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
- 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
- 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
- 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
- A crowdsourced set of curated structural variants for the human genome. PLoS computational biology. 2020 Academic Article GET IT
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The search for genetic determinants of human neural tube defects.
Current opinion in pediatrics.
2019
Information Resource
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Times cited: 14 -
Astrocyte-produced leukemia inhibitory factor expands the neural stem/progenitor pool following perinatal hypoxia-ischemia.
Journal of neuroscience research.
2016
Academic Article
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Times cited: 21 -
Profiling stem cell states in three-dimensional biomaterial niches using high content image informatics.
Acta biomaterialia.
2016
Academic Article
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Times cited: 16