Zhao-hui Gu

Shanghai, China

Last Updated: 09/26/2026

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Found 14 publications

Multiregion sequencing reveals the intratumor heterogeneity of driver mutations in TP53-driven non-small cell lung cancer.

Multiregion sequencing reveals the intratumor heterogeneity of driver mutations in TP53-driven non-small cell lung cancer.

Journal: International journal of cancer

Published: August 21, 2016

Mutations of Epigenetic Modifier Genes as a Poor Prognostic Factor in Acute Promyelocytic Leukemia Under Treatment With All-Trans Retinoic Acid and Arsenic Trioxide.

Mutations of Epigenetic Modifier Genes as a Poor Prognostic Factor in Acute Promyelocytic Leukemia Under Treatment With All-Trans Retinoic Acid and Arsenic Trioxide.

Journal: EBioMedicine

Published: March 20, 2015

Exome sequencing identifies somatic mutations of DDX3X in natural killer/T-cell lymphoma.

Exome sequencing identifies somatic mutations of DDX3X in natural killer/T-cell lymphoma.

Journal: Nature genetics

Published: February 11, 2015

Characterization of Somatic Mutations in Air Pollution-Related Lung Cancer.

Characterization of Somatic Mutations in Air Pollution-Related Lung Cancer.

Journal: EBioMedicine

Published: January 29, 2015

Genomic landscape of CD34+ hematopoietic cells in myelodysplastic syndrome and gene mutation profiles as prognostic markers.

Genomic landscape of CD34+ hematopoietic cells in myelodysplastic syndrome and gene mutation profiles as prognostic markers.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: May 23, 2014

DNMT3A Arg882 mutation drives chronic myelomonocytic leukemia through disturbing gene expression/DNA methylation in hematopoietic cells.

DNMT3A Arg882 mutation drives chronic myelomonocytic leukemia through disturbing gene expression/DNA methylation in hematopoietic cells.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: February 06, 2014

Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population.

Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population.

Journal: European journal of endocrinology

Published: October 23, 2013

GSTT1 deletion is related to polycyclic aromatic hydrocarbons-induced DNA damage and lymphoma progression.

GSTT1 deletion is related to polycyclic aromatic hydrocarbons-induced DNA damage and lymphoma progression.

Journal: PloS one

Published: September 26, 2013

Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.

Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.

Journal: Human genetics

Published: August 14, 2013

Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.

Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.

Journal: Human molecular genetics

Published: April 25, 2013

Whole-exome sequencing to identify novel somatic mutations in squamous cell lung cancers.

Whole-exome sequencing to identify novel somatic mutations in squamous cell lung cancers.

Journal: International journal of oncology

Published: March 25, 2013

A refined study of FCRL genes from a genome-wide association study for Graves' disease.

A refined study of FCRL genes from a genome-wide association study for Graves' disease.

Journal: PloS one

Published: October 20, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026