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Identifying patient-specific flow of signal transduction perturbed by multiple single-nucleotide alterations

Quantitative biology, 2020-12, Vol.8 (4), p.336-346

2020

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AM22, a novel synthetic microRNA, inhibits the proliferation of colorectal cancer cells by targeting core binding factor subunit β (CBFB)

Investigational new drugs, 2022-06, Vol.40 (3), p.469-477

2022

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Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein

Stem cell reports, 2021-04, Vol.16 (4), p.985-996

2021

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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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Single nucleotide alterations in MicroRNAs and human cancer-A not fully explored field

Non-coding RNA research, 2020-03, Vol.5 (1), p.27-31

Zhao, Dan

2020

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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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Comprehensive Analyses of Somatic Copy Number Alterations and Mutations Based on the Adenoma–Carcinoma Sequence

Genes chromosomes & cancer, 2024-09, Vol.63 (9), p.e23267-n/a

2024

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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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Precision Nutrition

2023

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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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Detection of DNA copy number alterations by matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of single nucleotide polymorphisms

Clinical chemistry and laboratory medicine, 2022-09, Vol.60 (10), p.1543-1550

2022

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Comparative Cytogenetic Analysis of Dog and Human Choroid Plexus Tumors Defines Syntenic Regions of Genomic Loss

Journal of neuropathology and experimental neurology, 2018-05, Vol.77 (5), p.413-419

2018

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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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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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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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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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The repertoire of copy number alteration signatures in human cancer

Briefings in bioinformatics, 2023-03, Vol.24 (2)

2023

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Identifying patient-specific flow of signal transduction perturbed by multiple single-nucleotide alterations

AM22, a novel synthetic microRNA, inhibits the proliferation of colorectal cancer cells by targeting core binding factor subunit β (CBFB)

Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein

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

Single nucleotide alterations in MicroRNAs and human cancer-A not fully explored field

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

Comprehensive Analyses of Somatic Copy Number Alterations and Mutations Based on the Adenoma–Carcinoma Sequence

Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project

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

Precision Nutrition

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

A comprehensive survey of genomic alterations in gastric cancer reveals systematic patterns of molecular exclusivity and co-occurrence among distinct therapeutic targets

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

Detection of DNA copy number alterations by matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of single nucleotide polymorphisms

Comparative Cytogenetic Analysis of Dog and Human Choroid Plexus Tumors Defines Syntenic Regions of Genomic Loss

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

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

Genetic alterations in hepatocellular carcinoma: An update

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

The repertoire of copy number alteration signatures in human cancer

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