MiR-137: an important player in neural development and neoplastic transformation

Untitled work

Bartel (2004) · doi:10.1016/s0092-8674(04)00045-5 · Cited by 34,714 · see citing works

MicroRNAs: Target Recognition and Regulatory Functions

Bartel, D. P. (2009) · Cell · doi:10.1016/j.cell.2009.01.002 · Cited by 20,068 · see citing works

MicroRNA expression profiles classify human cancers

Lü, J., Getz, G. A., Miska, E. A., Alvarez-Saavedra, E., Lamb, J., Peck, D., Sweet-Cordero, A., Ebert, B. L., Mak, R. H., Ferrando, A. A., et al. (2005) · Nature · doi:10.1038/nature03702 · Cited by 9,497 · see citing works

MicroRNA signatures in human cancers

Calin, G. A., & Croce, C. M. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1997 · Cited by 7,592 · see citing works

Biological insights from 108 schizophrenia-associated genetic loci

Schizophrenia Working Group of the Psychiatric Genomics Consortium (2014) · Nature · doi:10.1038/nature13595 · Cited by 7,577 · see citing works

DNA methylation patterns and epigenetic memory

Bird, A. (2002) · Genes & Development · doi:10.1101/gad.947102 · Cited by 7,124 · see citing works

Oncomirs — microRNAs with a role in cancer

Esquela‐Kerscher, A., & Slack, F. J. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1840 · Cited by 7,038 · see citing works

Untitled work

(2008) · doi:10.1038/nrg2290 · Cited by 5,199 · see citing works

The nuclear RNase III Drosha initiates microRNA processing

Lee, Y., Ahn, C., Han, J., Choi, H., Kim, J., Yim, J., Lee, J., Provost, P., Rådmark, O., Kim, S., et al. (2003) · Nature · doi:10.1038/nature01957 · Cited by 5,094 · see citing works

Identification of Novel Genes Coding for Small Expressed RNAs

Lagos-Quintana, M., Rauhut, R., Lendeckel, W., & Tuschl, T. (2001) · Science · doi:10.1126/science.1064921 · Cited by 4,956 · see citing works

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

The International Schizophrenia Consortium (2009) · Nature · doi:10.1038/nature08185 · Cited by 4,821 · see citing works

MicroRNA Gene Expression Deregulation in Human Breast Cancer

Iorio, M. V., Ferracin, M., Liu, C.-G., Veronese, A., Spizzo, R., Sabbioni, S., Magri, E., Pedriali, M., Fabbri, M., Campiglio, M., et al. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-1783 · Cited by 4,053 · see citing works

A Mammalian microRNA Expression Atlas Based on Small RNA Library Sequencing

Landgraf, P., Rusu, M., Sheridan, R., Sewer, A., Iovino, N., Aravin, A., Pfeffer, S., Rice, A., Kamphorst, A. O., Landthaler, M., et al. (2007) · Cell · doi:10.1016/j.cell.2007.04.040 · Cited by 3,626 · see citing works

The Versatile Role of microRNA-30a in Human Cancer

Wang, C., Yang, X., Chen, Y., & Chen, L. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000471111 · Cited by 3,409 · see citing works

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

(2013) · The Lancet · doi:10.1016/s0140-6736(12)62129-1 · Cited by 3,010 · see citing works

An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells

Hammond, S. M., Bernstein, E., Beach, D., & Hannon, G. J. (2000) · Nature · doi:10.1038/35005107 · Cited by 3,006 · see citing works

Identification of tissue-specific microRNAs from mouse

Lagos-Quintana, M., Rauhut, R., Yalcin, A., Meyer, J., Lendeckel, W., & Tuschl, T. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00809-6 · Cited by 2,859 · see citing works

Processing of primary microRNAs by the Microprocessor complex

Denli, A. M., Tops, B. B. J., Plasterk, R. H. A., Ketting, R. F., & Hannon, G. J. (2004) · Nature · doi:10.1038/nature03049 · Cited by 2,784 · see citing works

The Microprocessor complex mediates the genesis of microRNAs

Gregory, R. I., Yan, K.-P., Amuthan, G., Chendrimada, T. P., Doratotaj, B., Cooch, N. S., & Shiekhattar, R. (2004) · Nature · doi:10.1038/nature03120 · Cited by 2,724 · see citing works

Polycomb complexes repress developmental regulators in murine embryonic stem cells

Boyer, L. A., Plath, K., Zeitlinger, J., Brambrink, T., Medeiros, L. A., Lee, T. I., Levine, S. S., Wernig, M., Tajonar, A., Ray, M. K., et al. (2006) · Nature · doi:10.1038/nature04733 · Cited by 2,518 · see citing works

Control of Developmental Regulators by Polycomb in Human Embryonic Stem Cells

Lee, T. I., Jenner, R. G., Boyer, L. A., Guenther, M. G., Levine, S. S., Kumar, R., Chevalier, B. S., Johnstone, S. E., Cole, M. F., Isono, K., et al. (2006) · Cell · doi:10.1016/j.cell.2006.02.043 · Cited by 2,238 · see citing works

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

Lichtenstein, P., Yip, B. H., Björk, C., Pawitan, Y., Cannon, T. D., Sullivan, P. F., & Hultman, C. M. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60072-6 · Cited by 2,125 · see citing works

TRBP recruits the Dicer complex to Ago2 for microRNA processing and gene silencing

Chendrimada, T. P., Gregory, R. I., Kumaraswamy, E., Norman, J. A., Cooch, N. S., Nishikura, K., & Shiekhattar, R. (2005) · Nature · doi:10.1038/nature03868 · Cited by 2,103 · see citing works

Schizophrenia

van Os, J., & Kapur, S. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60995-8 · Cited by 1,971 · see citing works

Genome-wide association study identifies five new schizophrenia loci

The Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium (2011) · Nature Genetics · doi:10.1038/ng.940 · Cited by 1,919 · see citing works

A brain-specific microRNA regulates dendritic spine development

Schratt, G. M., Tuebing, F., Nigh, E. A., Kane, C. G., Sabatini, M. E., Kiebler, M., & Greenberg, M. E. (2006) · Nature · doi:10.1038/nature04367 · Cited by 1,786 · see citing works

MicroRNA dysregulation in cancer: diagnostics, monitoring and therapeutics. A comprehensive review

Iorio, M. V., & Croce, C. M. (2012) · EMBO Molecular Medicine · doi:10.1002/emmm.201100209 · Cited by 1,738 · see citing works

Identification of Mammalian microRNA Host Genes and Transcription Units

Rodriguez, A., Griffiths-Jones, S., Ashurst, J. L., & Bradley, A. (2004) · Genome Research · doi:10.1101/gr.2722704 · Cited by 1,732 · see citing works

Decreased Dendritic Spine Density on Prefrontal Cortical Pyramidal Neurons in Schizophrenia

Glantz, L. A., & Lewis, D. A. (2000) · Archives of General Psychiatry · doi:10.1001/archpsyc.57.1.65 · Cited by 1,636 · see citing works

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Multicenter Genetic Studies of Schizophrenia Consortium, Ripke, S., Psychosis Endophenotypes International Consortium, Wellcome Trust Case Control Consortium 2, O'Dushlaine, C., Chambert, K., Moran, J. L., Kähler, A. K., Akterin, S., Bergen, S. E., et al. (2013) · Nature Genetics · doi:10.1038/ng.2742 · Cited by 1,496 · see citing works

The microRNA miR-34a inhibits prostate cancer stem cells and metastasis by directly repressing CD44

Liu, C., Kelnar, K., Liu, B., Chen, X., Calhoun‐Davis, T., Li, H., Patrawala, L., Yan, H., Jeter, C. R., Honorio, S., et al. (2011) · Nature Medicine · doi:10.1038/nm.2284 · Cited by 1,401 · see citing works

MicroRNA control of signal transduction

Inui, M., Martello, G., & Piccolo, S. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2868 · Cited by 1,262 · see citing works

MicroRNAs in Development and Disease

Sayed, D. H., & Abdellatif, M. (2011) · Physiological Reviews · doi:10.1152/physrev.00006.2010 · Cited by 1,074 · see citing works

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

Malhotra, D., & Sebat, J. (2012) · Cell · doi:10.1016/j.cell.2012.02.039 · Cited by 854 · see citing works

Paxillin and focal adhesion signalling

Turner, C. E. (2000) · Nature Cell Biology · doi:10.1038/35046659 · Cited by 839 · see citing works

Illuminating the silence: understanding the structure and function of small RNAs

Rana, T. M. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2085 · Cited by 837 · see citing works

Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues.

Bandrés, E., Cubedo, E., Agirre, X., Malumbres, R., Zárate, R., Ramírez, N., Abajo, A., Navarro, A., Moreno, I., Monzó, M., et al. (2006) · Molecular Cancer · doi:10.1186/1476-4598-5-29 · Cited by 795 · see citing works

miR-124 and miR-137 inhibit proliferation of glioblastoma multiforme cells and induce differentiation of brain tumor stem cells

Silber, J., Lim, D. A., Petritsch, C., Persson, A. I., Maunakea, A. K., Yu, M., Vandenberg, S. R., Ginzinger, D. G., James, C. D., Costello, J. F., et al. (2008) · BMC Medicine · doi:10.1186/1741-7015-6-14 · Cited by 765 · see citing works

Increased dendritic spine densities on cortical projection neurons in autism spectrum disorders

Hutsler, J. J., & Zhang, H. (2010) · Brain Research · doi:10.1016/j.brainres.2009.09.120 · Cited by 765 · see citing works

Targeting of the Bmi-1 Oncogene/Stem Cell Renewal Factor by MicroRNA-128 Inhibits Glioma Proliferation and Self-Renewal

Godlewski, J. A., Nowicki, M. O., Bronisz, A., Williams, S. P., Otsuki, A., Nuovo, G. J., Ray‐Chaudhury, A., Newton, H. B., Chiocca, E. A., & Lawler, S. E. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-2629 · Cited by 702 · see citing works

Dual Role for Argonautes in MicroRNA Processing and Posttranscriptional Regulation of MicroRNA Expression

Diederichs, S., & Haber, D. A. (2007) · Cell · doi:10.1016/j.cell.2007.10.032 · Cited by 687 · see citing works

Histone lysine methylation: a signature for chromatin function

Sims, R. J., Nishioka, K., & Reinberg, D. (2003) · Trends in Genetics · doi:10.1016/j.tig.2003.09.007 · Cited by 684 · see citing works

Development of a Lung Cancer Therapeutic Based on the Tumor Suppressor MicroRNA-34

Wiggins, J. F., Ruffino, L., Kelnar, K., Omotola, M., Patrawala, L., Brown, D., & Bader, A. G. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-0655 · Cited by 679 · see citing works

Exploration of Tumor-Suppressive MicroRNAs Silenced by DNA Hypermethylation in Oral Cancer

Kozaki, K., Imoto, I., Mogi, S., Omura, K., & Inazawa, J. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-5194 · Cited by 612 · see citing works

Characterization of MicroRNA Expression Levels and Their Biological Correlates in Human Cancer Cell Lines

Gaur, A., Jewell, D. A., Liang, Y., Ridzon, D., Moore, J. H., Chen, C., Ambros, V. R., & Israel, M. A. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-2698 · Cited by 593 · see citing works

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

Wellcome Trust Case Control Consortium, Green, E. K., Grozeva, D., Jones, I., Jones, L., Kirov, G., Caesar, S., Gordon-Smith, K., Fraser, C., Forty, L., et al. (2010) · Molecular Psychiatry · doi:10.1038/mp.2009.49 · Cited by 526 · see citing works

Regression of murine lung tumors by the let-7 microRNA

Trang, P., Medina, P. P., Wiggins, J. F., Ruffino, L., Kelnar, K., Omotola, M., Homer, R., Brown, D., Bader, A. G., Weidhaas, J. B., et al. (2009) · Oncogene · doi:10.1038/onc.2009.445 · Cited by 502 · see citing works

Developing MicroRNA Therapeutics

van Rooij, E., Purcell, A. L., & Levin, A. A. (2012) · Circulation Research · doi:10.1161/circresaha.111.247916 · Cited by 498 · see citing works

Cross talk between microRNA and epigenetic regulation in adult neurogenesis

Szulwach, K. E., Li, X., Smrt, R. D., Li, Y., Luo, Y., Lin, L., Santistevan, N. J., Li, W., Zhao, X., & Jin, P. (2010) · Journal of Cell Biology · doi:10.1083/jcb.200908151 · Cited by 493 · see citing works

MicroRNAs as Regulators of Differentiation and Cell Fate Decisions

Ivey, K. N., & Srivastava, D. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.06.012 · Cited by 449 · see citing works

Schizophrenia is associated with an increase in cortical microRNA biogenesis

Beveridge, N. J., Gardiner, E. J., Carroll, A. P., Tooney, P. A., & Cairns, M. J. (2009) · Molecular Psychiatry · doi:10.1038/mp.2009.84 · Cited by 431 · see citing works

MicroRNAs and the cell cycle

Bueno, M. J., & Malumbres, M. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.02.002 · Cited by 409 · see citing works

MicroRNA miR-137 Regulates Neuronal Maturation by Targeting Ubiquitin Ligase Mind Bomb-1

Smrt, R. D., Szulwach, K. E., Pfeiffer, R. L., Li, X., Guo, W., Pathania, M., Teng, Z.-Q., Luo, Y., Peng, J., Bordey, A., et al. (2010) · Stem Cells · doi:10.1002/stem.431 · Cited by 404 · see citing works

Multiple microRNAs modulate p21Cip1/Waf1 expression by directly targeting its 3′ untranslated region

Wu, S., Huang, S., Ding, J., Zhao, Y., Liang, L., Liu, T., Zhan, R., & He, X. (2010) · Oncogene · doi:10.1038/onc.2010.34 · Cited by 394 · see citing works

A microRNA-based gene dysregulation pathway in Huntington's disease

Johnson, R., Zuccato, C., Belyaev, N. D., Guest, D. J., Cattaneo, E. F., & Buckley, N. J. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2007.11.001 · Cited by 360 · see citing works

Mef2‐mediated transcription of the miR379–410 cluster regulates activity‐dependent dendritogenesis by fine‐tuning Pumilio2 protein levels

Fiore, R., Khudayberdiev, S., Christensen, M., Siegel, G., Flavell, S. W., Kim, T., Greenberg, M. E., & Schratt, G. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.10 · Cited by 348 · see citing works

Redefining MicroRNA Targets

Seitz, H. (2009) · Current Biology · doi:10.1016/j.cub.2009.03.059 · Cited by 346 · see citing works

Differential Patterns of MicroRNA Expression in Neuroblastoma Are Correlated with Prognosis, Differentiation, and Apoptosis

Chen, Y., & Stallings, R. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-3667 · Cited by 341 · see citing works

MicroRNAs in apoptosis, autophagy and necroptosis

Su, Z., Yang, Z., Xu, Y., Chen, Y., & Yu, Q. (2015) · Oncotarget · doi:10.18632/oncotarget.3523 · Cited by 340 · see citing works

MicroRNA Expression Is Down-Regulated and Reorganized in Prefrontal Cortex of Depressed Suicide Subjects

Smalheiser, N. R., Lugli, G., Rizavi, H. S., Torvik, V. I., Turecki, G., & Dwivedi, Y. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033201 · Cited by 324 · see citing works

MicroRNAs: a developing story

Pasquinelli, A. E., Hunter, S. E., & Bracht, J. R. (2005) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2005.01.002 · Cited by 323 · see citing works

miR-137 forms a regulatory loop with nuclear receptor TLX and LSD1 in neural stem cells

Sun, G., Ye, P., Murai, K., Lang, M., Li, S., Zhang, H., Li, W., Fu, C., Yin, J., Wang, A., et al. (2011) · Nature Communications · doi:10.1038/ncomms1532 · Cited by 306 · see citing works

Differential Patterns of MicroRNA Expression in Neuroblastoma Are Correlated with Prognosis, Differentiation, and Apoptosis

Arceci, R. J. (2008) · Yearbook of Oncology · doi:10.1016/s1040-1741(08)79165-6 · Cited by 299 · see citing works

Epigenetic Silencing of miR-137 Is an Early Event in Colorectal Carcinogenesis

Balaguer, F., Link, A., Lozano, J. J., Cuatrecasas, M., Nagasaka, T., Boland, C. R., & Goel, A. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-0622 · Cited by 293 · see citing works

MicroRNA-137 Targets Microphthalmia-Associated Transcription Factor in Melanoma Cell Lines

Bemis, L., Chen, R., Amato, C. M., Classen, E. H., Robinson, S. E., Coffey, D. G., Erickson, P. F., Shellman, Y. G., & Robinson, W. A. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-2912 · Cited by 273 · see citing works

Genome-wide association study of recurrent early-onset major depressive disorder

Shi, J., Potash, J. B., Knowles, J. A., Weissman, M. M., Coryell, W. H., Scheftner, W. A., Lawson, W. B., DePaulo, J. R., Gejman, P. V., Sanders, A. R., et al. (2010) · Molecular Psychiatry · doi:10.1038/mp.2009.124 · Cited by 267 · see citing works

Trans-Synaptic Eph Receptor-Ephrin Signaling in Hippocampal Mossy Fiber LTP

Contractor, A., Rogers, C., Maron, C., Henkemeyer, M. J., Swanson, G. T., & Heinemann, S. F. (2002) · Science · doi:10.1126/science.1069081 · Cited by 262 · see citing works

Upregulation of Dicer and MicroRNA Expression in the Dorsolateral Prefrontal Cortex Brodmann Area 46 in Schizophrenia

Santarelli, D. M., Beveridge, N. J., Tooney, P. A., & Cairns, M. J. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.030 · Cited by 255 · see citing works

MicroRNA-137/181c Regulates Serine Palmitoyltransferase and In Turn Amyloid β, Novel Targets in Sporadic Alzheimer's Disease

Geekiyanage, H., & Chan, C. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3883-11.2011 · Cited by 254 · see citing works

Impact of microRNA regulation on variation in human gene expressionPreprint

Lü, J., & Clark, A. G. (2012) · Genome Research · doi:10.1101/gr.132514.111 · Cited by 254 · see citing works

Human TRBP and PACT Directly Interact with Each Other and Associate with Dicer to Facilitate the Production of Small Interfering RNA

Kok, K., Ng, M.-H. J., Ching, Y.-P., & Jin, D. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611768200 · Cited by 239 · see citing works

The schizophrenia risk gene product miR-137 alters presynaptic plasticity

Siegert, S., Seo, J., Kwon, E. J., Rudenko, A., Cho, S., Wang, W., Flood, Z., Martorell, A. J., Ericsson, M., Mungenast, A. E., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4023 · Cited by 224 · see citing works

Chromosome 1p21.3 microdeletions comprising <i>DPYD</i> and <i>MIR137</i> are associated with intellectual disability

Willemsen, M. H., Vallès, A., Kirkels, L. A. M. H., Mastebroek, M., Olde Loohuis, N., Kos, A., Wissink-Lindhout, W. M., de Brouwer, A. P. M., Nillesen, W. M., Pfundt, R., et al. (2011) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2011-100294 · Cited by 202 · see citing works

Validation of schizophrenia-associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR-137 targets

Kwon, E., Wang, W., & Tsai, L.-H. (2013) · Molecular Psychiatry · doi:10.1038/mp.2011.170 · Cited by 200 · see citing works

The Role of MicroRNAs in Biological Processes

Tüfekçi, K. U., Meuwissen, R. L. J., & Genç, Ş. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-748-8_2 · Cited by 195 · see citing works

MicroRNA-137 is downregulated in glioblastoma and inhibits the stemness of glioma stem cells by targeting RTVP-1

Bier, A., Giladi, N., Kronfeld, N., Lee, H. K., Cazacu, S., Finniss, S., Xiang, C., Poisson, L., deCarvalho, A. C., Slavin, S., et al. (2013) · Oncotarget · doi:10.18632/oncotarget.928 · Cited by 191 · see citing works

Genome-wide analysis reveals methyl-CpG–binding protein 2–dependent regulation of microRNAs in a mouse model of Rett syndrome

Wu, H., Tao, J., Chen, P. J., Shahab, A., Ge, W., Hart, R. P., Ruan, X., Ruan, Y., & Sun, Y. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005595107 · Cited by 180 · see citing works

miR‐137 targets Cdc42 expression, induces cell cycle G1 arrest and inhibits invasion in colorectal cancer cells

Liu, M., Lang, N., Qiu, M., Xu, F., Li, Q., Tang, Q., Chen, J., Chen, X., Zhang, S., Liu, Z., et al. (2010) · International Journal of Cancer · doi:10.1002/ijc.25452 · Cited by 166 · see citing works

Distinct roles for paxillin and Hic-5 in regulating breast cancer cell morphology, invasion, and metastasis

Deakin, N. O., & Turner, C. E. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-09-0790 · Cited by 165 · see citing works

miR‐137 inhibits the proliferation of lung cancer cells by targeting Cdc42 and Cdk6

Zhu, X., Li, Y., Shen, H., Li, H. R., Long, L., Hui, L., & Xu, W. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.11.004 · Cited by 162 · see citing works

Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia

Green, M. J., Cairns, M. J., Wu, J. Q., Dragović, M., Jablensky, A. V., Tooney, P. A., Scott, R. J., & Carr, V. J. (2012) · Molecular Psychiatry · doi:10.1038/mp.2012.84 · Cited by 150 · see citing works

miR-137 Inhibits the Invasion of Melanoma Cells through Downregulation of Multiple Oncogenic Target Genes

Luo, C., Tetteh, P. W., Merz, P., Dickes, E., Abukiwan, A., Hotz‐Wagenblatt, A., Holland-Cunz, S. G., Sinnberg, T. W., Schittek, B., Schadendorf, D., et al. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.357 · Cited by 142 · see citing works

miRNA 34a, 100, and 137 modulate differentiation of mouse embryonic stem cells

Tarantino, C., Paolella, G., Cozzuto, L., Minopoli, G., Pastore, L., Parisi, S., & Russo, T. (2010) · The FASEB Journal · doi:10.1096/fj.09-152207 · Cited by 137 · see citing works

L‐type calcium channels and psychiatric disorders: A brief review

Casamassima, F., Hay, A. C., Benedetti, A., Lattanzi, L., Cassano, G. B., & Perlis, R. H. (2010) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31122 · Cited by 136 · see citing works

Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder

Sarachana, T., & Hu, V. W. (2013) · Molecular Autism · doi:10.1186/2040-2392-4-14 · Cited by 135 · see citing works

MIR137 gene and target gene CACNA1C of miR-137 contribute to schizophrenia susceptibility in Han Chinese

Guan, F., Zhang, B., Yan, T., Li, L., Liu, F., Li, T., Feng, Z., Zhang, B., Liu, X., & Li, S. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.11.004 · Cited by 135 · see citing works

miR-137 Is Frequently Down-Regulated in Gastric Cancer and Is a Negative Regulator of Cdc42

Chen, Q., Chen, X., Zhang, M., Fan, Q., Luo, S., & Cao, X. (2011) · Digestive Diseases and Sciences · doi:10.1007/s10620-010-1536-3 · Cited by 135 · see citing works

Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex

Guella, I., Sequeira, A., Rollins, B. L., Morgan, L., Torri, F., van Erp, T. G. M., Myers, R., Barchas, J. D., Schatzberg, A. F., Watson, S. J., et al. (2013) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2013.05.021 · Cited by 132 · see citing works

miRNA expression profiling of lung adenocarcinomas: correlation with mutational status

Đačić, S., Kelly, L. M., Shuai, Y., & Nikiforova, M. N. (2010) · Modern Pathology · doi:10.1038/modpathol.2010.152 · Cited by 130 · see citing works

MicroRNA-137, an HMGA1 Target, Suppresses Colorectal Cancer Cell Invasion and Metastasis in Mice by Directly Targeting FMNL2

Li, L., Li, X., Zhang, X., Lv, Z., He, G., Zhao, W., Ren, X., Li, Y., Bian, X., Liao, W., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.11.033 · Cited by 126 · see citing works

Potential Impact of miR-137 and Its Targets in Schizophrenia

Wright, C., Turner, J., Calhoun, V., & Perrone-Bizzozero, N. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00058 · Cited by 124 · see citing works

Epigenetics, MicroRNAs, and Carcinogenesis: Functional Role of MicroRNA-137 in Uveal Melanoma

Chen, X., Wang, J., Shen, H., Lü, J., Li, C., Hu, D., Dong, X. D., Yan, D., & Tu, L. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-5272 · Cited by 124 · see citing works

MicroRNA-137 promoter methylation in oral rinses from patients with squamous cell carcinoma of the head and neck is associated with gender and body mass index

Langevin, S. M., Stone, R. A., Bunker, C. H., Grandis, J. R., Sobol, R. W., & Taioli, E. (2010) · Carcinogenesis · doi:10.1093/carcin/bgq051 · Cited by 123 · see citing works

MiR-137 Targets Estrogen-Related Receptor Alpha and Impairs the Proliferative and Migratory Capacity of Breast Cancer Cells

Zhao, Y., Li, Y., Lou, G., Zhao, L., Xu, Z., Zhang, Y., & He, F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039102 · Cited by 120 · see citing works

The genome-wide supported microRNA-137 variant predicts phenotypic heterogeneity within schizophrenia

Lett, T. A. P., Chakavarty, M. M., Felsky, D., Brandl, E. J., Tiwari, A. K., Gonçalves, V. F., Rajji, T. K., Daskalakis, Z. J., Meltzer, H. Y., Lieberman, J. A., et al. (2013) · Molecular Psychiatry · doi:10.1038/mp.2013.17 · Cited by 119 · see citing works

Identifying gene regulatory networks in schizophrenia

Potkin, S. G., Macciardi, F. M., Guffanti, G., Fallon, J. H., Wang, Q., Turner, J. A., Lakatos, A., Miles, M. F., Lander, A. D., Vawter, M. P., et al. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.036 · Cited by 112 · see citing works

MiR‐137 functions as a tumor suppressor in neuroblastoma by downregulating KDM1A

Althoff, K., Beckers, A., Odersky, A., Mestdagh, P., Köster, J., Bray, I. M., Bryan, K. R., Vandesompele, J., Speleman, F., Stallings, R. L., et al. (2013) · International Journal of Cancer · doi:10.1002/ijc.28091 · Cited by 109 · see citing works

miR-148 Regulates Mitf in Melanoma Cells

Haflidadóttir, B. S., Bergsteinsdóttir, K., Praetorius, C., & Steingrı́msson, E. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011574 · Cited by 109 · see citing works

MicroRNA‐137 promoter methylation is associated with poorer overall survival in patients with squamous cell carcinoma of the head and neck

Langevin, S. M., Stone, R. A., Bunker, C. H., Lyons‐Weiler, M. A., LaFramboise, W. A., Kelly, L. A., Seethala, R. R., Grandis, J. R., Sobol, R. W., & Taioli, E. (2010) · Cancer · doi:10.1002/cncr.25689 · Cited by 109 · see citing works

Micro-RNAs miR125b and miR137 are frequently upregulated in response to capecitabine chemoradiotherapy of rectal cancer

Svoboda (1992) · International Journal of Oncology · doi:10.3892/ijo_00000038 · Cited by 108 · see citing works

B-Ephrin Reverse Signaling Is Required for NMDA-Independent Long-Term Potentiation of Mossy Fibers in the Hippocampus

Armstrong, J. N., Saganich, M. J., Xu, N., Henkemeyer, M. J., Heinemann, S. F., & Contractor, A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4338-05.2006 · Cited by 108 · see citing works

miR-137 is frequently down-regulated in glioblastoma and is a negative regulator of Cox-2

Chen, L., Wang, X., Wang, H., Li, Y., Yan, W., Han, L., Zhang, K., Zhang, J., Wang, Y., Feng, Y., et al. (2012) · European Journal of Cancer · doi:10.1016/j.ejca.2012.02.007 · Cited by 107 · see citing works

FoxD3-regulated microRNA-137 suppresses tumour growth and metastasis in human hepatocellular carcinoma by targeting AKT2

Liu, L.-L., Lu, S.-X., Li, M., Li, L.-Z., Fu, J., Hu, W., Yang, Y., Luo, R.-Z., Zhang, C. Z., & Yun, J. (2014) · Oncotarget · doi:10.18632/oncotarget.2089 · Cited by 107 · see citing works

Ephrin reverse signaling in axon guidance and synaptogenesis

Xu, N., & Henkemeyer, M. J. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.10.024 · Cited by 102 · see citing works

MicroRNA Role in Thyroid Cancer Development

Marini, F., Luzi, E., & Brandi, M. L. (2011) · Journal of Thyroid Research · doi:10.4061/2011/407123 · Cited by 90 · see citing works

Experimental validation of candidate schizophrenia gene ZNF804A as target for hsa-miR-137

Kim, A. H., Parker, E. K., Williamson, V. S., McMichael, G. O., Fanous, A. H., & Vladimirov, V. I. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.06.038 · Cited by 90 · see citing works

MLK3 Regulates Paxillin Phosphorylation in Chemokine-Mediated Breast Cancer Cell Migration and Invasion to Drive Metastasis

Chen, J., & Gallo, K. A. (2012) · Cancer Research · doi:10.1158/0008-5472.can-12-0655 · Cited by 89 · see citing works

Review: Cancer and schizophrenia: is there a paradox?

Hodgson, R. E., Wildgust, H. J., & Bushe, C. (2010) · Journal of Psychopharmacology · doi:10.1177/1359786810385489 · Cited by 83 · see citing works

Impact of a microRNA MIR137 Susceptibility Variant on Brain Function in People at High Genetic Risk of Schizophrenia or Bipolar Disorder

Whalley, H. C., Papmeyer, M., Romaniuk, L., Sprooten, E., Johnstone, E. C., Hall, J., Lawrie, S. M., Evans, K. L., Blumberg, H. P., Sussmann, J. E., et al. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.137 · Cited by 81 · see citing works

Schizophrenia miR-137 Locus Risk Genotype Is Associated with Dorsolateral Prefrontal Cortex Hyperactivation

van Erp, T. G. M., Guella, I., Vawter, M. P., Turner, J. A., Brown, G. G., McCarthy, G., Greve, D. N., Glover, G. H., Calhoun, V. D., Lim, K. O., et al. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.06.016 · Cited by 77 · see citing works

Dysregulation of REST ‐regulated coding and non‐coding RNA s in a cellular model of Huntington's disease

Soldati, C., Bithell, A., Johnston, C., Wong, K., Stanton, L. W., & Buckley, N. J. (2012) · Journal of Neurochemistry · doi:10.1111/jnc.12090 · Cited by 76 · see citing works

Small RNAs Guide Hematopoietic Cell Differentiation and Function

Navarro, F., & Lieberman, J. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0902567 · Cited by 73 · see citing works

Epigenetic silencing of miR-137 is a frequent event in gastric carcinogenesis

Steponaitienė, R., Kupčinskas, J., Langner, C., Balaguer, F., Venclauskas, L., Paužas, H., Tamelis, A., Skiecevičienė, J., Kupčinskas, L., Malfertheiner, P., et al. (2015) · Molecular Carcinogenesis · doi:10.1002/mc.22287 · Cited by 69 · see citing works

MicroRNA-137 Targets Carboxyl-terminal Binding Protein 1 in Melanoma Cell Lines

Deng, Y., Deng, H., Bi, F., Liu, J., Bemis, L., Norris, D. A., Wang, X., & Zhang, Q. (2011) · International Journal of Biological Sciences · doi:10.7150/ijbs.7.133 · Cited by 69 · see citing works

Tumor suppressive microRNA-137 negatively regulates Musashi-1 and colorectal cancer progression

Smith, A. R., Marquez, R. T., Tsao, W.-C., Pathak, S., Roy, A. R., Ping, J., Wilkerson, B., Lan, L., Meng, W., Neufeld, K. L., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.3726 · Cited by 68 · see citing works

Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137

Cummings, E., Donohoe, G. J., Hargreaves, A., Moore, S., Fahey, C., Dinan, T. G., McDonald, C., O’Callaghan, E., O’Neill, F. A., Waddington, J. L., et al. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.08.065 · Cited by 68 · see citing works

Neurexin-1 and Frontal Lobe White Matter: An Overlapping Intermediate Phenotype for Schizophrenia and Autism Spectrum Disorders

Voineskos, A. N., Lett, T. A. P., Lerch, J. P., Tiwari, A. K., Ameis, S. H., Rajji, T. K., Müller, D. J., Mulsant, B. H., & Kennedy, J. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020982 · Cited by 67 · see citing works

miR-137 suppresses cell growth in ovarian cancer by targeting AEG-1

Guo, J., Xia, B., Meng, F., & Lou, G. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.10.052 · Cited by 60 · see citing works

A direct molecular link between the autism candidate gene RORa and the schizophrenia candidate MIR137

Devanna, P., & Vernes, S. C. (2014) · Scientific Reports · doi:10.1038/srep03994 · Cited by 59 · see citing works

Affinity purification of microRNA-133a with the cardiac transcription factor, Hand2

Vo, N., Dalton, R. P., Liu, N., Olson, E. N., & Goodman, R. H. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013162107 · Cited by 57 · see citing works

The impact of microRNA expression on cellular proliferation

Lenkala, D., LaCroix, B. L., Gamazon, E. R., Geeleher, P., Im, H. K., & Huang, R. S. (2014) · Human Genetics · doi:10.1007/s00439-014-1434-4 · Cited by 56 · see citing works

Regulation of Huntingtin Gene Expression by miRNA-137, -214, -148a, and Their Respective isomiRs

Kozłowska, E., Krzyżosiak, W. J., & Kościańska, E. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140816999 · Cited by 55 · see citing works

MicroRNA-137 represses Klf4 and Tbx3 during differentiation of mouse embryonic stem cells

Jiang, K., Ren, C., & Nair, V. D. (2013) · Stem Cell Research · doi:10.1016/j.scr.2013.09.001 · Cited by 53 · see citing works

Phenotypic effects of a bipolar liability gene among individuals with major depressive disorder

Casamassima, F., Huang, J., D, M. F. M., Sachs, G. S., Smoller, J. W., Cassano, G. B., Lattanzi, L., Fagerness, J., Stange, J. P., & Perlis, R. H. (2009) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30962 · Cited by 53 · see citing works

Transcriptional targets of the schizophrenia risk gene MIR137

Collins, A. L., Kim, Y., Bloom, R. J., Kelada, S. N. P., Sethupathy, P., & Sullivan, P. F. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.42 · Cited by 52 · see citing works

The Therapeutic Potential of microRNAs in Nervous System Damage, Degeneration, and Repair

Hutchison, E. R., Okun, E., & Mattson, M. P. (2009) · NeuroMolecular Medicine · doi:10.1007/s12017-009-8086-x · Cited by 51 · see citing works

MIR ‐137 Suppresses Growth and Invasion, is Downregulated in Oligodendroglial Tumors and Targets CSE1L

Li, K. K., Yang, L., Pang, J. C., Chan, A. K., Zhou, L., Mao, Y. Q., Wang, Y., Lau, K., Poon, W. S., Shi, Z., et al. (2012) · Brain Pathology · doi:10.1111/bpa.12015 · Cited by 49 · see citing works

miR‐137 inhibits proliferation of melanoma cells by targeting PAK 2

Hao, S., Luo, C., Abukiwan, A., Wang, G., He, J., Huang, L., Weber, C. E. M., Lv, N., Xiao, X., Eichmüller, S. B., et al. (2015) · Experimental Dermatology · doi:10.1111/exd.12812 · Cited by 44 · see citing works

Paxillin mutations affect focal adhesions and lead to altered mitochondrial dynamics

Kawada, I., Hasina, R., Lennon, F. E., Bindokas, V. P., Usatyuk, P. V., Tan, Y. C., Krishnaswamy, S., Arif, Q., Carey, G. B., Hseu, R. D., et al. (2013) · Cancer Biology & Therapy · doi:10.4161/cbt.25091 · Cited by 44 · see citing works

microRNAs and thyroid cancer: Biological and clinical significance

Leonardi, G. C., Candido, S., CARBONE, M., Colaianni, V., Garozzo, S. F., Cinà, D., & Libra, M. (2012) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2012.1089 · Cited by 43 · see citing works

microRNA-137 modulates pancreatic cancer cells tumor growth, invasion and sensitivity to chemotherapy.

Xiao, J., Peng, F., Yu, C., Wang, M., Li, X., Li, Z., Jiang, J., & Sun, C. (2014) · Europe PMC (PubMed Central) · Cited by 43 · see citing works

A GWAS SNP for Schizophrenia Is Linked to the Internal MIR137 Promoter and Supports Differential Allele-Specific Expression

Warburton, A., Breen, G. D., Bubb, V. J., & Quinn, J. P. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv144 · Cited by 40 · see citing works

miR-137 regulates epithelial-mesenchymal transition in gastrointestinal stromal tumor

Liu, S., Cui, J., Liao, G., Zhang, Y., Ye, K., Lu, T., Qi, J., & Wan, G. (2014) · Tumor Biology · doi:10.1007/s13277-014-2177-5 · Cited by 38 · see citing works

miR-137 impairs the proliferative and migratory capacity of human non-small cell lung cancer cells by targeting paxillin

Bi, Y., Han, Y. P., Bi, H., Gao, F., & Wang, X. (2013) · Human Cell · doi:10.1007/s13577-013-0085-4 · Cited by 35 · see citing works

Genetic association study of the P300 endophenotype in schizophrenia

Decoster, J., Binder, M. D., Viechtbauer, W., Nagels, G., Myin‐Germeys, I., Peuskens, J., van Os, J., & van Winkel, R. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.07.018 · Cited by 35 · see citing works

miR-137, a new target for post-stroke depression?

Zhao, L., Li, H., Guo, R.-Y., Ma, T., Hou, R., Ma, X., & Du, Y. (2013) · PubMed Central · doi:10.3969/j.issn.1673-5374.2013.26.005 · Cited by 34 · see citing works

Disruption of the MicroRNA 137 Primary Transcript Results in Early Embryonic Lethality in Mice

Crowley, J. J., Collins, A. L., Lee, R. J., Nonneman, R. J., Farrell, M. S., Ancalade, N., Mugford, J. W., Agster, K. L., Nikolova, V. D., Moy, S. S., et al. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.05.022 · Cited by 33 · see citing works

Ontogeny of small RNA in the regulation of mammalian brain development

Hollins, S. L., Goldie, B. J., Carroll, A. P., Mason, E. A., Walker, F. R., Eyles, D. W., & Cairns, M. J. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-777 · Cited by 30 · see citing works

MicroRNA-137 is downregulated in human osteosarcoma and regulates cell proliferation and migration through targeting FXYD6

Li, Z., Zhang, H., Wang, Y.-X., & Wang, W. (2015) · Journal of drug targeting · doi:10.3109/1061186x.2015.1057149 · Cited by 28 · see citing works

Developmental suppression of schizophrenia-associated miR-137 alters sensorimotor function in zebrafish

Giacomotto, J., Carroll, A. P., Rinkwitz, S., Mowry, B. J., Cairns, M. J., & Becker, T. S. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.88 · Cited by 24 · see citing works

Anti-epileptic effects of neuropeptide Y gene transfection into the rat brain

Zhao, W., Dong, C., Li, W., Lv, P., & Dong, X. (2013) · Neural Regeneration Research · doi:10.4103/1673-5374.121651 · Cited by 19 · see citing works

RNA-Dependent Intergenerational Inheritance of Enhanced Synaptic Plasticity After Environmental Enrichment

Benito, E., Kerimoglu, C., Ramachandran, B., Pena‐Centeno, T., Jain, G., Stilling, R. M., Islam, R., Capece, V., Zhou, Q., Edbauer, D., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.059 · Cited by 155 · see citing works

Neurobiological perspective of 22q11.2 deletion syndrome

Zinkstok, J., Boot, E., Bassett, A. S., Hiroi, N., Butcher, N. J., Vingerhoets, C., Vorstman, J. A. S., & van Amelsvoort, T. (2019) · The Lancet Psychiatry · doi:10.1016/s2215-0366(19)30076-8 · Cited by 132 · see citing works

Double-Edged Sword of Tumour Suppressor Genes in Schizophrenia

Zhuo, C., Wang, D., Zhou, C., Chen, C., Li, J., Tian, H., Li, S., Ji, F., Liu, C., Chen, M., et al. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00001 · Cited by 127 · see citing works

Increased miR‐34c mediates synaptic deficits by targeting synaptotagmin 1 through ROS‐JNK‐p53 pathway in Alzheimer’s Disease

Shi, Z., Zhang, K., Zhou, H., Jiang, L., Xie, B., Wang, R., Xia, W., Yin, Y., Gao, Z., Cui, D., et al. (2020) · Aging Cell · doi:10.1111/acel.13125 · Cited by 115 · see citing works

Sperm microRNAs confer depression susceptibility to offspring

Wang, Y., Chen, Z., Hu, H., Lei, J., Zhou, Z., Yao, B., Chen, L., Liang, G., Zhan, S., Zhu, X., et al. (2021) · Science Advances · doi:10.1126/sciadv.abd7605 · Cited by 108 · see citing works

LSD1/KDM1A, a Gate-Keeper of Cancer Stemness and a Promising Therapeutic Target

Karakaidos, P., Verigos, J., & Magklara, A. (2019) · Cancers · doi:10.3390/cancers11121821 · Cited by 108 · see citing works

Epigenomic Dysregulation in Schizophrenia: In Search of Disease Etiology and Biomarkers

Khavari, B., & Cairns, M. J. (2020) · Cells · doi:10.3390/cells9081837 · Cited by 106 · see citing works

miR-137 boosts the neuroprotective effect of endothelial progenitor cell-derived exosomes in oxyhemoglobin-treated SH-SY5Y cells partially via COX2/PGE2 pathway

Li, Y., Wang, J., Chen, S., Wu, P., Xu, S., Wang, C., Shi, H., & Bihl, J. C. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01836-y · Cited by 98 · see citing works

Mitochondrial, exosomal miR137-COX6A2 and gamma synchrony as biomarkers of parvalbumin interneurons, psychopathology, and neurocognition in schizophrenia

Khadimallah, I., Jenni, R., Cabungcal, J.-H., Cleusix, M., Fournier, M., Béard, E., Klauser, P., Knebel, J., Murray, M. M., Retsa, C., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01313-9 · Cited by 88 · see citing works

Circular RNA biogenesis is decreased in postmortem cortical gray matter in schizophrenia and may alter the bioavailability of associated miRNA

Mahmoudi, E., Fitzsimmons, C., Geaghan, M. P., Shannon Weickert, C., Atkins, J. R., Wang, X., & Cairns, M. J. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0348-1 · Cited by 73 · see citing works

Dysregulation of mi RNA and its potential therapeutic application in schizophrenia

Cao, T., & Zhen, X. (2018) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12840 · Cited by 71 · see citing works

Diagnostic value of blood-derived microRNAs for schizophrenia: results of a meta-analysis and validation

Liu, S., Zhang, F., Wang, X., Shugart, Y. Y., Zhao, Y., Li, X., Liu, Z., Sun, N., Yang, C., Zhang, K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-15751-5 · Cited by 69 · see citing works

Interpreting the impact of noncoding structural variation in neurodevelopmental disorders

D’haene, E., & Vergult, S. (2020) · Genetics in Medicine · doi:10.1038/s41436-020-00974-1 · Cited by 60 · see citing works

miR-137 attenuates Aβ-induced neurotoxicity through inactivation of NF-κB pathway by targeting TNFAIP1 in Neuro2a cells

He, D., Tan, J., & Zhang, J. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.06.144 · Cited by 61 · see citing works

MicroRNAs as critical biomarkers of major depressive disorder: a comprehensive perspective

Ortega, M. A., Alvarez-Mon, M. A., García-Montero, C., Fraile-Martinez, O., Lahera, G., Monserrat, J., Muñoz-Merida, L., Mora, F., Rodríguez-Jiménez, R., Fernandez-Rojo, S., et al. (2021) · Biomedicines · doi:10.3390/biomedicines9111659 · Cited by 57 · see citing works

Therapy resistance in neuroblastoma: Mechanisms and reversal strategies

Zhou, X., Wang, X., Li, N., Guo, Y. A., Yang, X., & Lei, Y. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1114295 · Cited by 56 · see citing works

Hippocampal TET1 and TET2 Expression and DNA Hydroxymethylation Are Affected by Physical Exercise in Aged Mice

Jessop, P., & Toledo‐Rodriguez, M. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00045 · Cited by 55 · see citing works

Mutant KRAS promotes liver metastasis of colorectal cancer, in part, by upregulating the MEK-Sp1-DNMT1-miR-137-YB-1-IGF-IR signaling pathway

Chu, P., Lin, P., Wu, H.-Y., Lin, K., Wu, C. S.-Y., Bekaii‐Saab, T., Lin, Y., Lee, C., Lee, J.-C., & Chen, C. (2018) · Oncogene · doi:10.1038/s41388-018-0222-3 · Cited by 54 · see citing works

Multi-biomarker responses to pesticides in an agricultural population from Central Brazil

Ramos, J. S. A., Pedroso, T. M. A., Godoy, F. R., Batista, R. E., de Almeida, F. B., Francelin, C., Ribeiro, F. L., Parise, M. R., & Silva, D. D. M. E. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.141893 · Cited by 54 · see citing works

The role of microRNAs in neurobiology and pathophysiology of the hippocampus

Rashidi, S. K., Kalirad, A., Rafie, S., Behzad, E., & Dezfouli, M. A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1226413 · Cited by 51 · see citing works

A comprehensive review of the genetic and biological evidence supports a role for MicroRNA‐137 in the etiology of schizophrenia

Sakamoto, K., & Crowley, J. J. (2017) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32554 · Cited by 48 · see citing works

A set of microRNAs coordinately controls tumorigenesis, invasion, and metastasis

Michael, I. P., Saghafinia, S., & Hanahan, D. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1913307116 · Cited by 52 · see citing works

Site‐specific metastasis: A cooperation between cancer cells and the metastatic microenvironment

Izraely, S., & Witz, I. P. (2020) · International Journal of Cancer · doi:10.1002/ijc.33247 · Cited by 49 · see citing works

M2 Microglia-Derived Exosomes Protect Against Glutamate-Induced HT22 Cell Injury via Exosomal miR-124-3p

Zhu, L., Ma, L., Du, X., Jiang, Y., Gao, J., Fan, Z., Zheng, H., Zhu, J., & Zhang, G. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04075-x · Cited by 45 · see citing works

MiR‐137 inhibited inflammatory response and apoptosis after spinal cord injury via targeting of MK2

Gao, L., Dai, C., Feng, Z., Zhang, L., & Zhang, Z. (2017) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26489 · Cited by 45 · see citing works

miR-137: A Novel Therapeutic Target for Human Glioma

Wang, Y., Chen, R., Zhou, X., Guo, R., Yin, J., Li, Y., & Ma, G. (2020) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2020.06.028 · Cited by 43 · see citing works

Targeted inhibition of HDAC8 increases the doxorubicin sensitivity of neuroblastoma cells via up regulation of miR-137

Zhao, G., Wang, G., Bai, H., Li, T., Gong, F., Yang, H., Wen, J., & Wang, W. (2017) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2017.02.035 · Cited by 41 · see citing works

Manipulating microRNAs for the Treatment of Malignant Pleural Mesothelioma: Past, Present and Future

Reid, G., Johnson, T. G., & van Zandwijk, N. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00105 · Cited by 41 · see citing works

Neurodevelopment regulators miR-137 and miR-34 family as biomarkers for early and adult onset schizophrenia

Chen, B.-Y., Lin, J., Lu, M.-K., Tan, H.-P., Jang, F.-L., & Lin, S. (2021) · Schizophrenia · doi:10.1038/s41537-021-00164-1 · Cited by 40 · see citing works

Redundant and incoherent regulations of multiple phenotypes suggest microRNAs’ role in stability controlPreprint

Liufu, Z., Zhao, Y., Guo, L., Miao, G., Xiao, J., Lyu, Y., Chen, Y., Shi, S., Tang, T., & Wu, C. (2017) · Genome Research · doi:10.1101/gr.222505.117 · Cited by 39 · see citing works

Brain Targeting of Citicoline Sodium via Hyaluronic Acid-Decorated Novel Nano-Transbilosomes for Mitigation of Alzheimer’s Disease in a Rat Model: Formulation, Optimization, in vitro and in vivo Assessment

AbouElhassan, K. M., Sarhan, H. A., Hussein, A. K., Taye, A., Ahmed, Y. M., & Safwat, M. A. (2022) · International Journal of Nanomedicine · doi:10.2147/ijn.s381353 · Cited by 40 · see citing works

LncRNA GAS5 and miR-137 Polymorphisms and Expression are Associated with Multiple Sclerosis Risk: Mechanistic Insights and Potential Clinical Impact

Senousy, M. A., Shaker, O. G., Sayed, N. H., Fathy, N., & Kortam, M. A. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00150 · Cited by 39 · see citing works

Exosome-based strategies for diagnosis and therapy of glioma cancer

Fath, M. K., Azami, J., Masoudi, A., Mosaddeghi-Heris, R., Rahmani, E., Alavi, F., Bahrami, A. A., Payandeh, Z., Khalesi, B., Dadkhah, M., et al. (2022) · Cancer Cell International · doi:10.1186/s12935-022-02642-7 · Cited by 39 · see citing works

A CREB2-targeting microRNA is required for long-term memory after single-trial learning

Korneev, S. A., Vavoulis, D. V., Naskar, S., Dyakonova, V. E., Kemenes, I., & Kemenes, G. (2018) · Scientific Reports · doi:10.1038/s41598-018-22278-w · Cited by 38 · see citing works

Schizophrenia-Associated MicroRNA–Gene Interactions in the Dorsolateral Prefrontal Cortex

Santarelli, D. M., Carroll, A. P., Cairns, H. M., Tooney, P. A., & Cairns, M. J. (2019) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2019.10.003 · Cited by 38 · see citing works

Dysregulation of circRNA expression in the peripheral blood of individuals with schizophrenia and bipolar disorder

Mahmoudi, E., Green, M. J., & Cairns, M. J. (2021) · Journal of Molecular Medicine · doi:10.1007/s00109-021-02070-6 · Cited by 37 · see citing works

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

Fiksinski, A., Schneider, M., Zinkstok, J., Baribeau, D. A., Chawner, S. J. R. A., & Vorstman, J. A. S. (2021) · Current Psychiatry Reports · doi:10.1007/s11920-021-01225-z · Cited by 38 · see citing works

An epigenetic basis for an omnigenic model of psychiatric disorders

Peedicayil, J., & Grayson, D. R. (2018) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2018.01.027 · Cited by 35 · see citing works

Multifaceted Regulation of MicroRNA Biogenesis: Essential Roles and Functional Integration in Neuronal and Glial Development

Suster, I., & Feng, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136765 · Cited by 37 · see citing works

MicroRNA-137 Drives Epigenetic Reprogramming in the Adult Amygdala and Behavioral Changes after Adolescent Alcohol Exposure

Kyzar, E. J., Bohnsack, J. P., Zhang, H., & Pandey, S. C. (2019) · eNeuro · doi:10.1523/eneuro.0401-19.2019 · Cited by 32 · see citing works

The Significant Role of microRNAs in Gliomas Angiogenesis: A Particular Focus on Molecular Mechanisms and Opportunities for Clinical Application

Mafi, A., Mannani, R., Khalilollah, S., Hedayati, N., Salami, R., Rezaee, M., Dehmordi, R. M., Ghorbanhosseini, S. S., Alimohammadi, M., & Akhavan‐Sigari, R. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01385-x · Cited by 33 · see citing works

The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratio

Holm, A., Possovre, M.-L., Bandarabadi, M., Moseholm, K. F., Justinussen, J. L., Bozic, I., Lemcke, R., Arribat, Y., Amati, F., Silahtaroglu, A., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2112225119 · Cited by 32 · see citing works

MiR-137 Deficiency Causes Anxiety-Like Behaviors in Mice

Yan, H., Sun, X., Wang, Z., Liu, P., Mi, T., Liu, C., Wang, Y., He, X., Du, H., Liu, C., et al. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00260 · Cited by 29 · see citing works

Ubiquitin Signaling Regulates RNA Biogenesis, Processing, and Metabolism

Thapa, P. S., Shanmugam, N., & Pokrzywa, W. (2019) · BioEssays · doi:10.1002/bies.201900171 · Cited by 29 · see citing works

MicroRNA-22 Controls Aberrant Neurogenesis and Changes in Neuronal Morphology After Status Epilepticus

Beamer, E. H., Jurado‐Arjona, J., Jimenez-Mateos, E. M., Morgan, J., Reschke, C. R., Kenny, A., de Leo, G., Olivos-Oré, L. A., Arribas-Blázquez, M., Madden, S. F., et al. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00442 · Cited by 27 · see citing works

Small nucleolar RNA host gene 1 promotes development and progression of colorectal cancer through negative regulation of miR‐137

Fu, Y., Yin, Y., Peng, S., Yang, G., Yu, Y., Guo, C., Qin, Y., Zhang, X., Xu, W., & Qin, Y. (2019) · Molecular Carcinogenesis · doi:10.1002/mc.23101 · Cited by 28 · see citing works

MicroRNA-22 exerts its neuroprotective and angiogenic functions via regulating PI3K/Akt signaling pathway in cerebral ischemia–reperfusion rats

Wang, X., Shi, C., Pan, H., Meng, X., & Ji, F. (2019) · Journal of Neural Transmission · doi:10.1007/s00702-019-02124-7 · Cited by 28 · see citing works

Artificial Intelligence and the detection of pediatric concussion using epigenomic analysis

Bahado-Singh, R. O., Vishweswaraiah, S., Er, A., Aydas, B., Türkoğlu, O., Taşkın, B. D., Duman, M., Yılmaz, D., & Radhakrishna, U. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146510 · Cited by 27 · see citing works

MiR-194-5p serves as a potential biomarker and regulates the proliferation and apoptosis of hippocampus neuron in children with temporal lobe epilepsy

Niu, X., Zhu, H., Liu, Q., Yan, J.-F., & Li, M.-L. (2021) · Journal of the Chinese Medical Association · doi:10.1097/jcma.0000000000000518 · Cited by 27 · see citing works

Current and Future Perspectives of Noncoding RNAs in Brain Function and Neuropsychiatric Disease

Kyzar, E. J., Bohnsack, J. P., & Pandey, S. C. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.08.013 · Cited by 27 · see citing works

D2 receptor-mediated miRNA-143 expression is associated with the effects of antipsychotic drugs on phencyclidine-induced schizophrenia-related locomotor hyperactivity and with Neuregulin-1 expression in mice

Wang, P., Cao, T., Chen, J., Jiang, Y., Wang, C., Waddington, J. L., & Zhen, X. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107675 · Cited by 27 · see citing works

A nanobiosensor based on graphene oxide and DNA binding dye for multi-microRNAs detection

Rahaie, M., & Noroozi, S. K. (2019) · Bioscience Reports · doi:10.1042/bsr20181404 · Cited by 27 · see citing works

Identification of miR-24 and miR-137 as novel candidate multiple sclerosis miRNA biomarkers using multi-staged data analysis protocol.

Ehya, F., Tehrani, H. A., Garshasbi, M., & Nabavi, S. M. (2017) · PubMed Central · doi:10.22099/mbrc.2017.24861.1256 · Cited by 26 · see citing works

Transgenic mice overexpressing miR-137 in the brain show schizophrenia-associated behavioral deficits and transcriptome profiles

Arakawa, Y., Yokoyama, K., Tasaki, S., Kato, J., Nakashima, K., Takeyama, M., Nakatani, A., & Suzuki, M. (2019) · PLoS ONE · doi:10.1371/journal.pone.0220389 · Cited by 26 · see citing works

miR-137 acts as a tumor suppressor via inhibiting CXCL12 in human glioblastoma

Li, D., Wei, S., Fang, Y., Wang, P., & Li, J. (2017) · Oncotarget · doi:10.18632/oncotarget.20589 · Cited by 24 · see citing works

Lessons Learned From Parsing Genetic Risk for Schizophrenia Into Biological Pathways

Pergola, G., Penzel, N., Sportelli, L., & Bertolino, A. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.10.009 · Cited by 24 · see citing works

Identifying the differentially expressed peripheral blood microRNAs in psychiatric disorders: a systematic review and meta-analysis

Liu, X., Dong, L., Jiang, Z., Song, M., & Yan, P. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1390366 · Cited by 24 · see citing works

SYNCRIP controls miR-137 and striatal learning in animal models of methamphetamine abstinence

Kim, B. S., Tag, S. H., Nam, E., Ham, S., Ahn, S., Kim, J., Cho, D., Lee, S.-J., Yang, Y., Lee, S. E., et al. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2022.02.030 · Cited by 23 · see citing works

Non-Coding RNAs in the Regulation of Hippocampal Neurogenesis and Potential Treatment Targets for Related Disorders

Tan, Z., Li, W., Cheng, X., Zhu, Q., & Zhang, X. (2022) · Biomolecules · doi:10.3390/biom13010018 · Cited by 24 · see citing works

Extracellular vesicles from medicated plasma of Buyang Huanwu decoction-preconditioned neural stem cells accelerate neurological recovery following ischemic stroke

Long, J., Gu, C., Zhang, Q., Liu, J., Huang, J., Li, Y., Zhang, Y., Li, R., Ahmed, W., Zhang, J., et al. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1096329 · Cited by 23 · see citing works

A direct regulatory link between microRNA-137 and SHANK2: implications for neuropsychiatric disorders

Cortabitarte, A. D. S., Berkel, S., Cristian, F.-B., Fischer, C., & Rappold, G. (2018) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-018-9233-1 · Cited by 23 · see citing works

The Impact of Environmental Factors on 5-Hydroxymethylcytosine in the Brain

Kochmanski, J. J., & Bernstein, A. I. (2020) · Current Environmental Health Reports · doi:10.1007/s40572-020-00268-3 · Cited by 21 · see citing works

MIR137 polygenic risk is associated with schizophrenia and affects functional connectivity of the dorsolateral prefrontal cortex

Liu, S., Li, A., Liu, Y., Li, J., Wang, M., Sun, Y., Qin, W., Yu, C., Jiang, T., & Liu, B. (2019) · Psychological Medicine · doi:10.1017/s0033291719001442 · Cited by 20 · see citing works

Cortical cellular diversity and development in schizophrenia

Price, A. J., Jaffe, A. E., & Weinberger, D. R. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0775-8 · Cited by 20 · see citing works

The “missing heritability”—Problem in psychiatry: Is the interaction of genetics, epigenetics and transposable elements a potential solution?

van Calker, D., & Serchov, T. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.03.019 · Cited by 19 · see citing works

Dysregulated miRNAs in bone cells of patients with Gorham‐Stout disease

Rossi, M., Rana, I., Buonuomo, P. S., Battafarano, G., Mariani, E., D’Agostini, M., Porzio, O., Martino, V. D., Minisola, S., Macchiaiolo, M., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202001904rr · Cited by 19 · see citing works

MicroRNA Methylome Signature and Their Functional Roles in Colorectal Cancer Diagnosis, Prognosis, and Chemoresistance

Baharudin, R., Bakarurraini, N. Q. R., Ismail, I., Lee, L., & Mutalib, N. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137281 · Cited by 18 · see citing works

Proliferation of bovine myoblast by LncPRRX1 via regulation of the miR-137/CDC42 axis

Zhang, W., Sun, B., Zhao, Y., Raza, S. H. A., Li, Y., Wang, J., Ma, X., Almohaimeed, H. M., Shaheen, S. Y., Al-Sarraj, F. M., et al. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.08.018 · Cited by 18 · see citing works

Exploring the Role of microRNAs in Glioma Progression, Prognosis, and Therapeutic Strategies

Tluli, O., Al-Maadhadi, M., Al-Khulaifi, A. A., Akomolafe, A. F., Al-Kuwari, S. Y., Al-Khayarin, R. S., Maccalli, C., & Pedersen, S. (2023) · Cancers · doi:10.3390/cancers15174213 · Cited by 18 · see citing works

From molecular pathogenesis to therapy: Unraveling non-coding RNAs/DNMT3A axis in human cancers

Huang, C., & Zarch, S. M. A. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116107 · Cited by 17 · see citing works

Synergistic effect of mesenchymal stem cell-derived extracellular vesicle and miR-137 alleviates autism-like behaviors by modulating the NF-κB pathway

Qin, Q., Shan, Z., Xing, L., Jiang, Y., Li, M., Fan, L., Zeng, X., Ma, X., Zheng, D., Wang, H., et al. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05257-w · Cited by 17 · see citing works

The role of exosomes derived from stem cells in nerve regeneration: A contribution to neurological repair

Zhang, Q., Liu, J., Wang, W., Lin, W., Waqas, A., Duan, W., Huang, S., Zhu, Z., & Chen, L. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114882 · Cited by 17 · see citing works

miR-137 functions as a tumor suppressor gene in pituitary adenoma by targeting AKT2.

Duan, J., Lu, G., Li, Y., Zhou, S., Zhou, D., & Tao, H. (2019) · Europe PMC (PubMed Central) · Cited by 17 · see citing works

The MIR137 VNTR rs58335419 Is Associated With Cognitive Impairment in Schizophrenia and Altered Cortical Morphology

Mahmoudi, E., Atkins, J., Quidé, Y., Reay, W., Cairns, H. M., Fitzsimmons, C., Carr, V., Green, M., & Cairns, M. (2020) · Schizophrenia bulletin · doi:10.1093/schbul/sbaa123 · Cited by 15 · see citing works

Bioinformatic analysis and in vitro validation of a five-microRNA signature as a prognostic biomarker of hepatocellular carcinoma

Li, W., Kong, X., Huang, T., Shen, L., Wu, P., & Chen, Q. (2020) · Annals of Translational Medicine · doi:10.21037/atm-20-2509 · Cited by 16 · see citing works

Non-coding RNAs involved in fibroblast-like synoviocyte functioning in arthritis rheumatoid: From pathogenesis to therapy

Peng, Y., Zhang, M., & Hu, J. (2023) · Cytokine · doi:10.1016/j.cyto.2023.156418 · Cited by 16 · see citing works

Exploring the biological role of postzygotic and germinal de novo mutations in ASD

Alonso-González, A., Calaza, M., Amigo, J., González‐Peñas, J., Martínez-Regueiro, R., Fernández‐Prieto, M., Parellada, M., Arango, C., Rodriguez‐Fontenla, C., & Carracedo, Á. (2021) · Scientific Reports · doi:10.1038/s41598-020-79412-w · Cited by 16 · see citing works

MiR-137 promotes cell growth and inhibits extracellular matrix protein expression in H2O2-induced human trabecular meshwork cells by targeting Src

Wang, L., Tian, Y., Cao, Y., Ma, Q., & Zhao, S. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135902 · Cited by 16 · see citing works

Association of MIR137 With Symptom Severity and Cognitive Functioning in Belarusian Schizophrenia Patients

Kandratsenka, H., Nestsiarovich, A., Goloenko, I., Даниленко, Н. Г., Makarevich, A., Obyedkov, V., Davydenko, O. G., & Waszkiewicz, N. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00295 · Cited by 16 · see citing works

A miR-137–Related Biological Pathway of Risk for Schizophrenia Is Associated With Human Brain Emotion Processing

Pergola, G., Rampino, A., Sportelli, L., Borcuk, C., Passiatore, R., Carlo, P. D., Marakhovskaia, A., Fazio, L., Amoroso, N., Castro, M. N., et al. (2023) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2023.11.001 · Cited by 17 · see citing works

MicroRNA-137-3p Protects PC12 Cells Against Oxidative Stress by Downregulation of Calpain-2 and nNOS

Tang, Y., Li, Y., Yu, G., Ling, Z., Zhong, K., Zilundu, P. L. M., Li, W., Fu, R., & Zhou, L. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00908-0 · Cited by 15 · see citing works

Bioinformatics Analysis Revealed Novel 3′UTR Variants Associated with Intellectual Disability

Yang, J., Liu, A., He, I., & Bai, Y. (2020) · Genes · doi:10.3390/genes11090998 · Cited by 15 · see citing works

Bioinformatics and network-based approaches for determining pathways, signature molecules, and drug substances connected to genetic basis of schizophrenia etiology

Khan, U., Rahman, M. H., Khan, M. S., Hossain, M. S., & Billah, M. M. (2022) · Brain Research · doi:10.1016/j.brainres.2022.147889 · Cited by 14 · see citing works

MicroRNAs influence and longevity

Eshkoor, S. A., Ghodsian, N., & Akhtari‐Zavare, M. (2022) · Egyptian Journal of Medical Human Genetics · doi:10.1186/s43042-022-00316-7 · Cited by 14 · see citing works

miRNA-Mediated Mechanisms in the Generation of Effective and Safe Oncolytic Viruses

Toropko, M., Chuvpilo, S. A., & Karabelsky, A. V. (2024) · Pharmaceutics · doi:10.3390/pharmaceutics16080986 · Cited by 14 · see citing works

microRNA Deficiency in VIP+ Interneurons Leads to Cortical Circuit Dysfunction

Qiu, F., Mao, X., Liu, P., Wu, J., Zhang, Y., Sun, D., Zhu, Y., Gong, L., Shao, M., Fan, K., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz236 · Cited by 15 · see citing works

Hypothesis: Exosomal microRNAs as potential biomarkers for schizophrenia

Raghavan, V., Bhomia, M., Torres, I., Jain, S., & Wang, K. (2017) · Medical Hypotheses · doi:10.1016/j.mehy.2017.04.003 · Cited by 14 · see citing works

MicroRNAs as potential diagnostic biomarkers for bipolar disorder

Martinez, B., & Peplow, P. V. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01588 · Cited by 13 · see citing works

Circulating microRNA miR-137 as a stable biomarker for methamphetamine abstinence

Kim, B., Tag, S. H., Kim, Y. S., Cho, S. N., & Im, H. (2022) · Psychopharmacology · doi:10.1007/s00213-022-06074-z · Cited by 13 · see citing works

CircHOMER1 aggravates oxidative stress, inflammation and extracellular matrix deposition in high glucose‐induced human mesangial cells

Shu, S., Zhongju, X., Lu, H., Li, Z., & Zhang, Y. (2022) · Nephrology · doi:10.1111/nep.14115 · Cited by 12 · see citing works

Cost-effective monitoring of microRNA-205 applied as a biomarker using G-quadruplex DNAzyme and 1,1’-oxalyldiimidazole chemiluminescence

Kim, K., Park, P., & Lee, J. H. (2019) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2019.112780 · Cited by 12 · see citing works

MicroRNA binding site variation is enriched in psychiatric disorders

Geaghan, M. P., Reay, W. R., & Cairns, M. J. (2022) · Human Mutation · doi:10.1002/humu.24481 · Cited by 11 · see citing works

Extracellular vesicles as biomarkers for traumatic brain injury using a 3D in vitro human brain tissue model

Hsi, P. T., Tandon, V., & Kaplan, D. L. (2025) · Scientific Reports · doi:10.1038/s41598-025-04835-2 · Cited by 11 · see citing works

Noncoding RNAs orchestrating the central dogma

Lozano‐Villada, S., & Puthanveettil, S. V. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110933 · Cited by 12 · see citing works

Scalable single-cell total RNA sequencing unifies coding and noncoding transcriptomics

Isakova, A., Liu, D. D., Cvijović, I., Sinha, R., Eastman, A. E., Saul, S., Detweiler, A. M., Neff, N. F., Einav, S., Weissman, I. L., et al. (2026) · Nature Biotechnology · doi:10.1038/s41587-026-03068-6 · Cited by 11 · see citing works

Gene Therapy for Neuropsychiatric Disorders: Potential Targets and Tools

Lotfi, M., Tambuwala, M. M., Shahcheraghi, S. H., Ayatollahi, J., Aljabali, A. A. A., Zoubi, M. S. A., Panda, P. K., Mishra, V. K., Satija, S., Charbe, N. B., et al. (2022) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527321666220304153719 · Cited by 13 · see citing works

The role of YAP/TAZ mechanosignaling in trabecular meshwork and Schlemm’s canal cell dysfunction

Ghosh, R., & Herberg, S. (2024) · Vision Research · doi:10.1016/j.visres.2024.108477 · Cited by 13 · see citing works

Recent Advances in the miRNA-Mediated Regulation of Neuronal Differentiation and Death

Patranabis, S. (2024) · NeuroMolecular Medicine · doi:10.1007/s12017-024-08820-2 · Cited by 12 · see citing works

Glucocorticoid receptor regulates expression of microRNA-22 and downstream signaling pathway in apoptosis of pancreatic acinar cells

Fu, Q., Liu, C., Zhang, X., Zhai, Z., Wang, Y.-Z., Hu, M., Xu, X.-L., Zhang, H., & Qin, T. (2018) · World Journal of Gastroenterology · doi:10.3748/wjg.v24.i45.5120 · Cited by 11 · see citing works

Effects of MiR‐137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls

Cosgrove, D., Mothersill, D., Whitton, L., Harold, D. H., Kelly, S., Holleran, L., Holland, J. F., Anney, R., Richards, A., Mantripragada, K. K., et al. (2018) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32620 · Cited by 11 · see citing works

miR-137: A New Player in Schizophrenia

Yin, J., Lin, J., Luo, X., Chen, Y., Li, Z., Ma, G., & Li, K. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15023262 · Cited by 98 · see citing works

www.mdpi.com/journal/ijms Review miR-137: A New Player in Schizophrenia

Yin, J., 林举达, Luo, X., Chen, Y., Li, Z., Ma, G., & Li, K. (2014)

The schizophrenia risk gene MIR137 acts as a hippocampal gene network node orchestrating the expression of genes relevant to nervous system development and function

Loohuis, N. F. M. O., Kasri, N. N., Glennon, J. C., van Bokhoven, H., Hébert, S. S., Kaplan, B. B., Martens, G. J. M., & Aschrafi, A. (2016) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2016.02.009 · Cited by 29 · see citing works

Participación del miR-137 en el cáncer

Cervantes-Ayala, A., Garrido, R. R.-E., & Velázquez-Flores, M. (2018)

Microrna 137 Plays A Critical Role in Early Embryonic Development and Synaptic Transmission

Crowley, J. J. (2017) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2016.09.594