Ömer Arda Çetinkaya

6PUBLICATIONS
32CO-AUTHORS
Anthropological geneticsCancer geneticsMedical biochemistry - proteins and peptides (incl. medical proteomics)Epigenetics (incl. genome methylation and epigenomics)Applied immunology (incl. antibody engineering, xenotransplantation and t-cell therapies)
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Publications (6)

|Jan 07, 2025
Extreme Phenotypic Variation in Siblings with Identical Homozygous Mutations Causing ADA2 Deficiency: A Case Series

Muhammed D Aksu, Seza Özen, Tekin Aksu

|Mar 26, 2024
Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria.

Naz Guleray Lafci, Mark van Goor, Semra Cetinkaya

|May 25, 2022
Defining mitochondrial protein functions through deep multiomic profiling.

Jarred W Rensvold, Evgenia Shishkova, Yuriy Sverchkov

|Feb 25, 2022
HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia.

Marie-Françoise O'Donohue, Lydie Da Costa, Marco Lezzerini

|Jul 14, 2020
Re: The Predictive Value of the Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratio in Patients with Recurrent Idiopathic Granulomatous Mastitis.

Ömer Arda Çetinkaya, Süleyman Utku Çelik, Serdar Gökay Terzioğlu

|Mar 22, 2017
Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg.

Arda Cetinkaya, Ali Karaman, Mehmet Burak Mutlu

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Frequent Collaborators

2 joint publications

Nurten A Akarsu

1 joint publications

Marie-Françoise O'Donohue

1 joint publications

Lydie Da Costa

1 joint publications

Marije Bartels