Zhongzhong Chen

Shanghai, China

Last Updated: 09/26/2026

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Found 30 publications

Correction: Novel evidence of CNV deletion in KCTD13 related to the severity of isolated hypospadias in Chinese population.

Correction: Novel evidence of CNV deletion in KCTD13 related to the severity of isolated hypospadias in Chinese population.

Journal: Frontiers in pediatrics
Published: November 24, 2025

Novel evidence of CNV deletion in KCTD13 related to the severity of isolated hypospadias in Chinese population.

Novel evidence of CNV deletion in KCTD13 related to the severity of isolated hypospadias in Chinese population.

Journal: Frontiers in pediatrics
Published: March 29, 2024

Progress and clinical prospect of genomic structural variants investigation.

Progress and clinical prospect of genomic structural variants investigation.

Journal: Science bulletin
Published: February 03, 2024

The interaction of endorepellin and neurexin triggers neuroepithelial autophagy and maintains neural tube development.

The interaction of endorepellin and neurexin triggers neuroepithelial autophagy and maintains neural tube development.

Journal: Science bulletin
Published: November 17, 2023

Systematic analysis and evaluation of chromosome aberrations in major birth defects associated with infertility.

Systematic analysis and evaluation of chromosome aberrations in major birth defects associated with infertility.

Journal: Intractable & rare diseases research
Published: October 29, 2023

An expanded view of infertility: The challenge of the changing profiling of major birth defects in China.

An expanded view of infertility: The challenge of the changing profiling of major birth defects in China.

Journal: Bioscience trends
Published: July 19, 2023

Rare loss-of-function variants reveal threshold and multifactorial inheritance of dextrocardia.

Rare loss-of-function variants reveal threshold and multifactorial inheritance of dextrocardia.

Journal: Science bulletin
Published: April 12, 2023

Urogenital sinus malformation: From development to management.

Urogenital sinus malformation: From development to management.

Journal: Intractable & rare diseases research
Published: March 29, 2023

Molecular genetics and general management of androgen insensitivity syndrome.

Molecular genetics and general management of androgen insensitivity syndrome.

Journal: Intractable & rare diseases research
Published: March 21, 2023

Whole-exome sequencing study of hypospadias.

Whole-exome sequencing study of hypospadias.

Journal: iScience
Published: December 21, 2022

Clinical Characteristics and Pathogenic Gene Identification in Chinese Patients With Paget's Disease of Bone.

Clinical Characteristics and Pathogenic Gene Identification in Chinese Patients With Paget's Disease of Bone.

Journal: Frontiers in endocrinology
Published: January 07, 2022

Re: Vuthy Ea, Anne Bergougnoux, Pascal Philibert, et al. How Far Should We Explore Hypospadias? Next-generation Sequencing Applied to a Large Cohort of Hypospadiac Patients. Eur Urol 2021;79:507-515.

Re: Vuthy Ea, Anne Bergougnoux, Pascal Philibert, et al. How Far Should We Explore Hypospadias? Next-generation Sequencing Applied to a Large Cohort of Hypospadiac Patients. Eur Urol 2021;79:507-515.

Journal: European urology
Published: February 23, 2021
Showing 1-12 of 30

Last Updated: 09/26/2026