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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 3
2010 2
2011 1
2012 3
2015 1
2016 2
2017 2
2018 1
2019 1
2020 1
2021 1
2022 1
2023 1
2024 0

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21 results

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Page 1
The present and future of gene profiling in breast cancer.
Espinosa E, Gámez-Pozo A, Sánchez-Navarro I, Pinto A, Castañeda CA, Ciruelos E, Feliu J, Vara JA. Espinosa E, et al. Among authors: sanchez navarro i. Cancer Metastasis Rev. 2012 Jun;31(1-2):41-6. doi: 10.1007/s10555-011-9327-7. Cancer Metastasis Rev. 2012. PMID: 22124734 Review.
Allelic overload and its clinical modifier effect in Bardet-Biedl syndrome.
Perea-Romero I, Solarat C, Blanco-Kelly F, Sanchez-Navarro I, Bea-Mascato B, Martin-Salazar E, Lorda-Sanchez I, Swafiri ST, Avila-Fernandez A, Martin-Merida I, Trujillo-Tiebas MJ, Carreño E, Jimenez-Rolando B, Garcia-Sandoval B, Minguez P, Corton M, Valverde D, Ayuso C. Perea-Romero I, et al. Among authors: sanchez navarro i. NPJ Genom Med. 2022 Jul 14;7(1):41. doi: 10.1038/s41525-022-00311-2. NPJ Genom Med. 2022. PMID: 35835773 Free PMC article.
The efficacy of a medication review programme conducted in an emergency department.
Santolaya-Perrín R, Calderón-Hernanz B, Jiménez-Díaz G, Galán-Ramos N, Moreno-Carvajal MT, Rodríguez-Camacho JM, Serra-Simó P, García-Ortiz JC, Tarradas-Torras J, Ginés-Palomares A, Sánchez-Navarro I. Santolaya-Perrín R, et al. Among authors: sanchez navarro i. Int J Clin Pharm. 2019 Jun;41(3):757-766. doi: 10.1007/s11096-019-00836-0. Epub 2019 Apr 26. Int J Clin Pharm. 2019. PMID: 31028596 Clinical Trial.
NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases.
Perea-Romero I, Blanco-Kelly F, Sanchez-Navarro I, Lorda-Sanchez I, Tahsin-Swafiri S, Avila-Fernandez A, Martin-Merida I, Trujillo-Tiebas MJ, Lopez-Rodriguez R, Rodriguez de Alba M, Iancu IF, Romero R, Quinodoz M, Hakonarson H, Garcia-Sandova B, Minguez P, Corton M, Rivolta C, Ayuso C. Perea-Romero I, et al. Among authors: sanchez navarro i. Hum Genet. 2021 Dec;140(12):1665-1678. doi: 10.1007/s00439-021-02343-7. Epub 2021 Aug 26. Hum Genet. 2021. PMID: 34448047 Free PMC article.
Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa.
Perez-Carro R, Corton M, Sánchez-Navarro I, Zurita O, Sanchez-Bolivar N, Sánchez-Alcudia R, Lelieveld SH, Aller E, Lopez-Martinez MA, López-Molina MI, Fernandez-San Jose P, Blanco-Kelly F, Riveiro-Alvarez R, Gilissen C, Millan JM, Avila-Fernandez A, Ayuso C. Perez-Carro R, et al. Among authors: sanchez navarro i. Sci Rep. 2016 Jan 25;6:19531. doi: 10.1038/srep19531. Sci Rep. 2016. PMID: 26806561 Free PMC article.
MALDI profiling of human lung cancer subtypes.
Gámez-Pozo A, Sánchez-Navarro I, Nistal M, Calvo E, Madero R, Díaz E, Camafeita E, de Castro J, López JA, González-Barón M, Espinosa E, Fresno Vara JA. Gámez-Pozo A, et al. Among authors: sanchez navarro i. PLoS One. 2009 Nov 5;4(11):e7731. doi: 10.1371/journal.pone.0007731. PLoS One. 2009. PMID: 19890392 Free PMC article.
Aurora kinases as prognostic biomarkers in ovarian carcinoma.
Mendiola M, Barriuso J, Mariño-Enríquez A, Redondo A, Domínguez-Cáceres A, Hernández-Cortés G, Pérez-Fernández E, Sánchez-Navarro I, Vara JA, Suárez A, Espinosa E, González-Barón M, Palacios J, Hardisson D. Mendiola M, et al. Among authors: sanchez navarro i. Hum Pathol. 2009 May;40(5):631-8. doi: 10.1016/j.humpath.2008.10.011. Epub 2009 Jan 20. Hum Pathol. 2009. PMID: 19157502
Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment.
García-García G, Sanchez-Navarro I, Aller E, Jaijo T, Fuster-Garcia C, Rodríguez-Munoz A, Vallejo E, Tellería JJ, Vázquez S, Beltrán S, Derdak S, Zurita O, Villaverde-Montero C, Avila-Fernández A, Corton M, Blanco-Kelly F, Hakonarson H, Millán JM, Ayuso C. García-García G, et al. Among authors: sanchez navarro i. Mol Vis. 2020 Mar 18;26:216-225. eCollection 2020. Mol Vis. 2020. PMID: 32214787 Free PMC article.
21 results