Muhammad Tariq - Concepedia

Author

Muhammad Tariq

Also Known As

M Tariq, M. TARIQ, M. Tariq, MUHAMMAD TARIQ, Mehreen Tariq, Muhammad Ali Tariq, Muhammad Haseeb Ali Tariq, Muhammad Tariq, Muhammad Wasim Tariq, Tariq Muhammad

107

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Quaid-i-Azam University Cincinnati Children's Hospital Medical Center Indiana University School of Medicine University of Tabuk Indiana University – Purdue University Indianapolis

About

Muhammad Tariq is an author at Quaid-i-Azam University specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	488
2	Biology	2	2	41
3	Cell Biology	2	2	161
4	Health Sciences	1	1	12
5	Genetic Medicine	1	1	54

Muhammad Tariq

Publications

818

Citations

H-Index

Page 1

	Year	Citations
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia You Li, Hisato Yagi, Ezenwa Obi Onuoha, PLoS Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsLeft-right Patterning	2016	135
SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing Muhammad Tariq, John W. Belmont, Seema R. Lalani, Genome biology	2011	65
Mutation in the <i>HPGD</i> gene encoding NAD<sup>+</sup> dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC) Muhammad Tariq, Zahid Azeem, Ghazanfar Ali, Journal of Medical Genetics	2008	57
Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study Stephanie M. Ware, James D. Wilkinson, Muhammad Tariq, Journal of the American Heart Association	2021	56
The genetic architecture of pediatric cardiomyopathy Stephanie M. Ware, Surbhi Bhatnagar, Phillip J. Dexheimer, The American Journal of Human Genetics CardiomyopathyHeart FailureGeneticsPediatric CardiomyopathyCongenital Heart Defect	2022	56
Genetic and Functional Analyses of<i>ZIC3</i>Variants in Congenital Heart Disease Jason Cowan, Muhammad Tariq, Stephanie M. Ware Human Mutation Genetic TestingDevelopmental BiologyAnalyzed Polyalanine ExpansionsCerebellum 3Genetic Disorder	2013	54
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3) Zahid Azeem, Musharraf Jelani, Gul Naz, Human Genetics Signal TransductionG Protein-coupled ReceptorGenetic DisorderGeneticsInherited Metabolic Disease	2008	49
Whole exome sequencing identified a novel zinc-finger gene <i>ZNF141</i> associated with autosomal recessive postaxial polydactyly type A Umme Kalsoom, Eva Klopocki, Naveed Wasif, Journal of Medical Genetics	2012	47
Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects Jason Cowan, Muhammad Tariq, Chad A. Shaw, Philosophical Transactions of the Royal Society B Biological Sciences Cnv AnalysisHigh Cnv YieldDevelopmental BiologyGenetic DisorderGenetics	2016	44
NOVEL PROTEIN-TRUNCATING MUTATIONS IN THE<i>ASPM</i>GENE IN FAMILIES WITH AUTOSOMAL RECESSIVE PRIMARY MICROCEPHALY Asma Gul, Muhammad Tariq, Muhammad Nasim Khan, Journal of Neurogenetics Neurodevelopmental DisordersPrimary MicrocephalyAspm GeneDevelopmental BiologyMendelian Disorder	2007	30

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