Wei Luo

49PUBLICATIONS
57CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Toxicology (incl. clinical toxicology)Haematological tumoursMedical infection agents (incl. prions)Pacific Peoples and disability
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Publications (49)

|Oct 28, 2026
Genetic Analysis of the SLC38A6 Gene in Chinese Patients with Essential Tremor: Not Causative, But Rather an Additional Susceptibility Gene?

|Oct 24, 2026
Temporomandibular Joint Disorder in Parkinson's Disease Patients.

|Aug 27, 2026
Brain calcification-associated JAM2 pathogenic mutations impair JAM2-JAM3 tight junction structure and the blood-brain barrier integrity.

|Aug 06, 2026
Rare Heterozygous Loss-of-Function Variants in MCOLN1 Identified in Two Sporadic Patients with α-Synucleinopathies.

|Jul 21, 2026
Breaking barriers and fighting inequality in Parkinson's disease care: Personal reflections of movement disorders clinicians.

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

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Frequent Collaborators

14 joint publications

Zhidong Cen

14 joint publications

Xinhui Chen

9 joint publications

Dehao Yang

8 joint publications

Haotian Wang