Muhammad Tariq
Muhammad Tariq
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DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia
Y Li, H Yagi, EO Onuoha, RR Damerla, R Francis, Y Furutani, M Tariq, ...
PLoS genetics 12 (2), e1005821, 2016
SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing
M Tariq, JW Belmont, S Lalani, T Smolarek, SM Ware
Genome biology 12 (9), 1-13, 2011
Genetic and Functional Analyses of ZIC3 Variants in Congenital Heart Disease
J Cowan, M Tariq, SM Ware
Human mutation 35 (1), 66-75, 2014
Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC)
M Tariq, Z Azeem, G Ali, MS Chishti, W Ahmad
Journal of Medical Genetics 46 (1), 14-20, 2009
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
Importance of genetic evaluation and testing in pediatric cardiomyopathy
M Tariq, SM Ware
World journal of cardiology 6 (11), 1156, 2014
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A
E Klopocki, N Wasif, M Tariq, S Khan, J Hecht, P Krawitz, S Mundlos, ...
Journal of medical genetics 50 (1), 47-53, 2013
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
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
Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects
JR Cowan, M Tariq, C Shaw, M Rao, JW Belmont, SR Lalani, ...
Philosophical Transactions of the Royal Society B: Biological Sciences 371 …, 2016
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families
M Tariq, M Ayub, M Jelani, S Basit, G Naz, N Wasif, SI Raza, AK Naveed, ...
British Journal of Dermatology 160 (5), 1006-1010, 2009
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins
P John, M Tariq, M Arshad Rafiq, M Amin-Ud-Din, D Muhammad, ...
Archives of dermatological research 298 (3), 135-137, 2006
Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy
J Schubert, M Tariq, G Geddes, S Kindel, EM Miller, SM Ware
Human Mutation 39 (12), 2083-2096, 2018
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
A novel 4-bp insertion mutation in EDA1 gene in a Pakistani family with X-linked hypohidrotic ectodermal dysplasia
M Tariq, N Wasif, M Ayub, W Ahmad
European Journal of Dermatology 17 (3), 209-212, 2007
A novel missense mutation in the TRPS1 gene underlies trichorhinophalangeal syndrome type III
M Tariq, S Ahmad, W Ahmad
British Journal of Dermatology 159 (2), 476-478, 2008
A novel deletion mutation in the EDAR gene in a Pakistani family with autosomal recessive hypohidrotic ectodermal dysplasia
M Tariq, N Wasif, W Ahmad
British Journal of Dermatology 157 (1), 207-209, 2007
Genetic causes of cardiomyopathy in children: first results from the pediatric cardiomyopathy genes study
SM Ware, JD Wilkinson, M Tariq, JA Schubert, A Sridhar, SD Colan, L Shi, ...
Journal of the American Heart Association 10 (9), e017731, 2021
A Novel Locus for Ectodermal Dysplasia of Hairs, Nails and Teeth Type Maps to Chromosome 18q22. 1–22.3
M Tariq, MS Chishti, G Ali, W Ahmad
Annals of human genetics 72 (1), 19-25, 2008
A novel missense mutation in the EVC gene underlies Ellis‐van Creveld syndrome in a Pakistani family
N Wasif, M Tariq, W Ahmad
Pediatrics International 52 (2), 240-246, 2010
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