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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31.
Funct Integr Genomics. 2022.
PMID: 35098403
Apolipoprotein E allelic variants and cerebral palsy.
Gümüş E, Aras BD, Çilingir O, Yarar C, Çarman KB, Laçiner-Gürlevik S, Koçak O, Artan S.
Gümüş E, et al. Among authors: aras bd.
Turk J Pediatr. 2018;60(4):361-371. doi: 10.24953/turkjped.2018.04.002.
Turk J Pediatr. 2018.
PMID: 30859759
Free article.
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NDE1-related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly.
Bas H, Saylisoy S, Cilingir O, Gokalp EE, Kocagil S, Yarar C, Aras BD, Artan S.
Bas H, et al. Among authors: aras bd.
Am J Med Genet A. 2022 Jan;188(1):326-331. doi: 10.1002/ajmg.a.62508. Epub 2021 Sep 25.
Am J Med Genet A. 2022.
PMID: 34562061
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A pediatric BAL case with double Ph chromosomes and trisomy 5.
Gunden G, Isik S, Ozdemir C, Cİlİngİr O, Bor O, Gokalp EE, Kocagil S, Artan S, Aras BD.
Gunden G, et al. Among authors: aras bd.
Cancer Genet. 2021 Nov;258-259:7-9. doi: 10.1016/j.cancergen.2021.06.005. Epub 2021 Jun 22.
Cancer Genet. 2021.
PMID: 34225100
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BCL2, BCL6, IGH, TP53, and MYC protein expression and gene rearrangements as prognostic markers in diffuse large B-cell lymphoma: a study of 44 Turkish patients.
Akay OM, Aras BD, Isiksoy S, Toprak C, Mutlu FS, Artan S, Oner U, Gulbas Z.
Akay OM, et al. Among authors: aras bd.
Cancer Genet. 2014 Mar;207(3):87-93. doi: 10.1016/j.cancergen.2014.02.001. Epub 2014 Feb 8.
Cancer Genet. 2014.
PMID: 24674866
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