Taner Karakaya

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 6

Top Topics

Intellectual Disability

Polycystic Kidney Disease

Top Venues

European journal of haematology

American journal of medical genetics. Part A

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

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)
Ayça Kocaaga, Yesim Özdemir Atikel, Mehtap Sak, Taner Karakaya
The genetic spectrum of polycystic kidney disease in children. Revista da Associacao Medica Brasileira (1992) 69 (11) (2023)
Taner Karakaya, Ayberk Turkyilmaz, Gunes Sager, Rahsan Inan, Oguzhan Yarali, Alper Han Cebi, Yasemin Akin
Molecular characterization of Turkish patients with demyelinating Charcot-Marie-Tooth disease. Neurogenetics 23 (3) (2022)
Taner Karakaya, Fatma Sılan, Ozturk Ozdemir
A New Mutation, Hb A 2 -Canakkale [δ10(A7)Ala→Val; HBD : c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A 2 Levels. Hemoglobin 46 (2) (2022)
Taner Karakaya, Ali Evren Bilgic, Deniz Eris, Burak Baser, Serdar Mermer, Onur Yildiz
Identification of a novel pathogenic variant in CKAP2L and literature review in a child with Filippi syndrome and congenital talipes equinovarus. American journal of medical genetics. Part A 185 (7) (2021)