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Genetic variants of VWF gene in type 2 von Willebrand disease.
Freitas SDS, Rezende SM, de Oliveira LC, Prezotti ANL, Renni MS, Corsini CA, Amorim MVA, Matosinho CGR, Carvalho MRS, Chaves DG. Freitas SDS, et al. Among authors: carvalho mrs. Haemophilia. 2019 Mar;25(2):e78-e85. doi: 10.1111/hae.13714. Epub 2019 Feb 28. Haemophilia. 2019. PMID: 30817071
Identification and in silico characterization of structural and functional impacts of genetic variants in milk protein genes in the Zebu breeds Guzerat and Gyr.
Matosinho CGR, Rosse IC, Fonseca PAS, de Oliveira FS, Dos Santos FG, Araújo FMG, de Matos Salim AC, Lopes BC, Arbex WA, Machado MA, Peixoto MGCD, da Silva Verneque R, Martins MF, da Silva MVGB, Oliveira G, Pires DEV, Carvalho MRS. Matosinho CGR, et al. Among authors: carvalho mrs. Trop Anim Health Prod. 2021 Oct 27;53(6):524. doi: 10.1007/s11250-021-02970-2. Trop Anim Health Prod. 2021. PMID: 34705124
NAToRA, a relatedness-pruning method to minimize the loss of dataset size in genetic and omics analyses.
Leal TP, Furlan VC, Gouveia MH, Saraiva Duarte JM, Fonseca PA, Tou R, Scliar MO, Araujo GS, Costa LF, Zolini C, Peixoto MGCD, Carvalho MRS, Lima-Costa MF, Gilman RH, Tarazona-Santos E, Rodrigues MR. Leal TP, et al. Among authors: carvalho mrs. Comput Struct Biotechnol J. 2022 Apr 9;20:1821-1828. doi: 10.1016/j.csbj.2022.04.009. eCollection 2022. Comput Struct Biotechnol J. 2022. PMID: 35521552 Free PMC article.
In deep bioinformatic characterization of a novel fumarate hydratase variant FH c.199T > G; (p.Tyr67Asp) in hereditary leiomyomatosis and renal cell carcinoma.
Chami A, de Souza Zózimo TR, Alves TM, Matosinho CGR, Santos C, Simões MM, Cabral WLR, de Paula Ricardo BF, da Silva Filho AL, Carvalho MRS, da Conceição Braga L. Chami A, et al. Among authors: carvalho mrs. Fam Cancer. 2023 Oct;22(4):481-486. doi: 10.1007/s10689-023-00335-2. Epub 2023 Jun 15. Fam Cancer. 2023. PMID: 37316640
46 results