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2022 Journal Article MUC1 mediated macrophage activation promotes colitis-associated colorectal cancer via activating the IL-6/STAT3 axisSheng, Yong H., Davies, Julie M., Wang, Ran, Wong, Kuan Yau, Giri, Rabina, Yang, Yuanhao, Begun, Jakob, Florin, Timothy H., Hasnain, Sumaira Z. and McGuckin, Michael A. (2022). MUC1 mediated macrophage activation promotes colitis-associated colorectal cancer via activating the IL-6/STAT3 axis. Cellular and Molecular Gastroenterology and Hepatology, 14 (4), 789-811. doi: 10.1016/j.jcmgh.2022.06.010 |
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2021 Journal Article Investigating the shared genetic architecture between multiple sclerosis and inflammatory bowel diseasesYang, Yuanhao, Musco, Hannah, Simpson-Yap, Steve, Zhu, Zhihong, Wang, Ying, Lin, Xin, Zhang, Jiawei, Taylor, Bruce, Gratten, Jacob and Zhou, Yuan (2021). Investigating the shared genetic architecture between multiple sclerosis and inflammatory bowel diseases. Nature Communications, 12 (1) 5641, 5641. doi: 10.1038/s41467-021-25768-0 |
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2021 Journal Article Mendelian randomization study reveals a population-specific putative causal effect of type 2 diabetes in risk of cataractZhang, Haoyang, Xiu, Xuehao, Xue, Angli, Yang, Yuedong, Yang, Yuanhao and Zhao, Huiying (2021). Mendelian randomization study reveals a population-specific putative causal effect of type 2 diabetes in risk of cataract. International Journal of Epidemiology, 50 (6), 2024-2037. doi: 10.1093/ije/dyab175 |
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2021 Journal Article Analysis of common genetic variation and rare CNVs in the Australian Autism BiobankYap, Chloe X., Alvares, Gail A., Henders, Anjali K., Lin, Tian, Wallace, Leanne, Farrelly, Alaina, McLaren, Tiana, Berry, Jolene, Vinkhuyzen, Anna A. E., Trzaskowski, Maciej, Zeng, Jian, Yang, Yuanhao, Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren, Leslie, Jodie, Levis Frenk, Mira, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Visscher, Peter M., Dawson, Paul A., Dissanayake, Cheryl ... Gratten, Jacob (2021). Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank. Molecular Autism, 12 (1) 12, 12. doi: 10.1186/s13229-020-00407-5 |
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2019 Conference Publication Common genetic variation explains a high proportion of the elevated risk of psychiatric disorders in children of younger mothersGratten, Jacob, Yang, Yuanhao, Trzaskowski, Maciej, Kemper, Kathryn, Yengo, Loic, Zheng, Zhili, Zhang, Futao, Zhu, Zhihong, Mcrae, Allan, Yang, Jian, Wray, Naomi and Visscher, Peter (2019). Common genetic variation explains a high proportion of the elevated risk of psychiatric disorders in children of younger mothers. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, Scotland, 11-15 October, 2018. Amsterdam, Netherlands: Elsevier BV. doi: 10.1016/j.euroneuro.2018.08.167 |
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2018 Journal Article Imprint of assortative mating on the human genomeYengo, Loic, Robinson, Matthew R., Keller, Matthew C., Kemper, Kathryn E., Yang, Yuanhao, Trzaskowski, Maciej, Gratten, Jacob, Turley, Patrick, Cesarini, David, Benjamin, Daniel J., Wray, Naomi R., Goddard, Michael E., Yang, Jian and Visscher, Peter M. (2018). Imprint of assortative mating on the human genome. Nature Human Behaviour, 2 (12), 948-954. doi: 10.1038/s41562-018-0476-3 |
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2018 Journal Article Molecular genetic overlap between migraine and major depressive disorderYang, Yuanhao, Zhao, Huiying, Boomsma, Dorret I., Ligthart, Lannie, Belin, Andrea C., Smith, George Davey, Esko, Tonu, Freilinger, Tobias M., Hansen, Thomas Folkmann, Ikram, M. Arfan, Kallela, Mikko, Kubisch, Christian, Paraskevi, Christofidou, Strachan, David P., Wessman, Maija, International Headache Genetics Consortium, van den Maagdenberg, Arn M. J. M., Terwindt, Gisela M. and Nyholt, Dale R. (2018). Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics, 26 (8), 1202-1216. doi: 10.1038/s41431-018-0150-2 |
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2017 Journal Article Improving the detection of pathways in genome-wide association studies by combined effects of SNPs from Linkage Disequilibrium blocksZhao, Huiying, Nyholt, Dale R., Yang, Yuanhao, Wang, Jihua and Yang, Yuedong (2017). Improving the detection of pathways in genome-wide association studies by combined effects of SNPs from Linkage Disequilibrium blocks. Scientific Reports, 7 (1) 3512. doi: 10.1038/s41598-017-03826-2 |
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2017 Journal Article A continuum of genetic liability for minor and major depressionCorfield, E. C., Yang, Y., Martin, N. G. and Nyholt, D. R. (2017). A continuum of genetic liability for minor and major depression. Translational Psychiatry, 7 (5) e1131, e1131-e1131. doi: 10.1038/tp.2017.99 |
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2016 Journal Article Familial aggregation of migraine and depression: insights from a large Australian twin sampleYang, Yuanhao, Zhao, Huiying, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G. and Nyholt, Dale R. (2016). Familial aggregation of migraine and depression: insights from a large Australian twin sample. Twin Research and Human Genetics, 19 (4), 312-321. doi: 10.1017/thg.2016.43 |
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2016 Journal Article Shared genetic factors underlie migraine and depressionYang, Yuanhao, Zhao, Huiying, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G. and Nyholt, Dale R. (2016). Shared genetic factors underlie migraine and depression. Twin Research and Human Genetics, 19 (4), 341-350. doi: 10.1017/thg.2016.46 |
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2016 Journal Article Genetic epidemiology of migraine and depressionYang, Yuanhao, Ligthart, Lannie, Terwindt, Gisela M., Boomsma, Dorret I., Rodriguez-Acevedo, Astrid J. and Nyholt, Dale R. (2016). Genetic epidemiology of migraine and depression. Cephalalgia, 36 (7), 679-691. doi: 10.1177/0333102416638520 |
