Jing H. Wong

Tokyo, Japan

Last Updated: 09/26/2026

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Found 11 publications

Comprehensive analysis of full-length transcripts reveals novel splicing abnormalities and oncogenic transcripts in liver cancer.

Comprehensive analysis of full-length transcripts reveals novel splicing abnormalities and oncogenic transcripts in liver cancer.

Journal: PLoS genetics

Published: April 19, 2022

Likely pathogenic structural variants in genetically unsolved patients with retinitis pigmentosa revealed by long-read sequencing.

Likely pathogenic structural variants in genetically unsolved patients with retinitis pigmentosa revealed by long-read sequencing.

Journal: Journal of medical genetics

Published: January 05, 2022

Characterization of intermediate-sized insertions using whole-genome sequencing data and analysis of their functional impact on gene expression.

Characterization of intermediate-sized insertions using whole-genome sequencing data and analysis of their functional impact on gene expression.

Journal: Human genetics

Published: February 02, 2021

Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer.

Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer.

Journal: Genome medicine

Published: June 30, 2020

Comprehensive analysis of indels in whole-genome microsatellite regions and microsatellite instability across 21 cancer types.

Comprehensive analysis of indels in whole-genome microsatellite regions and microsatellite instability across 21 cancer types.

Journal: Genome research

Published: July 23, 2019

eVIDENCE: a practical variant filtering for low-frequency variants detection in cell-free DNA.

eVIDENCE: a practical variant filtering for low-frequency variants detection in cell-free DNA.

Journal: Scientific reports

Published: May 01, 2019

Identification of intermediate-sized deletions and inference of their impact on gene expression in a human population.

Identification of intermediate-sized deletions and inference of their impact on gene expression in a human population.

Journal: Genome medicine

Published: March 21, 2019

Aberrant (pro)renin receptor expression induces genomic instability in pancreatic ductal adenocarcinoma through upregulation of SMARCA5/SNF2H.

Aberrant (pro)renin receptor expression induces genomic instability in pancreatic ductal adenocarcinoma through upregulation of SMARCA5/SNF2H.

Journal: Communications biology

Published: November 16, 2018

Whole Genome Sequencing of a Vietnamese Family from a Dioxin Contamination Hotspot Reveals Novel Variants in the Son with Undiagnosed Intellectual Disability.

Whole Genome Sequencing of a Vietnamese Family from a Dioxin Contamination Hotspot Reveals Novel Variants in the Son with Undiagnosed Intellectual Disability.

Journal: International journal of environmental research and public health

Published: October 19, 2018

Whole genome sequencing and mutation rate analysis of trios with paternal dioxin exposure.

Whole genome sequencing and mutation rate analysis of trios with paternal dioxin exposure.

Journal: Human mutation

Published: January 24, 2018

Identification of ITPA on chromosome 20 as a susceptibility gene for young-onset tuberculosis.

Identification of ITPA on chromosome 20 as a susceptibility gene for young-onset tuberculosis.

Journal: Human genome variation

Published: August 03, 2015

Showing 1-11 of 11

Last Updated: 09/26/2026