Absarul A. Haque

Jeddah, Saudi Arabia

Last Updated: 09/26/2026

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Found 47 publications

Exome Sequencing uncovers Homozygous Stop-Gained variant in the SYNE1 Gene Leading to Spinocerebellar Ataxia.

Exome Sequencing uncovers Homozygous Stop-Gained variant in the SYNE1 Gene Leading to Spinocerebellar Ataxia.

Journal: Pakistan journal of medical sciences

Published: January 20, 2026

Characterization of Desertihabitans sp. FB5, a halophyte associated Actinomycetes producing phytohormones.

Characterization of Desertihabitans sp. FB5, a halophyte associated Actinomycetes producing phytohormones.

Journal: Bioinformation

Published: November 01, 2025

Clinical Discovery and Molecular Analysis of Two Novel MSH2 Gene Mutations (p.Ala771Gly and p.Val797Gly) in Saudi Colorectal Cancer Patients: Potential Implications for Tumorigenesis.

Clinical Discovery and Molecular Analysis of Two Novel MSH2 Gene Mutations (p.Ala771Gly and p.Val797Gly) in Saudi Colorectal Cancer Patients: Potential Implications for Tumorigenesis.

Journal: Health science reports

Published: March 17, 2025

Phytochemical Profiling and Anticancer Potential of Fagonia cretica L. Extracts on Liver Cancer (HepG2) Cells using In vitro and In silico Approaches.

Phytochemical Profiling and Anticancer Potential of Fagonia cretica L. Extracts on Liver Cancer (HepG2) Cells using In vitro and In silico Approaches.

Journal: Anti-cancer agents in medicinal chemistry

Published: January 13, 2025

Effect of novel IL-8 gene mutation on its protein structure and stability among ovarian cancer patients in Saudi Arabia.

Effect of novel IL-8 gene mutation on its protein structure and stability among ovarian cancer patients in Saudi Arabia.

Journal: Bioinformation

Published: November 01, 2024

The mutational spectrum of NRAS gene discovers a novel frameshift mutation (E49R) in Saudi colorectal cancer patients.

The mutational spectrum of NRAS gene discovers a novel frameshift mutation (E49R) in Saudi colorectal cancer patients.

Journal: Cancer cell international

Published: April 18, 2024

KDM3A knockdown regulates COMP, LOX, COL8A1 and ACOT1 genes in myocardial fibrosis.

KDM3A knockdown regulates COMP, LOX, COL8A1 and ACOT1 genes in myocardial fibrosis.

Journal: Bioinformation

Published: April 01, 2024

Whole exome sequencing of a novel homozygous missense variant in PALB2 gene leading to Fanconi anaemia complementation group.

Whole exome sequencing of a novel homozygous missense variant in PALB2 gene leading to Fanconi anaemia complementation group.

Journal: Biomedical reports

Published: November 30, 2023

Discovery of a novel mutation F184S (c.551T>C) in GATA4 gene causing congenital heart disease in a consanguineous Saudi family.

Discovery of a novel mutation F184S (c.551T>C) in GATA4 gene causing congenital heart disease in a consanguineous Saudi family.

Journal: Heliyon

Published: November 27, 2023

A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family.

A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family.

Journal: Pakistan journal of medical sciences

Published: September 03, 2023

A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family.

A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family.

Journal: Genes

Published: January 13, 2023

A Systems Biology and LASSO-Based Approach to Decipher the Transcriptome-Interactome Signature for Predicting Non-Small Cell Lung Cancer.

A Systems Biology and LASSO-Based Approach to Decipher the Transcriptome-Interactome Signature for Predicting Non-Small Cell Lung Cancer.

Journal: Biology

Published: October 31, 2022

Showing 1-12 of 47

Last Updated: 09/26/2026