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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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Low-density lipoprotein receptor variants are associated with spontaneous and treatment-induced recovery from hepatitis C virus infection

Infection, genetics and evolution, 2009-09, Vol.9 (5), p.847-852

2009

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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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Single-cell Sequencing Reveals Variants in ARID1A , GPRC5A and MLL2 Driving Self-renewal of Human Bladder Cancer Stem Cells

European urology, 2017-01, Vol.71 (1), p.8-12

2017

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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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Molecular alterations in colorectal adenomas and intramucosal adenocarcinomas defined by high-density single-nucleotide polymorphism arrays

Journal of gastroenterology, 2017-11, Vol.52 (11), p.1158-1168

2017

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Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population

Nutrients, 2020-11, Vol.12 (11), p.3389

2020

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CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

BMC bioinformatics, 2016-08, Vol.17 (1), p.310-310, Article 310

2016

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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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Catecholaminergic Gene Polymorphisms Are Associated with GI Symptoms and Morphological Brain Changes in Irritable Bowel Syndrome

PloS one, 2015-08, Vol.10 (8), p.e0135910-e0135910

2015

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Genetic alterations in hepatocellular carcinoma: An update

World journal of gastroenterology : WJG, 2016-11, Vol.22 (41), p.9069-9095

2016

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Holocene population expansion of a tropical bee coincides with early human colonization of Fiji rather than climate change

Molecular ecology, 2021-08, Vol.30 (16), p.4005-4022

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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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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Molecular alterations in gastric cancer with special reference to the early-onset subtype

World journal of gastroenterology : WJG, 2016-02, Vol.22 (8), p.2460-2474

2016

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Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing

Experimental and molecular pathology, 2017-02, Vol.102 (1), p.156-161

2017

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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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A new approach to decode DNA methylome and genomic variants simultaneously from double strand bisulfite sequencing

Briefings in bioinformatics, 2021-11, Vol.22 (6)

2021

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Steroidogenic factor-1 (SF-1, NR5A1) and human disease

Molecular and cellular endocrinology, 2011-04, Vol.336 (1-2), p.198-205

2011

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Genetic alterations within the DENND1A gene in patients with polycystic ovary syndrome (PCOS)

PloS one, 2013-09, Vol.8 (9), p.e77186-e77186

2013

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Identification of genetic alterations in extramammary Paget disease using whole exome analysis

Journal of dermatological science, 2019-04, Vol.94 (1), p.229-235

2019

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Chromosomal Aberrations in Canine Gliomas Define Candidate Genes and Common Pathways in Dogs and Humans

Journal of neuropathology and experimental neurology, 2016-07, Vol.75 (7), p.700-710

2016

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Target genes discovery through copy number alteration analysis in human hepatocellular carcinoma

World journal of gastroenterology : WJG, 2013-12, Vol.19 (47), p.8873-8879

2013

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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

Low-density lipoprotein receptor variants are associated with spontaneous and treatment-induced recovery from hepatitis C virus infection

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

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

Single-cell Sequencing Reveals Variants in ARID1A , GPRC5A and MLL2 Driving Self-renewal of Human Bladder Cancer Stem Cells

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

Molecular alterations in colorectal adenomas and intramucosal adenocarcinomas defined by high-density single-nucleotide polymorphism arrays

Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population

CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

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

Catecholaminergic Gene Polymorphisms Are Associated with GI Symptoms and Morphological Brain Changes in Irritable Bowel Syndrome

Genetic alterations in hepatocellular carcinoma: An update

Holocene population expansion of a tropical bee coincides with early human colonization of Fiji rather than climate change

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

A clinically applicable molecular classification of oncocytic cell thyroid nodules

Molecular alterations in gastric cancer with special reference to the early-onset subtype

Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing

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

A new approach to decode DNA methylome and genomic variants simultaneously from double strand bisulfite sequencing

Steroidogenic factor-1 (SF-1, NR5A1) and human disease

Genetic alterations within the DENND1A gene in patients with polycystic ovary syndrome (PCOS)

Identification of genetic alterations in extramammary Paget disease using whole exome analysis

Chromosomal Aberrations in Canine Gliomas Define Candidate Genes and Common Pathways in Dogs and Humans

Target genes discovery through copy number alteration analysis in human hepatocellular carcinoma

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