检索结果 - Min, Josine
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GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals 由 Iotchkova, Valentina, Ritchie, Graham R.S., Geihs, Matthias, Morganella, Sandro, Min, Josine L., Walter, Klaudia, Timpson, Nicholas John, Dunham, Ian, Birney, Ewan, Soranzo, Nicole
出版 2019Text -
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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel 由 Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L., Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Gambaro, Giovanni, Richards, J. Brent, Durbin, Richard, Timpson, Nicholas J., Marchini, Jonathan, Soranzo, Nicole
出版 2015Text -
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Systematic identification of genetic influences on methylation across the human life course 由 Gaunt, Tom R., Shihab, Hashem A., Hemani, Gibran, Min, Josine L., Woodward, Geoff, Lyttleton, Oliver, Zheng, Jie, Duggirala, Aparna, McArdle, Wendy L., Ho, Karen, Ring, Susan M., Evans, David M., Davey Smith, George, Relton, Caroline L.
出版 2016Text -
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MicroRNA Expression in Abdominal and Gluteal Adipose Tissue Is Associated with mRNA Expression Levels and Partly Genetically Driven 由 Rantalainen, Mattias, Herrera, Blanca M., Nicholson, George, Bowden, Rory, Wills, Quin F., Min, Josine L., Neville, Matt J., Barrett, Amy, Allen, Maxine, Rayner, Nigel W., Fleckner, Jan, McCarthy, Mark I., Zondervan, Krina T., Karpe, Fredrik, Holmes, Chris C., Lindgren, Cecilia M.
出版 2011Text -
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DNA methylome-wide association study of genetic risk for depression implicates antigen processing and immune responses 由 Shen, Xueyi, Caramaschi, Doretta, Adams, Mark J., Walker, Rosie M., Min, Josine L., Kwong, Alex, Hemani, Gibran, Barbu, Miruna C., Whalley, Heather C., Harris, Sarah E., Deary, Ian J., Morris, Stewart W., Cox, Simon R., Relton, Caroline L., Marioni, Riccardo E., Evans, Kathryn L., McIntosh, Andrew M.
出版 2022Text -
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The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits 由 Min, Josine L., Taylor, Jennifer M., Richards, J. Brent, Watts, Tim, Pettersson, Fredrik H., Broxholme, John, Ahmadi, Kourosh R., Surdulescu, Gabriela L., Lowy, Ernesto, Gieger, Christian, Newton-Cheh, Chris, Perola, Markus, Soranzo, Nicole, Surakka, Ida, Lindgren, Cecilia M., Ragoussis, Jiannis, Morris, Andrew P., Cardon, Lon R., Spector, Tim D., Zondervan, Krina T.
出版 2011Text -
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Complex trait methylation scores in the prediction of major depressive disorder 由 Barbu, Miruna C., Amador, Carmen, Kwong, Alex S.F., Shen, Xueyi, Adams, Mark J., Howard, David M., Walker, Rosie M., Morris, Stewart W., Min, Josine L., Liu, Chunyu, van Dongen, Jenny, Ghanbari, Mohsen, Relton, Caroline, Porteous, David J., Campbell, Archie, Evans, Kathryn L., Whalley, Heather C., McIntosh, Andrew M.
出版 2022Text -
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Opportunities and Challenges in Functional Genomics Research in Osteoporosis: Report From a Workshop Held by the Causes Working Group of the Osteoporosis and Bone Research Academy... 由 Tobias, Jonathan H., Duncan, Emma L., Kague, Erika, Hammond, Chrissy L., Gregson, Celia L., Bassett, Duncan, Williams, Graham R., Min, Josine L., Gaunt, Tom R., Karasik, David, Ohlsson, Claes, Rivadeneira, Fernando, Edwards, James R., Hannan, Fadil M., Kemp, John P., Gilbert, Sophie J., Alonso, Nerea, Hassan, Neelam, Compston, Juliet E., Ralston, Stuart H.
出版 2021Text -
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Assessing the role of genome-wide DNA methylation between smoking and risk of lung cancer using repeated measurements: the HUNT study 由 Sun, Yi-Qian, Richmond, Rebecca C, Suderman, Matthew, Min, Josine L, Battram, Thomas, Flatberg, Arnar, Beisvag, Vidar, Nøst, Therese Haugdahl, Guida, Florence, Jiang, Lin, Wahl, Sissel Gyrid Freim, Langhammer, Arnulf, Skorpen, Frank, Walker, Rosie M, Bretherick, Andrew D, Zeng, Yanni, Chen, Yue, Johansson, Mattias, Sandanger, Torkjel M, Relton, Caroline L, Mai, Xiao-Mei
出版 2021Text -
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Genome-wide association meta-analysis identifies 29 new acne susceptibility loci 由 Mitchell, Brittany L., Saklatvala, Jake R., Dand, Nick, Hagenbeek, Fiona A., Li, Xin, Min, Josine L., Thomas, Laurent, Bartels, Meike, Jan Hottenga, Jouke, Lupton, Michelle K., Boomsma, Dorret I., Dong, Xianjun, Hveem, Kristian, Løset, Mari, Martin, Nicholas G., Barker, Jonathan N., Han, Jiali, Smith, Catherine H., Rentería, Miguel E., Simpson, Michael A.
出版 2022Text -
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Coexpression Network Analysis in Abdominal and Gluteal Adipose Tissue Reveals Regulatory Genetic Loci for Metabolic Syndrome and Related Phenotypes 由 Min, Josine L., Nicholson, George, Halgrimsdottir, Ingileif, Almstrup, Kristian, Petri, Andreas, Barrett, Amy, Travers, Mary, Rayner, Nigel W., Mägi, Reedik, Pettersson, Fredrik H., Broxholme, John, Neville, Matt J., Wills, Quin F., Cheeseman, Jane, Allen, Maxine, Holmes, Chris C., Spector, Tim D., Fleckner, Jan, McCarthy, Mark I., Karpe, Fredrik, Lindgren, Cecilia M., Zondervan, Krina T.
出版 2012Text -
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Epigenetic Regulation of F2RL3 Associates With Myocardial Infarction and Platelet Function 由 Corbin, Laura J., White, Stephen J., Taylor, Amy E., Williams, Christopher M., Taylor, Kurt, van den Bosch, Marion T., Teasdale, Jack E., Jones, Matthew, Bond, Mark, Harper, Matthew T., Falk, Louise, Groom, Alix, Hazell, Georgina G.J., Paternoster, Lavinia, Munafò, Marcus R., Nordestgaard, Børge G., Tybjærg-Hansen, Anne, Bojesen, Stig E., Relton, Caroline, Min, Josine L., Davey Smith, George, Mumford, Andrew D., Poole, Alastair W., Timpson, Nicholas J.
出版 2022Text -
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A Genome-Wide Metabolic QTL Analysis in Europeans Implicates Two Loci Shaped by Recent Positive Selection 由 Nicholson, George, Rantalainen, Mattias, Li, Jia V., Maher, Anthony D., Malmodin, Daniel, Ahmadi, Kourosh R., Faber, Johan H., Barrett, Amy, Min, Josine L., Rayner, N. William, Toft, Henrik, Krestyaninova, Maria, Viksna, Juris, Neogi, Sudeshna Guha, Dumas, Marc-Emmanuel, Sarkans, Ugis, Donnelly, Peter, Illig, Thomas, Adamski, Jerzy, Suhre, Karsten, Allen, Maxine, Zondervan, Krina T., Spector, Tim D., Nicholson, Jeremy K., Lindon, John C., Baunsgaard, Dorrit, Holmes, Elaine, McCarthy, Mark I., Holmes, Chris C.
出版 2011Text -
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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans 由 Timpson, Nicholas J., Walter, Klaudia, Min, Josine L., Tachmazidou, Ioanna, Malerba, Giovanni, Shin, So-Youn, Chen, Lu, Futema, Marta, Southam, Lorraine, Iotchkova, Valentina, Cocca, Massimiliano, Huang, Jie, Memari, Yasin, McCarthy, Shane, Danecek, Petr, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Perry, John R. B., Ring, Susan M., Gaye, Amadou, Dedoussis, George, Farmaki, Aliki-Eleni, Burton, Paul, Talmud, Philippa J., Gambaro, Giovanni, Spector, Tim D., Smith, George Davey, Durbin, Richard, Richards, J Brent, Humphries, Steve E., Zeggini, Eleftheria, Soranzo, Nicole
出版 2014Text -
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Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans 由 Timpson, Nicholas J., Walter, Klaudia, Min, Josine L., Tachmazidou, Ioanna, Malerba, Giovanni, Shin, So-Youn, Chen, Lu, Futema, Marta, Southam, Lorraine, Iotchkova, Valentina, Cocca, Massimiliano, Huang, Jie, Memari, Yasin, McCarthy, Shane, Danecek, Petr, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Perry, John R. B., Ring, Susan M., Gaye, Amadou, Dedoussis, George, Farmaki, Aliki-Eleni, Burton, Paul, Talmud, Philippa J., Gambaro, Giovanni, Spector, Tim D., Smith, George Davey, Durbin, Richard, Richards, J. Brent, Humphries, Steve E., Zeggini, Eleftheria, Soranzo, Nicole
出版 2015Text