Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families
Unal, E., Karakaya, A. A., Beştaş, A., Yıldırım, R., Taş, F. F., Onay, H., Özkınay, F., Haspolat, Y. K.
Published in Journal of endocrinological investigation (01.06.2021)
Published in Journal of endocrinological investigation (01.06.2021)
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Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel NAGLU gene mutations
Ozkinay, F., Emecen, D.A., Kose, M., Isik, E., Bozaci, A.E., Canda, E., Tuysuz, B., Zubarioglu, T., Atik, T., Onay, H.
Published in Molecular genetics and metabolism reports (01.06.2021)
Published in Molecular genetics and metabolism reports (01.06.2021)
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Journal Article
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations
Demir, T., Onay, H., Savage, D. B., Temeloglu, E., Uzum, A. K., Kadioglu, P., Altay, C., Ozen, S., Demir, L., Cavdar, U., Akinci, B.
Published in Diabetic medicine (01.10.2016)
Published in Diabetic medicine (01.10.2016)
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A novel mutation in steroidogenic factor (SF1/NR5A1) gene in a patient with 46 XY DSD without adrenal insufficiency
Tuhan, H., Anik, A., Catli, G., Onay, H., Aykut, A., Abaci, A., Bober, E.
Published in Andrologia (01.02.2017)
Published in Andrologia (01.02.2017)
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Journal Article
Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?
Schallreuter, K U, Bahadoran, P, Picardo, M, Slominski, A, Elassiuty, YE, Kemp, E H, Giachino, C, Liu, J B, Luiten, R M, Lambe, T, Le Poole, IC, Dammak, I, Onay, H, Zmijewski, MA, Dell'Anna, M L, Zeegers, M P, Cornall, R J, Paus, R, Ortonne, J P, Westerhof, W
Published in Experimental dermatology (01.02.2008)
Published in Experimental dermatology (01.02.2008)
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Journal Article
Superoxide dismutase 1 and 2 gene polymorphism in Turkish vitiligo patients
Tuna, A, Ozturk, G, Gerceker, TB, Karaca, E, Onay, H, Guvenc, SM, Cogulu, O
Published in Balkan journal of medical genetics (29.12.2017)
Published in Balkan journal of medical genetics (29.12.2017)
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Journal Article
Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?
Ralf Paus, Lübeck, Schallreuter, K. U., Bahadoran, P., Picardo, M., Slominski, A., Elassiuty, Y. E., Kemp, E. H., Giachino, C., Liu, J. B., Luiten, R. M., Lambe, T., Le Poole, I. C., Dammak, I., Onay, H., Zmijewski, M. A., Dell'Anna, M. L., Zeegers, M. P., Cornall, R. J., Paus, R., Ortonne, J. P., Westerhof, W.
Published in Experimental dermatology (01.02.2008)
Published in Experimental dermatology (01.02.2008)
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Journal Article
Evidence that the wider social environment moderates the association between familial liability and psychosis spectrum outcome
Binbay, T., Drukker, M., Alptekin, K., Elbi, H., Tanık, F. Aksu, Özkınay, F., Onay, H., Zağlı, N., van Os, J.
Published in Psychological medicine (01.12.2012)
Published in Psychological medicine (01.12.2012)
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Journal Article
Mutation analysis of the NRXN1 gene in autism spectrum disorders
Onay, H, Kacamak, D, Kavasoglu, AN, Akgun, B, Yalcinli, M, Kose, S, Ozbaran, B
Published in Balkan journal of medical genetics (01.12.2016)
Published in Balkan journal of medical genetics (01.12.2016)
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Journal Article
In vitro gene manipulation of spinal muscular atrophy fibroblast cell line using gene-targeting fragment for restoration of SMN protein expression
Rashnonejad, A, Gündüz, C, Süslüer, S Y, Onay, H, Durmaz, B, Bandehpour, M, Özkınay, F
Published in Gene therapy (01.01.2016)
Published in Gene therapy (01.01.2016)
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Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann–Pick disease patients: Mutation profile and description of a novel mutation
Aykut, A., Karaca, E., Onay, H., Kalkan Ucar, S., Coker, M., Cogulu, O., Ozkinay, F.
Published in Gene (10.09.2013)
Published in Gene (10.09.2013)
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Journal Article
Assessment of Toll-like receptor-4 gene polymorphism on pyelonephritis and renal scar
Akil, I., Ozkinay, F., Onay, H., Canda, E., Gumuser, G., Kavukcu, S.
Published in International journal of immunogenetics (01.08.2012)
Published in International journal of immunogenetics (01.08.2012)
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Journal Article
Which social environment is more important in the persistence of psychotic experiences? Differential impact of neighbourhood and family context in a six-year longitudinal population-based cohort
Binbay, T, Kırlı, U, Elbi, H, Kayahan, B, Onay, H, Ferda, Ö, Drukker, M, van Os, J, Alptekin, K
Published in European psychiatry (01.03.2016)
Published in European psychiatry (01.03.2016)
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A six-year longitudinal population-based cohort for the extended psychosis phenotype: An epidemiological study of the gene-environment interactions (TürkSch)
Alptekin, K, Binbay, T, Kırlı, U, Elbi, H, Kayahan, B, Onay, H, Özkınay, F, van Os, J
Published in European psychiatry (01.03.2016)
Published in European psychiatry (01.03.2016)
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Journal Article
Psychotic experiences, alcohol–cannabis abuse, stressful events and familial risk is associated with onset of clinical psychosis: Evidence from a 6-year longitudinal population-based cohort
Kirli, U, Binbay, T, Elbi, H, Kayahan, B, van Os, J, Onay, H, Ozkınay, F, Gokcelli, D.K, Alptekin, K
Published in European psychiatry (01.03.2016)
Published in European psychiatry (01.03.2016)
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Journal Article
558 Prader-Willi Syndrome Due to Maternal Uniparental Disomy following Assisted Reproductive Technology
Cogulu, O, Atik, T, Karaca, E, Onay, H, Ozkinay, F
Published in Archives of disease in childhood (01.10.2012)
Published in Archives of disease in childhood (01.10.2012)
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Journal Article
Low levels of mannose-binding lectin confers protection against tuberculosis in Turkish children
Cosar, H, Ozkinay, F, Onay, H, Bayram, N, Bakiler, A. R, Anıl, M, Can, D, Özkınay, C
Published in European journal of clinical microbiology & infectious diseases (01.12.2008)
Published in European journal of clinical microbiology & infectious diseases (01.12.2008)
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Journal Article
Clinical spectra of neuromuscular manifestations in patients with lipodystrophy: A multicenter study
Akinci, G, Topaloglu, H, Demir, T, Danyeli, A.E, Talim, B, Keskin, F.E, Kadioglu, P, Talip, E, Altay, C, Yaylali, G.F, Bilen, H, Nur, B, Demir, L, Onay, H, Akinci, B
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
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