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Featured

2016

Journal Article

Rare variants are common in schizophrenia

Gratten, Jacob (2016). Rare variants are common in schizophrenia. Nature Neuroscience, 19 (11), 1426-1428. doi: 10.1038/nn.4422

Rare variants are common in schizophrenia

Featured

2016

Journal Article

Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations

Gratten, Jacob, Wray, Naomi R., Peyrot, Wouter J., McGrath, John J., Visscher, Peter M. and Goddard, Michael E. (2016). Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations. Nature Genetics, 48 (7), 718-+. doi: 10.1038/ng.3577

Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations

Featured

2013

Journal Article

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

Gratten, Jacob, Visscher, Peter M., Mowry, Bryan J. and Wray, Naomi R. (2013). Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nature Genetics, 45 (3), 234-238. doi: 10.1038/ng.2555

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

2024

Journal Article

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

Trastulla, Lucia, Dolgalev, Georgii, Moser, Sylvain, Jiménez-Barrón, Laura T., Andlauer, Till F. M., von Scheidt, Moritz, Ruderfer, Douglas M., Ripke, Stephan, McQuillin, Andrew, Stahl, Eli A., Domenici, Enrico, Adolfsson, Rolf, Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau, Richard A., Bene, Judit, Bergen, Sarah E., Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Blackwood, Douglas H. R., Borglum, Anders D., Bramon, Elvira, Bruggeman, Richard ... Ziller, Michael J. (2024). Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nature Communications , 15 (1) 5534. doi: 10.1038/s41467-024-49338-2

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

2024

Conference Publication

Investigation Of De Novo Mutations In Schizophrenia Affected Indian Families

Periyasamy, Sathish, Youssef, Pierre, Qiongyi, Zhao, John, Sujit, Smith, Heather, Gratten, Jacob, Thara, Rangaswamy and Mowry, Bryan (2024). Investigation Of De Novo Mutations In Schizophrenia Affected Indian Families. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.285

Investigation Of De Novo Mutations In Schizophrenia Affected Indian Families

2024

Conference Publication

Spatial Transcriptomics Reveals Brain-wide Changes In Gene Expression Associated With Prophylactic Effects Of Nortriptyline In A Mouse Model Of Chronic Stress Exposure

Yang, Yuanhao, Tannenberg, Rudolph, Hafey, Katelyn, Zhou, Mei, Groves, Natalie, Jhaveri, Dhanisha and Gratten, Jacob (2024). Spatial Transcriptomics Reveals Brain-wide Changes In Gene Expression Associated With Prophylactic Effects Of Nortriptyline In A Mouse Model Of Chronic Stress Exposure. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.159

Spatial Transcriptomics Reveals Brain-wide Changes In Gene Expression Associated With Prophylactic Effects Of Nortriptyline In A Mouse Model Of Chronic Stress Exposure

2024

Journal Article

Absence of association between maternal adverse events and long-term gut microbiome outcomes in the Australian Autism Biobank

Vasileva, Svetlina, Yap, Chloe X., Whitehouse, Andrew J. O., Gratten, Jacob and Eyles, Darryl (2024). Absence of association between maternal adverse events and long-term gut microbiome outcomes in the Australian Autism Biobank. Brain, Behavior, and Immunity - Health, 39 100814. doi: 10.1016/j.bbih.2024.100814

Absence of association between maternal adverse events and long-term gut microbiome outcomes in the Australian Autism Biobank

2024

Journal Article

Association of number of siblings with preclinical markers of cardiovascular disease. the cardiovascular risk in Young Finns study

Pihlman, Jukka, Magnussen, Costan G., Laitinen, Tomi T., Ruohonen, Saku, Pahkala, Katja, Jokinen, Eero, Laitinen, Tomi P., Hutri-Kahonen, Nina, Tossavainen, Paivi, Taittonen, Leena, Kahonen, Mika, Viikari, Jorma SA., Raitakari, Olli T., Juonala, Markus and Nuotio, Joel (2024). Association of number of siblings with preclinical markers of cardiovascular disease. the cardiovascular risk in Young Finns study. International Journal of Cardiology Cardiovascular Risk and Prevention, 20 200227. doi: 10.1016/j.ijcrp.2023.200227

Association of number of siblings with preclinical markers of cardiovascular disease. the cardiovascular risk in Young Finns study

2024

Journal Article

Connecting clinical and genetic heterogeneity in ADHD

Yap, Chloe X. and Gratten, Jacob (2024). Connecting clinical and genetic heterogeneity in ADHD. Nature Genetics, 56 (2), 195-196. doi: 10.1038/s41588-024-01652-7

Connecting clinical and genetic heterogeneity in ADHD

2024

Journal Article

Connecting clinical and genetic heterogeneity in ADHD

Yap, Chloe X. and Gratten, Jacob (2024). Connecting clinical and genetic heterogeneity in ADHD. Nature Genetics, 56 (2), 195-196. doi: 10.1038/s41588-024-01652-7

Connecting clinical and genetic heterogeneity in ADHD

2024

Journal Article

Associations of the gut microbiome with treatment resistance in schizophrenia

Vasileva, Svetlina S., Yang, Yuanhao, Baker, Andrea, Siskind, Dan, Gratten, Jacob and Eyles, Darryl (2024). Associations of the gut microbiome with treatment resistance in schizophrenia. JAMA Psychiatry, 81 (3), 292-302. doi: 10.1001/jamapsychiatry.2023.5371

Associations of the gut microbiome with treatment resistance in schizophrenia

2024

Journal Article

A Proposed Pediatric Clinical Cardiovascular Health Reference Standard

Petito, Lucia C., Mccabe, Megan E., Pool, Lindsay R., Krefman, Amy E., Perak, Amanda M., Marino, Bradley S., Juonala, Markus, Kahonen, Mika, Lehtimaki, Terho, Bazzano, Lydia A., Liu, Lei, Pahkala, Katja, Laitinen, Tomi T., Raitakari, Olli T., Gooding, Holly C., Daniels, Stephen R., Skinner, Asheley C., Greenland, Philip, Davis, Matthew M., Wakschlag, Lauren S., Van Horn, Linda, Hou, Lifang, Lloyd-Jones, DonaldM., Labarthe, Darwin R. and Allen, Norrina B. (2024). A Proposed Pediatric Clinical Cardiovascular Health Reference Standard. American Journal of Preventive Medicine, 66 (2), 216-225. doi: 10.1016/j.amepre.2023.09.019

A Proposed Pediatric Clinical Cardiovascular Health Reference Standard

2024

Journal Article

Erratum: Autism-related dietary preferences mediate autism-gut microbiome associations (Cell (2021) 184(24) (5916–5931.e17), (S0092867421012319), (10.1016/j.cell.2021.10.015))

Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Wood, David L.A., Krause, Lutz, Tyson, Gene W., Restuadi, Restuadi, Wallace, Leanne, McLaren, Tiana, Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Frenk, Mira Levis, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Holtmann, Gerald, Strike, Lachlan T., de Zubicaray, Greig I. ... Gratten, Jacob (2024). Erratum: Autism-related dietary preferences mediate autism-gut microbiome associations (Cell (2021) 184(24) (5916–5931.e17), (S0092867421012319), (10.1016/j.cell.2021.10.015)). Cell, 187 (2), 495-510. doi: 10.1016/j.cell.2023.12.001

Erratum: Autism-related dietary preferences mediate autism-gut microbiome associations (Cell (2021) 184(24) (5916–5931.e17), (S0092867421012319), (10.1016/j.cell.2021.10.015))

2024

Other Outputs

TRS-BIOME

Eyles, Darryl, Vasileva, Svetlina, Siskind, Dan, Alexander, Suzy, Gratten, Jake, Ko, Pauline and Vasileva, Svetlina (2024). TRS-BIOME. The University of Queensland. (Dataset) doi: 10.48610/23fd2eb

TRS-BIOME

2023

Journal Article

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

Kavousi, Maryam, Bos, Maxime M., Barnes, Hanna J., Cardenas, Christian L. Lino, Wong, Doris, Lu, Haojie, Hodonsky, Chani J., Landsmeer, Lennart P. L., Turner, Adam W., Kho, Minjung, Hasbani, Natalie R., de Vries, Paul S., Bowden, Donald W., Chopade, Sandesh, Deelen, Joris, Benavente, Ernest Diez, Guo, Xiuqing, Hofer, Edith, Hwang, Shih-Jen, Lutz, Sharon M., Lyytikaeinen, Leo-Pekka, Slenders, Lotte, Smith, Albert V., Stanislawski, Maggie A., van Setten, Jessica, Wong, Quenna, Yanek, Lisa R., Becker, Diane M., Beekman, Marian ... Miller, Clint L. (2023). Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. Nature Genetics, 55 (10), 1651-1664. doi: 10.1038/s41588-023-01518-4

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

2023

Journal Article

Selection of cross-reactive T cells by commensal and food-derived yeasts drives cytotoxic T<sub>H</sub>1 cell responses in Crohn's disease

Martini, Gabriela Rios, Tikhonova, Ekaterina, Rosati, Elisa, Decelie, Meghan Bialt, Sievers, Laura Katharina, Tran, Florian, Lessing, Matthias, Bergfeld, Arne, Hinz, Sophia, Nikolaus, Susanna, Kuempers, Julia, Matysiak, Anna, Hofmann, Philipp, Saggau, Carina, Schneiders, Stephan, Kamps, Ann-Kristin, Jacobs, Gunnar, Lieb, Wolfgang, Maul, Jochen, Siegmund, Britta, Seegers, Barbara, Hinrichsen, Holger, Oberg, Hans-Heinrich, Wesch, Daniela, Bereswill, Stefan, Heimesaat, Markus M., Rupp, Jan, Kniemeyer, Olaf, Brakhage, Axel A. ... Bacher, Petra (2023). Selection of cross-reactive T cells by commensal and food-derived yeasts drives cytotoxic TH1 cell responses in Crohn's disease. Nature Medicine, 29 (10), 2602-2614. doi: 10.1038/s41591-023-02556-5

Selection of cross-reactive T cells by commensal and food-derived yeasts drives cytotoxic T<sub>H</sub>1 cell responses in Crohn's disease

2023

Journal Article

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Maury, Eduardo A., Sherman, Maxwell A., Genovese, Giulio, Gilgenast, Thomas G., Kamath, Tushar, Burris, S. J., Rajarajan, Prashanth, Flaherty, Erin, Akbarian, Schahram, Chess, Andrew, McCarroll, Steven A., Loh, Po-Ru, Phillips-Cremins, Jennifer E., Brennand, Kristen J., Macosko, Evan Z., Walters, James T.R., O'Donovan, Michael, Sullivan, Patrick, Marshall, Christian R., Merico, Daniele, Thiruvahindrapuram, Bhooma, Wang, Zhouzhi, Scherer, Stephen W., Howrigan, Daniel P, Ripke, Stephan, Bulik-Sullivan, Brendan, Farh, Kai-How, Fromer, Menachem, Goldstein, Jacqueline I. ... Walsh, Christopher A. (2023). Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions. Cell Genomics, 3 (8) 100356, 1-21. doi: 10.1016/j.xgen.2023.100356

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

2023

Journal Article

Genetic insights into resting heart rate and its role in cardiovascular disease

van de Vegte, Yordi, Eppinga, Ruben P., van der Ende, M. Yldau, Hagemeijer, Yanick, Mahendran, Yuvaraj V., Salfati, Elias Y., Smith, Albert E., Tan, Vanessa, Arking, Dan V., Ntalla, Ioanna, Appel, Emil A., Schurmann, Claudia, Brody, Jennifer, Rueedi, Rico, Polasek, Ozren, Sveinbjornsson, Gardar, Lecoeur, Cecile, Ladenvall, Claes, Zhao, Jing Hua, Isaacs, Aaron, Wang, Lihua, Luan, Jian'an, Hwang, Shih-Jen, Mononen, Nina U., Auro, Kirsi F., Jackson, Anne, Bielak, Lawrence, Zeng, Linyao, Shah, Nabi ... van der Harst, Pim (2023). Genetic insights into resting heart rate and its role in cardiovascular disease. Nature Communications, 14 (1) 4646, 1-21. doi: 10.1038/s41467-023-39521-2

Genetic insights into resting heart rate and its role in cardiovascular disease

2023

Journal Article

Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: a general population study

Saarinen, Aino, Hietala, Jarmo, Lyytikainen, Leo-Pekka, Mishra, Binisha Hamal, Sormunen, Elina, Kahonen, Mika, Rovio, Suvi, Viikari, Jorma, Raitakari, Olli, Lehtimaki, Terho and Keltikangas-Jarvinen, Liisa (2023). Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: a general population study. Psychiatry Research, 326 115355, 1-9. doi: 10.1016/j.psychres.2023.115355

Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: a general population study

2023

Journal Article

Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

Hsu, Yu-Han H., Pintacuda, Greta, Liu, Ruize, Nacu, Eugeniu, Kim, April, Tsafou, Kalliopi, Petrossian, Natalie, Crotty, William, Suh, Jung Min, Riseman, Jackson, Martin, Jacqueline M., Biagini, Julia C., Mena, Daya, Ching, Joshua K.T., Malolepsza, Edyta, Li, Taibo, Singh, Tarjinder, Ge, Tian, Egri, Shawn B., Tanenbaum, Benjamin, Stanclift, Caroline R., Apffel, Annie M., Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T.R., Farh, Kai-How, Holmans, Peter A., Lee, Phil ... Lage, Kasper (2023). Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia. iScience, 26 (5) 106701, 1-28. doi: 10.1016/j.isci.2023.106701

Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia