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Turki M. Sobahy

Observed names: Sobahy, Turki M., Turki M Sobahy, Turki Mohammed Sobahy Sobahy, Turki Sobahy
ORCID: 0000-0003-1797-3098
Observed ORCID: 0000-0003-1797-3098
OpenAlex ID: A5023914465
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden
2016 · Mohamed Abouelhoda, Turki Sobahy, et al. · Genetics in Medicine · 108
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The role of BRCA1/2 in hereditary and familial breast and ovarian cancers
2019 · Yousef M. Hawsawi, Nouf S. Al‐Numair, et al. · Molecular Genetics & Genomic Medicine · 46
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Synthesis and antitumorigenesis effect of novel 2-amino -3-cyano pyridine derivatives containing sulfonamide moiety against breast cancer
2023 · Rasha A. Zailaee, Samar A. Zailaie, et al. · Journal of Molecular Structure · 9
A heterozygous CEBPA mutation disrupting the bZIP domain in a RUNX1 and SRSF2 mutational background causes MDS disease progression
2025 · Ruba Almaghrabi, Yara Alyahyawi, et al. · Nature Communications · 7
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Quantitative DNA analysis of very low-level hepatitis B viremic patients reporting to the gastroenterology clinic
2011 · Mohammad S. Bamaga, Turki M. Sobahy, et al. · Saudi Medical Journal · 6
Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer
2022 · Jamal Zekri, Mohammed Abbas Baghdadi, et al. · ecancermedicalscience · 5
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Variants of Human Mucin Genes in Clear Cell Renal Cell Carcinoma and their Potential Prognostic and Predictive Values.
2023 · Jamal Zekri, Mohammed A Baghdadi, et al. · PubMed · 2
Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows
2022 · Turki M. Sobahy, Ghassan Tashkandi, et al. · BMC Medical Genomics · 2
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Pattern reversal visual evoked potentials (prVEPs) in autosomal recessive hereditary spastic paraplegia with thin corpus callosum (ARHSPTCC) patients with SPG 11 mutations in Saudi Arabia, cross section hospital base study
2022 · Nouf Alfaidi, Turki Sobahy, et al. · Journal of the Neurological Sciences · 2
SARS-COV-2 Triggers the Development of Class I and Class II HLA Antibodies in Recovered Convalescent Plasma Donors
2022 · Ashraf Dada, Khalid Elhassan, et al. · Intervirology · 2
CACSV: a computational web-sever that provides classification for cancer somatic genetic variants from different tissues
2023 · Nahla AlKurabi, Ahad AlGahtani, et al. · BMC Bioinformatics · 1
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Epigenetic Age Prediction Remains Stable Across Common Variants and Diverse Ancestries
2025 · Turki M. Sobahy, Estefania Huergo, et al. · medRxiv
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Detection of Novel Candidate Mutations as A Cause of Steroid-resistant Nephrotic Syndrome in Children using Next-generation Sequencing Techniques
2022 · Walaa F. Alsanie, Abdulhakeem S. Alamri, et al. · Indian Journal of Pharmaceutical Education and Research
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Additional file 3 of Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows
2022 · Sobahy, Turki M., Tashkandi, Ghassan, et al. · Figshare
Additional file 4 of Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows
2022 · Sobahy, Turki M., Tashkandi, Ghassan, et al. · Figshare
Additional file 1 of Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows
2022 · Sobahy, Turki M., Tashkandi, Ghassan, et al. · Figshare
Additional file 2 of Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows
2022 · Sobahy, Turki M., Tashkandi, Ghassan, et al. · Figshare
Clinically Actionable Cancer Somatic Variants (CACSV): A tumor interpreted dataset for analytical workflow
2021 · Turki M. Sobahy, Donya Bahussain, et al. · Research Square
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Novel genomic variants associated with polysplenia, situs inversus totalis, atrial septal defect and double outlet right ventricle in Saudi patient
2020 · Yousef Mohammedrabaa Hawsawi, Turki Mohammed Sobahy Sobahy, et al.
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Abstract P4-09-13: Spectrum analysis of the inherited mutations of BRCA1/-2 genes that associated with high risk breast cancer in Saudi population
2020 · Yousef MohammedRabaa Hawsawi, Abdelrazak Meliti, et al. · Cancer Research
Prognostic and predictive biomarkers for clear cell renal cell carcinoma utilizing next generation sequencing.
2019 · Jamal Zekri, Abdelrazak Meliti, et al. · Journal of Clinical Oncology
Abstract 3372: Mutations of mismatch repair genes in Her2 overexpressed breast cancer
2018 · Mohammed A. Baghdadi, Turki M. Sobahy, et al. · Cancer Research
Works count: 23
Citation count: 190
H-index: 5
I10-index: 2
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