Zhaowei Zhou
Key Laboratory For The Genetics Of Developmental And Neuropsychiatric Disorders
Shanghai, China
Shanghai, China
Last Updated: 09/26/2026
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Found 10 publications
The amino acid variants in HLA II molecules explain the major association with adult-onset Still's disease in the Han Chinese population.
Journal: Journal of autoimmunity
Published: July 19, 2020
Polymorphism of the PPARD Gene and Dynamic Balance Performance in Han Chinese Children.
Journal: Hereditas
Published: March 08, 2019
Both HLA class I and II regions identified as genome-wide significant susceptibility loci for adult-onset Still's disease in Chinese individuals.
Journal: Annals of the rheumatic diseases
Published: February 14, 2019
Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects.
Journal: Molecular genetics & genomic medicine
Published: January 11, 2019
Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review.
Journal: BMC medical genetics
Published: January 15, 2018
Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population.
Journal: Hereditas
Published: April 25, 2017
SHEsisPlus, a toolset for genetic studies on polyploid species.
Journal: Scientific reports
Published: October 28, 2015
Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese.
Journal: Nature communications
Published: December 07, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026