Gozde Yesil Sayın (Gozde Yesil, Gözde Yesil Sayın, Gözde Yeşil)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 11

Top Topics

Intellectual Disability

Top Venues

Movement disorders : official journal of the Movement Disorder Society

Pediatric nephrology (Berlin, Germany)

Annals of dermatology

The International journal of neuroscience

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

Publications

Rauan Kaiyrzhanov, Juan Dario Ortigoza-Escobar, Brett W Stringer, Manizha Ganieva, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al-Shammari, Mohammed Al-Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil Sayın, Turkan Uygur, Karen Pysden, Ian R Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden, Reza Maroofian
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 39 (6) (2024)
Rauan Kaiyrzhanov, Juan Dario Ortigoza-Escobar, Brett W Stringer, Manizha Ganieva, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al-Shammari, Mohammed Al-Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil Sayın, Turkan Uygur, Karen Pysden, Ian R Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden, Reza Maroofian
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 39 (6) (2024)
Rauan Kaiyrzhanov, Juan Dario Ortigoza-Escobar, Brett W Stringer, Manizha Ganieva, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al-Shammari, Mohammed Al-Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil Sayın, Turkan Uygur, Karen Pysden, Ian R Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden, Reza Maroofian
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 39 (6) (2024)
Rauan Kaiyrzhanov, Juan Dario Ortigoza-Escobar, Brett W Stringer, Manizha Ganieva, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al-Shammari, Mohammed Al-Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil Sayın, Turkan Uygur, Karen Pysden, Ian R Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden, Reza Maroofian
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society (2024)
Emrah Yücesan, Beyza Goncu, Cemil Ozgul, Arda Kebapci, Ayca Dilruba Aslanger, Enes Akyuz, Gozde Yesil Sayın
Functional Characterization of KCNMA1 mutation associated with dyskinesia, seizure, developmental delay, and cerebellar atrophy. The International journal of neuroscience (2023)
Naci Senkal, Istemi Serin, Sacide Pehlivan, Mustafa Pehlivan, Alpay Medetalibeyoglu, Timurhan Cebeci, Hilal Konyaoglu, Yasemin Oyacı, Gozde Yesil Sayın, Ummuhan Isoglu-Alkac, Tufan Tukek, Murat Köse
The effect of DNA repair gene variants on COVID-19 disease: susceptibility, severity, and clinical course. Nucleosides, nucleotides & nucleic acids (2023)
Ilayda Altun, Seha Kamil Saygili, Nur Canpolat, Yasemin Ozluk, Ozge Hurdogan, Gozde Yesil Sayın, Salim Caliskan, Fatma Lale Sever
Strong mesangial IgA staining-does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Answers. Pediatric nephrology (Berlin, Germany) 36 (7) (2021)
Sacide Pehlivan, Murat Köse, Sevim Meşe, Istemi Serin, Naci Şenkal, Yasemin Oyaci, Alpay Medetalibeyoglu, Mustafa Pehlivan, Gozde Yesil Sayın, Ummihan Isoglu-Alkac, Tufan Tukek
Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (-) patients. Pathogens and global health (2021)
Ayse B Kolemen, Enes Akyuz, Ali Toprak, Erdem Deveci, Gozde Yesil Sayın
Evaluation of the parents' anxiety levels before and after the diagnosis of their child with a rare genetic disease: the necessity of psychological support. Orphanet journal of rare diseases 16 (1) (2021)
Ilayda Altun, Seha Kamil Saygili, Nur Canpolat, Yasemin Ozluk, Ozge Hurdogan, Gozde Yesil Sayın, Salim Caliskan, Fatma Lale Sever
Strong mesangial IgA staining-does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Questions. Pediatric nephrology (Berlin, Germany) 36 (7) (2021)
Emin Özlü, Ayşe Serap Karadağ, Ibrahim Akalin, Gozde Yesil Sayın, Sarenur Yılmaz, İlkin Zindancı, Tugba Kevser Uzuncakmak, Seyma Ozkanlı, Necmettin Akdeniz
Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome. Annals of dermatology 31 (Suppl) (2019)