Brain

Journal Abbreviation: BRAIN
ISSN: 0006-8950
eISSN: 1460-2156
Publisher: Oxford University Press

Publications (47)

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Unpublished / Preprint

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Abstract

Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly (2022) Kloeckner C, Murray JPF, Tavasoli M, Sticht H, Stoltenburg-Didinger G, Scholle LM, Bakhtiari S, et al. Journal article Matrix metalloproteinase 10 is linked to the risk of progression to dementia of the Alzheimer's type (2022) Adami PVM, Orellana A, Garcia P, Kleineidam L, Alarcon-Martin E, Montrreal L, Aguilera N, et al. Journal article Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study (2022) Spitzer H, Ripart M, Whitaker K, D'Arco F, Mankad K, Chen AA, Napolitano A, et al. Journal article Next-generation antibody-based therapies in neurology (2021) Ruck T, Nimmerjahn F, Wiendl H, Luenemann JD Journal article, Review article The Developing Human Connectome Project: Typical and disrupted perinatal functional connectivity (2021) Eyre M, Fitzgibbon SP, Ciarrusta J, Cordero-Grande L, Price AN, Poppe T, Schuh A, et al. Journal article Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia (2020) Ebrahimi-Fakhari D, Teinert J, Behne R, Wimmer M, D'Amore A, Eberhardt K, Brechmann B, et al. Journal article Janus-faced spatacsin (SPG11): involvement in neurodevelopment and multisystem neurodegeneration (2020) Pozner T, Regensburger M, Engelhorn T, Winkler J, Winner B Journal article, Review article Modelling brain development to detect white matter injury in term and preterm born neonates (2020) O'Muircheartaigh J, Robinson EC, Pietsch M, Wolfers T, Aljabar P, Grande LC, Teixeira RPAG, et al. Journal article The coding and non-coding transcriptional landscape of subependymal giant cell astrocytomas (2020) Bongaarts A, Van Scheppingen J, Korotkov A, Mijnsbergen C, Anink JJ, Jansen FE, Spliet WG, et al. Journal article Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration (2020) Fagerberg CR, Taylor A, Distelmaier F, Schrøder HD, Kibæk M, Wieczorek D, Tarnopolsky M, et al. Journal article
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