The Mendelian Legacy to Mental and Behavioral Disorders

The Mendelian Legacy to Mental and Behavioral Disorders

Editorial

Guardado en:

International Journal of Psychological Research

2011-2084

2011-7922

Arcos-Burgos, Mauricio

Cuartas, Mauricio

UNIVERSIDAD DE SAN BUENAVENTURA

10.21500/20112084.4529

13

2020-01-20

6

8

Colombia

Trastornos del comportamiento

http://purl.org/coar/access_right/c_abf2

info:eu-repo/semantics/openAccess

International Journal of Psychological Research - 2020

id 50b95d2724351ad2820ed55fea550b09
record_format ojs
spelling The Mendelian Legacy to Mental and Behavioral Disorders
text/xml
Text
http://purl.org/coar/access_right/c_abf2
info:eu-repo/semantics/openAccess
http://purl.org/coar/version/c_970fb48d4fbd8a85
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:eu-repo/semantics/article
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.
International Journal of Psychological Research - 2020
https://creativecommons.org/licenses/by-nc-sa/4.0/
Español
https://revistas.usb.edu.co/index.php/IJPR/article/view/4529
The Mendelian Legacy to Mental and Behavioral Disorders
Publication
application/pdf
Editorial
Trastornos del comportamiento
Artículo de revista
International Journal of Psychological Research
Editorial
Arcos-Burgos, Mauricio
Cuartas, Mauricio
Behavioral Disorders
Journal article
13
Universidad San Buenaventura - USB (Colombia)
1
https://revistas.usb.edu.co/index.php/IJPR/article/download/4529/3654
8
https://revistas.usb.edu.co/index.php/IJPR/article/download/4529/3541
6
2020-01-20T22:24:32Z
https://doi.org/10.21500/20112084.4529
10.21500/20112084.4529
2020-01-20T22:24:32Z
2020-01-20
2011-2084
2011-7922
institution UNIVERSIDAD DE SAN BUENAVENTURA
thumbnail https://nuevo.metarevistas.org/UNIVERSIDADDESANBUENAVENTURA_COLOMBIA/logo.png
country_str Colombia
collection International Journal of Psychological Research
title The Mendelian Legacy to Mental and Behavioral Disorders
spellingShingle The Mendelian Legacy to Mental and Behavioral Disorders
Arcos-Burgos, Mauricio
Cuartas, Mauricio
Trastornos del comportamiento
Behavioral Disorders
title_short The Mendelian Legacy to Mental and Behavioral Disorders
title_full The Mendelian Legacy to Mental and Behavioral Disorders
title_fullStr The Mendelian Legacy to Mental and Behavioral Disorders
title_full_unstemmed The Mendelian Legacy to Mental and Behavioral Disorders
title_sort mendelian legacy to mental and behavioral disorders
description Editorial
description_eng Editorial
author Arcos-Burgos, Mauricio
Cuartas, Mauricio
author_facet Arcos-Burgos, Mauricio
Cuartas, Mauricio
topicspa_str_mv Trastornos del comportamiento
topic Trastornos del comportamiento
Behavioral Disorders
topic_facet Trastornos del comportamiento
Behavioral Disorders
citationvolume 13
citationissue 1
publisher Universidad San Buenaventura - USB (Colombia)
ispartofjournal International Journal of Psychological Research
source https://revistas.usb.edu.co/index.php/IJPR/article/view/4529
language Español
format Article
rights http://purl.org/coar/access_right/c_abf2
info:eu-repo/semantics/openAccess
International Journal of Psychological Research - 2020
https://creativecommons.org/licenses/by-nc-sa/4.0/
references 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.
type_driver info:eu-repo/semantics/article
type_coar http://purl.org/coar/resource_type/c_6501
type_version info:eu-repo/semantics/publishedVersion
type_coarversion http://purl.org/coar/version/c_970fb48d4fbd8a85
type_content Text
publishDate 2020-01-20
date_accessioned 2020-01-20T22:24:32Z
date_available 2020-01-20T22:24:32Z
url https://revistas.usb.edu.co/index.php/IJPR/article/view/4529
url_doi https://doi.org/10.21500/20112084.4529
issn 2011-2084
eissn 2011-7922
doi 10.21500/20112084.4529
citationstartpage 6
citationendpage 8
url4_str_mv https://revistas.usb.edu.co/index.php/IJPR/article/download/4529/3654
url2_str_mv https://revistas.usb.edu.co/index.php/IJPR/article/download/4529/3541
_version_ 1797376672188596224

Código QR

Estadísticas y Métricas Alternativas

Títulos similares