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Authors: Michael S Hildebrand
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Journal Article

Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40 Free

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Angela T Morgan and others
Brain, Volume 146, Issue 12, December 2023, Pages 5086–5097, https://doi.org/10.1093/brain/awad314
Published: 18 November 2023
Journal Article

Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy Open Access

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Luca Gozzelino and others
Brain, Volume 145, Issue 7, July 2022, Pages 2313–2331, https://doi.org/10.1093/brain/awac082
Published: 04 July 2022
Journal Article

UNC13B and focal epilepsy Free

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Timothy E. Green and others
Brain, Volume 145, Issue 3, March 2022, Pages e10–e12, https://doi.org/10.1093/brain/awab485
Published: 05 April 2022
Journal Article

Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes Open Access

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Line Skotte and others
Brain, Volume 145, Issue 2, February 2022, Pages 555–568, https://doi.org/10.1093/brain/awab260
Published: 12 January 2022
Journal Article

Atypical development of Broca’s area in a large family with inherited stuttering Free

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Daisy G Y Thompson-Lake and others
Brain, Volume 145, Issue 3, March 2022, Pages 1177–1188, https://doi.org/10.1093/brain/awab364
Published: 23 November 2021
Journal Article

Cerebrospinal fluid liquid biopsy for detecting somatic mosaicism in brain Open Access

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Zimeng Ye and others
Brain Communications, Volume 3, Issue 1, 2021, fcaa235, https://doi.org/10.1093/braincomms/fcaa235
Published: 21 January 2021
Journal Article

Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size Free

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Diana Le Duc and others
Brain, Volume 142, Issue 9, September 2019, Pages 2617–2630, https://doi.org/10.1093/brain/awz198
Published: 20 July 2019
Journal Article

Dorsal language stream anomalies in an inherited speech disorder Free

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Frédérique J Liégeois and others
Brain, Volume 142, Issue 4, April 2019, Pages 966–977, https://doi.org/10.1093/brain/awz018
Published: 23 February 2019
Journal Article

Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features Free

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Samuel F Berkovic and others
Brain, Volume 142, Issue 1, January 2019, Pages 59–69, https://doi.org/10.1093/brain/awy297
Published: 15 December 2018
Journal Article

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A Open Access

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Dalia Kasperavičiūtė and others
Brain, Volume 136, Issue 10, October 2013, Pages 3140–3150, https://doi.org/10.1093/brain/awt233
Published: 06 September 2013