Ömer Arda Çetinkaya (Arda Cetinkaya)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 6

Top Topics

Intellectual Disability

Dna Methylation

Saccharomyces Cerevisiae

Top Venues

European journal of human genetics : EJHG

Congenital anomalies

European journal of breast health

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

Publications

Naz Guleray Lafci, Mark van Goor, Semra Cetinkaya, Jenny van der Wijst, Melisa Acun, Fatma Kurt Colak, Ömer Arda Çetinkaya, Joost G J Hoenderop
Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria. European journal of human genetics : EJHG (2024)
Naz Guleray Lafci, Mark van Goor, Semra Cetinkaya, Jenny van der Wijst, Melisa Acun, Fatma Kurt Colak, Ömer Arda Çetinkaya, Joost G J Hoenderop
Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria. European journal of human genetics : EJHG (2024)
Jarred W Rensvold, Evgenia Shishkova, Yuriy Sverchkov, Ian J Miller, Ömer Arda Çetinkaya, Angela Pyle, Mateusz Manicki, Dain R Brademan, Yasemin Alanay, Julian Raiman, Adam Jochem, Paul D Hutchins, Sean R Peters, Vanessa Linke, Katherine A Overmyer, Austin Z Salome, Alexander S Hebert, Catherine E Vincent, Nicholas W Kwiecien, Matthew J P Rush, Michael S Westphall, Mark Craven, Nurten A Akarsu, Robert W Taylor, Joshua J Coon, David J Pagliarini
Defining mitochondrial protein functions through deep multiomic profiling. Nature 606 (7913) (2022)
Marie-Françoise O'Donohue, Lydie M Da Costa, Marco Lezzerini, Sule Unal, Clément Joret, Marije Bartels, Eva Brilstra, Marijn Scheijde-Vermeulen, Ludivine Wacheul, Kim De Keersmaecker, Stijn Vereecke, Veerle Labarque, Manon Saby, Sophie D Lefevre, Jessica Platon, Nathalie Montel-Lehry, Nathalie Laugero, Eric Lacazette, Koen van Gassen, Riekelt H L Houtkooper, Pelin Ozlem Simsek-Kiper, Thierry Leblanc, Nese Yarali, Ömer Arda Çetinkaya, Nurten A Akarsu, Pierre-Emmanuel Gleizes, Denis L J Lafontaine, Alyson W MacInnes
HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia. Blood 139 (21) (2022)
Ömer Arda Çetinkaya, Süleyman Utku Çelik, Serdar Gökay Terzioğlu, Aydan Eroğlu
Re: The Predictive Value of the Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratio in Patients with Recurrent Idiopathic Granulomatous Mastitis. European journal of breast health 16 (3) (2020)
Ömer Arda Çetinkaya, Ali Karaman, Mehmet Burak Mutlu, Taner Yavuz
Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg. Congenital anomalies 58 (1) (2017)