Irene J. Chang

Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia

Nynke Oosterhof, Irene J. Chang, Ehsan Ghayoor Karimiani et al. · The American Journal of Human Genetics · 2019 · 254 citations · Full text

Pediatric-onset Leukoencephalopathy, Homozygous Mutations, Neurological Disorder +10

Targeted long-read sequencing identifies missing disease-causing variation

Danny E. Miller, Arvis Sulovari, Tianyun Wang et al. · The American Journal of Human Genetics · 2021 · 227 citations · Full text

Long-read Sequencing, Long-read Sequencing Identifies, Next-generation Sequencing +4

Effect of an educational intervention on HPV knowledge and vaccine attitudes among urban employed women and female undergraduate students in China: a cross-sectional study

Irene J. Chang, Rong Huang, Wei He et al. · BMC Public Health · 2013 · 90 citations · Full text

Association of Variants in the <i>SPTLC1</i> Gene With Juvenile Amyotrophic Lateral Sclerosis

Janel O. Johnson, Ruth Chia, Danny E. Miller et al. · JAMA Neurology · 2021 · 78 citations · Full text

COQ2 nephropathy: a treatable cause of nephrotic syndrome in children

Michelle C. Starr, Irene J. Chang, Laura S. Finn et al. · Pediatric Nephrology · 2018 · 42 citations

Glomerular Disease, Glomerulonephritis, Renal Function +10