Dai, Li

The genetic architecture of down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

Korbel, J. O., Tirosh-Wagner, T., Urban, A. E., Chen, X.-N., Kasowski, M., Dai, L., Grubert, F., Erdman, C., Gao, M. C., Lange, K., et al. (2009) · Proceedings of the National Academy of Sciences

Down syndrome and intellectual disability researchGenomic variations and chromosomal abnormalities

Cited by 399

A human neurodevelopmental model for Williams syndrome

Chailangkarn, T., Trujillo, C. A., Freitas, B. C., Hrvoj-Mihic, B., Herai, R. H., Yu, D. X., Brown, T. T., Marchetto, M. C., Bardy, C., McHenry, L., et al. (2016) · Nature

Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders

Cited by 195

Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior

Dai, L., Carter, C. S., Ying, J., Bellugi, U., Pournajafi-Nazarloo, H., & Korenberg, J. R. (2012) · PLoS ONE

Williams Syndrome ResearchNeuroendocrine regulation and behavior

Cited by 119

Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex

Gao, M. C., Bellugi, U., Dai, L., Mills, D. L., Sobel, E. M., Lange, K., & Korenberg, J. R. (2010) · PLoS ONE

Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders

Cited by 42