| 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 | 108 | 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, 1-13, 2011 | 81 | 2011 |
| Importance of genetic evaluation and testing in pediatric cardiomyopathy M Tariq, SM Ware World journal of cardiology 6 (11), 1156, 2014 | 61 | 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 | 60 | 2009 |
| Genetic and Functional Analyses of ZIC3 Variants in Congenital Heart Disease J Cowan, M Tariq, SM Ware Human mutation 35 (1), 66-75, 2014 | 59 | 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 | 54 | 2013 |
| 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, 515-519, 2008 | 52 | 2008 |
| 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 | 38 | 2021 |
| 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 | 38 | 2007 |
| 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 | 31 | 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 | 30 | 2009 |
| The genetic architecture of pediatric cardiomyopathy SM Ware, S Bhatnagar, PJ Dexheimer, JD Wilkinson, A Sridhar, X Fan, ... The American Journal of Human Genetics 109 (2), 282-298, 2022 | 29 | 2022 |
| 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, 77-82, 2008 | 27 | 2008 |
| 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 | 25 | 2018 |
| 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, 135-137, 2006 | 25 | 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, 625-629, 2009 | 20 | 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 | 20 | 2007 |
| 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 | 15 | 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 | 13 | 2008 |
| 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 | 11 | 2008 |
