Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila YH Chao, LA Robak, F Xia, MK Koenig, A Adesina, CA Bacino, F Scaglia, ... Human molecular genetics 25 (9), 1846-1856, 2016 | 69 | 2016 |
Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse MF Wangler, YH Chao, V Bayat, N Giagtzoglou, AB Shinde, N Putluri, ... PLoS genetics 13 (6), e1006825, 2017 | 36 | 2017 |
A homozygous mutation in PEX16 identified by whole-exome sequencing ending a diagnostic odyssey CA Bacino, YH Chao, E Seto, T Lotze, F Xia, RO Jones, A Moser, ... Molecular genetics and metabolism reports 5, 15-18, 2015 | 20 | 2015 |
Dataset for a case report of a homozygous PEX16 F332del mutation C Bacino, YH Chao, E Seto, T Lotze, F Xia, RO Jones, A Moser, ... Data in Brief 6, 722-727, 2016 | 1 | 2016 |
Drosophila Models Uncover Substrate Channeling Effects on Phospholipids and Sphingolipids in Peroxisomal Biogenesis Disorders MF Wangler, YH Chao, M Roth, R Welti, J McNew bioRxiv, 2024.04. 26.591192, 2024 | | 2024 |
Identification and Functional Annotation of Novel Autism Candidate Genes Using an in Vivo High-Throughput Drosophila Genetic Screen H Chao, O Kanca, S Manivannan, X Luo, N Liu, S Saurabh, M Lagarde, ... ANNALS OF NEUROLOGY 80, S306-S307, 2016 | | 2016 |