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121. The basal interstitial nucleus (BIN) of the cerebellum provides diffuse ascending inhibitory input to the floccular granule cell layer.

Jaarsma D, Blot FGC, Wu B, Venkatesan S, Voogd J, Meijer D, Ruigrok TJH, Gao Z, Schonewille M, De Zeeuw CI
in The Journal of comparative neurology 2018

122. Long term neurodevelopmental consequences of intrauterine exposure to lithium and antipsychotics: a systematic review and meta-analysis.

Poels EM, Schrijver L, Kamperman AM, Hillegers MH, Hoogendijk WJ, Kushner SA, Roza SJ
in European Child & Adolescent Psychiatry 2018

123. Cerebellar learning properties are modulated by the CRF receptor in granular cells.

Ezra-Nevo G, Prestori F, Locatelli F, Soda T, Ten Brinke MM, Engel M, Boele HJ, Botta L, Leshkowitz D, Ramot A, Tsoory M, Biton IE, Deussing J, D'Angelo E, De Zeeuw CI, Chen A
in The Journal of neuroscience : the official journal of the Society for Neuroscience 2018

124. Psychotic-like experiences in pre-adolescence: what precedes the antecedent symptoms of severe mental illness?

Bolhuis K, Verhoeff ME, Blanken LM, Cibrev D, Jaddoe VWV, Verhulst FC, Hillegers MHJ, Kushner SA, Tiemeier H
in Acta Psychiatrica Scandinavica 2018

125. A Reconfigurable Ultrasound Transceiver ASIC With 24×40 Elements for 3-D Carotid Artery Imaging.

Eunchul Kang, Qing Ding, Maysam Shabanimotlagh, Pieter Kruizinga, Zu-yao Chang, Emile Noothout, Hendrik J. Vos, Johan G. Bosch, Martin D. Verweij, Nico de Jong, Michiel A. P. Pertijs
in J. Solid-State Circuits 2018

126. Differentiating Cerebellar Impact on Thalamic Nuclei.

Gornati SV, Schäfer CB, Eelkman Rooda OHJ, Nigg AL, De Zeeuw CI, Hoebeek FE
in Cell reports 2018

127. ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia.

Bouwkamp CG, Afawi Z, Fattal-Valevski A, Quadri M, Breedveld GJ, Masalha R, Mandel H, Abu Tailakh M, van Eijcken WF, Vernooij MW, Bonifati V, Kushner SA
in Neurology Genetics 2018

128. Chloride Homeostasis in Neurons With Special Emphasis on the Olivocerebellar System: Differential Roles for Transporters and Channels.

Rahmati N, Hoebeek FE, Peter S, De Zeeuw CI
in Frontiers in cellular neuroscience 2018

129. Single transcription factor based generation of oligodendrocytes from human pluripotent stem cells.

García-León JA, Kumar M, Boon R, Chau D, One J, Wolfs E, Eggermonts K, Berckmans P, Gunhanlar N, De Vrij FM, Pavie B, Corthout N, Kushner SA, Carlos J, Dávila C, Lambrichts I, Hu WS, Verfaillie CM
in Stem Cell Reports 2018

130. Cerebellar transcranial direct current stimulation interacts with BDNF Val66Met in motor learning.

van der Vliet R, Jonker ZD, Louwen SC, Heuvelman M, de Vreede L, Ribbers GM, De Zeeuw CI, Donchin O, Selles RW, van der Geest JN, Frens MA
in Brain stimulation 2018

131. Are infectious agents involved in the pathogenesis of postpartum psychosis?

De Witte LD, Snijders G, Litjens M, Kamperman AM, Kushner SA, Kahn RS, Bergink V
in Journal of Affective Disorders 2018

132. Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxia.

Chopra R, Wasserman AH, Pulst SM, De Zeeuw CI, Shakkottai VG
in Human molecular genetics 2018

133. Individual Differences in Motor Noise and Adaptation Rate Are Optimally Related.

134. Correction to: Cerebellar Modules and Their Role as Operational Cerebellar Processing Units: A Consensus paper.

Apps R, Hawkes R, Aoki S, Bengtsson F, Brown AM, Chen G, Ebner TJ, Isope P, Jörntell H, Lackey EP, Lawrenson C, Lumb B, Schonewille M, Sillitoe RV, Spaeth L, Sugihara I, Valera A, Voogd J, Wylie DR, Ruigrok TJH
in Cerebellum (London, England) 2018

135. Visual search accelerates during adolescence.

in Journal of vision 2018

136. Cerebellar Modules and Their Role as Operational Cerebellar Processing Units.

Apps R, Hawkes R, Aoki S, Bengtsson F, Brown AM, Chen G, Ebner TJ, Isope P, Jörntell H, Lackey EP, Lawrenson C, Lumb B, Schonewille M, Sillitoe RV, Spaeth L, Sugihara I, Valera A, Voogd J, Wylie DR, Ruigrok TJH
in Cerebellum (London, England) 2018

137. Pain Experience is Somatotopically Organized and Overlaps with Pain Anticipation in the Human Cerebellum.

Michelle Welman FHS, Smit AE, Jongen JLM, Tibboel D, van der Geest JN, Holstege JC
in Cerebellum (London, England) 2018

138. Nerve reinnervation and itch behavior in a rat burn wound model.

Saffari TM, Schüttenhelm BN, van Neck JW, Holstege JC
in Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society 2018

139. An anatomical study on the effectiveness of Arthrex Mini TightRope ligament reconstruction in an unstable trapeziometacarpal joint.

Friebel TR, Walbeehm ET, Kleinrensink GJ, Ray S, Zuidam JM
in Archives of orthopaedic and trauma surgery 2018

140. Optimal surgical approach for the treatment of Quervains disease: A surgical-anatomical study.

Poublon AR, Kleinrensink GJ, Kerver A, Coert JH, Walbeehm ET
in World journal of orthopedics 2018

141. Mesh versus suture repair of umbilical hernia in adults: a randomised, double-blind, controlled, multicentre trial.

Kaufmann R, Halm JA, Eker HH, Klitsie PJ, Nieuwenhuizen J, van Geldere D, Simons MP, van der Harst E, van 't Riet M, van der Holt B, Kleinrensink GJ, Jeekel J, Lange JF
in Lancet (London, England) 2018

142. Comparing different modalities for the diagnosis of incisional hernia: a systematic review.

Kroese LF, Sneiders D, Kleinrensink GJ, Muysoms F, Lange JF
in Hernia : the journal of hernias and abdominal wall surgery 2018

143. A cerebellar mechanism for learning prior distributions of time intervals.

Narain D, Remington E.D, De Zeeuw, C.I & Jazayeri M
in Nature Communications 2018

144. The Zinc Transporter SLC39A7 (ZIP7) Is Essential for Regulation of Cytosolic Zinc Levels.

Woodruff G, Bouwkamp CG, de Vrij FM, Lovenberg T, Bonaventure P, Kushner SA, Harrington AW
in Molecular pharmacology 2018

145. Employed family-based genetic discovery combining linkage analysis and exome sequencing to identify RCL1 as a novel candidate gene for depression, with independent replication in a population-based cohort.

Amin N, de Vrij FMS, Baghdadi M, Brouwer RWW, van Rooij JGJ, Jovanova O, Uitterlinden AG, Hofman A, Janssen HLA, Murad SD, Kraaij R, Stedehouder J, van den Hout MCGN, Kros JM, van IJcken WFJ, Tiemeier H, Kushner SA, van Duijn CM
in Molecular psychiatry 2018

146. Homozygous missense mutation associated with complicated hereditary spastic paraplegia

Bouwkamp CG, Afawi Z, Fattal-Valevski A, Krabbendam IE, Rivetti S, Masalha R, Quadri M, Breedveld GJ, Mandel H, Tailakh MA, Beverloo HB, Stevanin G, Brice A, van IJcken WFJ, Vernooij MW, Dolga AM, de Vrij FMS, Bonifati V, Kushner SA
in Neurology. Genetics 2018

147. Activity-Dependent Myelination of Parvalbumin Interneurons Mediated by Axonal Morphological Plasticity.

in The Journal of neuroscience : the official journal of the Society for Neuroscience 2018

148. SOX10 Single Transcription Factor-Based Fast and Efficient Generation of Oligodendrocytes from Human Pluripotent Stem Cells.

García-León JA, Kumar M, Boon R, Chau D, One J, Wolfs E, Eggermont K, Berckmans P, Gunhanlar N, de Vrij F, Lendemeijer B, Pavie B, Corthout N, Kushner SA, Dávila JC, Lambrichts I, Hu WS, Verfaillie CM
in Stem cell reports 2018

149. Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity.

Romano V, De Propris L, Bosman LW, Warnaar P, Ten Brinke MM, Lindeman S, Ju C, Velauthapillai A, Spanke JK, Middendorp Guerra E, Hoogland TM, Negrello M, D'Angelo E, De Zeeuw CI
in eLife 2018

150. Testing the Precedence Effect in the Median Plane Reveals Backward Spatial Masking of Sound.

Ege R, van Opstal AJ, Bremen P, van Wanrooij MM
in Scientific reports 2018

151. Cerebellar involvement in migraine.

Kros L, Angueyra Aristizábal CA, Khodakhah K
in Cephalalgia : an international journal of headache 2018

152. Increased susceptibility to cortical spreading depression and epileptiform activity in a mouse model for FHM2.

Kros L, Lykke-Hartmann K, Khodakhah K
in Scientific reports 2018

153. Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1.

Rietman AB, van der Vaart T, Plasschaert E, Nicholson BA, Oostenbrink R, Krab LC, Descheemaeker MJ, Wit MY, Moll HA, Legius E, Nijs PFA
in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017

154. De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability

Küry S, van Woerden GM, Besnard T, Proietti Onori M, Latypova X, Towne MC, Cho MT, Prescott TE, Ploeg MA, Sanders S, Stessman HAF, Pujol A, Distel B, Robak LA, Bernstein JA, Denommé-Pichon AS, Lesca G, Sellars EA, Berg J, Carré W, Busk ØL, van Bon BWM, Waugh JL, Deardorff M, Hoganson GE, Bosanko KB, Johnson DS, Dabir T, Holla ØL, Sarkar A, Tveten K, de Bellescize J, Braathen GJ, Terhal PA, Grange DK, van Haeringen A, Lam C, Mirzaa G, Burton J, Bhoj EJ, Douglas J, Santani AB, Nesbitt AI, Helbig KL, Andrews MV, Begtrup A, Tang S, van Gassen KLI, Juusola J, Foss K, Enns GM, Moog U, Hinderhofer K, Paramasivam N, Lincoln S, Kusako BH, Lindenbaum P, Charpentier E, Nowak CB, Cherot E, Simonet T, Ruivenkamp CAL, Hahn S, Brownstein CA, Xia F, Schmitt S, Deb W, Bonneau D, Nizon M, Quinquis D, Chelly J, Rudolf G, Sanlaville D, Parent P, Gilbert-Dussardier B, Toutain A, Sutton VR, Thies J, Peart-Vissers LELM, Boisseau P, Vincent M, Grabrucker AM, Dubourg C; Undiagnosed Diseases Network, Tan WH, Verbeek NE, Granzow M, Santen GWE, Shendure J, Isidor B, Pasquier L, Redon R, Yang Y, State MW, Kleefstra T, Cogné B; GEM HUGO; Deciphering Developmental Disorders Study, Petrovski S, Retterer K, Eichler EE, Rosenfeld JA, Agrawal PB, Bézieau S, Odent S, Elgersma Y, Mercier S
in Am J Hum Genet 2017

155. Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability.

Reijnders MRF, Kousi M, van Woerden GM, Klein M, Bralten J, Mancini GMS, van Essen T, Proietti-Onori M, Smeets EEJ, van Gastel M, Stegmann APA, Stevens SJC, Lelieveld SH, Gilissen C, Pfundt R, Tan PL, Kleefstra T, Franke B, Elgersma Y, Katsanis N, Brunner HG
in Nature communications 2017

156. A brain proteomic investigation of rapamycin effects in the mouse model.

Wesseling H, Elgersma Y, Bahn S
in Molecular autism 2017

157. Ub3a loss increases excitability and blunts orientation tuning in the visual cortex of Angelman syndrome model mice.

Wallace ML, van Woerden GM, Elgersma Y, Smith SL, Philpot BD
in Journal of neurophysiology 2017

158. A simplified protocol for differentiation of electrophysiologically mature neuronal networks from human induced pluripotent stem cells.

Gunhanlar N, Shpak G, van der Kroeg M, Gouty-Colomer LA, Munshi ST, Lendemeijer B, Ghazvini M, Dupont C, Hoogendijk WJG, Gribnau J, de Vrij FMS, Kushner SA
in Molecular psychiatry 2017

159. The SAC1 domain in synaptojanin is required for autophagosome maturation at presynaptic terminals.

Vanhauwaert R, Kuenen S, Masius R, Bademosi A, Manetsberger J, Schoovaerts N, Bounti L, Gontcharenko S, Swerts J, Vilain S, Picillo M, Barone P, Munshi ST, de Vrij FM, Kushner SA, Gounko NV, Mandemakers W, Bonifati V, Meunier FA, Soukup SF, Verstreken P
in The EMBO journal 2017

160. A rare missense variant in RCL1 segregates with depression in extended families.

Amin N, de Vrij FMS, Baghdadi M, Brouwer RWW, van Rooij JGJ, Jovanova O, Uitterlinden AG, Hofman A, Janssen HLA, Darwish Murad S, Kraaij R, Stedehouder J, van den Hout MCGN, Kros JM, van IJcken WFJ, Tiemeier H, Kushner SA, van Duijn CM
in Molecular psychiatry 2017