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Rubinstein-Taybi syndrome in diverse populations.
Am J Med Genet A. 2020 Dec;182(12):2939-2950. doi: 10.1002/ajmg.a.61888. Epub 2020 Sep 27.
Am J Med Genet A. 2020.
PMID: 32985117
Comorbidity of congenital heart defects and holoprosencephaly is likely genetically driven and gene-specific.
Tekendo-Ngongang C, Owosela B, Muenke M, Kruszka P.
Tekendo-Ngongang C, et al. Among authors: owosela b.
Am J Med Genet C Semin Med Genet. 2020 Mar;184(1):154-158. doi: 10.1002/ajmg.c.31770. Epub 2020 Feb 5.
Am J Med Genet C Semin Med Genet. 2020.
PMID: 32022405
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Exome Sequencing and Congenital Heart Disease in Sub-Saharan Africa.
Ekure EN, Adeyemo A, Liu H, Sokunbi O, Kalu N, Martinez AF, Owosela B, Tekendo-Ngongang C, Addissie YA, Olusegun-Joseph A, Ikebudu D, Berger SI, Muenke M, Han Z, Kruszka P.
Ekure EN, et al. Among authors: owosela b.
Circ Genom Precis Med. 2021 Feb;14(1):e003108. doi: 10.1161/CIRCGEN.120.003108. Epub 2021 Jan 15.
Circ Genom Precis Med. 2021.
PMID: 33448881
Free PMC article.
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Identifying and improving the "ground truth" of race in disparities research through improved EMR data reporting. A systematic review.
Owosela BO, Steinberg RS, Leslie SL, Celi LA, Purkayastha S, Shiradkar R, Newsome JM, Gichoya JW.
Owosela BO, et al.
Int J Med Inform. 2024 Feb;182:105303. doi: 10.1016/j.ijmedinf.2023.105303. Epub 2023 Nov 30.
Int J Med Inform. 2024.
PMID: 38088002
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