121. The incidence of extraction site incisional hernia after minimally invasive colorectal surgery: a systematic review and meta-analysis.
den Hartog FPJ, van Egmond S, Poelman MM, Menon AG, Kleinrensink GJ, Lange JF, Tanis PJ, Deerenberg EB
in Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland 2022
122. Addressing the inconsistent electric fields of tDCS by using patient-tailored configurations in chronic stroke: Implications for treatment.
van der Cruijsen J, Dooren RF, Schouten AC, Oostendorp TF, Frens MA, Ribbers GM, van der Helm FCT, Kwakkel G, Selles RW
in NeuroImage. Clinical 2022
123. Hallucinations and Brain Morphology Across Early Adolescence: A Longitudinal Neuroimaging Study.
Steenkamp LR, Blok E, Muetzel RL, White T, Hillegers MHJ, Blanken LME, Bolhuis K, Tiemeier H, Kushner SA
in Biological psychiatry 2022
124. Dissecting schizophrenia phenotypic variation: the contribution of genetic variation, environmental exposures, and gene-environment interactions.
125. EDEN: A High-Performance, General-Purpose, NeuroML-Based Neural Simulator.
in Frontiers in neuroinformatics 2022
126. Reply to Piochon et al.: NMDARs in Purkinje cells are not involved in parallel fiber-Purkinje cell synaptic plasticity or motor learning.
Schonewille M, Girasole AE, De Zeeuw CI, Bouvier G
in Proceedings of the National Academy of Sciences of the United States of America 2022
127. Myelination synchronizes cortical oscillations by consolidating parvalbumin-mediated phasic inhibition.
128. Long-term association of pregnancy and maternal brain structure: the Rotterdam Study.
Aleknaviciute J, Evans TE, Aribas E, de Vries MW, Steegers EAP, Ikram MA, Tiemeier H, Kavousi M, Vernooij MW, Kushner SA
in European journal of epidemiology 2022
129. Improving the Security of the IEEE 802.15.6 Standard for Medical BANs.
Muhammad Ali Siddiqi, Georg Hahn, Said Hamdioui, Wouter A. Serdijn, Christos Strydis
in IEEE Access 2022
130. Time and tide of cerebellar synchrony.
in Proceedings of the National Academy of Sciences of the United States of America 2022
131. Correction to: Deconvolution of the Functional Ultrasound Response in the Mouse Visual Pathway Using Block-Term Decomposition.
in Neuroinformatics 2022
132. A Systematic Review of Direct Outputs from the Cerebellum to the Brainstem and Diencephalon in Mammals.
in Cerebellum (London, England) 2022
133. Postsynaptic plasticity of Purkinje cells in mice is determined by molecular identity.
in Communications biology 2022
134. Tsc1 Haploinsufficiency Leads to Pax2 Dysregulation in the Developing Murine Cerebellum
Ines Serra, Ana Stravs, Catarina Osório, Maria Roa Oyaga, Martijn Schonewille, Christian Tudorache, and Aleksandra Badura
in Front Mol Neurosci. 2022
135. Applicability of devices available for the measurement of intracompartmental pressures: a cadaver study.
Vogels S, Ritchie ED, de Vries D, Kleinrensink GJ, Verhofstad MHJ, Hoencamp R
in Journal of experimental orthopaedics 2022
136. Adult gene reinstatement restores the learning and plasticity deficits of knockout mice.
Rigter PMF, Wallaard I, Aghadavoud Jolfaei M, Kingma J, Post L, Elgersma M, Elgersma Y, van Woerden GM
in iScience 2022
137. The Hippocampal Response to Acute Corticosterone Elevation Is Altered in a Mouse Model for Angelman Syndrome.
in International journal of molecular sciences 2022
138. Multidimensional analysis of behavior predicts genotype with high accuracy in a mouse model of Angelman syndrome.
Tanas JK, Kerr DD, Wang L, Rai A, Wallaard I, Elgersma Y, Sidorov MS
in Translational psychiatry 2022
139. Measuring Cerebellar Processing and Sensorimotor Functions in Non-Human Primates
140. Genetic barcoding systematically comparing genes in del(5q) MDS reveals a central role for CSNK1A1 in clonal expansion.
Stalmann USA, Ticconi F, Snoeren IAM, Li R, Gleitz H, Cowley G, McConkey ME, Wong AB, Schmitz S, Fuchs SNR, Sood S, Leimkühler NB, Martinez-Høyer S, Banjanin B, Root DE, Brümmendorf TH, Pearce J, Schuppert A, Bindels E, Essers M, Heckl D, Stiehl TP, Costa IG, Ebert BL, Schneider RK
in Blood advances 2022
141. Focused ultrasound neuromodulation on a multiwell MEA.
142. A custom interconnection multi-FPGA framework for distributed processing applications.
Carlos Salazar-García, Alfonso Chacón-Rodríguez, Renato Rimolo-Donadio, Ronny García-Ramírez, David Solórzano-Pacheco, Jeferson González-Gómez, Christos Strydis
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143. A cross-species spatiotemporal proteomic analysis identifies UBE3A-dependent signaling pathways and targets.
Pandya NJ, Meier S, Tyanova S, Terrigno M, Wang C, Punt AM, Mientjes EJ, Vautheny A, Distel B, Kremer T, Elgersma Y, Jagasia R
in Molecular psychiatry 2022
144. Detection of visual field defects using Eye Movement Pediatric Perimetry in children with intracranial lesions: feasibility and applicability.
Meethal NSK, Robben J, Mazumdar D, Loudon S, Naus N, Polling JR, van der Steen J, George R, Pel JJM
in Heliyon 2022
146. High-resolution micro-Doppler imaging during neurosurgical resection of an arteriovenous malformation: illustrative case
147. Automated causal inference in application to randomized controlled clinical trials.
Jiqing Wu, Nanda Horeweg, Marco de Bruyn, Remi A. Nout, Ina M. Jürgenliemk-Schulz, Ludy C. H. W. Lutgens, Jan J. Jobsen, Elzbieta M. van der Steen-Banasik, Hans W. Nijman, Vincent T. H. B. M. Smit, Tjalling Bosse, Carien L. Creutzberg, Viktor H. Koelzer
in Nat. Mach. Intell. 2022
148. Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.
Kaiser FMP, Gruenbacher S, Oyaga MR, Nio E, Jaritz M, Sun Q, van der Zwaag W, Kreidl E, Zopf LM, Dalm VASH, Pel J, Gaiser C, van der Vliet R, Wahl L, Rietman A, Hill L, Leca I, Driessen G, Laffeber C, Brooks A, Katsikis PD, Lebbink JHG, Tachibana K, van der Burg M, De Zeeuw CI, Badura A, Busslinger M
in The Journal of experimental medicine 2022
149. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
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in Nature genetics 2021
150. Schizophrenia polygenic risk is associated with child mental health problems through early childhood adversity: evidence for a gene-environment correlation.
Bolhuis K, Steenkamp LR, Blanken LME, Neumann A, Jansen PR, Hillegers MHJ, Cecil CAM, Tiemeier H, Kushner SA
in European child & adolescent psychiatry 2021
151. miR-142-3p Regulates Cortical Oligodendrocyte Gene Co-expression Networks Associated with Tauopathy.
Hinman JD, Ngo KJ, Kim D, Chen C, Abraham CR, Ghanbari M, Ikram MA, Kushner SA, Kawaguchi R, Coppola G, Goth K, Bellusci S, Hernandez I, Kosik KS, Fogel BL
in Human molecular genetics 2021
152. Monogenic Causes of Apparently Idiopathic Perinatal Intracranial Hemorrhage.
Hausman-Kedem M, Malinger G, Modai S, Kushner SA, Shiran SI, Ben-Sira L, Roth J, Constantini S, Fattal-Valevski A, Ben-Shachar S
in Annals of neurology 2021
153. Peer-reported bullying, rejection and hallucinatory experiences in childhood.
Steenkamp LR, Tiemeier H, Bolhuis K, Hillegers MHJ, Kushner SA, Blanken LME
in Acta psychiatrica Scandinavica 2021
154. Unlike dietary restriction, rapamycin fails to extend lifespan and reduce transcription stress in progeroid DNA repair-deficient mice.
Birkisdóttir MB, Jaarsma D, Brandt RMC, Barnhoorn S, van Vliet N, Imholz S, van Oostrom CT, Nagarajah B, Portilla Fernández E, Roks AJM, Elgersma Y, van Steeg H, Ferreira JA, Pennings JLA, Hoeijmakers JHJ, Vermeij WP, Dollé MET
in Aging cell 2021
155. The use of eye-movement recording in patients with anti-Hu antibody-associated paraneoplastic neurological syndromes to objectively determine extent and course of disease.
in European journal of neurology 2021
156. To Explore the Predictive Power of Visuomotor Network Dysfunctions in Mild Cognitive Impairment and Alzheimer's Disease.
157. Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutations.
in Human molecular genetics 2021
158. TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development.
van Woerden GM, Bos M, de Konink C, Distel B, Trezza RA, Shur NE, Barañano K, Mahida S, Chassevent A, Schreiber A, Erwin AL, Gripp KW, Rehman F, Brulleman S, Mc Cormack R, de Geus G, Kalsner L, Sorlin A, Bruel AL, Koolen DA, Gabriel MK, Rossi M, Fitzpatrick DR, Wilkie AOM, Calpena E, Johnson D, Brooks A, van Slegtenhorst M, Fleischer J, Groepper D, Lindstrom K, Micheil Innes A, Goodwin A, Humberson J, Noyes A, Langley KG, Telegrafi A, Blevins A, Hoffman J, Guillen Sacoto MJ, Juusola J, Monaghan KG, Punj S, Simon M, Pfundt R, Elgersma Y, Kleefstra T
in Human mutation 2021
159. UBE3A reinstatement as a disease-modifying therapy for Angelman syndrome.
160. Mono-ubiquitination of Rabphilin 3A by UBE3A serves a non-degradative function.
Avagliano Trezza R, Punt AM, Mientjes E, van den Berg M, Zampeta FI, de Graaf IJ, van der Weegen Y, Demmers JAA, Elgersma Y, Distel B
in Scientific reports 2021
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