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

Year Number of Results
2002 1
2009 1
2010 1
2011 1
2012 3
2013 1
2014 1
2015 5
2016 7
2017 8
2018 4
2019 7
2020 10
2021 9
2022 5
2023 6
2024 1

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62 results

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Page 1
Functional profiling of the Saccharomyces cerevisiae genome.
Giaever G, Chu AM, Ni L, Connelly C, Riles L, Véronneau S, Dow S, Lucau-Danila A, Anderson K, André B, Arkin AP, Astromoff A, El-Bakkoury M, Bangham R, Benito R, Brachat S, Campanaro S, Curtiss M, Davis K, Deutschbauer A, Entian KD, Flaherty P, Foury F, Garfinkel DJ, Gerstein M, Gotte D, Güldener U, Hegemann JH, Hempel S, Herman Z, Jaramillo DF, Kelly DE, Kelly SL, Kötter P, LaBonte D, Lamb DC, Lan N, Liang H, Liao H, Liu L, Luo C, Lussier M, Mao R, Menard P, Ooi SL, Revuelta JL, Roberts CJ, Rose M, Ross-Macdonald P, Scherens B, Schimmack G, Shafer B, Shoemaker DD, Sookhai-Mahadeo S, Storms RK, Strathern JN, Valle G, Voet M, Volckaert G, Wang CY, Ward TR, Wilhelmy J, Winzeler EA, Yang Y, Yen G, Youngman E, Yu K, Bussey H, Boeke JD, Snyder M, Philippsen P, Davis RW, Johnston M. Giaever G, et al. Among authors: benito r. Nature. 2002 Jul 25;418(6896):387-91. doi: 10.1038/nature00935. Nature. 2002. PMID: 12140549
Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY.
Mansouri L, Thorvaldsdottir B, Sutton LA, Karakatsoulis G, Meggendorfer M, Parker H, Nadeu F, Brieghel C, Laidou S, Moia R, Rossi D, Catherwood M, Kotaskova J, Delgado J, Rodríguez-Vicente AE, Benito R, Rigolin GM, Bonfiglio S, Scarfo L, Mattsson M, Davis Z, Gogia A, Rani L, Baliakas P, Foroughi-Asl H, Jylhä C, Skaftason A, Rapado I, Miras F, Martinez-Lopez J, de la Serna J, Rivas JMH, Thornton P, Larráyoz MJ, Calasanz MJ, Fésüs V, Mátrai Z, Bödör C, Smedby KE, Espinet B, Puiggros A, Gupta R, Bullinger L, Bosch F, Tazón-Vega B, Baran-Marszak F, Oscier D, Nguyen-Khac F, Zenz T, Terol MJ, Cuneo A, Hernández-Sánchez M, Pospisilova S, Mills K, Gaidano G, Niemann CU, Campo E, Strefford JC, Ghia P, Stamatopoulos K, Rosenquist R. Mansouri L, et al. Among authors: benito r. Leukemia. 2023 Feb;37(2):339-347. doi: 10.1038/s41375-022-01802-y. Epub 2022 Dec 24. Leukemia. 2023. PMID: 36566271 Free PMC article.
Inherited Thrombocytopenia Caused by Variants in Crucial Genes for Glycosylation.
Marín-Quílez A, Díaz-Ajenjo L, Di Buduo CA, Zamora-Cánovas A, Lozano ML, Benito R, González-Porras JR, Balduini A, Rivera J, Bastida JM. Marín-Quílez A, et al. Among authors: benito r. Int J Mol Sci. 2023 Mar 7;24(6):5109. doi: 10.3390/ijms24065109. Int J Mol Sci. 2023. PMID: 36982178 Free PMC article. Review.
Platelet transcriptome analysis in patients with germline RUNX1 mutations.
Palma-Barqueros V, Bastida JM, López Andreo MJ, Zámora-Cánovas A, Zaninetti C, Ruiz-Pividal JF, Bohdan N, Padilla J, Teruel-Montoya R, Marín-Quilez A, Revilla N, Sánchez-Fuentes A, Rodriguez-Alen A, Benito R, Vicente V, Iturbe T, Greinacher A, Lozano ML, Rivera J; Grupo Español de Alteraciones Plaquetarias Congénitas (GEAPC); Spanish Society of Thrombosis and Haemostasis (SETH). Palma-Barqueros V, et al. Among authors: benito r. J Thromb Haemost. 2023 May;21(5):1352-1365. doi: 10.1016/j.jtha.2023.01.023. Epub 2023 Feb 1. J Thromb Haemost. 2023. PMID: 36736831
Targeted genome editing in acute lymphoblastic leukemia: a review.
Montaño A, Forero-Castro M, Hernández-Rivas JM, García-Tuñón I, Benito R. Montaño A, et al. Among authors: benito r. BMC Biotechnol. 2018 Jul 17;18(1):45. doi: 10.1186/s12896-018-0455-9. BMC Biotechnol. 2018. PMID: 30016959 Free PMC article. Review.
Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders.
Bastida JM, Benito R, Lozano ML, Marín-Quilez A, Janusz K, Martín-Izquierdo M, Hernández-Sánchez J, Palma-Barqueros V, Hernández-Rivas JM, Rivera J, González-Porras JR. Bastida JM, et al. Among authors: benito r. Semin Thromb Hemost. 2019 Oct;45(7):695-707. doi: 10.1055/s-0039-1687889. Epub 2019 Apr 30. Semin Thromb Hemost. 2019. PMID: 31041795 Review.
Novel variants in GALE cause syndromic macrothrombocytopenia by disrupting glycosylation and thrombopoiesis.
Marín-Quílez A, Di Buduo CA, Díaz-Ajenjo L, Abbonante V, Vuelta E, Soprano PM, Miguel-García C, Santos-Mínguez S, Serramito-Gómez I, Ruiz-Sala P, Peñarrubia MJ, Pardal E, Hernández-Rivas JM, González-Porras JR, García-Tuñón I, Benito R, Rivera J, Balduini A, Bastida JM. Marín-Quílez A, et al. Among authors: benito r. Blood. 2023 Jan 26;141(4):406-421. doi: 10.1182/blood.2022016995. Blood. 2023. PMID: 36395340 Free PMC article.
NEMHESYS-European Perspective on the Implementation of Next-generation Sequencing Into Clinical Diagnostics.
Serramito-Gómez I, Clarke KM, Rodríguez-Vicente AE, McGimpsey JE, Abáigar M, Díez CB, Benito R, Bullinger L, Mills KI, Hernández Rivas JM. Serramito-Gómez I, et al. Among authors: benito r. Hemasphere. 2021 Feb 17;5(3):e541. doi: 10.1097/HS9.0000000000000541. eCollection 2021 Mar. Hemasphere. 2021. PMID: 33623883 Free PMC article. No abstract available.
aCGH-MAS: analysis of aCGH by means of multiagent system.
De Paz JF, Benito R, Bajo J, Rodríguez AE, Abáigar M. De Paz JF, et al. Among authors: benito r. Biomed Res Int. 2015;2015:194624. doi: 10.1155/2015/194624. Epub 2015 Mar 22. Biomed Res Int. 2015. PMID: 25874203 Free PMC article. Review.
62 results