Chuan Tan
The University of Adelaide(AU)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Genomics and Chromatin Dynamics, Epigenetics and DNA Methylation
Most-Cited Works
- → X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes(2015)302 cited
- → Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency(2015)100 cited
- → THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability(2015)78 cited
- → PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy(2018)50 cited
- → Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder(2014)34 cited
- → IncreasedSTAG2dosage defines a novel cohesinopathy with intellectual disability and behavioral problems(2015)32 cited
- → Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα)(2017)29 cited
- Next-generation sequencing in 248 families with X-linked intellectual disability(2011)
- → Protocadherin Mutations in Neurodevelopmental Disorders(2016)1 cited
- Update on X-linked intellectual disability(2015)