Xinhua Bao

Association between genetic variation of <i>CACNA1H</i> and childhood absence epilepsy

Yucai Chen, Jianjun Lu, Hong Pan et al. · Annals of Neurology · 2003 · 374 citations · Full text

The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy

Stephanie Fehr, Meredith Wilson, Jenny Downs et al. · European Journal of Human Genetics · 2012 · 304 citations · Full text

Autoimmune Disease, Neurological Disorder, Independent Clinical Entity +8

Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys

Yongchang Chen, Juehua Yu, Yuyu Niu et al. · Cell · 2017 · 194 citations · Full text

Knockout Mouse, Mendelian Disorder, Genetic Disorder +4

Rett syndrome-causing mutations compromise MeCP2-mediated liquid–liquid phase separation of chromatin

Liang Wang, Mingli Hu, Mei-Qing Zuo et al. · Cell Research · 2020 · 148 citations · Full text

Chromatin, Genome Instability, Chromatin Structure +11

POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders

Russell P. Saneto, Inn-Chi Lee, Mary Kay Koenig et al. · Seizure · 2010 · 140 citations · Full text

Genetic Testing, Pediatric Seizure Disorders, Polg Dna +7