Honorary Professor

Sarah Medland

Email: 

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

Applied economics Psychology

Search Professor Sarah Medland’s works on UQ eSpace

481 works between 2001 and 2025
All (481) Journal Article (411) Book Chapter (5) Conference Publication (64) Other Outputs (1)

221 - 240 of 481 works

2018

Journal Article

Anticytokine autoantibodies in a patient with a heterozygous <i>NFKB2</i> mutation

Ramakrishnan, Kesava A., Rae, William, Barcenas-Morales, Gabriela, Gao, Yifang, Pengelly, Reuben J., Patel, Sanjay V., Kumararatne, Dinakantha S., Ennis, Sarah, Doffinger, Rainer, Faust, Saul N. and Williams, Anthony P. (2018). Anticytokine autoantibodies in a patient with a heterozygous NFKB2 mutation. Journal of Allergy and Clinical Immunology, 141 (4), 1479-+. doi: 10.1016/j.jaci.2017.11.014

Anticytokine autoantibodies in a patient with a heterozygous <i>NFKB2</i> mutation

2018

Journal Article

Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins

Couvy-Duchesne, Baptiste, O'Callaghan, Victoria, Parker, Richard, Mills, Natalie, Kirk, Katherine M., Scott, Jan, Vinkhuyzen, Anna., Hermens, Daniel F., Lind, Penelope A., Davenport, Tracey A., Burns, Jane M., Connell, Melissa, Zietsch, Brendan P., Scott, James, Wright, Margaret J., Medland, Sarah E., McGrath, John, Martin, Nicholas G., Hickie, Ian B. and Gillespie, Nathan A. (2018). Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins. BMJ Open, 8 (3) e018959, 1-13. doi: 10.1136/bmjopen-2017-018959

Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins

2018

Journal Article

Publisher Correction: protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Turcot, Valérie, Lu, Yingchang, Highland, Heather M., Schurmann, Claudia, Justice, Anne E., Fine, Rebecca S., Bradfield, Jonathan P., Esko, Tõnu, Giri, Ayush, Graff, Mariaelisa, Guo, Xiuqing, Hendricks, Audrey E., Karaderi, Tugce, Lempradl, Adelheid, Locke, Adam E., Mahajan, Anubha, Marouli, Eirini, Sivapalaratnam, Suthesh, Young, Kristin L., Alfred, Tamuno, Feitosa, Mary F., Masca, Nicholas G. D., Manning, Alisa K., Medina-Gomez, Carolina, Mudgal, Poorva, Ng, Maggie C. Y., Reiner, Alex P., Vedantam, Sailaja, Willems, Sara M. ... Loos, Ruth J. F. (2018). Publisher Correction: protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics, 50 (5), 1-2. doi: 10.1038/s41588-018-0082-3

Publisher Correction: protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

2018

Journal Article

The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families

Bates, Timothy C., Maher, Brion S., Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2018). The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families. Twin Research and Human Genetics, 21 (2), 73-83. doi: 10.1017/thg.2018.11

The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families

2018

Journal Article

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

Mühleisen, Thomas W., Reinbold, Céline S., Forstner, Andreas J., Abramova, Lilia I., Alda, Martin, Babadjanova, Gulja, Bauer, Michael, Brennan, Paul, Chuchalin, Alexander, Cruceanu, Cristiana, Czerski, Piotr M., Degenhardt, Franziska, Fischer, Sascha B., Fullerton, Janice M., Gordon, Scott D., Grigoroiu-Serbanescu, Maria, Grof, Paul, Hauser, Joanna, Hautzinger, Martin, Herms, Stefan, Hoffmann, Per, Kammerer-Ciernioch, Jutta, Khusnutdinova, Elza, Kogevinas, Manolis, Krasnov, Valery, Lacour, André, Laprise, Catherine, Leber, Markus, Lissowska, Jolanta ... Cichon, Sven (2018). Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. Journal of Affective Disorders, 228, 20-25. doi: 10.1016/j.jad.2017.11.068

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

2018

Journal Article

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

Beaumont, Robin N., Warrington, Nicole M., Cavadino, Alana, Tyrrell, Jessica, Nodzenski, Michael, Horikoshi, Momoko, Geller, Frank, Myhre, Ronny, Richmond, Rebecca C., Paternoster, Lavinia, Bradfield, Jonathan P., Kreiner-Møller, Eskil, Huikari, Ville, Metrustry, Sarah, Lunetta, Kathryn L., Painter, Jodie N., Hottenga, Jouke-Jan, Allard, Catherine, Barton, Sheila J., Espinosa, Ana, Marsh, Julie A., Potter, Catherine, Zhang, Ge, Ang, Wei, Berry, Diane J., Bouchard, Luigi, Das, Shikta, Early Growth Genetics (EGG) Consortium, Hakonarson, Hakon ... Freathy, Rachel M. (2018). Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. Human Molecular Genetics, 27 (4) ddx429, 742-756. doi: 10.1093/hmg/ddx429

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

2018

Journal Article

No evidence of association of oxytocin polymorphisms with breastfeeding in 2 independent samples

Colodro-Conde, L., Sánchez-Romera, J. F., Lind, P. A., Zhu, G., Martin, N. G., Medland, S. E. and Ordoñana, J. R. (2018). No evidence of association of oxytocin polymorphisms with breastfeeding in 2 independent samples. Genes, Brain and Behavior, 17 (7) e12464, e12464. doi: 10.1111/gbb.12464

No evidence of association of oxytocin polymorphisms with breastfeeding in 2 independent samples

2018

Journal Article

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

Chang, H., Hoshina, N., Zhang, C., Ma, Y., Cao, H., Wang, Y., Wu, D. D., Bergen, S. E., Landén, M., Hultman, C. M., Preisig, M., Kutalik, Z., Castelao, E., Grigoroiu-Serbanescu, M., Forstner, A. J., Strohmaier, J., Hecker, J., Schulze, T. G., Müller-Myhsok, B., Reif, A., Mitchell, P. B., Martin, N. G., Schofield, P. R., Cichon, S., Nöthen, M. M., Walter, H., Erk, S., Heinz, A., Amin, N. ... MooDS Bipolar Consortium (2018). The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. Molecular Psychiatry, 23 (2), 400-412. doi: 10.1038/mp.2016.231

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

2018

Journal Article

Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair

Liu, Fan, Chen, Yan, Zhu, Gu, Hysi, Pirro G., Wu, Sijie, Adhikari, Kaustubh, Breslin, Krystal, Pośpiech, Ewelina, Hamer, Merel A., Peng, Fuduan, Muralidharan, Charanya, Acuna-Alonzo, Victor, Canizales-Quinteros, Samuel, Bedoya, Gabriel, Gallo, Carla, Poletti, Giovanni, Rothhammer, Francisco, Bortolini, Maria Catira, Gonzalez-Jose, Rolando, Zeng, Changqing, Xu, Shuhua, Jin, Li, Uitterlinden, André G., Arfan Ikram, M., van Duijn, Cornelia M., Nijsten, Tamar, Walsh, Susan, Branicki, Wojciech, Wang, Sijia ... Kayser, Manfred (2018). Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair. Human Molecular Genetics, 27 (3), 559-575. doi: 10.1093/hmg/ddx416

Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair

2018

Journal Article

Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for major depressive disorder and white matter microstructure in the UK Biobank

Barbu, Miruna C., Zeng, Yanni, Shen, Xueyi, Cox, Simon R., Clarke, Toni-Kim, Gibson, Jude, Adams, Mark J., Johnstone, Mandy, Haley, Chris S., Lawrie, Stephen M., Deary, Ian J., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F.M., Bacanu, Silviu-Alin, Bækvad-Hansen, Marie, Beekman, Aartjan T.F., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas H.R., Bryois, Julien ... Whalley, Heather C. (2018). Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for major depressive disorder and white matter microstructure in the UK Biobank. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, 4 (1), 91-100. doi: 10.1016/j.bpsc.2018.07.006

Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for major depressive disorder and white matter microstructure in the UK Biobank

2018

Conference Publication

Psychiatric Liability Genes are Linked to Oscillatory Brain Activity: A Genome-Wide Association Study

Smit, Dirk, Wright, Margareth, Meyers, Jacquelyn, Martin, Nicholas, Ho, Yvonne, Malone, Stephen, Zhang, Jian, Burwell, Scott, Chorlian, David, de Geus, Eco, Denys, Damiaan, Hansell, Narelle, Hottenga, Jouke-Jan, McGue, Matt, van Beijsterveldt, Catharina, Jehanshad, Neda, Thompson, Paul, Whelan, Chris, Medland, Sarah, Porjesz, Bernice, Iacono, William and Boomsma, Dorret (2018). Psychiatric Liability Genes are Linked to Oscillatory Brain Activity: A Genome-Wide Association Study. 73rd Annual Scientific Convention and Meeting of the Society-of-Biological-Psychiatry (SOBP), New York NY United States, 10-12 May 2017. New York NY United States: Elsevier . doi: 10.1016/j.biopsych.2018.02.865

Psychiatric Liability Genes are Linked to Oscillatory Brain Activity: A Genome-Wide Association Study

2018

Journal Article

Type I Error Rates and Parameter Bias in Multivariate Behavioral Genetic Models

Verhulst, Brad, Prom-Wormley, Elizabeth, Keller, Matthew, Medland, Sarah and Neale, Michael C. (2018). Type I Error Rates and Parameter Bias in Multivariate Behavioral Genetic Models. Behavior Genetics, 49 (1), 99-111. doi: 10.1007/s10519-018-9942-y

Type I Error Rates and Parameter Bias in Multivariate Behavioral Genetic Models

2018

Journal Article

Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels

Lupton, Michelle K., Medland, Sarah E., Gordon, Scott D., Goncalves, Tabatha, MacGregor, Stuart, Mackey, David A., Young, Terri L., Duffy, David L., Visscher, Peter M., Wray, Naomi R., Nyholt, Dale R., Bain, Lisa, Ferreira, Manuel A., Henders, Anjali K., Wallace, Leanne, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2018). Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels. Journal of Alzheimer's Disease, 64 (1), 49-54. doi: 10.3233/JAD-171104

Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels

2018

Book Chapter

Multisite metaanalysis of image-wide genome-wide associations with morphometry

Jahanshad, Neda, Roshchupkin, Gennady, Faskowitz, Joshua, Hibar, Derrek P., Gutman, Boris A., Adams, Hieab H. H., Niessen, Wiro J., Vernooij, Meike W., Ikram, M. Arfan, Zwiers, Marcel P., Arias-Vasquez, Alejandro, Franke, Barbara, Ing, Alex, Desrivieres, Sylvane, Schumann, Gunter, de Zubicaray, Greig I., McMahon, Katie L., Medland, Sarah E., Wright, Margaret J. and Thompson, Paul M. (2018). Multisite metaanalysis of image-wide genome-wide associations with morphometry. Imaging genetics. (pp. 1-23) edited by Adrian Dalca, Kayhan Batmanghelich, Mert Sabuncu and Li Shen. London, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-813968-4.00001-8

Multisite metaanalysis of image-wide genome-wide associations with morphometry

2018

Journal Article

Subclonal Evolution of Cancer-Related Gene Mutations in p53 Immunopositive Patches in Human Skin

Albibas, Amel A., Rose-Zerilli, Matthew J. J., Lai, Chester, Pengelly, Reuben J., Lockett, Gabrielle A., Theaker, Jeffrey, Ennis, Sarah, Holloway, John W. and Healy, Eugene (2018). Subclonal Evolution of Cancer-Related Gene Mutations in p53 Immunopositive Patches in Human Skin. Journal of Investigative Dermatology, 138 (1), 189-198. doi: 10.1016/j.jid.2017.07.844

Subclonal Evolution of Cancer-Related Gene Mutations in p53 Immunopositive Patches in Human Skin

2018

Journal Article

Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia

Nakahara, Soichiro, Medland, Sarah, Turner, Jessica A., Calhoun, Vince D., Lim, Kelvin O., Mueller, Bryon A., Bustillo, Juan R., O'Leary, Daniel S., Vaidya, Jatin G., McEwen, Sarah, Voyvodic, James, Belger, Aysenil, Mathalon, Daniel H., Ford, Judith M., Guffanti, Guia, Macciardi, Fabio, Potkin, Steven G. and van Erp, Theo G.M. (2018). Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Schizophrenia Research, 201, 393-399. doi: 10.1016/j.schres.2018.05.041

Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia

2018

Journal Article

Genomic kinship construction to enhance genetic analyses in the human connectome project data

Kochunov, Peter, Donohue, Brian, Mitchell, Braxton D., Ganjgahi, Habib, Adhikari, Bhim, Ryan, Meghann, Medland, Sarah E., Jahanshad, Neda, Thompson, Paul M., Blangero, John, Fieremans, Els, Novikov, Dmitry S., Marcus, Daniel, Van Essen, David C., Glahn, David C, Elliot Hong, L. and Nichols, Thomas E. (2018). Genomic kinship construction to enhance genetic analyses in the human connectome project data. Human Brain Mapping, 40 (5), 1677-1688. doi: 10.1002/hbm.24479

Genomic kinship construction to enhance genetic analyses in the human connectome project data

2017

Journal Article

Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence

Scott, Jan, Davenport, Tracey A., Parker, Richard, Hermens, Daniel F., Lind, Penelope A., Medland, Sarah E., Wright, Margaret J., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2017). Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence. Journal of Affective Disorders, 230, 1-6. doi: 10.1016/j.jad.2017.12.007

Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence

2017

Journal Article

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

Joshi, Peter K., Pirastu, Nicola, Kentistou, Katherine A., Fischer, Krista, Hofer, Edith, Schraut, Katharina E., Clark, David W., Nutile, Teresa, Barnes, Catriona L. K., Timmers, Paul R. H. J., Shen, Xia, Gandin, Ilaria, McDaid, Aaron F., Hansen, Thomas Folkmann, Gordon, Scott D., Giulianini, Franco, Boutin, Thibaud S., Abdellaoui, Abdel, Zhao, Wei, Medina-Gomez, Carolina, Bartz, Traci M., Trompet, Stella, Lange, Leslie A., Raffield, Laura, Van Der Spek, Ashley, Galesloot, Tessel E., Proitsi, Petroula, Yanek, Lisa R., Bielak, Lawrence F. ... Wilson, James F. (2017). Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nature Communications, 8 (1) 910, 910. doi: 10.1038/s41467-017-00934-5

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

2017

Journal Article

Genome-wide association studies of a broad spectrum of antisocial behavior

Tielbeek, Jorim J., Johansson, Ada, Polderman, Tinca J.C., Rautiainen, Marja-Riitta, Jansen, Philip, Taylor, Michelle, Tong, Xiaoran, Lu, Qing, Burt, Alexandra S., Tiemeier, Henning, Viding, Essi, Plomin, Robert, Martin, Nicholas G., Heath, Andrew C., Madden, Pamela A.F., Montgomery, Grant, Beaver, Kevin M., Waldman, Irwin, Gelernter, Joel, Kranzler, Henry R., Farrer, Lindsay A., Perry, John R.B., Munafò, Marcus, LoParo, Devon, Paunio, Tiina, Tiihonen, Jari, Mous, Sabine E., Pappa, Irene, De Leeuw, Christiaan ... Broad Antisocial Behavior Consortium (2017). Genome-wide association studies of a broad spectrum of antisocial behavior. JAMA Psychiatry, 74 (12), 1242-1250. doi: 10.1001/jamapsychiatry.2017.3069

Genome-wide association studies of a broad spectrum of antisocial behavior

Availability

Honorary Professor Sarah Medland is:
Available for supervision

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Supervision history

Current supervision

  • Doctor Philosophy

    Genetic and environmental risk factors influencing mood disorders

    Principal Advisor

  • Doctor Philosophy

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

    Principal Advisor

    Other advisors: Professor Nick Martin, Associate Professor Miguel Rentería

  • 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

Completed supervision

Enquiries

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