Hello! Describe your research question and I'll help you find matching datasets across 2,944 studies from AnVIL, BDC, CRDC, and KFDRC.

A Chromatin Accessibility Atlas of the Developing Human Telencephalon

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome

Yuyang Chen, R. Dawes, Hyung Chul Kim, et al. (2024). Nature. Cited 76 times. https://doi.org/10.1038/s41586-024-07773-7