Publications & Works

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

The impact and future of artificial intelligence in medical genetics and molecular medicine: an ongoing revolution

Özçelik F., Dundar M., Yıldırım A., Henehan G., Vicente O., Sanchez-Alcazar J. A., et al.
FUNCTIONAL & INTEGRATIVE GENOMICS , vol.24, no.4, 2024 (SCI-Expanded) identifier identifier identifier

Deciphering the host genetic factors conferring susceptibility to severe COVID-19 using exome sequencing

Uslu K., Ozcelik F., Zararsiz G., Eldem V., Cephe A., Sahin I. O., et al.
GENES AND IMMUNITY , vol.25, no.1, pp.14-42, 2024 (SCI-Expanded) Sustainable Development identifier identifier identifier

A case of autoimmune lymphoproliferative syndrome with a novel de novo FAS variant

ÖZÇELİK F., ASLAN K., Gok V., Ari M. B., ÖZCAN A., EKEN A., et al.
Pediatric Hematology and Oncology , vol.41, no.4, pp.301-309, 2024 (SCI-Expanded) identifier identifier identifier

PPM1K defects cause mild maple syrup urine disease: The second case in the literature

ÖZÇELİK F., ARSLAN S., Ozguc Caliskan B., KARDAŞ F., ÖZKUL Y., DÜNDAR M.
American Journal of Medical Genetics, Part A , vol.191, no.5, pp.1360-1365, 2023 (SCI-Expanded) identifier identifier identifier

A Case of Short Stature Caused by a Mutation in the ACAN Gene

KARATAŞ E., DEMİR M., ÖZÇELİK F., KARA L., Akyurek E., BERBER U., et al.
MOLECULAR SYNDROMOLOGY , vol.14, no.2, pp.123-128, 2023 (SCI-Expanded) identifier identifier identifier

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.
FUNCTIONAL & INTEGRATIVE GENOMICS , vol.22, no.3, pp.291-315, 2022 (SCI-Expanded) Sustainable Development identifier identifier identifier

A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A

SARIKAYA E., ÖZÇELİK F., GÜL ŞİRAZ Ü., HATİPOĞLU N., GÜNEŞ T., DÜNDAR M.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.6, pp.845-850, 2022 (SCI-Expanded) identifier identifier identifier

Refereed Congress / Symposium Publications in Proceedings

Self Mutilasyon Etiyolojisinde Nadir Vaka: PRX ve SCN9A Mutasyonu Bir Arada

Doğan Y. E., Canpolat M., Özçelik F., Öztürk S., Özbek Tezcan F., Dündar M.
65.Türkiye Milli Pediatri Derneği Kongresi, Antalya, Turkey, 3 - 07 November 2021, pp.77

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