Tong Cheng

Shanghai, China

Last Updated: 09/26/2026

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Found 11 publications

High Diagnostic Accuracy of Epigenetic Imprinting Biomarkers in Thyroid Nodules.

High Diagnostic Accuracy of Epigenetic Imprinting Biomarkers in Thyroid Nodules.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology

Published: November 15, 2022

Differences of adrenal-derived androgens in 5α-reductase deficiency versus androgen insensitivity syndrome.

Differences of adrenal-derived androgens in 5α-reductase deficiency versus androgen insensitivity syndrome.

Journal: Clinical and translational science

Published: July 07, 2021

Genetic Analysis of 25 Patients with 5α-Reductase Deficiency in Chinese Population.

Genetic Analysis of 25 Patients with 5α-Reductase Deficiency in Chinese Population.

Journal: BioMed research international

Published: November 04, 2019

Identification of three novel SRD5A2 mutations in Chinese patients with 5α-reductase 2 deficiency.

Identification of three novel SRD5A2 mutations in Chinese patients with 5α-reductase 2 deficiency.

Journal: Asian journal of andrology

Published: April 30, 2019

Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique.

Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique.

Journal: Molecular genetics & genomic medicine

Published: January 26, 2019

Oxidative stress increases the 17,20-lyase-catalyzing activity of adrenal P450c17 through p38α in the development of hyperandrogenism.

Oxidative stress increases the 17,20-lyase-catalyzing activity of adrenal P450c17 through p38α in the development of hyperandrogenism.

Journal: Molecular and cellular endocrinology

Published: June 26, 2018

Clinical behaviors of rare variants of papillary thyroid carcinoma are associated with survival: a population-level analysis.

Clinical behaviors of rare variants of papillary thyroid carcinoma are associated with survival: a population-level analysis.

Journal: Cancer management and research

Published: March 23, 2018

Next-generation sequencing reveals genetic landscape in 46, XY disorders of sexual development patients with variable phenotypes.

Next-generation sequencing reveals genetic landscape in 46, XY disorders of sexual development patients with variable phenotypes.

Journal: Human genetics

Published: November 23, 2017

Polymorphism in the Alternative Donor Site of the Cryptic Exon of LHCGR: Functional Consequences and Associations with Testosterone Level.

Polymorphism in the Alternative Donor Site of the Cryptic Exon of LHCGR: Functional Consequences and Associations with Testosterone Level.

Journal: Scientific reports

Published: July 14, 2016

Aromatase deficiency: a novel compound heterozygous mutation identified in a Chinese girl with severe phenotype and obvious maternal virilization.

Aromatase deficiency: a novel compound heterozygous mutation identified in a Chinese girl with severe phenotype and obvious maternal virilization.

Journal: Molecular and cellular endocrinology

Published: March 16, 2016

Clinical and molecular manifestation of fifteen 17OHD patients: a novel mutation and a founder effect.

Clinical and molecular manifestation of fifteen 17OHD patients: a novel mutation and a founder effect.

Journal: Endocrine

Published: December 28, 2015

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Last Updated: 09/26/2026