Publications Directory


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Experimental


G

401. GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility

Judson, M. C., Wallace, M. L., Sidorov, M. S., Burette, A. C., Gu, B., van Woerden, G. M., King, I. F., Han, J. E., Zylka, M. J., Elgersma, Y., Weinberg, R. J. and Philpot, B. D.
in Neuron 2016

402. Gait patterns associated with thyroid function: The Rotterdam Study

Bano, A., Chaker, L., Darweesh, S. K. L., Korevaar, T. I. M., Mattace-Raso, F. U. S., Dehghan, A., Franco, O. H., Van Der Geest, J. N., Ikram, M. A.
in Scientific Reports 2016

403. Gait Patterns in a Community-Dwelling Population Aged 50 Years and Older

Verlinden, V. J. A., J. N. van der Geest, Y. Y. Hoogendam, A. Hofman, M. M. B. Breteler, and M. A. Ikram
in Gait and Posture 2012

404. Gait patterns in COPD: The Rotterdam study

Lahousse L., Verlinden V. J. A., Van Der Geest J. N., Joos G. F. , Hofman A., Stricker B. H. C., Brusselle G. G., Ikram M. A.
in European Respiratory Journal 2015

405. Gait shows a sex-specific pattern of associations with daily functioning in a community-dwelling population of older people.

Verlinden VJ, van der Geest JN, Heeringa J, Hofman A, Ikram MA
in Gait & posture 2014

406. Gating of Long-Term Potentiation by Nicotinic Acetylcholine Receptors at the Cerebellum Input Stage

Prestori, F., Bonardi, C., Mapelli, L., Lombardo, P., Goselink, R., De Stefano, M. E., Gandolfi, D., Mapelli, J., Bertrand, D., Schonewille, M., De Zeeuw, C., & D'Angelo, E.
in PLoS ONE 2013

407. Gene expression changes in cerebellum induced by dietary restriction.

Van't Sant LJ, Birkisdóttir MB, Ozinga RA, Gyenis Á, Hoeijmakers JHJ, Vermeij WP, Jaarsma D
in Frontiers in molecular neuroscience 2023

408. 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

409. Genetic dissection of the function of hindbrain axonal commissures

Renier N, Schonewille M, Giraudet F, Badura A, Tessier-Lavigne M, Avan P, De Zeeuw CI, Chédotal A
in PLoS Biol 2010

410. Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome.

Manoubi W, Mahdouani M, Hmida D, Kdissa A, Rouissi A, Turki I, Gueddiche N, Soyah N, Saad A, Bouwkamp C, Elgersma Y, Mougou-Zerelli S, Gribaa M
in World journal of clinical cases 2024

411. Genetic risk for Alzheimer disease in children: Evidence from early-life IQ and brain white-matter microstructure.

Vinueza-Veloz MF, Martín-Román C, Robalino-Valdivieso MP, White T, Kushner SA, De Zeeuw CI
in Genes, brain, and behavior 2020

412. GenNet framework: interpretable deep learning for predicting phenotypes from genetic data.

van Hilten A, Kushner SA, Kayser M, Arfan Ikram M, Adams HHH, Klaver CCW, Niessen WJ, Roshchupkin GV
in Communications biology 2021

413. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.

Mullins N, Forstner AJ, O'Connell KS, Coombes B, Coleman JRI, Qiao Z, Als TD, Bigdeli TB, Børte S, Bryois J, Charney AW, Drange OK, Gandal MJ, Hagenaars SP, Ikeda M, Kamitaki N, Kim M, Krebs K, Panagiotaropoulou G, Schilder BM, Sloofman LG, Steinberg S, Trubetskoy V, Winsvold BS, Won HH, Abramova L, Adorjan K, Agerbo E, Al Eissa M, Albani D, Alliey-Rodriguez N, Anjorin A, Antilla V, Antoniou A, Awasthi S, Baek JH, Bækvad-Hansen M, Bass N, Bauer M, Beins EC, Bergen SE, Birner A, Bøcker Pedersen C, Bøen E, Boks MP, Bosch R, Brum M, Brumpton BM, Brunkhorst-Kanaan N, Budde M, Bybjerg-Grauholm J, Byerley W, Cairns M, Casas M, Cervantes P, Clarke TK, Cruceanu C, Cuellar-Barboza A, Cunningham J, Curtis D, Czerski PM, Dale AM, Dalkner N, David FS, Degenhardt F, Djurovic S, Dobbyn AL, Douzenis A, Elvsåshagen T, Escott-Price V, Ferrier IN, Fiorentino A, Foroud TM, Forty L, Frank J, Frei O, Freimer NB, Frisén L, Gade K, Garnham J, Gelernter J, Giørtz Pedersen M, Gizer IR, Gordon SD, Gordon-Smith K, Greenwood TA, Grove J, Guzman-Parra J, Ha K, Haraldsson M, Hautzinger M, Heilbronner U, Hellgren D, Herms S, Hoffmann P, Holmans PA, Huckins L, Jamain S, Johnson JS, Kalman JL, Kamatani Y, Kennedy JL, Kittel-Schneider S, Knowles JA, Kogevinas M, Koromina M, Kranz TM, Kranzler HR, Kubo M, Kupka R, Kushner SA, Lavebratt C, Lawrence J, Leber M, Lee HJ, Lee PH, Levy SE, Lewis C, Liao C, Lucae S, Lundberg M, MacIntyre DJ, Magnusson SH, Maier W, Maihofer A, Malaspina D, Maratou E, Martinsson L, Mattheisen M, McCarroll SA, McGregor NW, McGuffin P, McKay JD, Medeiros H, Medland SE, Millischer V, Montgomery GW, Moran JL, Morris DW, Mühleisen TW, O'Brien N, O'Donovan C, Olde Loohuis LM, Oruc L, Papiol S, Pardiñas AF, Perry A, Pfennig A, Porichi E, Potash JB, Quested D, Raj T, Rapaport MH, DePaulo JR, Regeer EJ, Rice JP, Rivas F, Rivera M, Roth J, Roussos P, Ruderfer DM, Sánchez-Mora C, Schulte EC, Senner F, Sharp S, Shilling PD, Sigurdsson E, Sirignano L, Slaney C, Smeland OB, Smith DJ, Sobell JL, Søholm Hansen C, Soler Artigas M, Spijker AT, Stein DJ, Strauss JS, Świątkowska B, Terao C, Thorgeirsson TE, Toma C, Tooney P, Tsermpini EE, Vawter MP, Vedder H, Walters JTR, Witt SH, Xi S, Xu W, Yang JMK, Young AH, Young H, Zandi PP, Zhou H, Zillich L, Adolfsson R, Agartz I, Alda M, Alfredsson L, Babadjanova G, Backlund L, Baune BT, Bellivier F, Bengesser S, Berrettini WH, Blackwood DHR, Boehnke M, Børglum AD, Breen G, Carr VJ, Catts S, Corvin A, Craddock N, Dannlowski U, Dikeos D, Esko T, Etain B, Ferentinos P, Frye M, Fullerton JM, Gawlik M, Gershon ES, Goes FS, Green MJ, Grigoroiu-Serbanescu M, Hauser J, Henskens F, Hillert J, Hong KS, Hougaard DM, Hultman CM, Hveem K, Iwata N, Jablensky AV, Jones I, Jones LA, Kahn RS, Kelsoe JR, Kirov G, Landén M, Leboyer M, Lewis CM, Li QS, Lissowska J, Lochner C, Loughland C, Martin NG, Mathews CA, Mayoral F, McElroy SL, McIntosh AM, McMahon FJ, Melle I, Michie P, Milani L, Mitchell PB, Morken G, Mors O, Mortensen PB, Mowry B, Müller-Myhsok B, Myers RM, Neale BM, Nievergelt CM, Nordentoft M, Nöthen MM, O'Donovan MC, Oedegaard KJ, Olsson T, Owen MJ, Paciga SA, Pantelis C, Pato C, Pato MT, Patrinos GP, Perlis RH, Posthuma D, Ramos-Quiroga JA, Reif A, Reininghaus EZ, Ribasés M, Rietschel M, Ripke S, Rouleau GA, Saito T, Schall U, Schalling M, Schofield PR, Schulze TG, Scott LJ, Scott RJ, Serretti A, Shannon Weickert C, Smoller JW, Stefansson H, Stefansson K, Stordal E, Streit F, Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Waldman ID, Weickert TW, Werge T, Wray NR, Zwart JA, Biernacka JM, Nurnberger JI, Cichon S, Edenberg HJ, Stahl EA, McQuillin A, Di Florio A, Ophoff RA, Andreassen OA
in Nature genetics 2021

414. Gestalt Perception in Children With Visual Impairments: Item-Specific Performance and Looking Behavior

van der Zee YJ, Kooiker MJ, Talamante Ojeda M, Pel JJ
in DEVELOPMENTAL NEUROPSYCHOLOGY 2019

415. Gestalt Perception in Children With Visual Impairments: Item-Specific Performance and Looking Behavior.

van der Zee YJ, Kooiker MJG, Talamante Ojeda M, Pel JJM
in Dev Neuropsychol 2019

416. Glissades Are Altered by Lesions to the Oculomotor Vermis but Not by Saccadic Adaptation

Flierman N.A., Ignashchenkova A., Negrello M., Their P., De Zeeuw C.I., Badura A.
in Frontiers in Behavioral Neuroscience 2019

417. Golgi fragmentation precedes neuromuscular denervation and is associated with endosome abnormalities in SOD1-ALS mouse motor neurons

van Dis, V., Kuijpers, M., Haasdijk, E. D., Teuling, E., Oakes, S. A., Hoogenraad, C. C. and Jaarsma, D.
in Acta neuropathologica communications 2014

418. Graded error signals in eyeblink conditioning.

in Neurobiology of learning and memory 2019

H

419. 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

420. HCN channels are a novel therapeutic target for cognitive dysfunction in Neurofibromatosis type 1.

Omrani A, van der Vaart T, Mientjes E, van Woerden GM, Hojjati MR, Li KW, Gutmann DH, Levelt CN, Smit AB, Silva AJ, Kushner SA, Elgersma Y
in Molecular psychiatry 2015

421. Headplate and cranial window surgery for two-photon imaging of inferior colliculus in transgenic mice.

Wong, A.B. Borst, J.G.G.
in Bio-protocol 2021

422. Headplate Installation and Craniotomy for Awake In Vivo Electrophysiological Recordings or Two-Photon Imaging of the Mouse Inferior Colliculus

Kraakman, B., Solovjova, S., Borst, J. G. G. and Wong, A. B.
in Bio-protocol 2023

423. Health-related quality of life in children with neurofibromatosis type 1: contribution of demographic factors, disease-related factors, and behavior.

Krab LC, Oostenbrink R, de Goede-Bolder A, Aarsen FK, Elgersma Y, Moll HA
in The Journal of pediatrics 2008

424. Hepatitis E Virus Infects Neurons and Brains.

Zhou X, Huang F, Xu L, Lin Z, de Vrij FMS, Ayo-Martin AC, van der Kroeg M, Zhao M, Yin Y, Wang W, Cao W, Wang Y, Kushner SA, Marie Peron J, Alric L, de Man RA, Jacobs BC, van Eijk JJ, Aronica EMA, Sprengers D, Metselaar HJ, de Zeeuw CI, Dalton HR, Kamar N, Peppelenbosch MP, Pan Q
in The Journal of infectious diseases 2017

425. Heritability and genome-wide association analyses of human gait suggest contribution of common variants.

Adams H. H. H., Verlinden V. J. A., Callisaya M. L., van Duijn C. M., Hofman A., Thomson R., Uitterlinden A. G., Vernooij M. W., van der Geest J. N., Srikanth V.
in The Journals of Gerontology Series A: Biological Sciences and Medical Sciences: glv081. 2015

426. Heterogeneous encoding of temporal stimuli in the cerebellar cortex

De Zeeuw, C.*. Koppen, J.*, Bregman, G.G.B., Runge, M., & Narain, D.
in Nature Communications 2023

427. Heterogeneous expression of t-type ca2+ channels defines different neuronal populations in the inferior olive of the mouse

Bazzigaluppi, P. and De Jeu, M. T. G.
in Frontiers in Cellular Neuroscience 2016

428. Heuristic search for adaptive, defect-tolerant multiprocessor arrays.

Vasileios Vasilikos, Georgios Smaragdos, Christos Strydis, Ioannis Sourdis
in ACM Trans. Embedded Comput. Syst. 2013

429. High Bandwidth Synaptic Communication and Frequency Tracking in Human Neocortex

Testa-Silva, G., Verhoog, M. B., Linaro, D., de Kock, C. P. J., Baayen, J. C., Meredith, R. M., De Zeeuw, C. I., Giugliano, M. and Mansvelder, H. D.
in PLoS Biology 2014

430. High cortical spreading depression susceptibility and migraine‐associated symptoms in Cav2.1 S218L mice

AMJM van den Maagdenberg, T Pizzorusso, S Kaja, N Terpolilli, M Shapovalova, F E Hoebeek, C F Barrett, L Gherardini, R van de Ven, B Todorov, L Broos, A Tottene, Z Gao, M Fodor, C I De Zeeuw, R R Frants, N Plesnila, J J Plomp, D Pietrobon, M D Ferrari
in Annals of neurology 2010

431. High frequency burst firing of granule cells ensures transmission at the parallel fiber to purkinje cell synapse at the cost of temporal coding.

in Frontiers in neural circuits 2013

432. High frequency switched-mode stimulation can evoke post synaptic responses in cerebellar principal neurons

van Dongen, M. N., F. E. Hoebeek, S. K. E. Koekkoek, C. I. De Zeeuw and W. A. Serdijn
in Frontiers in Neuroengineering 2015

433. High-definition imaging of carotid artery wall dynamics.

Kruizinga P, Mastik F, van den Oord SC, Schinkel AF, Bosch JG, de Jong N, van Soest G, van der Steen AF
in Ultrasound in medicine & biology 2014

434. High-resolution micro-Doppler imaging during neurosurgical resection of an arteriovenous malformation: illustrative case

Soloukey, S., Verhoef, L., Jan van Doormaal, P., Generowicz, B. S., Dirven, C. M. F., De Zeeuw, C. I., Koekkoek, S. K. E., Kruizinga, P., Vincent, A. J. P. E., & Schouten, J. W.
in Journal Of Neurosurgery 2022

435. Hippocampal-cerebellar interaction during spatio-temporal prediction

436. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder.

Niggl E, Bouman A, Briere LC, Hoogenboezem RM, Wallaard I, Park J, Admard J, Wilke M, Harris-Mostert EDRO, Elgersma M, Bain J, Balasubramanian M, Banka S, Benke PJ, Bertrand M, Blesson AE, Clayton-Smith J, Ellingford JM, Gillentine MA, Goodloe DH, Haack TB, Jain M, Krantz I, Luu SM, McPheron M, Muss CL, Raible SE, Robin NH, Spiller M, Starling S, Sweetser DA, Thiffault I, Vetrini F, Witt D, Woods E, Zhou D, Elgersma Y, van Esbroeck ACM
in American journal of human genetics 2023

437. Homologous organization of cerebellar pathways to sensory, motor, and associative forebrain.

Pisano TJ, Dhanerawala ZM, Kislin M, Bakshinskaya D, Engel EA, Hansen EJ, Hoag AT, Lee J, de Oude NL, Venkataraju KU, Verpeut JL, Hoebeek FE, Richardson BD, Boele HJ, Wang SS
in Cell reports 2021

438. 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

439. How Do Short-Term Changes at Synapses Fine-Tune Information Processing?

Klug, A., J. G. G. Borst, B. A. Carlson, C. Kopp-Scheinpflug, V. A. Klyachko, and M. A. Xu-Friedman
in Journal of Neuroscience 2012

440. How inhibitory and excitatory inputs gate output of the inferior olive.

Loyola S, Hoogland TM, Hoedemaker H, Romano V, Negrello M, De Zeeuw CI
in eLife 2023