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Concomitant inhibition of B7-H3 and PD-L1 expression by a novel and synthetic microRNA delivers potent antitumor activities in colorectal tumor models

Investigational new drugs, 2021-10, Vol.39 (5), p.1267-1274

2021

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Evaluation of cell-free DNA approaches for multi-cancer early detection

Cancer cell, 2022-12, Vol.40 (12), p.1537-1549.e12

2022

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Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data

Annals of oncology, 2015-01, Vol.26 (1), p.64-70

2015

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Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis

Leukemia, 2010-02, Vol.24 (2), p.438-449

2010

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A genome‐wide study of the relationship between chromosomal abnormalities and gene expression in colorectal tumors

Genes chromosomes & cancer, 2021-04, Vol.60 (4), p.250-262

2021

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Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer

The Journal of pathology, 2022-05, Vol.257 (1), p.68-81

2022

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A clinically applicable molecular classification of oncocytic cell thyroid nodules

Endocrine-related cancer, 2023-09, Vol.30 (9), p.1

2023

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The Clinical Utility of Optical Genome Mapping for the Assessment of Genomic Aberrations in Acute Lymphoblastic Leukemia

Cancers, 2021-08, Vol.13 (17), p.4388

2021

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Conjunctival melanoma copy number alterations and correlation with mutation status, tumor features, and clinical outcome

Pigment cell and melanoma research, 2019-07, Vol.32 (4), p.564-575

2019

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Kasumi leukemia cell lines: characterization of tumor genomes with ethnic origin and scales of genomic alterations

Human cell : official journal of Human Cell Research Society, 2020-07, Vol.33 (3), p.868-876

2020

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Genomic characterization of a large panel of patient-derived hepatocellular carcinoma xenograft tumor models for preclinical development

Oncotarget, 2015-08, Vol.6 (24), p.20160-20176

2015

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Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays

Oncogene, 2008-03, Vol.27 (13), p.1951-1960

2008

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Somatic copy number alterations predict response to platinum therapy in epithelial ovarian cancer

Gynecologic oncology, 2014-12, Vol.135 (3), p.415-422

2014

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Genome-wide single-nucleotide polymorphism array-based karyotyping in myelodysplastic syndrome and chronic myelomonocytic leukemia and its impact on treatment outcomes following decitabine treatment

Annals of hematology, 2013-04, Vol.92 (4), p.459-469

2013

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Targeted or whole genome sequencing of formalin fixed tissue samples: potential applications in cancer genomics

Oncotarget, 2015-09, Vol.6 (28), p.25943-25961

2015

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Comprehensive Assessment of Copy Number Alterations Uncovers Recurrent AIFM3 and DLK1 Copy Gain in Medullary Thyroid Carcinoma

Cancers, 2021-01, Vol.13 (2), p.218

2021

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Comprehensive analysis of somatic copy number alterations in clear cell renal cell carcinoma

Molecular carcinogenesis, 2020-04, Vol.59 (4), p.412-424

2020

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Prognostic gene alterations and clonal changes in childhood B-ALL

Leukemia research, 2019-08, Vol.83, p.106159-106159, Article 106159

2019

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Genomic profiling of colorectal cancer with isolated lung metastasis

Cancer cell international, 2020-07, Vol.20 (1), p.281-13, Article 281

2020

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Molecular Alterations in Dog Pheochromocytomas and Paragangliomas

Cancers, 2019-04, Vol.11 (5), p.607

2019

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Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation

Cancers, 2022-03, Vol.14 (7), p.1629

2022

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Frequent genomic loss at chr16p13.2 is associated with poor prognosis in colorectal cancer

International journal of cancer, 2011-10, Vol.129 (8), p.1848-1858

2011

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Whole-genome sequencing identifies new genetic alterations in meningiomas

Oncotarget, 2017-03, Vol.8 (10), p.17070-17080

2017

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TP53 alterations in primary and secondary Sézary syndrome: A diagnostic tool for the assessment of malignancy in patients with erythroderma

PloS one, 2017-03, Vol.12 (3), p.e0173171-e0173171

2017

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An integrated analysis of germline and somatic, genetic and epigenetic alterations at 9p21.3 in glioblastoma

Cancer, 2012-01, Vol.118 (1), p.232-240

2012

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Concomitant inhibition of B7-H3 and PD-L1 expression by a novel and synthetic microRNA delivers potent antitumor activities in colorectal tumor models

Evaluation of cell-free DNA approaches for multi-cancer early detection

Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data

Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis

A genome‐wide study of the relationship between chromosomal abnormalities and gene expression in colorectal tumors

Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer

A clinically applicable molecular classification of oncocytic cell thyroid nodules

The Clinical Utility of Optical Genome Mapping for the Assessment of Genomic Aberrations in Acute Lymphoblastic Leukemia

Conjunctival melanoma copy number alterations and correlation with mutation status, tumor features, and clinical outcome

Kasumi leukemia cell lines: characterization of tumor genomes with ethnic origin and scales of genomic alterations

Genomic characterization of a large panel of patient-derived hepatocellular carcinoma xenograft tumor models for preclinical development

Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays

Somatic copy number alterations predict response to platinum therapy in epithelial ovarian cancer

Genome-wide single-nucleotide polymorphism array-based karyotyping in myelodysplastic syndrome and chronic myelomonocytic leukemia and its impact on treatment outcomes following decitabine treatment

Targeted or whole genome sequencing of formalin fixed tissue samples: potential applications in cancer genomics

Comprehensive Assessment of Copy Number Alterations Uncovers Recurrent AIFM3 and DLK1 Copy Gain in Medullary Thyroid Carcinoma

Comprehensive analysis of somatic copy number alterations in clear cell renal cell carcinoma

Prognostic gene alterations and clonal changes in childhood B-ALL

Genomic profiling of colorectal cancer with isolated lung metastasis

Molecular Alterations in Dog Pheochromocytomas and Paragangliomas

Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation

Frequent genomic loss at chr16p13.2 is associated with poor prognosis in colorectal cancer

Whole-genome sequencing identifies new genetic alterations in meningiomas

TP53 alterations in primary and secondary Sézary syndrome: A diagnostic tool for the assessment of malignancy in patients with erythroderma

An integrated analysis of germline and somatic, genetic and epigenetic alterations at 9p21.3 in glioblastoma

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