Alavanda C - Search Results

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

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.

3

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.

4

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

5

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.

6

Mutation Spectrum of Familial Adenomatous Polyposis Patients in Turkish Population: Identification of 3 Novel APC Mutations.

Arslan Ateş E, Alavanda C, Demir Ş, Keklikkıran Ç, Attaallah W, Özdoğan OC, Güney Aİ. Arslan Ateş E, et al. Among authors: alavanda c. Turk J Gastroenterol. 2022 Feb;33(2):81-87. doi: 10.5152/tjg.2021.201068. Turk J Gastroenterol. 2022. PMID: 35238777 Free PMC article.

7

[No title available]

[No authors listed] [No authors listed] PMID: 36876326

8

Novel, homozygous RAB3GAP1 c.2606 + 1G>A, p.Glu830ValfsTer9 variant and chromosome 3q29 duplication in a Turkish individual with Warburg micro syndrome.

Geckinli B, Turkyilmaz A, Alavanda C, Sager G, Arslan Ates E, Soylemez MA, Arman A. Geckinli B, et al. Among authors: alavanda c. Clin Dysmorphol. 2023 Apr 1;32(2):55-61. doi: 10.1097/MCD.0000000000000454. Epub 2023 Feb 17. Clin Dysmorphol. 2023. PMID: 36876345

9

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

10

Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS-CoV-2 from 946 whole-exome sequencing data in the Turkish population.

Duman N, Tuncel G, Bisgin A, Bozdogan ST, Sag SO, Gul S, Kiraz A, Balta B, Erdogan M, Uyanik B, Canbek S, Ata P, Geckinli BB, Arslan Ates E, Alavanda C, Yesim Ozdemir S, Sezer O, Ozgon GO, Gurkan H, Guler K, Boga I, Kaya N, Alemdar A, Sayan M, Dundar M, Ergoren MC, Temel SG. Duman N, et al. Among authors: alavanda c. J Med Virol. 2022 Nov;94(11):5225-5243. doi: 10.1002/jmv.27976. Epub 2022 Jul 22. J Med Virol. 2022. PMID: 35811452 Free PMC article.

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