Elliott Sherr
10PUBLICATIONS
94CO-AUTHORS
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Publications (10)
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|Nov 06, 2024
Basic helix-loop-helix transcription factor <i>BHLHE22</i> monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, tone and movement abnormalities.Carolyn Le, Emanuela Argilli, Elizabeth George
|Jul 10, 2024
Monoallelic de novo <i>AJAP1</i> loss-of-function variants disrupt trans-synaptic control of neurotransmitter release.Simon Früh, Sami Boudkkazi, Peter Koppensteiner
|Jun 12, 2024
Discovering the gene-brain-behavior link in autism via generative machine learning.Shinjini Kundu, Haris Sair, Elliott H Sherr
|May 04, 2021
DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation.Laura Morcom, Timothy J Edwards, Eric Rider
|Apr 19, 2021
DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation.Laura Morcom, Ilan Gobius, Ashley Pl Marsh
|Dec 03, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients.Laura Bryant, Dong Li, Samuel G Cox
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Frequent Collaborators
4 joint publications
Pratik Mukherjee
3 joint publications
Srikantan S Nagarajan
2 joint publications
Jeffrey Berman
2 joint publications
Jonathan Wc Lim
2 joint publications
Yunan Ye
2 joint publications
Rodrigo Suárez
2 joint publications
Wendy K Chung
2 joint publications
Timothy P L Roberts
2 joint publications
Laura Morcom
2 joint publications
Anne M Findlay
