Hüseyin Onay (Huseyin Onay, H Onay)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 17

Top Topics

Intellectual Disability

Chemotherapy Induced

Top Venues

Journal of clinical research in pediatric endocrinology

Journal of pediatric endocrinology & metabolism : JPEM

Cardiovascular diagnosis and therapy

Turkish journal of haematology : official journal of Turkish Society of Haematology

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

Publications

Sandra Marques E Silva, Andrea Virginia Ferreira Chaves, Murillo Antunes, Juan Pablo Costabel, Armando Alves da Fonseca, Adriana Furtado, Juan Esteban Gomez-Mesa, Francisco Javier Marin Gutiérrez, Oren Caspi, Irina Maksimova, Manish Maski, Cecilia Micheletti, José Luiz Barros Pena, Márcia Gonçalves Ribeiro, Maria Juliana Rodríguez-González, Omac Tufekcioglu, Hüseyin Onay
Multinational experience with next-generation sequencing: opportunity to identify transthyretin cardiac amyloidosis and Fabry disease. Cardiovascular diagnosis and therapy 14 (2) (2024)
Ferda Evin, Tahir Atik, Hüseyin Onay, Ruhsar Damla Gökşen Şimşek, Şükran Darcan, Ozgur Cogulu, Samim Özen
Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta. Journal of pediatric endocrinology & metabolism : JPEM (2024)
Ilayda Korkmaz, Sema Kalkan Uçar, Hüseyin Onay, Eser Yıldırım Sözmen, Mahmut Çoker, Melis Palamar
Ocular Manifestations of Fabry Disease: Report from a Tertiary Eye Care Center in Türkiye. Turkish journal of ophthalmology 54 (3) (2024)
Ferda Evin, Tahir Atik, Hüseyin Onay, Ruhsar Damla Gökşen Şimşek, Şükran Darcan, Ozgur Cogulu, Samim Özen
Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta. Journal of pediatric endocrinology & metabolism : JPEM 37 (8) (2024)
Sandra Marques E Silva, Andrea Virginia Ferreira Chaves, Murillo Antunes, Juan Pablo Costabel, Armando Alves da Fonseca, Adriana Furtado, Juan Esteban Gomez-Mesa, Francisco Javier Marin Gutiérrez, Oren Caspi, Irina Maksimova, Manish Maski, Cecilia Micheletti, José Luiz Barros Pena, Márcia Gonçalves Ribeiro, Maria Juliana Rodríguez-González, Omac Tufekcioglu, Hüseyin Onay
Multinational experience with next-generation sequencing: opportunity to identify transthyretin cardiac amyloidosis and Fabry disease. Cardiovascular diagnosis and therapy 14 (2) (2024)
Ferda Evin, Esra Isik, Hüseyin Onay, Samim Özen, Şükran Darcan, Ruhsar Damla Gökşen Şimşek
ABCC8-related maturity-onset diabetes of the young: switching from insulin to sulphonylurea therapy: how long do we need for a good metabolic control? Journal of pediatric endocrinology & metabolism : JPEM (2023)
Taylan Öztürk, Ezgi Karataş Yiğitaslan, Pelin Teke Kisa, Hüseyin Onay, Ali Osman Saatci
Lipemia Retinalis Diagnosed Incidentally After Laser Photocoagulation Treatment for Retinopathy of Prematurity Turkish journal of ophthalmology 51 (5) (2022)
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)
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)
Duygu Tekin, Gökengin Deniz, Hüseyin Onay, Memnune Selda Erensoy, Rüçhan Sertöz
Investigation of drug resistance against protease, reverse transcriptase, and integrase inhibitors by next-generation sequencing in HIV-positive patients. Journal of medical virology 93 (6) (2020)
Nihal Mete Gökmen, César Rodríguez-Alcalde, Okan Gülbahar, Margarita Lopez-Trascasa, Hüseyin Onay, Alberto López-Lera
Novel homozygous variants in the SERPING1 gene in two Turkish families with hereditary angioedema of recessive inheritance. Immunology and cell biology 98 (8) (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)
Edip Unal, Ruken Yıldırım, Funda Feryal Taş, Vasfiye Demir, Hüseyin Onay, Yusuf Kenan Haspolat
Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene Journal of clinical research in pediatric endocrinology 10 (4) (2018)
Edip Unal, Ruken Yıldırım, Suat Tekin, Vasfiye Demir, Hüseyin Onay, Yusuf Kenan Haspolat
A Novel Mutation of AMHR2 in Two Siblings with Persistent Müllerian Duct Syndrome Journal of clinical research in pediatric endocrinology 10 (4) (2018)
Lale Olcay, Şule Ünal, Hüseyin Onay, Esra Erdemli, Ayşenur Öztürk, Deniz Billur, Ayse Metin, Hamza Okur, Zeynep Yildiz Yildirmak, Yahya Buyukasik, Aydan İkincioğulları, Mesude Falay, Gülsüm Özet, Sevgi Yetgin
Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death Turkish journal of haematology : official journal of Turkish Society of Haematology 35 (4) (2018)