Ceren Alavanda[Author] - Search Results

Year	Number of Results
2020	1
2021	7
2022	10
2023	7
2024	0

1

Dirimtekin E, Mortoglou M, Alavanda C, Benomar Yemlahi A, Arslan Ates E, Guney I, Uysal-Onganer P. Dirimtekin E, et al. Among authors: alavanda c. ACS Omega. 2023 Jul 18;8(30):27743-27750. doi: 10.1021/acsomega.3c03867. eCollection 2023 Aug 1. ACS Omega. 2023. PMID: 37546627 Free PMC article.

2

Clinical and genetic characterization of children with cubilin variants.

Cicek N, Alpay H, Guven S, Alavanda C, Türkkan ÖN, Pul S, Demirci E, Yıldız N, Ata P, Gokce I. Cicek N, et al. Among authors: alavanda c. Pediatr Nephrol. 2023 Apr;38(4):1381-1385. doi: 10.1007/s00467-022-05730-y. Epub 2022 Sep 16. Pediatr Nephrol. 2023. PMID: 36112210

3

Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf-Yang syndrome.

Alavanda C, Arslan Ateş E, Yavaş Abalı Z, Geçkinli BB, Turan S, Arman A. Alavanda C, et al. Clin Genet. 2023 Jul;104(1):127-132. doi: 10.1111/cge.14320. Epub 2023 Mar 9. Clin Genet. 2023. PMID: 36843439

4

Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty.

Kırkgöz T, Kaygusuz SB, Alavanda C, Helvacıoğlu D, Abalı ZY, Tosun BG, Eltan M, Menevşe TS, Guran T, Arman A, Turan S, Bereket A. Kırkgöz T, et al. Among authors: alavanda c. J Pediatr Endocrinol Metab. 2023 Mar 9;36(4):401-408. doi: 10.1515/jpem-2022-0645. Print 2023 Apr 25. J Pediatr Endocrinol Metab. 2023. PMID: 36883204

5

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity.

Turan S, Mumm S, Alavanda C, Kaygusuz BS, Gurpinar Tosun B, Arman A, Huskey M, Guran T, Duan S, Bereket A, Whyte MP. Turan S, et al. Among authors: alavanda c. JBMR Plus. 2022 Jul 28;6(8):e10663. doi: 10.1002/jbm4.10663. eCollection 2022 Aug. JBMR Plus. 2022. PMID: 35991533 Free PMC article.

6

Phenotypic and genotypic characteristics of children with Bartter syndrome.

Güven S, Gökçe İ, Alavanda C, Çiçek N, Demirci EB, Sak M, Pul S, Türkkan ÖN, Yıldız N, Ata P, Alpay H. Güven S, et al. Among authors: alavanda c. Turk J Pediatr. 2022;64(5):825-838. doi: 10.24953/turkjped.2021.4697. Turk J Pediatr. 2022. PMID: 36305432 Free article.

7

Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients.

Arslan Ates E, Turkyilmaz A, Alavanda C, Yildirim O, Guney AI. Arslan Ates E, et al. Among authors: alavanda c. Medeni Med J. 2022 Jun 23;37(2):150-158. doi: 10.4274/MMJ.galenos.2022.22556. Medeni Med J. 2022. PMID: 35734982 Free PMC article.

8

Meckel-Gruber Syndrome: Clinical and Molecular Genetic Profiles in Two Fetuses and Review of the Current Literature.

Turkyilmaz A, Geckinli BB, Alavanda C, Arslan Ates E, Buyukbayrak EE, Eren SF, Arman A. Turkyilmaz A, et al. Among authors: alavanda c. Genet Test Mol Biomarkers. 2021 Jun;25(6):445-451. doi: 10.1089/gtmb.2020.0311. Epub 2021 Jun 4. Genet Test Mol Biomarkers. 2021. PMID: 34096792 Review.

9

Enostosis in a patient with KBG syndrome caused by a novel missense ANKRD11 variant.

Geckinli BB, Alavanda C, Arslan Ates E, Yildirim O, Arman A. Geckinli BB, et al. Among authors: alavanda c. Clin Dysmorphol. 2022 Jul 1;31(3):153-156. doi: 10.1097/MCD.0000000000000421. Epub 2022 Apr 8. Clin Dysmorphol. 2022. PMID: 35394473 No abstract available.

10

Secondary findings in 622 Turkish clinical exome sequencing data.

Arslan Ateş E, Türkyilmaz A, Yıldırım Ö, Alavanda C, Polat H, Demir Ş, Çebi AH, Geçkinli BB, Güney Aİ, Ata P, Arman A. Arslan Ateş E, et al. Among authors: alavanda c. J Hum Genet. 2021 Nov;66(11):1113-1119. doi: 10.1038/s10038-021-00936-8. Epub 2021 May 28. J Hum Genet. 2021. PMID: 34050257

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