Alper O - Search Results

1

Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2.

Ramzan M, Zafeer MF, Abad C, Guo S, Owrang D, Alper O, Mutlu A, Atik T, Duman D, Bademci G, Vona B, Kalcioglu MT, Walz K, Tekin M. Ramzan M, et al. Among authors: alper o. Eur J Hum Genet. 2024 Jun;32(6):639-646. doi: 10.1038/s41431-024-01562-6. Epub 2024 Feb 19. Eur J Hum Genet. 2024. PMID: 38374469

2

Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss.

Ramzan M, Duman D, Hendricks LCP, Guo S, Mutlu A, Kalcioglu MT, Seyhan S, Carranza C, Bonyadi M, Mahdieh N, Yildirim-Baylan M, Figueroa-Ildefonso E, Alper O, Atik T, Ayral A, Bozan N, Balta B, Rivas C, Manzoli GN, Huesca-Hernandez F, Kuchay RAH, Durgut M, Bademci G, Tekin M. Ramzan M, et al. Among authors: alper o. J Hum Genet. 2023 Oct;68(10):657-669. doi: 10.1038/s10038-023-01159-9. Epub 2023 May 22. J Hum Genet. 2023. PMID: 37217689

3

Novel Gene Variants Associated with Primary Ciliary Dyskinesia.

Demir Eksi D, Yilmaz E, Basaran AE, Erduran G, Nur B, Mihci E, Karadag B, Bingol A, Alper OM. Demir Eksi D, et al. Among authors: alper om. Indian J Pediatr. 2022 Jul;89(7):682-691. doi: 10.1007/s12098-022-04098-z. Epub 2022 Mar 3. Indian J Pediatr. 2022. PMID: 35239159

4

Association Between Cystic Fibrosis Severity Markers and CFTR Genotypes in Turkish Children.

Başaran AE, Başaran A, Kocacik Uygun DF, Yılmaz E, Moballegh A, Öz L, Alper Ö, Bingöl A. Başaran AE, et al. Among authors: alper o. Turk Thorac J. 2021 Nov;22(6):426-431. doi: 10.5152/TurkThoracJ.2021.20282. Turk Thorac J. 2021. PMID: 35110256 Free PMC article.

5

Initial regional evaluation of the Cystic Fibrosis Newborn Screening Program: data from the Mediterranean coast of Turkey.

Başaran AE, Başaran A, Kocacik DF, Alper Ö, Acican D, Bingöl A. Başaran AE, et al. Among authors: alper o. Turk J Med Sci. 2019 Dec 16;49(6):1655-1661. doi: 10.3906/sag-1904-198. Turk J Med Sci. 2019. PMID: 31655510 Free PMC article.

6

Recent Advances in Craniosynostosis.

Yilmaz E, Mihci E, Nur B, Alper ÖM, Taçoy Ş. Yilmaz E, et al. Among authors: alper om. Pediatr Neurol. 2019 Oct;99:7-15. doi: 10.1016/j.pediatrneurol.2019.01.018. Epub 2019 Feb 2. Pediatr Neurol. 2019. PMID: 31421914 Review.

7

Coronal craniosynostosis due to TCF12 mutations in patients from Turkey.

Yilmaz E, Mihci E, Nur B, Alper OM. Yilmaz E, et al. Among authors: alper om. Am J Med Genet A. 2019 Nov;179(11):2241-2245. doi: 10.1002/ajmg.a.61311. Epub 2019 Jul 28. Am J Med Genet A. 2019. PMID: 31353793

8

Clinical and genetic findings of two cases with Apert syndrome.

Cammarata-Scalisi F, Yilmaz E, Callea M, Avendaño A, Mıhçı E, Alper OM. Cammarata-Scalisi F, et al. Among authors: alper om. Bol Med Hosp Infant Mex. 2019;76(1):44-48. doi: 10.24875/BMHIM.18000053. Bol Med Hosp Infant Mex. 2019. PMID: 30657466 English.

9

Large expert-curated database for benchmarking document similarity detection in biomedical literature search.

Brown P; RELISH Consortium; Zhou Y. Brown P, et al. Database (Oxford). 2019 Jan 1;2019:baz085. doi: 10.1093/database/baz085. Database (Oxford). 2019. PMID: 33326193 Free PMC article.

10

A novel AXIN2 gene mutation in sagittal synostosis.

Yilmaz E, Mihci E, Guzel Nur B, Alper OM. Yilmaz E, et al. Among authors: alper om. Am J Med Genet A. 2018 Sep;176(9):1976-1980. doi: 10.1002/ajmg.a.40373. Epub 2018 Aug 8. Am J Med Genet A. 2018. PMID: 30088857

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