J. García

发表

Molecular Characterization of the Region 7q22.1 in Splenic Marginal Zone Lymphomas

J. Martinez-Climent, M. Piris, Jesús M. Hernández, 2011, PloS one.

Malignant Lymphomas Splenic marginal zone B-cell lymphomas : two cytogenetic subtypes , one with gain of 3 q and the other with loss of 7 q

J. Climent, S. Serrano, I. Benet, 2022 .

Pseudomesotheliomatous carcinoma of the lung with a distinct morphology, immunohistochemistry, and comparative genomic hybridization profile.

E. de Álava, J. García, A. Panizo, 2007, Annals of diagnostic pathology.

The value of fluorescence in situ hybridization for the detection of 11q in multiple myeloma.

J. Hernández, N. Gutiérrez, J. S. San Miguel, 2004, Haematologica.

Imatinib therapy of chronic myeloid leukemia restores the expression levels of key genes for DNA damage and cell-cycle progression

N. Gutiérrez, M. Delgado, C. Robledo, 2012, Pharmacogenetics and genomics.

P53 deletion may drive the clinical evolution and treatment response in multiple myeloma

T. Flores, N. Gutiérrez, J. S. San Miguel, 2010, European journal of haematology.

Immunomodulatory effect of 5-azacytidine (5-azaC): potential role in the transplantation setting.

F. J. Gonzalez, E. Ballestar, B. Blanco, 2010, Blood.

Comparative genomic hybridization analysis of basal cell carcinoma

R. González-Sarmiento, J. García, E. Fernández‐López, 2019, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.

Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes

J. Hernández-Rivas, A. Kohlmann, M. D. del Cañizo, 2016, PloS one.

Clinical applications of BAC array-CGH to the study of diffuse large B-cell lymphomas.

J. Hernández, C. Robledo, J. García, 2013, Methods in molecular biology.

Array comparative genomic hybridization identifies genetic regions associated with outcome in aggressive diffuse large B‐cell lymphomas

Marcos González, J. Hernández, M. Piris, 2009, Cancer.

Transient t(11;17)(q14;q12) in patient with chronic myelogenous leukemia in complete molecular response.

Marcos González, J. Hernández, N. Gutiérrez, 2008, Cancer genetics and cytogenetics.

Effects of imatinib mesylate on normal bone marrow cells from chronic myeloid leukemia patients in complete cytogenetic response.

J. Miguel, Jesús M. Hernández, N. Gutiérrez, 2009, Leukemia research.

Commentary: Genomic Analysis Reveals Heterogeneity Between Lesions in Synchronous Primary Right-Sided and Left-Sided Colon Cancer

M. Urioste, R. González-Sarmiento, L. Corchete, 2022, Frontiers in Molecular Biosciences.

Toward a Molecular Classification of Synchronous Colorectal Cancer: Clinical and Molecular Characterization

M. Urioste, J. García, D. Rueda, 2017, Clinical colorectal cancer.

Genome-wide profiling of methylation identifies novel targets with aberrant hyper-methylation and reduced expression in low-risk myelodysplastic syndromes

J. Hernández-Rivas, S. Aibar, Jesús M. Hernández, 2012 .

Long-read sequencing resolves structural variants in SERPINC1 causing antithrombin deficiency and identifies a complex rearrangement and a retrotransposon insertion not characterized by routine diagnostic methods

Nicholas S. Gleadall, W. Ouwehand, P. Morange, 2020, bioRxiv.

Heterogeneity of structural abnormalities in the 7q31.3∼q34 region in myeloid malignancies

F. Solé, J. Hernández, J. Miguel, 2004 .

Response to imatinib mesylate in patients with hypereosinophilic syndrome

J. Hernández-Rivas, N. Gutiérrez, J. Rodríguez, 2012, International Journal of Hematology.

Incidence and clinical characteristics of myeloproliferative neoplasms displaying a PDGFRB rearrangement

N. Gutiérrez, J. García, P. Giraldo, 2012, European journal of haematology.

Recurrent NOMO1 Gene Deletion Is a Potential Clinical Marker in Early-Onset Colorectal Cancer and Is Involved in the Regulation of Cell Migration

R. González-Sarmiento, M. Sánchez-Martín, L. Corchete, 2022, Cancers.

Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency

Nicholas S. Gleadall, W. Ouwehand, P. Morange, 2022, Thrombosis and haemostasis.

Long-Read Sequencing Identi ﬁ es the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin De ﬁ ciency

Nicholas S. Gleadall, W. Ouwehand, P. Morange, 2022 .

Comment on ‘Wild-type APC prediction of poor prognosis in microsatellite-stable proximal colorectal cancer differs according to the age of onset'

M. Urioste, R. González-Sarmiento, J. García, 2016, British Journal of Cancer.

Imatinib mesylate elicits positive clinical response in atypical chronic myeloid leukemia involving the platelet-derived growth factor receptor beta.

J. Hernández, N. Gutiérrez, J. S. San Miguel, 2003, Blood.

Artículo 6 : “ Autophagy modulation in head and neck squamous cell carcinoma cell lines : a new target for cancer treatment ”

J. García, B. Pérez, Hernández, 2018 .

Analysis of chromosomal imbalances in an elderly woman with a giant cell tumour

J. Hernández, T. Flores, C. Robledo, 2005, Virchows Archiv.

Onychomatricoma: genome-wide analyses of a rare nail matrix tumor.

C. Robledo, J. García, Á. Santos-Briz, 2011, Journal of the American Academy of Dermatology.

Atypical chronic myeloid leukemia (aCML)

Jesús M. Hernández, J. García, M. Arefi, 2011 .

CRISPR/Cas9-generated models uncover therapeutic vulnerabilities of del(11q) CLL cells to dual BCR and PARP inhibition

J. Hernández-Rivas, Catherine J. Wu, I. García-Tuñón, 2020, Leukemia.

Expression of VAV1 in the tumour microenvironment of glioblastoma multiforme

Jesús M. Hernández, J. Couceiro, X. Bustelo, 2012, Journal of Neuro-Oncology.

Molecular analysis of ex-vivo CD133+ GBM cells revealed a common invasive and angiogenic profile but different proliferative signatures among high grade gliomas

J. Hernández-Rivas, R. González-Sarmiento, M. Pérez-Caro, 2010, BMC Cancer.

Post-transcriptional Modifications Contribute to the Upregulation of Cyclin D2 in Multiple Myeloma

I. Sánchez-García, L. Corchete, N. Gutiérrez, 2015, Clinical Cancer Research.

A high number of losses in 13q14 chromosome band is associated with a worse outcome and biological differences in patients with B-cell chronic lymphoid leukemia

C. Fontanillo, F. Ortuño, N. Gutiérrez, 2009, Haematologica.

Early-onset colorectal cancer: a separate subset of colorectal cancer.

J. García, D. Rueda, J. Perea, 2014, World journal of gastroenterology.

TET2 Overexpression in Chronic Lymphocytic Leukemia Is Unrelated to the Presence of TET2 Variations

Marcos González, J. Hernández-Rivas, A. Kohlmann, 2014, BioMed research international.

Molecular Characterization of Chronic Lymphocytic Leukemia Patients with a High Number of Losses in 13q14

Marcos González, J. Hernández-Rivas, N. Gutiérrez, 2012, PloS one.

The presence of genomic imbalances is associated with poor outcome in patients with burkitt lymphoma treated with dose‐intensive chemotherapy including rituximab

L. Escoda, M. Tormo, J. Hernández-Rivas, 2016, British journal of haematology.

Primary Mixed Squamous Carcinoma and Osteosarcoma (Carcinosarcomas) of the Lung Have a CGH Mapping Similar to Primitive Squamous Carcinomas and Osteosarcomas

E. Álava, J. García, A. Panizo, 2008, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Genomic analysis of clonal eosinophils by CGH arrays reveals new genetic regions involved in chronic eosinophilia

J. Hernández-Rivas, C. Robledo, J. García, 2014, European journal of haematology.

17265 Healthcare-associatedhepatitisCvirusinfection

Y. Doki, E. Maccaroni, R. Berardi, 2014 .

Chromosomal imbalances identified by comparative genomic hybridization in sporadic parathyroid adenomas.

Jesús M. Hernández, J. R. Polo, J. Tardío, 2002, European journal of endocrinology.

Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome

J. Hernández-Rivas, J. Rodríguez, J. Labrador, 2016, PloS one.

Prognostic and biologic significance of chromosomal imbalances assessed by comparative genomic hybridization in multiple myeloma.

J. Hernández, A. Órfão, N. Gutiérrez, 2004, Blood.

Cimp-Positive Status is More Representative in Multiple Colorectal Cancers than in Unique Primary Colorectal Cancers

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2019, Scientific Reports.

Clinical and Molecular Comparative Study of Colorectal Cancer Based on Age-of-Onset and Tumor Location: Two Main Criteria for Subclassifying Colorectal Cancer

M. Urioste, R. González-Sarmiento, L. Inglada-Perez, 2019, International journal of molecular sciences.

VRK2 identifies a subgroup of primary high-grade astrocytomas with a better prognosis

I. Rodriguez-Hernandez, R. González-Sarmiento, P. Lazo, 2013, BMC Clinical Pathology.

Molecular analysis of non-culture CD 133 + GBM cells revealed different signatures among high grade gliomas

J. Hernández-Rivas, R. González-Sarmiento, M. Pérez-Caro, 2010 .

Molecular dissection of structural variations involved in antithrombin deficiency.

W. Ouwehand, J. Hernández-Rivas, J. Corral, 2022, The Journal of molecular diagnostics : JMD.

Copy neutral loss of heterozygosity (cnLOH) patterns in synchronous colorectal cancer

M. Urioste, R. González-Sarmiento, L. Corchete, 2020, European Journal of Human Genetics.

Intermediate molecular phenotypes to identify genetic markers of anthracycline-induced cardiotoxicity risk

D. Lambrechts, A. González-Neira, G. Pita, 2023, bioRxiv.

Cytogenetic and genomic analysis of a patient with turner syndrome and t(2;12): a case report

J. Hernández-Rivas, A. López-Cortés, C. Paz-y-Miño, 2020, Molecular cytogenetics.

Ring chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature

Jesús M. Hernández, J. Guevara-Aguirre, C. Paz-y-Miño, 2018, Journal of Medical Case Reports.

Integrative analysis of DNA copy number, DNA methylation and gene expression in multiple myeloma reveals alterations related to relapse

J. Hernández-Rivas, J. Miguel, L. Corchete, 2016, Oncotarget.

MicroRNA-223 is a novel negative regulator of HSP90B1 in CLL

Juan F. de Paz, Marcos González, J. Hernández-Rivas, 2015, BMC Cancer.

Integration of Global Spectral Karyotyping, CGH Arrays, and Expression Arrays Reveals Important Genes in the Pathogenesis of Glioblastoma Multiforme

C. Elosua, Jesús M. Hernández, N. Gutiérrez, 2012, Annals of Surgical Oncology.

Intermediate-onset colorectal cancer: A clinical and familial boundary between both early and late-onset colorectal cancer

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2019, PloS one.

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

M. Urioste, J. Benítez, J. Hernández, 2016, Molecular carcinogenesis.

Integrated Analysis of Mismatch Repair System in Malignant Astrocytomas

I. Rodriguez-Hernandez, R. González-Sarmiento, J. Martín-Vallejo, 2013, PloS one.

De Novo Duplication of Chromosome 9p in a Female Infant: Phenotype and Genotype Correlation

Jesús M. Hernández, A. López-Cortés, C. Paz-y-Miño, 2019, Journal of Pediatric Genetics.

NOMO-1 gene is deleted in early-onset colorectal cancer

M. Urioste, R. González-Sarmiento, J. García, 2017, Oncotarget.

Analysis of DNA repair gene polymorphisms in glioblastoma.

I. Rodriguez-Hernandez, R. González-Sarmiento, J. García, 2014, Gene.

Novel Dominant KCNQ2 Exon 7 Partial In-Frame Duplication in a Complex Epileptic and Neurodevelopmental Delay Syndrome

R. González-Sarmiento, P. Lazo, P. Gómez-Puertas, 2020, International journal of molecular sciences.

Clinical, cytogenetic, and molecular findings in a patient with ring chromosome 4: case report and literature review

J. Hernández-Rivas, C. Paz-y-Miño, J. García, 2019, BMC Medical Genomics.

Redefining synchronous colorectal cancers based on tumor clonality

M. Urioste, L. Corchete, D. García-Olmo, 2018, International journal of cancer.

MOLECULAR CLASSIFICATION OF SYNCHRONOUS COLORECTAL CANCER : CLINICAL AND MOLECULAR CHARACTERIZATION Running title : Characterization of synchronous colorectal cancer

M. Urioste, J. García, D. Rueda, 2016 .

Overexpression of the VAV proto‐oncogene product is associated with B‐cell chronic lymphocytic leukaemia displaying loss on 13q

J. Hernández, J. Miguel, X. Bustelo, 2006, British journal of haematology.

Germinal centre protein HGAL promotes lymphoid hyperplasia and amyloidosis via BCR-mediated Syk activation

Ash A. Alizadeh, Michael R. Green, I. Lossos, 2012, Nature Communications.

Unsupervised Analysis of Array Comparative Genomic Hybridization Data from Early-Onset Colorectal Cancer Reveals Equivalence with Molecular Classification and Phenotypes1

M. Urioste, R. González-Sarmiento, J. García, 2016, Neoplasia.

Topological Analysis of Amplicon Structure in Comparative Genomic Hybridization (CGH) Data: An Application to ERBB2/HER2/NEU Amplified Tumors

Sergio Ardanza-Trevijano, Georgina Gonzalez, Tyler Borrman, 2016, CTIC.

Possible Exiguobacterium sibiricum Skin Infection in Human

J. García, J. Sáez-Nieto, D. Tena, 2014, Emerging infectious diseases.

Heterogeneity of structural abnormalities in the 7q31.3 approximately q34 region in myeloid malignancies.

F. Solé, J. Hernández, M. Calasanz, 2004, Cancer genetics and cytogenetics.

Multicolor fluorescence in situ hybridization studies in multiple myeloma and monoclonal gammopathy of undetermined significance.

J. Hernández, N. Gutiérrez, J. S. San Miguel, 2003, The hematology journal : the official journal of the European Haematology Association.

Cutaneous intraneural perineurioma: a case report.

T. Mentzel, J. García, Á. Santos-Briz, 2013, The American Journal of dermatopathology.

Geographic differences in the incidence of cytogenetic abnormalities of acute myelogenous leukemia (AML) in Spain.

M. Odero, M. Calasanz, Jesús M. Hernández, 2006, Leukemia research.

Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore.

M. Urioste, J. Benítez, R. González-Sarmiento, 2015, American journal of cancer research.

Detection of the Mbcr/abl translocation in chronic myeloid leukemia by fluorescence in situ hybridization: comparison with conventional cytogenetics and implications for minimal residual disease detection.

J. Hernández, A. Órfão, J. Wiegant, 1997, Human pathology.

Clinical, biological, and immunophenotypical characteristics of B-cell chronic lymphocytic leukemia with trisomy 12 by fluorescence in situ hybridization.

A. Órfão, J. Wiegant, A. Raap, 1995, Cytometry.

Increased number of chromosomal imbalances and high-level DNA amplifications in mantle cell lymphoma are associated with blastoid variants.

A. López-Guillermo, F. Bosch, E. Campo, 1999, Blood.

Splenic marginal zone B-cell lymphomas: two cytogenetic subtypes, one with gain of 3q and the other with loss of 7q.

J. Climent, S. Serrano, I. Benet, 2001, Haematologica.

Characterization of breast cancer by array comparative genomic hybridization.

J. Climent, J. Arsuaga, J. García, 2007, Biochemistry and cell biology = Biochimie et biologie cellulaire.

Novel genomic imbalances in B-cell splenic marginal zone lymphomas revealed by comparative genomic hybridization and cytogenetics.

J. Martinez-Climent, M. Piris, J. García, 2001, The American journal of pathology.

Differential clinicopathological and molecular features within late-onset colorectal cancer according to tumor location

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2018, Oncotarget.

Frequency and impact of KRAS mutation in early onset colorectal cancer.

M. Urioste, R. González-Sarmiento, J. García, 2017, Human pathology.

Hematological, immunophenotypic, and cytogenetic characteristics of acute myeloblastic leukemia with trisomy 11.

N. Gutiérrez, J. S. San Miguel, M. Vidriales, 2005, Cancer genetics and cytogenetics.

Both expanded and uncultured mesenchymal stem cells from MDS patients are genomically abnormal, showing a specific genetic profile for the 5q− syndrome

J. Hernández-Rivas, J. García, F. Sánchez-Guijo, 2009, Leukemia.

Cimp-Positive Status is More Representative in Multiple Colorectal Cancers than in Unique Primary Colorectal Cancers

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2019, Scientific Reports.

Trisomies 8 and 20 in desmoid tumors.

P. van Eyken, P. Cin, R. Sciot, 1996, Cancer genetics and cytogenetics.

Clinical, molecular and biochemical characterization of nine Spanish families with Conradi–Hünermann–Happle syndrome: new insights into X‐linked dominant chondrodysplasia punctata with a comprehensive review of the literature

F. Martínez, R. González-Sarmiento, J. Rosell, 2012, The British journal of dermatology.

GSK3-SCFFBXW7 targets JunB for degradation in G2 to preserve chromatid cohesion before anaphase

A. Pineda-Lucena, R. Farràs, M. Piechaczyk, 2013, Oncogene.

Clinical, hematological and cytogenetic characteristics of atypical chronic myeloid leukemia.

J. García, A. Cuneo, G. Castoldi, 2000, Annals of oncology : official journal of the European Society for Medical Oncology.

Association of Polyps with Early-Onset Colorectal Cancer and Throughout Surveillance: Novel Clinical and Molecular Implications

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2019, Cancers.

Immunomodulatory effect of 5-azacytidine (5-azaC): potential role in the transplantation setting.

F. J. Gonzalez, E. Ballestar, B. Blanco, 2010, Blood.

SLUG (SNAI2) overexpression in embryonic development

P. A. Pérez-Mancera, I. González-Herrero, T. Flores, 2006, Cytogenetic and Genome Research.

Epidermal growth factor receptor expression is associated with poor outcome in cutaneous squamous cell carcinoma

J. Pérez-Losada, A. Castellanos-Martín, J. García, 2017, The British journal of dermatology.

A clinico-pathological and molecular analysis reveals differences between solitary (early and late-onset) and synchronous rectal cancer

M. Urioste, R. González-Sarmiento, L. Corchete, 2021, Scientific Reports.