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Author/Creator Campos, Olga

1. Comprehensive analysis and ACMG‐based classification of CHEK2 variants in hereditary cancer patients. Issue 12 (14th October 2020)

Authors:
Vargas‐Parra, Gardenia; del Valle, Jesús; Rofes, Paula; Gausachs, Mireia; Stradella, Agostina; Moreno‐Cabrera, José M.; Velasco, Angela; Tornero, Eva; Menéndez, Mireia; Muñoz, Xavier; Iglesias, Silvia; López‐Doriga, Adriana; Azuara, Daniel; Campos, Olga; Cuesta, Raquel; Darder, Esther; de Cid, Ra...
Journal:
Human mutation
Issue:
Volume 41:Issue 12(2020)
Page Start:
2128
Record Type:
Journal Article
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2. Does multilocus inherited neoplasia alleles syndrome have severe clinical expression?. Issue 8 (22nd December 2018)

Authors:
Stradella, Agostina; del Valle, Jesús; Rofes, Paula; Feliubadaló, Lídia; Grau Garces, Èlia; Velasco, Àngela; González, Sara; Vargas, Gardenia; Izquierdo, Ángel; Campos, Olga; Tornero, Eva; Navarro, Matilde; Balmaña-Gelpi, Judith; Capellá, Gabriel; Pineda, Marta; Brunet, Joan; Lázaro, Conxi
Journal:
Journal of medical genetics
Issue:
Volume 56:Issue 8(2019)
Page Start:
521
Record Type:
Journal Article
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3. Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype. Issue 2 (1st April 2014)

Authors:
Seguí, Nuria; Navarro, Matilde; Pineda, Marta; Köger, Nicole; Bellido, Fernando; González, Sara; Campos, Olga; Iglesias, Silvia; Valdés-Mas, Rafael; López-Doriga, Adriana; Gut, Marta; Blanco, Ignacio; Lázaro, Conxi; Capellá, Gabriel; Puente, Xose S; Plotz, Guido; Valle, Laura
Journal:
Gut
Issue:
Volume 64:Issue 2(2015)
Page Start:
355
Record Type:
Journal Article
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4. ICO Amplicon NGS Data Analysis: A Web Tool for Variant Detection in Common High‐Risk Hereditary Cancer Genes Analyzed by Amplicon GS Junior Next‐Generation Sequencing. Issue 3 (6th December 2013)

Authors:
Lopez‐Doriga, Adriana; Feliubadaló, Lídia; Menéndez, Mireia; Lopez‐Doriga, Sergio; Morón‐Duran, Francisco D.; del Valle, Jesús; Tornero, Eva; Montes, Eva; Cuesta, Raquel; Campos, Olga; Gómez, Carolina; Pineda, Marta; González, Sara; Moreno, Victor; Capellá, Gabriel; Lázaro, Conxi
Journal:
Human mutation
Issue:
Volume 35:Issue 3(2014:Mar.)
Page Start:
271
Record Type:
Journal Article
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5. Primary constitutional MLH1 epimutations: a focal epigenetic event. Issue 8 (16th October 2018)

Authors:
Dámaso, Estela; Castillejo, Adela; Arias, María del Mar; Canet-Hermida, Julia; Navarro, Matilde; del Valle, Jesús; Campos, Olga; Fernández, Anna; Marín, Fátima; Turchetti, Daniela; García-Díaz, Juan de Dios; Lázaro, Conxi; Genuardi, Maurizio; Rueda, Daniel; Alonso, Ángel; Soto, Jose; Hitchins, Me...
Journal:
British journal of cancer
Issue:
Volume 119:Issue 8(2018)
Page Start:
978
Record Type:
Journal Article
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6. Screening of CNVs using NGS data improves mutation detection yield and decreases costs in genetic testing for hereditary cancer. Issue 1 (20th November 2020)

Authors:
Moreno-Cabrera, José Marcos; del Valle, Jesús; Feliubadaló, Lidia; Pineda, Marta; González, Sara; Campos, Olga; Cuesta, Raquel; Brunet, Joan; Serra, Eduard; Capellà, Gabriel; Gel, Bernat; Lázaro, Conxi
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 1(2022)
Page Start:
75
Record Type:
Journal Article
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