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

547 works between 2001 and 2025
All (547) Journal Article (464) Other Outputs (1) Conference Publication (77) Book Chapter (5)

301 - 320 of 547 works

2017

Journal Article

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Macé, Aurélien, Tuke, Marcus A., Deelen, Patrick, Kristiansson, Kati, Mattsson, Hannele, Nõukas, Margit, Sapkota, Yadav, Schick, Ursula, Porcu, Eleonora, Rüeger, Sina, McDaid, Aaron F., Porteous, David, Winkler, Thomas W., Salvi, Erika, Shrine, Nick, Liu, Xueping, Ang, Wei Q., Zhang, Weihua, Feitosa, Mary F., Venturini, Cristina, Van Der Most, Peter J., Rosengren, Anders, Wood, Andrew R., Beaumont, Robin N., Jones, Samuel E., Ruth, Katherine S., Yaghootkar, Hanieh, Tyrrell, Jessica, Havulinna, Aki S. ... Kutalik, Zoltán (2017). CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nature Communications, 8 (1) 744, 744. doi: 10.1038/s41467-017-00556-x

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

2017

Journal Article

Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals

St Pourcain, Beate, Eaves, Lindon J, Ring, Susan M, Fisher, Simon E, Medland, Sarah, Evans, David M and Davey Smith, George (2017). Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals. Biological psychiatry, 83 (7), 598-606. doi: 10.1016/j.biopsych.2017.09.020

Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals

2017

Journal Article

Autoimmunity/inflammation in a monogenic primary immunodeficiency cohort

Rae, William, Ward, Daniel, Mattocks, Christopher J., Gao, Yifang, Pengelly, Reuben J., Patel, Sanjay V., Ennis, Sarah, Faust, Saul N. and Williams, Anthony P. (2017). Autoimmunity/inflammation in a monogenic primary immunodeficiency cohort. Clinical & Translational Immunology, 6 e155. doi: 10.1038/cti.2017.38

Autoimmunity/inflammation in a monogenic primary immunodeficiency cohort

2017

Journal Article

Hidden heritability due to heterogeneity across seven populations

Tropf, Felix C., Lee, S Hong, Verweij, Renske M., Stulp, Gert, van der Most, Peter J., de Vlaming, Ronald, Bakshi, Andrew, Briley, Daniel A., Rahal, Charles, Hellpap, Robert, Nyman, Anastasia, Esko, Tõnu, Metspalu, Andres, Medland, Sarah E., Martin, Nicholas G., Barban, Nicola, Snieder, Harold, Robinson, Matthew R. and Mills, Melinda C. (2017). Hidden heritability due to heterogeneity across seven populations. Nature Human Behaviour, 1 (10), 757-765. doi: 10.1038/s41562-017-0195-1

Hidden heritability due to heterogeneity across seven populations

2017

Journal Article

Genome-Wide Association shows that pigmentation genes play a role in skin aging

Law, Matthew H., Medland, Sarah E., Zhu, Gu, Yazar, Seyhan, Vinuela, Ana, Wallace, Leanne, Shekar, Sri Niranjan, Duffy, David L., Bataille, Veronique, Glass, Dan, Spector, Tim D., Wood, Diane, MuTHER Consortium, Gordon, Scott D., Barbour, Julie M., Henders, Anjali K., Hewitt, Alex W., Montgomery, Grant W., Sturm, Richard A., Mackey, David A., Green, Adele C., Martin, Nicholas G. and MacGregor, Stuart (2017). Genome-Wide Association shows that pigmentation genes play a role in skin aging. Journal of Investigative Dermatology, 137 (9), 1887-1894. doi: 10.1016/j.jid.2017.04.026

Genome-Wide Association shows that pigmentation genes play a role in skin aging

2017

Journal Article

Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1

Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, Backlund, Lena, Frisén, Louise, Lavebratt, Catharina, Schalling, Martin, Ösby, Urban ... MooDS Consortium (2017). Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1. Molecular Neurobiology, 54 (7), 5166-5176. doi: 10.1007/s12035-016-0041-x

Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1

2017

Journal Article

Neuroticism and the Overlap between Autistic and ADHD Traits: Findings from a Population Sample of Young Adult Australian Twins

Park, Shin-Ho, Guastella, Adam J., Lynskey, Michael, Agrawal, Arpana, Constantino, John N., Medland, Sarah E., Song, Yun Ju C., Martin, Nicholas G. and Colodro-Conde, Lucía (2017). Neuroticism and the Overlap between Autistic and ADHD Traits: Findings from a Population Sample of Young Adult Australian Twins. Twin Research and Human Genetics, 20 (4), 319-329. doi: 10.1017/thg.2017.38

Neuroticism and the Overlap between Autistic and ADHD Traits: Findings from a Population Sample of Young Adult Australian Twins

2017

Journal Article

Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts

Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Yokoyama, Yoshie, Hur, Yoon-Mi, Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Honda, Chika, Inui, Fujio, Iwatani, Yoshinori, Watanabe, Mikio, Tomizawa, Rie, Pietilainen, Kirsi H., Rissanen, Aila, Siribaddana, Sisira H., Hotopf, Matthew, Sumathipala, Athula, Rijsdijk, Fruhling, Tan, Qihua, Zhang, Dongfeng, Pang, Zengchang, Piirtola, Maarit, Aaltonen, Sari, Oncel, Sevgi Y., Aliev, Fazil, Rebato, Esther, Hjelmborg, Jacob B., Christensen, Kaare ... Kaprio, Jaakko (2017). Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts. American Journal of Clinical Nutrition, 106 (2), 457-466. doi: 10.3945/ajcn.117.153643

Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts

2017

Journal Article

A direct test of the diathesis–stress model for depression

Colodro-Conde, L., Couvy-Duchesne, B., Zhu, G., Coventry, W. L., Byrne, E. M., Gordon, S., Wright, M. J., Montgomery, G. W., Madden, P. A. F., Ripke, S., Eaves, L. J., Heath, A. C., Wray, N. R., Medland, S. E. and Martin, N. G. (2017). A direct test of the diathesis–stress model for depression. Molecular Psychiatry, 23 (7), 1590-1596. doi: 10.1038/mp.2017.130

A direct test of the diathesis–stress model for depression

2017

Journal Article

No genetic overlap between circulating iron levels and Alzheimer's disease

Lupton, Michelle K., Benyamin, Beben, Proitsi, Petroula, Nyholt, Dale R., Ferreira, Manuel A., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A., Medland, Sarah E., Gordon, Scott D., Lovestone, Simon, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Vellas, Bruno, Powell, John F., Bush, Ashley I., Wright, Margaret J., Martin, Nicholas G. and Whitfield, John B. (2017). No genetic overlap between circulating iron levels and Alzheimer's disease. Journal of Alzheimers Disease, 59 (1), 85-99. doi: 10.3233/JAD-170027

No genetic overlap between circulating iron levels and Alzheimer's disease

2017

Journal Article

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Weiner, Daniel J., Wigdor, Emilie M., Ripke, Stephan, Walters, Raymond K., Kosmicki, Jack A., Grove, Jakob, Samocha, Kaitlin E., Goldstein, Jacqueline I., Okbay, Aysu, Bybjerg-Grauholm, Jonas, Werge, Thomas, Hougaard, David M, Taylor, Jacob, Skuse, David, Devlin, Bernie, Anney, Richard, Sanders, Stephan J, Bishop, Somer, Mortensen, Preben Bo, Børglum, Anders D, Smith, George Davey, Daly, Mark J, Robinson, Elise B., Bækvad-Hansen, Marie, Dumont, Ashley, Hansen, Christine, Hansen, Thomas F., Howrigan, Daniel, Mattheisen, Manuel ... iPSYCH-Broad Autism Grp ; Psychiat Genomics Consortium (2017). Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nature Genetics, 49 (7), 978-985. doi: 10.1038/ng.3863

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

2017

Journal Article

16S sequencing and functional analysis of the fecal microbiome during treatment of newly diagnosed pediatric inflammatory bowel disease

Ashton, James J., Colquhoun, Catherine M., Cleary, David W., Coelho, Tracy, Haggarty, Rachel, Mulder, Imke, Batra, Akshay, Afzal, Nadeem A., Beattie, R. Mark, Scott, Karen P. and Ennis, Sarah (2017). 16S sequencing and functional analysis of the fecal microbiome during treatment of newly diagnosed pediatric inflammatory bowel disease. Medicine, 96 (26) e7347. doi: 10.1097/MD.0000000000007347

16S sequencing and functional analysis of the fecal microbiome during treatment of newly diagnosed pediatric inflammatory bowel disease

2017

Journal Article

Obstetrical, pregnancy and socio-economic predictors for new-onset severe postpartum psychiatric disorders in primiparous women

Meltzer-Brody, S., Maegbaek, M. L., Medland, S. E., Miller, W. C., Sullivan, P. and Munk-Olsen, T. (2017). Obstetrical, pregnancy and socio-economic predictors for new-onset severe postpartum psychiatric disorders in primiparous women. Psychological Medicine, 47 (8), 1427-1441. doi: 10.1017/S0033291716003020

Obstetrical, pregnancy and socio-economic predictors for new-onset severe postpartum psychiatric disorders in primiparous women

2017

Journal Article

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Anney, Richard J. L., Ripke, Stephan, Anttila, Verneri, Grove, Jakob, Holmans, Peter, Huang, Hailiang, Klei, Lambertus, Lee, Phil H., Medland, Sarah E., Neale, Benjamin, Robinson, Elise, Weiss, Lauren A., Zwaigenbaum, Lonnie, Yu, Timothy W., Wittemeyer, Kerstin, Willsey, A.Jeremy, Wijsman, Ellen M., Werge, Thomas, Wassink, Thomas H., Waltes, Regina, Walsh, Christopher A., Wallace, Simon, Vorstman, Jacob A. S., Vieland, Veronica J., Vicente, Astrid M., Vanengeland, Herman, Tsang, Kathryn, Thompson, Ann P., Szatmari, Peter ... The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium (2017). Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Molecular Autism, 8 (1) 21. doi: 10.1186/s13229-017-0137-9

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

2017

Conference Publication

Investigating the Overlap between Common Genetic Factors for ADHD Risk and Brain Volume Measures

Klein, Marieke, Stein, Jason L., Thompson, Paul, Faraone, Steve, Borglum, Anders, Faraone, Stephen V., Thompson, Paul M., Medland, Sarah E., Arias-Vasquez, Alejandro and Franke, Barbara (2017). Investigating the Overlap between Common Genetic Factors for ADHD Risk and Brain Volume Measures. 72nd Annual Scientific Convention and Meeting of the Society-of-Biological-Psychiatry (SOBP), San Diego Ca, May 18-20, 2017. NEW YORK: ELSEVIER SCIENCE INC. doi: 10.1016/j.biopsych.2017.02.112

Investigating the Overlap between Common Genetic Factors for ADHD Risk and Brain Volume Measures

2017

Journal Article

Subcortical brain structure and suicidal behaviour in major depressive disorder: a meta-analysis from the ENIGMA-MDD working group

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

Subcortical brain structure and suicidal behaviour in major depressive disorder: a meta-analysis from the ENIGMA-MDD working group

2017

Journal Article

Does the sex of one’s co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts

Bogl, Leonie H., Jelenkovic, Aline, Vuoksimaa, Eero, Ahrenfeldt, Linda, Pietiläinen, Kirsi H., Stazi, Maria A., Fagnani, Corrado, D’Ippolito, Cristina, Hur, Yoon-Mi, Jeong, Hoe-Uk, Silberg, Judy L., Eaves, Lindon J., Maes, Hermine H., Bayasgalan, Gombojav, Narandalai, Danshiitsoodol, Cutler, Tessa L., Kandler, Christian, Jang, Kerry L., Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O., Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Derom, Catherine A., Vlietinck, Robert F., Nelson, Tracy L., Whitfield, Keith E., Corley, Robin P. ... Kaprio, Jaakko (2017). Does the sex of one’s co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts. Biology of Sex Differences, 8 (1) 14. doi: 10.1186/s13293-017-0134-x

Does the sex of one’s co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts

2017

Journal Article

Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway

Andreoletti, Gaia, Shakhnovich, Valentina, Christenson, Kathy, Coelho, Tracy, Haggarty, Rachel, Afzal, Nadeem A., Batra, Akshay, Petersen, Britt-Sabina, Mort, Matthew, Beattie, R. Mark and Ennis, Sarah (2017). Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway. Scientific Reports, 7 46454. doi: 10.1038/srep46454

Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway

2017

Journal Article

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

Day, Felix R., Thompson, Deborah J., Helgason, Hannes, Chasman, Daniel I., Finucane, Hilary, Sulem, Patrick, Ruth, Katherine S., Whalen, Sean, Sarkar, Abhishek K., Albrecht, Eva, Altmaier, Elisabeth, Amini, Marzyeh, Barbieri, Caterina M., Boutin, Thibaud, Campbell, Archie, Demerath, Ellen, Giri, Ayush, He, Chunyan, Hottenga, Jouke J., Karlsson, Robert, Kolcic, Ivana, Loh, Po-Ru, Lunetta, Kathryn L., Mangino, Massimo, Marco, Brumat, McMahon, George, Medland, Sarah E., Nolte, Ilja M., Noordam, Raymond ... Perry, John R. B. (2017). Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nature Genetics, 49 (6), 834-841. doi: 10.1038/ng.3841

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

2017

Journal Article

Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysis

Hoogman, Martine, Bralten, Janita, Hibar, Derrek P, Mennes, Maarten, Zwiers, Marcel P, Schweren, Lizanne S J, van Hulzen, Kimm J E, Medland, Sarah E, Shumskaya, Elena, Jahanshad, Neda, Zeeuw, Patrick de, Szekely, Eszter, Sudre, Gustavo, Wolfers, Thomas, Onnink, Alberdingk M H, Dammers, Janneke T, Mostert, Jeanette C, Vives-Gilabert, Yolanda, Kohls, Gregor, Oberwelland, Eileen, Seitz, Jochen, Schulte-Rüther, Martin, Ambrosino, Sara, Doyle, Alysa E, Høvik, Marie F, Dramsdahl, Margaretha, Tamm, Leanne, van Erp, Theo G M, Dale, Anders ... Franke, Barbara (2017). Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysis. The Lancet Psychiatry, 4 (4), 310-319. doi: 10.1016/S2215-0366(17)30049-4

Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysis

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

    Other advisors: Professor Dan Siskind

  • 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 and environmental risk factors influencing mood disorders

    Principal Advisor

  • 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

Enquiries

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