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De novo variants in exomes of congenital heart disease patients identify risk genes and pathways.
Genome Med. 2020 Jan 15;12(1):9. doi: 10.1186/s13073-019-0709-8.
Genome Med. 2020.
PMID: 31941532
Free PMC article.
Identifying disease-causing mutations in genomes of single patients by computational approaches.
Sevim Bayrak C, Itan Y.
Sevim Bayrak C, et al.
Hum Genet. 2020 Jun;139(6-7):769-776. doi: 10.1007/s00439-020-02179-7. Epub 2020 May 13.
Hum Genet. 2020.
PMID: 32405658
Review.
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Identification of discriminative gene-level and protein-level features associated with pathogenic gain-of-function and loss-of-function variants.
Sevim Bayrak C, Stein D, Jain A, Chaudhary K, Nadkarni GN, Van Vleck TT, Puel A, Boisson-Dupuis S, Okada S, Stenson PD, Cooper DN, Schlessinger A, Itan Y.
Sevim Bayrak C, et al.
Am J Hum Genet. 2021 Dec 2;108(12):2301-2318. doi: 10.1016/j.ajhg.2021.10.007. Epub 2021 Nov 10.
Am J Hum Genet. 2021.
PMID: 34762822
Free PMC article.
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RAG-3D: a search tool for RNA 3D substructures.
Zahran M, Sevim Bayrak C, Elmetwaly S, Schlick T.
Zahran M, et al. Among authors: sevim bayrak c.
Nucleic Acids Res. 2015 Oct 30;43(19):9474-88. doi: 10.1093/nar/gkv823. Epub 2015 Aug 24.
Nucleic Acids Res. 2015.
PMID: 26304547
Free PMC article.
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