Investigating DNA methylation as a potential mediator between pigmentation genes, pigmentary traits and skin cancer

por Bonilla, Carolina, Bertoni, Bernardo, Min, Josine L., Hemani, Gibran, Elliott, Hannah R.
Publicado 2020

Triangulating Molecular Evidence to Prioritize Candidate Causal Genes at Established Atopic Dermatitis Loci

por Sobczyk, Maria K., Richardson, Tom G., Zuber, Verena, Min, Josine L., Gaunt, Tom R., Paternoster, Lavinia
Publicado 2021

The Effect of Pre-Analytical Conditions on Blood Metabolomics in Epidemiological Studies

por Santos Ferreira, Diana L., Maple, Hannah J., Goodwin, Matt, Brand, Judith S., Yip, Vikki, Min, Josine L., Groom, Alix, Lawlor, Debbie A., Ring, Susan
Publicado 2019

An interactive genome browser of association results from the UK10K cohorts project

por Geihs, Matthias, Yan, Ying, Walter, Klaudia, Huang, Jie, Memari, Yasin, Min, Josine L., Mead, Daniel, Hubbard, Tim J., Timpson, Nicholas J., Down, Thomas A., Soranzo, Nicole
Publicado 2015

Variability of gene expression profiles in human blood and lymphoblastoid cell lines

por Min, Josine L, Barrett, Amy, Watts, Tim, Pettersson, Fredrik H, Lockstone, Helen E, Lindgren, Cecilia M, Taylor, Jennifer M, Allen, Maxine, Zondervan, Krina T, McCarthy, Mark I
Publicado 2010

Characterisation of ethnic differences in DNA methylation between UK-resident South Asians and Europeans

por Elliott, Hannah R., Burrows, Kimberley, Min, Josine L., Tillin, Therese, Mason, Dan, Wright, John, Santorelli, Gillian, Davey Smith, George, Lawlor, Deborah A., Hughes, Alun D., Chaturvedi, Nishi, Relton, Caroline L.
Publicado 2022

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

por 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
Publicado 2015

Systematic identification of genetic influences on methylation across the human life course

por 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.
Publicado 2016

MicroRNA Expression in Abdominal and Gluteal Adipose Tissue Is Associated with mRNA Expression Levels and Partly Genetically Driven

por 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.
Publicado 2011

DNA methylome-wide association study of genetic risk for depression implicates antigen processing and immune responses

por 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.
Publicado 2022

The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits

por 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.
Publicado 2011

Complex trait methylation scores in the prediction of major depressive disorder

por 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.
Publicado 2022

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...

por 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.
Publicado 2021

Assessing the role of genome-wide DNA methylation between smoking and risk of lung cancer using repeated measurements: the HUNT study

por 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
Publicado 2021

Genome-wide association meta-analysis identifies 29 new acne susceptibility loci

por 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.
Publicado 2022

Coexpression Network Analysis in Abdominal and Gluteal Adipose Tissue Reveals Regulatory Genetic Loci for Metabolic Syndrome and Related Phenotypes

por 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.
Publicado 2012

Epigenetic Regulation of F2RL3 Associates With Myocardial Infarction and Platelet Function

por 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.
Publicado 2022

A Genome-Wide Metabolic QTL Analysis in Europeans Implicates Two Loci Shaped by Recent Positive Selection

por 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.
Publicado 2011

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

por 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
Publicado 2014

Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

por 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
Publicado 2015