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Mert Pekerbaş

Observed name: Mert Pekerbas
ORCID: 0000-0003-0515-2858
Observed ORCID: 0000-0003-0515-2858
OpenAlex ID: A5074117922
Epigenetic signatures in gastric cancer: current knowledge and future perspectives
2022 · Fatma Sogutlu, Mert Pekerbas, et al. · Expert Review of Molecular Diagnostics · 20
The anticancer potential of Origanum onites L. in gastric cancer through epigenetic alterations
2025 · Fatma Sogutlu, Mert Pekerbas, et al. · BMC Complementary Medicine and Therapies · 7
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Complex karyotype with double Philadelphia chromosome and T315I mutation results in blastic phase and extensive extramedullary infiltration in a chronic myeloid leukemia patient
2022 · Eren Arslan Davulcu, Mert Pekerbas, et al. · Cancer Genetics · 4
Integrative and systematic genomic approaches to improve diagnosis in rare and undiagnosed diseases: results from the RareBoost project
2026 · Ayca Yigit, Mert Pekerbas, et al. · European Journal of Human Genetics · 2
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The Role of Serum Vitamin D Levels and Vitamin D Receptor (VDR) Gene Variants on Dental Caries
2024 · Ece Şengün Berber, Feyza Umay Koç, et al. · Children · 2
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Expanding mutational landscape and clinical phenotype of the CASK-related neurological disorders
2026 · Mert Pekerbas, Kutay Bulut, et al. · Journal of Human Genetics
A novel 270 kb deletion upstream of LMNB1 overlapping the ADLD critical regulatory region in two siblings with adult-onset leukodystrophy
2026 · Ayca Yigit, Mert Pekerbas, et al. · BMC Neurology
Clinical, biochemical, and genetic perspectives in hepatic glycogen storage diseases: HEPA-GSD study
2026 · Özlem Ünal Uzun, Gülhan Karakaya Molla, et al. · Molecular Genetics and Metabolism
RareBoost: A Research-Integrated Program for Rare and Undiagnosed Diseases in Türkiye
2026 · Mehmet Mert Topaloğlu, Ayca Yigit, et al. · Research Square
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Grange‐Like Phenotype Associated With an RNF213 Pathogenic Variant: Expanding the Vasculopathy Spectrum
2026 · Serife Ozturk Yilmaz, Ayca Yigit, et al. · American Journal of Medical Genetics Part A
A rare case of Yersinia pseudotuberculosis liver abscess and bacteremia in a heterozygous carrier of HFE1 H63D and MPEG1 mutations in Turkiye
2024 · Muhammed Alper Ozarslan, Hasan Selcuk Ozkan, et al. · Hepatology forum/Hepatology forum (Online)
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Works count: 11
Citation count: 35
H-index: 3
I10-index: 1
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