J. M. Rosa-Rosa

发表

Histological changes secondary to wire coil placement in breast tissue and lymph nodes

M. E. Reguero, J. Palacios, B. Pérez-Mies, 2018, Virchows Archiv.

The Clonal Relationship Between the Ductal and Lobular Components of Mixed Ductal-Lobular Carcinomas Suggested a Ductal Origin in Most Tumors

David Pizarro, M. Biscuola, M. López-García, 2022, The American journal of surgical pathology.

Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.

M. Urioste, J. Benítez, A. González-Neira, 2009, American journal of human genetics.

Detection of kinase domain mutations in BCR::ABL1 leukemia by ultra-deep sequencing of genomic DNA

S. Mercadal, E. Barragán, L. Villalón, 2022, Scientific Reports.

A method for resequencing from minimal amounts of starting DNA.

A. Ashworth, M. Zvelebil, I. Kozarewa, 2012 .

Mutational Screening of BRCA1/2 Genes as a Predictive Factor for Therapeutic Response in Epithelial Ovarian Cancer: A Consensus Guide from the Spanish Society of Pathology (SEAP-IAP) and the Spanish Society of Human Genetics (AEGH)

J. Cigudosa, F. Rojo, A. Osorio, 2019, Virchows Archiv.

NGS-Based Molecular Karyotyping of Multiple Myeloma: Results from the GEM12 Clinical Trial

M. Calasanz, X. Agirre, A. Oriol, 2022, Cancers.

Molecular Basis of Tumor Heterogeneity in Endometrial Carcinosarcoma

S. Ong, M. Biscuola, J. Palacios, 2019, Cancers.

Treating KRAS-mutant NSCLC: latest evidence and clinical consequences

F. López-Ríos, J. Palacios, P. Garrido, 2017, Therapeutic advances in medical oncology.

Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles

J. Benítez, M. Southey, F. Odefrey, 2013, PloS one.

A core microRNA signature associated with inducers of the epithelial‐to‐mesenchymal transition

A. Díaz-López, G. Moreno-Bueno, J. Palacios, 2014, The Journal of pathology.

VGLL1 expression is associated with a triple-negative basal-like phenotype in breast cancer.

J. Benítez, A. Calcabrini, J. Palacios, 2014, Endocrine-related cancer.

Pleomorphic lobular carcinoma of the breast with osteoclast-like giant cells: a case report and review of the literature

N. Martínez-Jáñez, M. E. Reguero-Callejas, J. Palacios, 2018, Diagnostic Pathology.

High Frequency of ERBB2 Activating Mutations in Invasive Lobular Breast Carcinoma with Pleomorphic Features

P. Garrido, E. Holgado, E. López-Miranda, 2019, Cancers.

Deep Sequencing of Target Linkage Assay-Identified Regions in Familial Breast Cancer: Methods, Analysis Pipeline and Troubleshooting

Z. Xuan, J. Benítez, G. Hannon, 2010, PloS one.

Molecular Pathology of Uterine Carcinosarcoma

M. Biscuola, S. Leskelä, J. Palacios, 2017 .

Dedifferentiated endometrial carcinomas with neuroendocrine features: a clinicopathologic, immunohistochemical, and molecular genetic study.

J. Prat, I. Espinosa, E. D'angelo, 2018, Human pathology.

The Frequency and Prognostic Significance of the Histologic Type in Early-stage Ovarian Carcinoma

J. López-Guerrero, A. Poveda, D. Hardisson, 2019, The American journal of surgical pathology.

Next generation sequencing to decipher concurrent loss of PMS2 and MSH6 in colorectal cancer

C. Guillén, C. Perna, J. Palacios, 2020, Diagnostic Pathology.

Mismatch Repair Deficiency in Ovarian Carcinoma

J. López-Guerrero, J. Ibarra, R. Guarch, 2020, The American journal of surgical pathology.

Modified SureSelectQXT Target Enrichment Protocol for Illumina Multiplexed Sequencing of FFPE Samples

J. Palacios, P. Garrido, S. Leskelä, 2018, Biological Procedures Online.

Molecular genetic heterogeneity in undifferentiated endometrial carcinomas

X. Matías-Guiu, J. Prat, R. Soslow, 2016, Modern Pathology.

Molecular genetic heterogeneity in undifferentiated endometrial carcinomas

X. Matías-Guiu, J. Prat, R. Soslow, 2016, Modern Pathology.

Real-life disease monitoring in follicular lymphoma patients using liquid biopsy ultra-deep sequencing and PET/CT

T. Baumann, I. Rapado, M. Mollejo, 2023, Leukemia.

A Modified Method for Whole Exome Resequencing from Minimal Amounts of Starting DNA

A. Ashworth, M. Zvelebil, G. Morgan, 2012, PloS one.

Molecular Heterogeneity of Endometrioid Ovarian Carcinoma

J. López-Guerrero, A. Poveda, S. Montes, 2020, The American journal of surgical pathology.

A 7 Mb region within 11q13 may contain a high penetrance gene for breast cancer

Peter Devilee, Javier Benitez, Roger L. Milne, 2009, Breast Cancer Research and Treatment.

Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies

J. Benítez, M. Southey, P. Devilee, 2007, BMC Genomics.

Identification of Immunoglobulin Gene Rearrangement Biomarkers in Multiple Myeloma through cfDNA-Based Liquid Biopsy Using tchDNA-Seq

J. Martínez-López, Natalia Buenache, J. M. Rosa-Rosa, 2023, Cancers.

Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies

J. Benítez, M. Southey, P. Devilee, 2007, BMC Genomics.

Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.

M. Urioste, J. Benítez, A. González-Neira, 2009, American journal of human genetics.