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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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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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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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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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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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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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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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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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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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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

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

Precision Nutrition

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

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

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

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

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

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

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

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

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