Articoli con mandati relativi all'accesso pubblico - Ignacio BlancoUlteriori informazioni
Non disponibili pubblicamente: 11
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Diagnostic accuracy of the faecal immunochemical test for colorectal cancer in symptomatic patients: comparison with NICE and SIGN referral criteria
J Cubiella, M Salve, M Díaz‐Ondina, P Vega, MT Alves, F Iglesias, ...
Colorectal Disease 16 (8), O273-O282, 2014
Mandati: Government of Spain
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Analysis of intratumor heterogeneity in Neurofibromatosis type 1 plexiform neurofibromas and neurofibromas with atypical features: Correlating histological and genomic findings
M Carrió, B Gel, E Terribas, AC Zucchiatti, T Moliné, I Rosas, Á Teulé, ...
Human mutation 39 (8), 1112-1125, 2018
Mandati: Government of Spain
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Comprehensive functional assessment of MLH1 variants of unknown significance
E Borràs, M Pineda, A Brieger, I Hinrichsen, C Gómez, M Navarro, ...
Human mutation 33 (11), 1576-1588, 2012
Mandati: Government of Spain
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Assessing the RNA effect of 26 DNA variants in the BRCA1 and BRCA2 genes
M Menéndez, J Castellsagué, M Mirete, E Pros, L Feliubadaló, A Osorio, ...
Breast cancer research and treatment 132, 979-992, 2012
Mandati: Government of Spain
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Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers
J Zugazagoitia, P Pérez-Segura, A Manzano, I Blanco, A Vega, ...
Breast cancer research and treatment 148, 415-421, 2014
Mandati: Government of Spain
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Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype
N Seguí, M Navarro, M Pineda, N Köger, F Bellido, S González, ...
Gut 64 (2), 355-356, 2015
Mandati: Government of Spain
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Evidence for a link between TNFRSF11A and risk of breast cancer
N Bonifaci, M Palafox, P Pellegrini, A Osorio, J Benitez, P Peterlongo, ...
Breast cancer research and treatment 129, 947-954, 2011
Mandati: Government of Spain
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Identification of a founder EPCAM deletion in Spanish Lynch syndrome families
P Mur, M Pineda, A Romero, J Del Valle, E Borras, A Canal, M Navarro, ...
Clinical Genetics 85 (3), 260-266, 2014
Mandati: Government of Spain
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Chromosomal translocations inactivating CDKN2A support a single path for malignant peripheral nerve sheath tumor initiation
M Magallón-Lorenz, J Fernández-Rodríguez, E Terribas, ...
Human Genetics 140 (8), 1241-1252, 2021
Mandati: US National Institutes of Health, Government of Spain
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Revisiting the UK Genetic Severity Score for NF2: a proposal for the addition of a functional genetic component
N Catasús, B Garcia, I Galván-Femenía, A Plana, A Negro, I Rosas, A Ros, ...
Journal of Medical Genetics 59 (7), 678-686, 2022
Mandati: Government of Spain
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Identification of a new complex rearrangement affecting exon 20 of BRCA1
J Del Valle, O Campos, A Velasco, E Darder, M Menéndez, L Feliubadaló, ...
Breast cancer research and treatment 130, 341-344, 2011
Mandati: Government of Spain
Disponibili pubblicamente: 136
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Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
HFA Vasen, I Blanco, K Aktan-Collan, JP Gopie, A Alonso, S Aretz, ...
Gut 62 (6), 812-823, 2013
Mandati: Cancer Research UK
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Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
N Mavaddat, D Barrowdale, IL Andrulis, SM Domchek, D Eccles, ...
Cancer Epidemiology, Biomarkers & Prevention 21 (1), 134-147, 2012
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
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Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer
KL Bolton, G Chenevix-Trench, C Goh, S Sadetzki, SJ Ramus, BY Karlan, ...
Jama 307 (4), 382-389, 2012
Mandati: US National Institutes of Health, Cancer Research UK, Government of Spain
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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
SE Bojesen, KA Pooley, SE Johnatty, J Beesley, K Michailidou, JP Tyrer, ...
Nature genetics 45 (4), 371-384, 2013
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
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Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
P Møller, TT Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 67 (7), 1306-1316, 2018
Mandati: National Health and Medical Research Council, Australia, Swedish Research …
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Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
TR Rebbeck, N Mitra, F Wan, OM Sinilnikova, S Healey, L McGuffog, ...
Jama 313 (13), 1347-1361, 2015
Mandati: US National Institutes of Health, Cancer Research UK, National Institute for …
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Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
P Møller, T Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 66 (3), 464-472, 2017
Mandati: Cancer Research UK, UK Medical Research Council, National Institute for …
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
M Dominguez-Valentin, JR Sampson, TT Seppälä, SW Ten Broeke, ...
Genetics in Medicine 22 (1), 15-25, 2020
Mandati: US National Institutes of Health, National Institute for Health Research, UK …
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Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths
P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ...
Science immunology 6 (62), eabl4340, 2021
Mandati: US National Institutes of Health, Howard Hughes Medical Institute, National …
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