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Arcos-Burgos, M., & Cuartas, M. (2020). The Mendelian Legacy to Mental and Behavioral Disorders. International Journal of Psychological Research, 13(1), 6–8. https://doi.org/10.21500/20112084.4529
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The editorial board reserves the right of amendments deemed necessary in the application of the rules of publication.
To give up copyright, the authors allow that, International Journal of Psychological Research, distribute the work more broadly, check for the reuse by others and take care of the necessary procedures for the registration and administration of copyright; at the same time, our editorial board represents the interests of the author and allows authors to re-use his work in various forms. In response to the above, authors transfer copyright to the journal, International Journal of Psychological Research. This transfer does not imply other rights which are not those of authorship (for example those that concern about patents). Likewise, preserves the authors rights to use the work integral or partially in lectures, books and courses, as well as make copies for educational purposes. Finally, the authors may use freely the tables and figures in its future work, wherever make explicit reference to the previous publication in International Journal of Psychological Research. The assignment of copyright includes both virtual rights and forms of the article to allow the editorial to disseminate the work in the manner which it deems appropriate.
The editorial board reserves the right of amendments deemed necessary in the application of the rules of publication.
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Referencias
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.
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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