Ning Wang

26PUBLICATIONS
85CO-AUTHORS
Gene mappingNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Medical biochemistry - proteins and peptides (incl. medical proteomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (26)

|Oct 23, 2026
SLC20A2 Intragenic Structural Variants as a Cause of Primary Brain Calcification.

|Oct 13, 2026
Stage-Specific Patterns of Imaging and Non-Motor Biomarkers in Spinocerebellar Ataxia Type 3.

|Oct 04, 2026
Integrated genetic and epigenetic diagnosis of facioscapulohumeral muscular dystrophy using Oxford Nanopore long-read sequencing.

|Sep 14, 2026
A De Novo 16p13.3 Triplication Underlying Early-Onset Complex Neurodegeneration.

|Sep 06, 2026
De Novo Facioscapulohumeral Muscular Dystrophy: A Severe Subtype Driven by D4Z4 Repeat Contractions.

|May 21, 2026
Biallelic loss-of-function mutations in BPNT1 cause vitamin B12-dependent megaloblastic anemia.

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Frequent Collaborators

9 joint publications

Wan-Jin Chen

4 joint publications

Zhiqiang Wang

4 joint publications

Naiqing Cai

3 joint publications

Shi-Rui Gan