Doç. Dr. TİMUR TUNCALI

ATLAS Yayın Analitiği

Makaleler 15

1. Post-Treatment Persistent Erythrocytosis in Patients with Hodgkin Lymphoma: Molecular Mechanisms Underlying the Pathogenesis of Erythrocytosis.

Koyun D., Yüksel S., Civriz Bozdağ S., Tuncalı T., Kuzu I., Özcan M.

Cancers , cilt.18, sa.15, 2026 (SCI-Expanded, Scopus)

2. **Innate immunogenetic synergy between KIR and Neanderthal-derived OAS variants predicts COVID-19 outcomes**

Akin H. Y., Tuncali T., Gencer E. B., Cengiz Seval G., Saricaoglu E. M., Gulten E., et al.

PLOS ONE , cilt.21, sa.5, 2026 (SCI-Expanded, Scopus)

3. Somatic variants and frequencies of familial myeloma germline predisposition genes among patients within the CoMMpass dataset

AKKUŞ E., TUNCALI T., Akin H. Y., Beksaç M.

Expert Review of Hematology , cilt.19, sa.1, ss.79-88, 2026 (SCI-Expanded, Scopus)

4. Diagnostic Yield and Clinical Utility of Genetic Testing in Turkish Adults with Suspected Inherited Kidney Disease: Insights from a Population with High Parental Consanguinity

KUMRU G., ALTINER Ş., KARAKAYA A., EKİNCİ S., TUNCALI T., KUTLAY N., et al.

Journal of clinical practice and research , 2026 (ESCI, TRDizin)

5. Familial Multiple Myeloma: Insights From Epidemiology and Underlying Germline Genetic Predisposition to the Clinic

Akkus E., TUNCALI T., Beksac M.

Clinical Lymphoma, Myeloma and Leukemia , cilt.25, sa.6, 2025 (SCI-Expanded, Scopus)

6. A Germline Variant of BNIP1 Gene (rs28199) is Associated with Familial Multiple Myeloma

AKKUŞ E., TUNCALI T., Akin H. Y., SALİHOĞLU A., Sevindik O. G., Kirkizlar H. O., et al.

CLINICAL LYMPHOMA MYELOMA & LEUKEMIA , 2024 (SCI-Expanded, Scopus)

7. Germline genetic variants in Turkish familial multiple myeloma/monoclonal gammopathy of undetermined significance cases

AKKUŞ E., TUNCALI T., Akin H. Y., Aydin Y., Besisik S. K., GÜRKAN E., et al.

BRITISH JOURNAL OF HAEMATOLOGY , cilt.204, sa.3, ss.931-938, 2024 (SCI-Expanded, Scopus)

8. X-linked Dyskeratosis Congenita Case with Mutation 1058C>T(p.Ala353Val) in Dyskerine Gene

ÖKTEM A., KUŞÇU D. D., TUNCALI T., Kahraman U., ÖZBOLAT S.

Indian Journal of Dermatology , cilt.69, sa.1, ss.106, 2024 (SCI-Expanded, Scopus)

9. Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

Kiraz A., Sezer O., ALEMDAR A., Canbek S., Duman N., BİŞGİN A., et al.

Journal of medical virology , cilt.95, sa.2, 2023 (SCI-Expanded, Scopus)

10. **Phenotypic and molecular characterization of five patients with PIK3CA-related overgrowth spectrum (PROS)**

Ili E., Tasdelen E., Durmaz C. D., ALTINER Ş., TUNCALI T., Martinez-Glez V., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.188, sa.6, ss.1792-1800, 2022 (SCI-Expanded, Scopus)

11. Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.

FUNCTIONAL & INTEGRATIVE GENOMICS , cilt.22, sa.3, ss.291-315, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

12. Clinical findings in 22q11.2 microdeletion syndrome: case series

ALTINER Ş., TUNCALI T., KUTLAY N., KARABULUT H. G., ILGIN RUHİ H.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.30, sa.SUPPL 1, ss.325, 2022 (SCI-Expanded, Scopus)

13. A case report of an atypical FIP1L1-PDGFRA fusion in a patient with hypereosinophilia

EKİNCİ S., CENGİZ SEVAL G., KARABULUT H. G., Vicdan A., YÜKSEL S., KUZU I., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.30, sa.SUPPL 1, ss.222, 2022 (SCI-Expanded, Scopus)

14. Evaluation of Plasma Cell Molecular Cytogenetic Findings of Myeloma Patients: One-Year Single-Center Experience

KAPLAN İ., CESUR BALTACI H. N., ALTINER Ş., EKİNCİ S., VİCDAN N. A., KARABULUT H. G., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.30, sa.SUPPL 1, ss.413, 2022 (SCI-Expanded, Scopus)

15. ROHMM-A flexible hidden Markov model framework to detect runs of homozygosity from genotyping data

Celik G., TUNCALI T.

HUMAN MUTATION , cilt.43, sa.2, ss.158-168, 2022 (SCI-Expanded, Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 6

1. Pnömoniden Genetik Tanıya: ICF Sendromu

alpkıray m. f., İSLAMOĞLU C., ÖZTÜRK A. G., bal s., ERMAN B., TUNCALI T., et al.

31.Ulusal Alerji ve Klinik İmmünoloji Kongresi, Antalya, Türkiye, 25 Kasım 2025, ss.100-98, (Tam Metin Bildiri)

2. Kronik Lenfositik Lösemi Hastalarında Ighv Somatik Hipermutasyon Profili: Tek Merkez Deneyimi

İLBASMIŞ H., ALTINER Ş., TUNCALI T., KUTLAY N., KARABULUT H. G., EKİNCİ S., et al.

3. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 27 - 30 Ekim 2025, (Özet Bildiri)

3. Senkopta EKG tekrarının önemi: Uzun QT sendromu olgu sunumu

NAS G. N., ALTINTAŞ M., YILMAZ M. M., RAMOĞLU M. G., HARTUÇ İ., TUNCALI T., et al.

2.Ankara Pediatri Kongresi, Ankara, Türkiye, 7 Kasım - 10 Mart 2024, cilt.78, ss.99, (Özet Bildiri)

4. BRCA1 and BRCA2 Germline Sequence Analysis Data: A Single-Center Experience

LEBLEBİCİ C. B., KUTLAY N., ILGIN RUHİ H., TUNCALI T., KARABULUT H. G., EKİNCİ S., et al.

International hereditary cancer congress, Antalya, Türkiye, 6 - 09 Şubat 2025, (Özet Bildiri)

5. Could VUS be important in AML?

KUTLAY N., KARABULUT H. G., TUNCALI T., ILGIN RUHİ H., EKİNCİ S., ALTINER Ş., et al.

ESHG Conference Berlin 1-4 June 2024, Berlin, Almanya, 01 Haziran 2024, cilt.32, ss.923, (Özet Bildiri)

6. Evaluation of the results of cytogenetic, molecular cytogenetic and molecular analysis in non-Hodgkin lymphoma

LEBLEBİCİ C. B., KUTLAY N., VİCDAN N. A., EKİNCİ S., ILGIN RUHİ H., TUNCALI T., et al.

ESHG Conference Berlin 1-4 June 2024, Berlin, Almanya, 1 Haziran - 01 Nisan 2024, (Özet Bildiri)

Metrikler

Yayın

105

Yayın (WoS)

Yayın (Scopus)

Atıf (WoS)

283

H-İndeks (WoS)

Atıf (Scopus)

362

H-İndeks (Scopus)

Atıf (Scholar)

H-İndeks (Scholar)

Proje

Tez Danışmanlığı

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

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