The DOI matches its Crossref record; 334 of the 341 references it cites were found in a registry or an index.
Dendritic spine actin cytoskeleton in autism spectrum disorder
Abstract
Dendritic spines are small actin-rich protrusions from neuronal dendrites that form the postsynaptic part of most excitatory synapses. Changes in the shape and size of dendritic spines correlate with the functional changes in excitatory synapses and are heavily dependent on the remodeling of the underlying actin cytoskeleton. Recent evidence implicates synapses at dendritic spines as important substrates of pathogenesis in neuropsychiatric disorders, including autism spectrum disorder (ASD). Although synaptic perturbations are not the only alterations relevant for these diseases, understanding the molecular underpinnings of the spine and synapse pathology may provide insight into their etiologies and could reveal new drug targets. In this review, we will discuss recent findings of defective actin regulation in dendritic spines associated with ASD.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“ASD exhibits a strong genetic basis, and increasing evidence from inherited and de novo gene variations suggests a notable convergence on synapse pathophysiology in ASD, particularly dysfunction of excitatory synaptic transmission 1, 2.”
From Autism-like social deficit generated by Dock4 deficiency is rescued by restoration of Rac1 activity and NMDA receptor function. (2021) · cites this paper as [2]
Citations
Cites
Items 201–334 of 334
Carlson, B. R., Lloyd, K. E., Kruszewski, A., Kim, I.-H., Rodriguiz, R. M., Heindel, C., Faytell, M., Dudek, S. M., Wetsel, W. C., & Soderling, S. H. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4433-10.2011 · Cited by 119
Celestino-Soper, P. B. S., Shaw, C. A., Sanders, S., Li, J., Murtha, M. T., Ercan‐Sencicek, A. G., Davis, L. K., Thomson, S. A. M., Gambin, T., Chinault, A. C., et al. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr363 · Cited by 116
Shank3 Deficiency Induces NMDA Receptor Hypofunction via an Actin-Dependent Mechanism
Duffney, L. J., Wei, J., Cheng, J., Liu, W., Smith, K. R., Kittler, J. T., & Yan, Z. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1175-13.2013 · Cited by 115
Drebrin contains a cryptic F-actin–bundling activity regulated by Cdk5 phosphorylation
Worth, D. C., Daly, C. N., Geraldo, S., Oozeer, F., & Gordon‐Weeks, P. R. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201303005 · Cited by 115
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
The Wave complex is intrinsically inactive
Derivery, E., Lombard, B., Loew, D., & Gautreau, A. M. (2009) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20342 · Cited by 114
Toma, C., Torrico, B., Hervás, A., Valdés-Mas, R., Tristán-Noguero, A., Padillo, V, Maristany, M., Salgado, M., Arenas, C., Puente, X. S., et al. (2014) · Molecular Psychiatry · doi:10.1038/mp.2013.106 · Cited by 114
DISC1 genetics, biology and psychiatric illness
Thomson, P. A., Malavasi, E. L. V., Grünewald, E., Soares, D. C., Borkowska, M., & Millar, J. K. (2012) · Frontiers in Biology · doi:10.1007/s11515-012-1254-7 · Cited by 112
Roberts, J., Hovanes, K., Dasouki, M., Manzardo, A. M., & Butler, M. G. (2013) · Gene · doi:10.1016/j.gene.2013.10.020 · Cited by 111
CYFIP family proteins between autism and intellectual disability: links with Fragile X syndrome
Abekhoukh, S., & Bardoni, B. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00081 · Cited by 110
Ting, J. T., Peça, J., & Feng, G. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150442 · Cited by 110
Lee, E., Lee, H., Huang, T., Chung, C., Shin, W., Kim, K., Koh, J., Hsueh, Y., & Kim, E. (2015) · Nature Communications · doi:10.1038/ncomms8168 · Cited by 110
Ivanov, A., Esclapez, M., Pellegrino, C., Shirao, T., & Ferhat, L. (2009) · Journal of Cell Science · doi:10.1242/jcs.033464 · Cited by 109
Fauchereau, F. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00078-2 · Cited by 109
van der Zwaag, B., Staal, W. G., Hochstenbach, R., Poot, M., Spierenburg, H. A., de Jonge, M. V., Verbeek, N. E., van 't Slot, R., van Es, M. A., Staal, F. J., et al. (2010) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31055 · Cited by 108
The striatin family: A new signaling platform in dendritic spines
Benoist, M., Gaillard, S., & Castets, F. (2006) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2005.12.006 · Cited by 104
A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
Florio, M., Namba, T., Pääbo, S., Hiller, M., & Huttner, W. Β. (2016) · Science Advances · doi:10.1126/sciadv.1601941 · Cited by 100
Phosphoinositide Binding Inhibits α-Actinin Bundling Activity
Fraley, T. S., Tran, T. C., Corgan, A. M., Nash, C. A., Hao, J., Critchley, D. R., & Greenwood, J. A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m213288200 · Cited by 100
Clement, J. P., Ozkan, E. D., Aceti, M., Miller, C. A., & Rumbaugh, G. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0765-13.2013 · Cited by 99
Nakano-Kobayashi, A., Kasri, N. N., Newey, S. E., & Aelst, L. V. (2009) · Current Biology · doi:10.1016/j.cub.2009.05.022 · Cited by 99
A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons
Lin, Y., Frei, J. A., Kilander, M. B. C., Shen, W., & Blatt, G. J. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00263 · Cited by 97
Cellular and synaptic network defects in autism
Peça, J., & Feng, G. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.02.015 · Cited by 96
Feliciano, D. M., Lin, T. V., Hartman, N. W., Bartley, C. M., Kubera, C., Hsieh, L. S., Lafourcade, C., O’Keefe, R. A., & Bordey, A. (2013) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2013.02.008 · Cited by 95
Quitsch, A., Berhörster, K., Liew, C. W., Richter, D., & Kreienkamp, H.-J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2699-04.2005 · Cited by 95
Mimura, N., & Asano, A. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)61254-2 · Cited by 93
Bongmba, O. Y. N., Martinez, L. A., Elhardt, M. E., Butler, K., & Tejada-Simon, M. V. (2011) · Brain Research · doi:10.1016/j.brainres.2011.05.020 · Cited by 91
SynGAP isoforms exert opposing effects on synaptic strength
McMahon, A. C., Barnett, M. W., O'Leary, T. S., Stoney, P. N., Collins, M. O., Papadia, S., Choudhary, J. S., Komiyama, N. H., Grant, S. G. N., Hardingham, G. E., et al. (2012) · Nature Communications · doi:10.1038/ncomms1900 · Cited by 91
Dosunmu, R., Alashwal, H., & Zawia, N. H. (2012) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2012.05.003 · Cited by 91
Wang, C.-C., Held, R. G., & Hall, B. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083941 · Cited by 90
Drebrin-induced Stabilization of Actin Filaments
Mikati, M. A., Grintsevich, E. E., & Reisler, E. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.472647 · Cited by 90
Ca2+ Regulation of Gelsolin Activity: Binding and Severing of F-actin
Kinosian, H. J., Newman, J., Lincoln, B., Selden, L. A., Gershman, L. C., & Estes, J. E. (1998) · Biophysical Journal · doi:10.1016/s0006-3495(98)77751-3 · Cited by 90
Chen, Y.-K., & Hsueh, Y.-P. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4405-11.2012 · Cited by 90
Nakamura, F. (2013) · Biochemical Journal · doi:10.1042/bj20130290 · Cited by 88
Liu, A., Zhou, Z., Dang, R., Zhu, Y., Qi, J., He, G., Leung, C., Pak, D. T. S., Jia, Z., & Xie, W. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201509023 · Cited by 87
Haeckel, A., Ahuja, R., Gundelfinger, E. D., Qualmann, B., & Kessels, M. M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.0336-08.2008 · Cited by 85
Curatolo, P., Napolioni, V., & Moavero, R. (2010) · Journal of Child Neurology · doi:10.1177/0883073810361789 · Cited by 84
Insulin receptor substrate of 53 kDa links postsynaptic shank to PSD‐95
Soltau, M., Berhörster, K., Kindler, S., Buck, F., Richter, D., & Kreienkamp, H. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02523.x · Cited by 84
Jiang-Xie, L.-F., Liao, H., Chen, C., Chen, Y.-T., Ho, S., Lu, D., Lee, L., Liou, H., Fu, W., & Gau, S. S. (2014) · Molecular Autism · doi:10.1186/2040-2392-5-32 · Cited by 84
Hodges, J., Litwa, K., Asmussen, H., Vicente‐Manzanares, M., & Horwitz, A. R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024149 · Cited by 84
The actin cytoskeleton in presynaptic assembly
Nelson, J. C., Stavoe, A. K., & Colón‐Ramos, D. A. (2013) · Cell Adhesion & Migration · doi:10.4161/cam.24803 · Cited by 83
Scotto-Lomassese, S., Nissant, A., Mota, T., Néant-Féry, M., Oostra, B. A., Greer, C. A., Lledo, P.-M., Trembleau, A., & Caillé, I. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5514-10.2011 · Cited by 80
PRICKLE1 Contributes to Cancer Cell Dissemination through Its Interaction with mTORC2
Daulat, A. M., Bertucci, F., Audebert, S., Sergé, A., Finetti, P., Josselin, E., Castellano, R., Birnbaum, D., Angers, S., & Borg, J. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.04.011 · Cited by 80
Knuesel, I., Zuellig, R. A., SCHAUB, M. C., & Fritschy, J. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01476.x · Cited by 78
Joensuu, M., Padmanabhan, P., Durisic, N., Bademosi, A. T., Cooper, E. J., Morrow, I. C., Harper, C. B., Jung, W., Parton, R. G., Goodhill, G. J., et al. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201604001 · Cited by 78
Self-citationSant'Ana, J. A. A. P., Ennion, S. J., Sargeant, A. J., Moorman, A. F. M., & Goldspink, G. (1997) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240050495 · Cited by 76
Allen, D. L., Harrison, B. C., Sartorius, C. A., Byrnes, W. C., & Leinwand, L. A. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.280.3.c637 · Cited by 76
NYAP: a phosphoprotein family that links PI3K to WAVE1 signalling in neurons
Yokoyama, K., Tezuka, T., Kotani, M., Nakazawa, T., Hoshina, N., Shimoda, Y., Kakuta, S., Sudo, K., Watanabe, K., Iwakura, Y., et al. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.348 · Cited by 75
Cerri, C., Fabbri, A., Vannini, E., Spolidoro, M., Costa, M., Maffei, L., Fiorentini, C., & Caleo, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2617-11.2011 · Cited by 75
A double hit implicates DIAPH3 as an autism risk gene
Vorstman, J. A. S., van Daalen, E., Jalali, G. R., Schmidt, E. R. E., Pasterkamp, R. J., de Jonge, M., Hennekam, E. A. M., Janson, E., Staal, W. G., van der Zwaag, B., et al. (2011) · Molecular Psychiatry · doi:10.1038/mp.2010.26 · Cited by 74
Neuronal Rho GEFs in Synaptic Physiology and Behavior
Miller, M. B., Yan, Y., Eipper, B. A., & Mains, R. E. (2013) · The Neuroscientist · doi:10.1177/1073858413475486 · Cited by 74
Xiang, S., Kim, E. Y., Connelly, J. J., Nassar, N. N., Kirsch, J., Winking, J., Schwarz, G., & Schindelin, H. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.03.019 · Cited by 73
Akshoomoff, N. A., Mattson, S. N., & Grossfeld, P. (2014) · Genetics in Medicine · doi:10.1038/gim.2014.86 · Cited by 73
Lü, L., Timofeyev, V., Li, N., Rafizadeh, S., Singapuri, A., Harris, T. R., & Chiamvimonvat, N. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908207106 · Cited by 73
Cory, G. O. C., & Ridley, A. J. (2002) · Nature · doi:10.1038/418732a · Cited by 72
Shank3-Rich2 Interaction Regulates AMPA Receptor Recycling and Synaptic Long-Term Potentiation
Raynaud, F., Janossy, A., Dahl, J., Bertaso, F., Perroy, J., Varrault, A., Vidal, M., Worley, P. F., Boeckers, T. M., Bockaert, J., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2725-12.2013 · Cited by 71
Isolation and characterization of cortactin isoforms and a novel cortactin‐binding protein, CBP90
Ohoka, Y., & Takai, Y. (1998) · Genes to Cells · doi:10.1046/j.1365-2443.1998.00216.x · Cited by 71
Cukovic, D., Lu, G. W. K., Wible, B. A., Steele, D. F., & Fedida, D. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)02505-4 · Cited by 70
Marta Ribasés, A., Bosch, R., Amaia Hervas, G., Ramos‐Quiroga, J. A., Sánchez‐Mora, C., Bielsa, A., Gastaminza, X., Guijarro, S., Nogueira, M., Gómez-Barros, N., et al. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.06.024 · Cited by 68
Connolly, J. J., Glessner, J., & Hakonarson, H. H. (2012) · Child Development · doi:10.1111/j.1467-8624.2012.01838.x · Cited by 66
Chen, Y., Chen, C.-Y., Hu, H., & Hsueh, Y. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-05-0365 · Cited by 66
Burket, J. A., Herndon, A. L., Winebarger, E. E., Jacome, L. F., & Deutsch, S. I. (2011) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2011.08.001 · Cited by 65
Kılınçaslan, A., Kök, B. E., Tektürk, P., Yalçınkaya, C., Özkara, Ç., & Yapıcı, Z. (2016) · Journal of Child and Adolescent Psychopharmacology · doi:10.1089/cap.2016.0100 · Cited by 65
van den Boom, F., Düßmann, H., Uhlenbrock, K., Abouhamed, M., & Bähler, M. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-08-0771 · Cited by 64
Nakazawa, T., Kuriu, T., Tezuka, T., Umemori, H., Okabe, S., & Yamamoto, T. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05335.x · Cited by 63
Dong, T., He, J., Wang, S., Wang, L., Cheng, Y., & Zhong, Y. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1602152113 · Cited by 62
Kalinowska, M., Chávez, A. E., Lutzu, S., Castillo, P. E., Bukauskas, F. F., & Francesconi, A. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.640136 · Cited by 61
Topical Review : Neuropsychiatric Problems in Tuberous Sclerosis Complex
Asato, M. R., & Hardan, A. Y. (2004) · Journal of Child Neurology · doi:10.1177/088307380401900401 · Cited by 60
Bacon, C., Endris, V., & Rappold, G. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.21955 · Cited by 59
Chien, W., Gau, S. S., Wu, Y., Huang, Y., Fang, J., Chen, Y., Soong, W., Chiu, Y., & Chen, C. (2010) · Clinical Genetics · doi:10.1111/j.1399-0004.2010.01395.x · Cited by 58
Patel, K. G., Liu, C., Cameron, P. L., & Cameron, R. S. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-20-07954.2001 · Cited by 56
Autism spectrum disorders: Integration of the genome, transcriptome and the environment
Vijayakumar, N. T., & Judy, M. V. (2016) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2016.03.026 · Cited by 56
Liu, Y. F., Sowell, S. M., Luo, Y. Y., Chaubey, A., Cameron, R. S., Kim, H.-G., & Srivastava, A. K. (2015) · PLoS ONE · doi:10.1371/journal.pone.0123106 · Cited by 55
Control of interneuron dendritic growth through NRG1/erbB4-mediated kalirin-7 disinhibition
Cahill, M. E., Jones, K. A., Rafalovich, I., Xie, Z., Barros, C. S., Müller, U., & Penzes, P. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.35 · Cited by 53
Rosário, M., Schuster, S., Jüttner, R., Parthasarathy, S., Tarabykin, V. S., & Birchmeier, W. (2012) · Genes & Development · doi:10.1101/gad.191593.112 · Cited by 53
Cheung, J., Petek, E., Nakabayashi, K., Tsui, L., Vincent, J. B., & Scherer, S. W. (2001) · Genomics · doi:10.1006/geno.2001.6651 · Cited by 51
Hodges, J., Martín‐Vílchez, S., Asmussen, H., Whitmore, L. A., & Horwitz, A. R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101770 · Cited by 50
Nakazawa, T., Hashimoto, R., Sakoori, K., Sugaya, Y., Tanimura, A., Hashimotodani, Y., Ohi, K., Yamamori, H., Yasuda, Y., Umeda‐Yano, S., et al. (2016) · Nature Communications · doi:10.1038/ncomms10594 · Cited by 50
Lesca, G., Till, M., Labalme, A., Vallée, D., Hugonenq, C., Philip, N., Edery, P., & Sanlaville, D. (2011) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.34004 · Cited by 48
Role of Rho GTPases in the Morphogenesis and Motility of Dendritic Spines
Tashiro, A., & Yuste, R. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(07)00421-1 · Cited by 47
PRICKLE1 Interaction with SYNAPSIN I Reveals a Role in Autism Spectrum Disorders
Paemka, L., Mahajan, V. B., Skeie, J. M., Sowers, L. P., Ehaideb, S. N., Gonzalez‐Alegre, P., Sasaoka, T., Tao, H., Miyagi, A., Ueno, N., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080737 · Cited by 47
Cortactin binding protein 2 increases microtubule stability and regulates dendritic arborization
Shih, P.-Y., Lee, S., Chen, Y., & Hsueh, Y. (2014) · Journal of Cell Science · doi:10.1242/jcs.149476 · Cited by 47
The Childhood Muscular Dystrophies: Diseases Sharing a Common Pathogenesis of Membrane Instability
Mendell, J. R., Sahenk, Z., & Prior, T. W. (1995) · Journal of Child Neurology · doi:10.1177/088307389501000219 · Cited by 47
Li, J., Cai, T., Jiang, Y., Chen, H., He, X., Chen, C., Li, X., Shao, Q., Ran, X., Li, Z., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.58 · Cited by 47
Rho GTPases in neurodegeneration diseases
DeGeer, J., & Lamarche-Vane, N. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.06.016 · Cited by 46
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders
Özgen, M. H., van Daalen, E., Bolton, P., Maloney, V. K., Huang, S., Cresswell, L., van den Boogaard, M. H., Eleveld, M. J., Slot, R. V. ‘., Hochstenbach, R., et al. (2009) · Clinical Genetics · doi:10.1111/j.1399-0004.2009.01254.x · Cited by 46
Impact of Actin Filament Stabilization on Adult Hippocampal and Olfactory Bulb Neurogenesis
Kronenberg, G., Gertz, K. R., Baldinger, T., Kirste, I., Eckart, S., Yildirim, F., Ji, S., Heuser, I., Schröck, H., Hörtnagl, H., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4231-09.2010 · Cited by 46
Nie, D. A., Chen, Z., Ebrahimi‐Fakhari, D., Nardo, A. D., Jülich, K., Robson, V. K., Cheng, Y.-C., Woolf, C. J., Heiman, M., & Şahin, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4796-14.2015 · Cited by 45
Targeted treatments in autism and fragile X syndrome
Gürkan, C. K., & Hagerman, R. J. (2012) · Research in Autism · doi:10.1016/j.rasd.2012.05.007 · Cited by 45
The cellular function of srGAP3 and its role in neuronal morphogenesis
Bacon, C., Endris, V., & Rappold, G. (2012) · Mechanisms of Development · doi:10.1016/j.mod.2012.10.005 · Cited by 45
Wang, J., Tao, Y., Song, F., Sun, Y., Ott, J., & Saffen, D. (2015) · Annals of Human Genetics · doi:10.1111/ahg.12121 · Cited by 45
Wiśniowiecka‐Kowalnik, B., Kastory-Bronowska, M., Bartnik, M., Derwińska, K., Dymczak-Domini, W., Szumbarska, D., Ziemka, E., Szczałuba, K., Sykulski, M., Gambin, T., et al. (2012) · European Journal of Human Genetics · doi:10.1038/ejhg.2012.219 · Cited by 44
Myosin IIb controls actin dynamics underlying the dendritic spine maturation
Koskinen, M., Bertling, E., Hotulainen, R., Tanhuanpää, K., & Hotulainen, P. (2014) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2014.05.008 · Cited by 44
Self-citationIdentification and characterization of ARHGAP24 and ARHGAP25 genes in silico
Katoh, M., & Katoh, M. (2004) · International Journal of Molecular Medicine · doi:10.3892/ijmm.14.2.333 · Cited by 44
Brett, M., McPherson, J. R., Zang, Z. J., Lai, A., Tan, E. S., Ng, I., Ong, L.-C., Cham, B., Tan, P., Rozen, S., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093409 · Cited by 43
Zamboni, V., Armentano, M., Sarò, G., Ciraolo, E., Ghigo, A., Germena, G., Umbach, A., Valnegri, P., Passafaro, M., Carabelli, V., et al. (2016) · Scientific Reports · doi:10.1038/srep34877 · Cited by 43
Powell, A. D., Gill, K. K., Saintot, P., Jiruška, P., Chelly, J., Billuart, P., & Jefferys, J. G. R. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.219907 · Cited by 42
Postsynaptic distribution of IRSp53 in spiny excitatory and inhibitory neurons
Burette, A. C., Park, H., & Weinberg, R. J. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23526 · Cited by 42
Santos-Rebouças, C. B., Belet, S., de Almeida, L. G., Ribeiro, M. G., Medina‐Acosta, E., Bahia, P. R. V., da Silva, A. F. A., dos Santos, F. L., de Lacerda, G. C. B., Pimentel, M. M. G., et al. (2013) · European Journal of Human Genetics · doi:10.1038/ejhg.2013.216 · Cited by 42
Machado, C. D. O. F., Griesi‐Oliveira, K., Rosenberg, C., Kok, F., Martins, S., Passos‐Bueno, M. R., & Sertie, A. L. (2015) · European Journal of Human Genetics · doi:10.1038/ejhg.2015.69 · Cited by 41
Connolly, S., Anney, R., Gallagher, L., & Heron, E. A. (2016) · European Journal of Human Genetics · doi:10.1038/ejhg.2016.153 · Cited by 41
Mulatinho, M. V., Serao, C. L. C., Scalco, F. B., Hardekopf, D. W., Peková, Š., Mrasek, K., Liehr, T., Weise, A., Rao, N. P., & Llerena, J. C. (2012) · Molecular Cytogenetics · doi:10.1186/1755-8166-5-30 · Cited by 40
Papadopoulos, T. G., Schemm, R., Grubmüller, H., & Brose, N. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.633024 · Cited by 39
Khelfaoui, M., Gambino, F., Houbaert, X., Ragazzon, B., Müller, C. R., Carta, M., Lanore, F., Srikumar, B. N., Gastrein, P., Lepleux, M., et al. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0160 · Cited by 39
Yoshii, A., Zhao, J.-P., Pandian, S., van Zundert, B., & Constantine‐Paton, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4585-12.2013 · Cited by 38
Lin, L.-F., Lo, L. H.-Y., Lyu, Q., & Lai, K. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.772442 · Cited by 38
Novel copy number variants in children with autism and additional developmental anomalies
Davis, L. K., Meyer, K. J., Rudd, D. S., Librant, A. L., Epping, E. A., Sheffield, V. C., & Wassink, T. H. (2009) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-009-9013-z · Cited by 37
Narayan, S., Nakajima, K., & Sawa, A. (2013) · The Neuroscientist · doi:10.1177/1073858412470168 · Cited by 37
Claudio Toma, A., Amaia Hervas, G., Balmaña, N., Vilella, E., Aguilera, F., Cuscó, I., Campo, M. D., Caballero‐Andaluz, R., de Diego‐Otero, Y., Ribasés, M., et al. (2010) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2010.09.001 · Cited by 37
Turk, J. (2011) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e328349bb77 · Cited by 35
Krasowska, E., Zabłocki, K., Górecki, D. C., & Swinny, J. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108364 · Cited by 35
Nakano-Kobayashi, A., Tai, Y., Kasri, N. N., & Aelst, L. V. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0894-14.2014 · Cited by 34
Kneussel, M., Engelkamp, D., & Betz, H. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2000.01411.x · Cited by 32
Multiple CaMKII Binding Modes to the Actin Cytoskeleton Revealed by Single-Molecule Imaging
Khan, S., Conte, I. L., Carter, T. D., Bayer, K. U., & Molloy, J. E. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.06.007 · Cited by 31
Liu, L., Sun, L., Li, Z., Li, H., Wei, L., Wang, Y., & Qian, Q. (2013) · Behavioral and Brain Functions · doi:10.1186/1744-9081-9-48 · Cited by 30
Implication of Rho GTPases in Neurodegenerative Diseases
Antoine‐Bertrand, J., Villemure, J.-F., & Lamarche‐Vane, N. (2011) · Current Drug Targets · doi:10.2174/138945011795906543 · Cited by 30
Radu, M., Rawat, S. J., Beeser, A. E., Iliuk, A. B., Tao, W. A., & Chernoff, J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.459719 · Cited by 27
Pirozzi, F., Raimo, F. R. D., Zanni, G., Bertini, E., Billuart, P., Tartaglione, T., Tabolacci, E., Brancaccio, A., Neri, G., & Chiurazzi, P. (2011) · Human Mutation · doi:10.1002/humu.21567 · Cited by 26
NOMA-GAP/ARHGAP33 regulates synapse development and autistic-like behavior in the mouse
Schuster, S., Rivalan, M., Strauß, U., Stoenica, L., Trimbuch, T., Rademacher, N., Parthasarathy, S., Lajkó, D., Rosenmund, C., Shoichet, S. A., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.42 · Cited by 26
Clinical and genetic study of a family with a paternally inherited 15q11–q13 duplication
Marini, C., Cecconi, A., Contini, E., Pantaleo, M., Metitieri, T., Guarducci, S., Giglio, S., Guerrini, R., & Genuardi, M. (2013) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.35907 · Cited by 26
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder
Bhat, G., LaGrave, D., Millson, A., Herriges, J. C., Lamb, A. N., & Matalon, R. K. (2016) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2016.05.014 · Cited by 26
Is MYO9B the missing link between schizophrenia and celiac disease?
Jungerius, B. J., Bakker, S. C., Monsuur, A. J., Sinke, R. J., Kahn, R. S., & Wijmenga, C. (2007) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30605 · Cited by 24
Differential distribution of dystrophin in postsynaptic densities of spine synapses
Jancsik, V., & Hajós, F. (1998) · Neuroreport · doi:10.1097/00001756-199807130-00018 · Cited by 24
Myo9b and RICS Modulate Dendritic Morphology of Cortical Neurons
Long, H., Zhu, X., Yang, P., Gao, Q., Chen, Y., & Ma, L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr378 · Cited by 21
Allegra, M., Spalletti, C., Vignoli, B., Azzimondi, S., Busti, I., Billuart, P., Canossa, M., & Caleo, M. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.01.003 · Cited by 20
Wibawa, T., Takeshima, Y., Mitsuyoshi, I., Wada, H., Surono, A., Nakamura, H., & Matsuo, M. (2000) · Brain and Development · doi:10.1016/s0387-7604(99)00126-6 · Cited by 19
The emerging neuroscience of autism spectrum disorders
Buxbaum, J. D., & Hof, P. R. (2011) · Brain Research · doi:10.1016/j.brainres.2011.02.030 · Cited by 18
Convergent synaptic and circuit substrates underlying autism genetic risks
McGee, A. W., Li, G., Lu, Z., & Qiu, S. (2014) · Frontiers in Biology · doi:10.1007/s11515-014-1298-y · Cited by 17
Crystal Structure of the alpha-Actinin Rod: Four Spectrin Repeats Forming a Thight Dimer.
Ylänne, J., Scheffzek, K., Young, P., & Saraste, M. (2001) · PubMed · Cited by 17
Griscelli syndrome type 1: a report of two cases and review of the literature
Thomas, E., Walker, L., Pullaperuma, S., Cooper, B., Brueton, L. A., Basile, G. D. S., Suri, M., & Brady, A. F. (2009) · Clinical Dysmorphology · doi:10.1097/mcd.0b013e328317b870 · Cited by 16
Marco, E. J., Abidi, F., Bristow, J. D., Dean, W. B., Cotter, P. D., Jeremy, R. J., Schwartz, C., & Sherr, E. H. (2009) · BMJ Case Reports · doi:10.1136/bcr.06.2009.1999 · Cited by 12
De novo autosomal dominant mutation in SYNGAP1
Cook, E. H. (2011) · Autism Research · doi:10.1002/aur.198 · Cited by 7
TC10β/CDC42 GTPase activating protein is required for the growth of cortical neuron dendrites
Shen, P.-C., Xu, D., Liu, J.-W., Li, K., Lin, M.-H., Wang, H.-T., Wang, R., & Zheng, J. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.053 · Cited by 6
Irwin (2001) · doi:10.1002/1096-8628(20010115)98:2
Huttenlocher (1997) · doi:10.1002/(sici)1096-9861(19971020)387:2
Research works printed but not linked: 2
- Wang, 2016, De novo genic mutations among a Chinese autism spectrum disorder cohort, Nat. Commun., 7, 10.1038/ncomms13316 · DOI
- Wisniowiecka-Kowalnik, 2013, Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders, Eur. J. Hum. Genet., 21, 620, 10.1038/ejhg.2012.219 · DOI
Cited by
Sorted by citations
A synaptic perspective of fragile X syndrome and autism spectrum Disorders.
Bagni, C., & Zukin, R. S. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.041 · Cited by 326
Plasticity of Spine Structure: Local Signaling, Translation and Cytoskeletal Reorganization
Nakahata, Y., & Yasuda, R. (2018) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2018.00029 · Cited by 209
Borovac, J., Bosch, M., & Okamoto, K. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.07.001 · Cited by 193
Carmona, A., Roudeau, S., & Ortega, R. (2021) · Toxics · doi:10.3390/toxics9090198 · Cited by 119
Integrin activity in neuronal connectivity
Lilja, J., & Ivaska, J. (2018) · Journal of Cell Science · doi:10.1242/jcs.212803 · Cited by 107
Metadata
- Authors
- Joensuu, M., Lanoue, V., & Hotulainen, P.
- Affiliations
- The University of Queensland (AU)
- Minerva Foundation (FI)
- Corresponding author
- Hotulainen, Pirta
- Venue
- Progress in Neuro-Psychopharmacology and Biological Psychiatry
- Publisher
- Elsevier BV
- Published
- 2018-06
- Volume
- 84
- Issue
- Pt B
- Pages
- 362-381
- ISSN
- 0278-5846 (ISSN-L)
- OpenAlex
- W2751324602
- Cited by
- 65
- References
- 341
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 4 · 2023: 6 · 2022: 7 · 2021: 14 · 2020: 9 · 2019: 5 · 2018: 10
- FWCI
- 0.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Progress in Neuro-Psychopharmacology and Biological Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Academy of Finland (298124)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Keywords
- dendritic spines, actin cytoskeleton, autism spectrum disorder, excitatory synapses, synaptic plasticity, actin regulation, neuropsychiatric disorders, therapeutic target
- MeSH terms
- Autism Spectrum Disorder, Animals, Humans, Actin Cytoskeleton, Synapses, Dendritic Spines
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review