Mr Miguel Renteria Rodriguez
Honorary Fellow
School of Biomedical Sciences
Book Chapter
Renteria, Miguel E., Cortes, Adrian and Medland, Sarah E. (2013).Using PLINK for genome-wide association studies (GWAS) and data analysis. Genome-Wide Association Studies and Genomic Prediction. (pp. 193-213) edited by Cedric Gondro, Julius van der Werf and Ben Hayes.New York, NY, United States: Humana Press. doi:10.1007/978-1-62703-447-0_8
Journal Articles
Campos, Adrian I., Verweij, Karin J. H., Statham, Dixie J., Madden, Pamela A. F., Maciejewski, Dominique F., Davis, Katrina A. S., John, Ann, Hotopf, Matthew, Heath, Andrew C., Martin, Nicholas G. and Rentería, Miguel E. (2020). Genetic aetiology of self-harm ideation and behaviour. Scientific Reports, 10 (1) 9713, doi:10.1038/s41598-020-66737-9
Schmaal, Lianne, Pozzi, Elena, C. Ho, Tiffany, van Velzen, Laura S., Veer, Ilya M., Opel, Nils, Van Someren, Eus J. W., Han, Laura K. M., Aftanas, Lybomir, Aleman, André, Baune, Bernhard T., Berger, Klaus, Blanken, Tessa F., Capitão, Liliana, Couvy-Duchesne, Baptiste, R. Cullen, Kathryn, Dannlowski, Udo, Davey, Christopher, Erwin-Grabner, Tracy, Evans, Jennifer, Frodl, Thomas, Fu, Cynthia H. Y., Godlewska, Beata, Gotlib, Ian H., Goya-Maldonado, Roberto, Grabe, Hans J., Groenewold, Nynke A., Grotegerd, Dominik, Gruber, Oliver, Gutman, Boris A. and Hall, Geoffrey B. (2020). ENIGMA MDD: seven years of global neuroimaging studies of major depression through worldwide data sharing. Translational Psychiatry, 10 (1) 172, doi:10.1038/s41398-020-0842-6
Mitchell, Brittany L., Cuéllar-Partida, Gabriel, Grasby, Katrina L., Campos, Adrian I., Strike, Lachlan T., Hwang, Liang-Dar, Okbay, Aysu, Thompson, Paul M., Medland, Sarah E., Martin, Nicholas G., Wright, Margaret J. and Rentería, Miguel E. (2020). Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory. NeuroImage, 212116691, doi:10.1016/j.neuroimage.2020.116691
Thompson, Paul M., Jahanshad, Neda, Ching, Christopher R. K., Salminen, Lauren E., Thomopoulos, Sophia I., Bright, Joanna, Baune, Bernhard T., Bertolín, Sara, Bralten, Janita, Bruin, Willem B., Bülow, Robin, Chen, Jian, Chye, Yann, Dannlowski, Udo, de Kovel, Carolien G. F., Donohoe, Gary, Eyler, Lisa T., Faraone, Stephen V., Favre, Pauline, Filippi, Courtney A., Frodl, Thomas, Garijo, Daniel, Gil, Yolanda, Grabe, Hans J., Grasby, Katrina L., Hajek, Tomas, Han, Laura K. M., Hatton, Sean N., Hilbert, Kevin, Ho, Tiffany C. and Holleran, Laurena (2020). ENIGMA and global neuroscience: a decade of large-scale studies of the brain in health and disease across more than 40 countries. Translational psychiatry, 10 (1) 100, doi:10.1038/s41398-020-0705-1
Rentería, Miguel E., Mitchell, Brittany L. and Manrique de Lara, Amaranta (2020). Genetic testing for Alzheimerʼs disease : trends, challenges and ethical considerations. Current Opinion in Psychiatry, 33 (2) 136-140. doi:10.1097/yco.0000000000000573
Campos, Adrián I., García-Marín, Luis M., Byrne, Enda M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2020). Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Nature Communications, 11 (1) 817, doi:10.1038/s41467-020-14625-1
Leon-Apodaca, Ana V., Chiu-Han, Enrique, Ortega-Mora, Ivett, Román-López, Talía V., Caballero-Sánchez, Ulises, Aldana-Assad, Oscar, Campos, Adrián I., Cuellar-Partida, Gabriel, Ruiz-Contreras, Alejandra E., Alcauter, Sarael, Rentería, Miguel E. and Medina-Rivera, Alejandra (2019). TwinsMX: uncovering the basis of health and disease in the Mexican population. Twin Research and Human Genetics, 22 (6) 611-616. doi:10.1017/thg.2019.112
Satizabal, Claudia L., Adams, Hieab H. H., Hibar, Derrek P., White, Charles C., Knol, Maria J., Stein, Jason L., Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V., Smith, Albert V., Bis, Joshua C., Jian, Xueqiu, Luciano, Michelle, Hofer, Edith, Teumer, Alexander, van der Lee, Sven J., Yang, Jingyun, Yanek, Lisa R., Lee, Tom V., Li, Shuo, Hu, Yanhui, Koh, Jia Yu, Eicher, John D., Desrivières, Sylvane, Arias-Vasquez, Alejandro, Chauhan, Ganesh, Athanasiu, Lavinia, Rentería, Miguel E., Kim, Sungeun and Hoehn, David (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics, 51 (11) 1624-1636. doi:10.1038/s41588-019-0511-y
Mullins, Niamh, Bigdeli, Tim B., Børglum, Anders D., Coleman, Jonathan R.I., Demontis, Ditte, Mehta, Divya, Power, Robert A., Ripke, Stephan, Stahl, Eli A., Starnawska, Anna, Anjorin, Adebayo, Corvin, Aiden, Sanders, Alan R., Forstner, Andreas J., Reif, Andreas, Koller, Anna C., Tkowska, Beata Swia, Baune, Bernhard T., Müller-Myhsok, Bertram, Penninx, Brenda W.J.H., Pato, Carlos, Zai, Clement, Rujescu, Dan, Hougaard, David M., Quested, Digby, Levinson, Douglas F., Binder, Elisabeth B., Byrne, Enda M., Agerbo, Esben, Streit, Fabian and Mayoral, Fermin (2019). GWAS of suicide attempt in psychiatric disorders and association with major depression polygenic risk scores. American Journal of Psychiatry, 176 (8) 651-660. doi:10.1176/appi.ajp.2019.18080957
Campos, Adrian I., Mitchell, Brittany L. and Rentería, Miguel E. (2019). Twins can help us understand how genes and the environment shape us. Frontiers for Young Minds, 7 doi:10.3389/frym.2019.00059
Mitchell, Brittany L., Zhu, Gu, Medland, Sarah E., Renteria, Miguel. E., Eyles, Darryl W., Grasby, Katrina L., McGrath, John J. and Martin, Nicholas G. (2019). Half the genetic variance in vitamin D concentration is shared with skin colour and sun exposure genes. Behavior Genetics, 49 (4) 386-398. doi:10.1007/s10519-019-09954-x
Mitchell, Brittany L., Campos, Adrian I., Rentería, Miguel E., Parker, Richard, Sullivan, Lenore, McAloney, Kerrie, Couvy-Duchesne, Baptiste, Medland, Sarah E., Gillespie, Nathan A., Scott, Jan, Zietsch, Brendan P., Lind, Penelope A., Martin, Nicholas G. and Hickie, Ian B. (2019). Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study. Twin Research and Human Genetics, 22 (03) 154-163. doi:10.1017/thg.2019.27
Manrique de Lara, Amaranta, Soto-Gómez, Liliana, Núñez-Acosta, Elisa, Saruwatari-Zavala, Garbiñe and Rentería, Miguel E. (2018). Ethical issues in susceptibility genetic testing for late-onset neurodegenerative diseases. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 180 (8) 609-621. doi:10.1002/ajmg.b.32699
Dominguez-Baleon, Carmen, Gutierrez-Mondragon, Luis F., Campos-Gonzalez, Adrian I. and Renteria, Miguel E. (2018). Neuroimaging studies of suicidal behavior and non-suicidal self-injury in psychiatric patients: a systematic review. Frontiers in Psychiatry, 9 (OCT) 500, doi:10.3389/fpsyt.2018.00500
Gillespie, Nathan A., Neale, Michael C., Bates, Timothy C., Eyler, Lisa T., Fennema-Notestine, Christine, Vassileva, Jasmin, Lyons, Michael J., Prom-Wormley, Elizabeth C., McMahon, Katie L., Thompson, Paul M., de Zubicaray, Greig., Hickie, Ian B., McGrath, John J., Strike, Lachlan T., Rentería, Miguel E., Panizzon, Matthew S., Martin, Nicholas G., Franz, Carol E., Kremen, William S. and Wright, Margaret J. (2018). Testing associations between cannabis use and subcortical volumes in two large population-based samples. Addiction, 113 (9) 1661-1672. doi:10.1111/add.14252
Guadalupe, Tulio, Mathias, Samuel R., vanErp, Theo G. M., Whelan, Christopher D., Zwiers, Marcel P., Abe, Yoshinari, Abramovic, Lucija, Agartz, Ingrid, Andreassen, Ole A., Arias-Vásquez, Alejandro, Aribisala, Benjamin S., Armstrong, Nicola J., Arolt, Volker, Artiges, Eric, Ayesa-Arriola, Rosa, Baboyan, Vatche G., Banaschewski, Tobias, Barker, Gareth, Bastin, Mark E., Baune, Bernhard T., Blangero, John, Bokde, Arun L.W., Boedhoe, Premika S.W., Bose, Anushree, Brem, Silvia, Brodaty, Henry, Bromberg, Uli, Brooks, Samantha, Büchel, Christian, Buitelaar, Jan and Calhoun, Vince D. (2017). Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex. Brain Imaging and Behavior, 11 (5) 1497-1514. doi:10.1007/s11682-016-9629-z
Renteria, M. E., Schmaal, L., Hibar, D. P., Couvy-Duchesne, B., Strike, L. T., Mills, N. T., de Zubicaray, G. I., McMahon, K. L., Medland, S. E., Gillespie, N. A., Hatton, S. N., Lagopoulos, J., Veltman, D. J., van der Wee, N., van Erp, T. G. M., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Voelzke, H., Veer, I. M., Walter, H., Schnell, K., Schramm, E., Normann, C., Schoepf, D., Konrad, C., Zurowski, B., Godlewska, B. R., Cowen, P. J. and Penninx, B. W. J. H. (2017). Subcortical brain structure and suicidal behaviour in major depressive disorder: a meta-analysis from the ENIGMA-MDD working group. Translational Psychiatry, 7 (5) e1116, e1116-e1116. doi:10.1038/tp.2017.84
Hibar, Derrek P., Adams, Hieab H. H., Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L., Hofer, Edith, Renteria, Miguel E., Bis, Joshua C., Arias-Vasquez, Alejandro, Ikram, M. Kamran, Desrivieres, Sylvane, Vernooij, Meike W., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beecham, Ashley H., Beiser, Alexa, Bernard, Manon, Blanton, Susan H., Bohlken, Marc M., Boks, Marco P., Bralten, Janita, Brickman, Adam M., Carmichael, Owen and Chakravarty, M. Mallar (2017). Novel genetic loci associated with hippocampal volume. Nature Communications, 8 (1) 13624, doi:10.1038/ncomms13624
Adams, Hieab H. H., Hibar, Derrek P., Chouraki, Vincent, Stein, Jason L., Nyquist, Paul A., Renteria, Miguel E., Trompet, Stella, Arias-Vasquez, Alejandro, Seshadri, Sudha, Desrivieres, Sylvane, Beecham, Ashley H., Jahanshad, Neda, Wittfeld, Katharina, Van der Lee, Sven J., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beiser, Alexa, Bernard, Manon, Bis, Joshua C., Blanken, Laura M. E., Blanton, SusanH., Bohlken, Marc M., Boks, Marco P. and Bralten, Janita (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 (12) 1569-1582. doi:10.1038/nn.4398
Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, Breslin, Paul A. S., Reed, Danielle R., Macgregor, Stuart, Gharahkhani, Puya, Martin, Nicholas G. and Renteria, Miguel E. (2016). Sweet taste perception is associated with body mass index at the phenotypic and genotypic level. Twin Research and Human Genetics, 19 (5) 465-471. doi:10.1017/thg.2016.60
Maciejewski, Dominique F., Renteria, Miguel E., Abdellaoui, Abdel, Medland, Sarah E., Few, Lauren R., Gordon, Scott D., Madden, Pamela A. F., Montgomery, Grant, Trull, Timothy J., Heath, Andrew C., Statham, Dixie J., Martin, Nicholas G., Zietsch, Brendan P. and Verweij, Karin J. H. (2016). The association of genetic predisposition to depressive symptoms with non-suicidal and suicidal self-injuries. Behavior Genetics, 47 (1) 1-8. doi:10.1007/s10519-016-9809-z
Becker, Martin, Guadalupe, Tulio, Franke, Barbara, Hibar, Derrek P., Renteria, Miguel E., Stein, Jason L., Thompson, Paul M., Francks, Clyde, Vernes, Sonja C. and Fisher, Simon E. (2016). Early developmental gene enhancers affect subcortical volumes in the adult human brain. Human Brain Mapping, 37 (5) 1788-1800. doi:10.1002/hbm.23136
Schmaal, L., Hibar, D. P., Samann, P. G., Hall, G. B., Baune, B. T., Jahanshad, N., Cheung, J. W., van Erp, T. G. M., Bos, D., Ikram, M. A., Vernooij, M. W., Niessen, W. J., Tiemeier, H., Hofman, A., Wittfeld, K., Grabe, H. J., Janowitz, D., Bulow, R., Selonke, M., Volzke, H., Grotegerd, D., Dannlowski, U., Arolt, V., Opel, N., Heindel, W., Kugel, H., Hoehn, D., Czisch, M., Couvy-Duchesne, B., Renteria, M. E. and Strike, L. T. (2016). Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group. Molecular Psychiatry, 22 (6) 900-909. doi:10.1038/mp.2016.60
Schmaal, L., Veltman, D. J., van Erp, T. G. M., Sämann, P. G., Frodl, T., Jahanshad, N., Loehrer, E., Tiemeier, H., Hofman, A., Niessen, W. J., Vernooij, M. W., Ikram, M. A., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Völzke, H., Hoehn, D., Czisch, M., Lagopoulos, J., Hatton, S. N., Hickie, I. B., Goya-Maldonado, R., Krämer, B., Gruber, O., Couvy-Duchesne, B., Rentería, M. E., Strike, L. T., Mills, N. T., De Zubicaray, G. I. and McMahon, K. L. (2016). Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group. Molecular Psychiatry, 21 (6) 806-812. doi:10.1038/mp.2015.69
Hibar, Derrek P, Stein, Jason L, Renteria, Miguel E, Arias-Vasquez, Alejandro, Desrivieres, Sylvane, Jahanshad, Neda, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Andersson, Micael, Aribisala, Benjamin S, Armstrong, Nicola J, Bernard, Manon, Bohlken, Marc M, Boks, Marco P, Bralten, Janita, Brown, Andrew A, Mallar Chakravarty M., Chen, Qiang, Ching, Christopher R.K., Cuellar-Partida, Gabriel, Den Braber, Anouk, Giddaluru, Sudheer, Goldman, Aaron L, Grimm, Oliver, Guadalupe, Tulio, Hass, Johanna, Woldehawariat, Girma, Holmes, Avram J, Hoogman, Martine and Janowitz, Deborah (2015). Common genetic variants influence human subcortical brain structures. Nature, 520 (7546) 224-229. doi:10.1038/nature14101
Cuellar-Partida, Gabriel, Renteria, Miguel E. and MacGregor, Stuart (2015). LocusTrack: integrated visualization of GWAS results and genomic annotation. Source Code for Biology and Medicine, 10 (1) 1, 1.1-1.4. doi:10.1186/s13029-015-0032-8
Rentería, M. E., Hansell, N. K., Strike, L. T., McMahon, K. L., de Zubicaray, G. I., Hickie, Ian B., Thompson, Paul M., Martin, N. G., Medland, S. E. and Wright, M. J. (2014). Genetic architecture of subcortical brain regions: common and region-specific genetic contributions. Genes, Brain and Behavior, 13 (8) 821-830. doi:10.1111/gbb.12177
Thompson, Paul M., Stein, Jason L., Medland, Sarah E., Hibar, Derrek P., Arias Vasquez, Alejandro, Renteria, Miguel E., Toro, Roberto, Jahanshad, Neda, Schumann, Gunter, Franke, Barbara, Wright, Margaret J., Martin, Nicholas G., Agartz, Ingrid, Alda, Martin, Alhusaini, Saud, Almasy, Laura, Almeida, Jorge, Alpert, Kathryn, Andreasen, Nancy C., Andreassen, Ole A., Apostolova, Liana G., Appel, Katja, Armstrong, Nicola J., Aribisala, Benjamin, Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Bergmann, Ørjan, Binder, Elisabeth B., Blangero, John and Bockholt, Henry J. (2014). The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 8 (2) 153-182. doi:10.1007/s11682-013-9269-5
Rentería, Miguel E., Coolen, Marcel W., Statham, Aaron L., Choi, R. Seong Min, Qu, Wenjia, Campbell, Megan J., Smith, Sara, Henders, Anjali K., Montgomery, Grant W., Clark, Susan J., Martin, Nicholas G. and Medland, Sarah E. (2013). GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. Twin Research and Human Genetics, 16 (4) 767-781. doi:10.1017/thg.2013.30
Renteria, Miguel E. (2012). Cerebral assymmetry: a quantitative, multifactorial, and plastic brain phenotype. Twin Research and Human Genetics, 15 (3) 401-413. doi:10.1017/thg.2012.13
Stein, Jason L., Medland, Sarah E., Vasquez, Alejandro Arias, Hibar, Derrek P., Senstad, Rudy E., Winkler, Anderson M., Toro, Roberto, Appel, Katja, Bartecek, Richard, Bergmann, Ørjan, Bernard, Manon, Brown, Andrew A., Cannon, Dara M., Chakravarty, M. Mallar, Christoforou, Andrea, Domin, Martin, Grimm, Oliver, Hollinshead, Marisa, Holmes, Avram J., Homuth, Georg, Hottenga, Jouke-Jan, Langan, Camilla, Lopez, Lorna M., Hansell, Narelle K., Hwang, Kristy S., Kim, Sungeun, Laje, Gonzalo, Lee, Phil H., Liu, Xinmin, Loth, Eva and Lourdusamy, Anbarasu (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics, 44 (5) 552-561. doi:10.1038/ng.2250
Renteria, Miguel E., Gandhi, Neha S., Vinuesa, Pablo, Helmerhorst, Erik and Mancera, Ricardo L. (2008). A comparative structural bioinformatics analysis of the insulin receptor family ectodomain based on phylogenetic information. PLoS One, 3 (11) doi:10.1371/journal.pone.0003667
Conference Papers
Lundberg, Mischa, Campos, Adrian, Rentería, Miguel, Ngo, Trung and Cuéllar-Partida, Gabriel (2019). Dissecting the genetic architecture of chronic pain using CTG-VL — Complex-Traits Genetics Virtual Lab. In: Behavior Genetics Association 49th Annual Meeting Abstracts. 49th Annual Meeting of the Behavior Genetics Association, Stockholm, Sweden, (517). 26–29 June 2019. doi:10.1007/s10519-019-09973-8
Cuéllar-Partida, Gabriel, Lundberg, Mischa, Campos-González, Adrian I., Kho, Pik Fang, D’Urso, Shannon, Hwang, Liang-Dar, Ngo, Trung Thanh and Rentería, Miguel E. (2019). Complex-Traits Genetics Virtual Lab: A community-driven web platform for post-GWAS analyses. In: American Society of Human Genetics 69th Annual Meeting Poster Abstracts. American Society of Human Genetics (ASHG) 69th Annual Meeting, Houston, TX United States, (3006). 15–19 October 2019.
Ngo, Trung T. , Rentería, Miguel E. and Cuéllar-Partida, Gabriel (2018).Advancing a neurogenomics oscillator model of bistable affective-cognitive states, behaviour and disorders. 5th Annual Australasian Society for Social & Affective Neuroscience Conference, Brisbane QLD, Australia, 20–21 June 2018.
Ngo, Trung T. , Rentería, Miguel E. and Cuéllar-Partida, Gabriel (2018).E-mental health transdiagnostic stratification: A cloud-based platform for multi-phenotyping and genetic analyses. 40th Annual Society for Mental Health Research Conference, Noosa Heads, QLD Australia, 28–30 November 2018.
Cuéllar-Partida, Gabriel, Ngo, Trung T., Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017).A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait. BLiSS 2017 — Brisbane Life Science ECR Symposium, Translational Research Institute, Brisbane, 24 November 2017.
Ngo, Trung T., Cuéllar-Partida, Gabriel, Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017).GWAS of complementary perceptual endophenotype measures: How do they rate?. Australasian Society for Bipolar & Depressive Disorders (ASBDD) 2017 Conference, Deakin Edge, Melbourne, 15–17 September 2017.
Thesis
Rentería Rodríguez, Miguel Enrique (2013). Mapping the genetic architecture of subcortical brain anatomy. PhD Thesis, School of Psychology, The University of Queensland.