selected publications
- A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele. Human molecular genetics. 2023 Academic Article GET IT
-
Astrocytes derived from ASD individuals alter behavior and destabilize neuronal activity through aberrant Ca2+ signaling.
Molecular psychiatry.
2022
Academic Article
GET IT
Times cited: 12 -
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk.
Proceedings of the National Academy of Sciences of the United States of America.
2021
Academic Article
GET IT
Times cited: 5 -
Unraveling the complex genetics of neural tube defects: From biological models to human genomics and back.
Genesis (New York, N.Y. : 2000).
2021
Review
GET IT
Times cited: 8 -
Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida.
Genetics in medicine : official journal of the American College of Medical Genetics.
2021
Academic Article
GET IT
Times cited: 5 -
A crowdsourced set of curated structural variants for the human genome.
PLoS computational biology.
2020
Academic Article
GET IT
Times cited: 2 -
The search for genetic determinants of human neural tube defects.
Current opinion in pediatrics.
2019
Review
GET IT
Times cited: 11 -
Astrocyte-produced leukemia inhibitory factor expands the neural stem/progenitor pool following perinatal hypoxia-ischemia.
Journal of neuroscience research.
2016
Academic Article
GET IT
Times cited: 20 -
Profiling stem cell states in three-dimensional biomaterial niches using high content image informatics.
Acta biomaterialia.
2016
Academic Article
GET IT
Times cited: 15