Ferda Özkınay (Ferda Ozkinay, F Özkınay)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Venues

Journal of clinical research in pediatric endocrinology

American journal of medical genetics. Part A

European journal of haematology

Journal of endocrinological investigation

Ege Universitesi

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

Affiliation History

Ege Universitesi Jun 01 1979

Turkey

Prof :: Medical Genetics, Pediatrics

Publications

Esra Isik, Yesim Aydinok, Canan Albayrak, Basak Durmus, Zeynep Karakas, Mehmet Fatih Orhan, Nazan Sarper, Sultan Aydin Köker, Selma Unal, Yeşim Oymak, Nihal Karadaş, Ayşen Türedi Yıldırım, Davut Albayrak, Funda Tayfun Küpesiz, Deniz Tuğcu, Serap Karaman, Mahmut Töbü, Ekrem Ünal, Alper Ozcan, Sule Unal, Tekin Aksu, Ayşegül Ünüvar, Mustafa Bilici, Fatih Mehmet Azık, Yilmaz Ay, Sema Aylan Gelen, Emine Zengin, Esin Albudak, Ibrahim Eker, Taner Karakaya, Ozgur Cogulu, Ferda Özkınay, Tahir Atik
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis. European journal of haematology (2024)
Esra Isik, Yesim Aydinok, Canan Albayrak, Basak Durmus, Zeynep Karakas, Mehmet Fatih Orhan, Nazan Sarper, Sultan Aydin Köker, Selma Unal, Yeşim Oymak, Nihal Karadaş, Ayşen Türedi Yıldırım, Davut Albayrak, Funda Tayfun Küpesiz, Deniz Tuğcu, Serap Karaman, Mahmut Töbü, Ekrem Ünal, Alper Ozcan, Sule Unal, Tekin Aksu, Ayşegül Ünüvar, Mustafa Bilici, Fatih Mehmet Azık, Yilmaz Ay, Sema Aylan Gelen, Emine Zengin, Esin Albudak, Ibrahim Eker, Taner Karakaya, Ozgur Cogulu, Ferda Özkınay, Tahir Atik
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis. European journal of haematology 113 (1) (2024)
Gokcen Karamik, Beyhan Tüysüz, Esra Isik, Aysegul Yilmaz, Yasemin Alanay, Evrim Cifci Sunamak, Enise Avci Durmusalioglu, Ferda Özkınay, Gökhan Ozan Çetin, Nuray Ozturk, Ercan Mihci, Banu Nur
The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review. American journal of medical genetics. Part A (2023)
Mehmet Burak Durmaz, Hilmi Bolat, Zehra Cengisiz, Fuat Akercan, Tuba Sözen Türk, Erhan Parıltay, Aslı Ece Solmaz, Mert Kazandi, Emin Karaca, Asude Alpman Durmaz, Ayça Aykut, Sermet Sağol, Haluk Akın, Ferda Özkınay, Ozgur Cogulu
20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey Turkish journal of medical sciences 51 (4) (2021)
Guner Ozenen Gizem, Zümrüt Şahbudak Bal, Zuhal Umit, Nimet Melis Bilen, Yildirim Arslan Sema, Ali Yurtseven, Eylem Ulas Saz, Barutcuoglu Burcu, Rüçhan Sertöz, Nuri Zafer Kurugöl, Ferda Özkınay
Demographic, clinical, and laboratory features of COVID-19 in children: The role of mean platelet volume in predicting hospitalization and severity. Journal of medical virology 93 (5) (2021)
Birsen Şentürk Pilan, Nazlı Burcu Özbaran, Didem Çelik, Tuğçe Özcan, Samim Özen, Ruhsar Damla Gökşen Şimşek, İbrahim Ulman, Ali Avanoğlu, Sibel Tiryaki, Hüseyin Onay, Ozgur Cogulu, Ferda Özkınay, Şükran Darcan
Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Tahir Atik, Esra Işık, Hüseyin Onay, Bilçağ Akgün, Moharram Shamsali, Kaan Kavaklı, Melike Sezgin Evim, Gülen Tüysüz, Namık Yaşar Özbek, Fahri Şahin, Zafer Salcıoğlu, Canan Albayrak, Yeşim Oymak, Ekrem Ünal, Fatma Burcu Belen, Ebru Yılmaz Keskin, Can Balkan, Birol Baytan, Alphan Küpesiz, Vildan Culha, Tuba Nur Tahtakesen, Adalet Meral Güneş, Ferda Özkınay
Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations Turkish journal of haematology : official journal of Turkish Society of Haematology 37 (3) (2020)
Esra Isik, Duygu Arican, Tahir Atik, Joo Enn Ooi, Şükran Darcan, Samim Özen, Pelin Özlem Şimsek Kiper, Gülen Eda Utine, Ozgur Cogulu, Ferda Özkınay
A rare cause of syndromic short stature: 3M syndrome in three families. American journal of medical genetics. Part A 185 (2) (2020)
Edip Unal, Amine Aktar Karakaya, Aslı Beştaş, Ruken Yıldırım, Funda Feryal Taş, Hüseyin Onay, Ferda Özkınay, Yusuf Kenan Haspolat
Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families. Journal of endocrinological investigation 44 (6) (2020)
Asude Alpman Durmaz, Ayça Aykut, Tahir Atik, Samim Özen, Durdugül Ayyıldız Emecen, Aysun Ata, Esra Isik, Ruhsar Damla Gökşen Şimşek, Ozgur Cogulu, Ferda Özkınay
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Esra Isik, Hüseyin Onay, Tahir Atik, Aslı Ece Solmaz, Samim Özen, Ozgur Cogulu, Şükran Darcan, Ferda Özkınay
A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia Journal of clinical research in pediatric endocrinology 12 (1) (2019)
Samim Özen, Tahir Atik, Özlem Korkmaz, Hüseyin Onay, Damla Gökşen, Ferda Özkınay, Ozgur Cogulu, Şükran Darcan
Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene Journal of clinical research in pediatric endocrinology 12 (1) (2019)

Ferda Özkınay.css-eqlu8i{font-size:small;padding-left:4px;} (Ferda Ozkinay, F Özkınay)

Publication Activity (10 Years)

Top Topics

Top Venues

Ferda Özkınay (Ferda Ozkinay, F Özkınay)