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Honorary Professor

Sarah Medland

Email: 

Overview

Background

Professor Sarah Medland (OAM, FASSA, FAHMS, PhD) is a Psychiatric and Statistical Geneticist working in Neuroimaging and Mental health genetics. Her work bridges Genetics, Psychology, Neuro-Imaging, Health Economics and applied Statistics with a focus on understanding the genetic and environmental contributions to human behaviour and disease. She chairs the genetics working group of the ENIGMA neuroimaging consortium and is an active member of the Psychiatric Genomics Consortium.

Primary Appointment: Coordinator of the Mental Health Research Program and Group Leader (Psychiatric Genetics) QIMR Berghofer Medical Research Institute.

ORCID: 0000-0003-1382-380X

ResearcherID: C-7630-2013

Scopus Author ID: 34571085600

Email: sarah.medland@qimrberghofer.edu.au

Qualifications

2006 PhD (Psychology), University of Queensland

Dean's Award for Outstanding Research Higher Degree Thesis

2000 BA Hons (Psychology), University of Queensland, 2000 (Psychology Double Major, English Minor)

Availability

Honorary Professor Sarah Medland is:
Available for supervision

Fields of research

Works

Search Professor Sarah Medland’s works on UQ eSpace

545 works between 2001 and 2025

181 - 200 of 545 works

2020

Journal Article

The genetic architecture of sporadic and multiple consecutive miscarriage

Laisk, Triin, Soares, Ana Luiza G., Ferreira, Teresa, Painter, Jodie N., Censin, Jenny C., Laber, Samantha, Bacelis, Jonas, Chen, Chia-Yen, Lepamets, Maarja, Lin, Kuang, Liu, Siyang, Millwood, Iona Y., Ramu, Avinash, Southcombe, Jennifer, Andersen, Marianne S., Yang, Ling, Becker, Christian M., Børglum, Anders D., Gordon, Scott D., Bybjerg-Grauholm, Jonas, Helgeland, Øyvind, Hougaard, David M., Jin, Xin, Johansson, Stefan, Juodakis, Julius, Kartsonaki, Christiana, Kukushkina, Viktorija, Lind, Penelope A., Metspalu, Andres ... Lindgren, Cecilia M. (2020). The genetic architecture of sporadic and multiple consecutive miscarriage. Nature Communications, 11 (1) 5980, 1-12. doi: 10.1038/s41467-020-19742-5

The genetic architecture of sporadic and multiple consecutive miscarriage

2020

Journal Article

Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts

Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Latvala, Antti, Honda, Chika, Inui, Fujio, Tomizawa, Rie, Watanabe, Mikio, Sakai, Norio, Rebato, Esther, Busjahn, Andreas, Tyler, Jessica, Hopper, John L., Ordoñana, Juan R., Sánchez-Romera, Juan F., Colodro-Conde, Lucia, Calais-Ferreira, Lucas, Oliveira, Vinicius C., Ferreira, Paulo H., Medda, Emanuela, Nisticò, Lorenza, Toccaceli, Virgilia, Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Siribaddana, Sisira H., Hotopf, Matthew, Sumathipala, Athula, Rijsdijk, Fruhling ... Kaprio, Jaakko (2020). Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts. Scientific Reports, 10 (1) 12681, 12681. doi: 10.1038/s41598-020-69526-6

Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts

2020

Journal Article

A large-scale genome-wide association study meta-analysis of cannabis use disorder

Johnson, Emma C., Demontis, Ditte, Thorgeirsson, Thorgeir E., Walters, Raymond K., Polimanti, Renato, Hatoum, Alexander S., Sanchez-Roige, Sandra, Paul, Sarah E., Wendt, Frank R., Clarke, Toni-Kim, Lai, Dongbing, Reginsson, Gunnar W., Zhou, Hang, He, June, Baranger, David A. A., Gudbjartsson, Daniel F., Wedow, Robbee, Adkins, Daniel E., Adkins, Amy E., Alexander, Jeffry, Bacanu, Silviu-Alin, Bigdeli, Tim B., Boden, Joseph, Brown, Sandra A., Bucholz, Kathleen K., Bybjerg-Grauholm, Jonas, Corley, Robin P., Degenhardt, Louisa, Dick, Danielle M. ... Agrawal, Arpana (2020). A large-scale genome-wide association study meta-analysis of cannabis use disorder. The Lancet Psychiatry, 7 (12), 1032-1045. doi: 10.1016/S2215-0366(20)30339-4

A large-scale genome-wide association study meta-analysis of cannabis use disorder

2020

Journal Article

Distinctive features of orbital adipose tissue (OAT) in Graves' Orbitopathy

Zhang, Lei, Evans, Anna, von Ruhland, Chris, Draman, Mohd Shazli, Edkins, Sarah, Vincent, Amy E., Berlinguer-Palmini, Rolando, Rees, D. Aled, Haridas, Anjana S., Morris, Dan, Tee, Andrew R., Ludgate, Marian, Turnbull, Doug M., Karpe, Fredrik and Dayan, Colin M. (2020). Distinctive features of orbital adipose tissue (OAT) in Graves' Orbitopathy. International Journal of Molecular Sciences, 21 (23) 9145, 1-18. doi: 10.3390/ijms21239145

Distinctive features of orbital adipose tissue (OAT) in Graves' Orbitopathy

2020

Conference Publication

Modifiable risk factors and miscarriage: a Mendelian Randomization analysis

Painter, Jodie N., Martin, Nick G. and Medland, Sarah E. (2020). Modifiable risk factors and miscarriage: a Mendelian Randomization analysis. 50th Annual Meeting of the Behavior-Genetics-Association (BGA), Electr Network, Jun 26, 2020. NEW YORK: SPRINGER.

Modifiable risk factors and miscarriage: a Mendelian Randomization analysis

2020

Conference Publication

Symptom-level genetic modelling identifies novel risk loci and unravels the shared genetic architecture of anxiety and depression

Thorp, Jackson G., Campos, Adrian I., Grotzinger, Andrew D., Gerring, Zachary, An, Jiyuan, Ong, Jue-Sheng, Wang, Wei, Shringarpure, Suyash, Byrne, Enda M., MacGregor, Stuart, Martin, Nicholas G., Medland, Sarah E., Middeldorp, Christel M. and Derks, Eske M. (2020). Symptom-level genetic modelling identifies novel risk loci and unravels the shared genetic architecture of anxiety and depression. 50th Annual Meeting of the Behavior-Genetics-Association (BGA), Electr Network, Jun 26, 2020. NEW YORK: SPRINGER.

Symptom-level genetic modelling identifies novel risk loci and unravels the shared genetic architecture of anxiety and depression

2020

Conference Publication

The relationship between comorbid chronic pain and poorer self-reported antidepressant efficacy is partly mediated by genetics

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.

The relationship between comorbid chronic pain and poorer self-reported antidepressant efficacy is partly mediated by genetics

2020

Journal Article

Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature

Ho, Yvonne Y. W., Mina-Vargas, Angela, Zhu, Gu, Brims, Mark, Mcnevin, Dennis, Montgomery, Grant W., Martin, Nicholas G., Medland, Sarah E. and Painter, Jodie N. (2020). Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature. Twin Research and Human Genetics, 23 (5) PII S183242742000078X, 271-277. doi: 10.1017/thg.2020.78

Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature

2020

Journal Article

Genome-wide association study identifies 48 common genetic variants associated with handedness

Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., Boyd, Heather A., Breteler, Monique M. B., Campbell, Harry, Chasman, Daniel I., Cherkas, Lynn F., Davies, Gail, de Geus, Eco J. C., Deary, Ian J., Deloukas, Panos, Dick, Danielle M., Duffy, David L., Eriksson, Johan G., Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D., Han, Jiali ... Medland, Sarah E. (2020). Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour, 5 (1), 59-70. doi: 10.1038/s41562-020-00956-y

Genome-wide association study identifies 48 common genetic variants associated with handedness

2020

Journal Article

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

Hofer, Edith, Roshchupkin, Gennady V., Adams, Hieab H. H., Knol, Maria J., Lin, Honghuang, Li, Shuo, Zare, Habil, Ahmad, Shahzad, Armstrong, Nicola J., Satizabal, Claudia L., Bernard, Manon, Bis, Joshua C., Gillespie, Nathan A., Luciano, Michelle, Mishra, Aniket, Scholz, Markus, Teumer, Alexander, Xia, Rui, Jian, Xueqiu, Mosley, Thomas H., Saba, Yasaman, Pirpamer, Lukas, Seiler, Stephan, Becker, James T., Carmichael, Owen, Rotter, Jerome I., Psaty, Bruce M., Lopez, Oscar L., Amin, Najaf ... Hansell, Narelle K. (2020). Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nature Communications, 11 (1) 4796, 4796. doi: 10.1038/s41467-020-18367-y

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

2020

Journal Article

Septic shock: a genomewide association study and polygenic risk score analysis

D'Urso, Shannon, Rajbhandari, Dorrilyn, Peach, Elizabeth, De Guzman, Erika, Li, Qiang, Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Ligthart, Symen, Brown, Matthew A., Powell, Joseph, McArthur, Colin, Rhodes, Andrew, Meyer, Jason, Finfer, Simon, Myburgh, John, Blumenthal, Antje, Cohen, Jeremy, Venkatesh, Balasubramanian, Cuellar-Partida, Gabriel and Evans, David M. (2020). Septic shock: a genomewide association study and polygenic risk score analysis. Twin Research and Human Genetics, 23 (4) PII S1832427420000602, 204-213. doi: 10.1017/thg.2020.60

Septic shock: a genomewide association study and polygenic risk score analysis

2020

Journal Article

Challenges in the diagnosis and discovery of rare genetic disorders using contemporary sequencing technologies

Seaby, Eleanor G. and Ennis, Sarah (2020). Challenges in the diagnosis and discovery of rare genetic disorders using contemporary sequencing technologies. Briefings in Functional Genomics, 19 (4), 243-258. doi: 10.1093/bfgp/elaa009

Challenges in the diagnosis and discovery of rare genetic disorders using contemporary sequencing technologies

2020

Journal Article

Cohort profile: the Australian genetics of depression study

Byrne, Enda M., Kirk, Katherine M., Medland, Sarah E., McGrath, John J., Colodro-Conde, Lucia, Parker, Richard, Cross, Simone, Sullivan, Lenore, Statham, Dixie J., Levinson, Douglas F., Licinio, Julio, Wray, Naomi R, Hickie, Ian B. and Martin, Nicholas G. (2020). Cohort profile: the Australian genetics of depression study. BMJ Open, 10 (5) e032580, e032580. doi: 10.1136/bmjopen-2019-032580

Cohort profile: the Australian genetics of depression study

2020

Journal Article

Brain aging in major depressive disorder: results from the ENIGMA major depressive disorder working group

Han, Laura K. M., Dinga, Richard, Hahn, Tim, Ching, Christopher R. K., Eyler, Lisa T., Aftanas, Lyubomir, Aghajani, Moji, Aleman, André, Baune, Bernhard T., Berger, Klaus, Brak, Ivan, Filho, Geraldo Busatto, Carballedo, Angela, Connolly, Colm G., Couvy-Duchesne, Baptiste, Cullen, Kathryn R., Dannlowski, Udo, Davey, Christopher G., Dima, Danai, Duran, Fabio L. S., Enneking, Verena, Filimonova, Elena, Frenzel, Stefan, Frodl, Thomas, Fu, Cynthia H. Y., Godlewska, Beata R., Gotlib, Ian H., Grabe, Hans J., Groenewold, Nynke A. ... Schmaal, Lianne (2020). Brain aging in major depressive disorder: results from the ENIGMA major depressive disorder working group. Molecular Psychiatry, 26 (9), 5124-5139. doi: 10.1038/s41380-020-0754-0

Brain aging in major depressive disorder: results from the ENIGMA major depressive disorder working group

2020

Journal Article

Mapping brain asymmetry in health and disease through the ENIGMA consortium

Kong, Xiang-Zhen, Postema, Merel C., Guadalupe, Tulio, de Kovel, Carolien, Boedhoe, Premika S. W., Hoogman, Martine, Mathias, Samuel R., van Rooij, Daan, Schijven, Dick, Glahn, David C., Medland, Sarah E., Jahanshad, Neda, Thomopoulos, Sophia I., Turner, Jessica A., Buitelaar, Jan, van Erp, Theo G. M., Franke, Barbara, Fisher, Simon E., van den Heuvel, Odile A., Schmaal, Lianne, Thompson, Paul M. and Francks, Clyde (2020). Mapping brain asymmetry in health and disease through the ENIGMA consortium. Human Brain Mapping, 43 (1) hbm.25033, 167-181. doi: 10.1002/hbm.25033

Mapping brain asymmetry in health and disease through the ENIGMA consortium

2020

Journal Article

Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory

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

Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory

2020

Journal Article

Curly questions

Medland, Sarah E. (2020). Curly questions. Twin Research and Human Genetics, 23 (2) PII S1832427420000237, 98-99. doi: 10.1017/thg.2020.23

Curly questions

2020

Journal Article

Editorial

Evans, David, Medland, Sarah E. and Gillespie, Nathan (2020). Editorial. Twin Research and Human Genetics, 23 (2), 67-67. doi: 10.1017/thg.2020.45

Editorial

2020

Journal Article

ENIGMA and global neuroscience: a decade of large-scale studies of the brain in health and disease across more than 40 countries

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

ENIGMA and global neuroscience: a decade of large-scale studies of the brain in health and disease across more than 40 countries

2020

Journal Article

The genetic architecture of the human cerebral cortex

Grasby, Katrina L., Jahanshad, Neda, Painter, Jodie N., Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P., Lind, Penelope A., Pizzagalli, Fabrizio, Ching, Christopher R. K., McMahon, Mary Agnes B., Shatokhina, Natalia, Zsembik, Leo C. P., Thomopoulos, Sophia I., Zhu, Alyssa H., Strike, Lachlan T., Agartz, Ingrid, Alhusaini, Saud, Almeida, Marcio A. A., Alnæs, Dag, Amlien, Inge K., Andersson, Micael, Ard, Tyler, Armstrong, Nicola J., Ashley-Koch, Allison, Atkins, Joshua R., Bernard, Manon, Brouwer, Rachel M., Buimer, Elizabeth E. L., Bülow, Robin ... Medland, Sarah E. (2020). The genetic architecture of the human cerebral cortex. Science, 367 (6484) aay6690, 1-17. doi: 10.1126/science.aay6690

The genetic architecture of the human cerebral cortex

Supervision

Availability

Honorary Professor Sarah Medland is:
Available for supervision

Looking for a supervisor? Read our advice on how to choose a supervisor.

Supervision history

Current supervision

  • Doctor Philosophy

    Genetic determinants of treatment outcomes in mental health: harnessing the shared genetic etiology of mental disorders for precision psychiatry.

    Principal Advisor

  • Doctor Philosophy

    Genetic and environmental risk factors influencing mood disorders

    Principal Advisor

  • Master Philosophy

    Novel efficient statistical methods for biobank-scale prediction from brain imaging

    Principal Advisor

  • Doctor Philosophy

    Unveiling the Complexities of Psychotic Disorders: Enhancing Treatment Safety and Understanding Heterogeneity Through Biomarkers, Genetic Analysis, and Multimodal Data Integration

    Principal Advisor

    Other advisors: Professor Dan Siskind

  • Doctor Philosophy

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

    Associate Advisor

    Other advisors: Professor Nick Martin, Associate Professor Miguel Rentería

Completed supervision

Media

Enquiries

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