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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 1
2001 2
2002 6
2003 7
2004 11
2005 14
2006 7
2007 12
2008 11
2009 9
2010 9
2011 11
2012 7
2013 6
2014 9
2015 9
2016 6
2017 10
2018 15
2019 18
2020 23
2021 23
2022 27
2023 36
2024 8

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256 results

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Page 1
High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population.
Mitani T, Isikay S, Gezdirici A, Gulec EY, Punetha J, Fatih JM, Herman I, Akay G, Du H, Calame DG, Ayaz A, Tos T, Yesil G, Aydin H, Geckinli B, Elcioglu N, Candan S, Sezer O, Erdem HB, Gul D, Demiral E, Elmas M, Yesilbas O, Kilic B, Gungor S, Ceylan AC, Bozdogan S, Ozalp O, Cicek S, Aslan H, Yalcintepe S, Topcu V, Bayram Y, Grochowski CM, Jolly A, Dawood M, Duan R, Jhangiani SN, Doddapaneni H, Hu J, Muzny DM; Baylor-Hopkins Center for Mendelian Genomics; Marafi D, Akdemir ZC, Karaca E, Carvalho CMB, Gibbs RA, Posey JE, Lupski JR, Pehlivan D. Mitani T, et al. Among authors: ceylan ac. Am J Hum Genet. 2021 Oct 7;108(10):1981-2005. doi: 10.1016/j.ajhg.2021.08.009. Epub 2021 Sep 28. Am J Hum Genet. 2021. PMID: 34582790 Free PMC article.
Neuromuscular disease genetics in under-represented populations: increasing data diversity.
Wilson LA, Macken WL, Perry LD, Record CJ, Schon KR, Frezatti RSS, Raga S, Naidu K, Köken ÖY, Polat I, Kapapa MM, Dominik N, Efthymiou S, Morsy H, Nel M, Fassad MR, Gao F, Patel K, Schoonen M, Bisschoff M, Vorster A, Jonvik H, Human R, Lubbe E, Nonyane M, Vengalil S, Nashi S, Srivastava K, Lemmers RJLF, Reyaz A, Mishra R, Töpf A, Trainor CI, Steyn EC, Mahungu AC, van der Vliet PJ, Ceylan AC, Hiz AS, Çavdarlı B, Semerci Gündüz CN, Ceylan GG, Nagappa M, Tallapaka KB, Govindaraj P, van der Maarel SM, Narayanappa G, Nandeesh BN, Wa Somwe S, Bearden DR, Kvalsund MP, Ramdharry GM, Oktay Y, Yiş U, Topaloğlu H, Sarkozy A, Bugiardini E, Henning F, Wilmshurst JM, Heckmann JM, McFarland R, Taylor RW, Smuts I, van der Westhuizen FH, Sobreira CFDR, Tomaselli PJ, Marques W Jr, Bhatia R, Dalal A, Srivastava MVP, Yareeda S, Nalini A, Vishnu VY, Thangaraj K, Straub V, Horvath R, Chinnery PF, Pitceathly RDS, Muntoni F, Houlden H, Vandrovcova J, Reilly MM, Hanna MG. Wilson LA, et al. Among authors: ceylan ac. Brain. 2023 Dec 1;146(12):5098-5109. doi: 10.1093/brain/awad254. Brain. 2023. PMID: 37516995 Free PMC article.
Malonyl coenzyme A decarboxylase deficiency with a novel mutation.
Kasapkara CS, Civelek Ürey B, Ceylan AC, Ünal Uzun Ö, Çetin II. Kasapkara CS, et al. Among authors: ceylan ac. Cardiol Young. 2021 Sep;31(9):1535-1537. doi: 10.1017/S104795112100113X. Epub 2021 Mar 22. Cardiol Young. 2021. PMID: 33745485
ALG11-CDG: novel variant and review of the literature.
Erdal AE, Ceylan AC, Gücüyener K, Öktem RM, Kıreker Köylü O, Kasapkara ÇS. Erdal AE, et al. Among authors: ceylan ac. J Pediatr Endocrinol Metab. 2023 Feb 28;36(4):409-413. doi: 10.1515/jpem-2022-0480. Print 2023 Apr 25. J Pediatr Endocrinol Metab. 2023. PMID: 36843332 Review.
An extrahepatic hydatid cyst with the fat-fluid level.
Yildirim F, Turan A, Guven S, Ceylan A. Yildirim F, et al. Among authors: ceylan a. BJR Case Rep. 2021 Nov 26;8(1):20210059. doi: 10.1259/bjrcr.20210059. eCollection 2022 Jan 1. BJR Case Rep. 2021. PMID: 35136632 Free PMC article.
Cardiomyocyte-specific deletion of endothelin receptor A (ETA) obliterates cardiac aging through regulation of mitophagy and ferroptosis.
Zou R, Shi W, Ceylan AF, Dong M, Zhang M, Zou Z, Peng B, Dong F, Turdi S, Lin J, Zhang Y, Wang G, Fan X, Ren J. Zou R, et al. Among authors: ceylan af. Biochim Biophys Acta Mol Basis Dis. 2024 Feb;1870(2):166958. doi: 10.1016/j.bbadis.2023.166958. Epub 2023 Nov 12. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 37963542
Predictors of ileus following colorectal resections.
Sapci I, Hameed I, Ceylan A, Oktem A, Rencuzogullari A, Hull TL, Liska D, Delaney CP, Gorgun E. Sapci I, et al. Among authors: ceylan a. Am J Surg. 2020 Mar;219(3):527-529. doi: 10.1016/j.amjsurg.2019.10.002. Epub 2019 Oct 5. Am J Surg. 2020. PMID: 31604485
256 results