Publications by authors named "Rafaqat Ishaq"

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Exploring novel amides as efflux pump inhibitors for overcoming antibiotic resistance in multidrug-resistant .
Fahad Ullah, Maqsood Ali, Falak Niaz, Israr Ali Khan, Sher Wali Khan, Rafaqat Ishaq

Iran J Microbiol· August 2025

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Whole-Exome sequencing identifies GYS2 biallelic variants in individuals with suspected epilepsy.
Muhammad Ilyas, Dorothea Holzwarth, Rafaqat Ishaq, Yasir Ali, Umme Habiba

Seizure· March 2024

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Whole exome sequencing identifies variable expressivity of CLN6 variants in Progressive myoclonic epilepsy affected families.
Muhammad Ilyas, Faiza Tariq, Rafaqat Ishaq, Umme Habiba, Farah Bibi

Epilepsy Res· March 2024

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Whole Exome Sequencing Reveals Clustering of Variants of Known Vitiligo Genes in Multiplex Consanguineous Pakistani Families.
Rafaqat Ishaq, Muhammad Ilyas, Umme Habiba, Muhammad Noor Ul Amin, Sadia Saeed

Genes (Basel)· May 2023

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Differential Treatment Responses in Pakistani Schizophrenia Samples: Correlation with Sociodemographic Parameters, Drug Addiction, Attitude to the Treatment and Antipsychotic Agents.
Umme Habiba, Aafia Malik, Ghazala Kaukab Raja, Muhammad Raza Memon, Asad Tameezud Din Nizami, Rafaqat Ishaq

Brain Sci· February 2023

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Pathogenic variants of AIPL1, MERTK, GUCY2D, and FOXE3 in Pakistani families with clinically heterogeneous eye diseases.
Muhammad Rashid, Muhammad Qasim, Rafaqat Ishaq, Shazia Anwer Bukhari, Zureesha Sajid

PLoS One· November 2020

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Multi-omic studies on missense PLG variants in families with otitis media.
Tori C Bootpetch, Lena Hafrén, Christina L Elling, Erin E Baschal, Ani W Manichaikul, Rafaqat Ishaq

Sci Rep· September 2020

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Novel Mutations in , , , and Identified in Familial Cases of Prelingual Hearing Loss.
Saba Zafar, Mohsin Shahzad, Rafaqat Ishaq, Ayesha Yousaf, Rehan S Shaikh

Genes (Basel)· August 2020

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Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani Families.
Muhammad Noman, Rafaqat Ishaq, Shazia A Bukhari, Zubair M Ahmed, Saima Riazuddin

Genes (Basel)· December 2019

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