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Dr Yuanhao Yang
Dr

Yuanhao Yang

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Overview

Background

Dr. Yuanhao Yang is a senior research fellow at Mater Research Institute, with high-level expertise in computational and statistical genetics and genomics. His research field focuses on understanding the genetic and genomic etiology of human complex traits and common diseases, such as multiple sclerosis, depression and autism, through large-scale genetic/genomic and multi-omics data, including 1) revealing the genetic architecture of complex traits and common diseases using advanced genome-wide association study (GWAS)-based quantitative genetics methods; and 2) identifying potential relationships between disease risk and cellular genotypes/pathways using single-cell RNA sequence/spatial transcriptomics data and technology.

Availability

Dr Yuanhao Yang is:
Available for supervision

Qualifications

  • Bachelor of Biotechnology, Sun Yat-sen University
  • Masters (Coursework) of Biostatistics, The University of Manchester
  • Doctor of Philosophy, Queensland University of Technology

Works

Search Professor Yuanhao Yang’s works on UQ eSpace

27 works between 2016 and 2024

1 - 20 of 27 works

2024

Journal Article

β-resorcylic acid released by Limosilactobacillus reuteri protects against cisplatin-induced ovarian toxicity and infertility

Feng, Yinglin, Zheng, Huimin, Yin, Chunhua, Liang, Dong, Zhang, Siyou, Chen, Jingrui, Mai, Feihong, Lan, Zixin, Zhu, Menglin, Mai, Zhensheng, Shen, Sj, Jayawardana, Thisun, Wu, Rong, Tang, Wenli, Zhang, Renfang, He, Xiaoyun, Zheng, Shanshan, Hu, Qian, Han, Yubin, Yang, Yuanhao, Gong, Shenhai, Wang, Zhang, El-Omar, Emad M., Luo, Wei, Chen, Xueqin, Chen, Guoqiang, Li, Pan and Chen, Xia (2024). β-resorcylic acid released by Limosilactobacillus reuteri protects against cisplatin-induced ovarian toxicity and infertility. Cell Reports Medicine, 5 (8) 101678, 101678. doi: 10.1016/j.xcrm.2024.101678

β-resorcylic acid released by Limosilactobacillus reuteri protects against cisplatin-induced ovarian toxicity and infertility

2024

Journal Article

Brain cell-type shifts in Alzheimer’s disease, autism, and schizophrenia interrogated using methylomics and genetics

Yap, Chloe X., Vo, Daniel D., Heffel, Matthew G., Bhattacharya, Arjun, Wen, Cindy, Yang, Yuanhao, Kemper, Kathryn E., Zeng, Jian, Zheng, Zhili, Zhu, Zhihong, Hannon, Eilis, Vellame, Dorothea Seiler, Franklin, Alice, Caggiano, Christa, Wamsley, Brie, Geschwind, Daniel H., Zaitlen, Noah, Gusev, Alexander, Pasaniuc, Bogdan, Mill, Jonathan, Luo, Chongyuan and Gandal, Michael J. (2024). Brain cell-type shifts in Alzheimer’s disease, autism, and schizophrenia interrogated using methylomics and genetics. Science Advances, 10 (21) adn7655. doi: 10.1126/sciadv.adn7655

Brain cell-type shifts in Alzheimer’s disease, autism, and schizophrenia interrogated using methylomics and genetics

2024

Journal Article

Genetic evidence for T-wave area from 12-lead electrocardiograms to monitor cardiovascular diseases in patients taking diabetes medications

Qi, Mengling, Zhang, Haoyang, Xiu, Xuehao, He, Dan, Cooper, David N., Yang, Yuanhao and Zhao, Huiying (2024). Genetic evidence for T-wave area from 12-lead electrocardiograms to monitor cardiovascular diseases in patients taking diabetes medications. Human Genetics. doi: 10.1007/s00439-024-02661-6

Genetic evidence for T-wave area from 12-lead electrocardiograms to monitor cardiovascular diseases in patients taking diabetes medications

2023

Journal Article

Inferring the genetic relationship between brain imaging-derived phenotypes and risk of complex diseases by Mendelian randomization and genome-wide colocalization

Lin, Siying, Zhang, Haoyang, Qi, Mengling, Cooper, David N., Yang, Yuedong, Yang, Yuanhao and Zhao, Huiying (2023). Inferring the genetic relationship between brain imaging-derived phenotypes and risk of complex diseases by Mendelian randomization and genome-wide colocalization. NeuroImage, 279 120325, 120325. doi: 10.1016/j.neuroimage.2023.120325

Inferring the genetic relationship between brain imaging-derived phenotypes and risk of complex diseases by Mendelian randomization and genome-wide colocalization

2023

Journal Article

Improved concordance of challenging human epidermal growth factor receptor 2 dual in-situ hybridisation cases with the use of a digital image analysis algorithm in breast cancer

Gough, Madeline, Liu, Cheng, Srinivasan, Bhuvana, Wilkinson, Lisa, Dunk, Louisa, Yang, Yuanhao, Schreiber, Veronika, Tuffaha, Haitham, Kryza, Thomas, Hooper, John D., Lakhani, Sunil R. and Snell, Cameron E. (2023). Improved concordance of challenging human epidermal growth factor receptor 2 dual in-situ hybridisation cases with the use of a digital image analysis algorithm in breast cancer. Histopathology, 83 (4), 647-656. doi: 10.1111/his.15000

Improved concordance of challenging human epidermal growth factor receptor 2 dual in-situ hybridisation cases with the use of a digital image analysis algorithm in breast cancer

2023

Journal Article

Novel plasma and brain proteins that are implicated in multiple sclerosis

Lin, Xin, Yang, Yuanhao, Gresle, Melissa, Cuellar-Partida, Gabriel, Han, Xikun, Stankovich, Jim, Fuh-Ngwa, Valery, Charlesworth, Jac, Burdon, Kathryn P, Butzkueven, Helmut, Taylor, Bruce V, Zhou, Yuan and AusLong/Ausimmune Investigators Group Steve Simpson-Yap (2023). Novel plasma and brain proteins that are implicated in multiple sclerosis. Brain, 146 (6) awac420, 2464-2475. doi: 10.1093/brain/awac420

Novel plasma and brain proteins that are implicated in multiple sclerosis

2023

Conference Publication

HER2 in situ hybridization testing in breast cancer: applying algorithm-assisted assessment to reduce interobserver variability in difficult cases

Gough, Madeline, Liu, Cheng, Srinivasan, Bhuvana, Wilkinson, Lisa, Dunk, Louisa, Yang, Yuanhao, Tuffaha, Haitham, Kryza, Thomas, Hooper, John D., Lakhani, Sunil R. and Snell, Cameron Edward (2023). HER2 in situ hybridization testing in breast cancer: applying algorithm-assisted assessment to reduce interobserver variability in difficult cases. 2023 ASCO Annual Meeting, Chicago, IL United States, 2-6 June 2023. Alexandria, VA United States: American Society of Clinical Oncology. doi: 10.1200/jco.2023.41.16_suppl.e13561

HER2 in situ hybridization testing in breast cancer: applying algorithm-assisted assessment to reduce interobserver variability in difficult cases

2023

Journal Article

Interactions between the lipidome and genetic and environmental factors in autism

Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Giles, Corey, Huynh, Kevin, Nguyen, Anh, Wallace, Leanne, McLaren, Tiana, Yang, Yuanhao, Hernandez, Leanna M., Gandal, Michael J., Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Levis Frenk, Mira, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Strike, Lachlan T. ... The Busselton Health Study Investigators (2023). Interactions between the lipidome and genetic and environmental factors in autism. Nature Medicine, 29 (4), 936-949. doi: 10.1038/s41591-023-02271-1

Interactions between the lipidome and genetic and environmental factors in autism

2023

Journal Article

Neural biomarker diagnosis and prediction to mild cognitive impairment and Alzheimer's disease using EEG technology

Jiao, Bin, Li, Rihui, Zhou, Hui, Qing, Kunqiang, Liu, Hui, Pan, Hefu, Lei, Yanqin, Fu, Wenjin, Wang, Xiaoan, Xiao, Xuewen, Liu, Xixi, Yang, Qijie, Liao, Xinxin, Zhou, Yafang, Fang, Liangjuan, Dong, Yanbin, Yang, Yuanhao, Jiang, Haiyan, Huang, Sha and Shen, Lu (2023). Neural biomarker diagnosis and prediction to mild cognitive impairment and Alzheimer's disease using EEG technology. Alzheimer's Research and Therapy, 15 (1) 32, 32. doi: 10.1186/s13195-023-01181-1

Neural biomarker diagnosis and prediction to mild cognitive impairment and Alzheimer's disease using EEG technology

2023

Journal Article

The shared genetic landscape of blood cell traits and risk of neurological and psychiatric disorders

Yang, Yuanhao, Zhou, Yuan, Nyholt, Dale R., Yap, Chloe X., Tannenberg, Rudolph K., Wang, Ying, Wu, Yang, Zhu, Zhihong, Taylor, Bruce V. and Gratten, Jacob (2023). The shared genetic landscape of blood cell traits and risk of neurological and psychiatric disorders. Cell Genomics, 3 (2) 100249, 100249. doi: 10.1016/j.xgen.2022.100249

The shared genetic landscape of blood cell traits and risk of neurological and psychiatric disorders

2023

Journal Article

Genetically determined serum serine level has a novel causal effect on multiple sclerosis risk and predicts disability progression

Lin, Xin, Yang, Yuanhao, Fuh-Ngwa, Valery, Yin, Xianyong, Simpson-Yap, Steve, van der Mei, Ingrid, Broadley, Simon A, Ponsonby, Anne-Louise, Burdon, Kathryn P, Taylor, Bruce V, Zhou, Yuan and Ausimmune/ AusLong Investigators Group (2023). Genetically determined serum serine level has a novel causal effect on multiple sclerosis risk and predicts disability progression. Journal of Neurology, Neurosurgery and Psychiatry, 94 (7) jnnp-2022-330259, 1-6. doi: 10.1136/jnnp-2022-330259

Genetically determined serum serine level has a novel causal effect on multiple sclerosis risk and predicts disability progression

2023

Journal Article

GPR183 antagonism reduces macrophage infiltration in influenza and SARS-CoV-2 infection

Foo, Cheng Xiang, Bartlett, Stacey, Chew, Keng Yih, Ngo, Minh Dao, Bielefeldt-Ohmann, Helle, Jayakody Arachchige, Buddhika, Matthews, Benjamin, Reed, Sarah, Wang, Ran, Smith, Christian, Sweet, Matthew J., Burr, Lucy, Bisht, Kavita, Shatunova, Svetlana, Sinclair, Jane E., Parry, Rhys, Yang, Yuanhao, Lévesque, Jean-Pierre, Khromykh, Alexander, Rosenkilde, Mette Marie, Short, Kirsty R. and Ronacher, Katharina (2023). GPR183 antagonism reduces macrophage infiltration in influenza and SARS-CoV-2 infection. European Respiratory Journal, 61 (3) 2201306, 1-15. doi: 10.1183/13993003.01306-2022

GPR183 antagonism reduces macrophage infiltration in influenza and SARS-CoV-2 infection

2023

Journal Article

Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans

Lu, Zhiya, Zhang, Haoyang, Yang, Yuanhao and Zhao, Huiying (2023). Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans. Human Genetics, 142 (7), 965-980. doi: 10.1007/s00439-023-02573-x

Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans

2022

Journal Article

Genetic evidence for a causal relationship between type 2 diabetes and peripheral artery disease in both Europeans and East Asians

Xiu, Xuehao, Zhang, Haoyang, Xue, Angli, Cooper, David N., Yan, Li, Yang, Yuedong, Yang, Yuanhao and Zhao, Huiying (2022). Genetic evidence for a causal relationship between type 2 diabetes and peripheral artery disease in both Europeans and East Asians. BMC Medicine, 20 (1) 300, 1-16. doi: 10.1186/s12916-022-02476-0

Genetic evidence for a causal relationship between type 2 diabetes and peripheral artery disease in both Europeans and East Asians

2022

Journal Article

Integrating Genetic Structural Variations and Whole-Genome Sequencing Into Clinical Neurology

Lin, Xin, Yang, Yuanhao, Melton, Phillip E., Singh, Vikrant, Simpson-Yap, Steve, Burdon, Kathryn P., Taylor, Bruce V. and Zhou, Yuan (2022). Integrating Genetic Structural Variations and Whole-Genome Sequencing Into Clinical Neurology. Neurology: Genetics, 8 (4) e200005, 1-12. doi: 10.1212/NXG.0000000000200005

Integrating Genetic Structural Variations and Whole-Genome Sequencing Into Clinical Neurology

2022

Journal Article

MUC1 mediated macrophage activation promotes colitis-associated colorectal cancer via activating the IL-6/STAT3 axis

Sheng, 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

MUC1 mediated macrophage activation promotes colitis-associated colorectal cancer via activating the IL-6/STAT3 axis

2021

Journal Article

Investigating the shared genetic architecture between multiple sclerosis and inflammatory bowel diseases

Yang, 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

Investigating the shared genetic architecture between multiple sclerosis and inflammatory bowel diseases

2021

Journal Article

Mendelian randomization study reveals a population-specific putative causal effect of type 2 diabetes in risk of cataract

Zhang, 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

Mendelian randomization study reveals a population-specific putative causal effect of type 2 diabetes in risk of cataract

2021

Journal Article

Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank

Yap, 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

Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank

2019

Conference Publication

Common genetic variation explains a high proportion of the elevated risk of psychiatric disorders in children of younger mothers

Gratten, 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

Common genetic variation explains a high proportion of the elevated risk of psychiatric disorders in children of younger mothers

Funding

Current funding

  • 2023 - 2027
    Unravelling the interplay between EBV genomics and host T cell immune regulation in multiple sclerosis (Ex-led UTas MRFF MS grant)
    University of Tasmania
    Open grant

Supervision

Availability

Dr Yuanhao Yang is:
Available for supervision

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Supervision history

Current supervision

Media

Enquiries

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