Guven Y - Search Results

1

Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis.

Du R, Dinckan N, Song X, Coban-Akdemir Z, Jhangiani SN, Guven Y, Aktoren O, Kayserili H, Petty LE, Muzny DM, Below JE, Boerwinkle E, Wu N, Gibbs RA, Posey JE, Lupski JR, Letra A, Uyguner ZO. Du R, et al. Among authors: guven y. Hum Genet. 2018 Sep;137(9):689-703. doi: 10.1007/s00439-018-1907-y. Epub 2018 Jul 26. Hum Genet. 2018. PMID: 30046887 Free PMC article.

2

Orodental findings of a family with lacrimo-auriculo-dento digital (LADD) syndrome.

Guven Y, Rosti RO, Tuna EB, Kayserili H, Aktoren O. Guven Y, et al. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008 Dec;106(6):e33-44. doi: 10.1016/j.tripleo.2008.07.019. Epub 2008 Sep 17. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008. PMID: 18801668

3

A study on neonatal factors and eruption time of primary teeth.

Aktoren O, Tuna EB, Guven Y, Gokcay G. Aktoren O, et al. Among authors: guven y. Community Dent Health. 2010 Mar;27(1):52-6. Community Dent Health. 2010. PMID: 20426262

4

Success rates of mineral trioxide aggregate, ferric sulfate, and formocresol pulpotomies: a 24-month study.

Erdem AP, Guven Y, Balli B, Ilhan B, Sepet E, Ulukapi I, Aktoren O. Erdem AP, et al. Among authors: guven y. Pediatr Dent. 2011 Mar-Apr;33(2):165-70. Pediatr Dent. 2011. PMID: 21703067 Clinical Trial.

5

A novel c.1255G>T (p.D419Y) mutation in SH3BP2 gene causes cherubism in a Turkish family.

Dinckan N, Guven Y, Kayserili H, Aktoren O, Uyguner OZ. Dinckan N, et al. Among authors: guven y. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Nov;114(5):e42-6. doi: 10.1016/j.oooo.2012.01.031. Epub 2012 May 12. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012. PMID: 23083484

6

Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI.

Kantaputra PN, Kayserili H, Güven Y, Kantaputra W, Balci MC, Tanpaiboon P, Uttarilli A, Dalal A. Kantaputra PN, et al. Among authors: guven y. J Inherit Metab Dis. 2014 Mar;37(2):263-8. doi: 10.1007/s10545-013-9645-8. Epub 2013 Aug 22. J Inherit Metab Dis. 2014. PMID: 23974652

7

Shear bond strength and ultrastructural interface analysis of different adhesive systems to Er:YAG laser-prepared dentin.

Guven Y, Aktoren O. Guven Y, et al. Lasers Med Sci. 2015 Feb;30(2):769-78. doi: 10.1007/s10103-013-1424-0. Epub 2013 Aug 28. Lasers Med Sci. 2015. PMID: 23982720

8

C5orf42 is the major gene responsible for OFD syndrome type VI.

Lopez E, Thauvin-Robinet C, Reversade B, Khartoufi NE, Devisme L, Holder M, Ansart-Franquet H, Avila M, Lacombe D, Kleinfinger P, Kaori I, Takanashi J, Le Merrer M, Martinovic J, Noël C, Shboul M, Ho L, Güven Y, Razavi F, Burglen L, Gigot N, Darmency-Stamboul V, Thevenon J, Aral B, Kayserili H, Huet F, Lyonnet S, Le Caignec C, Franco B, Rivière JB, Faivre L, Attié-Bitach T. Lopez E, et al. Among authors: guven y. Hum Genet. 2014 Mar;133(3):367-77. doi: 10.1007/s00439-013-1385-1. Epub 2013 Nov 1. Hum Genet. 2014. PMID: 24178751

9

Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation.

Guven Y, Altunoglu U, Aktoren O, Uyguner ZO, Kayserili H, Kaewkahya M, Kantaputra PN. Guven Y, et al. Eur J Med Genet. 2014 Apr;57(5):240-6. doi: 10.1016/j.ejmg.2014.02.014. Epub 2014 Mar 12. Eur J Med Genet. 2014. PMID: 24631696

10

Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations.

Kantaputra PN, Kayserili H, Guven Y, Kantaputra W, Balci MC, Tanpaiboon P, Tananuvat N, Uttarilli A, Dalal A. Kantaputra PN, et al. Among authors: guven y. Am J Med Genet A. 2014 Jun;164A(6):1443-53. doi: 10.1002/ajmg.a.36489. Epub 2014 Mar 27. Am J Med Genet A. 2014. PMID: 24677745

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