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Author/Creator Cuesta, Raquel

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. 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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3. 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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