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Epigenome signatures landscaped by histone H3K9me3 are associated with the synaptic dysfunction in Alzheimer's disease

Aging cell, 2020-06, Vol.19 (6), p.e13153-n/a

2020

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Integrative analysis of genomic and transcriptomic characteristics associated with progression of aggressive thyroid cancer

Nature communications, 2019-06, Vol.10 (1), p.2764-12, Article 2764

2019

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Comprehensive Analysis of the Transcriptional and Mutational Landscape of Follicular and Papillary Thyroid Cancers

PLoS genetics, 2016-08, Vol.12 (8), p.e1006239-e1006239

2016

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A transforming KIF5B and RET gene fusion in lung adenocarcinoma revealed from whole-genome and transcriptome sequencing

Genome research, 2012-03, Vol.22 (3), p.436

2012

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The transcriptional landscape and mutational profile of lung adenocarcinoma

Genome research, 2012-11, Vol.22 (11), p.2109

2012

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The tumor immune microenvironmental analysis of 2,033 transcriptomes across 7 cancer types

Scientific reports, 2020-06, Vol.10 (1), p.9536-9536, Article 9536

2020

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Comprehensive analysis of the tumor immune micro-environment in non-small cell lung cancer for efficacy of checkpoint inhibitor

Scientific reports, 2018-10, Vol.8 (1), p.14576-14, Article 14576

2018

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Integrative analysis of oncogenic fusion genes and their functional impact in colorectal cancer

British journal of cancer, 2018-07, Vol.119 (2), p.230-240

2018

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Genomic and transcriptomic analyses reveal a tandem amplification unit of 11 genes and mutations in mismatch repair genes in methotrexate-resistant HT-29 cells

Experimental and Molecular Medicine, 2021, 53(0), , pp.1-12

2021

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Alterations of transcriptome signatures in head trauma-related neurodegenerative disorders

Scientific reports, 2020-06, Vol.10 (1), p.8811-8811, Article 8811

2020

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Two distinct mechanisms of silencing by the KvDMR1 imprinting control region

The EMBO journal, 2008-01, Vol.27 (1), p.168-178

2008

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ClinPharmSeq: A targeted sequencing panel for clinical pharmacogenetics implementation

PloS one, 2022-07, Vol.17 (7), p.e0272129-e0272129

2022

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Comprehensive characterization of maternal, fetal, and neonatal microbiomes supports prenatal colonization of the gastrointestinal tract

Scientific reports, 2023-03, Vol.13 (1), p.4652-4652, Article 4652

2023

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Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis

Scientific reports, 2018-06, Vol.8 (1), p.8678-7, Article 8678

2018

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RNA editing in RHOQ promotes invasion potential in colorectal cancer

The Journal of experimental medicine, 2014-04, Vol.211 (4), p.613-621

2014

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An epigenomic roadmap to induced pluripotency reveals DNA methylation as a reprogramming modulator

Nature communications, 2014-12, Vol.5 (1), p.5619-5619, Article 5619

2014

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Development of a common platform for the noninvasive prenatal diagnosis of X‐linked diseases

Prenatal diagnosis, 2018-10, Vol.38 (11), p.835-840

2018

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Identification of novel mutations in FFPE lung adenocarcinomas using DEPArray sorting technology and next-generation sequencing

Journal of applied genetics, 2018-08, Vol.59 (3), p.269-277

2018

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Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis

BMC cancer, 2016-02, Vol.16 (170), p.170-170, Article 170

2016

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NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants

Genome medicine, 2019-10, Vol.11 (1), p.64-64, Article 64

2019

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Targeted sequencing of cancer-related genes in colorectal cancer using next-generation sequencing

PloS one, 2013-05, Vol.8 (5), p.e64271

2013

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Glutaminase 2 expression is associated with regional heterogeneity of 5-aminolevulinic acid fluorescence in glioblastoma

Scientific reports, 2017-09, Vol.7 (1), p.12221-11, Article 12221

2017

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Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson's disease

Human genomics, 2021-08, Vol.15 (1), p.58-58, Article 58

2021

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Indigenous Ancestry and Admixture in the Uruguayan Population

Frontiers in genetics, 2021-09, Vol.12, p.733195-733195

2021

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Epigenome signatures landscaped by histone H3K9me3 are associated with the synaptic dysfunction in Alzheimer's disease

Integrative analysis of genomic and transcriptomic characteristics associated with progression of aggressive thyroid cancer

Comprehensive Analysis of the Transcriptional and Mutational Landscape of Follicular and Papillary Thyroid Cancers

A transforming KIF5B and RET gene fusion in lung adenocarcinoma revealed from whole-genome and transcriptome sequencing

The transcriptional landscape and mutational profile of lung adenocarcinoma

The tumor immune microenvironmental analysis of 2,033 transcriptomes across 7 cancer types

Comprehensive analysis of the tumor immune micro-environment in non-small cell lung cancer for efficacy of checkpoint inhibitor

Integrative analysis of oncogenic fusion genes and their functional impact in colorectal cancer

Genomic and transcriptomic analyses reveal a tandem amplification unit of 11 genes and mutations in mismatch repair genes in methotrexate-resistant HT-29 cells

Alterations of transcriptome signatures in head trauma-related neurodegenerative disorders

Two distinct mechanisms of silencing by the KvDMR1 imprinting control region

ClinPharmSeq: A targeted sequencing panel for clinical pharmacogenetics implementation

Comprehensive characterization of maternal, fetal, and neonatal microbiomes supports prenatal colonization of the gastrointestinal tract

Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis

RNA editing in RHOQ promotes invasion potential in colorectal cancer

An epigenomic roadmap to induced pluripotency reveals DNA methylation as a reprogramming modulator

Development of a common platform for the noninvasive prenatal diagnosis of X‐linked diseases

Identification of novel mutations in FFPE lung adenocarcinomas using DEPArray sorting technology and next-generation sequencing

Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis

Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals

NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants

Targeted sequencing of cancer-related genes in colorectal cancer using next-generation sequencing

Glutaminase 2 expression is associated with regional heterogeneity of 5-aminolevulinic acid fluorescence in glioblastoma

Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson's disease

Indigenous Ancestry and Admixture in the Uruguayan Population

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