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Nature Methods|November 1, 2018
Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Nature Methods|January 4, 2019
Publisher Correction: Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Nature Methods|March 2, 2019
Author Correction: Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Acta Neuropathologica|May 13, 2022
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibilityKatri Silvennoinen, Kinga Gawel, Despina Tsortouktzidis, et al.Human Molecular Genetics|June 19, 2014
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsyEva M Reinthaler, Dennis Lal, Sebastien Lebon, et al.American Journal of Human Genetics|November 22, 2016
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair SyndromeF Buket Ü Basmanav, Laura Cau, Aylar Tafazzoli, et al.Nature Communications|January 24, 2015
Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampusMichael R Johnson, Jacques Behmoaras, Leonardo Bottolo, et al.Brain : a Journal of Neurology|September 10, 2013
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1ADalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.Science (New York, N.Y.)|June 23, 2018
Analysis of shared heritability in common disorders of the brain, Verneri Anttila, Brendan Bulik-Sullivan, et al.Pageof 12