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441. Gait Patterns in a Community-Dwelling Population Aged 50 Years and Older
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442. 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.
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443. Gait shows a sex-specific pattern of associations with daily functioning in a community-dwelling population of older people.
444. 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
445. 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
446. 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
447. Genetic dissection of the function of hindbrain axonal commissures
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448. 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
449. 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
450. 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
451. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
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452. Genomics yields biological and phenotypic insights into bipolar disorder.
O'Connell KS, Koromina M, van der Veen T, Boltz T, David FS, Yang JMK, Lin KH, Wang X, Coleman JRI, Mitchell BL, McGrouther CC, Rangan AV, Lind PA, Koch E, Harder A, Parker N, Bendl J, Adorjan K, Agerbo E, Albani D, Alemany S, Alliey-Rodriguez N, Als TD, Andlauer TFM, Antoniou A, Ask H, Bass N, Bauer M, Beins EC, Bigdeli TB, Pedersen CB, Boks MP, Børte S, Bosch R, Brum M, Brumpton BM, Brunkhorst-Kanaan N, Budde M, Bybjerg-Grauholm J, Byerley W, Cabana-Domínguez J, Cairns MJ, Carpiniello B, Casas M, Cervantes P, Chatzinakos C, Chen HC, Clarence T, Clarke TK, Claus I, Coombes B, Corfield EC, Cruceanu C, Cuellar-Barboza A, Czerski PM, Dafnas K, Dale AM, Dalkner N, Degenhardt F, DePaulo JR, Djurovic S, Drange OK, Escott-Price V, Fanous AH, Fellendorf FT, Ferrier IN, Forty L, Frank J, Frei O, Freimer NB, Fullard JF, Garnham J, Gizer IR, Gordon SD, Gordon-Smith K, Greenwood TA, Grove J, Guzman-Parra J, Ha TH, Hahn T, Haraldsson M, Hautzinger M, Havdahl A, Heilbronner U, Hellgren D, Herms S, Hickie IB, Hoffmann P, Holmans PA, Huang MC, Ikeda M, Jamain S, Johnson JS, Jonsson L, Kalman JL, Kamatani Y, Kennedy JL, Kim E, Kim J, Kittel-Schneider S, Knowles JA, Kogevinas M, Kranz TM, Krebs K, Kushner SA, Lavebratt C, Lawrence J, Leber M, Lee HJ, Liao C, Lucae S, Lundberg M, MacIntyre DJ, Maier W, Maihofer AX, Malaspina D, Manchia M, Maratou E, Martinsson L, Mattheisen M, McGregor NW, McInnis MG, McKay JD, Medeiros H, Meyer-Lindenberg A, Millischer V, Morris DW, Moutsatsou P, Mühleisen TW, O'Donovan C, Olsen CM, Panagiotaropoulou G, Papiol S, Pardiñas AF, Park HY, Perry A, Pfennig A, Pisanu C, Potash JB, Quested D, Rapaport MH, Regeer EJ, Rice JP, Rivera M, Schulte EC, Senner F, Shadrin A, Shilling PD, Sigurdsson E, Sindermann L, Sirignano L, Siskind D, Slaney C, Sloofman LG, Smeland OB, Smith DJ, Sobell JL, Soler Artigas M, Stein DJ, Stein F, Su MH, Sung H, Świątkowska B, Terao C, Tesfaye M, Tesli M, Thorgeirsson TE, Thorp JG, Toma C, Tondo L, Tooney PA, Tsai SJ, Tsermpini EE, Vawter MP, Vedder H, Vreeker A, Walters JTR, Winsvold BS, Witt SH, Won HH, Ye R, Young AH, Zandi PP, Zillich L, Adolfsson R, Alda M, Alfredsson L, Backlund L, Baune BT, Bellivier F, Bengesser S, Berrettini WH, Biernacka JM, Boehnke M, Børglum AD, Breen G, Carr VJ, Catts S, Cichon S, Corvin A, Craddock N, Dannlowski U, Dikeos D, Etain B, Ferentinos P, Frye M, Fullerton JM, Gawlik M, Gershon ES, Goes FS, Green MJ, Grigoroiu-Serbanescu M, Hauser J, Henskens FA, Hjerling-Leffler J, Hougaard DM, Hveem K, Iwata N, Jones I, Jones LA, Kahn RS, Kelsoe JR, Kircher T, Kirov G, Kuo PH, Landén M, Leboyer M, Li QS, Lissowska J, Lochner C, Loughland C, Luykx JJ, Martin NG, Mathews CA, Mayoral F, McElroy SL, McIntosh AM, McMahon FJ, Medland SE, Melle I, Milani L, Mitchell PB, Morken G, Mors O, Mortensen PB, Müller-Myhsok B, Myers RM, Myung W, Neale BM, Nievergelt CM, Nordentoft M, Nöthen MM, Nurnberger JI, O'Donovan MC, Oedegaard KJ, Olsson T, Owen MJ, Paciga SA, Pantelis C, Pato CN, Pato MT, Patrinos GP, Pawlak JM, Ramos-Quiroga JA, Reif A, Reininghaus EZ, Ribasés M, Rietschel M, Ripke S, Rouleau GA, Roussos P, Saito T, Schall U, Schalling M, Schofield PR, Schulze TG, Scott LJ, Scott RJ, Serretti A, Smoller JW, Squassina A, Stahl EA, Stefansson H, Stefansson K, Stordal E, Streit F, Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Waldman ID, Weickert CS, Weickert TW, Werge T, Whiteman DC, Zwart JA, Edenberg HJ, McQuillin A, Forstner AJ, Mullins N, Di Florio A, Ophoff RA, Andreassen OA
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453. Gestalt Perception in Children With Visual Impairments: Item-Specific Performance and Looking Behavior
454. Gestalt Perception in Children With Visual Impairments: Item-Specific Performance and Looking Behavior.
455. Gestalt, Navon and Kanizsa illusion processing in CVI, ADHD, and dyslexia Children with Normal verbal IQ.
in Frontiers in human neuroscience 2024
456. Glissades Are Altered by Lesions to the Oculomotor Vermis but Not by Saccadic Adaptation
in Frontiers in Behavioral Neuroscience 2019
458. Graded error signals in eyeblink conditioning.
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459. 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
460. 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
461. Headplate and cranial window surgery for two-photon imaging of inferior colliculus in transgenic mice.
462. Headplate Installation and Craniotomy for Awake In Vivo Electrophysiological Recordings or Two-Photon Imaging of the Mouse Inferior Colliculus
in Bio-protocol 2023
463. 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
464. 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
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465. 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
466. Heterogeneous encoding of temporal stimuli in the cerebellar cortex
in Nature Communications 2023
467. Heterogeneous expression of t-type ca2+ channels defines different neuronal populations in the inferior olive of the mouse
468. Heterogeneous spatial tuning in the auditory pathway of the Mongolian Gerbil (Meriones unguiculatus).
469. Heuristic search for adaptive, defect-tolerant multiprocessor arrays.
Vasileios Vasilikos, Georgios Smaragdos, Christos Strydis, Ioannis Sourdis
in ACM Trans. Embedded Comput. Syst. 2013
471. 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
472. 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
473. High frequency switched-mode stimulation can evoke post synaptic responses in cerebellar principal neurons
in Frontiers in Neuroengineering 2015
474. 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
475. High-resolution micro-Doppler imaging during neurosurgical resection of an arteriovenous malformation: illustrative case
476. Hippocampal-cerebellar interaction during spatio-temporal prediction
in Cerebral Cortex 2013
477. 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
478. Homeostatic bidirectional plasticity in upbound and downbound micromodules in a model of the olivocerebellar loop.
in PLoS computational biology 2025
479. 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
480. 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
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