Wei M. Ye
Changsha, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 15 publications
Identification of novel mutations in TSC1 and TSC2 for tuberous sclerosis complex by targeted next-generation sequencing and ACMG guidelines.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: June 26, 2020
Corrigendum to "Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3" [Stem Cell Research Vol 40 (2019) 101555].
Journal: Stem cell research
Published: February 03, 2020
Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3.
Journal: Stem cell research
Published: August 08, 2019
Identifying SYNE1 Ataxia With Novel Mutations in a Chinese Population.
Journal: Frontiers in neurology
Published: September 16, 2018
Association of TNF-α rs1799964 and IL-1β rs16944 polymorphisms with multiple system atrophy in Chinese Han population.
Journal: The International journal of neuroscience
Published: December 19, 2017
Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease.
Journal: Brain : a journal of neurology
Published: March 24, 2017
Alteration of methylation status in the ATXN3 gene promoter region is linked to the SCA3/MJD.
Journal: Neurobiology of aging
Published: June 15, 2016
(CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China.
Journal: Brain : a journal of neurology
Published: April 17, 2016
Identification of a de novo DYNC1H1 mutation via WES according to published guidelines.
Journal: Scientific reports
Published: August 19, 2015
Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective.
Journal: PloS one
Published: May 13, 2015
Last Updated: 09/26/2026