Jan Ching Chun Hu
University of Michigan
H-index: 65
North America-United States
Top articles of Jan Ching Chun Hu
Association of Structural Forms of 17q21. 31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes
medRxiv
2024/2/28
Hui Wang
H-Index: 2
Kurt Farrell
H-Index: 7
Catriona Mclean
H-Index: 62
Ulrich Müller
H-Index: 28
Lili-Naz Hazrati
H-Index: 29
Irene Litvan
H-Index: 62
Douglas Galasko
H-Index: 78
Edward B Lee
H-Index: 44
Huw R Morris
H-Index: 51
Yuk Yee Leung
H-Index: 12
Giovanni Coppola
H-Index: 6
Li-San Wang
H-Index: 42
Jung-Ying Tzeng
H-Index: 16
Correlation of lipocalin 2 and glycolipid metabolism and body composition in a large cohort of children with osteogenesis imperfecta
Journal of Endocrinological Investigation
2024/1
Genotype–phenotype relationship and comparison between eastern and western patients with osteogenesis imperfecta
Journal of Endocrinological Investigation
2024/1
FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome
International Endodontic Journal
2023/8
PAX9 mutations and genetic synergism in familial tooth agenesis
Annals of the New York Academy of Sciences
2023/6
Dentin defects caused by a Dspp−1 frameshift mutation are associated with the activation of autophagy
Scientific Reports
2023/4/19
Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta
Journal of Personalized Medicine
2023/2/14
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy
medRxiv
2023/12/30
Phenotypic variability in LAMA3‐associated amelogenesis imperfecta
Oral Diseases
2023/11
Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations
Scientific Reports
2022/10/1
Translated Mutant DSPP mRNA Expression Level Impacts the Severity of Dentin Defects
Journal of Personalized Medicine
2022/6/19
The Modified Shields Classification and 12 Families with Defined DSPP Mutations
Genes
2022/5/12
Novel homozygous KREMEN1 mutation causes ectodermal dysplasia
Oral diseases
2022/4
Novel KLK4 Mutations Cause Hypomaturation Amelogenesis Imperfecta
Journal of Personalized Medicine
2022/1/24
Novel Mutations in GPR68 and SLC24A4 Cause Hypomaturation Amelogenesis Imperfecta
Journal of Personalized Medicine
2021/12/28
A genetic model for the secretory stage of dental enamel formation
2021/12/1
Analyses of oligodontia phenotypes and genetic etiologies
International journal of oral science
2021/12
Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis
Journal of Personalized Medicine
2021/11/17
Mouse Dspp frameshift model of human dentinogenesis imperfecta
Scientific Reports
2021/10/19
MMP20-generated amelogenin cleavage products prevent formation of fan-shaped enamel malformations
Scientific Reports
2021/5/19