The Mendelian Legacy to Mental and Behavioral Disorders
Editorial
- Autores:
-
Arcos-Burgos, Mauricio
Cuartas, Mauricio
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2020
- Institución:
- Universidad de San Buenaventura
- Repositorio:
- Repositorio USB
- Idioma:
- spa
- OAI Identifier:
- oai:bibliotecadigital.usb.edu.co:10819/25842
- Acceso en línea:
- https://hdl.handle.net/10819/25842
https://doi.org/10.21500/20112084.4529
- Palabra clave:
- Behavioral Disorders
Trastornos del comportamiento
- Rights
- openAccess
- License
- International Journal of Psychological Research - 2020
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The Mendelian Legacy to Mental and Behavioral Disorders |
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The Mendelian Legacy to Mental and Behavioral Disorders |
| title |
The Mendelian Legacy to Mental and Behavioral Disorders |
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The Mendelian Legacy to Mental and Behavioral Disorders Behavioral Disorders Trastornos del comportamiento |
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The Mendelian Legacy to Mental and Behavioral Disorders |
| title_full |
The Mendelian Legacy to Mental and Behavioral Disorders |
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The Mendelian Legacy to Mental and Behavioral Disorders |
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The Mendelian Legacy to Mental and Behavioral Disorders |
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The Mendelian Legacy to Mental and Behavioral Disorders |
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Arcos-Burgos, Mauricio Cuartas, Mauricio |
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Arcos-Burgos, Mauricio Cuartas, Mauricio |
| dc.subject.eng.fl_str_mv |
Behavioral Disorders |
| topic |
Behavioral Disorders Trastornos del comportamiento |
| dc.subject.spa.fl_str_mv |
Trastornos del comportamiento |
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Editorial |
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2020 |
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2020-01-20T22:24:32Z 2025-07-31T16:12:16Z |
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2020-01-20T22:24:32Z 2025-07-31T16:12:16Z |
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2011-2084 |
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Acosta, M. T., Arcos-Burgos, M., & Muenke, M. (2004). Attention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype? Genet Med, 6 (1), 1–15. doi:10.1097/01.gim.0000110413.07490.0b. Acosta, M. T., Velez, J. I., Bustamante, M. L., Balog, J. Z., Arcos-Burgos, M., & Muenke, M. (2011). A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome. Transl Psychiatry, 6 (1), e17. doi:10.1038/tp.2011.14. Arcos-Burgos, M., & Acosta, M. T. (2007). Tuning major gene variants conditioning human behavior: the anachronism of ADHD. Curr Opin Genet Dev, 17 (3), 234–238. doi:10.1016/j.gde.2007.04.011. Arcos-Burgos, M., & Muenke, M. (2010). Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHD. Atten Defic Hyperact Disord, 2 (3), 139– 147. doi:10.1007/s12402-010-0030-2. Arias, J. M. C., Acosta, C. A. P., Valencia, J. G., Montoya, G. J., Viana, J. C. A., Nieto, O. C., & Achury, J. G. (2011). Exploring epistasis in candidate genes for antisocial personality disorder. Psychiatric genetics, 21 (3), 115–124. Feldman, M. W., & Ramachandran, S. (2018). Missing compared to what? Revisiting heritability, genes and culture. Philos Trans R Soc Lond B Biol Sci, 373 (1743), 20170064. doi:10.1098/rstb.2017.0064. International Schizophrenia Consortium, Purcell, S. M., Wray, N. R., Stone, J. L., Visscher, P. M., O’Donovan, M. C., & Sklar, P. (2009). Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature, 460 (7256), 748–752. doi:10.1038/nature08185. Jain, M., Velez, J. I., Acosta, M. T., Palacio, L. G., Balog, J., Roessler, E., & Muenke, M. (2012). A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD. Mol Psychiatry, 17 (7), 741–747. doi:10.1038/mp.2011.59. Lam, M., Chen, C. Y., Li, Z., Martin, A. R., Bryois, J., Ma, X., & Huang, H. (2019). Comparative genetic architectures of schizophrenia in East Asian and European populations. Nat Genet, 51 (12), 1670– 1678. doi:10.1038/s41588-019-0512-x. Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Attention Deficit/Hyperactivity Disorder Working Group of the iPsych-Broad-Pgc Consortium, A. S. D. W. G. o. t. i.-B.-P. G. C. C. B. D. W. G., Tourette Syndrome Working Group of the Pgc, S. C. S. U. D. W. G. o. t. P. G. C., & Polderman, T. J. C. (2019). Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM. Psychol Med, 49 (2), 351. doi:10.1017/S0033291718002945. Pulver, A. E., Karayiorgou, M., Wolyniec, P. S., Lasseter, V. K., Kasch, L., Nestadt, G., . . . others (1994). Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12-q13. 1: Part 1. American journal of medical genetics, 54 (1), 36–43. doi:10.1002/ajmg.1320540108. Ruiz, A., Blanco, R., Arcos, M., Santander, J., & San Martin, A. (1997). Complex segregation analysis of schizophrenia in Santiago, Chile. Schizophr Res, 26 (1), 65–69. doi:10.1016/s0920-9964(97)00038-8. Straub, R. E., MacLean, C. J., Walsh, D., & Kendler, K. S. (1996). Support for schizophrenia vulnerability loci on chromosomes 6p and 8p from Irish families. Cold Spring Harb Symp Quant Biol, 61, 823–833. Valencia, M., & Cuartas Arias, J. M. (2016). Potential biomarkers in personality disorders: current state and future research. International Journal of Psychological Research, 9 (1), 98–112. Vinkhuyzen, A. A., Wray, N. R., Yang, J., Goddard, M. E., & Visscher, P. M. (2013). Estimation and partition of heritability in human populations using whole-genome analysis methods. Annu Rev Genet, 47 , 75–95. doi:10.1146/annurev-genet-111212-133258 Wong, M. L., Dong, C., Andreev, V., Arcos-Burgos, M.,& Licinio, J. (2012). Prediction of susceptibilityto major depression by a model of interactions of multiple functional genetic variants and environmental factors. Mol Psychiatry, 17 (6), 624–633. doi:10.1038/mp.2012.13. |
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Arcos-Burgos, MauricioCuartas, Mauricio2020-01-20T22:24:32Z2025-07-31T16:12:16Z2020-01-20T22:24:32Z2025-07-31T16:12:16Z2020-01-20EditorialEditorialapplication/pdftext/xml10.21500/20112084.45292011-79222011-2084https://hdl.handle.net/10819/25842https://doi.org/10.21500/20112084.4529spaUniversidad San Buenaventura - USB (Colombia)https://revistas.usb.edu.co/index.php/IJPR/article/download/4529/3541https://revistas.usb.edu.co/index.php/IJPR/article/download/4529/365481613International Journal of Psychological ResearchAcosta, M. T., Arcos-Burgos, M., & Muenke, M. (2004). Attention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype? Genet Med, 6 (1), 1–15. doi:10.1097/01.gim.0000110413.07490.0b. Acosta, M. T., Velez, J. I., Bustamante, M. L., Balog, J. Z., Arcos-Burgos, M., & Muenke, M. (2011). A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome. Transl Psychiatry, 6 (1), e17. doi:10.1038/tp.2011.14. Arcos-Burgos, M., & Acosta, M. T. (2007). Tuning major gene variants conditioning human behavior: the anachronism of ADHD. Curr Opin Genet Dev, 17 (3), 234–238. doi:10.1016/j.gde.2007.04.011. Arcos-Burgos, M., & Muenke, M. (2010). Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHD. Atten Defic Hyperact Disord, 2 (3), 139– 147. doi:10.1007/s12402-010-0030-2. Arias, J. M. C., Acosta, C. A. P., Valencia, J. G., Montoya, G. J., Viana, J. C. A., Nieto, O. C., & Achury, J. G. (2011). Exploring epistasis in candidate genes for antisocial personality disorder. Psychiatric genetics, 21 (3), 115–124. Feldman, M. W., & Ramachandran, S. (2018). Missing compared to what? Revisiting heritability, genes and culture. Philos Trans R Soc Lond B Biol Sci, 373 (1743), 20170064. doi:10.1098/rstb.2017.0064. International Schizophrenia Consortium, Purcell, S. M., Wray, N. R., Stone, J. L., Visscher, P. M., O’Donovan, M. C., & Sklar, P. (2009). Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature, 460 (7256), 748–752. doi:10.1038/nature08185. Jain, M., Velez, J. I., Acosta, M. T., Palacio, L. G., Balog, J., Roessler, E., & Muenke, M. (2012). A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD. Mol Psychiatry, 17 (7), 741–747. doi:10.1038/mp.2011.59. Lam, M., Chen, C. Y., Li, Z., Martin, A. R., Bryois, J., Ma, X., & Huang, H. (2019). Comparative genetic architectures of schizophrenia in East Asian and European populations. Nat Genet, 51 (12), 1670– 1678. doi:10.1038/s41588-019-0512-x. Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Attention Deficit/Hyperactivity Disorder Working Group of the iPsych-Broad-Pgc Consortium, A. S. D. W. G. o. t. i.-B.-P. G. C. C. B. D. W. G., Tourette Syndrome Working Group of the Pgc, S. C. S. U. D. W. G. o. t. P. G. C., & Polderman, T. J. C. (2019). Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM. Psychol Med, 49 (2), 351. doi:10.1017/S0033291718002945. Pulver, A. E., Karayiorgou, M., Wolyniec, P. S., Lasseter, V. K., Kasch, L., Nestadt, G., . . . others (1994). Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12-q13. 1: Part 1. American journal of medical genetics, 54 (1), 36–43. doi:10.1002/ajmg.1320540108. Ruiz, A., Blanco, R., Arcos, M., Santander, J., & San Martin, A. (1997). Complex segregation analysis of schizophrenia in Santiago, Chile. Schizophr Res, 26 (1), 65–69. doi:10.1016/s0920-9964(97)00038-8. Straub, R. E., MacLean, C. J., Walsh, D., & Kendler, K. S. (1996). Support for schizophrenia vulnerability loci on chromosomes 6p and 8p from Irish families. Cold Spring Harb Symp Quant Biol, 61, 823–833. Valencia, M., & Cuartas Arias, J. M. (2016). Potential biomarkers in personality disorders: current state and future research. International Journal of Psychological Research, 9 (1), 98–112. Vinkhuyzen, A. A., Wray, N. R., Yang, J., Goddard, M. E., & Visscher, P. M. (2013). Estimation and partition of heritability in human populations using whole-genome analysis methods. Annu Rev Genet, 47 , 75–95. doi:10.1146/annurev-genet-111212-133258 Wong, M. L., Dong, C., Andreev, V., Arcos-Burgos, M.,& Licinio, J. (2012). Prediction of susceptibilityto major depression by a model of interactions of multiple functional genetic variants and environmental factors. Mol Psychiatry, 17 (6), 624–633. doi:10.1038/mp.2012.13.International Journal of Psychological Research - 2020info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2https://creativecommons.org/licenses/by-nc-sa/4.0/https://revistas.usb.edu.co/index.php/IJPR/article/view/4529Behavioral DisordersTrastornos del comportamientoThe Mendelian Legacy to Mental and Behavioral DisordersThe Mendelian Legacy to Mental and Behavioral DisordersArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85Textinfo:eu-repo/semantics/articleJournal articleinfo:eu-repo/semantics/publishedVersionPublicationOREORE.xmltext/xml2544https://bibliotecadigital.usb.edu.co/bitstreams/05dcf909-63f6-4b6e-9c95-1c6456110c5d/download58eed75c06d2b916f633325c44163b26MD5110819/25842oai:bibliotecadigital.usb.edu.co:10819/258422025-07-31 11:12:16.513https://creativecommons.org/licenses/by-nc-sa/4.0/https://bibliotecadigital.usb.edu.coRepositorio Institucional Universidad de San Buenaventura Colombiabdigital@metabiblioteca.com |