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Tayfun Ozcelik
Tayfun Ozcelik
Bilkent University, Department of Molecular Biology and Genetics
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Cited by
Year
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Q Zhang, P Bastard, Z Liu, J Le Pen, M Moncada-Velez, J Chen, M Ogishi, ...
Science 370 (6515), eabd4570, 2020
21202020
Trembler mouse carries a point mutation in a myelin gene
U Suter, AA Welcher, T Özcelik, GJ Snipes, B Kosaras, U Francke, ...
Nature 356 (6366), 241-244, 1992
4991992
Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths
P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ...
Science immunology 6 (62), eabl4340, 2021
4292021
Mutation of the human circadian clock gene CRY1 in familial delayed sleep phase disorder
A Patke, PJ Murphy, OE Onat, AC Krieger, T Özçelik, SS Campbell, ...
Cell 169 (2), 203-215. e13, 2017
3462017
X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19
T Asano, B Boisson, F Onodi, D Matuozzo, M Moncada-Velez, ...
Science immunology 6 (62), eabl4348, 2021
3252021
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region
T Özçelik, S Leff, W Robinson, T Donlon, M Lalande, E Sanjines, ...
Nature genetics 2 (4), 265-269, 1992
3221992
Human MLH1 Deficiency Predisposes to Hematological Maligancy and Neurofibromatosis Type
MD Ricciardone, T Ozçelik, B Cevher, H Ozdag, M Tuncer, A Gürgey, ...
Cancer research 59 (2), 290-293, 1999
3111999
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region
SE Leff, CI Brannan, ML Reed, T Özçelik, U Francke, NG Copeland, ...
Nature genetics 2 (4), 259-264, 1992
3071992
Structural and functional conservation of synaptotagmin (p65) in Drosophila and humans.
MS Perin, PA Johnston, T Ozcelik, R Jahn, U Francke, TC Südhof
Journal of Biological Chemistry 266 (1), 615-622, 1991
2961991
Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization
O Ibraghimov-Beskrovnaya, A Milatovich, T Ozcelik, B Yang, K Koepnick, ...
Human molecular genetics 2 (10), 1651-1657, 1993
2921993
A structural homologue of the N-formyl peptide receptor. Characterization and chromosome mapping of a peptide chemoattractant receptor family.
PM Murphy, T Ozcelik, RT Kenney, HL Tiffany, D McDermott, U Francke
Journal of Biological Chemistry 267 (11), 7637-7643, 1992
2751992
Circulating endothelial progenitor cells in multiple myeloma: implications and significance
H Zhang, V Vakil, M Braunstein, ELP Smith, J Maroney, L Chen, K Dai, ...
Blood 105 (8), 3286-3294, 2005
2552005
A global effort to define the human genetics of protective immunity to SARS-CoV-2 infection
JL Casanova, HC Su, L Abel, A Aiuti, S Almuhsen, AA Arias, P Bastard, ...
Cell 181 (6), 1194-1199, 2020
2512020
Coagulation factor V gene mutation increases the risk of venous thrombosis in Behçet's disease
A Gül, U Özbek, C Öztürk, M Inanc, M Konice, T Özçelik
Rheumatology 35 (11), 1178-1180, 1995
2051995
Skewed X chromosome inactivation in blood cells of women with scleroderma
Z Özbalkan, S Baǧışlar, S Kiraz, CB Akyerli, HTE Özer, Ş Yavuz, AM Birlik, ...
Arthritis & Rheumatism 52 (5), 1564-1570, 2005
1902005
Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant
S Boisson-Dupuis, N Ramirez-Alejo, Z Li, E Patin, G Rao, G Kerner, ...
Science immunology 3 (30), eaau8714, 2018
1682018
Structures and chromosomal localizations of two human genes encoding synaptobrevins 1 and 2.
BT Archer 3rd, T Ozcelik, R Jahn, U Francke, TC Südhof
Journal of Biological Chemistry 265 (28), 17267-17273, 1990
1641990
Mitochondrial serine protease HTRA2 p. G399S in a kindred with essential tremor and Parkinson disease
H Unal Gulsuner, S Gulsuner, FN Mercan, OE Onat, T Walsh, H Shahin, ...
Proceedings of the National Academy of Sciences 111 (51), 18285-18290, 2014
1572014
Structure and chromosomal localization of the mammalian agrin gene
F Rupp, T Ozcelik, M Linial, K Peterson, U Francke, R Scheller
Journal of Neuroscience 12 (9), 3535-3544, 1992
1441992
Molecular evolution of the human interleukin–8 receptor gene cluster
SK Ahuja, T Özçelik, A Milatovitch, U Francke, PM Murphy
Nature genetics 2 (1), 31-36, 1992
1441992
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