Rafaqat Ishaq

Mehr Ali, PB, Pakistan

Last Updated: 09/26/2026

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Found 9 publications

Exploring novel amides as efflux pump inhibitors for overcoming antibiotic resistance in multidrug-resistant Pseudomonas aeruginosa.

Exploring novel amides as efflux pump inhibitors for overcoming antibiotic resistance in multidrug-resistant Pseudomonas aeruginosa.

Journal: Iranian journal of microbiology

Published: August 11, 2025

Whole exome sequencing identifies variable expressivity of CLN6 variants in Progressive myoclonic epilepsy affected families.

Whole exome sequencing identifies variable expressivity of CLN6 variants in Progressive myoclonic epilepsy affected families.

Journal: Epilepsy research

Published: October 04, 2023

Whole Exome Sequencing Reveals Clustering of Variants of Known Vitiligo Genes in Multiplex Consanguineous Pakistani Families.

Whole Exome Sequencing Reveals Clustering of Variants of Known Vitiligo Genes in Multiplex Consanguineous Pakistani Families.

Journal: Genes

Published: April 13, 2023

Whole-Exome sequencing identifies GYS2 biallelic variants in individuals with suspected epilepsy.

Whole-Exome sequencing identifies GYS2 biallelic variants in individuals with suspected epilepsy.

Journal: Seizure

Published: February 08, 2023

Differential Treatment Responses in Pakistani Schizophrenia Samples: Correlation with Sociodemographic Parameters, Drug Addiction, Attitude to the Treatment and Antipsychotic Agents.

Differential Treatment Responses in Pakistani Schizophrenia Samples: Correlation with Sociodemographic Parameters, Drug Addiction, Attitude to the Treatment and Antipsychotic Agents.

Journal: Brain sciences

Published: January 12, 2023

Pathogenic variants of AIPL1, MERTK, GUCY2D, and FOXE3 in Pakistani families with clinically heterogeneous eye diseases.

Pathogenic variants of AIPL1, MERTK, GUCY2D, and FOXE3 in Pakistani families with clinically heterogeneous eye diseases.

Journal: PloS one

Published: August 02, 2020

Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss.

Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss.

Journal: Genes

Published: July 30, 2020

Multi-omic studies on missense PLG variants in families with otitis media.

Multi-omic studies on missense PLG variants in families with otitis media.

Journal: Scientific reports

Published: November 18, 2019

Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani Families.

Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani Families.

Journal: Genes

Published: November 06, 2019

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Last Updated: 09/26/2026