Yayınlar & Eserler

Yayın Ağı
Makaleler 27
Tümü (27)
SCI-E, SSCI, AHCI (19)
SCI-E, SSCI, AHCI, ESCI (26)
ESCI (3)
Scopus (27)
TRDizin (2)

1. PRR11 expression in early ER+/HER2‑low breast cancer: Association with estrogen receptor positivity and exploratory analysis of prognostic significance

Turkel A., DOĞAN M., Irkkan S. C., ERDEM H. B., BOZDOĞAN N., Bahsi T.
Oncology Letters , cilt.32, sa.3, 2026 (SCI-Expanded, Scopus) Creative Commons License

2. Efficacy of risperidone and behavioral delineation in METTL5-related syndrome: a pooled analysis of literature and report of a novel variant

Gündoğdu Öğütlü Ö. B., Baştan F., Erdem Z. S., Öğütlü H., ERDEM H. B.
Acta Neurologica Belgica , cilt.126, sa.4, ss.1347-1354, 2026 (SCI-Expanded, Scopus)

3. Rare Coexistence of Hidradenitis Suppurativa and Hyper-IgD Syndrome With Homozygous MVK V377I and Compound Heterozygous MEFV (M680I/E148Q) Mutations

Tas-Aygar G., GÖNÜL M., Sunar Yayla E. N., ERDEM H. B., KARTAL S. P.
Pediatric Dermatology , cilt.43, sa.2, ss.398-401, 2026 (SCI-Expanded, Scopus)

4. Decoding Genomic Variants in a Turkish Cohort of Patients with Spasticity

Bakır A., Saat H., ERDEM H. B., Sezer A., Taşdelen E., Bir F. D., et al.
Bratislava Medical Journal , cilt.126, sa.10, ss.2688-2697, 2025 (SCI-Expanded, Scopus)

5. Design, Development, and Clinical Validation of a Novel Kit for Cell-Free DNA Extraction

Çelik E., Güner H., Kayalı G., ERDEM H. B., Bahsi T., KAZAN H. H.
Diagnostics , cilt.15, sa.15, 2025 (SCI-Expanded, Scopus) Creative Commons License

6. Evaluation of Mutation Profiles of Cardiomyopathy Patients in the Turkish Cohort

Bakir A., Saat H., ERDEM H. B., Tolunay H., KAZAN H. H.
Bratislava Medical Journal , cilt.126, sa.5, ss.811-817, 2025 (SCI-Expanded, Scopus)

7. Effects of BRCA variation on prognosis in patients with nonmetastatic breast cancer

Türkel A., Onur I. D., Anik H., Öner I., ERDEM H. B., Bahsi T., et al.
Annals of Human Genetics , cilt.88, sa.6, ss.436-444, 2024 (SCI-Expanded, Scopus)

8. Higher TP53 somatic mutation prevalence from liquid biopsy analysis in ever smoker non-small-cell lung cancer patients

ERDEM H. B., Alay M. T., Özdemir Z., Çevik E., ATEŞ Ö., Karaçin C., et al.
Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis , cilt.828, 2024 (Scopus)

9. Report of a progressive leukoencephalopathy with ovarian failure (LKENP) case with compound heterozygous genotype and a novel variant: AARS2:c.2358_2364+7dup

Duzkale N., Lafci O., Ayaz R., ERDEM H. B., Ates M. P., ÖNDER H.
Neurology Asia , cilt.29, sa.4, ss.1181-1185, 2024 (SCI-Expanded, Scopus) Creative Commons License

10. Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling

Özdemir Z., Çevik E., Öksüzoğlu Ö. B. Ç., DOĞAN M., ATEŞ Ö., Esin E., et al.
Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis , cilt.827, 2023 (SCI-Expanded, Scopus)

11. Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy

Saat H., Şahin İ., ERDEM H. B., ÖZGÜR S., Tokgöz S. T., Bahsi T.
Anatolian Journal of Cardiology , cilt.26, sa.6, ss.460-465, 2022 (SCI-Expanded, Scopus, TRDizin)

12. Liquid biopsy: Novel perspectives on the importance and spectrum of pik3ca, pten and ret mutations in solid tumors

Sahin I., Saat H., AKSOY S., DİZDAR Ö., ERDEM H. B., Bahsi T.
Molecular and Clinical Oncology , cilt.16, sa.1, 2022 (ESCI, Scopus) Creative Commons License

13. Face masks and polycythemia is the standard hemoglobin cutoff valid in the pandemic?

Yaman S., BAŞCI S., Turan G., Ulu B. U., YİĞENOĞLU T. N., Bahsi T., et al.
Iraqi Journal of Hematology , cilt.11, sa.2, ss.130-133, 2022 (Scopus)

14. Non-Invasive Cancer Genotyping: A Single-Center Experience on the Challenges, Limitations, and Methods

Sahin I., Saat H., ERDEM H. B., Bahsi T.
Gazi Medical Journal , cilt.33, sa.2, ss.146-150, 2022 (Scopus)

15. Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature

Ceylan A. C., Acar Arslan E., ERDEM H. B., Kavus H., ARSLAN M., Topaloğlu H.
Acta Neurologica Belgica , cilt.121, sa.6, ss.1457-1462, 2021 (SCI-Expanded, Scopus)

16. High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

Mitani T., Isikay S., Gezdirici A., Gulec E. Y., Punetha J., Fatih J. M., et al.
American Journal of Human Genetics , cilt.108, sa.10, ss.1981-2005, 2021 (SCI-Expanded, Scopus)

17. Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies

Dworschak G. C., Punetha J., Kalanithy J. C., Mingardo E., ERDEM H. B., Akdemir Z. C., et al.
Genetics in Medicine , cilt.23, sa.9, ss.1715-1725, 2021 (SCI-Expanded, Scopus)

18. High Expression of Stem Cell-Related Genes in Polyps with Villous Features and High-Grade Dysplasia Support Malignant Phenotype and Colorectal Carcinogenesis

Sahin I., GÜNDOĞDU B., CEYLAN A. C., ERDEM H. B., TATAR A.
Asian Pacific Journal of Cancer Prevention , cilt.22, sa.8, ss.2429-2435, 2021 (Scopus) Creative Commons License

19. Function of telomere in aging and age related diseases

ERDEM H. B., Bahsi T., ERGÜN M. A.
Environmental Toxicology and Pharmacology , cilt.85, 2021 (SCI-Expanded, Scopus)

20. Genetic diagnosis in chronic myeloid leukemia Kronik Miyeloid Lösemide Genetik Tanı

ERDEM H. B., Kaymak A. Ö.
Gazi Medical Journal , cilt.31, sa.2, ss.224-226, 2020 (ESCI, Scopus)

21. Evaluation of clinical outcome and mixed chimerism follow-up after allogeneic hematopoietic stem cell transplantation in hematological malignancies

Bahsi T., YİĞENOĞLU T. N., ERDEM H. B., KIZIL ÇAKAR M., DAL M. S., ALTUNTAŞ F.
Gazi Medical Journal , cilt.31, sa.1, ss.52-55, 2020 (ESCI, Scopus)

22. Spectrum of BRCA1/BRCA2 variants in 1419 Turkish breast and ovarian cancer patients: A single center study 1419 Türk meme ve over kanseri hastasında BRCA1/BRCA2 varyantlarının dağılımı: Tek merkez çalışması

Bahsi T., ERDEM H. B.
Turkish Journal of Biochemistry , cilt.45, sa.1, ss.83-90, 2020 (SCI-Expanded, Scopus, TRDizin)

23. The Frequency of Monocyte Chemoattractant Protein-1 Gene Polymorphism in Obstructive Sleep Apnea Syndrome

Kerget B., ARAZ Ö., ERDEM H. B., Akgün M.
Lung , cilt.197, sa.5, ss.585-592, 2019 (SCI-Expanded, Scopus)

24. A De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child

GÜRLEK GÖKÇEBAY D., Akpinar-Tekgunduz S., ERDEM H. B., Yarali N.
Hemoglobin , cilt.43, sa.4-5, ss.277-279, 2019 (SCI-Expanded, Scopus)

25. The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance

Pehlivan D., Bayram Y., Gunes N., Coban Akdemir Z., Shukla A., Bierhals T., et al.
American Journal of Human Genetics , cilt.105, sa.1, ss.132-150, 2019 (SCI-Expanded, Scopus)

26. Comparison of RT-qPCR and RT-Digital PCR for detection and quantification of BCR-ABL1 transcripts in chronic myeloid leukemia RT-qPCR ve RT-Dijital PCR Yöntemlerinin Kronik Myeloid Lösemi'de BCR-ABL1 Transkriptlerini Tespit Etme ve Ölçümleme Basarilarinin Karsilastirilmasi

Bahsi T., ERDEM H. B.
Gazi Medical Journal , cilt.30, sa.4A, ss.421-424, 2019 (Scopus) Creative Commons License

27. Mitochondrial DNA copy number alterations in familial mediterranean fever patients

ERDEM H. B., CEYLAN A. N., ŞAHİN İ. F., Sever-Erdem Z., ÇİTLİ Ş., TATAR A.
Bratislava Medical Journal , cilt.119, sa.7, ss.425-428, 2018 (SCI-Expanded, Scopus)
Metrikler

Yayın

27

Yayın (WoS)

26

Yayın (Scopus)

27

H-İndeks (WoS)

6

Atıf (Scopus)

272

H-İndeks (Scopus)

6

Atıf (TrDizin)

10

H-İndeks (TrDizin)

1

Atıf (Diğer Toplam)

10

Proje

1

Tez Danışmanlığı

3

Açık Erişim

8