Mohiuddin M. Taher

Umm al-Qura University — Saudi Arabia

Medicine · Health Sciences

21h-index1.8kcitations82works1.72yr avg
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Research Topics

Lipoproteins and Cardiovascular Health(12), Protein Kinase Regulation and GTPase Signaling(6), Cancer Genomics and Diagnostics(6), Diabetes, Cardiovascular Risks, and Lipoproteins(5), Genetic factors in colorectal cancer(5)

Publications78 total

Identification of variants in exon 4 of the LDLR gene and assessment of their effects on the produced proteins in saudi women with metabolic syndrome
Diabetology & Metabolic Syndrome·2025Open Access
The effect of mephedrone on human neuroblastoma and astrocytoma cells
Saudi Pharmaceutical Journal·2024· 4 citedOpen Access
Next-Generation DNA Sequencing of Grade 1 Meningioma Tumours: A Case Report of Angiomatous and Psammomatous Meningiomas
Cureus·2024· 1 citedOpen Access
Supratentorial Sporadic Hemangioblastoma: A Case Report With Mutation Profiling Using Next-Generation DNA Sequencing
Cureus·2023· 2 citedOpen Access
Editorial
Journal of Umm Al-Qura University for Medical Sciences·2023Open Access
Arterial Tortuosity Syndrome in a Newborn: A Case Report With Literature Review
Cureus·2023Open Access
Arterial Tortuosity Syndrome in a Newborn: A Case Report With Literature Review
Cureus·2022· 4 citedOpen Access
Profile of Male Breast Cancer in Makkah Region of Saudi Arabia: A 4-Year Retrospective Analysis of Radiology and Histopathology
International Journal of Breast Cancer·2022· 2 citedOpen Access
Identification of Novel and Known LDLR Variants Triggering SevereFamilial Hypercholesterolemia in Saudi Families
Current Vascular Pharmacology·2022· 3 cited
Design and optimization of 18-gene Ion AmpliSeq panel of Next-generation sequencing for gene mutation analysis causing pain insensitivity
Journal of Umm Al-Qura University for Medical Sciences·2022· 2 citedOpen Access
Mutation Profiling of Intracranial Myxopapillary Ependymoma by Next Generation DNA Sequencing.
PubMed·2021· 2 cited
Compound A Increases Cell Infiltration in Target Organs of Acute Graft-versus-Host Disease (aGVHD) in a Mouse Model
Molecules·2021· 2 citedOpen Access
Next Generation Exome Sequencing of Pediatric Asthma Identifies Rare and Novel Variants in Candidate Genes
Disease Markers·2021· 11 citedOpen Access
A unique case of multiple calvarial hemangiomas with one large symplastic hemangioma
BMC Neurology·2021· 4 citedOpen Access
Identification of PKHD1 mutations in Brain, Breast and Rectal tumors by Next Generation DNA Sequencing.
PubMed·2021
The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing
Frontiers in Genetics·2020· 10 citedOpen Access
EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma
Oncology Letters·2020· 6 citedOpen Access
Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population
Saudi Journal of Biological Sciences·2020· 13 citedOpen Access
Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing
F1000Research·2020· 10 citedOpen Access
Next Generation Exome Sequencing of paediatric Asthma Identifies Rare and Novel Variants in Candidate Genes
Research Square (Research Square)·2020· 1 citedOpen Access
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Frequent Co-authors

Faisal A. Al-Allaf(24), Zainularifeen Abduljaleel(15), Mohammad Athar(15), Abdellatif Bouazzaoui(15), Kristoffer Valerie(11), Neda M. Bogari(8), Wajahatullah Khan(6), Chad Hershey(5), Muhammad Saeed(5), Tahani Nageeti(5), Amr A. Amin(5), Hala Abalkhail(4), Abdullah Al‐Ashwal(4), Khalid AlQuthami(4), Ashwag Aljohani(4), Anwar S. Abd‐Elfattah(4), V. Natarajan(3), Faisal A. Ba-Hammam(3), Guido Lammering(3), Ahmad F. Al-Allaf(3)