Berk Ozyilmaz[Author] - Search Results

Year	Number of Results
2015	2
2017	2
2018	5
2019	12
2020	8
2021	4
2022	7
2023	2
2024	2

1

Experiences in the molecular genetic and histopathological evaluation of calpainopathies.

Ozyilmaz B, Kirbiyik O, Ozdemir TR, Ozer OK, Kutbay YB, Erdogan KM, Guvenc MS, Arıkan Ş, Turk TS, Kale MY, Uludag IF, Baydan F, Sertpoyraz F, Gencpinar P, Diniz G. Ozyilmaz B, et al. Neurogenetics. 2022 Apr;23(2):103-114. doi: 10.1007/s10048-022-00687-4. Epub 2022 Feb 14. Neurogenetics. 2022. PMID: 35157181

2

A hypomyelinating leukodystrophy with calcification: oculodentodigital dysplasia.

Cavusoglu D, Dundar NO, Arican P, Ozyilmaz B, Gencpinar P. Cavusoglu D, et al. Among authors: ozyilmaz b. Acta Neurol Belg. 2020 Oct;120(5):1177-1179. doi: 10.1007/s13760-019-01178-4. Epub 2019 Jun 25. Acta Neurol Belg. 2020. PMID: 31240666 No abstract available.

3

Assessment of mimicking by EBV-CMV immunoglobulin M of anti-HLA antibodies.

Güleç RD, Arslan FD, Özyılmaz B, Yılmaz N, Hancı SY, Köse Ş. Güleç RD, et al. Among authors: ozyilmaz b. J Immunol Methods. 2023 Dec;523:113577. doi: 10.1016/j.jim.2023.113577. Epub 2023 Oct 20. J Immunol Methods. 2023. PMID: 37865308

4

Fetal HLA-G alleles and their effect on miscarriage.

Koc A, Kirbiyik O, Kutbay YB, Ozyilmaz B, Ozdemir TR, Kaya OO, Kubat G, Koc ZP. Koc A, et al. Among authors: ozyilmaz b. Adv Clin Exp Med. 2018 Sep;27(9):1233-1237. doi: 10.17219/acem/69692. Adv Clin Exp Med. 2018. PMID: 29809322 Free article.

5

Gilbert Syndrome and Genetic Findings in Children: A Tertiary-Center Experience from Turkey.

Çağan Appak Y, Aksoy B, Özyılmaz B, Özdemir TR, Baran M. Çağan Appak Y, et al. Among authors: ozyilmaz b. Turk Arch Pediatr. 2022 May;57(3):295-299. doi: 10.5152/TurkArchPediatr.2022.21291. Turk Arch Pediatr. 2022. PMID: 35781232 Free PMC article.

6

Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant.

Catli G, Gao W, Foley C, Özyilmaz B, Edeer N, Diniz G, Losekoot M, van Doorn J, Dauber A, Dundar BN, Wit JM, Hwa V. Catli G, et al. Among authors: ozyilmaz b. Mol Cell Endocrinol. 2023 Jan 1;559:111799. doi: 10.1016/j.mce.2022.111799. Epub 2022 Oct 17. Mol Cell Endocrinol. 2023. PMID: 36265659

7

ALK, ROS1 and EGFR status of lung cancers in the Aegean Region of Turkey.

Diniz G, Komurcuoglu B, Ozyilmaz B, Ozguzer A, Yucel N, Kirbiyik O. Diniz G, et al. Among authors: ozyilmaz b. Indian J Pathol Microbiol. 2022 Apr-Jun;65(2):305-310. doi: 10.4103/IJPM.IJPM_1129_20. Indian J Pathol Microbiol. 2022. PMID: 35435363 Free article.

8

Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability.

Arican P, Olgac Dundar N, Ozyilmaz B, Cavusoglu D, Gencpinar P, Erdogan KM, Saka Guvenc M. Arican P, et al. Among authors: ozyilmaz b. J Pediatr Genet. 2019 Mar;8(1):1-9. doi: 10.1055/s-0038-1676583. Epub 2018 Dec 14. J Pediatr Genet. 2019. PMID: 30775046 Free PMC article.

9

First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss.

Özyılmaz B, Mercan GC, Kırbıyık Ö, Özdemir TR, Özkara S, Kaya ÖÖ, Kutbay YB, Erdoğan KM, Güvenç MS, Koç A. Özyılmaz B, et al. Turk Arch Otorhinolaryngol. 2019 Sep;57(3):140-148. doi: 10.5152/tao.2019.4320. Epub 2019 Sep 1. Turk Arch Otorhinolaryngol. 2019. PMID: 31620696 Free PMC article.

10

QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey.

Özer Kaya Ö, Koç A, Özdemir TR, Kirbiyik Ö, Özyilmaz B, Özeren M, Öztekin DC, Taner CE, Kutbay YB. Özer Kaya Ö, et al. Among authors: ozyilmaz b. Turk J Med Sci. 2017 Feb 27;47(1):142-147. doi: 10.3906/sag-1511-157. Turk J Med Sci. 2017. PMID: 28263482 Free article.

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