (2), 105-110, 2006
|A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly|
A Gul, MJ Hassan, S Hussain, SI Raza, MS Chishti, W Ahmad
Journal of human genetics 51 (9), 760-764, 2006
|Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly|
R Kousar, MJ Hassan, B Khan, S Basit, S Mahmood, A Mir, W Ahmad, ...
BMC neurology 11 (1), 1-6, 2011
|Previously described sequence variant in CDK5RAP2gene in a Pakistani family with autosomal recessive primary microcephaly|
MJ Hassan, M Khurshid, Z Azeem, P John, G Ali, MS Chishti, W Ahmad
BMC medical genetics 8 (1), 1-7, 2007
|Autosomal-recessive hearing impairment due to rare missense variants within S1PR2|
RLP Santos-Cortez, R Faridi, AU Rehman, K Lee, M Ansar, X Wang, ...
The American Journal of Human Genetics 98 (2), 331-338, 2016
|Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability|
RLP Santos-Cortez, V Khan, FS Khan, ZN Mughal, I Chakchouk, K Lee, ...
Human genetics 137 (9), 735-752, 2018
|In silico analysis of SIGMAR1 variant (rs4879809) segregating in a consanguineous Pakistani family showing amyotrophic lateral sclerosis without frontotemporal lobar dementia|
MI Ullah, A Ahmad, SI Raza, A Amar, A Ali, A Bhatti, P John, A Mohyuddin, ...
Neurogenetics 16 (4), 299-306, 2015
|Novel protein-truncating mutations in the ASPM gene in families with autosomal recessive primary microcephaly|
A Gul, M Tariq, MN Khan, MJ Hassan, G Ali, W Ahmad
Journal of neurogenetics 21 (3), 153-163, 2007
|Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients|
MJ Hassan, S Mahmood, G Ali, N Bibi, I Waheed, MA Rafiq, M Ansar, ...
Pediatrics International 50 (2), 162-166, 2008
|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 syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11. 22–q11. 2|
MJ Hassan, MS Chishti, SM Jamal, M Tariq, W Ahmad
Human genetics 123 (1), 77-82, 2008
|DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13. 2|
RLP Santos, MJ Hassan, S Sikandar, K Lee, G Ali, PE Martin, ...
Human genetics 120 (1), 85-92, 2006
|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
|What drives interest rate spreads of commercial banks in Pakistan? Empirical evidence based on panel data|
M Hassan, B Khan
SBP Research Bulletin 6 (2), 16-32, 2010
|A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26. 2‐q26. 31|
A Wali, P John, A Gul, K Lee, MS Chishti, G Ali, MJ Hassan, SM Leal, ...
Clinical genetics 70 (3), 233-239, 2006
|A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25. 1-p24. 3|
MJ Hassan, RLP Santos, MA Rafiq, MH Chahrour, TL Pham, M Wajid, ...
Human genetics 118 (5), 605-610, 2006
|Association between tumour necrosis‐α gene polymorphisms and acne vulgaris in a P akistani population|
NM Aisha, J Haroon, S Hussain, CM Tahir, M Ikramullah, H Rahim, ...
Clinical and Experimental Dermatology 41 (3), 297-301, 2016