| Year |
Citation |
Score |
| 2024 |
Küry S, Stanton JE, van Woerden G, Hsieh TC, Rosenfelt C, Scott-Boyer MP, Most V, Wang T, Papendorf JJ, de Konink C, Deb W, Vignard V, Studencka-Turski M, Besnard T, Hajdukowicz AM, et al. Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene in neurodevelopmental proteasomopathies. Medrxiv : the Preprint Server For Health Sciences. PMID 38293138 DOI: 10.1101/2024.01.13.24301174 |
0.635 |
|
| 2023 |
Ebstein F, Küry S, Most V, Rosenfelt C, Scott-Boyer MP, van Woerden GM, Besnard T, Papendorf JJ, Studencka-Turski M, Wang T, Hsieh TC, Golnik R, Baldridge D, Forster C, de Konink C, et al. PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production. Science Translational Medicine. 15: eabo3189. PMID 37256937 DOI: 10.1126/scitranslmed.abo3189 |
0.572 |
|
| 2022 |
Rigter PMF, Wallaard I, Aghadavoud Jolfaei M, Kingma J, Post L, Elgersma M, Elgersma Y, van Woerden GM. Adult gene reinstatement restores the learning and plasticity deficits of knockout mice. Iscience. 25: 105303. PMID 36304100 DOI: 10.1016/j.isci.2022.105303 |
0.656 |
|
| 2022 |
van Woerden GM, Senden R, de Konink C, Trezza RA, Baban A, Bassetti JA, van Bever Y, Bird LM, van Bon BW, Brooks AS, Guan Q, Klee EW, Marcelis C, Rosado JM, Schimmenti LA, et al. The MAP3K7 gene: further delineation of clinical characteristics and genotype/phenotype correlations. Human Mutation. PMID 35730652 DOI: 10.1002/humu.24425 |
0.57 |
|
| 2021 |
Proietti Onori M, Koene LMC, Schäfer CB, Nellist M, de Brito van Velze M, Gao Z, Elgersma Y, van Woerden GM. RHEB/mTOR hyperactivity causes cortical malformations and epileptic seizures through increased axonal connectivity. Plos Biology. 19: e3001279. PMID 34038402 DOI: 10.1371/journal.pbio.3001279 |
0.764 |
|
| 2021 |
Proietti Onori M, van Woerden GM. Role of calcium/calmodulin-dependent kinase 2 in neurodevelopmental disorders. Brain Research Bulletin. 171: 209-220. PMID 33774142 DOI: 10.1016/j.brainresbull.2021.03.014 |
0.771 |
|
| 2021 |
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, et al. TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development. Human Mutation. PMID 33565190 DOI: 10.1002/humu.24176 |
0.638 |
|
| 2020 |
Sonzogni M, Zhai P, Mientjes EJ, van Woerden GM, Elgersma Y. Assessing the requirements of prenatal UBE3A expression for rescue of behavioral phenotypes in a mouse model for Angelman syndrome. Molecular Autism. 11: 70. PMID 32948244 DOI: 10.1186/s13229-020-00376-9 |
0.593 |
|
| 2019 |
Tonazzini I, Van Woerden GM, Masciullo C, Mientjes EJ, Elgersma Y, Cecchini M. The role of ubiquitin ligase E3A in polarized contact guidance and rescue strategies in UBE3A-deficient hippocampal neurons. Molecular Autism. 10: 41. PMID 31798818 DOI: 10.1186/s13229-019-0293-1 |
0.616 |
|
| 2019 |
Heimer G, van Woerden GM, Barel O, Marek-Yagel D, Kol N, Munting BJ, Borghei M, Atawneh OM, Nissenkorn A, Rechavi G, Anikster Y, Elgersma Y, Kushner SA, Ben Zeev B. Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia. Human Mutation. PMID 31692205 DOI: 10.1002/Humu.23945 |
0.601 |
|
| 2019 |
Avagliano Trezza R, Sonzogni M, Bossuyt SNV, Zampeta FI, Punt AM, van den Berg M, Rotaru DC, Koene LMC, Munshi ST, Stedehouder J, Kros JM, Williams M, Heussler H, de Vrij FMS, Mientjes EJ, ... van Woerden GM, et al. Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome. Nature Neuroscience. PMID 31235931 DOI: 10.1038/S41593-019-0425-0 |
0.62 |
|
| 2019 |
Sonzogni M, Hakonen J, Bernabé Kleijn M, Silva-Santos S, Judson MC, Philpot BD, van Woerden GM, Elgersma Y. Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes. Molecular Autism. 10: 23. PMID 31143434 DOI: 10.1186/S13229-019-0277-1 |
0.6 |
|
| 2019 |
Kool MJ, Onori MP, Borgesius NZ, van de Bree JE, Elgersma-Hooisma M, Nio E, Bezstarosti K, Buitendijk GHS, Aghadavoud Jolfaei M, Demmers JAA, Elgersma Y, van Woerden GM. CAMK2-dependent signaling in neurons is essential for survival. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 31064859 DOI: 10.1523/JNEUROSCI.1341-18.2019 |
0.653 |
|
| 2018 |
Sonzogni M, Wallaard I, Santos SS, Kingma J, du Mee D, van Woerden GM, Elgersma Y. A behavioral test battery for mouse models of Angelman syndrome: a powerful tool for testing drugs and novel mutants. Molecular Autism. 9: 47. PMID 30220990 DOI: 10.1186/s13229-018-0231-7 |
0.561 |
|
| 2018 |
Onori MP, Koopal B, Everman DB, Worthington JD, Jones JR, Ploeg MA, Mientjes E, van Bon BW, Kleefstra T, Schulman H, Kushner SA, Küry S, Elgersma Y, van Woerden GM. The intellectual disability-associated CAMK2G p.Arg292Pro mutation acts as a pathogenic gain-of-function. Human Mutation. PMID 30184290 DOI: 10.1002/Humu.23647 |
0.582 |
|
| 2018 |
Rotaru DC, van Woerden GM, Wallaard I, Elgersma Y. Adult gene reinstatement restores the electrophysiological deficits of prefrontal cortex layer 5 neurons in a mouse model of Angelman syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 30082419 DOI: 10.1523/JNEUROSCI.0083-18.2018 |
0.646 |
|
| 2017 |
Wang T, van Woerden GM, Elgersma Y, Borst JGG. Enhanced Transmission at the Calyx of Held Synapse in a Mouse Model for Angelman Syndrome. Frontiers in Cellular Neuroscience. 11: 418. PMID 29354033 DOI: 10.3389/fncel.2017.00418 |
0.637 |
|
| 2017 |
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, et al. De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. American Journal of Human Genetics. 101: 768-788. PMID 29100089 DOI: 10.1016/J.Ajhg.2017.10.003 |
0.793 |
|
| 2017 |
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, et al. Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability. Nature Communications. 8: 1052. PMID 29051493 DOI: 10.1038/S41467-017-00933-6 |
0.571 |
|
| 2017 |
Wallace ML, van Woerden GM, Elgersma Y, Smith SL, Philpot BD. UBE3A loss increases excitability and blunts orientation tuning in the visual cortex of Angelman syndrome model mice. Journal of Neurophysiology. jn.00618.2016. PMID 28468997 DOI: 10.1152/Jn.00618.2016 |
0.605 |
|
| 2016 |
Kool MJ, van de Bree JE, Bodde HE, Elgersma Y, van Woerden GM. The molecular, temporal and region-specific requirements of the beta isoform of Calcium/Calmodulin-dependent protein kinase type 2 (CAMK2B) in mouse locomotion. Scientific Reports. 6: 26989. PMID 27244486 DOI: 10.1038/srep26989 |
0.607 |
|
| 2016 |
Judson MC, Wallace ML, Sidorov MS, Burette AC, Gu B, van Woerden GM, King IF, Han JE, Zylka MJ, Elgersma Y, Weinberg RJ, Philpot BD. GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility. Neuron. PMID 27021170 DOI: 10.1016/j.neuron.2016.02.040 |
0.606 |
|
| 2016 |
Tonazzini I, Meucci S, Van Woerden GM, Elgersma Y, Cecchini M. Impaired Neurite Contact Guidance in Ubiquitin Ligase E3a (Ube3a)-Deficient Hippocampal Neurons on Nanostructured Substrates. Advanced Healthcare Materials. PMID 26845073 DOI: 10.1002/adhm.201500815 |
0.608 |
|
| 2015 |
Omrani A, van Woerden GM, Elgersma Y. Neurofibromin regulates HCN activity in Parvalbumin-positive interneurons. Molecular Psychiatry. 20: 1263. PMID 26487477 DOI: 10.1038/mp.2015.154 |
0.636 |
|
| 2015 |
Bruinsma CF, Schonewille M, Gao Z, Aronica EM, Judson MC, Philpot BD, Hoebeek FE, van Woerden GM, De Zeeuw CI, Elgersma Y. Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model. The Journal of Clinical Investigation. 125: 4305-15. PMID 26485287 DOI: 10.1172/Jci83541 |
0.785 |
|
| 2015 |
Bruinsma CF, Savelberg SM, Kool MJ, Jolfaei MA, van Woerden GM, Baarends WM, Elgersma Y. An essential role for UBE2A/HR6A in learning and memory and mGLUR-dependent long-term depression. Human Molecular Genetics. PMID 26476408 DOI: 10.1093/Hmg/Ddv436 |
0.788 |
|
| 2015 |
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. HCN channels are a novel therapeutic target for cognitive dysfunction in Neurofibromatosis type 1. Molecular Psychiatry. PMID 25917366 DOI: 10.1038/Mp.2015.48 |
0.761 |
|
| 2015 |
Silva-Santos S, van Woerden GM, Bruinsma CF, Mientjes E, Jolfaei MA, Distel B, Kushner SA, Elgersma Y. Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model. The Journal of Clinical Investigation. 125: 2069-76. PMID 25866966 DOI: 10.1172/Jci80554 |
0.785 |
|
| 2015 |
Goorden SM, Abs E, Bruinsma CF, Riemslagh FW, van Woerden GM, Elgersma Y. Intact neuronal function in Rheb1 mutant mice: implications for TORC1-based treatments. Human Molecular Genetics. 24: 3390-8. PMID 25759467 DOI: 10.1093/Hmg/Ddv087 |
0.779 |
|
| 2014 |
Achterberg KG, Buitendijk GH, Kool MJ, Goorden SM, Post L, Slump DE, Silva AJ, van Woerden GM, Kushner SA, Elgersma Y. Temporal and region-specific requirements of αCaMKII in spatial and contextual learning. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 11180-7. PMID 25143599 DOI: 10.1523/Jneurosci.0640-14.2014 |
0.781 |
|
| 2014 |
Gao Z, van Woerden GM, Elgersma Y, De Zeeuw CI, Hoebeek FE. Distinct roles of α- and βCaMKII in controlling long-term potentiation of GABAA-receptor mediated transmission in murine Purkinje cells. Frontiers in Cellular Neuroscience. 8: 16. PMID 24550776 DOI: 10.3389/fncel.2014.00016 |
0.611 |
|
| 2011 |
Borgesius NZ, van Woerden GM, Buitendijk GH, Keijzer N, Jaarsma D, Hoogenraad CC, Elgersma Y. βCaMKII plays a nonenzymatic role in hippocampal synaptic plasticity and learning by targeting αCaMKII to synapses. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 10141-8. PMID 21752990 DOI: 10.1523/JNEUROSCI.5105-10.2011 |
0.62 |
|
| 2011 |
van der Vaart T, van Woerden GM, Elgersma Y, de Zeeuw CI, Schonewille M. Motor deficits in neurofibromatosis type 1 mice: the role of the cerebellum. Genes, Brain, and Behavior. 10: 404-9. PMID 21352477 DOI: 10.1111/J.1601-183X.2011.00685.X |
0.763 |
|
| 2011 |
Goorden SM, Hoogeveen-Westerveld M, Cheng C, van Woerden GM, Mozaffari M, Post L, Duckers HJ, Nellist M, Elgersma Y. Rheb is essential for murine development. Molecular and Cellular Biology. 31: 1672-8. PMID 21321084 DOI: 10.1128/MCB.00985-10 |
0.743 |
|
| 2009 |
van Woerden GM, Hoebeek FE, Gao Z, Nagaraja RY, Hoogenraad CC, Kushner SA, Hansel C, De Zeeuw CI, Elgersma Y. betaCaMKII controls the direction of plasticity at parallel fiber-Purkinje cell synapses. Nature Neuroscience. 12: 823-5. PMID 19503086 DOI: 10.1038/Nn.2329 |
0.571 |
|
| 2008 |
Denayer E, Ahmed T, Brems H, Van Woerden G, Borgesius NZ, Callaerts-Vegh Z, Yoshimura A, Hartmann D, Elgersma Y, D'Hooge R, Legius E, Balschun D. Spred1 is required for synaptic plasticity and hippocampus-dependent learning. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 14443-9. PMID 19118178 DOI: 10.1523/Jneurosci.4698-08.2008 |
0.659 |
|
| 2008 |
Olijslagers JE, de Kloet ER, Elgersma Y, van Woerden GM, Joëls M, Karst H. Rapid changes in hippocampal CA1 pyramidal cell function via pre- as well as postsynaptic membrane mineralocorticoid receptors. The European Journal of Neuroscience. 27: 2542-50. PMID 18547242 DOI: 10.1111/j.1460-9568.2008.06220.x |
0.558 |
|
| 2007 |
Goorden SM, van Woerden GM, van der Weerd L, Cheadle JP, Elgersma Y. Cognitive deficits in Tsc1+/- mice in the absence of cerebral lesions and seizures. Annals of Neurology. 62: 648-55. PMID 18067135 DOI: 10.1002/ana.21317 |
0.762 |
|
| 2007 |
Hojjati MR, van Woerden GM, Tyler WJ, Giese KP, Silva AJ, Pozzo-Miller L, Elgersma Y. Kinase activity is not required for alphaCaMKII-dependent presynaptic plasticity at CA3-CA1 synapses. Nature Neuroscience. 10: 1125-7. PMID 17660813 DOI: 10.1038/Nn1946 |
0.718 |
|
| 2007 |
van Woerden GM, Harris KD, Hojjati MR, Gustin RM, Qiu S, de Avila Freire R, Jiang YH, Elgersma Y, Weeber EJ. Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation. Nature Neuroscience. 10: 280-2. PMID 17259980 DOI: 10.1038/Nn1845 |
0.734 |
|
| 2005 |
Kushner SA, Elgersma Y, Murphy GG, Jaarsma D, van Woerden GM, Hojjati MR, Cui Y, LeBoutillier JC, Marrone DF, Choi ES, De Zeeuw CI, Petit TL, Pozzo-Miller L, Silva AJ. Modulation of presynaptic plasticity and learning by the H-ras/extracellular signal-regulated kinase/synapsin I signaling pathway. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 9721-34. PMID 16237176 DOI: 10.1523/Jneurosci.2836-05.2005 |
0.76 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2024 |
Rigter PMF, de Konink C, Dunn MJ, Proietti Onori M, Humberson JB, Thomas M, Barnes C, Prada CE, Weaver KN, Ryan TD, Caluseriu O, Conway J, Calamaro E, Fong CT, Wuyts W, ... ... van Woerden GM, et al. Role of CAMK2D in neurodevelopment and associated conditions. American Journal of Human Genetics. PMID 38272033 DOI: 10.1016/j.ajhg.2023.12.016 |
0.299 |
|
| 2014 |
Lourenço J, Pacioni S, Rebola N, van Woerden GM, Marinelli S, DiGregorio D, Bacci A. Non-associative potentiation of perisomatic inhibition alters the temporal coding of neocortical layer 5 pyramidal neurons. Plos Biology. 12: e1001903. PMID 25003184 DOI: 10.1371/Journal.Pbio.1001903 |
0.296 |
|
| 2020 |
Moro A, van Woerden GM, Toonen RF, Verhage M. CaMKII controls neuromodulation via neuropeptide gene expression and axonal targeting of neuropeptide vesicles. Plos Biology. 18: e3000826. PMID 32776935 DOI: 10.1371/Journal.Pbio.3000826 |
0.279 |
|
| 2023 |
Rigter PMF, de Konink C, van Woerden GM. Loss of CAMK2G affects intrinsic and motor behavior but has minimal impact on cognitive behavior. Frontiers in Neuroscience. 16: 1086994. PMID 36685241 DOI: 10.3389/fnins.2022.1086994 |
0.275 |
|
| 2022 |
Dwyer BK, Veenma DCM, Chang K, Schulman H, Van Woerden GM. Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a Mutation in the Gene (c.328G>A p.Glu110Lys). Frontiers in Pharmacology. 13: 794008. PMID 35620293 DOI: 10.3389/fphar.2022.794008 |
0.258 |
|
| 2019 |
Vargas JY, Loria F, Wu YJ, Córdova G, Nonaka T, Bellow S, Syan S, Hasegawa M, van Woerden GM, Trollet C, Zurzolo C. The Wnt/Ca pathway is involved in interneuronal communication mediated by tunneling nanotubes. The Embo Journal. e101230. PMID 31625188 DOI: 10.15252/Embj.2018101230 |
0.206 |
|
| 2021 |
Pellikaan K, van Woerden GM, Kleinendorst L, Rosenberg AGW, Horsthemke B, Grosser C, van Zutven LJCM, van Rossum EFC, van der Lely AJ, Resnick JL, Brüggenwirth HT, van Haelst MM, de Graaff LCG. The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous Variant; Bio-Molecular Analysis and Review of the Literature. Genes. 12. PMID 34200226 DOI: 10.3390/genes12060875 |
0.206 |
|
| 2022 |
Palmelund LB, van Woerden GM, Bräuner-Osborne H, Wellendorph P. Development of a medium throughput whole-cell microtiter plate Thr286 autophosphorylation assay for CaMKIIα using ELISA. Journal of Pharmacological and Toxicological Methods. 107226. PMID 36174932 DOI: 10.1016/j.vascn.2022.107226 |
0.196 |
|
| 2021 |
Leurs U, Klein AB, McSpadden ED, Griem-Krey N, Solbak SMØ, Houlton J, Villumsen IS, Vogensen SB, Hamborg L, Gauger SJ, Palmelund LB, Larsen ASG, Shehata MA, Kelstrup CD, Olsen JV, ... ... van Woerden GM, et al. GHB analogs confer neuroprotection through specific interaction with the CaMKIIα hub domain. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34330837 DOI: 10.1073/pnas.2108079118 |
0.194 |
|
| 2022 |
Saccher M, Kawasaki S, Onori MP, van Woerden GM, Giagka V, Dekker R. Focused ultrasound neuromodulation on a multiwell MEA. Bioelectronic Medicine. 8: 2. PMID 35081966 DOI: 10.1186/s42234-021-00083-7 |
0.182 |
|
| 2019 |
Tetenborg S, Yadav SC, Brüggen B, Zoidl GR, Hormuzdi SG, Monyer H, van Woerden GM, Janssen-Bienhold U, Dedek K. Localization of Retinal Ca/Calmodulin-Dependent Kinase II-β (CaMKII-β) at Bipolar Cell Gap Junctions and Cross-Reactivity of a Monoclonal Anti-CaMKII-β Antibody With Connexin36. Frontiers in Molecular Neuroscience. 12: 206. PMID 31555090 DOI: 10.3389/Fnmol.2019.00206 |
0.176 |
|
| 1990 |
Abbenhuis MA, Raaijmakers WG, Raaijmakers JG, van Woerden GJ. Episodic memory in dementia of the Alzheimer type and in normal ageing: similar impairment in automatic processing. The Quarterly Journal of Experimental Psychology. a, Human Experimental Psychology. 42: 569-83. PMID 2236633 DOI: 10.1080/14640749008401237 |
0.105 |
|
| 2019 |
van Woerden GM. Measuring Electroencephalography: The Ups and Downs of Delta and Beta Bands as Biomarkers for 15q11-q13-Related Disorders. Biological Psychiatry. 85: e45-e46. PMID 30999987 DOI: 10.1016/j.biopsych.2019.03.002 |
0.06 |
|
| 2016 |
Van Woerden G, Van Den Brand CL, Den Hartog CF, Idenburg FJ, Grootendorst DC, Van Der Linden MC. Increased analgesia administration in emergency medicine after implementation of revised guidelines International Journal of Emergency Medicine. 9: 1-7. DOI: 10.1186/s12245-016-0102-y |
0.026 |
|
| 2016 |
Van Woerden G, Van Den Brand CL, Den Hartog CF, Idenburg FJ, Grootendorst DC, Van Der Linden MC. Increased analgesia administration in emergency medicine after implementation of revised guidelines. International Journal of Emergency Medicine. 9: 4. PMID 26860533 DOI: 10.1186/s12245-016-0102-y |
0.025 |
|
| 2020 |
van Veldhuisen SL, van Woerden G, Hemels MEW, America YGCJ, de Boer RA, Rienstra M, van Veldhuisen DJ, Hazebroek EJ. Preoperative cardiac screening using NT-proBNP in obese patients 50 years and older undergoing bariatric surgery: a study of 310 consecutive patients. Surgery For Obesity and Related Diseases : Official Journal of the American Society For Bariatric Surgery. PMID 33036941 DOI: 10.1016/j.soard.2020.08.036 |
0.024 |
|
| 2020 |
Gorter TM, van Woerden G, Rienstra M, Dickinson MG, Hummel YM, Voors AA, Hoendermis ES, van Veldhuisen DJ. Epicardial Adipose Tissue and Invasive Hemodynamics in Heart Failure With Preserved Ejection Fraction. Jacc. Heart Failure. PMID 32653444 DOI: 10.1016/j.jchf.2020.06.003 |
0.017 |
|
| 2021 |
Tromp J, Bryant JA, Jin X, van Woerden G, Asali S, Yiying H, Liew OW, Ching JCP, Jaufeerally F, Loh SY, Sim D, Lee S, Soon D, Tay WT, Packer M, et al. Epicardial fat in heart failure with reduced versus preserved ejection fraction. European Journal of Heart Failure. PMID 33724596 DOI: 10.1002/ejhf.2156 |
0.01 |
|
| Hide low-probability matches. |