Author

Na Chen

Central South UniversityORCID 0000-0001-8797-8535Unclaimed ORCID profile · follow to get notified of new preprints

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Na Chen2 papers · Chinese Academy of Sciences

Biology Disciplines

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Cell Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:proteomics· 1 Organism:rat· 1 Approach:statistical model· 1

Frequent Co-Authors

Cheng XuiD· 1 shared Chunyan Ye· 1 shared Dandan WangiD· 1 shared E WangiD· 1 shared Gang Qin· 1 shared Jian QiuiD· 1 shared Kun XiaiD· 1 shared Lizhe GuoiD· 1 shared

Activity by Year

2017-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperCell Biology

Cheng XuORCID

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintApr 14, 2025

SND1 Impairs Calcium Homeostasis in Right Ventricular Failure by Binding and Destabilizing SERCA2a in Cardiomyocytes

Lizhe Guo, Xingyang Liu, Lu Wang…·E Wang

This study identifies SND1 as a reactivated fetal gene that contributes to right ventricular failure by destabilizing SERCA2a, impairing calcium handling, and reducing cardiomyocyte contractility and survival.

DOI 10.1101/2025.04.14.648853

𝕏 PostBluesky

GeneticsbioRxivPreprintOct 8, 2017

Neolithic super-grandfather Y haplotypes, their related surnames, and autism spectrum disorder

Pei He, Na Chen, Zhengmao Hu…·Shi Huang

The paper links Neolithic Y haplotypes to autism spectrum disorder (ASD) by showing higher frequencies of low SES haplotypes in ASD fathers and a male-biased ASD ratio in related surnames.

3 citations

humanstatistical model

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