Associate Professor Miguel Rentería
Honorary Senior Fellow
School of Biomedical Sciences
Researcher biography
I am a genetic epidemiologist specialising in the genetics of neurodegenerative diseases, with a particular focus on Parkinson's disease, chronic pain, and other age-related conditions. I lead a dynamic team of scientists dedicated to understanding how genetic and environmental factors influence neurodegeneration, brain health, and related health outcomes. My research is interdisciplinary, integrating advanced statistical genetics, bioinformatics, and data science to unravel disease mechanisms, improve patient stratification, and identify potential therapeutic targets.
In 2020, I founded the Australian Parkinson's Genetics Study (APGS), now the largest Parkinson's cohort in Australia with over 10,000 participants. This landmark study has positioned Australia as a key contributor to global Parkinson's genetics research. I am also actively involved in the Global Parkinson's Genetics Program (GP2), where I contribute to large-scale data analysis and work within the underrepresented populations working group to enhance diversity in genetic research worldwide.
Committed to training the next generation of researchers, I have supervised over 16 students, including several PhD candidates who have gone on to successful careers in academia and industry. Two of my recent PhD graduates received the Outstanding Thesis Award, and another received the AIPS Florey Next Generation Award.
I have published consistently in prominent journals, including Nature, Nature Genetics, Nature Communications, BRAIN, Biological Psychiatry, and SLEEP. To date, I have authored over 100 academic articles, which have been widely cited, and I have secured competitive funding from NHMRC, MRFF, The Michael J. Fox Foundation for Parkinson's Research, Shake It Up Australia Foundation, the US National Institutes of Health, and the Alzheimer's Association. My work has been recognised with several prestigious awards, including the 2023 Al & Val Rosenstrauss Fellowship from the Rebecca L Cooper Medical Research Foundation, the 2021 Enrico Greppi International Migraine Research Award, and the 2024 Adele Green Emerging Leader Award from QIMR Berghofer Medical Research Institute. I am also a Global Atlantic Fellow for Equity in Brain Health, a program by the University of California San Francisco and Trinity College Dublin, which supports my commitment to promoting brain health equity worldwide.
Book Chapters
García-Marín, Luis M., Ceja, Zuriel, Rentería, Miguel E. and Galaburda, Albert M. (2024). Cerebral Lateralization and Hemispheric Specialization. The Sage Handbook of Cognitive and Systems Neuroscience. (pp. 259-276) London, United Kingdom: SAGE Publications. doi: 10.4135/9781529616613.n17
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
Diaz-Torres, Santiago, Lee, Samantha Sze-Yee, García-Marín, Luis M., Campos, Adrian I., Lingham, Garreth, Ong, Jue-Sheng, Mackey, David A., Burdon, Kathryn P., Hunter, Michael, Dong, Xianjun, MacGregor, Stuart, Gharahkhani, Puya and Rentería, Miguel E. (2024). Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysis. Nature Communications, 15 (1) 9116, 1-10. doi: 10.1038/s41467-024-53212-6
García-Marín, Luis M., Campos, Adrian I., Diaz-Torres, Santiago, Rabinowitz, Jill A., Ceja, Zuriel, Mitchell, Brittany L., Grasby, Katrina L., Thorp, Jackson G., Agartz, Ingrid, Alhusaini, Saud, Ames, David, Amouyel, Philippe, Andreassen, Ole A., Arfanakis, Konstantinos, Arias-Vasquez, Alejandro, Armstrong, Nicola J., Athanasiu, Lavinia, Bastin, Mark E., Beiser, Alexa S., Bennett, David A., Bis, Joshua C., Boks, Marco P. M., Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Buitelaar, Jan K., Burkhardt, Ralph, Cahn, Wiepke, Calhoun, Vince D. ... Rentería, Miguel E. (2024). Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries. Nature Genetics, 56 (11), 1-12. doi: 10.1038/s41588-024-01951-z
Ceja, Zuriel, Van Velzen, Laura S., Campos, Adrian I., Jahanshad, Neda, Medland, Sarah E., Edwards, Alexis C., Schmaal, Lianne and Rentería, Miguel E. (2024). Recent breakthroughs in genetic and brain structural correlates of suicidal behaviours: A short review. Biological Psychiatry. doi: 10.1016/j.biopsych.2024.09.010
Diaz-Torres, Santiago, Lee, Samantha Sze-Yee, Ogonowski, Natalia S., Mackey, David A., MacGregor, Stuart, Gharahkhani, Puya and Renteria, Miguel E. (2024). Macular structural integrity estimates are associated with Parkinson’s disease genetic risk. Acta Neuropathologica Communications, 12 (1) 130, 130. doi: 10.1186/s40478-024-01841-9
Reyes-Pérez, Paula, Hernández-Ledesma, Ana Laura, Román-López, Talía V., García-Vilchis, Brisa, Ramírez-González, Diego, Lázaro-Figueroa, Alejandra, Martinez, Domingo, Flores-Ocampo, Victor, Espinosa-Méndez, Ian M., Tinajero-Nieto, Lizbet, Peña-Ayala, Angélica, Morelos-Figaredo, Eugenia, Guerra-Galicia, Carlos M., Torres-Valdez, Estefania, Gordillo-Huerta, María Vanessa, Gandarilla-Martínez, Nadia A, Salinas-Barboza, Karla, Félix-Rodríguez, Guillermo, Frontana-Vázquez, Gabriel, Matuk-Pérez, Yamil, Estrada-Bellmann, Ingrid, Alpizar-Rodríguez, Deshiré, Rodríguez-Violante, Mayela, Rentería, Miguel E., Ruíz-Contreras, Alejandra E., Alcauter, Sarael and Medina-Rivera, Alejandra (2024). Building national patient registries in Mexico: insights from the MexOMICS Consortium. Frontiers in Digital Health, 6 1344103. doi: 10.3389/fdgth.2024.1344103
García-Vilchis, Brisa, Román-López, Talia V., Ramírez-González, Diego, López-Camaño, Xanat J., Murillo-Lechuga, Vanessa, Díaz-Téllez, Xóchitl, Sánchez-Moncada, C. Itzamná, Espinosa-Méndez, Ian M., Zenteno-Morales, Diego, Espinosa-Valdes, Zaida X., Pradel-Jiménez, Sofia, Tapia-Atilano, Andrea, Zanabria-Pérez, Ana V., Livas-Gangas, Federica, Aldana-Assad, Oscar, Caballero-Sánchez, Ulises, Dominguez-Frausto, César A., Rentería, Miguel E., Medina-Rivera, Alejandra, Alcauter, Sarael and Ruiz-Contreras, Alejandra E. (2024). TwinsMX: Exploring the Genetic and Environmental Influences on Health Traits in the Mexican Population. Twin Research and Human Genetics, 27 (2), 1-12. doi: 10.1017/thg.2024.18
Knol, Maria J., Poot, Raymond A., Evans, Tavia E., Satizabal, Claudia L., Mishra, Aniket, Sargurupremraj, Muralidharan, van der Auwera, Sandra, Duperron, Marie-Gabrielle, Jian, Xueqiu, Hostettler, Isabel C., van Dam-Nolen, Dianne H.K., Lamballais, Sander, Pawlak, Mikolaj A., Lewis, Cora E., Carrion-Castillo, Amaia, van Erp, Theo G.M., Reinbold, Céline S., Shin, Jean, Scholz, Markus, Håberg, Asta K., Kämpe, Anders, Li, Gloria H.Y., Avinun, Reut, Atkins, Joshua R., Hsu, Fang-Chi, Amod, Alyssa R., Lam, Max, Tsuchida, Ami, Teunissen, Mariël W.A. ... Adams, Hieab H.H. (2024). Genetic variants for head size share genes and pathways with cancer. Cell Reports Medicine, 5 (5) 101529, 101529. doi: 10.1016/j.xcrm.2024.101529
García-Marín, Luis M. and Rentería, Miguel E. (2024). Fighting plastic pollution with a circular economy roadmap and strategy: Addressed to the United Nations Environment Programme. Journal of Science Policy & Governance, 24 (01). doi: 10.38126/jspg240107
Ogonowski, Natalia S., García-Marín, Luis M., Fernando, Amali S., Flores-Ocampo, Victor and Rentería, Miguel E. (2024). Impact of genetic predisposition to late-onset neurodegenerative diseases on early life outcomes and brain structure. Translational Psychiatry, 14 (1) 185, 185. doi: 10.1038/s41398-024-02898-9
Reyes-Pérez, Paula, García-Marín, Luis M., Aman, Asma M., Antar, Tarek, Flores-Ocampo, Victor, Mitchell, Brittany L., Medina-Rivera, Alejandra and Rentería, Miguel E. (2024). Investigating the Shared Genetic Etiology Between Parkinson’s Disease and Depression. Journal of Parkinson's Disease, 14 (3), 1-11. doi: 10.3233/jpd-230176
Martinez-Levy, Gabriela A., Maya-Martínez, Mateo, García-Marín, Luis M., Díaz-Torres, Santiago, Gómez, Lina M., Benjet, Corina, Rentería, Miguel E., Cruz-Fuentes, Carlos S. and Rabinowitz, Jill A. (2024). Associations of externalizing polygenic scores with externalizing disorders among Mexican youth. Journal of Psychiatric Research, 171, 346-353. doi: 10.1016/j.jpsychires.2024.01.030
Meng, Xiangrui, Navoly, Georgina, Giannakopoulou, Olga, Levey, Daniel F., Koller, Dora, Pathak, Gita A., Koen, Nastassja, Lin, Kuang, Adams, Mark J., Rentería, Miguel E., Feng, Yanzhe, Gaziano, J. Michael, Stein, Dan J., Zar, Heather J., Campbell, Megan L., van Heel, David A., Trivedi, Bhavi, Finer, Sarah, McQuillin, Andrew, Bass, Nick, Chundru, V. Kartik, Martin, Hilary C., Huang, Qin Qin, Valkovskaya, Maria, Chu, Chia-Yi, Kanjira, Susan, Kuo, Po-Hsiu, Chen, Hsi-Chung, Tsai, Shih-Jen ... BioBank Japan Project (2024). Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Nature Genetics, 56 (2), 222-233. doi: 10.1038/s41588-023-01596-4
Chen, Huadong, Buziau, Amée M, Rentería, Miguel E, Simons, Pomme I H G and Brouwers, Martijn C G J (2024). Fructose intake from sugar-sweetened beverages is associated with a greater risk of hyperandrogenism in women: UK Biobank cohort study. European Journal of Endocrinology, 190 (1), 104-112. doi: 10.1093/ejendo/lvae006
Palmer, Emily OC, Ker, Sheryl, Rentería, Miguel E., Carmody, Thomas and Rush, A. John (2024). Psychometric evaluation and linking of the PHQ-9, QIDS-C, and VQIDS-C in a real-world population with major depressive disorder. Neuropsychiatric Disease and Treatment, 20, 671-687. doi: 10.2147/NDT.S444223
Mbarek, Hamdi, Gordon, Scott D., Duffy, David L., Hubers, Nikki, Mortlock, Sally, Beck, Jeffrey J., Hottenga, Jouke-Jan, Pool, René, Dolan, Conor V., Actkins, Ky’Era V., Gerring, Zachary F., Van Dongen, Jenny, Ehli, Erik A., Iacono, William G., Mcgue, Matt, Chasman, Daniel I., Gallagher, C. Scott, Schilit, Samantha L. P., Morton, Cynthia C., Paré, Guillaume, Willemsen, Gonneke, Whiteman, David C., Olsen, Catherine M., Derom, Catherine, Vlietinck, Robert, Gudbjartsson, Daniel, Cannon-Albright, Lisa, Krapohl, Eva, Plomin, Robert ... Martin, Nicholas G. (2024). Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity. Human Reproduction, 39 (1), 240-257. doi: 10.1093/humrep/dead247
Lázaro-Figueroa, Alejandra, Hernández-Medrano, Ana Jimena, Ramírez-Pineda, Diana Berenice, Navarro Cadavid, Andrés, Makarious, Mary, Foo, Jia Nee, Alvarado, Chelsea X., Bandres-Ciga, Sara, Periñan, Maria Teresa, Gatto, Emilia M., Kauffman, Marcelo, Khachatryan, Samson, Tavadyan, Zaruhi, Shepherd, Claire E., Hunter, Julie, Kumar, Kishore, Ellis, Melina, Rentería, Miguel E., Koks, Sulev, Zimprich, Alexander, Schumacher-Schuh, Artur F., Rieder, Carlos, Awad, Paula Saffie, Tumas, Vitor, Camargos, Sarah, Fon, Edward A., Monchi, Oury, Fon, Ted, Galleguillos, Benjamin Pizarro ... Atadzhanov, Masharip (2024). Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?. Movement Disorders, 39 (11), 2117-2119. doi: 10.1002/mds.29719
García-Marín, Luis M., Ogonowski, Natalia S., Han, Laura K.M., Maya-Martínez, Mateo, Mitchell, Brittany L., Schmaal, Lianne, Martin, Nicholas G. and Rentería, Miguel E. (2024). Investigating the genetic relationship of intracranial and subcortical brain volumes with depression and other psychiatric disorders. Imaging Neuroscience, 2, 1-16. doi: 10.1162/imag_a_00291
Kim, Jonggeol Jeffrey, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Cannon, Paul, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Fitch, Alison, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Granka, Julie M., Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M. ... Mata, Ignacio (2023). Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease. Nature Genetics, 56 (1), 27-36. doi: 10.1038/s41588-023-01584-8
Lange, Lara M., Avenali, Micol, Ellis, Melina, Illarionova, Anastasia, Keller Sarmiento, Ignacio J., Tan, Ai-Huey, Madoev, Harutyun, Galandra, Caterina, Junker, Johanna, Roopnarain, Karisha, Solle, Justin, Wegel, Claire, Fang, Zih-Hua, Heutink, Peter, Kumar, Kishore R., Lim, Shen-Yang, Valente, Enza Maria, Nalls, Mike, Blauwendraat, Cornelis, Singleton, Andrew, Mencacci, Niccolo, Lohmann, Katja, Klein, Christine, Gatto, Emilia M., Kauffman, Marcelo, Khachatryan, Samson, Tavadyan, Zaruhi, Shepherd, Claire E., Hunter, Julie ... Atadzhanov, Masharip (2023). Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9). npj Parkinson's Disease, 9 (1) 133. doi: 10.1038/s41531-023-00560-7
Towns, Clodagh, Richer, Madeleine, Jasaityte, Simona, Stafford, Eleanor J., Joubert, Julie, Antar, Tarek, Martinez-Carrasco, Alejandro, Makarious, Mary B., Casey, Bradford, Vitale, Dan, Levine, Kristin, Leonard, Hampton, Pantazis, Caroline B., Screven, Laurel A., Hernandez, Dena G., Wegel, Claire E., Solle, Justin, Nalls, Mike A., Blauwendraat, Cornelis, Singleton, Andrew B., Tan, Manuela M. X., Iwaki, Hirotaka, Morris, Huw R., Gatto, Emilia M., Kauffman, Marcelo, Khachatryan, Samson, Tavadyan, Zaruhi, Shepherd, Claire E., Hunter, Julie ... Atadzhanov, Masharip (2023). Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2). npj Parkinson's Disease, 9 (1) 131. doi: 10.1038/s41531-023-00533-w
Garcia-Marin, Luis M., Mulcahy, Aoibhe, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Chafota, Freddy, Lind, Penelope A., Martin, Nicholas G., Hickie, Ian B., Rentería, Miguel E. and Campos, Adrian I. (2023). Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants. Annals of General Psychiatry, 22 (1) 49, 1-8. doi: 10.1186/s12991-023-00480-z
Rizig, Mie, Bandres-Ciga, Sara, Makarious, Mary B, Ojo, Oluwadamilola Omolara, Crea, Peter Wild, Abiodun, Oladunni Victoria, Levine, Kristin S, Abubakar, Sani Atta, Achoru, Charles Obiora, Vitale, Dan, Adeniji, Olaleye Akinmola, Agabi, Osigwe Paul, Koretsky, Mathew J, Agulanna, Uchechi, Hall, Deborah A, Akinyemi, Rufus Olusola, Xie, Tao, Ali, Mohammed Wulgo, Shamim, Ejaz A, Ani-Osheku, Ifeyinwa, Padmanaban, Mahesh, Arigbodi, Ohwotemu Michael, Standaert, David G, Bello, Abiodun Hamzat, Dean, Marissa N, Erameh, Cyril Oshomah, Elsayed, Inas, Farombi, Temitope Hannah, Okunoye, Olaitan ... Tavadyan, Zaruhi (2023). Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study. The Lancet Neurology, 22 (11), 1015-1025. doi: 10.1016/S1474-4422(23)00283-1
Román-López, Talía V., García-Vilchis, Brisa, Murillo-Lechuga, Vanessa, Chiu-Han, Enrique, López-Camaño, Xanat, Aldana-Assad, Oscar, Diaz-Torres, Santiago, Caballero-Sánchez, Ulises, Ortega-Mora, Ivett, Ramírez-González, Diego, Zenteno, Diego, Espinosa-Valdés, Zaida, Tapia-Atilano, Andrea, Pradel-Jiménez, Sofía, Rentería, Miguel E., Medina-Rivera, Alejandra, Ruiz-Contreras, Alejandra E. and Alcauter, Sarael (2023). Estimating the genetic contribution to astigmatism and myopia in the Mexican population. Twin Research and Human Genetics, 26 (4-5), 1-9. doi: 10.1017/thg.2023.41
Patel, Rashmi, Chan, Kelly M.Y., Palmer, Emily O.C., Valko, Matthew, Guruswamy, Guruprabha, Ker, Sheryl, Batra, Gunjan, Rentería, Miguel E. and Kollins, Scott H. (2023). Associations of comorbid substance use disorders with clinical outcomes in schizophrenia using electronic health record data. Schizophrenia Research, 260, 191-197. doi: 10.1016/j.schres.2023.08.023
Docherty, Anna R., Mullins, Niamh, Ashley-Koch, Allison E., Qin, Xuejun, Coleman, Jonathan R.I., Shabalin, Andrey, Kang, JooEun, Murnyak, Balasz, Wendt, Frank, Adams, Mark, Campos, Adrian I., DiBlasi, Emily, Fullerton, Janice M., Kranzler, Henry R., Bakian, Amanda V., Monson, Eric T., Rentería, Miguel E., Walss-Bass, Consuelo, Andreassen, Ole A., Behera, Chittaranjan, Bulik, Cynthia M., Edenberg, Howard J., Kessler, Ronald C., Mann, J. John, Nurnberger, John I., Pistis, Giorgio, Streit, Fabian, Ursano, Robert J., Polimanti, Renato ... German Borderline Genomics Consortium (2023). GWAS meta-analysis of suicide attempt: identification of 12 genome-wide significant loci and implication of genetic risks for specific health factors. American Journal of Psychiatry, 180 (10), 723-738. doi: 10.1176/appi.ajp.21121266
Rabinowitz, Jill A., Reboussin, Beth A., Sosnowski, David W., Kuo, Sally I-Chun, Strickland, Justin C., García-Marín, Luis M., Rentería, Miguel E., Gillespie, Nathan, Maher, Brion, Ialongo, Nicholas S., Thorpe, Roland J. and Uhl, George (2023). Associations of polygenic risk scores for smoking heaviness and lifetime cannabis use with tobacco and cannabis co-use trajectories among African Americans. Drug and Alcohol Dependence, 250 110895, 1-8. doi: 10.1016/j.drugalcdep.2023.110895
Wang, Tao, Rentería, Miguel E., Tian, Zhen and Peng, Jiajie (2023). Editorial: data mining and statistical methods for knowledge discovery in diseases based on multimodal omics, volume II. Frontiers in Genetics, 14 1270862, 1-3. doi: 10.3389/fgene.2023.1270862
Han, Xikun, Gharahkhani, Puya, Hamel, Andrew R., Ong, Jue Sheng, Rentería, Miguel E., Mehta, Puja, Dong, Xianjun, Pasutto, Francesca, Hammond, Christopher, Young, Terri L., Hysi, Pirro, Lotery, Andrew J., Jorgenson, Eric, Choquet, Hélène, Hauser, Michael, Cooke Bailey, Jessica N., Nakazawa, Toru, Akiyama, Masato, Shiga, Yukihiro, Fuller, Zachary L., Wang, Xin, Hewitt, Alex W., Craig, Jamie E., Pasquale, Louis R., Mackey, David A., Wiggs, Janey L., Khawaja, Anthony P., Segrè, Ayellet V., MacGregor, Stuart ... International Glaucoma Genetics Consortium (2023). Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci. Nature Genetics, 55 (7), 1116-1125. doi: 10.1038/s41588-023-01428-5
Diaz-Torres, Santiago, Ogonowski, Natalia, García-Marín, Luis M., Bonham, Luke W., Duran-Aniotz, Claudia, Yokoyama, Jennifer S. and Rentería, Miguel E. (2023). Genetic overlap between cortical brain morphometry and frontotemporal dementia risk. Cerebral Cortex, 33 (12), 7428-7435. doi: 10.1093/cercor/bhad049
García-Marín, Luis M., Reyes-Pérez, Paula, Diaz-Torres, Santiago, Medina-Rivera, Alejandra, Martin, Nicholas G., Mitchell, Brittany L. and Rentería, Miguel E. (2023). Shared molecular genetic factors influence subcortical brain morphometry and Parkinson’s disease risk. npj Parkinson's Disease, 9 (1) 73, 73. doi: 10.1038/s41531-023-00515-y
Wang, Jiao, Campos, Adrian I., Rentería, Miguel E. and Xu, Lin (2023). Causal associations of sleep apnea, snoring with cardiovascular diseases, and the role of body mass index: a two-sample Mendelian randomization study. European Journal of Preventive Cardiology, 30 (7), 552-560. doi: 10.1093/eurjpc/zwad005
Farrell, Scott F., Sterling, Michele, Klyne, David M., Mustafa, Sanam, Campos, Adrián I., Kho, Pik-Fang, Lundberg, Mischa, Rentería, Miguel E., Ngo, Trung Thanh and Cuéllar-Partida, Gabriel (2023). Genetic impact of blood C-reactive protein levels on chronic spinal and widespread pain. European Spine Journal, 32 (6), 2078-2085. doi: 10.1007/s00586-023-07711-7
Wee, Soon Nan, Liman, Christian, Waters, Heidi C., Houle, Christy R., Renteria, Miguel, Mukherjee, Sankha S, Surendran, Subina, Marcovici, Joshua, Brubaker, Malaak, Rasmussen Meehan, Stine, de Jong-Laird, Anne, Rush, A John and Sarkar, Joydeep (2023). Life engagement improvement following initiation of brexpiprazole treatment in patients with mdd: a naturalistic, retrospective real-world study. ClinicoEconomics and Outcomes Research, 15, 195-208. doi: 10.2147/ceor.s395255
Farrell, Scott F., Kho, Pik-Fang, Lundberg, Mischa, Campos, Adrián I., Rentería, Miguel E., de Zoete, Rutger M.J., Sterling, Michele, Ngo, Trung Thanh and Cuéllar-Partida, Gabriel (2023). A shared genetic signature for common chronic pain conditions and its impact on biopsychosocial traits. The Journal of Pain, 24 (3), 369-386. doi: 10.1016/j.jpain.2022.10.005
Campos, Adrian I., Ingold, Nathan, Huang, Yunru, Mitchell, Brittany L., Kho, Pik-Fang, Han, Xikun, García-Marín, Luis M., Ong, Jue-Sheng, 23andMe Research Team, Law, Matthew H., Yokoyama, Jennifer S., Martin, Nicholas G., Dong, Xianjun, Cuellar-Partida, Gabriel, MacGregor, Stuart, Aslibekyan, Stella and Rentería, Miguel E. (2023). Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep, 46 (3) zsac308, 1-14. doi: 10.1093/sleep/zsac308
Campos, Adrian I., Van Velzen, Laura S., Veltman, Dick J., Pozzi, Elena, Ambrogi, Sonia, Ballard, Elizabeth D., Banaj, Nerisa, Başgöze, Zeynep, Bellow, Sophie, Benedetti, Francesco, Bollettini, Irene, Brosch, Katharina, Canales-Rodríguez, Erick J., Clarke-Rubright, Emily K., Colic, Lejla, Connolly, Colm G., Courtet, Philippe, Cullen, Kathryn R., Dannlowski, Udo, Dauvermann, Maria R., Davey, Christopher G., Deverdun, Jeremy, Dohm, Katharina, Erwin-Grabner, Tracy, Goya-Maldonado, Roberto, Fani, Negar, Fortea, Lydia, Fuentes-Claramonte, Paola, Gonul, Ali Saffet ... Rentería, Miguel E. (2023). Concurrent validity and reliability of suicide risk assessment instruments: A meta-analysis of 20 instruments across 27 international cohorts. Neuropsychology, 37 (3), 315-329. doi: 10.1037/neu0000850
Wang, Jiao, Campos, Adrian I., García‐Marín, Luis M., Rentería, Miguel E. and Xu, Lin (2023). Causal associations of sleep apnea and snoring with type 2 diabetes and glycemic traits and the role of BMI. Obesity, 31 (3), 652-664. doi: 10.1002/oby.23669
Jayarathna, Dulari K., Rentería, Miguel E., Batra, Jyotsna and Gandhi, Neha S. (2023). Integrative competing endogenous RNA network analyses identify novel lncRNA and genes implicated in metastatic breast cancer. Scientific Reports, 13 (1) 2423, 1-10. doi: 10.1038/s41598-023-29585-x
Waters, Heidi C., Touya, Maelys, Wee, Soon Nan, Ng, Michelle, Thadani, Simran, Surendran, Subina, Rentería, Miguel, Rush, A. John, Patel, Rashmi, Sarkar, Joydeep, Fitzgerald, Heather M. and Han, Xue (2023). Psychiatric healthcare resource utilization following initiation of aripiprazole once-monthly: a retrospective real-world study. Current Medical Research and Opinion, 39 (2), 299-306. doi: 10.1080/03007995.2022.2148461
Gomez, Lina, Díaz-Torres, Santiago, Colodro-Conde, Lucía, Garcia-Marin, Luis M., Yap, Chloe X., Byrne, Enda M., Yengo, Loic, Lind, Penelope A., Wray, Naomi R., Medland, Sarah E., Hickie, Ian B., Lupton, Michelle K., Rentería, Miguel E., Martin, Nicholas G. and Campos, Adrian I. (2022). Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study. European Archives of Psychiatry and Clinical Neuroscience, 273 (6), 1359-1368. doi: 10.1007/s00406-022-01527-0
Jayarathna, Dulari K., Rentería, Miguel E., Kho, Pik Fang, Batra, Jyotsna and Gandhi, Neha S. (2022). Dehydroepiandrosterone sulfate and colorectal cancer risk: a mendelian randomization analysis. Twin Research and Human Genetics, 25 (4-5) PII S1832427422000317, 180-186. doi: 10.1017/thg.2022.31
Castruita, Patricia Alejandra, Piña-Escudero, Stefanie Danielle, Rentería, Miguel E. and Yokoyama, Jennifer S. (2022). Genetic, Social, and Lifestyle Drivers of Healthy Aging and Longevity. Current Genetic Medicine Reports, 10 (3), 25-34. doi: 10.1007/s40142-022-00205-w
van Velzen, Laura S., Dauvermann, Maria R., Colic, Lejla, Villa, Luca M., Savage, Hannah S., Toenders, Yara J., Zhu, Alyssa H., Bright, Joanna K., Campos, Adrián I., Salminen, Lauren E., Ambrogi, Sonia, Ayesa-Arriola, Rosa, Banaj, Nerisa, Başgöze, Zeynep, Bauer, Jochen, Blair, Karina, Blair, Robert James, Brosch, Katharina, Cheng, Yuqi, Colle, Romain, Connolly, Colm G., Corruble, Emmanuelle, Couvy-Duchesne, Baptiste, Crespo-Facorro, Benedicto, Cullen, Kathryn R., Dannlowski, Udo, Davey, Christopher G., Dohm, Katharina, Fullerton, Janice M. ... Schmaal, Lianne (2022). Structural brain alterations associated with suicidal thoughts and behaviors in young people: results from 21 international studies from the ENIGMA Suicidal Thoughts and Behaviours consortium. Molecular Psychiatry, 27 (11), 1-11. doi: 10.1038/s41380-022-01734-0
Aman, Asma M., García-Marín, Luis M., Thorp, Jackson G., Campos, Adrian I., Cuellar-Partida, Gabriel, Martin, Nicholas G.. and Rentería, Miguel E. (2022). Phenome-wide screening of the putative causal determinants of depression using genetic data. Human Molecular Genetics, 31 (17), 2887-2898. doi: 10.1093/hmg/ddac081
Mitchell, Brittany L., Diaz-Torres, Santiago, Bivol, Svetlana, Cuellar-Partida, Gabriel, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H. ... International Headache Genetics Consortium (2022). Elucidating the relationship between migraine risk and brain structure using genetic data. Brain, 145 (9), 3214-3224. doi: 10.1093/brain/awac105
Mitchell, Brittany L., Hansell, Narelle K., McAloney, Kerrie, Martin, Nicholas G., Wright, Margaret J., Renteria, Miguel E. and Grasby, Katrina L. (2022). Polygenic influences associated with adolescent cognitive skills. Intelligence, 94 101680, 1-9. doi: 10.1016/j.intell.2022.101680
Wang, Jiao, Huang, Yingyue, Yang, Huiling, Lin, Zihong, Campos, Adrian I., Rentería, Miguel E. and Xu, Lin (2022). Plasma polyunsaturated fatty acid concentrations and sleep apnea risk: a two-sample Mendelian randomization study. Frontiers in Nutrition, 9 956900, 1-8. doi: 10.3389/fnut.2022.956900
Campos, Adrian I., Byrne, Enda M., Iorfino, Frank, Fabbri, Chiara, Hickie, Ian B., Lewis, Cathryn M., Wray, Naomi R., Medland, Sarah E., Rentería, Miguel E. and Martin, Nicholas G. (2022). Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 189 (6), 196-206. doi: 10.1002/ajmg.b.32913
Jayarathna, Dulari K., Rentería, Miguel E., Batra, Jyotsna and Gandhi, Neha S. (2022). A supervised machine learning approach identifies gene‐regulating factor‐mediated competing endogenous RNA networks in hormone‐dependent cancers. Journal of Cellular Biochemistry, 123 (8), 1394-1408. doi: 10.1002/jcb.30300
García-Marín, Luis M., Rabinowitz, Jill A., Ceja, Zuriel, Alcauter, Sarael, Medina-Rivera, Alejandra and Rentería, Miguel E. (2022). The pharmacogenomics of selective serotonin reuptake inhibitors. Pharmacogenomics, 23 (10), 597-607. doi: 10.2217/pgs-2022-0037
Wang, Tao, Rentería, Miguel E. and Peng, Jiajie (2022). Editorial: Data Mining and Statistical Methods for Knowledge Discovery in Diseases Based on Multimodal Omics. Frontiers in Genetics, 13 895796. doi: 10.3389/fgene.2022.895796
Patel, Rashmi, Wee, Soon Nan, Ramaswamy, Rajagopalan, Thadani, Simran, Tandi, Jesisca, Garg, Ruchir, Calvanese, Nathan, Valko, Matthew, Rush, A. John, Rentería, Miguel E., Sarkar, Joydeep and Kollins, Scott H. (2022). NeuroBlu, an electronic health record (EHR) trusted research environment (TRE) to support mental healthcare analytics with real-world data. BMJ Open, 12 (4) e057227, 1-11. doi: 10.1136/bmjopen-2021-057227
Campos, Adrian I., Garcia-Marin, Luis M., Christensen, Helen, Batterham, Philip J., van Velzen, Laura S., Schmaal, Lianne, Rabinowitz, Jill A., Jahanshad, Neda, Martin, Nicholas G., Cuellar-Partida, Gabriel, Ruderfer, Douglas, Mullins, Niamh, Rentería, Miguel E. and The International Suicide Genetics Consortium (2022). Genomics-driven screening for causal determinants of suicide attempt. Australian and New Zealand Journal of Psychiatry, 57 (3) ARTN 00048674221091499, 48674221091499-431. doi: 10.1177/00048674221091499
Rabinowitz, Jill A., Jin, Jin, Kuo, Sally I-Chun, Campos, Adrian I., Rentería, Miguel E., Huhn, Andrew S., Thrul, Johannes, Reboussin, Beth A., Benke, Kelly, Domingue, Benjamin, Ialongo, Nicholas S., Maher, Brion S., Kertes, Darlene, Troiani, Vanessa and Uhl, George (2022). Positive associations between cannabis and alcohol use polygenic risk scores and phenotypic opioid misuse among African-Americans. PloS One, 17 (4) e0266384, e0266384. doi: 10.1371/journal.pone.0266384
Pain, Oliver, Hodgson, Karen, Trubetskoy, Vassily, Ripke, Stephan, Marshe, Victoria S., Adams, Mark J., Byrne, Enda M., Campos, Adrian I., Carrillo-Roa, Tania, Cattaneo, Annamaria, Als, Thomas D., Souery, Daniel, Dernovsek, Mojca Z., Fabbri, Chiara, Hayward, Caroline, Henigsberg, Neven, Hauser, Joanna, Kennedy, James L., Lenze, Eric J., Lewis, Glyn, Müller, Daniel J., Martin, Nicholas G., Mulsant, Benoit H., Mors, Ole, Perroud, Nader, Porteous, David J., Rentería, Miguel E., Reynolds, Charles F., Rietschel, Marcella ... Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2022). Identifying the Common Genetic Basis of Antidepressant Response. Biological Psychiatry Global Open Science, 2 (2), 115-126. doi: 10.1016/j.bpsgos.2021.07.008
Rabinowitz, Jill A., Campos, Adrian I., Ong, Jue-Sheng, García-Marín, Luis M., Alcauter, Sarael, Mitchell, Brittany L, Grasby, Katrina L, Cuéllar-Partida, Gabriel, Gillespie, Nathan A, Huhn, Andrew S, Martin, Nicholas G, Thompson, Paul M, Medland, Sarah E, Maher, Brion S and Rentería, Miguel E (2022). Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use. Cerebral Cortex, 32 (4), 796-807. doi: 10.1093/cercor/bhab243
van Velzen, Laura S., Toenders, Yara J., Avila-Parcet, Aina, Dinga, Richard, Rabinowitz, Jill A., Campos, Adrián I., Jahanshad, Neda, Rentería, Miguel E. and Schmaal, Lianne (2022). Classification of suicidal thoughts and behaviour in children: results from penalised logistic regression analyses in the Adolescent Brain Cognitive Development study. The British Journal of Psychiatry, 220 (4), 1-9. doi: 10.1192/bjp.2022.7
Mitchell, Brittany L., Saklatvala, Jake R., Dand, Nick, Hagenbeek, Fiona A., Li, Xin, Min, Josine L., Thomas, Laurent, Bartels, Meike, Jan Hottenga, Jouke, Lupton, Michelle K., Boomsma, Dorret I., Dong, Xianjun, Hveem, Kristian, Løset, Mari, Martin, Nicholas G., Barker, Jonathan N., Han, Jiali, Smith, Catherine H., Rentería, Miguel E. and Simpson, Michael A. (2022). Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. Nature Communications, 13 (1) 702, 702. doi: 10.1038/s41467-022-28252-5
Mullins, Niamh, Kang, JooEun, Campos, Adrian I., Coleman, Jonathan R I, Edwards, Alexis C., Galfalvy, Hanga, Levey, Daniel F., Lori, Adriana, Shabalin, Andrey, Starnawska, Anna, Su, Mei-Hsin, Watson, Hunna J., Adams, Mark, Awasthi, Swapnil, Gandal, Michael, Hafferty, Jonathan D., Hishimoto, Akitoyo, Kim, Minsoo, Okazaki, Satoshi, Otsuka, Ikuo, Ripke, Stephan, Ware, Erin B., Bergen, Andrew W., Berrettini, Wade H., Bohus, Martin, Brandt, Harry, Chang, Xiao, Chen, Wei J., Chen, Hsi-Chung ... Ruderfer, Douglas M. (2022). Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors. Biological Psychiatry, 91 (3), 313-327. doi: 10.1016/j.biopsych.2021.05.029
Bivol, Svetlana, Mellick, George D., Gratten, Jacob, Parker, Richard, Mulcahy, Aoibhe, Mosley, Philip E., Poortvliet, Peter C., Campos, Adrian I., Mitchell, Brittany L., Garcia-Marin, Luis M., Cross, Simone, Ferguson, Mary, Lind, Penelope A., Loesch, Danuta Z., Visscher, Peter M., Medland, Sarah E., Scherzer, Clemens R., Martin, Nicholas G. and Rentería, Miguel E. (2022). Australian Parkinson’s Genetics Study (APGS): pilot (n=1532). BMJ Open, 12 (2) e052032, e052032. doi: 10.1136/bmjopen-2021-052032
Campos, Adrian I., Byrne, Enda M., Mitchell, Brittany L., Wray, Naomi R., Lind, Penelope A., Licinio, Julio, Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B. and Rentería, Miguel E. (2022). Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study. The Pharmacogenomics Journal, 22 (2), 130-135. doi: 10.1038/s41397-022-00267-7
Ingold, Nathan, Campos, Adrian I., Han, Xikun, Ong, Jue-Sheng, Gharahkhani, Puya, Mackey, David A., Rentería, Miguel E., Law, Matthew H. and MacGregor, Stuart (2022). Is genetic risk for sleep apnea causally linked With glaucoma susceptibility?. Investigative ophthalmology & visual science, 63 (1) 25, 25. doi: 10.1167/iovs.63.1.25
Ogonowski, Natalia, Salcidua, Stefanny, Leon, Tomas, Chamorro-Veloso, Nayaret, Valls, Cristian, Avalos, Constanza, Bisquertt, Alejandro, Rentería, Miguel E., Orellana, Paulina and Duran-Aniotz, Claudia (2022). Systematic Review: microRNAs as Potential Biomarkers in Mild Cognitive Impairment Diagnosis. Frontiers in Aging Neuroscience, 13 807764, 807764. doi: 10.3389/fnagi.2021.807764
Farrell, Scott F, Campos, Adrián I, Kho, Pik-Fang, de Zoete, Rutger M J, Sterling, Michele, Rentería, Miguel E, Ngo, Trung Thanh and Cuéllar-Partida, Gabriel (2021). Genetic basis to structural grey matter associations with chronic pain. Brain, 144 (12), 3611-3622. doi: 10.1093/brain/awab334
García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide analysis highlights putative causal relationships between self-reported migraine and other complex traits. Journal of Headache and Pain, 22 (1) 66, 66. doi: 10.1186/s10194-021-01284-w
Domínguez-Baleón, Carmen, Ong, Jue-Sheng, Scherzer, Clemens R., Rentería, Miguel E. and Dong, Xianjun (2021). Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study. Scientific Reports, 11 (1) 13980. doi: 10.1038/s41598-021-93105-y
García-Marín, Luis M., Campos, Adrián I., Cuéllar-Partida, Gabriel, Medland, Sarah E., Kollins, Scott H. and Rentería, Miguel E. (2021). Large-scale genetic investigation reveals genetic liability to multiple complex traits influencing a higher risk of ADHD. Scientific Reports, 11 (1) 22628, 22628. doi: 10.1038/s41598-021-01517-7
Martinez‐Levy, Gabriela A., Campos, Adrian I., Rabinowitz, Jill A., García‐Marín, Luis M., Benjet, Corina, Méndez, Enrique, Rentería, Miguel E. and Cruz‐Fuentes, Carlos S. (2021). Suicidal ideation and planning among Mexican adolescents are associated with depression polygenic risk scores. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 186 (8) ajmg.b.32864, 476-484. doi: 10.1002/ajmg.b.32864
Campos, Adrian I., Mulcahy, Aoibhe, Thorp, Jackson G., Wray, Naomi R., Byrne, Enda M., Lind, Penelope A., Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B. and Rentería, Miguel E. (2021). Understanding genetic risk factors for common side effects of antidepressant medications. Communications Medicine, 1 (1) 45, 1-10. doi: 10.1038/s43856-021-00046-8
Jayarathna, Dulari K., Rentería, Miguel E., Sauret, Emilie, Batra, Jyotsna and Gandhi, Neha S. (2021). Identifying complex lncRNA/Pseudogene–miRNA–mRNA crosstalk in hormone-dependent cancers. Biology, 10 (10) 1014, 1014. doi: 10.3390/biology10101014
Ker, Sheryl, Hsu, Jennifer, Balani, Anisha, Mukherjee, Sankha Subhra, Rush, A John, Khan, Mehreen, Elchehabi, Sara, Huffhines, Seth, DeMoss, Dustin, Rentería, Miguel E and Sarkar, Joydeep (2021). Factors that affect patient attrition in buprenorphine treatment for opioid use disorder: a retrospective real-world study using electronic health records. Neuropsychiatric Disease and Treatment, 17, 3229-3244. doi: 10.2147/ndt.s331442
Miles, Amy E., Dos Santos, Fernanda C., Byrne, Enda M., Renteria, Miguel E., McIntosh, Andrew M., Adams, Mark J., Pistis, Giorgio, Castelao, Enrique, Preisig, Martin, Baune, Bernhard T., Schubert, K. Oliver, Lewis, Cathryn M., Jones, Lisa A., Jones, Ian, Uher, Rudolf, Smoller, Jordan W., Perlis, Roy H., Levinson, Douglas F., Potash, James B., Weissman, Myrna M., Shi, Jianxin, Lewis, Glyn, Penninx, Brenda W. J. H., Boomsma, Dorret I., Hamilton, Steven P., Sibille, Etienne, Hariri, Ahmad R., Nikolova, Yuliya S. and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2021). Transcriptome-based polygenic score links depression-related corticolimbic gene expression changes to sex-specific brain morphology and depression risk. Neuropsychopharmacology, 46 (13), 2304-2311. doi: 10.1038/s41386-021-01189-x
Jayarathna, Dulari K., Rentería, Miguel E., Malik, Adil, Sauret, Emilie, Batra, Jyotsna and Gandhi, Neha S. (2021). Integrative transcriptome-wide analyses uncover novel risk-associated MicroRNAs in hormone-dependent cancers. Frontiers in Genetics, 12 716236. doi: 10.3389/fgene.2021.716236
Campos, Adrian I., Kho, Pik, Vazquez-Prada, Karla X., García-Marín, Luis M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Genetic susceptibility to pneumonia: a GWAS meta-analysis between the UK Biobank and FinnGen. Twin Research and Human Genetics, 24 (3) PII S183242742100027X, 145-154. doi: 10.1017/thg.2021.27
Campos, Adrián I., Ngo, Trung Thanh, Medland, Sarah E., Wray, Naomi R., Hickie, Ian B., Byrne, Enda M., Martin, Nicholas G. and Rentería, Miguel E. (2021). Genetic risk for chronic pain is associated with lower antidepressant effectiveness: converging evidence for a depression subtype. Australian and New Zealand Journal of Psychiatry, 56 (9) ARTN 00048674211031491, 1-10. doi: 10.1177/00048674211031491
Rabinowitz, Jill A., Jin, Jin, Kahn, Geoffrey, Kuo, Sally I.‐Chun, Campos, Adrian, Renteria, Miguel, Benke, Kelly, Wilcox, Holly, Ialongo, Nicholas S., Maher, Brion S., Kertes, Darlene, Eaton, William, Uhl, George, Wagner, Barry M. and Cohen, Daniel (2021). Genetic propensity for risky behavior and depression and risk of lifetime suicide attempt among urban African Americans in adolescence and young adulthood. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 186 (8) ajmg.b.32866, 456-468. doi: 10.1002/ajmg.b.32866
García-Marín, Luis M., Campos, Adrián I., Kho, Pik-Fang, Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide screening of GWAS data reveals the complex causal architecture of obesity. Human Genetics, 140 (8), 1253-1265. doi: 10.1007/s00439-021-02298-9
Roughan, William H., Campos, Adrián I., García-Marín, Luis M., Cuéllar-Partida, Gabriel, Lupton, Michelle K., Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Byrne, Enda M., Ngo, Trung Thanh, Martin, Nicholas G. and Rentería, Miguel E. (2021). Comorbid chronic pain and depression: shared risk factors and differential antidepressant effectiveness. Frontiers in Psychiatry, 12 643609, 1-13. doi: 10.3389/fpsyt.2021.643609
Garcia-Marin, Luis M., Alcauter, Sarael, Campos, Adrian I., Mulcahy, Aoibhe, Kho, Pik-Fang, Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Evidence of genetic overlap between circadian preference and brain white matter microstructure. Twin Research and Human Genetics, 24 (1) PII S1832427421000049, 1-6. doi: 10.1017/thg.2021.4
Campos, Adrian I., Thompson, Paul M., Veltman, Dick J., Pozzi, Elena, van Veltzen, Laura S., Jahanshad, Neda, Adams, Mark J., Baune, Bernhard T., Berger, Klaus, Brosch, Katharina, Bülow, Robin, Connolly, Colm G., Dannlowski, Udo, Davey, Christopher G., de Zubicaray, Greig I., Dima, Danai, Erwin-Grabner, Tracy, Evans, Jennifer W., Fu, Cynthia H.Y., Gotlib, Ian H., Goya-Maldonado, Roberto, Grabe, Hans J., Grotegerd, Dominik, Harris, Matthew A., Harrison, Ben J., Hatton, Sean N., Hermesdorf, Marco, Hickie, Ian B., Ho, Tiffany C. ... Rentería, Miguel E. (2021). Brain correlates of suicide attempt in 18,925 participants across 18 international cohorts. Biological Psychiatry, 90 (4), 243-252. doi: 10.1016/j.biopsych.2021.03.015
García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Inference of causal relationships between sleep-related traits and 1,527 phenotypes using genetic data. Sleep, 44 (1) zsaa154. doi: 10.1093/sleep/zsaa154
Rabinowitz, Jill A., Campos, Adrian I., Benjet, Corina, Su, Jinni, Macias-Kauffer, Luis, Méndez, Enrique, Martinez-Levy, Gabriela A., Cruz-Fuentes, Carlos S. and Rentería, Miguel E. (2020). Depression polygenic scores are associated with major depressive disorder diagnosis and depressive episode in Mexican adolescents. Journal of Affective Disorders Reports, 2 100028. doi: 10.1016/j.jadr.2020.100028
Haworth, Simon, Kho, Pik Fang, Holgerson, Pernilla Lif, Hwang, Liang-Dar, Timpson, Nicholas J., Rentería, Miguel E., Johansson, Ingegerd and Cuellar-Partida, Gabriel (2020). Assessment and visualization of phenome-wide causal relationships using genetic data: an application to dental caries and periodontitis. European Journal of Human Genetics, 29 (2), 300-308. doi: 10.1038/s41431-020-00734-4
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, 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 ... Veltman, Dick J. (2020). ENIGMA MDD: seven years of global neuroimaging studies of major depression through worldwide data sharing. Translational Psychiatry, 10 (1) 172, 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, 212 116691, 116691. 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 ... Zelman, Vladimir (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, 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, 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. ... Ikram, M. Arfan (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 ... Lewis, Cathryn M. (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) PII S1832427419000276, 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, 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 ... Francks, Clyde (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. ... Hickie, I. B. (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. ... Ikram, M. Arfan (2017). Novel genetic loci associated with hippocampal volume. Nature Communications, 8 (1) 13624, 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. ... Thompson, Paul M. (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. ... Veltman, D. J. (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. ... Hibar, D. P. (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 ... Medland, Sarah E (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. ... Saguenay Youth Study (SYS) Group (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 ... Brown, Matthew A. (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) e3667, e3667. doi: 10.1371/journal.pone.0003667
Conference Papers
Ceja, Zuriel, Edwards, Alexis, Martin, Nick, Hickie, Ian, Medland, Sarah E. and Rentería, Miguel E. (2024). Genetic And Psychological Predictors Of Suicidal Behavior: Insights From Polygenic Risk Scores And Mental Health Diagnoses. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.324
Yeow, Dennis, Rudaks, Laura I, García-Marín, Luis M, Flores-Ocampo, Victor, Morales-Briceño, Hugo, Yau, Wai Y, Kõks, Sulev, Mellick, George D, Fung, Victor SC, Tisch, Stephen, Wu, Kathy HC, Schofield, Deborah, Willis, Amanda M, Klein, Christine, Sue, Carolyn M, Davis, Ryan L, Young, Mary-Anne, Rentería, Miguel E, Kumar, Kishore R and Global Parkinson’s Genetics Program (GP2) Investigators and MonoPDAus Investigators (2024). Monogenic Parkinson’s Disease Australia (MonoPDAus) initiative: study protocol. ANZAN Annual Scientific Meeting, Jakarta, Indonesia, 10-14 September 2024. London, United Kingdom: BMJ Group. doi: 10.1136/bmjno-2024-anzan.60
Lupton, Michelle K., Gomez, Lina, Mitchell, Brittany L., Adsett, Jessica, García‐Marín, Luis M., Renteria, Miguel E., McAloney, Kerrie, Ceslis, Amelia, Thienel, Renate, Robinson, Gail, Breakspear, Michael and Martin, Nicholas G (2023). Poorer online cognitive performance is associated with genetic risk for Alzheimer’s disease and brain phenotypes in healthy mid‐life and older adults. AAIC 2023 Abstracts, Amsterdam, Netherlands, 16-20 July 2023. Hoboken, NJ USA: Wiley. doi: 10.1002/alz.078078
Escudero, Stefanie Danielle Pina, Franco, Teresita Ramos, Archila, Oscar Robles, Renteria, Miguel E., Ibanez, Agustin, Slachevsky, Andrea and Yokoyama, Jennifer S. (2023). Online abridged behavioral neurology training for specialists in Latin America: EduBrainLat. Alzheimer’s Association International Conference AAIC 2023, Amsterdam, Netherlands, 16-20 July 2023. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.080679
Diaz‐Torres, Santiago, Ogonowski, Natalia, García‐Marín, Luis M., Bonham, Luke W., Duran‐Aniotz, Claudia, Yokoyama, Jennifer S. and Renteria, Miguel E. (2023). Genetic overlap between cortical brain morphometry and frontotemporal dementia risk. Alzheimer’s Association International Conference AAIC 2023, Amsterdam, Netherlands, 16-20 July 2023. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.080759
Martinez-Levy, Gabriela, Maya-Martínez, Mateo, Garcia-Marin, Luis, Gómez, Lina, Benjet, Corina, Rentería, Miguel E., Cruz-Fuentes, Carlos S. and Rabinowits, Jill A. (2023). European Externalizing Polygenic Risk Scores Predicts Adhd Among Mexican Youth. World Congress of Psychiatric Genetics WCPG 2023, Montreal, QC Canada, 10-14 October 2023. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2023.08.236
Mitchell, B., Saklatvala, J., Martin, N.G., Smith, C., Barker, J., Renteria, M. and Simpson, M. (2022). Exploring the relationship between acne and mental health. 51st Annual ESDR Meeting, Amsterdam, Netherlands, 28 September-1 October 2022. Oxford, United Kingdom: Elsevier. doi: 10.1016/j.jid.2022.09.318
Hernandez-Ledesma, A. L., Nunez-Reza, K. J., Tapia-Atilano, A. Y., Flores-Ocampo, V., del Moral, J. E. Villarreal, Roman-Lopez, T. V., del Valle, S. V. Vera, Dominguez-Zuniga, D., Torres-Valdez, E., Frontana-Vazquez, G., Alcauter, S., Renteria, M. E., Ruiz-Contreras, A. E., Alpizar-Rodriguez, D. and Medina-Rivera, A. (2022). HEALTH RELATED QUALITY OF LIFE IN PATIENTS WITH SYSTEMIC LUPUS ERYTHEMATOSUS: DATA AND POTENTIAL APPLICATIONS OF THE MEXICAN REGISTER OF LUPUS. Annual European Congress of Rheumatology (EULAR), Copenhagen Denmark, Jun 01-04, 2022. LONDON: BMJ PUBLISHING GROUP. doi: 10.1136/annrheumdis-2022-eular.350
Campos, Adrian I., Garcia-Marin, Luis M., Christensen, Helen, Batterham, Philip J., van Velzen, Laura S., Schmaal, Lianne, Rabinowitz, Jill A., Jahanshad, Neda, Martin, Nicholas G., Cuellar-Partida, Gabriel, Ruderfer, Douglas M., Mullins, Niamh and Renteria, Miguel E. (2022). Genomics Driven Screening for Causal Determinants of Suicide Attempt. SOBP 77th Annual Scientific Meeting, New Orleans, LA United States, 28-30 April 2022. Philadelphia, PA United States: Elsevier.
van Velzen, Laura, Jahanshad, Neda, Campos, Adrian, Salminen, Lauren, Renteria, Miguel and Schmaal, Lianne (2021). Structural Brain Alterations Associated With Suicidal Ideation and Attempt: Mega-Analytic Results Across 37 International Studies. Society of Biological Psychiatry’s 2021 Annual Scientific Convention and Meeting, New Orleans, LA United States, 28-30 April 2022. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.biopsych.2021.02.072
Campos, Adrián I., Roughan, William H., García-Marin, Luis M., Cuéllar-Partida, Gabriel, Lupton, Michelle K., Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Byrne, Enda M., Ngo, Trung T., Martin, Nicholas G. and Rentería, Miguel E. (2020). The relationship between comorbid chronic pain and poorer self-reported antidepressant efficacy is partly mediated by genetics. Virtual 2020 World Congress of Psychiatric Genetics (WCPG), Online, 16–22 October 2020.
Ngo, Trung Thanh, Zhu, Guohun, Rentería, Miguel E. and Cuéllar-Partida, Gabriel (2020). Elucidating a phylogenetic switching model of sleep, vision & mental health with computational biology and complex network analyses. Systems & Computational Neuroscience Down Under (SCiNDU) 2020 meeting, St Lucia, QLD Australia, 29–31 January 2020.
Lundberg, Mischa, Campos, Adrian I., Farrell, Scott F., Wang, Geng, Sterling, Michele M., Rentería, Miguel E., Ngo, Trung Thanh and Cuéllar-Partida, Gabriel (2020). Genetic, lifestyle and environmental risk factors for chronic pain revealed through GWAS. 50th Annual Meeting of the Behavior Genetics Association, Online, 26 June 2020. NEW YORK: SPRINGER.
Lundberg, Mischa, Campos, Adrian, Renteria, Miguel, Trung Ngo, and Partida, Gabriel Cuellar (2019). Dissecting the genetic architecture of chronic pain using CTG-VL: complex-traits genetics virtual lab. 49th Annual Meeting of the Behavior-Genetics-Association (BGA), Stockholm Sweden, Jun 26-29, 2019. NEW YORK: SPRINGER.
Ngo, Trung T. , Rentería, Miguel E. and Cuéllar-Partida, Gabriel (2019). Precision switch medicine: transdiagnostic stratification of bipolar and related disorders with an integrated phenotyping and genetics analysis cloud platform. 21st Annual ISBD Conference: Global Advances in Bipolar Disorder and Depression, International Convention Centre, Sydney, Australia, 20–23 March 2019. Hoboken, NJ, United States: Wiley-Blackwell. doi: 10.1111/bdi.12746
Campos, Adrian, Renteria, Miguel E., Byrne, Enda, Medland, Sarah E., Wray, Naomi, Hickie, Ian B. and Martin, Nick (2019). Assessing clinical, demographic and genetic risk factors for treatment attributed suicidality in > 20,000 Australian adults on antidepressants. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, United States, 26-31 October 2019. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2019.07.212
Mitchell, Brittany, Renteria, Miguel E., Byrne, Enda, Conde, Lucia Colodro, Han, Xikun, Medland, Sarah E., Wray, Naomi and Martin, Nick (2019). Examining the shared genetics between educational attainment and depression: results from the Australian Genetics of Depression Study. 27th World Congress of Psychiatric Genetics, Los Angeles, United States, 26-31 October 2019. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2019.07.172
Mitchell, Brittany, Partida, Gabriel Cuellar, Grasby, Katrina, Strike, Lachlan, Thompson, Paul, Medland, Sarah, Martin, Nicholas, Wright, Margaret and Renteria, Miguel (2019). Educational attainment polygenic risk scores predict surface area of cortical regions important for language and memory. 49th Annual Meeting of the Behavior Genetics Association (BGA), Stockholm, Sweden, 26-29 June, 2019. New York, NY, United States: Springer New York LLC. doi: 10.1007/s10519-019-09973-8
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. 49th Annual Meeting of the Behavior Genetics Association, Stockholm, Sweden, 26–29 June 2019. New York, NY United States: Springer Nature. 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. American Society of Human Genetics (ASHG) 69th Annual Meeting, Houston, TX United States, 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.
Trung Ngo,, Renteria, Miguel E., Conde, Lucia Colodro, Couvy-Duchesne, Baptiste, Cuellar-Partida, Gabriel, Hansen, Narelle K., Medland, Sarah E., Miller, Steven M., Wright, Margaret J. and Martin, Nicholas G. (2017). Binocular rivalry rate as a novel candidate endophenotype for bipolar disorder. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto, Canada, 16-20 October 2015. Amsterdam, Netherlands: Elsevier.
Schmaal, L., Veltman, D. J., Van Erp, T. G., Saemann, 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., Voelzke, H., Hoehn, D., Czisch, M., Lagopoulos, J., Hatton, S. N., Hickie, I. B., Goya-Maldonado, R., Kraemer, B., Gruber, O., Couvy-Duchesne, B., Renteria, M. E., Strike, L. T., Mills, N. T. ... Hibar, D. P. (2015). Structural brain alterations in major depression: findings from the ENIGMA Major Depressive Disorder Working Group. 28th Congress of the European College of Neuropsychopharmacology (ECNP), Amsterdam Netherlands, Aug 29-Sep 01, 2015. Amsterdam, Netherlands: Elsevier BV. doi: 10.1016/S0924-977X(15)30517-4
Thesis
Rentería Rodríguez, Miguel Enrique (2013). Mapping the genetic architecture of subcortical brain anatomy. PhD Thesis, School of Psychology, The University of Queensland.