Hadia Gul

Dera Ismail Khan, KP 29050, Pakistan

Last Updated: 09/26/2026

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Found 8 publications

Expanding the ethnic and clinical spectrum of the IDS c.1122C>T mutation: first report from Pakistan.

Expanding the ethnic and clinical spectrum of the IDS c.1122C>T mutation: first report from Pakistan.

Journal: Neurogenetics

Published: July 01, 2025

A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.

A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.

Journal: Genetics and molecular biology

Published: February 13, 2025

SEC24D gene as a biomarker in human cancers and its association with CD8+ T cell immune cell infiltration.

SEC24D gene as a biomarker in human cancers and its association with CD8+ T cell immune cell infiltration.

Journal: American journal of translational research

Published: July 09, 2022

Ethnoveterinary uses of forage plants for domesticated ruminants in Malakand agency, Pakistan.

Ethnoveterinary uses of forage plants for domesticated ruminants in Malakand agency, Pakistan.

Journal: Journal of animal physiology and animal nutrition

Published: June 22, 2022

Homozygosity mapping coupled with whole-exome sequencing and protein modelling identified a novel missense mutation in GUCY2D in a consanguineous Pakistani family with Leber congenital amaurosis.

Homozygosity mapping coupled with whole-exome sequencing and protein modelling identified a novel missense mutation in GUCY2D in a consanguineous Pakistani family with Leber congenital amaurosis.

Journal: Journal of genetics

Published: September 02, 2021

Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations.

Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations.

Journal: Annals of human genetics

Published: August 04, 2018

Ophthalmo-genetic analysis of Pakistani patients with nonsyndromic oculocutaneous albinism through whole exome sequencing.

Ophthalmo-genetic analysis of Pakistani patients with nonsyndromic oculocutaneous albinism through whole exome sequencing.

Journal: JPMA. The Journal of the Pakistan Medical Association

Published: May 17, 2017

Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population.

Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population.

Journal: Scientific reports

Published: October 31, 2016

Showing 1-8 of 8

Last Updated: 09/26/2026