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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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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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Precision Nutrition

2023

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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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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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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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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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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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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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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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Genomic Analysis Made It Possible to Identify Gene-Driver Alterations Covering the Time Window between Diagnosis of Neuroblastoma 4S and the Progression to Stage 4

International journal of molecular sciences, 2022-06, Vol.23 (12), p.6513

2022

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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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SNP in Chalcone Synthase gene is associated with variation of 6-gingerol content in contrasting landraces of Zingiber officinale.Roscoe

Gene, 2015-07, Vol.566 (2), p.184-188

2015

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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 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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Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing

Annals of human genetics, 2021-01, Vol.85 (1), p.18-26

2021

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Serum folate concentration and the incidence of lung cancer

PloS one, 2017-05, Vol.12 (5), p.e0177441-e0177441

2017

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A strong association between VEGF-A rs28357093 and amyotrophic lateral sclerosis: a brazilian genetic study

Molecular biology reports, 2022-09, Vol.49 (9), p.9129-9133

2022

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

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

Precision Nutrition

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

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

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

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

A clinically applicable molecular classification of oncocytic cell thyroid nodules

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

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

Genomic Analysis Made It Possible to Identify Gene-Driver Alterations Covering the Time Window between Diagnosis of Neuroblastoma 4S and the Progression to Stage 4

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

SNP in Chalcone Synthase gene is associated with variation of 6-gingerol content in contrasting landraces of Zingiber officinale.Roscoe

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

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

Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing

Serum folate concentration and the incidence of lung cancer

A strong association between VEGF-A rs28357093 and amyotrophic lateral sclerosis: a brazilian genetic study

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