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Zeng W, Hu B, Tang L, You YY, Toderici M, Eugenia de la Morena-Barrio M, Corral J, Hu Y. Correction: Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency. Oncotarget. 2018 Feb 16;9(13):11428. doi: 10.18632/oncotarget.24519. eCollection 2018 Feb 16. PubMed PMID: 29542734; PubMed Central PMCID: PMC5834269.
AÑO: 2018
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29542734
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Abad-Navarro F, de la Morena-Barrio ME, Fernández-Breis JT, Corral J. Lost in translation: bioinformatic analysis of variations affecting the translation initiation codon in the human genome. Bioinformatics. 2018 Nov 15;34(22):3788-3794. doi: 10.1093/bioinformatics/bty453. PubMed PMID: 29868922.
AÑO: 2018; IF: 4.531
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Salloum-Asfar S, de la Morena-Barrio ME, Esteban J, Miñano A, Aroca C, Vicente V, Roldán V, Corral J. Assessment of two contact activation reagents for the diagnosis of congenital factor XI deficiency. Thromb Res. 2018 Mar;163:64-70. doi: 10.1016/j.thromres.2017.12.023. Epub 2018 Jan 3. PubMed PMID: 29367083.
AÑO: 2018; IF: 3.266
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de la Morena-Barrio ME, Ballesta-Martínez MJ, López-Gálvez R, Antón AI, López-González V, Martínez-Ribot L, Padilla J, Miñano A, García-Algar O, Del Campo M, Corral J, Guillén-Navarro E, Vicente V. Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation. Pediatr Res. 2018 Jan;83(1-1):119-127. doi: 10.1038/pr.2017.201. Epub 2017 Sep 20. PubMed PMID: 28820871.
AÑO: 2018; IF: 2.88
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Navarro-Fernández J, Eugenia de la Morena-Barrio M, Martínez-Alonso E, Dybedal I, Toderici M, Bohdan N, Miñano A, Heimdal K, Abildgaard U, Martínez-Menárguez JÁ, Corral J, Vicente V. Biochemical and cellular consequences of the antithrombin p.Met1? mutation identified in a severe thrombophilic family. Oncotarget. 2018 Sep 4;9(69):33202-33214. doi: 10.18632/oncotarget.26059. eCollection 2018 Sep 4. PubMed PMID: 30237862; PubMed Central PMCID: PMC6145704.
AÑO: 2018
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