Tuğba Kalaycı (Tuğba Kalayci, Tugba Kalayci)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 14

Top Topics

Multiple Myeloma

Intellectual Disability

Muscular Dystrophy

Top Venues

Clinical rheumatology

Clinical genetics

American journal of medical genetics. Part A

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)
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)
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)
Ece Çepni, Esra Börklü, Sahin Avci, Tuğba Kalaycı, Serpil Eraslan, Hülya Kayserili
Revisiting TOP2B-related phenotypes: Three new cases and literature review. Clinical genetics (2023)
Arjan F Theil, Alex Pines, Tuğba Kalaycı, José M Heredia-Genestar, Anja Raams, Marion H Rietveld, Sriram Sridharan, Sabine Ej Tanis, Klaas W Mulder, Nesimi Buyukbabani, Birsen Karaman, Zehra O Uyguner, Hülya Kayserili, Jan Hj Hoeijmakers, Hannes Lans, Jeroen Aa Demmers, Joris Pothof, Umut Altunoglu, Abdoelwaheb El Ghalbzouri, Wim Vermeulen
Trichothiodystrophy-associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiation. EMBO molecular medicine (2023)
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tuğba Kalaycı, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies. Genes 13 (12) (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)
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tuğba Kalaycı, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies. Genes 13 (12) (2022)
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tuğba Kalaycı, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies. Genes 13 (12) (2022)
Ahmet Burak Dirim, Tuğba Kalaycı, Seda Safak, Nurana Güller, Burak Gultekin, Ozge Hurdogan, Seyhun Solakoglu, Halil Yazici, Kıvanç Çefle, Şükrü Öztürk, Alaattin Yildiz
Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature. Clinical rheumatology 42 (2) (2022)
Ahmet Burak Dirim, Tuğba Kalaycı, Seda Safak, Nurana Güller, Burak Gultekin, Ozge Hurdogan, Seyhun Solakoglu, Halil Yazici, Kıvanç Çefle, Şükrü Öztürk, Alaattin Yildiz
Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature. Clinical rheumatology 42 (2) (2022)
Ahmet Burak Dirim, Tuğba Kalaycı, Seda Safak, Nurana Güller, Burak Gultekin, Ozge Hurdogan, Seyhun Solakoglu, Halil Yazici, Kıvanç Çefle, Şükrü Öztürk, Alaattin Yildiz
Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature. Clinical rheumatology 42 (2) (2022)
Ahmet Burak Dirim, Tuğba Kalaycı, Seda Safak, Nurana Güller, Burak Gultekin, Ozge Hurdogan, Seyhun Solakoglu, Halil Yazici, Kıvanç Çefle, Şükrü Öztürk, Alaattin Yildiz
Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature. Clinical rheumatology (2022)
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tuğba Kalaycı, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies. Genes 13 (12) (2022)