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2019 Journal Article The rs2516839 variation of USF1 gene is associated with 4-year mortality of nonagenarian women: the Vitality 90+studyOzsait-Selcuk, B., Komurcu-Bayrak, E., Jylha, M., Luukkaala, T., Perola, M., Kristiansson, K., Mononen, N., Hurme, M., Kahonen, M., Goebeler, S., Laaksonen, R., Hervonen, A., Erginel-Unaltuna, N., Karhunen, P. J. and Lehtimaki, T. (2019). The rs2516839 variation of USF1 gene is associated with 4-year mortality of nonagenarian women: the Vitality 90+study. Annals of Human Genetics, 83 (1), 34-45. doi: 10.1111/ahg.12282 |
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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 Study protocol for the Australian autism biobank: an international resource to advance autism discovery researchAlvares, Gail A., Dawson, Paul A., Dissanayake, Cheryl, Eapen, Valsamma, Gratten, Jacob, Grove, Rachel, Henders, Anjali, Heussler, Helen, Lawson, Lauren, Masi, Anne, Raymond, Emma, Rose, Felicity, Wallace, Leanne, Wray, Naomi R. and Whitehouse, Andrew J. O. (2018). Study protocol for the Australian autism biobank: an international resource to advance autism discovery research. BMC Pediatrics, 18 (1) 284, 284. doi: 10.1186/s12887-018-1255-z |
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2018 Journal Article Salbutamol-induced Decrease in Augmentation Index is Related to the Parallel Increase in Heart RateTikkakoski, Antti J., Kangas, Pauliina, Suojanen, Lauri, Tahvanainen, Anna M., Eraranta, Arttu, Kahonen, Mika A. P., Sipila, Kalle, Mustonen, Jukka T. and Porsti, Ilkka H. (2018). Salbutamol-induced Decrease in Augmentation Index is Related to the Parallel Increase in Heart Rate. Basic & Clinical Pharmacology & Toxicology, 123 (2), 161-173. doi: 10.1111/bcpt.12988 |
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2018 Journal Article Age at first birth in women is genetically associated with increased risk of schizophreniaNi, Guiyan, Gratten, Jacob, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Wray, Naomi R. and Lee, Sang Hong (2018). Age at first birth in women is genetically associated with increased risk of schizophrenia. Scientific Reports, 8 (1) 10168, 10168. doi: 10.1038/s41598-018-28160-z |
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2018 Journal Article Serum proteomic profiling to identify biomarkers of premature carotid atherosclerosisBhosale, Santosh D., Moulder, Robert, Venalainen, Mikko S., Koskinen, Juhani S., Pitkanen, Niina, Juonala, Markus T., Kahonen, Mika A. P., Lehtimaki, Terho J., Viikari, Jorma S. A., Elo, Laura L., Goodlett, David R., Lahesmaa, Riitta and Raitakari, Olli T. (2018). Serum proteomic profiling to identify biomarkers of premature carotid atherosclerosis. Scientific Reports, 8 (1) 9209. doi: 10.1038/s41598-018-27265-9 |
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2018 Journal Article Trans-eQTLs identified in whole blood have limited influence on complex disease biologyYap, Chloe X., Lloyd-Jones, Luke, Holloway, Alexander, Smartt, Peter, Wray, Naomi R., Gratten, Jacob and Powell, Joseph E. (2018). Trans-eQTLs identified in whole blood have limited influence on complex disease biology. European Journal of Human Genetics, 26 (9), 1-8. doi: 10.1038/s41431-018-0174-7 |
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2018 Journal Article Sizing up whole-genome sequencing studies of common diseasesWray, Naomi R. and Gratten, Jacob (2018). Sizing up whole-genome sequencing studies of common diseases. Nature Genetics, 50 (5), 635-637. doi: 10.1038/s41588-018-0113-0 |
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2018 Journal Article Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysisMcKeown, Nicola M., Dashti, Hassan S., Ma, Jiantao, Haslam, Danielle E., Kiefte-de Jong, Jessica C., Smith, Caren E., Tanaka, Toshiko, Graff, Mariaelisa, Lemaitre, Rozenn N., Rybin, Denis, Sonestedt, Emily, Frazier-Wood, Alexis C., Mook-Kanamori, Dennis O., Li, Yanping, Wang, Carol A., Leermakers, Elisabeth T. M., Mikkila, Vera, Young, Kristin L., Mukamal, Kenneth J., Cupples, L. Adrienne, Schulz, Christina-Alexandra, Chen, Tzu-An, Li-Gao, Ruifang, Huang, Tao, Oddy, Wendy H., Raitakari, Olli, Rice, Kenneth, Meigs, James B., Ericson, Ulrika ... Herman, Mark A. (2018). Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis. Diabetologia, 61 (2), 317-330. doi: 10.1007/s00125-017-4475-0 |
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2017 Journal Article Gene networks associated with non-syndromic intellectual disabilityLee, Soohyun, Rudd, Stephen, Gratten, Jacob, Visscher, Peter M., Prins, Johannes B. and Dawson, Paul A. (2017). Gene networks associated with non-syndromic intellectual disability. Journal of Neurogenetics, 32 (1), 6-14. doi: 10.1080/01677063.2017.1404058 |
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2017 Journal Article Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in ChineseGratten, Jacob, Zhao, Qiongyi, Benyamin, Beben, Garton, Fleur, He, Ji, Leo, Paul J., Mangelsdorf, Marie, Anderson, Lisa, Zhang, Zong-Hong, Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Edson, Janette, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K., Jin, Zi-Bing, Li, Zhongshan, Lin, Yong, Liu, Xiaolu, Marshall, Mhairi, Mowry, Bryan J., Ran, Shu, Reutens, David C., Song, Sharon, Tan, Li-Jun, Tang, Lu, Wallace, Robyn H. ... Fan, Dongsheng (2017). Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese. Genome Medicine, 9 (97) 97, 97. doi: 10.1186/s13073-017-0487-0 |
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2017 Journal Article Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosisBenyamin, Beben, He, Ji, Zhao, Qiongyi, Gratten, Jacob, Garton, Fleur, Leo, Paul J., Liu, Zhijun, Mangelsdorf, Marie, Al-Chalabi, Ammar, Anderson, Lisa, Butler, Timothy J., Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Devine, Matthew, Edson, Janette, Fifita, Jennifer A., Furlong, Sarah, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K., Jeffree, Rosalind L., Jin, Zi-Bing, Li, Zhongshan, Li, Ting, Li, Mengmeng, Lin, Yong, Liu, Xiaolu ... Fan, Dongsheng (2017). Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. Nature Communications, 8 (1) 611, 611. doi: 10.1038/s41467-017-00471-1 |
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2017 Journal Article Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohortGarton, Fleur C., Benyamin, Beben, Zhao, Qiongyi, Liu, Zhijun, Gratten, Jacob, Henders, Anjali K., Zhang, Zong-Hong, Edson, Janette, Furlong, Sarah, Morgan, Sarah, Heggie, Susan, Thorpe, Kathryn, Pfluger, Casey, Mather, Karen A., Sachdev, Perminder S., McRae, Allan F., Robinson, Matthew R., Shah, Sonia, Visscher, Peter M., Mangelsdorf, Marie, Henderson, Robert D., Wray, Naomi R. and McCombe, Pamela A. (2017). Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort. Molecular Genetics and Genomic Medicine, 5 (4), 418-428. doi: 10.1002/mgg3.302 |
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2017 Journal Article Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel diseaseJi, Sun-Gou, Juran, Brian D., Mucha, Soeren, Folseraas, Trine, Jostins, Luke, Melum, Espen, Kumasaka, Natsuhiko, Atkinson, Elizabeth J., Schlicht, Erik M., Liu, Jimmy Z., Shah, Tejas, Gutierrez-Achury, Javier, Boberg, Kirsten M., Bergquist, Annika, Vermeire, Severine, Eksteen, Bertus, Durie, Peter R., Farkkila, Martti, Mueller, Tobias, Schramm, Christoph, Sterneck, Martina, Weismueller, Tobias J., Gotthardt, Daniel N., Ellinghaus, David, Braun, Felix, Teufel, Andreas, Laudes, Mattias, Lieb, Wolfgang, Jacobs, Gunnar ... Anderson, Carl A. (2017). Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease. Nature Genetics, 49 (2), 269-273. doi: 10.1038/ng.3745 |
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2016 Journal Article Metabolic profiling of pregnancy: cross-sectional and longitudinal evidenceWang, Qin, Wurtz, Peter, Auro, Kirsi, Makinen, Ville-Petteri, Kangas, Antti J., Soininen, Pasi, Tiainen, Mika, Tynkkynen, Tuulia, Jokelainen, Jari, Santalahti, Kristiina, Salmi, Marko, Blankenberg, Stefan, Zeller, Tanja, Viikari, Jorma, Kahonen, Mika, Lehtimaki, Terho, Salomaa, Veikko, Perola, Markus, Jalkanen, Sirpa, Jarvelin, Marjo-Riitta, Raitakari, Olli T., Kettunen, Johannes, Lawlor, Debbie A. and Ala-Korpela, Mika (2016). Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence. Bmc Medicine, 14 205. doi: 10.1186/s12916-016-0733-0 |
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2016 Journal Article Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (vol 48, pg 624, 2016)Okbay, Aysu, Baselmans, Bart M. L., De Neve, Jan-Emmanuel, Turley, Patrick, Nivard, Michel G., Fontana, Mark Alan, Meddens, S. Fleur W., Linner, Richard Karlsson, Rietveld, Cornelius A., Derringer, Jaime, Gratten, Jacob, Lee, James J., Liu, Jimmy Z., de Vlaming, Ronald, Ahluwalia, Tarunveer S., Buchwald, Jadwiga, Cavadino, Alana, Frazier-Wood, Alexis C., Furlotte, Nicholas A., Garfield, Victoria, Geisel, Marie Henrike, Gonzalez, Juan R., Haitjema, Saskia, Karlsson, Robert, van der Laan, Sander W., Ladwig, Karl-Heinz, Lahti, Jari, van der Lee, Sven J., Lind, Penelope A. ... Cesarini, David (2016). Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (vol 48, pg 624, 2016). Nature Genetics, 48 (12), 1591-1591. doi: 10.1038/ng1216-1587b |
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2016 Journal Article Genome-wide analysis identifies 12 loci influencing human reproductive behaviorBarban, Nicola, Jansen, Rick, de Vlaming, Ronald, Vaez, Ahmad, Mandemakers, Jornt J., Tropf, Felix C., Shen, Xia, Wilson, James F., Chasman, Daniel I., Nolte, Illa M., Tragante, Vinicius, van der Laan, Sander W., Perry, John R. B., Kong, Augustine, Ahluwalia, Tarunveer S., Albrecht, Eva, Yerges-Armstrong, Laura, Atzmon, Gil, Auro, Kirsi, Ayers, Kristin, Bakshi, Andrew, Ben-Avraham, Danny, Berger, Klaus, Bergman, Aviv, Bertram, Lars, Bielak, Lawrence F., Bjornsdottir, Gyda, Bonder, Marc Jan, Broer, Linda ... Mills, Melinda C. (2016). Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nature Genetics, 48 (12), 1462-1472. doi: 10.1038/ng.3698 |
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2016 Journal Article Genome-Wide Meta-Analysis of Sciatica in Finnish PopulationLemmela, Susanna, Solovieva, Svetlana, Shiri, Rahman, Benner, Christian, Heliovaara, Markku, Kettunen, Johannes, Anttila, Verneri, Ripatti, Samuli, Perola, Markus, Seppala, Ilkka, Juonala, Markus, Kahonen, Mika, Salomaa, Veikko, Viikari, Jorma, Raitakari, Olli T., Lehtimaki, Terho, Palotie, Aarno, Viikari-Juntura, Eira and Husgafvel-Pursiainen, Kirsti (2016). Genome-Wide Meta-Analysis of Sciatica in Finnish Population. Plos One, 11 (10) e0163877. doi: 10.1371/journal.pone.0163877 |
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2016 Journal Article Genome-wide associations for birth weight and correlations with adult diseaseHorikoshi, Momoko, Beaumont, Robin N., Day, Felix R., Warrington, Nicole M., Kooijman, Marjolein N., Fernandez-Tajes, Juan, Feenstra, Bjarke, van Zuydam, Natalie R., Gaulton, Kyle J., Grarup, Niels, Bradfield, Jonathan P., Strachan, David P., Li-Gao, Ruifang, Ahluwalia, Tarunveer S., Kreiner, Eskil, Rueedi, Rico, Lyytikainen, Leo-Pekka, Cousminer, Diana L., Wu, Ying, Thiering, Elisabeth, Wang, Carol A., Have, Christian T., Hottenga, Jouke-Jan, Vilor-Tejedor, Natalia, Joshi, Peter K., Boh, Eileen Tai Hui, Ntalla, Ioanna, Pitkanen, Niina, Mahajan, Anubha ... Freathy, Rachel M. (2016). Genome-wide associations for birth weight and correlations with adult disease. Nature, 538 (7624), 248-252. doi: 10.1038/nature19806 |
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2016 Journal Article No association of coronary artery disease with X-chromosomal variants in comprehensive international meta-analysisLoley, Christina, Alver, Maris, Assimes, Themistocles L., Bjonnes, Andrew, Goel, Anuj, Gustafsson, Stefan, Hernesniemi, Jussi, Hopewell, Jemma C., Kanoni, Stavroula, Kleber, Marcus E., Lau, King Wai, Lu, Yingchang, Lyytikainen, Leo-Pekka, Nelson, Christopher P., Nikpay, Majid, Qu, Liming, Salfati, Elias, Scholz, Markus, Tukiainen, Taru, Willenborg, Christina, Won, Hong-Hee, Zeng, Lingyao, Zhang, Weihua, Anand, Sonia S., Beutner, Frank, Bottinger, Erwin P., Clarke, Robert, Dedoussis, George, Do, Ron ... Koenig, Inke R. (2016). No association of coronary artery disease with X-chromosomal variants in comprehensive international meta-analysis. Scientific Reports, 6 35278. doi: 10.1038/srep35278 |
