Teresa Ramon Y Cajal - Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau

M.A. Rezqallah Aron,L. Duran-Lozano, A. López-Fernández,E. Darder, R. Alfonso, M. Cartró, A.R. Jiménez-Macedo, A. Bareas,M. Cruellas Lapena, A. Moles-Fernández, M. Torres, A. Vallmajó,G. Llort Pursals, A. Roqué Lloveras, C. Llorente,M. Espinosa-Bravo, N. Tuset,T. Ramon y Cajal,J.M. Brunet Vidal, J. Balmaña Gelpi

ESMO Open (2024)

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Erratum to ‘The benefit of adding polygenic risk scores, lifestyle factors, and breast density to family history and genetic status for breast cancer risk and surveillance classification of unaffected women from germline CHEK2 c.1100delC families’ [The Breast 73 (2024) 103611]

Maartje A.C. Schreurs,Teresa Ramón y Cajal,Muriel A. Adank,J. Margriet Collée,Antoinette Hollestelle,Jeroen van Rooij,Marjanka K. Schmidt,Maartje J. Hooning

The Breast (2024): 103723

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Open-source Bioinformatic Pipeline to Improve PMS2 Genetic Testing Using Short-Read NGS Data

Elisabet Munte,Lidia Feliubadalo,Jesus Del Valle,Sara Gonzalez, Mireia Ramos-Muntada,Judith Balmana,Teresa Ramon y Caja,Noemi Tuset,Gemma Llort,Juan Cadinanos,Joan Brunet,Gabriel Capella,Conxi Lazaro,Marta Pineda

JOURNAL OF MOLECULAR DIAGNOSTICS（2024）

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Clinical Relevance of Tumour-Infiltrating Immune Cells in HER2-Negative Breast Cancer Treated with Neoadjuvant Therapy

Cristina Arqueros,Alberto Gallardo,Silvia Vidal,Ruben Osuna-Gomez,Ariadna Tibau,Olga Lidia Bell,Teresa Cajal,Enrique Lerma, Barbara Lobato-Delgado,Juliana Salazar,Agusti Barnadas

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCESno. 5 (2024)

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Genetic and Clinical Characterization of a Novel FH Founder Mutation in Families with Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome

Ana Beatriz Sánchez-Heras,Estela Dámaso,Adela Castillejo,Mercedes Robledo,Alexandre Teulé,Conxi Lázaro,Rosario Sánchez-Martínez,Ángel Zúñiga,Adrià López-Fernández,Judith Balmaña,Luis Robles,Teresa Ramon y Cajal,M. Isabel Castillejo, Raquel Perea Ibañez, Carmen Martínez Sevila, Andrea Sánchez-Mira,Inés Escandell,Luís Gómez,Pere Berbel,José Luis Soto

Orphanet journal of rare diseasesno. 1 (2024): 26-26

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