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992 results

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Page 1
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.
Delgado-Vega AM, Cederroth H, Taylan F, Ekholm K, Ek M, Thonberg H, Jemt A, Nilsson D, Eisfeldt J, Bilgrav Saether K, Höijer I, Akgun-Dogan O, Asano Y, Barakat TS, Batkovskyte D, Baynam G, Bodamer O, Chetruengchai W, Corcoran P, Couse M, Danis D, Demidov G, Dohi E, Erhardsson M, Fernandez-Luna L, Fujiwara T, Garg N, Giugliani R, Gonzaga-Jauregui C, Grigelioniene G, Groza T, Gunnarsson C, Hammarsjö A, Hammond CK, Hatirnaz Ng Ö, Hesketh S, Hettiarachchi D, Johansson Soller M, Kirmani UA, Kjellberg M, Kvarnung M, Kvlividze O, Lagerstedt-Robinson K, Lasko P, Lassmann T, Lau LYS, Laurie S, Lim WK, Liu Z, Lysenkova Wiklander M, Makay P, Maiga AB, Maya-González C, Meyn MS, Neethiraj R, Nigro V, Nordgren F, Nordlund J, Orrsjö S, Ottosson J, Ozbek U, Özdemir Ö, Partin C, Pearce DA, Peck R, Pedersen A, Pettersson M, Pongpanich M, Posada de la Paz M, Ramani A, Romero JA, Romero VI, Rosenquist R, Saw AM, Spencer M, Stattin EL, Srichomthong C, Tapia-Paez I, Taruscio D, Taylor JP, Tkemaladze T, Tully I, Tümer Z, van Zelst-Stams WAG, Verloes A, Västerviga E, Wang S, Yang R, Yamamoto S, Yépez VA, Zhang Q, Shotelersuk V, Wiafe SA, Alanay Y, Botto LD, Kirmani S, Lumaka A, Palmer EE, Puri RD,… See abstract for full author list ➔ Delgado-Vega AM, et al. Among authors: ozdemir o. Nat Genet. 2024 Nov;56(11):2287-2294. doi: 10.1038/s41588-024-01941-1. Nat Genet. 2024. PMID: 39433890 No abstract available.
Bromodomain-containing protein 2 gene in photosensitive epilepsy.
Yavuz EN, Ozdemir O, Catal S, Bebek N, Ozbek U, Baykan B. Yavuz EN, et al. Among authors: ozdemir o. Seizure. 2012 Oct;21(8):646-8. doi: 10.1016/j.seizure.2012.06.008. Epub 2012 Jul 4. Seizure. 2012. PMID: 22766109 Free article.
The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.
Haryanyan G, Ozdemir O, Tutkavul K, Dervent A, Ayta S, Ozkara C, Salman B, Yucesan E, Kesim Y, Susgun S, Ozbek U, Baykan B, Ugur Iseri SA, Bebek N. Haryanyan G, et al. Among authors: ozdemir o. J Hum Genet. 2021 Dec;66(12):1145-1151. doi: 10.1038/s10038-021-00944-8. Epub 2021 Jun 11. J Hum Genet. 2021. PMID: 34117373
Obstacles and expectations of rare disease patients and their families in Türkiye: ISTisNA project survey results.
Hatirnaz Ng O, Sahin I, Erbilgin Y, Ozdemir O, Yucesan E, Erturk N, Yemenici M, Akgun Dogan O, Ugur Iseri SA, Satman I, Alanay Y, Ozbek U. Hatirnaz Ng O, et al. Among authors: ozdemir o. Front Public Health. 2023 Jan 4;10:1049349. doi: 10.3389/fpubh.2022.1049349. eCollection 2022. Front Public Health. 2023. PMID: 36684907 Free PMC article.
Impact of deep phenotyping: high diagnostic yield in a diverse pediatric population of 172 patients through clinical whole-genome sequencing at a single center.
Akgun-Dogan O, Tuc Bengur E, Ay B, Ozkose GS, Kar E, Bengur FB, Bulut AS, Yigit A, Aydin E, Esen FN, Ozdemir O, Yesilyurt A, Alanay Y. Akgun-Dogan O, et al. Among authors: ozdemir o. Front Genet. 2024 Mar 15;15:1347474. doi: 10.3389/fgene.2024.1347474. eCollection 2024. Front Genet. 2024. PMID: 38560291 Free PMC article.
Rapid genome sequencing for critically ill infants: an inaugural pilot study from Turkey.
Guner Yilmaz B, Akgun-Dogan O, Ozdemir O, Yuksel B, Hatirnaz Ng O, Bilguvar K, Ay B, Ozkose GS, Aydin E, Yigit A, Bulut A, Esen FN, Beken S, Aktas S, Demirel A, Arcagok BC, Kazanci E, Bingol İ, Umur O, Sik G, Isik U, Ersoy M, Korkmaz A, Citak A, Mardinoglu A, Ozbek U, Alanay Y. Guner Yilmaz B, et al. Among authors: ozdemir o. Front Pediatr. 2024 Jul 4;12:1412880. doi: 10.3389/fped.2024.1412880. eCollection 2024. Front Pediatr. 2024. PMID: 39026936 Free PMC article.
Molecular and In Silico Analysis of the CHEK2 Gene in Individuals with High Risk of Cancer Predisposition from Türkiye.
Ozdemir O, Bychkovsky BL, Unal B, Onder G, Amanvermez U, Aydin E, Ergun B, Sahin I, Gokbayrak M, Ugurtas C, Koroglu MN, Cakir B, Kalay I, Cine N, Ozbek U, Rana HQ, Hatirnaz Ng O, Agaoglu NB. Ozdemir O, et al. Cancers (Basel). 2024 Nov 20;16(22):3876. doi: 10.3390/cancers16223876. Cancers (Basel). 2024. PMID: 39594831 Free PMC article.
992 results