Muhammad Tariq - Genetic Mutations

Author Information

Muhammad Tariq is affiliated with the Human Molecular Genetics Laboratory at the National Institute for Biotechnology and Genetic Engineering (NIBGE) College, PIEAS, Faisalabad, Pakistan. His research primarily focuses on genetic disorders and their underlying molecular mechanisms.

Research Contributions

Muhammad Tariq has made significant contributions to the field of genetics, particularly in understanding genetic disorders in consanguineous Pakistani families. His work includes identifying novel genetic variants associated with various conditions such as microcephaly, cardiomyopathy, limb-girdle muscular dystrophy, and primary ovarian insufficiency. His research often employs whole exome sequencing to uncover the genetic basis of these disorders. One of his notable works involves the identification of a novel variant in the GPR56/ADGRG1 gene. His studies also extend to the investigation of modifier genes exacerbating primary conditions caused by biallelic mutations.

Aliases

Muhammad Tariq is also known by other names including M Tariq and M. Tariq.

Publication and Citation Metrics

Metric	Value
Citation Count	1253
h-index	21
Paper Count	72

Publications:

Corrigendum

DOI: 10.1111/cge.14092

Year: 2022

Identification of a novel variant in GPR56/ADGRG1 gene through whole exome sequencing in a consanguineous Pakistani family

DOI: 10.1016/j.jocn.2021.09.027

Year: 2021

A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family

DOI: 10.3390/genes12101494

Year: 2021

A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family

DOI: 10.3390/genes12081282

Year: 2021

Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ

DOI: 10.3390/genes12050731

Year: 2021

Updates on Clinical and Genetic Heterogeneity of ASPM in 12 Autosomal Recessive Primary Microcephaly Families in Pakistani Population

DOI: 10.3389/fped.2021.695133

Year: 2021

Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study

DOI: 10.1161/JAHA.120.017731

Year: 2021

A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss.

DOI: 10.1007/s00439-021-02380-2

Year: 2021

Whole exome sequencing reveals a homozygous SGCB variant in a Pakhtun family with limb girdle muscular dystrophy (LGMDR4) phenotype

DOI: 10.1016/j.genrep.2020.101014

Year: 2021

A 24‐generation‐old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome

DOI: 10.1111/cge.14028

Year: 2021

What Are the Treatment Options?

Is There Any Treatment or Management Required?

How Do Mutagens Cause Genetic Mutations?

What Causes Sickle Cell Disease?

What are the Future Directions?

Can Genetics Explain Individual Differences in Cognitive Abilities?

What Are the Regulatory Guidelines for Benzene Exposure?

What are Synonymous Codons?

What Are the Risks Associated with Prenatal Screening and Diagnostic Tests?

How are Harmful Mutations Detected?

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