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Genetic and Epigenetic Networks in Intellectual Disabilities
Abstract
Mutations in more than 450 different genes have been associated with intellectual disability (ID) and related cognitive disorders (CDs), such as autism. It is to be expected that this number will increase three to fourfold in the next years due to the rapid implementation of innovative high-throughput sequencing technology in genetics labs. Numerous functional relationships have been identified between the products of individual ID genes, and common molecular and cellular pathways onto which these networks converge are beginning to emerge. Prominent examples are genes involved in synaptic plasticity, Ras and Rho GTPase signaling, and epigenetic genes that encode modifiers of the chromatin structure. It thus seems that there might be common pathological patterns in ID, despite its bewildering genetic heterogeneity. These common pathways provide attractive opportunities for knowledge-based therapeutic interventions.
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“Various genetic approaches have been successful in identifying the causes of more than 1,000 Mendelian, and fewer non-Mendelian, forms of neurodevelopmental disorders: prototypical examples are intellectual disability62–68, autism spectrum disorder (ASD)69–77, epilepsy78,79 and schizophrenia80–82.”
From Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders (2015) · cites this paper as [63]
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Cites
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U., & Zoghbi, H. Y. (1999) · Nature Genetics · doi:10.1038/13810 · Cited by 4,990
No health without mental health
Prince, M. J., Patel, V., Saxena, S., Maj, M., Maselko, J., Phillips, M. R., & Rahman, A. (2007) · The Lancet · doi:10.1016/s0140-6736(07)61238-0 · Cited by 4,028
Verkerk, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., et al. (1991) · Cell · doi:10.1016/0092-8674(91)90397-h · Cited by 3,481
Miller, D. T., Adam, M. P., Aradhya, S., Biesecker, L. G., Brothman, A. R., Carter, N. P., Church, D. M., Crolla, J. A., Eichler, E. E., Epstein, C. J., et al. (2010) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2010.04.006 · Cited by 2,882
AMPA Receptor Trafficking and Synaptic Plasticity
Malinow, R., & Malenka, R. C. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142758 · Cited by 2,588
Liaw, D., Marsh, D. J., Li, J., Dahia, P. L. M., Wang, S. I., Zheng, Z., Bose, S., Call, K. M., Tsou, H. C., Peacoke, M., et al. (1997) · Nature Genetics · doi:10.1038/ng0597-64 · Cited by 2,067
Functional impact of global rare copy number variation in autism spectrum disorders
Pinto, D., Pagnamenta, A. T., Klei, L., Anney, R., Merico, D., Regan, R., Conroy, J., Magalhaes, T. R., Correia, C., Abrahams, B. S., et al. (2010) · Nature · doi:10.1038/nature09146 · Cited by 2,013
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
Study, P. A. R. I. S., Jamain, S., Quach, H., Betancur, C., Råstam, M., Colineaux, C., Gillberg, I. C., Soderstrom, H., Giros, B., Leboyer, M., et al. (2003) · Nature Genetics · doi:10.1038/ng1136 · Cited by 1,851
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
Tartaglia, M., Mehler, E. L., Goldberg, R. B., Zampino, G., Brunner, H. G., Kremer, H., van der Burgt, I., Crosby, A. H., Ion, A., Jeffery, S., et al. (2001) · Nature Genetics · doi:10.1038/ng772 · Cited by 1,736
Common variants conferring risk of schizophrenia
†Genetic Risk and Outcome in Psychosis (GROUP), Stefansson, H., Ophoff, R. A., Steinberg, S., Andreassen, O. A., Cichon, S., Rujescu, D., Werge, T., Pietiläinen, O. P. H., Mors, O., et al. (2009) · Nature · doi:10.1038/nature08186 · Cited by 1,677
Research works printed but not linked: 2
- American Psychiatric Association. 1994.The Diagnostic and Statistical Manual of Mental Disorders(DSM)fourth edition(DSM-IV)
- 10.1037//0033-2909.96.3.518 · DOI
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de Ligt, J., Willemsen, M. H., van Bon, B. W. M., Kleefstra, T., Yntema, H. G., Kroes, T., Vulto-van Silfhout, A. T., Koolen, D. A., de Vries, P., Gilissen, C., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1206524 · Cited by 1,546
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Parikshak, N. N., Luo, R., Zhang, A., Won, H., Lowe, J. K., Chandran, V., Horvath, S., & Geschwind, D. H. (2013) · Cell · doi:10.1016/j.cell.2013.10.031 · Cited by 1,039
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Parenti, I., Rabaneda, L. G., Schoen, H., & Novarino, G. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.05.004 · Cited by 687
Stessman, H. A. F., Xiong, B., Coe, B. P., Wang, T., Hoekzema, K., Fenckova, M., Kvarnung, M., Gerdts, J., Trinh, S., Cosemans, N., et al. (2017) · Nature Genetics · doi:10.1038/ng.3792 · Cited by 559
From neural development to cognition: unexpected roles for chromatin
Ronan, J. L., Wu, W., & Crabtree, G. R. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3413 · Cited by 544
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Yu, T. W., Chahrour, M. H., Coulter, M. E., Jiralerspong, S., Okamura-Ikeda, K., Ataman, B., Schmitz-Abe, K., Harmin, D. A., Adli, M., Malik, A. N., et al. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.002 · Cited by 442
Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders
Parikshak, N. N., Gandal, M. J., & Geschwind, D. H. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3934 · Cited by 430
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome
Santen, G. W. E., Aten, E., Sun, Y., Almomani, R., Gilissen, C., Nielsen, M., Kant, S. G., Snoeck, I. N., Peeters, E. A. J., Hilhorst-Hofstee, Y., et al. (2012) · Nature Genetics · doi:10.1038/ng.2217 · Cited by 347
Xue, Y., Ankala, A., Wilcox, W. R., & Hegde, M. (2014) · Genetics in Medicine · doi:10.1038/gim.2014.122 · Cited by 359
The GABAA Receptor as a Therapeutic Target for Neurodevelopmental Disorders
Braat, S., & Kooy, R. F. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.042 · Cited by 294
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Tarailo-Graovac, M., Shyr, C., Ross, C. J., Horvath, G. A., Salvarinova, R., Ye, X. C., Zhang, L.-H., Bhavsar, A. P., Lee, J. J. Y., Drögemöller, B. I., et al. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1515792 · Cited by 281
Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability
Kleefstra, T., Kramer, J. M., Neveling, K., Willemsen, M. H., Koemans, T. S., Vissers, L. E. L. M., Wissink-Lindhout, W. M., Fencková, M., van den Akker, W. M. R., Kasri, N. N., et al. (2012) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2012.05.003 · Cited by 264
Intellectual disability and autism spectrum disorders: Causal genes and molecular mechanisms
Srivastava, A. K., & Schwartz, C. E. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.02.015 · Cited by 273
Glutamate Synapses in Human Cognitive Disorders
Volk, L. J., Chiu, S., Sharma, K., & Huganir, R. L. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-033821 · Cited by 256
Neurological Aspects of Human Glycosylation Disorders
Freeze, H. H., Eklund, E. A., Ng, B. G., & Patterson, M. C. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034019 · Cited by 243
Meredith, R. M. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.12.001 · Cited by 262
A Quantitative Framework to Evaluate Modeling of Cortical Development by Neural Stem Cells
Stein, J. L., de la Torre-Ubieta, L., Tian, Y., Parikshak, N. N., Hernández, I. A., Marchetto, M. C., Baker, D. K., Lu, D., Hinman, C. R., Lowe, J. K., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.035 · Cited by 201
Harrington, A. J., Raissi, A., Rajkovich, K., Berto, S., Kumar, J., Molinaro, G., Raduazzo, J., Guo, Y., Loerwald, K., Konopka, G., et al. (2016) · eLife · doi:10.7554/elife.20059 · Cited by 193
Astrocytes and Microglia and Their Potential Link with Autism Spectrum Disorders
Petrelli, F., Pucci, L., & Bezzi, P. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00021 · Cited by 192
Willemsen, M. H., Vulto-van Silfhout, A. T., Nillesen, W. M., Wissink-Lindhout, W. M., van Bokhoven, H., Philip, N., Berry-Kravis, E. M., Kini, U., van Ravenswaaij-Arts, C. M. A., Delle Chiaie, B., et al. (2011) · Molecular Syndromology · doi:10.1159/000335648 · Cited by 185
Activation of the ISR mediates the behavioral and neurophysiological abnormalities in Down syndrome
Zhu, P., Khatiwada, S., Cui, Y., Reineke, L. C., Dooling, S. W., Kim, J., Li, W., Walter, P., & Costa‐Mattioli, M. (2019) · Science · doi:10.1126/science.aaw5185 · Cited by 171
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Moreno-De-Luca, A., Ledbetter, D. H., & Martin, C. L. (2012) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70287-3 · Cited by 196
Iqbal, Z., Vandeweyer, G., van der Voet, M., Waryah, A., Zahoor, M., Besseling, J., Roca, L. T., Silfhout, A. T. V.-V., Nijhof, B., Kramer, J. M., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt043 · Cited by 175
Grozeva, D., Carss, K., Spasić-Bošković, O., Parker, M. J., Archer, H. L., Firth, H. V., Park, S., Canham, N. L. E., Holder, S., Wilson, M., et al. (2014) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.03.006 · Cited by 168
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UK10K, Riazuddin, S. A., Hussain, M., Razzaq, A., Iqbal, Z., Shahzad, M., Polla, D. L., Song, Y., van Beusekom, E., Khan, A. A., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.109 · Cited by 164
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Schubert, D., Martens, G. J. M., & Kolk, S. M. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.147 · Cited by 157
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Medic, N., Ziauddeen, H., Ersche, K. D., Farooqi, I. S., Bullmore, E. T., Nathan, P. J., Ronan, L., & Fletcher, P. C. (2016) · International Journal of Obesity · doi:10.1038/ijo.2016.42 · Cited by 135
Kuechler, A., Zink, A. M., Wieland, T., Lüdecke, H.-J., Cremer, K., Salviati, L., Magini, P., Najafi, K., Zweier, C., Czeschik, J. C., et al. (2014) · European Journal of Human Genetics · doi:10.1038/ejhg.2014.165 · Cited by 140
Iwase, S., Brookes, E., Agarwal, S., Badeaux, A. I., Ito, H., Vallianatos, C. N., Tomassy, G. S., Kasza, T., Lin, G. R., Thompson, A., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2015.12.091 · Cited by 132
Schuurs-Hoeijmakers, J. H. M., Oh, E. C. T., Vissers, L. E. L. M., Swinkels, M. E. M., Gilissen, C., Willemsen, M. A. A. P., Holvoet, M., Steehouwer, M., Veltman, J. A., Vries, B. B. A. D., et al. (2012) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2012.10.013 · Cited by 131
Courcet, J.-B., Faivre, L., Malzac, P., Masurel-Paulet, A., Lopez, E., Callier, P., Lambert, L., Lemesle, M., Thevenon, J., Gigot, N., et al. (2012) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2012-101251 · Cited by 121
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Siu, M. T., & Weksberg, R. (2017) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-319-53889-1_4 · Cited by 121
ROCK1 and 2 differentially regulate actomyosin organization to drive cell and synaptic polarity
Litwa, K., Badoual, M., Asmussen, H., Patel, H., Whitmore, L. A., & Horwitz, A. R. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201504046 · Cited by 127
Beal, M. A., Yauk, C. L., & Marchetti, F. (2017) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2017.04.001 · Cited by 129
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Reiner, O., Karzbrun, E., Kshirsagar, A., & Kaibuchi, K. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13403 · Cited by 129
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Bögershausen, N., Shahrzad, N., Chong, J. X., von Kleist-Retzow, J., Stanga, D., Li, Y., Bernier, F. P., Loucks, C. M., Wirth, R., Puffenberger, E. G., et al. (2013) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2013.05.028 · Cited by 118
Jeyabalan, N., & Clement, J. P. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00032 · Cited by 130
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Reichard, J., & Zimmer‐Bensch, G. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.776809 · Cited by 118
Hunt, D., Leventer, R. J., Simons, C., Taft, R., Swoboda, K. J., Gawne-Cain, M., study, T. D., Magee, A. C., Turnpenny, P. D., & Baralle, D. (2014) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2014-102798 · Cited by 104
Rho GTPase signaling at the synapse: Implications for intellectual disability
Ba, W., van der Raadt, J., & Kasri, N. N. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.05.033 · Cited by 114
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Ghosh, A., Michalon, A., Lindemann, L., Fontoura, P., & Santarelli, L. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd4102 · Cited by 108
Fass, D. M., Reis, S. A., Ghosh, B., Hennig, K. M., Joseph, N. F., Zhao, W., Nieland, T. J. F., Guan, J., Kuhnle, C. G., Tang, W., et al. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.06.043 · Cited by 111
Bronicki, L. M., Redin, C., Drunat, S., Piton, A., Lyons, M., Passemard, S., Baumann, C., Faivre, L., Thevenon, J., Rivière, J.-B., et al. (2015) · European Journal of Human Genetics · doi:10.1038/ejhg.2015.29 · Cited by 105
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Srour, M., & Shevell, M. I. (2013) · Archives of Disease in Childhood · doi:10.1136/archdischild-2013-304063 · Cited by 102
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Zucchelli, S., Fasolo, F., Russo, R., Cimatti, L., Patrucco, L., Takahashi, H., Jones, M. H., Santoro, C., Sblattero, D., Cotella, D., et al. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00174 · Cited by 101
Chilian, B., Abdollahpour, H., Bierhals, T., Haltrich, I., Fekete, G., Nagel, I., Rosenberger, G., & Kutsche, K. (2013) · Clinical Genetics · doi:10.1111/cge.12105 · Cited by 85
Wirth, B., Garbes, L., & Rießland, M. (2013) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2013.03.003 · Cited by 96
Tian, Y., Voineagu, I., Paşca, S. P., Won, H., Chandran, V., Horvath, S., Dolmetsch, R. E., & Geschwind, D. H. (2014) · Genome Medicine · doi:10.1186/s13073-014-0075-5 · Cited by 93
Shah, S., Molinaro, G., Liu, B., Wang, R., Huber, K. M., & Richter, J. D. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.02.076 · Cited by 95
Juvenile‐Onset Huntington Disease Pathophysiology and Neurodevelopment: A Review
Bakels, H. S., Roos, R. A. C., van Roon‐Mom, W., & de Bot, S. T. (2021) · Movement Disorders · doi:10.1002/mds.28823 · Cited by 95
Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse
Ung, D. C., Iacono, G., Méziane, H., Blanchard, E., Papon, M.-A., Selten, M. M., van Rhijn, J. R., Montjean, R., Rucci, J., Lorenzo, S. M., et al. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.39 · Cited by 91
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Pengelly, R. J., Greville-Heygate, S. L., Schmidt, S., Seaby, E. G., Jabalameli, M. R., Mehta, S. G., Parker, M. J., Goudie, D. R., Fagotto‐Kaufmann, C., Mercer, C., et al. (2016) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2016-103942 · Cited by 82
Davarnia, B., Hu, H., Kahrizi, K., Musante, L., Fattahi, Z., Hosseini, M., Maqsoud, F., Farajollahi, R., Wienker, T. F., Ropers, H., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129631 · Cited by 83
Gregorio, E. D., Riberi, E., Belligni, E. F., Biamino, E., Spielmann, M., Ala, U., Calcia, A., Bagnasco, I., Carli, D., Gai, G., et al. (2017) · Clinical Genetics · doi:10.1111/cge.13009 · Cited by 83
Rho GTPases in Intellectual Disability: From Genetics to Therapeutic Opportunities
Zamboni, V., Jones, R., Umbach, A., Ammoni, A., Passafaro, M., Hirsch, E., & Merlo, G. R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061821 · Cited by 83
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Kessi, M., Chen, B., Peng, J., Yan, F., Yang, L., & Yin, F. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-01850-0 · Cited by 84
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Dall’Aglio, L., Muka, T., Cecil, C. A. M., Bramer, W. M., Verbiest, M. M. P. J., Nano, J., Hidalgo, A. P. C., Franco, O. H., & Tiemeier, H. W. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.07.011 · Cited by 85
Balemans, M. C. M., Kasri, N. N., Kopanitsa, M. V., Afinowi, N. O., Ramakers, G. J. A., Peters, T. A., Beynon, A. J., Janssen, S. M., van Summeren, R. C. J., Eeftens, J. M., et al. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds490 · Cited by 78
The Genetics of Intellectual Disability
Jansen, S., Vissers, L. E. L. M., & de Vries, B. B. A. (2023) · Brain Sciences · doi:10.3390/brainsci13020231 · Cited by 81
Goodwin, L. R., & Picketts, D. J. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.10.008 · Cited by 76
Study, D. D. D. (., Zweier, M., Begemann, A., McWalter, K., Cho, M. T., Abela, L., Banka, S., Behring, B., Berger, A., Brown, C. W., et al. (2019) · European Journal of Human Genetics · doi:10.1038/s41431-018-0331-z · Cited by 71
Impaired Dendritic Development and Memory inSorbs2Knock-Out Mice
Zhang, Q., Gao, X., Li, C., Feliciano, C., Wang, D., Zhou, D., Yuan, M., Monteiro, P., Anand, M., Itohara, S., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2528-15.2016 · Cited by 74
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van deVondervoort, I. I. G. M., Gordebeke, P. M., Khoshab, N., Tiesinga, P. H. E., Buitelaar, J. K., Kozicz, T., Aschrafi, A., & Glennon, J. C. (2013) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2013.00053 · Cited by 73
Chia, P. H., Zhong, F. L., Niwa, S., Bonnard, C., Utami, K. H., Zeng, R., Lee, H., Eskin, A., Nelson, S. F., Xie, W. H., et al. (2018) · eLife · doi:10.7554/elife.32451 · Cited by 71
Desrivières, S., Lourdusamy, A., Tao, C., Toro, R., Jia, T., Loth, E., Medina, L. M., Kepa, A., Fernandes, A. R., Ruggeri, B., et al. (2014) · Molecular Psychiatry · doi:10.1038/mp.2013.197 · Cited by 70
Mutations in ARID2 are associated with intellectual disabilities
Shang, L., Cho, M. T., Retterer, K., Folk, L., Humberson, J. B., Rohena, L. O., Sidhu, A., Saliganan, S., Iglesias, A. D., Vitazka, P., et al. (2015) · Neurogenetics · doi:10.1007/s10048-015-0454-0 · Cited by 70
Willemsen, M. H., Nijhof, B., Fencková, M., Nillesen, W. M., Bongers, E. M. H. F., Castells‐Nobau, A., Asztalos, L., Viràgh, E., van Bon, B. W. M., Tezel, E., et al. (2013) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2012-101490 · Cited by 68
Epigenetic mechanisms underlying nervous system diseases
Qureshi, I., & Mehler, M. F. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63233-3.00005-1 · Cited by 70
The neurodevelopmental spectrum of synaptic vesicle cycling disorders
John, A., Ng‐Cordell, E., Hanna, N., Brkić, D., & Baker, K. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15135 · Cited by 65
Yasumura, M., Yoshida, T., Yamazaki, M., Abe, M., Natsume, R., Kanno, K., Uemura, T., Takao, K., Sakimura, K., Kikusui, T., et al. (2014) · Scientific Reports · doi:10.1038/srep06613 · Cited by 69
Nijhof, B., Castells‐Nobau, A., Wolf, L., Gooyert, J. M. S.-D., Monedero, I., Torroja, L., Coromina, L., van der Laak, J. A. W. M., & Schenck, A. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004823 · Cited by 66
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Takashi, H., Yoshida, T., Ra, M., Taguchi, R., & Mishina, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066254 · Cited by 64
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Gupta, C., Chandrashekar, P. B., Jin, T., He, C., Khullar, S., Chang, Q., & Wang, D. (2022) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-022-09438-w · Cited by 66
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Metadata
- Authors
- van Bokhoven, H.
- Affiliations
- Molecular Neurogenetics Unit, Department of Human Genetics, Nijmegen Center for Molecular Life Sciences, and Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition, and Behavior, Radboud University, Nijmegen Medical Center, 6500 HB Nijmegen, The Netherlands;
- Venue
- Annual Review of Genetics
- Publisher
- Annual Reviews
- Published
- 2011-12-15
- Volume
- 45
- Issue
- 1
- Pages
- 81-104
- ISSN
- 0066-4197 (ISSN-L)
- 1545-2948
- OpenAlex
- W2160616996
- Semantic Scholar
- cebf2b88230f016c9d33fe39a870dc47be6bc913
- Cited by
- 382
- References
- 210
- Citations by year
- 2026: 12 · 2025: 12 · 2024: 15 · 2023: 17 · 2022: 19 · 2021: 34 · 2020: 30 · 2019: 20 · 2018: 28 · 2017: 29 · 2016: 33 · 2015: 36 · 2014: 44 · 2013: 33 · 2012: 18
- FWCI
- 3.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Genetics (publishedVersion)
- PubMed (publishedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Down syndrome and intellectual disability research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- intellectual disability, cognitive disorders, autism spectrum disorder, gene networks, epigenetic networks, synaptic plasticity, Ras signaling, Rho GTPase signaling, chromatin structure, genetic heterogeneity, therapeutic target
- MeSH terms
- Autistic Disorder, Chromosome Aberrations, Chromosomes, Human, Cognition Disorders, Cytoskeletal Proteins, Humans, Intellectual Disability, Mutation, Spine, Synapses, Transcription, Genetic, Signal Transduction, Genetic Diseases, Inborn, Epigenesis, Genetic, Gene Regulatory Networks
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