Zehra Oya Uyguner (Oya Uyguner, Z O Uyguner)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 16

Top Topics

Mild Cognitive Impairment

Top Venues

Journal of endocrinological investigation

American journal of medical genetics. Part A

Clinical genetics

Journal of clinical research in pediatric endocrinology

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

Publications

Gozde Tutku Turgut, Umut Altunoglu, Cagri Gulec, Tugba Sarac Sivrikoz, Tuğba Kalaycı, Guven Toksoy, Şahin Avcı, Behiye Tuğçe Yıldırım, Gözde Yeşil Sayın, Ibrahim Halil Kalelioglu, Birsen Karaman, Recep Has, Seher Başaran, Atil Yuksel, Hülya Kayserili, Zehra Oya Uyguner
Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures. Clinical genetics (2024)
Volkan Karaman, Esin Karakılıc Ozturan, Şükran Poyrazoğlu, Metin Yusuf Gelmez, Firdevs Baş, Feyza Darendelıler, Zehra Oya Uyguner
Novel variants ensued genomic imprinting in familial central precocious puberty. Journal of endocrinological investigation 47 (8) (2024)
Gozde Tutku Turgut, Umut Altunoglu, Cagri Gulec, Tugba Sarac Sivrikoz, Tuğba Kalaycı, Guven Toksoy, Şahin Avcı, Behiye Tuğçe Yıldırım, Gözde Yeşil Sayın, Ibrahim Halil Kalelioglu, Birsen Karaman, Recep Has, Seher Başaran, Atil Yuksel, Hülya Kayserili, Zehra Oya Uyguner
Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures. Clinical genetics (2024)
Volkan Karaman, Esin Karakılıc Ozturan, Şükran Poyrazoğlu, Metin Yusuf Gelmez, Firdevs Baş, Feyza Darendelıler, Zehra Oya Uyguner
Novel variants ensued genomic imprinting in familial central precocious puberty. Journal of endocrinological investigation (2024)
Volkan Karaman, Esin Karakılıc Ozturan, Şükran Poyrazoğlu, Metin Yusuf Gelmez, Firdevs Baş, Feyza Darendelıler, Zehra Oya Uyguner
Novel variants ensued genomic imprinting in familial central precocious puberty. Journal of endocrinological investigation 47 (8) (2024)
Gozde Tutku Turgut, Umut Altunoglu, Cagri Gulec, Tugba Sarac Sivrikoz, Tuğba Kalaycı, Guven Toksoy, Şahin Avcı, Behiye Tuğçe Yıldırım, Gözde Yeşil Sayın, Ibrahim Halil Kalelioglu, Birsen Karaman, Recep Has, Seher Başaran, Atil Yuksel, Hülya Kayserili, Zehra Oya Uyguner
Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures. Clinical genetics 105 (6) (2024)
Volkan Karaman, Esin Karakılıc Ozturan, Şükran Poyrazoğlu, Metin Yusuf Gelmez, Firdevs Baş, Feyza Darendelıler, Zehra Oya Uyguner
Novel variants ensued genomic imprinting in familial central precocious puberty. Journal of endocrinological investigation 47 (8) (2024)
Volkan Karaman, Esin Karakılıc Ozturan, Şükran Poyrazoğlu, Metin Yusuf Gelmez, Firdevs Baş, Feyza Darendelıler, Zehra Oya Uyguner
Novel variants ensued genomic imprinting in familial central precocious puberty. Journal of endocrinological investigation 47 (8) (2024)
Irem Kalay, Cagri Gulec, Mehmet Cihan Balcı, Guven Toksoy, Gulden Gokcay, Seher Basaran, Mubeccel Demirkol, Zehra Oya Uyguner
Novel GALT variations and genetic spectrum in Turkish population with the correlation of genotype and phenotype. Annals of human genetics (2023)
Esin Karakılıc Ozturan, Umut Altunoglu, Ayse Pinar Ozturk, Asli Derya Kardelen Al, Zehra Yavaş Abalı, Sahin Avci, Bernd Wollnik, Şükran Poyrazoğlu, Firdevs Baş, Zehra Oya Uyguner, Hülya Kayserili, Feyza Darendelıler
Evaluation of growth, puberty, osteoporosis, and the response to long-term bisphosphonate therapy in four patients with osteoporosis-pseudoglioma syndrome. American journal of medical genetics. Part A 188 (7) (2022)
Tuğba Kalaycı, Umut Altunoglu, Aytul Çorbacioglu Esmer, Sahin Avci, Tugba Sarac Sivrikoz, Birsen Karaman, İbrahim Kalelioğlu, Recep Has, Zehra Oya Uyguner, Atıl Yüksel, Seher Başaran, Hülya Kayserili
Fetal skeletal dysplasia cohort of a single tertiary referral center in Istanbul, Turkey. American journal of medical genetics. Part A (2022)
Gozde Tutku Turgut, Umut Altunoglu, Tugba Sarac Sivrikoz, Guven Toksoy, Tuğba Kalaycı, Şahin Avcı, Birsen Karaman, Cagri Gulec, Seher Başaran, Gözde Yeşil Sayın, Hülya Kayserili, Zehra Oya Uyguner
Functional loss of ubiquitin-specific protease 14 may lead to a novel distal arthrogryposis phenotype. Clinical genetics 101 (4) (2022)
Neşe Akcan, Zehra Oya Uyguner, Firdevs Baş, Umut Altunoglu, Güven Toksoy, Birsen Karaman, Sahin Avci, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Agharza Aghayev, Volkan Karaman, Rüveyde Bundak, Seher Başaran, Feyza Darendelıler
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD Journal of clinical research in pediatric endocrinology 14 (2) (2022)
Dilek Uludağ Alkaya, Zehra Oya Uyguner, Nilay Güneş, Beyhan Tüysüz
Long-term follow-up findings in a Turkish girl with osteogenesis imperfecta type XX caused by a homozygous MESD variant. American journal of medical genetics. Part A 188 (5) (2022)
Gamze Guven, Bedia Samanci, Cagri Gulec, Hasmet Hanagasi, Hakan I Gürvit, Ebru Erzurumluoglu Gokalp, Fatih Tepgec, Suleyman Guler, Zehra Oya Uyguner, Basar Bilgiç
A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer's disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 42 (6) (2021)
Ezgi Gizem Berkay, Leyla Elkanova, Tuğba Kalaycı, Dilek Uludağ Alkaya, Umut Altunoglu, Kıvanç Cefle, Ercan Mıhçı, Banu Nur, Elifcan Taşdelen, Zuhal Bayramoğlu, Volkan Karaman, Güven Toksoy, Nilay Güneş, Şükrü Öztürk, Şükrü Palandüz, Hülya Kayserili, Beyhan Tüysüz, Zehra Oya Uyguner
Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey. American journal of medical genetics. Part A 185 (8) (2021)