Dr. Öğr. Üyesi ZUHAL ALTINTAŞ
- Yöksis ID 16456
- Researcher ID K-8514-2015
- ORCID ID 0000-0001-9805-6624
- Scopus ID 24802268100
- Scholar ID
- E-posta altintaszmert@mersin.edu.tr
- Dahili Telefon 22616, 1132
Birim
TIP FAKÜLTESİ
DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
TIBBİ GENETİK ANABİLİM DALI
DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
TIBBİ GENETİK ANABİLİM DALI
ÜAK Temel Alan Bilgisi
Sağlık Bilimleri Temel Alanı
Tıbbi Genetik
Tıbbi Genetik
Son 5 Makale
Association of LDLR and SCARB1 gene polymorphisms with hepatocellular carcinoma: a case-control study proposing a 'double-hit' model
LIPIDS IN HEALTH AND DISEASE, vol. 25, no. 1, pp. – Link 2026
Case Report: unmasking pseudo-homozygosity in CYP21A2: intergenerational gene conversion expansion and the necessity of multimodal genetic testing
Frontiers in Endocrinology, vol. 17, no. , pp. 1–8 Link 2026
Clinical and Genetic Determinants of Hepatocellular Carcinoma in a Turkish Cohort: Impact of SLCO1B1 and SLCO1B3 Germline Variations and Demographic Risk Factors
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 27, no. 14, pp. 6214– Link 2026
Clinical and Genetic Determinants of Hepatocellular Carcinoma in a Turkish Cohort: Impact of SLCO1B1 and SLCO1B3 Germline Variations and Demographic Risk Factors
International Journal of Molecular Sciences, vol. 27, no. , pp. 1–16 Link 2026
OATP1B3 c.699G>A Predicts a 6.3-Fold Increased Risk of Hyperbilirubinemia During OPrD Therapy for HCV
CURRENT ISSUES IN MOLECULAR BIOLOGY, vol. 48, no. 5, pp. 452– Link 2026
LIPIDS IN HEALTH AND DISEASE, vol. 25, no. 1, pp. – Link 2026
Case Report: unmasking pseudo-homozygosity in CYP21A2: intergenerational gene conversion expansion and the necessity of multimodal genetic testing
Frontiers in Endocrinology, vol. 17, no. , pp. 1–8 Link 2026
Clinical and Genetic Determinants of Hepatocellular Carcinoma in a Turkish Cohort: Impact of SLCO1B1 and SLCO1B3 Germline Variations and Demographic Risk Factors
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 27, no. 14, pp. 6214– Link 2026
Clinical and Genetic Determinants of Hepatocellular Carcinoma in a Turkish Cohort: Impact of SLCO1B1 and SLCO1B3 Germline Variations and Demographic Risk Factors
International Journal of Molecular Sciences, vol. 27, no. , pp. 1–16 Link 2026
OATP1B3 c.699G>A Predicts a 6.3-Fold Increased Risk of Hyperbilirubinemia During OPrD Therapy for HCV
CURRENT ISSUES IN MOLECULAR BIOLOGY, vol. 48, no. 5, pp. 452– Link 2026
Son 5 Bildiri
Prenatal Diagnosis of Rhombencephalosynapsis Associated With
Multiple Fetal Anomalies and a Maternally Inherited EP300 Gene Variant:
A Case Report
23rd World Congress in Fetal Medicine 2026, (28.06.2026 - ) Link 2026
Genotip ve Fenotip Uyumsuzluğu Olan 3 Hastanın Sitogenetik ve Moleküler Yönden Değerlendirilmesi
8. Bahar Pediatri Kongresi (26.03.2026 - ) Link 2026
Aneuploidy mosaicism in peripheral blood sample with Inv5(q)(q22q33.3) in a girl patient who presented with short stature
18th Medical Biology and Genetisc Congress (26.10.2023 - 29.10.2023) Link 2023
OATP1B3 699A>G Varyantına Sahip olmak Ombitasvir/Paritaprevir/Ritonavir+Dasabuvir İle Tedavi Edilen Hepatit C Hastalarında Hiperbilirubinemi İle İlişkilidir
14. Ulusal Hepatoloji Kongresi (17.05.2023 - 21.05.2023) 2023
Different aneuploidy mosaicism in peripheral blood sample with Inv5(q)(q22q33.3) in a girl patient who presented with short stature
XVIII. Tıbbi Biyoloji ve Genetik Kongresi (26.10.2023 - 29.10.2023) Link 2023
23rd World Congress in Fetal Medicine 2026, (28.06.2026 - ) Link 2026
Genotip ve Fenotip Uyumsuzluğu Olan 3 Hastanın Sitogenetik ve Moleküler Yönden Değerlendirilmesi
8. Bahar Pediatri Kongresi (26.03.2026 - ) Link 2026
Aneuploidy mosaicism in peripheral blood sample with Inv5(q)(q22q33.3) in a girl patient who presented with short stature
18th Medical Biology and Genetisc Congress (26.10.2023 - 29.10.2023) Link 2023
OATP1B3 699A>G Varyantına Sahip olmak Ombitasvir/Paritaprevir/Ritonavir+Dasabuvir İle Tedavi Edilen Hepatit C Hastalarında Hiperbilirubinemi İle İlişkilidir
14. Ulusal Hepatoloji Kongresi (17.05.2023 - 21.05.2023) 2023
Different aneuploidy mosaicism in peripheral blood sample with Inv5(q)(q22q33.3) in a girl patient who presented with short stature
XVIII. Tıbbi Biyoloji ve Genetik Kongresi (26.10.2023 - 29.10.2023) Link 2023