Minna Luo

5PUBLICATIONS
8CO-AUTHORS
Cell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsGenetic immunologyDevelopmental genetics (incl. sex determination)
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Publications (5)

|Oct 16, 2026
Functional Validation of a CC2D2A Non-Canonical Splice-Site Variant Supports Prenatal Molecular Testing in Joubert Syndrome.

|Aug 06, 2026
A De Novo DHX16 Variant Associated With Neuromuscular Oculoauditory Syndrome Regulates Pre-mRNA Splicing In Vitro.

|Sep 29, 2025
Novel Pathogenic Biallelic Variants in KIAA0586 Expand the Variant Spectrum of Ciliopathies.

Yue Shen, Ruida He, Chao Lu

|Apr 06, 2021
Clinical heterogeneity and intrafamilial variability of Joubert syndrome in two siblings with CPLANE1 variants.

Xiujuan Zhang, Yue Shen, Ping Li

|Oct 19, 2019
Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndrome.

Minna Luo, Li Cao, Zongfu Cao

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Frequent Collaborators

3 joint publications

Yue Shen

2 joint publications

Xu Ma

2 joint publications

Zongfu Cao

1 joint publications

Muqing Cao