Yucesan E - Search Results

1

Biallelic loss of EEF1D function links heat shock response pathway to autosomal recessive intellectual disability.

Ugur Iseri SA, Yucesan E, Tuncer FN, Calik M, Kesim Y, Altiokka Uzun G, Ozbek U. Ugur Iseri SA, et al. Among authors: yucesan e. J Hum Genet. 2019 May;64(5):421-426. doi: 10.1038/s10038-019-0570-z. Epub 2019 Feb 21. J Hum Genet. 2019. PMID: 30787422

2

Parathyroid allotransplantation in rabbits without cultivation.

Can I, Aysan E, Yucesan E, Sayitoglu M, Ozbek U, Ercivan M, Atasoy H, Buyukpinarbasili N, Muslumanoglu M. Can I, et al. Among authors: yucesan e. Int J Clin Exp Med. 2014 Jan 15;7(1):280-4. eCollection 2014. Int J Clin Exp Med. 2014. PMID: 24482717 Free PMC article.

3

Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation.

Kesim YF, Uzun GA, Yucesan E, Tuncer FN, Ozdemir O, Bebek N, Ozbek U, Iseri SA, Baykan B. Kesim YF, et al. Among authors: yucesan e. Epilepsy Res. 2016 Feb;120:73-8. doi: 10.1016/j.eplepsyres.2015.12.006. Epub 2015 Dec 12. Epilepsy Res. 2016. PMID: 26773249

4

SYNE1 related cerebellar ataxia presents with variable phenotypes in a consanguineous family from Turkey.

Yucesan E, Ugur Iseri SA, Bilgic B, Gormez Z, Bakir Gungor B, Sarac A, Ozdemir O, Sagiroglu M, Gurvit H, Hanagasi H, Ozbek U. Yucesan E, et al. Neurol Sci. 2017 Dec;38(12):2203-2207. doi: 10.1007/s10072-017-3049-8. Epub 2017 Jul 7. Neurol Sci. 2017. PMID: 28687974

5

Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.

Yücel-Yılmaz D, Yücesan E, Yalnızoğlu D, Oğuz KK, Sağıroğlu MŞ, Özbek U, Serdaroğlu E, Bilgiç B, Erdem S, İşeri SAU, Hanağası H, Gürvit H, Özgül RK, Dursun A. Yücel-Yılmaz D, et al. Among authors: yucesan e. Brain Dev. 2018 Jun;40(6):458-464. doi: 10.1016/j.braindev.2018.02.013. Epub 2018 Mar 12. Brain Dev. 2018. PMID: 29544888

6

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals.

Epi25 Collaborative. Electronic address: s.berkovic@unimelb.edu.au; Epi25 Collaborative. Epi25 Collaborative. Electronic address: s.berkovic@unimelb.edu.au, et al. Am J Hum Genet. 2019 Aug 1;105(2):267-282. doi: 10.1016/j.ajhg.2019.05.020. Epub 2019 Jul 18. Am J Hum Genet. 2019. PMID: 31327507 Free PMC article.

7

Polygenic burden in focal and generalized epilepsies.

Leu C, Stevelink R, Smith AW, Goleva SB, Kanai M, Ferguson L, Campbell C, Kamatani Y, Okada Y, Sisodiya SM, Cavalleri GL, Koeleman BPC, Lerche H, Jehi L, Davis LK, Najm IM, Palotie A, Daly MJ, Busch RM; Epi25 Consortium; Lal D. Leu C, et al. Brain. 2019 Nov 1;142(11):3473-3481. doi: 10.1093/brain/awz292. Brain. 2019. PMID: 31608925 Free PMC article.

8

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.

Niestroj LM, Perez-Palma E, Howrigan DP, Zhou Y, Cheng F, Saarentaus E, Nürnberg P, Stevelink R, Daly MJ, Palotie A, Lal D; Epi25 Collaborative. Niestroj LM, et al. Brain. 2020 Jul 1;143(7):2106-2118. doi: 10.1093/brain/awaa171. Brain. 2020. PMID: 32568404 Free PMC article.

9

Copy-number variations in adult patients with chronic immune thrombocytopenia.

Yucesan E, Hatirnaz Ng O, Yalniz FF, Yilmaz H, Salihoglu A, Sudutan T, Eskazan AE, Ongoren S, Baslar Z, Soysal T, Ozbek U, Sayitoglu M, Ar MC. Yucesan E, et al. Expert Rev Hematol. 2020 Nov;13(11):1277-1287. doi: 10.1080/17474086.2020.1819786. Epub 2020 Sep 23. Expert Rev Hematol. 2020. PMID: 32885695

10

Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations.

Stevelink R, Luykx JJ, Lin BD, Leu C, Lal D, Smith AW, Schijven D, Carpay JA, Rademaker K, Rodrigues Baldez RA, Devinsky O, Braun KPJ, Jansen FE, Smit DJA, Koeleman BPC; International League Against Epilepsy Consortium on Complex Epilepsies; Epi25 Collaborative. Stevelink R, et al. Epilepsia. 2021 Jul;62(7):1518-1527. doi: 10.1111/epi.16922. Epub 2021 May 18. Epilepsia. 2021. PMID: 34002374 Free PMC article.

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