Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration
Bilguvar, Kaya, Tyagi, Navneet K., Ozkara, Cigdem, Tuysuz, Beyhan, Bakircioglu, Mehmet, Choi, Murim, Delil, Sakir, Caglayan, Ahmet O., Baranoski, Jacob F., Erturk, Ozdem, Yalcinkaya, Cengiz, Karacorlu, Murat, Dincer, Alp, Johnson, Michele H., Mane, Shrikant, Chandra, Sreeganga S., Louvi, Angeliki, Boggon, Titus J., Lifton, Richard P., Horwich, Arthur L., Gunel, Murat
Published in Proceedings of the National Academy of Sciences - PNAS (26.02.2013)
Published in Proceedings of the National Academy of Sciences - PNAS (26.02.2013)
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Journal Article
Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly
Sgourdou, Paraskevi, Mishra-Gorur, Ketu, Saotome, Ichiko, Henagariu, Octavian, Tuysuz, Beyhan, Campos, Cynthia, Ishigame, Keiko, Giannikou, Krinio, Quon, Jennifer L., Sestan, Nenad, Caglayan, Ahmet O., Gunel, Murat, Louvi, Angeliki
Published in Scientific reports (08.03.2017)
Published in Scientific reports (08.03.2017)
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Journal Article
Selection of techniques for reducing shipping NOx and SOx emissions
Yang, Z.L., Zhang, D., Caglayan, O., Jenkinson, I.D., Bonsall, S., Wang, J., Huang, M., Yan, X.P.
Published in Transportation research. Part D, Transport and environment (01.08.2012)
Published in Transportation research. Part D, Transport and environment (01.08.2012)
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Journal Article
A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP
Çağlayan, Ahmet O, Tüysüz, Beyhan, Coşkun, Süleyman, Quon, Jennifer, Harmancı, Akdes S, Baranoski, Jacob F, Baran, Burçin, Erson-Omay, E Zeynep, Henegariu, Octavian, Mane, Shrikant M, Bilgüvar, Kaya, Yasuno, Katsuhito, Günel, Murat
Published in Journal of human genetics (01.05.2016)
Published in Journal of human genetics (01.05.2016)
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Journal Article
Oxidative stress markers in young patients with polycystic ovary syndrome, the relationship between insulin resistances
Karadeniz, M, Erdoğan, M, Tamsel, S, Zengi, A, Alper, G E, Cağlayan, O, Saygili, F, Yilmaz, C
Published in Experimental and clinical endocrinology & diabetes (01.04.2008)
Published in Experimental and clinical endocrinology & diabetes (01.04.2008)
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Journal Article
A novel DNA biosensor based on ellipsometry
Demirel, Gökhan, Çağlayan, Mustafa O., Garipcan, Bora, Pişkin, Erhan
Published in Surface science (15.02.2008)
Published in Surface science (15.02.2008)
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Journal Article
Thrombin-activatable fibrinolysis inhibitor and cardiovascular risk factors in polycystic ovary syndrome
Erdoğan, M, Karadeniz, M, Alper, G E, Tamsel, S, Uluer, H, Cağlayan, O, Saygili, F, Yilmaz, C
Published in Experimental and clinical endocrinology & diabetes (01.03.2008)
Published in Experimental and clinical endocrinology & diabetes (01.03.2008)
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Journal Article
Macroeconomic risk and hedge fund returns
Bali, Turan G., Brown, Stephen J., Caglayan, Mustafa O.
Published in Journal of financial economics (01.10.2014)
Published in Journal of financial economics (01.10.2014)
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Journal Article
Hot potatoes: Underpricing of stocks following extreme negative returns
Caglayan, Mustafa O., Lawrence, Edward, Reyes-Peña, Robinson
Published in Journal of banking & finance (01.04.2023)
Published in Journal of banking & finance (01.04.2023)
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Journal Article
DNA damage and its relationship with other oxidative stress parameters in Behcet’s disease
Sezer, E. D., Aksu, K., Caglayan, O., Keser, G., Karabulut, G., Ercan, G.
Published in Rheumatology international (2012)
Published in Rheumatology international (2012)
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Journal Article
Increased oxidative DNA damage in lean normoglycemic offspring of type 2 diabetic patients
Zengi, A, Ercan, G, Caglayan, O, Tamsel, S, Karadeniz, M, Simsir, I, Harman, E, Kahraman, C, Orman, M, Cetinkalp, S, Ozgen, G
Published in Experimental and clinical endocrinology & diabetes (01.09.2011)
Published in Experimental and clinical endocrinology & diabetes (01.09.2011)
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Journal Article
Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum
Caglayan, AO, Per, H, Akgumus, G, Gumus, H, Baranoski, J, Canpolat, M, Calik, M, Yikilmaz, A, Bilguvar, K, Kumandas, S, Gunel, M
Published in Clinical genetics (01.10.2013)
Published in Clinical genetics (01.10.2013)
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Journal Article
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey
Kalb, S, Caglayan, AO, Degerliyurt, A, Schmid, S, Ceylaner, S, Hatipoglu, N, Hinderhofer, K, Rehder, H, Kurtoglu, S, Ceylaner, G, Zschocke, J, Witsch-Baumgartner, M
Published in Clinical genetics (01.06.2012)
Published in Clinical genetics (01.06.2012)
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Journal Article