Jing-yu Liu
Union Hospital
Wuhan, 430022, China
Wuhan, 430022, China
Last Updated: 09/26/2026
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Found 10 publications
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcification.
Journal: Brain : a journal of neurology
Published: August 15, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor.
Journal: Brain : a journal of neurology
Published: June 09, 2019
Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from China.
Journal: Parkinsonism & related disorders
Published: January 02, 2019
Coding mutations in NUS1 contribute to Parkinson's disease.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: October 24, 2018
Evaluation of MYORG mutations as a novel cause of primary familial brain calcification.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 03, 2018
Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy.
Journal: Journal of medical genetics
Published: May 14, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Journal: Human molecular genetics
Published: January 20, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Journal: Human molecular genetics
Published: October 12, 2017
PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B.
Journal: Scientific reports
Published: February 27, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026