Meta-analyses of RELN variants in neuropsychiatric disorders
Abstract
Reelin is a critical extracellular matrix glycoprotein and implicated in neurodevelopment and psychiatric disorders in animal model studies. The genetic polymorphism of RELN has also been reported to be associated with several psychiatric disorders, but the results remain controversial. Here, we conducted meta-analyses of RELN gene SNPs and related neuropsychiatric disorders (schizophrenia, autistic spectrum disorders, attention-deficit hyperactivity disorder, Alzheimer's disease and bipolar disorders). A total of 12 SNPs (rs736707, rs362691, rs607755, rs2229864, rs7341475, rs262355, rs362719, rs11496125, g.-888G>C, rs2299356, rs528528, and rs4298437) in RELN gene were included into meta-analyses. Subgroup analyses based on ethnicity were performed. We found that RELN rs736707 was significantly related with psychiatric disorders (schizophrenia, autism spectrum disorders and attention-deficit hyperactivity disorder) in Asian group (C vs T, OR=1.26, 95% CI=1.13-1.41, P<0.01, FDR<0.01), and rs7341475 was only significantly associated with reduced risk of schizophrenia in Caucasian (A vs G, OR=0.88, 95% CI=0.82-0.95, P<0.01, FDR<0.01). No association of other SNPs and psychiatric disorders is found. These findings suggest a role of RELN SNPs in psychiatric diseases, and indicate that further researches in populations with different genetic background and studies with larger sample size are of great value.
Integrity signals
Registry
Cites
Statistics
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?
Axonal guidance and reelin signaling are important pathways for nervous system development and have been implicated in neuropsychiatric disorders such as bipolar, SCZ, and ADHD.
“Axonal guidance and reelin signaling are important pathways for nervous system development and have been implicated in neuropsychiatric disorders such as bipolar, SCZ, and ADHD [64–68]”
From An integrated analysis of genes and functional pathways for aggression in human and rodent models (2019) · cites this paper as [65]
Cites
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482 · see citing works
A protein related to extracellular matrix proteins deleted in the mouse mutant reeler
D'Arcangelo, G., G. Miao, G., Chen, S.-C., Scares, H. D., Morgan, J. I., & Curran, T. (1995) · Nature · doi:10.1038/374719a0 · Cited by 1,748 · see citing works
Hakak, Y., Walker, J. R., Li, C., Wong, W. H., Davis, K. L., Buxbaum, J. D., Haroutunian, V., & Fienberg, A. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081071198 · Cited by 1,192 · see citing works
Maternal influenza infection causes marked behavioral and pharmacological changes in the offspring
Shi, L., Fatemi, S. H., Sidwell, R. W., & Patterson, P. H. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00297.2003 · Cited by 1,025 · see citing works
Neuroanatomic observations of the brain in autism: a review and future directions
Bauman, M. L., & Kemper, T. L. (2005) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2004.09.006 · Cited by 919 · see citing works
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
Hong, S. E., Shugart, Y. Y., Huang, D. T.-C., Shahwan, S. A., Grant, P. E., Hourihane, J. O., Martin, N. D. T., & Walsh, C. A. (2000) · Nature Genetics · doi:10.1038/79246 · Cited by 878 · see citing works
A decrease of reelin expression as a putative vulnerability factor in schizophrenia
Impagnatiello, F., Guidotti, A. R., Pesold, C., Dwivedi, Y., Caruncho, H. J., Pisu, M. G., Uzunov, D. P., Smalheiser, N. R., Davis, J. M., Pandey, G. N., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.26.15718 · Cited by 753 · see citing works
Tissir, F., & Goffinet, A. M. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1113 · Cited by 748 · see citing works
Akbarian, S. (1993) · Archives of General Psychiatry · doi:10.1001/archpsyc.1993.01820150007001 · Cited by 679 · see citing works
Fatemi, S. H., Earle, J. A., & McMenomy, T. (2000) · Molecular Psychiatry · doi:10.1038/sj.mp.4000783 · Cited by 447 · see citing works
Neurochemical markers for schizophrenia, bipolar disorder, and major depression in postmortem brains
Torrey, E. F., Barci, B. M., Webster, M. J., Bartko, J. J., Meador-Woodruff, J. H., & Knable, M. B. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.10.019 · Cited by 426 · see citing works
Shifman, S., Johannesson, M., Bronstein, M., Chen, S. X., Collier, D. A., Craddock, N. J., Kendler, K. S., Li, T., O’Donovan, M. C., O’Neill, F. A., et al. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.0040028 · Cited by 345 · see citing works
Reelin expression and glycosylation patterns are altered in Alzheimer’s disease
Botella-López, A., Burgaya, F., Gavín, R., García-Ayllón, M. S., Gómez-Tortosa, E., Peña-Casanova, J., Ureña, J. M., Del Río, J. A., Blesa, R., Soriano, E., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601279103 · Cited by 221 · see citing works
Epigenetic GABAergic targets in schizophrenia and bipolar disorder
Guidotti, A., Auta, J., Chen, Y., Davis, J. M., Dong, E., Gavin, D. P., Grayson, D. R., Matrisciano, F., Pinna, G., Satta, R., et al. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.10.021 · Cited by 220 · see citing works
Cognitive disruption and altered hippocampus synaptic function in Reelin haploinsufficient mice
QIU, S., KORWEK, K., PRATTDAVIS, A., PETERS, M., BERGMAN, M., & WEEBER, E. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.11.001 · Cited by 202 · see citing works
Reduction of synapsin in the hippocampus of patients with bipolar disorder and schizophrenia
Vawter, M. P., Thatcher, L. N., Usen, N., Hyde, T. M., Kleinman, J. E., & Freed, W. J. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001158 · Cited by 188 · see citing works
Hamburgh, M. (1963) · Developmental Biology · doi:10.1016/0012-1606(63)90040-x · Cited by 149 · see citing works
The human reelin gene: isolation, sequencing, and mapping on chromosome 7.Preprint
DeSilva, U., D’Arcangelo, G., Braden, V. V., Chen, J., Miao, G. G., Curran, T., & Green, E. D. (1997) · Genome Research · doi:10.1101/gr.7.2.157 · Cited by 144 · see citing works
Towards understanding the schizophrenia code: an expanded convergent functional genomics approach
Le‐Niculescu, H., Balaraman, Y., Patel, S., Tan, J., Sidhu, K., Jerome, R. E., Edenberg, H. J., Kuczenski, R., Geyer, M. A., Nurnberger, J. I., et al. (2007) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30481 · Cited by 137 · see citing works
Lacor, P. N., Grayson, D. R., Auta, J., Sugaya, I., Costa, E., & Guidotti, A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.050589597 · Cited by 110 · see citing works
Boyle, M. P., Bernard, A., Thompson, C. L., Ng, L., Boe, A. F., Mortrud, M. T., Hawrylycz, M., Jones, A. R., Hevner, R. F., & Lein, E. S. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22655 · Cited by 107 · see citing works
Cellular Basis of Reduced Cortical Reelin Expression in Schizophrenia
Eastwood, S. L., & Harrison, P. J. (2006) · American Journal of Psychiatry · doi:10.1176/appi.ajp.163.3.540 · Cited by 104 · see citing works
Maloku, E., Covelo, I. R., Hanbauer, I., Guidotti, A., Kadriu, B., Hu, Q., Davis, J. M., & Costa, E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914483107 · Cited by 103 · see citing works
Neural ECM molecules in synaptic plasticity, learning, and memory
Senkov, O., Anđjus, P. R., Radenović, L., Soriano, E., & Dityatev, A. E. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63486-3.00003-7 · Cited by 94 · see citing works
Lacor, P. N., Grayson, D. R., Auta, J., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.7.3556 · Cited by 80 · see citing works
The Genetic Variation of RELN Expression in Schizophrenia and Bipolar Disorder
Ovadia, G., & Shifman, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019955 · Cited by 79 · see citing works
Altered levels of cerebrospinal fluid reelin in frontotemporal dementia and Alzheimer's disease
Sáez‐Valero, J., Costell, M., Sjögren, M. J. C., Andreasen, N., Blennow, K., & Luque, J. M. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10554 · Cited by 78 · see citing works
Li, H., Li, Y., Shao, J., Li, R., Qin, Y., Xie, C., & Zhao, Z. (2007) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30584 · Cited by 70 · see citing works
Sex‐specific association of the reelin gene with bipolar disorder
Goes, F. S., Willour, V. L., Zandi, P. P., Belmonte, P. L., MacKinnon, D. F., Mondimore, F. M., Schweizer, B., National Institute of Mental Health Genetics Initiative Bipolar Disorder Consortium, DePaulo, J. R., Gershon, E. S., et al. (2010) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31018 · Cited by 67 · see citing works
Reelin Glycoprotein in Autism and Schizophrenia
Fatemi, S. H. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)71008-4 · Cited by 59 · see citing works
Liu, Y., Chen, P.-L., McGrath, J. A., Wolyniec, P. S., Fallin, M. D., Nestadt, G., Liang, K., Pulver, A. E., Valle, D. L., & Avramopoulos, D. (2010) · Psychiatric Genetics · doi:10.1097/ypg.0b013e32833a220b · Cited by 47 · see citing works
The associations between ADHD and asthma in Korean children
Kwon, H., Lee, M.-Y., Ha, M., Yoo, S., Paik, K., Lim, J.-H., Sakong, J., Lee, C., Kang, D., Hong, S.-J., et al. (2014) · BMC Psychiatry · doi:10.1186/1471-244x-14-70 · Cited by 44 · see citing works
Apolipoprotein E genotype in schizophrenia
Arnold, S. E., Joo, E.-J., Martinoli, M., Roy, N., Trojanowski, J. Q., Gur, R. E., Cannon, T. D., & Price, R. A. (1997) · Neuroreport · doi:10.1097/00001756-199704140-00040 · Cited by 40 · see citing works
Dutta, S., Sinha, S., Ghosh, S., Chatterjee, A., Ahmed, S., & Rajamma, U. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.06.022 · Cited by 39 · see citing works
Li, M., Luo, X., Xiao, X., Shi, L., Liu, X., Yin, L.-D., Ma, X., Yang, S.-Y., Pu, X., Yu, J. S., et al. (2011) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2011.587891 · Cited by 34 · see citing works
He, Y., Xun, G., Xia, K., Hu, Z., Lv, L., Deng, Z., & Zhao, J. (2010) · Psychiatry Research · doi:10.1016/j.psychres.2010.04.051 · Cited by 32 · see citing works
Association of SLC18A1, TPH1, and RELN gene polymorphisms with risk of paranoid schizophrenia
Galaktionova, D. Y., Эмировна, Г. А., Хуснутдинова, Э. К., & Nasedkina, T. V. (2014) · Molecular Biology · doi:10.1134/s0026893314030042 · Cited by 20 · see citing works
Pisanté, A., Bronstein, M., Yakir, B., & Darvasi, A. (2009) · Psychiatric Genetics · doi:10.1097/ypg.0b013e32832cebe6 · Cited by 16 · see citing works
Galaktionova, D. I., Гареева, А. Э., Хуснутдинова, Э. К., & Tv, N. (2014) · PubMed · Cited by 14 · see citing works
Association study of the reelin (RELN) gene with Chinese Va schizophrenia
Yang, X. B., Kang, C., Liu, H., & Yang, J. (2012) · Psychiatric Genetics · doi:10.1097/ypg.0b013e32835d705c · Cited by 11 · see citing works
Mirnics, K., Middleton, F. A., Lewis, D. A., & Levitt, P. R. (2001) · The Scientific World JOURNAL · doi:10.1100/tsw.2001.17 · Cited by 9 · see citing works
[Association of RELN SNP rs7341475 with schizophrenia in the Chinese population].
Liu, X., Li, M., Yang, S.-Y., Su, B., & Yin, L.-D. (2011) · PubMed · doi:10.3724/sp.j.1141.2011.05499 · Cited by 8 · see citing works
Georgieva, V., Sivkov, S. T., Akabaliev, V., Koeva, Y. A., Angelova, R. Y., & Deneva, T. I. (2007) · PubMed · Cited by 2 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Microglia and Neurodevelopmental Disorders
Lukens, J. R., & Eyo, U. B. (2022) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110920-023056 · Cited by 165 · see citing works
An integrated analysis of genes and functional pathways for aggression in human and rodent models
Zhang-James, Y., Fernàndez-Castillo, N., Hess, J. L., Malki, K., Glatt, S. J., Cormand, B., & Faraone, S. V. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0068-7 · Cited by 98 · see citing works
Genetics of autism spectrum disorder: an umbrella review of systematic reviews and meta-analyses
Qiu, S., Qiu, Y., Li, Y., & Cong, X. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02009-6 · Cited by 84 · see citing works
Multisensory cortical processing and dysfunction across the neuropsychiatric spectrum
Hornix, B., Havekes, R., & Kas, M. J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.02.010 · Cited by 60 · see citing works
Wei, H., Zhu, Y., Wang, T., Zhang, X., Zhang, K., & Zhang, Z. (2021) · Journal of Neural Transmission · doi:10.1007/s00702-021-02360-w · Cited by 51 · see citing works
Reelin Signaling in Neurodevelopmental Disorders and Neurodegenerative Diseases
Joly‐Amado, A., Kulkarni, N., & Nash, K. R. (2023) · Brain Sciences · doi:10.3390/brainsci13101479 · Cited by 43 · see citing works
Rosato, M., Stringer, S., Gebuis, T., Paliukhovich, I., Li, K. W., Posthuma, D., Sullivan, P. F., Smit, A. B., & van Kesteren, R. E. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0436-y · Cited by 38 · see citing works
Identification of exon skipping events associated with Alzheimer’s disease in the human hippocampus
Initiative, A. D. N., Han, S., Miller, J. E., Byun, S., Kim, D., Risacher, S. L., Saykin, A. J., Lee, Y., & Nho, K. T. (2019) · BMC Medical Genomics · doi:10.1186/s12920-018-0453-8 · Cited by 34 · see citing works
Blaylock, R. L., Strunecká, A., Patočka, J., & Strunecký, O. (2018) · Surgical Neurology International · doi:10.4103/sni.sni_407_17 · Cited by 35 · see citing works
The Pathophysiological Link Between Reelin and Autism: Overview and New Insights
Scala, M., Grasso, E. A., Cara, G. D., Riva, A., Striano, P., & Verrottı, A. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.869002 · Cited by 25 · see citing works
Monoallelic and biallelic mutations inRELNunderlie a graded series of neurodevelopmental disorders
Donato, N. D., Guerrini, R., Billington, C. J., Barkovich, A. J., Dinkel, P., Freri, E., Heide, M., Gershon, E. S., Gertler, T. S., Hopkin, R. J., et al. (2022) · Brain · doi:10.1093/brain/awac164 · Cited by 23 · see citing works
Female gender specific association of the Reelin (RELN) gene rs7341475 variant with schizophrenia
Sözügüzel, M. D., Sazcı, A., & Yıldız, M. (2019) · Molecular Biology Reports · doi:10.1007/s11033-019-04803-w · Cited by 20 · see citing works
New Strategies for the Treatment of Neuropsychiatric Disorders Based on Reelin Dysfunction
Tsuneura, Y., NAKAI, T., Mizoguchi, H., & Yamada, K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031829 · Cited by 19 · see citing works
de Guglielmo, G., Iemolo, A., Nur, A., Turner, A. V., Montilla‐Perez, P., Martinez, A. R., Crook, C., Roberts, A. J., & Telese, F. (2022) · Genes Brain & Behavior · doi:10.1111/gbb.12828 · Cited by 18 · see citing works
Genetic etiology of autism spectrum disorder in the African population: a scoping review
Hakizimana, O., Hitayezu, J., Uyisenga, J. P., Onohuean, H., Palmeira, L., Bours, V., Alagbonsi, A. I., & Uwineza, A. (2024) · Frontiers in Genetics · doi:10.3389/fgene.2024.1431093 · Cited by 17 · see citing works
Guo, J., Riley, K. W., Durham, T., Margolis, A. E., Wang, S., Perera, F. P., & Herbstman, J. B. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.871820 · Cited by 15 · see citing works
Marzan, S., Aziz, M. A., & Islam, M. S. (2020) · Journal of Molecular Neuroscience · doi:10.1007/s12031-020-01696-4 · Cited by 15 · see citing works
Nawa, Y., Kimura, H., Mori, D., Kato, H., Toyama, M., Furuta, S., Yu, Y., Ishizuka, K., Kushima, I., Aleksić, B., et al. (2020) · Human Genome Variation · doi:10.1038/s41439-020-00125-7 · Cited by 14 · see citing works
Mpoulimari, I., & Zintzaras, E. (2022) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000316 · Cited by 14 · see citing works
Estrogen receptor beta and neural development
Nalvarte, I., Varshney, M., Inzunza, J., & Gustafsson, J.-Α. (2021) · Vitamins and hormones · doi:10.1016/bs.vh.2021.02.007 · Cited by 12 · 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
Wang, G., Ye, S., Gao, L., Han, Y., Guo, X., Dong, X., Su, Y., & Zhang, X. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.04.048 · Cited by 11 · see citing works
Genetic Variation and Autism: A Field Synopsis and Systematic Meta-Analysis
Lee, J., Son, M. J., Son, C. Y., Jeong, G. H., Lee, K. H., Lee, K. S., Ko, Y., Kim, J. Y., Lee, J. Y., Raduà, J., et al. (2020) · Brain Sciences · doi:10.3390/brainsci10100692 · Cited by 10 · see citing works
Association between RELN polymorphisms and schizophrenia in a Han population from Northeast China
Bai, W., Fu, Y., Yu, X., Zhu, B., Duan, R., Yu, Y., & Kou, C. (2019) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000235 · Cited by 9 · see citing works
Fotoh, W. M. M. A. E., Bayomy, N. R., Kasemy, Z. A. A., Barain, A. M., Shalaby, B. M., & Naby, S. A. A. E. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00136 · Cited by 8 · see citing works
Genetic predictors of severe intraventricular hemorrhage in extremely low-birthweight infants
Thornburg, C. D., Erickson, S. W., Page, G. P., Clark, E., DeAngelis, M. M., Hartnett, M. E., Goldstein, R. F., Dagle, J. M., Murray, J. C., Poindexter, B. B., et al. (2020) · Journal of Perinatology · doi:10.1038/s41372-020-00821-w · Cited by 7 · see citing works
Martínez‐Magaña, J. J., Mendoza, A. D. G., González-Covarrubias, V., Jiménez-Guenchi, J., Galindo-Chávez, A. G., Roche-Bergua, A., Castañeda-González, C., Lanzagorta, N., Soberón, X., & Nicolini, H. (2019) · Revista de investigaci�n Cl�nica · doi:10.24875/ric.19002923 · Cited by 6 · see citing works
Correlation of Four Single Nucleotide Polymorphisms of the RELN Gene With Schizophrenia
Ping, J., Zhang, J., Wan, J., Banerjee, A., Huang, C., Yu, J., Jiang, T., & Du, B. (2021) · East Asian Archives of Psychiatry · doi:10.12809/eaap2168 · Cited by 6 · see citing works
Ali, Z. A., Yasseen, A. A., McAllister, K. A., Al-Dujaili, A. H., Al-Karaqully, A. J., & Jumaah, A. S. (2022) · Molecular Biology Reports · doi:10.1007/s11033-022-07388-z · Cited by 6 · see citing works
Brietzke, E. M., Trevizol, A. P., Fries, G. R., Subramaniapillai, M., Kapczinski, F. P., McIntyre, R. S., & Mansur, R. B. (2018) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2018.04.012 · Cited by 6 · see citing works
Pattie, E. A., & Iffland, P. H. (2025) · Brain Sciences · doi:10.3390/brainsci16010054 · Cited by 5 · see citing works
Safety of Anti-Reelin Therapeutic Approaches for Chronic Inflammatory Diseases
Calvier, L., Alexander, A., Marckx, A. T., Kounnas, M. Z., Durakoglugil, M. S., & Herz, J. (2024) · Cells · doi:10.3390/cells13070583 · Cited by 6 · see citing works
Kara, B., Şahın, N., Kara, M., Çetin, E. S., & Topal, H. (2018) · Psychiatry and Clinical Psychopharmacology · doi:10.1080/24750573.2018.1478192 · Cited by 2 · see citing works
RELN rs7341475 Associates with Brain Structure in Japanese Healthy Females
Yamaguchi, R., Matsudaira, I. Y., Takeuchi, H., Imanishi, T., Kimura, R., Tomita, H., Kawashima, R., & Taki, Y. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.05.007 · Cited by 1 · see citing works
Sigurðardóttir, H., Eriksson, S., Niazi, A., Rhodin, M., Albertsdóttir, E., Kristjánsson, Þ., & Lindgren, G. (2025) · Scientific Reports · doi:10.1038/s41598-025-95593-8 · Cited by 1 · see citing works
Алфимова, М. В., Kondratyev, N. V., Golov, A. K., Golubev, S. A., Galaktionova, D. Y., Nasedkina, T. V., & Голимбет, В. Е. (2018) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro201811809171 · Cited by 1 · see citing works
Li, X., Hu, H., Johansen, N., & Quon, G. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.11.516161 · Cited by 1 · see citing works
The Genetic Basis of Human Cognition: Intelligence, Learning and Memory
Avgan, N. (2018) · Queensland University of Technology · doi:10.5204/thesis.eprints.122903
Алфимова, М. В., Kondratyev, N. V., Golov, A. K., Golubev, S. A., Galaktionova, D. Y., Nasedkina, T. V., & Голимбет, В. Е. (2019) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-019-00838-5
Heritability and Genetic Correlations Along the Corticospinal Tract
Gari, I. B., Bhatt, R. R., Yeh, F.-C. F., & Jahanshad, N. (2025) · Lecture notes in computer science · doi:10.1007/978-3-031-86920-4_18
REELIN-COLBOS (H3447R) in Colombian oldest-old individuals, a case series
Vásquez, D., Aguillon, D. F., Perez-Corredor, P. A., Alzate, D., Zuluaga, Y., Baena, A. Y., Madrigal, L., Hincapié, L., Ramirez-Gomez, L. A., Martinez, L., et al. (2025) · ScienceBank · doi:10.61340/rccoop
Litif, C. G., Libster, A., Desfor, S., Huang, T., Liaw, L., Cheng, A., & Telese, F. (2026) · bioRxiv · doi:10.64898/2026.02.21.707172
Etude du rôle de la kinésine KIF21B au cours du développement cortical
Asselin, L. (2019) · theses.fr (ABES) · doi:10.70675/bd543948zdb0fz4298zae3fzf4fc50923d78
Litif, C. G., Libster, A., Desfor, S., Huang, T., Liaw, L., Cheng, A., & Telese, F. (2026) · Genes, Brain and Behavior · doi:10.1111/gbb.70072 · Cited by 1 · see citing works
- Authors
- Chen, N., Bao, Y., Xue, Y., Sun, Y., Hu, D., Meng, S., Lu, L., & Shi, J.
- Affiliations
- Peking University (CN)
- Corresponding author
- Shi, Jie
- Venue
- Behavioural Brain Research
- Publisher
- Elsevier BV
- Published
- 2017-08
- Volume
- 332
- Pages
- 110-119
- ISSN
- 0166-4328 (ISSN-L)
- OpenAlex
- W2613466142
- Cited by
- 44
- References
- 43
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 2 · 2023: 1 · 2022: 12 · 2021: 3 · 2020: 5 · 2019: 7 · 2018: 8
- FWCI
- 0.83
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Behavioural Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Keywords
- reelin, single nucleotide polymorphisms, neuropsychiatric disorders, schizophrenia, autism spectrum disorder, attention deficit hyperactivity disorder, Alzheimer's disease, bipolar disorder, genetic association, ethnic subgroup differences
- MeSH terms
- Reelin Protein, Mental Disorders, Humans, Nerve Tissue Proteins, Serine Endopeptidases, Cell Adhesion Molecules, Neuronal, Extracellular Matrix Proteins, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide
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