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Muhammad Tariq

Observed names: M Tariq, M. Tariq, MUHAMMAD TARIQ, Muhammad Umer Tariq, Tariq Muhammad, Tariq, Muhammad
Observed institutions: Uppsala University, Quaid-i-Azam University, Cincinnati Children's Hospital Medical Center, National Institute for Biotechnology and Genetic Engineering, Pakistan Institute of Engineering and Applied Sciences, Pir Mehr Ali Shah Arid Agriculture University, Higher Education Commission, Indiana University Indianapolis, Indiana University School of Medicine, Pakistan Institute of Medical Sciences, Indiana University – Purdue University Indianapolis, University of Cincinnati, University of Tabuk
ORCID: 0000-0002-5334-403X
Observed ORCIDs: 0000-0002-5334-403X, 0000-0002-8430-7549
OpenAlex ID: A5100730883
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia
2016 · You Li, Hisato Yagi, et al. · PLoS Genetics · 141
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CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly
2013 · Muhammad S. Hussain, Shahid M. Baig, et al. · Human Molecular Genetics · 131
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations
2023 · Dongjing Liu, Dara Meyer, et al. · Nature Genetics · 82
Abolished InsP3R2 function inhibits sweat secretion in both humans and mice
2014 · Joakim Klar, Chihiro Hisatsune, et al. · Journal of Clinical Investigation · 77
The genetic architecture of pediatric cardiomyopathy
2022 · Stephanie M. Ware, Surbhi Bhatnagar, et al. · The American Journal of Human Genetics · 73
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Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study
2021 · Stephanie M. Ware, James D. Wilkinson, et al. · Journal of the American Heart Association · 73
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Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage
2017 · Joakim Klar, Jörg Piontek, et al. · PLoS Genetics · 70
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WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome
2009 · Sadia Nawaz, Joakim Klar, et al. · European Journal of Human Genetics · 69
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SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing
2011 · Muhammad Tariq, John W Belmont, et al. · Genome biology · 67
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Genetic and Functional Analyses ofZIC3Variants in Congenital Heart Disease
2013 · Jason Cowan, Muhammad Tariq, et al. · Human Mutation · 61
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Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC)
2008 · M Tariq, Z Azeem, et al. · Journal of Medical Genetics · 56
Importance of genetic evaluation and testing in pediatric cardiomyopathy
2014 · Muhammad Tariq, Stephanie M Ware · World Journal of Cardiology · 54
Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutation
2014 · Tahir Naeem Khan, Joakim Klar, et al. · European Journal of Human Genetics · 52
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Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)
2008 · Zahid Azeem, Musharraf Jelani, et al. · Human Genetics · 51
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A
2012 · Umm-e- Kalsoom, Eva Klopocki, et al. · Journal of Medical Genetics · 47
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Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects
2016 · Jason R. Cowan, Muhammad Tariq, et al. · Philosophical Transactions of the Royal Society B Biological Sciences · 43
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan
2020 · Sajida Rasool, Jamshaid Mahmood Baig, et al. · Molecular Genetics & Genomic Medicine · 39
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A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss
2021 · Farid Ullah, Waqar Rauf, et al. · Human Genetics · 35
A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia
2008 · Mahmood Rasool, Jens Schuster, et al. · Journal of Human Genetics · 35
A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency
2014 · Muhammad Jameel, Joakim Klar, et al. · BMC Medical Genetics · 31
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CRISPR/Cas9: targeted genome editing for the treatment of hereditary hearing loss
2020 · Rimsha Farooq, Khadim Hussain, et al. · Journal of Applied Genetics · 30
Novel Protein-truncating Mutations in Theaspmgene in Families With Autosomal Recessive Primary Microcephaly
2007 · Asma Gul, Muhammad Tariq, et al. · Journal of Neurogenetics · 30
Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy
2018 · Jeffrey Schubert, Muhammad Tariq, et al. · Human Mutation · 29
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A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22–q11.2
2007 · Muhammad Jawad Hassan, Muhammad Salman Chishti, et al. · Human Genetics · 27
CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly
2016 · Salil K. Sukumaran, Maria Stumpf, et al. · Molecular Genetics and Genomics · 26
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Works count: 104
Citation count: 1,894
H-index: 25
I10-index: 45
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