Merve Saka Güvenç (Merve S Güvenç, Merve Saka Guvenc)

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 6

Top Topics

Congenital Heart Disease

Mitochondrial Dna

Epidermal Growth Factor Receptor

Top Venues

Turkish journal of urology

The clinical respiratory journal

Annals of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Havva Yazıcı, Gunes Ak, Merve Yoldas Çelik, Fehime Erdem, Ayse Yuksel Yanbolu, Esra Er, Ayse Ergul Bozaci, Merve Saka Güvenç, Ayça Aykut, Asude Alpman Durmaz, Ebru Canda, Sema Kalkan Uçar, Mahmut Coker
Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form. Journal of pediatric endocrinology & metabolism : JPEM (2023)
Evren Gumus, Ebru Tuncez, Ozlem Oz, Merve Saka Güvenç
Response to Letter to the Editor: "Atrioventricular canal defect is an infrequent congenital heart disease that can be observed in Bardet-Biedl syndrome". Annals of human genetics 85 (3-4) (2021)
Hayrullah Manyas, Berna Eroğlu Filibeli, İlkay Ayrancı, Merve Saka Güvenç, Bumin Nuri Dündar, Gönül Çatli
Early and late diagnoses of 17β-Hydroxysteroid dehydrogenase type-3 deficiency in two unrelated patients. Andrologia 53 (6) (2021)
Sinem Ermin, Özgür Batum, Merve Saka Güvenç, Ayşe Gülden Diniz, Aysu Ayrancı, Kadri Murat Erdoğan, Nur Yücel, Eylem Yıldırım, Taha Reşid Özdemir, Alev Gülşah Hacar, Filiz Güldaval, Altug Koc, Zekiye Aydoğdu, Günseli Balcı, Berk Özyilmaz, Hacer Akşit Yaşar, Özge Özer Kaya, Mine Gayaf, Ozgur Kirbiyik, Nimet Aksel, Yaşar Bekir Kutbay, Tuba Nihal Ursavaş, Gülistan Karadeniz, Gulru Polat, Berna Kömürcüoğlu, Ali Kadri Çırak, Ufuk Yılmaz
The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosis. The clinical respiratory journal 15 (2) (2020)
Berk Özyilmaz, Gül Caner Mercan, Ozgur Kirbiyik, Taha Reşid Özdemir, Samira Özkara, Özge Özer Kaya, Yaşar Bekir Kutbay, Kadri Murat Erdoğan, Merve Saka Güvenç, Altug Koc
First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss. Turkish archives of otorhinolaryngology 57 (3) (2019)
Taha Reşid Özdemir, Berk Özyilmaz, Özgür Çakmak, Özge Özer Kaya, Can Köse, Ozgur Kirbiyik, Mehmet Zeynel Keskin, Altug Koc, Tuğba Zeyrek, Yaşar Bekir Kutbay, Kadri Murat Erdoğan, Merve Saka Güvenç
Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study. Turkish journal of urology 46 (2) (2019)