Dr Gabriel Cuellar Partida
Honorary Fellow
The University of Queensland Diamantina Institute
Visiting Academic
Journal Articles
García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Inference of causal relationships between sleep-related traits and 1,527 phenotypes using genetic data. Sleep, 44 (1). doi: 10.1093/sleep/zsaa154
Hwang, Liang-Dar, Tubbs, Justin D., Luong, Justin, Lundberg, Mischa, Moen, Gunn-Helen, Wang, Geng, Warrington, Nicole M., Sham, Pak C., Cuellar-Partida, Gabriel and Evans, David M. (2020). Estimating indirect parental genetic effects on offspring phenotypes using virtual parental genotypes derived from sibling and half sibling pairs. PLoS Genetics, 16 (10) e1009154, e1009154. doi: 10.1371/journal.pgen.1009154
Haworth, Simon, Kho, Pik Fang, Holgerson, Pernilla Lif, Hwang, Liang-Dar, Timpson, Nicholas J., Rentería, Miguel E., Johansson, Ingegerd and Cuellar-Partida, Gabriel (2020). Assessment and visualization of phenome-wide causal relationships using genetic data: an application to dental caries and periodontitis. European Journal of Human Genetics, 29 (2), 300-308. doi: 10.1038/s41431-020-00734-4
Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., Boyd, Heather A., Breteler, Monique M. B., Campbell, Harry, Chasman, Daniel I., Cherkas, Lynn F., Davies, Gail, de Geus, Eco J. C., Deary, Ian J., Deloukas, Panos, Dick, Danielle M., Duffy, David L., Eriksson, Johan G., Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D., Han, Jiali ... Medland, Sarah E. (2020). Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour, 5 (1), 59-70. doi: 10.1038/s41562-020-00956-y
D'Urso, Shannon, Rajbhandari, Dorrilyn, Peach, Elizabeth, De Guzman, Erika, Li, Qiang, Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Ligthart, Symen, Brown, Matthew A., Powell, Joseph, McArthur, Colin, Rhodes, Andrew, Meyer, Jason, Finfer, Simon, Myburgh, John, Blumenthal, Antje, Cohen, Jeremy, Venkatesh, Balasubramanian, Cuellar-Partida, Gabriel and Evans, David M. (2020). Septic shock: a genomewide association study and polygenic risk score analysis. Twin Research and Human Genetics, 23 (4), 204-213. doi: 10.1017/thg.2020.60
Shi, Xiu-Yu, Wang, Geng, Li, Ting, Li, Zhixiu, Leo, Paul, Liu, Zhisheng, Wu, Gefei, Zhu, Hongmin, Zhang, Yuqin, Li, Dong, Gao, Li, Yang, Liu, Wang, Wei, Liao, Jianxiang, Wang, Jiwen, Zhou, Shuizhen, Wang, Hua, Li, Xiaojing, Gao, Jingyun, Zhang, Li, Shu, Xiaomei, Li, Dan, Li, Yan, Chen, Chunhong, Zhang, Xiuju, Partida, Gabriel Cuellar, Lundberg, Mischa, Reutens, David, Bartlett, Perry ... Xu, Huji (2020). Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population. EBioMedicine, 57 102840, 102840. doi: 10.1016/j.ebiom.2020.102840
Mitchell, Brittany L., Cuéllar-Partida, Gabriel, Grasby, Katrina L., Campos, Adrian I., Strike, Lachlan T., Hwang, Liang-Dar, Okbay, Aysu, Thompson, Paul M., Medland, Sarah E., Martin, Nicholas G., Wright, Margaret J. and Rentería, Miguel E. (2020). Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory. NeuroImage, 212 116691, 116691. doi: 10.1016/j.neuroimage.2020.116691
Campos, Adrián I., García-Marín, Luis M., Byrne, Enda M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2020). Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Nature Communications, 11 (1) 817, 817. doi: 10.1038/s41467-020-14625-1
Leon-Apodaca, Ana V., Chiu-Han, Enrique, Ortega-Mora, Ivett, Román-López, Talía V., Caballero-Sánchez, Ulises, Aldana-Assad, Oscar, Campos, Adrián I., Cuellar-Partida, Gabriel, Ruiz-Contreras, Alejandra E., Alcauter, Sarael, Rentería, Miguel E. and Medina-Rivera, Alejandra (2019). TwinsMX: uncovering the basis of health and disease in the Mexican population. Twin Research and Human Genetics, 22 (6), 611-616. doi: 10.1017/thg.2019.112
Satizabal, Claudia L., Adams, Hieab H. H., Hibar, Derrek P., White, Charles C., Knol, Maria J., Stein, Jason L., Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V., Smith, Albert V., Bis, Joshua C., Jian, Xueqiu, Luciano, Michelle, Hofer, Edith, Teumer, Alexander, van der Lee, Sven J., Yang, Jingyun, Yanek, Lisa R., Lee, Tom V., Li, Shuo, Hu, Yanhui, Koh, Jia Yu, Eicher, John D., Desrivières, Sylvane, Arias-Vasquez, Alejandro, Chauhan, Ganesh, Athanasiu, Lavinia, Rentería, Miguel E. ... Ikram, M. Arfan (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics, 51 (11), 1624-1636. doi: 10.1038/s41588-019-0511-y
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. (2019). Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (Nature Genetics, (2018), 50, 1, (26-41), 10.1038/s41588-017-0011-x). Nature Genetics, 51 (7), 1191-1192. doi: 10.1038/s41588-019-0447-2
Hwang, Liang-Dar, Lin, Cailu, Gharahkhani, Puya, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, An, Jiyuan, Gordon, Scott D., Zhu, Gu, MacGregor, Stuart, Lawlor, Deborah A., Breslin, Paul A. S., Wright, Margaret J., Martin, Nicholas G. and Reed, Danielle R. (2019). New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. The American Journal of Clinical Nutrition, 109 (6), 1724-1737. doi: 10.1093/ajcn/nqz043
Cuellar Partida, Gabriel, Laurin, Charles, Ring, Susan M., Gaunt, Tom R., McRae, Allan, Visscher, Peter M., Montgomery, Grant W., Martin, Nicholas G., Hemani, Gibran, Suderman, Matthew, Relton, Caroline L., Davey Smith, George and Evans, David M. (2018). Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans. Human Molecular Genetics, 27 (16), 2927-2939. doi: 10.1093/hmg/ddy206
Tedja, Milly S., Wojciechowski, Robert, Hysi, Pirro G., Eriksson, Nicholas, Furlotte, Nicholas A., Verhoeven, Virginie J. M., Iglesias, Adriana I., Meester-Smoor, Magda A., Tompson, Stuart W., Fan, Qiao, Khawaja, Anthony P., Cheng, Ching-Yu, Höhn, René, Yamashiro, Kenji, Wenocur, Adam, Grazal, Clare, Haller, Toomas, Metspalu, Andres, Wedenoja, Juho, Jonas, Jost B., Wang, Ya Xing, Xie, Jing, Mitchell, Paul, Foster, Paul J., Klein, Barbara E. K., Klein, Ronald, Paterson, Andrew D., Hosseini, S. Mohsen, Shah, Rupal L. ... UK Biobank Eye and Vision Consortium (2018). Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nature Genetics, 50 (6), 834-848. doi: 10.1038/s41588-018-0127-7
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
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). Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics, 50 (1), 26-41. doi: 10.1038/s41588-017-0011-x
Cuellar-Partida, Gabriel, Williams, Katie M., Yazar, Seyhan, Guggenheim, Jeremy A., Hewitt, Alex W., Williams, Cathy, Wang, Jie Jin, Kho, Pik-Fang, Saw, Seang Mei, Cheng, Ching-Yu, Wong, Tien Yin, Aung, Tin, Young, Terri L., Tideman, J. Willem L., Jonas, Jost B., Mitchell, Paul, Wojciechowski, Robert, Stambolian, Dwight, Hysi, Pirro, Hammond, Christopher J., Mackey, David A., Lucas, Robyn M. and MacGregor, Stuart (2017). Genetically low vitamin D concentrations and myopic refractive error: a Mendelian randomization study. International Journal of Epidemiology, 46 (6), 1882-1890. doi: 10.1093/ije/dyx068
Ong, Jue-Sheng, Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Martin, Nicholas G., Chenevix-Trench, Georgia, Quinn, Michael C. J., Cornelis, Marilyn C., Gharahkhani, Puya, Webb, Penelope M., MacGregor, Stuart and Ovarian Cancer Association Consortium (2017). Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study. International Journal of Epidemiology, 47 (2), 450-459. doi: 10.1093/ije/dyx236
Laurin, Charles, Cuellar-Partida, Gabriel, Hemani, Gibran, Smith, George Davey, Yang, Jian and Evans, David M. (2017). Partitioning phenotypic variance due to parent-of-origin effects using genomic relatedness matrices. Behavior Genetics, 48 (1), 67-79. doi: 10.1007/s10519-017-9880-0
Marouli, Eirini, Graff, Mariaelisa, Medina-Gomez, Carolina, Lo, Ken Sin, Wood, Andrew R., Kjaer, Troels R., Fine, Rebecca S., Lu, Yingchang, Schurmann, Claudia, Highland, Heather M. , Rueger, Sina, Thorleifsson, Gudmar, Justice, Anne E., Lamparter, David, Stirrups, Kathleen E., Turcot, Valérie, Young, Kristin L., Winkler, Thomas W., Esko, Tõnu, Karaderi, Tugce, Locke, Adam E., Masca, Nicholas G. D., Ng, Maggie C. Y., Mudgal, Poorva, Rivas, Manuel A., Vedantam, Sailaja, Mahajan, Anubha, Guo, Xiuqing, Abecasis, Goncalo ... Lettre, Guillaume (2017). Rare and low-frequency coding variants alter human adult height. Nature, 542 (7640), 186-190. doi: 10.1038/nature21039
Hibar, Derrek P., Adams, Hieab H. H., Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L., Hofer, Edith, Renteria, Miguel E., Bis, Joshua C., Arias-Vasquez, Alejandro, Ikram, M. Kamran, Desrivieres, Sylvane, Vernooij, Meike W., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beecham, Ashley H., Beiser, Alexa, Bernard, Manon, Blanton, Susan H., Bohlken, Marc M., Boks, Marco P., Bralten, Janita, Brickman, Adam M. ... Ikram, M. Arfan (2017). Novel genetic loci associated with hippocampal volume. Nature Communications, 8 (1) 13624, 13624. doi: 10.1038/ncomms13624
Springelkamp, Henriet, Iglesias, Adriana I., Mishra, Aniket, Hoehn, Rene, Wojciechowski, Robert, Khawaja, Anthony P., Nag, Abhishek, Wang, Ya Xing, Wang, Jie Jin, Cuellar-Partida, Gabriel, Gibson, Jane, Bailey, Jessica N. Cooke, Vithana, Eranga N., Gharahkhani, Puya, Boutin, Thibaud, Ramdas, Wishal D., Zeller, Tanja, Luben, Robert N., Yonova-Doing, Ekaterina, Viswanathan, Ananth C., Yazar, Seyhan, Cree, Angela J., Haines, Jonathan L., Koh, Jia Yu, Souzeau, Emmanuelle, Wilson, James F., Amin, Najaf, Mueller, Christian, Venturini, Cristina ... MacGregor, Stuart (2017). New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics. Human Molecular Genetics, 26 (2), 438-453. doi: 10.1093/hmg/ddw399
Adams, Hieab H. H., Hibar, Derrek P., Chouraki, Vincent, Stein, Jason L., Nyquist, Paul A., Renteria, Miguel E., Trompet, Stella, Arias-Vasquez, Alejandro, Seshadri, Sudha, Desrivieres, Sylvane, Beecham, Ashley H., Jahanshad, Neda, Wittfeld, Katharina, Van der Lee, Sven J., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beiser, Alexa, Bernard, Manon, Bis, Joshua C., Blanken, Laura M. E., Blanton, SusanH., Bohlken, Marc M. ... Thompson, Paul M. (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 (12), 1569-1582. doi: 10.1038/nn.4398
Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, Breslin, Paul A. S., Reed, Danielle R., Macgregor, Stuart, Gharahkhani, Puya, Martin, Nicholas G. and Renteria, Miguel E. (2016). Sweet taste perception is associated with body mass index at the phenotypic and genotypic level. Twin Research and Human Genetics, 19 (5), 465-471. doi: 10.1017/thg.2016.60
Ong, Jue-Sheng, Cuellar-Partida, Gabriel, Lu, Yi, Fasching, Peter A., Hein, Alexander, Burghaus, Stefanie, Beckmann, Matthias W., Lambrechts, Diether, Van Nieuwenhuysen, Els, Vergote, Ignace, Vanderstichele, Adriaan, Doherty, Jennifer Anne, Rossing, Mary Anne, Chang-Claude, Jenny, Eilber, Ursula, Rudolph, Anja, Wang-Gohrke, Shan, Goodman, Marc T., Bogdanova, Natalia, Dork, Thilo, Durst, Matthias, Hillemanns, Peter, Runnebaum, Ingo B., Antonenkova, Natalia, Butzow, Ralf, Leminen, Arto, Nevanlinna, Heli, Pelttari, Liisa M., Edwards, Robert P. ... MacGregor, Stuart (2016). Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study. International Journal of Epidemiology, 45 (5), 1619-1630. doi: 10.1093/ije/dyw207
Cuellar-Partida, G., Lu, Y., Dixon, S.C., Australian Ovarian Cancer Study, Fasching, P.A., Hein, A., Burghaus, S., Beckmann, M.W., Lambrechts, D., van Nieuwenhuysen, E., Vergote, I., Vanderstichele, A., Doherty, J.A., Rossing, M.A., Chang-Claude, J., Rudolph, A., Wang-Gohrke, S., Goodman, M.T., Bogdanova, N., Dork, T., Durst, M., Hillemanns, P., Runnebaum, I.B., Antonenkova, N., Butzow, R., Leminen, A., Nevanlinna, H., Pelttari, L.M., Edwards, R.P. ... MacGregor, S. (2016). Assessing the genetic architecture of epithelial ovarian cancer histological subtypes. Human Genetics, 135 (7), 741-756. doi: 10.1007/s00439-016-1663-9
Cuellar-Partida, Gabriel, Craig, Jamie E., Burdon, Kathryn P., Wang, Jie Jin, Vote, Brendan J., Souzeau, Emmanuelle, McAllister, Ian L., Isaacs, Timothy, Lake, Stewart, Mackey, David A., Constable, Ian J., Mitchell, Paul, Hewitt, Alex W. and MacGregor, Stuart (2016). Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration. Scientific Reports, 6 (1) 26885. doi: 10.1038/srep26885
Cuellar-Partida, Gabriel, Lu, Yi, Kho, Pik Fang, Hewitt, Alex W., Wichmann, H. -Erich, Yazar, Seyhan, Stambolian, Dwight, Bailey-Wilson, Joan E., Wojciechowski, Robert, Wang, Jie Jin, Mitchell, Paul, Mackey, David A. and MacGregor, Stuart (2016). Assessing the genetic predisposition of education on myopia: a Mendelian randomization study. Genetic Epidemiology, 40 (1), 66-72. doi: 10.1002/gepi.21936
Cuellar-Partida, Gabriel, Springelkamp, Henriet, Lucas, Sionne E. M., Yazar, Seyhan, Hewitt, Alex W., Iglesias, Adriana I., Montgomery, Grant W., Martin, Nicholas G., Pennell, Craig E., van Leeuwen, Elisabeth M., Verhoeven, Virginie J. M., Hofman, Albert, Uitterlinden, Andre G., Ramdas, Wishal D., Wolfs, Roger. C. W., Vingerling, Johannes R., Brown, Matthew A., Mills, Richard A., Craig, Jamie E., Klaver, Caroline C. W., van Duijn, Cornelia M., Burdon, Kathryn P., MacGregor, Stuart and Mackey, David A. (2015). WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness. Human Molecular Genetics, 24 (17), 5060-5068. doi: 10.1093/hmg/ddv211
Lu, Yi, Cuellar-Partida, Gabriel, Painter, Jodie N., Nyholt, Dale R., Morris, Andrew P., Fasching, Peter A., Hein, Alexander, Burghaus, Stefanie, Beckmann, Matthias W., Lambrechts, Diether, Van Nieuwenhuysen, Els, Vergote, Ignace, Vanderstichele, Adriaan, Doherty, Jennifer Anne, Rossing, Mary Anne, Wicklund, Kristine G., Chang-Claude, Jenny, Eilber, Ursula, Rudolph, Anja, Wang-Gohrke, Shan, Goodman, Marc T., Bogdanova, Natalia, Doerk, Thilo, Duerst, Matthias, Hillemanns, Peter, Runnebaum, Ingo B., Antonenkova, Natalia, Butzow, Ralf, Leminen, Arto ... Visscher, Peter M. (2015). Shared genetics underlying epidemiological association between endometriosis and ovarian cancer. Human Molecular Genetics, 24 (20), 5955-5964. doi: 10.1093/hmg/ddv306
Springelkamp, Henriet, Iglesias, Adriana I., Cuellar-Partida, Gabriel, Amin, Najaf, Burdon, Kathryn P., van Leeuwen, Elisabeth M., Gharahkhani, Puya, Mishra, Aniket, van der Lee, Sven J., Hewitt, Alex W., Rivadeneira, Fernando, Viswanathan, Ananth C., Wolfs, Roger C. W., Martin, Nicholas G., Ramdas, Wishal D., van Koolwijk, Leonieke M., Pennell, Craig E., Vingerling, Johannes R., Mountain, Jenny E., Uitterlinden, Andre G., Hofman, Albert, Mitchell, Paul, Lemij, Hans G., Wang, Jie Jin, Klaver, Caroline C. W., Mackey, David A., Craig, Jamie E., van Duijn, Cornelia M. and MacGregor, Stuart (2015). ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure. Human Molecular Genetics, 24 (9), 2689-2699. doi: 10.1093/hmg/ddv027
Hibar, Derrek P, Stein, Jason L, Renteria, Miguel E, Arias-Vasquez, Alejandro, Desrivieres, Sylvane, Jahanshad, Neda, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Andersson, Micael, Aribisala, Benjamin S, Armstrong, Nicola J, Bernard, Manon, Bohlken, Marc M, Boks, Marco P, Bralten, Janita, Brown, Andrew A, Mallar Chakravarty M., Chen, Qiang, Ching, Christopher R.K., Cuellar-Partida, Gabriel, Den Braber, Anouk, Giddaluru, Sudheer, Goldman, Aaron L, Grimm, Oliver, Guadalupe, Tulio, Hass, Johanna, Woldehawariat, Girma, Holmes, Avram J ... Medland, Sarah E (2015). Common genetic variants influence human subcortical brain structures. Nature, 520 (7546), 224-229. doi: 10.1038/nature14101
Yazar, Seyhan, Cuellar-Partida, Gabriel, McKnight, Charlotte M., Quach-Thanissorn, Piriya, Mountain, Jenny A., Coroneo, Minas T., Pennell, Craig E., Hewitt, Alex W., MacGregor, Stuart and Mackey, David A. (2015). Genetic and environmental factors in conjunctival UV autofluorescence. JAMA Ophthalmology, 133 (4), 406-412. doi: 10.1001/jamaophthalmol.2014.5627
Miyake, Masahiro, Yamashiro, Kenji, Tabara, Yasuharu, Suda, Kenji, Morooka, Satoshi, Nakanishi, Hideo, Khor, Chiea-Chuen, Chen, Peng, Qiao, Fan, Nakata, Isao, Akagi-Kurashige, Yumiko, Gotoh, Norimoto, Tsujikawa, Akitaka, Meguro, Akira, Kusuhara, Sentaro, Polasek, Ozen, Hayward, Caroline, Wright, Alan F., Campbell, Harry, Richardson, Andrea J., Schache, Maria, Takeuchi, Masaki, Mackey, David A., Hewitt, Alex W., Cuellar, Gabriel, Shi, Yi, Huang, Luling, Yang, Zhenglin, Leung, Kim Hung ... Yoshimura, Nagahisa (2015). Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. Nature Communications, 6 (1) 6689. doi: 10.1038/ncomms7689
Strike, Lachlan T, Couvy-Duchesne, Baptiste, Hansell, Narelle K, Cuellar-Partida, Gabriel, Medland, Sarah E and Wright, Margaret J (2015). Genetics and brain morphology. Neuropsychology Review, 25 (1), 63-96. doi: 10.1007/s11065-015-9281-1
Cuellar-Partida, Gabriel, Renteria, Miguel E. and MacGregor, Stuart (2015). LocusTrack: integrated visualization of GWAS results and genomic annotation. Source Code for Biology and Medicine, 10 (1) 1, 1.1-1.4. doi: 10.1186/s13029-015-0032-8
Hysi, Pirro G., Cheng, Ching-Yu, Springelkamp, Henriet, Macgregor, Stuart, Bailey, Jessica N. Cooke, Wojciechowski, Robert, Vitart, Veronique, Nag, Abhishek, Hewitt, Alex W., Hohn, Rene, Venturini, Cristina, Mirshahi, Alireza, Ramdas, Wishal D., Thorleifsson, Gudmar, Vithana, Eranga, Khor, Chiea-Chuen, Stefansson, Arni B., Liao, Jiemin, Haines, Jonathan L., Amin, Najaf, Wang, Ya Xing, Wild, Philipp S., Ozel, Ayse B., Li, Jun Z., Fleck, Brian W., Zeller, Tanja, Staffieri, Sandra E., Teo, Yik-Ying, Cuellar-Partida, Gabriel ... Aung, Tin (2014). Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nature Genetics, 46 (10), 1126-1130. doi: 10.1038/ng.3087
McLeay, Robert C., Lesluyes, Tom, Partida, Gabriel Cuellar and Bailey, Timothy L. (2012). Genome-wide in silico prediction of gene expression. Bioinformatics, 28 (21), 2789-2796. doi: 10.1093/bioinformatics/bts529
Cuellar-Partida, Gabriel, Buske, Fabian A., McLeay, Robert C., Whitington, Tom, Noble, William Stafford and Bailey, Timothy L. (2012). Epigenetic priors for identifying active transcription factor binding sites. Bioinformatics, 28 (1) btr614, 56-62. doi: 10.1093/bioinformatics/btr614
Conference Papers
Lundberg, Mischa, Campos, Adrian I., Farrell, Scott F., Wang, Geng, Sterling, Michele M., Rentería, Miguel E., Ngo, Trung Thanh and Cuéllar-Partida, Gabriel (2020). Genetic, lifestyle and environmental risk factors for chronic pain revealed through GWAS. 50th Annual Meeting of the Behavior Genetics Association, Online, 26 June 2020. NEW YORK: SPRINGER.
Ngo, Trung Thanh, Zhu, Guohun, Rentería, Miguel E. and Cuéllar-Partida, Gabriel (2020). Elucidating a phylogenetic switching model of sleep, vision & mental health with computational biology and complex network analyses. Systems & Computational Neuroscience Down Under (SCiNDU) 2020 meeting, St Lucia, QLD Australia, 29–31 January 2020.
Cuéllar-Partida, Gabriel, Lundberg, Mischa, Campos-González, Adrian I., Kho, Pik Fang, D’Urso, Shannon, Hwang, Liang-Dar, Ngo, Trung Thanh and Rentería, Miguel E. (2019). Complex-Traits Genetics Virtual Lab: A community-driven web platform for post-GWAS analyses. American Society of Human Genetics (ASHG) 69th Annual Meeting, Houston, TX United States, 15–19 October 2019.
Ngo, Trung T. , Rentería, Miguel E. and Cuéllar-Partida, Gabriel (2019). Precision switch medicine: transdiagnostic stratification of bipolar and related disorders with an integrated phenotyping and genetics analysis cloud platform. 21st Annual ISBD Conference: Global Advances in Bipolar Disorder and Depression, International Convention Centre, Sydney, Australia, 20–23 March 2019. Hoboken, NJ, United States: Wiley-Blackwell. doi: 10.1111/bdi.12746
Lundberg, Mischa, Campos, Adrian, Rentería, Miguel, Ngo, Trung and Cuéllar-Partida, Gabriel (2019). Dissecting the genetic architecture of chronic pain using CTG-VL — Complex-Traits Genetics Virtual Lab. 49th Annual Meeting of the Behavior Genetics Association, Stockholm, Sweden, 26–29 June 2019. New York, NY United States: Springer Nature. doi: 10.1007/s10519-019-09973-8
Ngo, Trung Thanh, Lundberg, Mischa, Campos-González, Adrian, Kho, Pik Fang, D’Urso, Shannon, Hwang, Liang-Dar, Rentería, Miguel and Cuéllar-Partida, Gabriel (2019). Genetic epidemiology of back pain: Examining causality with Complex Traits Virtual Lab. Australasian Epidemiological Association 2019 Annual Scientific Meeting — 'Epidemiology in the real world', South Brisbane, QLD Australia, 23–25 October 2019.
Ngo, Trung T. , Rentería, Miguel E. and Cuéllar-Partida, Gabriel (2018). E-mental health transdiagnostic stratification: A cloud-based platform for multi-phenotyping and genetic analyses. 40th Annual Society for Mental Health Research Conference, Noosa Heads, QLD Australia, 28–30 November 2018.
Ngo, Trung T. , Rentería, Miguel E. and Cuéllar-Partida, Gabriel (2018). Advancing a neurogenomics oscillator model of bistable affective-cognitive states, behaviour and disorders. 5th Annual Australasian Society for Social & Affective Neuroscience Conference, Brisbane QLD, Australia, 20–21 June 2018.
Ngo, Trung T., Cuéllar-Partida, Gabriel, Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). GWAS of complementary perceptual endophenotype measures: How do they rate?. Australasian Society for Bipolar & Depressive Disorders (ASBDD) 2017 Conference, Deakin Edge, Melbourne, 15–17 September 2017.
Cuéllar-Partida, Gabriel, Ngo, Trung T., Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait. BLiSS 2017 — Brisbane Life Science ECR Symposium, Translational Research Institute, Brisbane, 24 November 2017.
Ngo, T. T., Couvy-Duchesne, B., Cuéllar-Partida, G., Rentería, M. E., Colodro Conde, L., Gordon, S. D., Hansell, N. K., Law, P. C. F., Miller, S. M., Medland, S. E., Wright, M. J. and Martin, N. G. (2016). Association of psychiatric profile measures with binocular rivalry rate (BRR): Implications for slow BRR as an endophenotype for bipolar disorder. International Society for Twin Studies Satellite Meeting, QIMR Berghofer Medical Research Institute, Brisbane, Australia, 20 June 2016. Cambridge, United Kingdom: Cambridge University Press. doi: 10.1017/thg.2016.66
Thesis
Cuellar Partida, Gabriel (2016). Complex trait genetics: mapping, correlation and causation. PhD Thesis, School of Medicine, The University of Queensland. doi: 10.14264/uql.2016.342