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Hon Assoc Professor Miguel Rentería
Hon Assoc Professor

Miguel Rentería

Email: 

Overview

Background

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.

Availability

Hon Assoc Professor Miguel Rentería is:
Available for supervision
Media expert

Qualifications

  • Bachelor (Honours) of Genomics, Universidad Nacional Autónoma de México (UNAM)
  • Doctor of Philosophy of Genetics, The University of Queensland
  • Masters (Coursework) of Public Policy, University of Oxford

Works

Search Professor Miguel Rentería’s works on UQ eSpace

190 works between 2008 and 2026

1 - 20 of 190 works

2026

Journal Article

Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations (npj Parkinson's Disease, (2025), 11, 1, (348), 10.1038/s41531-025-01180-z)

Sun, Wenhua, Schulte, Claudia, Gasser, Thomas, Tan, Manuela, Atadzhanov, Masharip, Nguyen, Toan, Nguyen, Duan, Foroud, Tatiana, Xie, Tao, Walker, Ruth, Alcalay, Roy, Albin, Roger, Shulman, Lisa, Dean, Marissa, Ruffrage, Lauren, Chahine, Lana M., Marek, Kenneth, Markopoulou, Katerina, Kieburtz, Karl, Nuytemans, Karen, Shulman, Joshua, Inca-Martinez, Miguel, Jankovic, Joseph, Lubbe, Steven, Mencacci, Niccolò E., Sarmiento, Ignacio Juan Keller, Chen, Honglei, Beach, Thomas, Serrano, Geidy E. ... Pihlstrøm, Lasse (2026). Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations (npj Parkinson's Disease, (2025), 11, 1, (348), 10.1038/s41531-025-01180-z). npj Parkinson's Disease, 12 (1) 93. doi: 10.1038/s41531-026-01351-6

Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations (npj Parkinson's Disease, (2025), 11, 1, (348), 10.1038/s41531-025-01180-z)

2026

Journal Article

Cumulative traumatic brain injury as a predictor of Parkinson's disease with sex-related differences

Lázaro-Figueroa, Alejandra, Garza-Flores, Stephanie, Reyes-Pérez, Paula, Morales De Arcia, Andrés, Esquivias, Juan, Caballero-Sánchez, Ulises, Guerra-Galicia, Carlos M., Estrada-Bellmann, Ingrid, Oropeza, Dante, Matuk-Pérez, Yamil, Morelos-Figaredo, Eugenia, Gandarilla-Martínez, Nadia A., Portillo-Sánchez, Antinea, Salinas-Barboza, Karla, López-Pintor, Araliz, Angulo-Arrieta, Ana, Nolasco-López, Miriam, Zayas-Del Moral, Alejandra, Rentería, Miguel E., Alcauter, Sarael, Hernandez-Ponce, Fatima, González-González, Mirna, Luna-Rangel, Francisco A., Medina-Rivera, Alejandra, Martinez-Ramirez, Daniel and Ruiz-Contreras, Alejandra E. (2026). Cumulative traumatic brain injury as a predictor of Parkinson's disease with sex-related differences. Parkinsonism and Related Disorders, 148 108334, 1-6. doi: 10.1016/j.parkreldis.2026.108334

Cumulative traumatic brain injury as a predictor of Parkinson's disease with sex-related differences

2026

Journal Article

Proteomic and genetic insights into ancestry‐specific associations in Parkinson's disease

Lim, Amanda Wei‐Yin, Foo, Jia‐Nee, Chew, Elaine Guo‐Yan, Lim, Shen‐Yang, Tan, Ai Huey, Hwang, Liang‐Dar, MacGregor, Stuart, Rentería, Miguel E. and Ong, Jue‐Sheng (2026). Proteomic and genetic insights into ancestry‐specific associations in Parkinson's disease. Movement Disorders, 41 (4) mds.70169, 981-991. doi: 10.1002/mds.70169

Proteomic and genetic insights into ancestry‐specific associations in Parkinson's disease

2026

Journal Article

Relationship between neurologic symptoms and signs and FMR1 genotype in premutation carriers

Tassone, Flora, Chafota, Freddy, Renteria, Miguel E., Hagerman, Randi J., Santos, Ellery, Atkinson, Anna, Martin, Nicholas G., Storey, Elsdon and Loesch, Danuta Z. (2026). Relationship between neurologic symptoms and signs and FMR1 genotype in premutation carriers. Annals of Clinical and Translational Neurology acn3.70375. doi: 10.1002/acn3.70375

Relationship between neurologic symptoms and signs and FMR1 genotype in premutation carriers

2026

Journal Article

CD8+ T cells sustain vaccination-induced immunity against dissemination of contained tuberculosis in immunosuppressed hosts

Miranda-Hernandez, Socorro, Kumar, Manoharan, Henderson, Alec, Graham, Erin, Tan, Xiao, Taylor, Jim, Meehan, Michael T., Ceja, Zuriel, del Pozo-Ramos, Lidia, Pan, Yi, Tsui, Ellen, Donovan, Meg L., Rentería, Miguel E., Flores-Valdez, Mario Alberto, Blumenthal, Antje, Nguyen, Quan, Subbian, Selvakumar, Field, Matt A. and Kupz, Andreas (2026). CD8+ T cells sustain vaccination-induced immunity against dissemination of contained tuberculosis in immunosuppressed hosts. Nature Communications, 17 (1) 4476, 1-17. doi: 10.1038/s41467-026-70911-4

CD8+ T cells sustain vaccination-induced immunity against dissemination of contained tuberculosis in immunosuppressed hosts

2026

Journal Article

Unique and shared internalizing and externalizing genetic factors associated with suicidal thoughts and behaviors: Findings from the adolescent brain cognitive development study

Thomas, Nathaniel S., Hung, I-Tzu, Ceja, Zuriel, García-Marín, Luis M., Stephenson, Mallory, Castro-de-Araujo, Luis Silva, Lannoy, Séverine, Thorp, Jackson, Rentería, Miguel E., Edwards, Alexis C. and Rabinowitz, Jill A. (2026). Unique and shared internalizing and externalizing genetic factors associated with suicidal thoughts and behaviors: Findings from the adolescent brain cognitive development study. Journal of Affective Disorders, 397 120931, 1-11. doi: 10.1016/j.jad.2025.120931

Unique and shared internalizing and externalizing genetic factors associated with suicidal thoughts and behaviors: Findings from the adolescent brain cognitive development study

2026

Journal Article

Genome-wide assessment reveals ancestral differences in homozygosity patterns potentially linked to Parkinson's Disease etiology

Step, Kathryn, Hernández, Carlos F., Khani, Marzieh, Eltaraifee, Esraa, Hernández-Medrano, Ana Jimena, Kung, Pin-Jui, Ostrožovičová, Miriam, Zirra, Alexandra, Pérez-Palma, Eduardo, Mencacci, Niccolò E., Keller Sarmiento, Ignacio J., Morris, Huw R., Mata, Ignacio F., Acosta-Uribe, Juliana, Fang, Zih-Hua, Bandres-Ciga, Sara, Mecheri, Yasser, Sofiane, Bouchetara Mohamed, Traki, Benhassine, Gatto, Emilia Mabel, Kauffman, Marcelo, Capparelli, Federico, Muller, Maria Valentina, Tela, Marcela Susana, Adamec, Dario Sergio, Avila, Cesar, Khachatryan, Samson, Tavadyan, Zaruhi, Isayan, Mariam ... Atadzhanov, Masharip (2026). Genome-wide assessment reveals ancestral differences in homozygosity patterns potentially linked to Parkinson's Disease etiology. Movement Disorders, 41 (5), 1128-1140. doi: 10.1002/mds.70182

Genome-wide assessment reveals ancestral differences in homozygosity patterns potentially linked to Parkinson's Disease etiology

2026

Journal Article

Insights from a cross-sectional population-based study of 10,929 Australians living with Parkinson's disease: risk factors, comorbidities, and sex differences

Cao, Fangyuan, McAloney, Kerrie, Ogonowski, Natalia S., García-Marín, Luis M., Díaz-Torres, Santiago, Flores-Ocampo, Victor, Ceja, Zuriel, Chafota, Freddy, Parker, Richard, Ferguson, Mary, Cicero, Rebekah A., List-Armitage, Susan E., Miller, Vicki, Campbell, Clyde, Sue, Carolyn M., Kumar, Kishore R., Mellick, George D., Martin, Nicholas G. and Rentería, Miguel E. (2026). Insights from a cross-sectional population-based study of 10,929 Australians living with Parkinson's disease: risk factors, comorbidities, and sex differences. The Lancet Regional Health - Western Pacific, 68 101816, 1-14. doi: 10.1016/j.lanwpc.2026.101816

Insights from a cross-sectional population-based study of 10,929 Australians living with Parkinson's disease: risk factors, comorbidities, and sex differences

2026

Journal Article

CRISPR screens identify PRMT7 as a therapeutic target to enhance T cell-mediated killing in breast cancer

Shi, Wei, Luo, Yi, Wang, Yizhuo, Burrows, Jacqueline M., Black, Debra, Civitarese, Andrew, Perlaza-Jimenez, Laura, Zhang, Ping, Manning, Murray, Tuano, Natasha, Rentería, Miguel E., Xiao, Christos, Tey, Siok-Keen, Rosenbluh, Joseph, Smith, Corey, Chenevix-Trench, Georgia and Beesley, Jonathan (2026). CRISPR screens identify PRMT7 as a therapeutic target to enhance T cell-mediated killing in breast cancer. npj Breast Cancer, 12 (1) 24. doi: 10.1038/s41523-025-00888-8

CRISPR screens identify PRMT7 as a therapeutic target to enhance T cell-mediated killing in breast cancer

2026

Journal Article

Genetic exploration of the relationship between liability to psychiatric disorders and acne vulgaris

Mitchell, Brittany L., Lupton, Michelle K., Rentería, Miguel E., Simpson, Michael A. and Reay, William R. (2026). Genetic exploration of the relationship between liability to psychiatric disorders and acne vulgaris. European Journal of Human Genetics, 34 (4) PMID 9302235, 565-573. doi: 10.1038/s41431-026-02028-7

Genetic exploration of the relationship between liability to psychiatric disorders and acne vulgaris

2026

Journal Article

Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onset

Lim, Kai Shi, Periñan, Maria Teresa, Chew, Elaine Guo Yan, Lee, Paul Suhwan, Akçimen, Fulya, Lim, Jia Lun, Koretsky, Mathew J., Funayama, Manabu, Yoshino, Hiroyo, Hattori, Nobutaka, Kaiyrzhanov, Rauan, Houlden, Henry, Isayan, Mariam, Tay, Yi Wen, Toh, Tzi Shin, Lit, Lei-Cheng, Khairul Anuar, Anis Nadhirah, Ding, Hans Xing, Screven, Laurel, Ibrahim, Norlinah Mohamed, Lin, Chin-Hsien, Kim, Han-Joon, Lee, Jee-Young, Chung, Sun Ju, Foo, Jia Nee, Tan, Eng-King, Lim, Shen-Yang, Tan, Ai Huey, Bandres-Ciga, Sara ... Yan Chew, Elaine Guo (2026). Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onset. npj Parkinson's Disease, 12 (1) 51. doi: 10.1038/s41531-026-01265-3

Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onset

2026

Conference Publication

TRANSDIAGNOSTIC COMPARISON OF SLEEP MEASURES ACROSS CHRONIC PHYSICAL AND MENTAL HEALTH DISORDERS USING FITBIT DATA IN THE ALL OF US DATASET

Huang, X., Hsieh, C., Nguyen, Q., Renteria, M. E. and Gharahkhani, P. (2026). TRANSDIAGNOSTIC COMPARISON OF SLEEP MEASURES ACROSS CHRONIC PHYSICAL AND MENTAL HEALTH DISORDERS USING FITBIT DATA IN THE ALL OF US DATASET. AMSTERDAM: ELSEVIER.

TRANSDIAGNOSTIC COMPARISON OF SLEEP MEASURES ACROSS CHRONIC PHYSICAL AND MENTAL HEALTH DISORDERS USING FITBIT DATA IN THE ALL OF US DATASET

2026

Journal Article

Transdiagnostic comparison of sleep measures across chronic physical and mental health disorders using FitBit data in the All of Us dataset

Huang, X., Hsieh, C., Nguyen, Q., Rentería, M.E. and Gharahkhani, P. (2026). Transdiagnostic comparison of sleep measures across chronic physical and mental health disorders using FitBit data in the All of Us dataset. Sleep Medicine, 138 108633, 108633. doi: 10.1016/j.sleep.2025.108633

Transdiagnostic comparison of sleep measures across chronic physical and mental health disorders using FitBit data in the All of Us dataset

2026

Journal Article

Genetic analysis of APOE reveals distinct origins and distribution of ancestry-enrichment haplotypes in the Mexican Biobank

Barberena-Jonas, Carmina, Flores-Ocampo, Victor, Ogonowski, Natalia S., Piña-Escudero, Stefanie Danielle, Mata, Ignacio F., Yokoyama, Jennifer S., García-García, Lourdes, Aguilar Salinas, Carlos Alberto, Tusié-Luna, María Teresa, Moreno-Estrada, Andrés and Rentería, Miguel E. (2026). Genetic analysis of APOE reveals distinct origins and distribution of ancestry-enrichment haplotypes in the Mexican Biobank. Genes and Diseases, 13 (1) 101542, 1-4. doi: 10.1016/j.gendis.2025.101542

Genetic analysis of APOE reveals distinct origins and distribution of ancestry-enrichment haplotypes in the Mexican Biobank

2026

Journal Article

Decoding chronic pain: integrating genetics, neuroimaging, and AI for precision management

Uckac, Bade, Ogonowski, Natalia S., García-Marín, Luis M., Diaz-Torres, Santiago, Farrell, Scott F., Nyholt, Dale R. and Rentería, Miguel E. (2026). Decoding chronic pain: integrating genetics, neuroimaging, and AI for precision management. Frontiers in Pain Research, 7 1747942, 7. doi: 10.3389/fpain.2026.1747942

Decoding chronic pain: integrating genetics, neuroimaging, and AI for precision management

2026

Journal Article

Genome-wide meta-analyses of non-response to antidepressants provide insights into underlying molecular genetics and suggest potential pharmacotherapies

Koch, Elise, Puusepp, Tuuli, Einarsson, Guðmundur, Mitchell, Brittany L., Harder, Arvid, Lin, Yuhao, García-Marín, Luis M., Krebs, Kristi, Shadrin, Alexey A., Xiong, Ying, Estonian Biobank Research Team, Metspalu, Andres, Esko, Tõnu, Mägi, Reedik, Nelis, Mari, Hudjashov, Georgi, Frei, Oleksandr, Lu, Yi, Hägg, Sara, Rentería, Miguel E., Medland, Sarah E., Wray, Naomi R., Martin, Nicholas G., Hübel, Christopher, Breen, Gerome, Thorgeirsson, Thorgeir, Stefánsson, Hreinn, Stefánsson, Kári, Lehto, Kelli ... O’Connell, Kevin S. (2026). Genome-wide meta-analyses of non-response to antidepressants provide insights into underlying molecular genetics and suggest potential pharmacotherapies. Molecular Psychiatry, 31 (4), 2005-2013. doi: 10.1038/s41380-025-03357-7

Genome-wide meta-analyses of non-response to antidepressants provide insights into underlying molecular genetics and suggest potential pharmacotherapies

2025

Journal Article

TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations

Sun, Wenhua, Schulte, Claudia, Gasser, Thomas, Tan, Manuela, Atadzhanov, Masharip, Nguyen, Toan, Nguyen, Duan, Foroud, Tatiana, Xie, Tao, Walker, Ruth, Alcalay, Roy, Albin, Roger, Shulman, Lisa, Dean, Marissa, Ruffrage, Lauren, Chahine, Lana M., Marek, Kenneth, Markopoulou, Katerina, Kieburtz, Karl, Nuytemans, Karen, Shulman, Joshua, Inca-Martinez, Miguel, Jankovic, Joseph, Lubbe, Steven, Mencacci, Niccolò E., Sarmiento, Ignacio Juan Keller, Chen, Honglei, Beach, Thomas, Serrano, Geidy E. ... Pihlstrøm, Lasse (2025). TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations. npj Parkinson's Disease, 11 (1) 348. doi: 10.1038/s41531-025-01180-z

TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations

2025

Journal Article

The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population

Lange, Lara M., Levine, Kristin, Fox, Susan H., Marras, Connie, Ahmed, Nazish, Kuznetsov, Nicole, Vitale, Dan, Iwaki, Hirotaka, Lohmann, Katja, Marsili, Luca, Espay, Alberto J., Bauer, Peter, Beetz, Christian, Martin, Jessica, Factor, Stewart A., Higginbotham, Lenora A., Chen, Honglei, Leonard, Hampton, Nalls, Mike A., Mencacci, Niccolo E., Morris, Huw R., Singleton, Andrew B., Klein, Christine, Blauwendraat, Cornelis, Fang, Zih-Hua, Atadzhanov, Masharip, Nguyen, Toan, Nguyen, Duan, Koretsky, Mathew ... Gatto, Emilia M. (2025). The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population. npj Parkinson's Disease, 11 (1) 58. doi: 10.1038/s41531-025-00896-2

The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population

2025

Journal Article

Unravelling the causal link between gut microbiota and acne risk using a genetic approach

Cao, Fangyuan, Ogonowski, Natalia S., Díaz-Torres, Santiago, Mitchell, Brittany L., Gharhakhani, Puya, Martin, Nicholas G., Simpson, Michael A., Ong, Jue-Sheng and Rentería, Miguel E. (2025). Unravelling the causal link between gut microbiota and acne risk using a genetic approach. Skin Health and Disease, 5 (6), 448-459. doi: 10.1093/skinhd/vzaf077

Unravelling the causal link between gut microbiota and acne risk using a genetic approach

2025

Journal Article

Transdiagnostic alterations in white matter microstructure associated with suicidal thoughts and behaviours in the ENIGMA Suicidal Thoughts and Behaviours consortium

van Velzen, Laura S., Colic, Lejla, Ceja, Zuriel, Dauvermann, Maria R., Villa, Luca M., Savage, Hannah S., Toenders, Yara J., Dehestani, Niousha, Zhu, Alyssa H., Campos, Adrian I., Salminen, Lauren E., Alda, Martin, Agartz, Ingrid, Alexander, Nina, Ayesa-Arriola, Rosa, Ballard, Elizabeth D., Banaj, Nerisa, Barkhau, Carlotta, Başgöze, Zeynep, Bauer, Jochen, Benedetti, Francesco, Berger, Klaus, Besteher, Bianca, Brosch, Katharina, Canal-Rivero, Manuel, Cervenka, Simon, Colle, Romain, Connolly, Colm G., Corruble, Emmanuelle ... Schmaal, Lianne (2025). Transdiagnostic alterations in white matter microstructure associated with suicidal thoughts and behaviours in the ENIGMA Suicidal Thoughts and Behaviours consortium. Translational Psychiatry, 15 (1) 429, 1-11. doi: 10.1038/s41398-025-03602-1

Transdiagnostic alterations in white matter microstructure associated with suicidal thoughts and behaviours in the ENIGMA Suicidal Thoughts and Behaviours consortium

Supervision

Availability

Hon Assoc Professor Miguel Rentería is:
Available for supervision

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Supervision history

Current supervision

  • Doctor Philosophy

    Monogenic Parkinson's disease among individuals from underrepresented backgrounds in Australia and Mexico

    Principal Advisor

  • Doctor Philosophy

    Genetic Aetiology of Cognitive and Speech-Related Features in Parkinson's Disease

    Principal Advisor

  • Doctor Philosophy

    Genetic architecture of differences in symptomatology and treatment response in major depressive disorder

    Principal Advisor

    Other advisors: Honorary Professor Sarah Medland, Honorary Professor Nick Martin

  • Doctor Philosophy

    Bridging gaps on the genetics of age-related disorder among under-represented populations

    Associate Advisor

  • Doctor Philosophy

    Application of machine learning techniques on longitudinal fitness tracker data to augment disease risk prediction

    Associate Advisor

    Other advisors: Dr Quan Nguyen

  • Doctor Philosophy

    Understanding the genetic aetiology of age-related diseases in diverse populations

    Associate Advisor

  • Doctor Philosophy

    From Genes to Brain Networks: AI Approaches to Understanding the Genetic Foundations of Brain Functionality in Health and Disease

    Associate Advisor

Completed supervision

Media

Enquiries

Contact Hon Assoc Professor Miguel Rentería directly for media enquiries about:

  • Human genetics
  • Parkinson's disease

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