Brain, 0006-8950


  1. 2020
  2. Bongaarts, A., van Scheppingen, J., Korotkov, A., Mijnsbergen, C., Anink, J. J., Jansen, F. E., ... Aronica, E. (2020). The coding and non-coding transcriptional landscape of subependymal giant cell astrocytomas. Brain, 143(1), 131-149.
  3. 2019
  4. van den Heuvel, M. P., Scholtens, L. H., de Lange, S. C., Pijnenburg, R., Cahn, W., van Haren, N. E. M., ... Rilling, J. K. (2019). Evolutionary modifications in human brain connectivity associated with schizophrenia. Brain, 142, 3991-4002.
  5. Abdelgabar, A. R., Suttrup, J., Broersen, R., Bhandari, R., Picard, S., Keysers, C., ... Gazzola, V. (2019). Action perception recruits the cerebellum and is impaired in patients with spinocerebellar ataxia. Brain, 142, 3791-3805.
  6. Kruszka, P., Berger, S., Casa, V., Dekker, M. R., Gaesser, J., Weiss, K., ... Muenke, M. (2019). Cohesin complex-associated holoprosencephaly. Brain, 142, 2631-2643.
  7. Schieving, J. H., de Bot, S. T., van de Pol, L. A., Wolf, N. I., Brilstra, E. H., Frints, S. G., ... Willemsen, M. A. (2019). De novo SPAST mutations may cause a complex SPG4 phenotype. Brain, 142(7).
  8. Vandervore, L. V., Schot, R., Kasteleijn, E., Oegema, R., Stouffs, K., Gheldof, A., ... Mancini, G. M. S. (2019). Corrigendum: Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics (vol 142, pg 867, 2019). Brain, 142.
  9. Vandervore, L. V., Schot, R., Kasteleijn, E., Oegema, R., Stouffs, K., Gheldof, A., ... Mancini, G. M. S. (2019). Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics. Brain, 142(4), 867-884.
  10. GRIN2A Study Grp, Strehlow, V., Heyne, H. O., Vlaskamp, D. R. M., Marwick, K. F. M., Rudolf, G., ... Lemke, J. R. (2019). GRIN2A-related disorders: genotype and functional consequence predict phenotype. Brain, 142(1), 80-92.
  11. FREX Consortium, GoNL Consortium, Kim, A., Savary, C., Dubourg, C., Carre, W., ... David, V. (2019). Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly. Brain, 142(1), 35-49.
  12. Ros, T., Enriquez Geppert, S., Young, K., Wood, G., Vuilleumier, P., Whitfield-Gabrieli, S., ... Thibault, R. T. (Accepted/In press). Consensus on the reporting and experimental design of clinical and cognitive-behavioural neurofeedback studies (CRED-nf checklist). Brain.
  13. 2018
  14. 2017
  15. Bustos, F. J., Ampuero, E., Jury, N., Aguilar, R., Falahi, F., Toledo, J., ... van Zundert, B. (2017). Epigenetic editing of the Dlg4/PSD95 gene improves cognition in aged and Alzheimer's disease mice. Brain, 140, 3252-3268.
  16. Nibbeling, E. A. R., Duarri, A., Verschuuren-Bemelmans, C. C., Fokkens, M. R., Karjalainen, J. M., Smeets, C. J. L. M., ... Verbeek, D. S. (2017). Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. Brain, 140(11), 2860-2878.
  17. Fovet, T., Micoulaud-Franchi, J-A., Vialatte, F-B., Lotte, F., Daudet, C., Batail, J-M., ... Ros, T. (2017). On assessing neurofeedback effects: Should double-blind replace neurophysiological mechanisms? Brain, 140(10), [e63].
  18. Tinkhauser, G., Pogosyan, A., Little, S., Beudel, M., Herz, D. M., Tan, H., & Brown, P. (2017). The modulatory effect of adaptive deep brain stimulation on beta bursts in Parkinson's disease. Brain, 140(4), 1053-1067.
  19. Wolff, M., Johannesen, K. M., Hedrich, U. B. S., Masnada, S., Rubboli, G., Gardella, E., ... Møller, R. S. (2017). Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders. Brain, 140(5), 1316-1336.
  20. 2016
  21. van Campen, J. S., Hompe, E. L., Jansen, F. E., Velis, D. N., Otte, W. M., van de Berg, F., ... Zijlmans, M. (2016). Cortisol fluctuations relate to interictal epileptiform discharges in stress sensitive epilepsy. Brain, 139, 1673-1679.
  22. Oswal, A., Beudel, M., Zrinzo, L., Limousin, P., Hariz, M., Foltynie, T., ... Brown, P. (2016). Deep brain stimulation modulates synchrony within spatially and spectrally distinct resting state networks in Parkinson's disease. Brain, 139, 1482-1496.
  23. 2015
  24. Schoels, L., Reimold, M., Seidel, K., Globas, C., Brockmann, K., Hauser, T. K., ... Rueb, U. (2015). No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra. Brain, 138, 3316–3326.
  25. Buijink, A. W. G., van der Stouwe, A. M. M., Broersma, M., Sharifi, S., Groot, P. F. C., Speelman, J. D., ... van Rootselaar, A-F. (2015). Motor network disruption in essential tremor: A functional and effective connectivity study. Brain, 138, 2934-2947.
  26. van Campen, J. S., Jansen, F. E., Pet, M. A., Otte, W. M., Hillegers, M. H. J., Joels, M., & Braun, K. P. J. (2015). Relation between stress-precipitated seizures and the stress response in childhood epilepsy. Brain, 138, 2234-2248.
  27. van Luijn, M. M., Kreft, K. L., Jongsma, M. L., Mes, S. W., Wierenga-Wolf, A. F., van Meurs, M., ... Hintzen, R. Q. (2015). Multiple sclerosis-associated CLEC16A controls HLA class II expression via late endosome biogenesis. Brain, 138(6), 1531-1547.
  28. 2014
  29. Niethammer, M., Tang, C. C., Feigin, A., Allen, P. J., Heinen, L., Hellwig, S., ... Eidelberg, D. (2014). A disease-specific metabolic brain network associated with corticobasal degeneration. Brain, 137, 3036-3046.
  30. van Lutterveld, R., van den Heuvel, M. P., Diederen, K. M. J., de Weijer, A. D., Begemann, M. J. H., Brouwer, R. M., ... Sommer, I. E. (2014). Cortical thickness in individuals with non-clinical and clinical psychotic symptoms. Brain, 137, 2664-2669.
  31. Fokke, C., van den Berg, B., Drenthen, J., Walgaard, C., van Doorn, P. A., & Jacobs, B. C. (2014). Diagnosis of Guillain-Barre syndrome and validation of Brighton criteria. Brain, 137, 33-43.
  32. 2013
  33. Stoffels, J. M. J., de Jonge, J. C., Stancic, M., Nomden, A., van Strien, M. E., Ma, D., ... Baron, W. (2013). Fibronectin aggregation in multiple sclerosis lesions impairs remyelination. Brain, 136, 116-131.
  34. Weterman, M. A. J., Barth, P. G., van Spaendonck-Zwarts, K. Y., Aronica, E., Poll-The, B-T., Brouwer, O. F., ... Baas, F. (2013). Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy. Brain, 136, 282-293.
  35. 2012
  36. van Gassen, K. L. I., van der Heijden, C. D. C. C., de Bot, S. T., den Dunnen, W. F. A., van den Berg, L. H., Verschuuren - Bemelmans, C. C., ... van de Warrenburg, B. P. (2012). Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort. Brain, 135, 2994-3004.
  37. 2011
  38. Rolyan, H., Scheffold, A., Heinrich, A., Begus-Nahrmann, Y., Langkopf, B. H., Hoelter, S. M., ... Rudolph, K. L. (2011). Telomere shortening reduces Alzheimer's disease amyloid pathology in mice. Brain, 134, 2044-2056.
  39. Ackermans, L., Duits, A., van der Linden, C., Tijssen, M., Schruers, K., Temel, Y., ... Visser-Vandewalle, V. (2011). Double-blind clinical trial of thalamic stimulation in patients with Tourette syndrome. Brain, 134, 832-844.
  40. Namavar, Y., Barth, P. G., Kasher, P. R., van Ruissen, F., Brockmann, K., Bernert, G., ... Sival, D. (2011). Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia. Brain, 134(Pt 1), 143-56.
  41. Fierstra, J., Conklin, J., Krings, T., Slessarev, M., Han, J. S., Fisher, J. A., ... Mikulis, D. J. (2011). Impaired peri-nidal cerebrovascular reserve in seizure patients with brain arteriovenous malformations. Brain, 134, 100-109.
  42. 2010
  43. Diederen, K. M. J., De Weijer, A. D., Daalman, K., Blom, J. D., Neggers, S. F. W., Kahn, R. S., & Sommer, I. E. C. (2010). Decreased language lateralization is characteristic of psychosis, not auditory hallucinations. Brain, 133, 3734-3744.
  44. Morava, E., Wevers, R. A., Cantagrel, V., Hoefsloot, L. H., Al-Gazali, L., Schoots, J., ... Lefeber, D. J. (2010). A novel cerebello-ocular syndrome with abnormal glycosylation due to abnormalities in dolichol metabolism. Brain, 133, 3210-3220.
  45. van der Schot, A. C., Vonk, R., Brouwer, R. M., van Baal, G. C. M., Brans, R. G. H., van Haren, N. E. M., ... Kahn, R. S. (2010). Genetic and environmental influences on focal brain density in bipolar disorder. Brain, 133, 3080-3092.
  46. Steenweg, M. E., Vanderver, A., Blaser, S., Bizzi, A., de Koning, T. J., Mancini, G. M. S., ... van der Knaap, M. S. (2010). Magnetic resonance imaging pattern recognition in hypomyelinating disorders. Brain, 133(10), 2971-82.
  47. Timmermann, L., Pauls, K. A. M., Wieland, K., Jech, R., Kurlemann, G., Sharma, N., ... Peker, S. (2010). Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulation. Brain, 133, 701-712.
  48. Leen, W. G., Klepper, J., Verbeek, M. M., Leferink, M., Hofste, T., van Engelen, B. G., ... Willemsen, M. A. (2010). Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder. Brain, 133, 655-670.
  49. 2009
  50. Lindroos, M. M., Borra, R. J., Parkkola, R., Virtanen, S. M., Lepomaki, V., Bucci, M., ... Majamaa, K. (2009). Cerebral oxygen and glucose metabolism in patients with mitochondrial m.3243A > G mutation. Brain, 132(12), 3274-3284.
  51. Rotthier, A., Baets, J., De Vriendt, E., Jacobs, A., Auer-Grumbach, M., Levy, N., ... Timmerman, V. (2009). Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain, 132, 2699-2711.
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