Zhimin Chen

7PUBLICATIONS
14CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Socio-economic development
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Publications (7)

|Sep 26, 2026
A Candidate MEST Splice-Site Variant in a Patient with Silver-Russell Syndrome-like Phenotype: First Report and Literature Review.

|Sep 24, 2026
Progress and Prospects of Newborn Screening in China.

|Aug 27, 2026
De Novo ZNF292 Variants Cause Neurodevelopmental Disorder with Short Stature: A Clinical Case Series of Eight Individuals.

|Aug 27, 2026
Ocular Nystagmus as the Initial Presenting Feature in a Patient with Complete CLTC Deletion: Expanding the Genotype-Phenotype Spectrum of CLTC-Related Disorder.

|Jul 28, 2026
Novel and Known DHX37 Variants in 46,XY DSD: Expanding the Genotypic and Phenotypic Spectrum.

|May 11, 2026
Advancements and insights into newborn screening with tandem mass spectrometry in China: a comprehensive descriptive analysis (2017-2021).

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Frequent Collaborators

1 joint publications

Daqing Ma

1 joint publications

Huidan Wu

1 joint publications

Chen Liu

1 joint publications

Zhengyan Zhao