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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.
Epilepsia|February 7, 2017
Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new casesJoseph D Symonds, Shelagh Joss, Kay A Metcalfe, 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.
Brain : a Journal of Neurology|February 9, 2022
Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphologySiddharth Banka, Abigail Bennington, Martin J Baker, et al.
American Journal of Medical Genetics. Part A|September 27, 2016
Clinical and genetic aspects of KBG syndromeKaren Low, Tazeen Ashraf, Natalie Canham, et al.
Nature Ecology & Evolution|November 1, 2017
Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi ArmillariaGyörgy Sipos, Arun N Prasanna, Mathias C Walter, et al.
Nature Ecology & Evolution|February 11, 2018
Author Correction: Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi ArmillariaGyörgy Sipos, Arun N Prasanna, Mathias C Walter, et al.
Nature Methods|December 22, 2023
The Cousa objective: a long-working distance air objective for multiphoton imaging in vivoChe-Hang Yu, Yiyi Yu, Liam M Adsit, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 22, 2022
Clustered variants in the 5' coding region of TRA2B cause a distinctive neurodevelopmental syndromeFrancis Ramond, Caroline Dalgliesh, Mona Grimmel, et al.
European Journal of Human Genetics : EJHG|April 16, 2009
BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defectsEmma Hilton, Jennifer Johnston, Sandra Whalen, et al.
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