Real-world evaluation of UK high hyperdiploidy profile using a large cohort of patients provided by HARMONY data platform

por Enshaei, Amir, Martinez Elicegui, Javier, Anguiano, Esther, Gibson, Jude, Lawal, Sulaiman, Ampatzidou, Mirella, Doubek, Michael, Fielding, Adele K., La Sala, Edoardo, Middleton, Elizabeth, Rijneveld, Anita W., Turki, Amin T., Zimmermann, Martin, Vora, Ajay, Moorman, Anthony V.
Publicado 2023

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

por Barbu, Miruna C., Zeng, Yanni, Shen, Xueyi, Cox, Simon R., Clarke, Toni-Kim, Gibson, Jude, Adams, Mark J., Johnstone, Mandy, Haley, Chris S., Lawrie, Stephen M., Deary, Ian J., McIntosh, Andrew M., Whalley, Heather C.
Publicado 2019

Insulin resistance: Genetic associations with depression and cognition in population based cohorts

por Frangou, Sophia, Shirali, Masoud, Adams, Mark J., Howard, David M., Gibson, Jude, Hall, Lynsey S., Smith, Blair H., Padmanabhan, Sandosh, Murray, Alison D., Porteous, David J., Haley, Chris S., Deary, Ian J., Clarke, Toni-Kim, McIntosh, Andrew M.
Publicado 2019

Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease

por McCartney, Daniel L., Stevenson, Anna J., Walker, Rosie M., Gibson, Jude, Morris, Stewart W., Campbell, Archie, Murray, Alison D., Whalley, Heather C., Porteous, David J., McIntosh, Andrew M., Evans, Kathryn L., Deary, Ian J., Marioni, Riccardo E.
Publicado 2018

Genetic and environmental exposures constrain epigenetic drift over the human life course

por Shah, Sonia, McRae, Allan F., Marioni, Riccardo E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Starr, John M., Wray, Naomi R., Deary, Ian J., Visscher, Peter M.
Publicado 2014

The epigenetic clock is correlated with physical and cognitive fitness in the Lothian Birth Cohort 1936

por Marioni, Riccardo E, Shah, Sonia, McRae, Allan F, Ritchie, Stuart J, Muniz-Terrera, Graciela, Harris, Sarah E, Gibson, Jude, Redmond, Paul, Cox, Simon R, Pattie, Alison, Corley, Janie, Taylor, Adele, Murphy, Lee, Starr, John M, Horvath, Steve, Visscher, Peter M, Wray, Naomi R, Deary, Ian J
Publicado 2015

Identification of 55,000 Replicated DNA Methylation QTL

por McRae, Allan F., Marioni, Riccardo E., Shah, Sonia, Yang, Jian, Powell, Joseph E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Bowdler, Lisa, Painter, Jodie N., Murphy, Lee, Martin, Nicholas G., Starr, John M., Wray, Naomi R., Deary, Ian J., Visscher, Peter M., Montgomery, Grant W.
Publicado 2018

Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank

por Hall, Lynsey S., Adams, Mark J., Arnau-Soler, Aleix, Clarke, Toni-Kim, Howard, David M., Zeng, Yanni, Davies, Gail, Hagenaars, Saskia P., Maria Fernandez-Pujals, Ana, Gibson, Jude, Wigmore, Eleanor M., Boutin, Thibaud S., Hayward, Caroline, Scotland, Generation, Porteous, David J., Deary, Ian J., Thomson, Pippa A., Haley, Chris S., McIntosh, Andrew M.
Publicado 2018

A meta-analysis of genome-wide association studies of epigenetic age acceleration

por Gibson, Jude, Russ, Tom C., Clarke, Toni-Kim, Howard, David M., Hillary, Robert F., Evans, Kathryn L., Walker, Rosie M., Bermingham, Mairead L., Morris, Stewart W., Campbell, Archie, Hayward, Caroline, Murray, Alison D., Porteous, David J., Horvath, Steve, Lu, Ake T., McIntosh, Andrew M., Whalley, Heather C., Marioni, Riccardo E.
Publicado 2019

Integrative genomic analysis of childhood acute lymphoblastic leukaemia lacking a genetic biomarker in the UKALL2003 clinical trial

por Schwab, Claire, Cranston, Ruth E., Ryan, Sarra L., Butler, Ellie, Winterman, Emily, Hawking, Zoe, Bashton, Matthew, Enshaei, Amir, Russell, Lisa J., Kingsbury, Zoya, Peden, John F., Barretta, Emilio, Murray, James, Gibson, Jude, Hinchliffe, Andrew C., Bain, Robert, Vora, Ajay, Bentley, David R., Ross, Mark T., Moorman, Anthony V., Harrison, Christine J.
Publicado 2022

Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

por Howard, David M., Adams, Mark J., Shirali, Masoud, Clarke, Toni-Kim, Marioni, Riccardo E., Davies, Gail, Coleman, Jonathan R. I., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Wigmore, Eleanor M., Gibson, Jude, Hagenaars, Saskia P., Lewis, Cathryn M., Ward, Joey, Smith, Daniel J., Sullivan, Patrick F., Haley, Chris S., Breen, Gerome, Deary, Ian J., McIntosh, Andrew M.
Publicado 2018

Addendum: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

por Howard, David M., Adams, Mark J., Shirali, Masoud, Clarke, Toni-Kim, Marioni, Riccardo E., Davies, Gail, Coleman, Jonathan R. I., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Wigmore, Eleanor M., Gibson, Jude, Hagenaars, Saskia P., Lewis, Cathryn M., Ward, Joey, Smith, Daniel J., Sullivan, Patrick F., Haley, Chris S., Breen, Gerome, Deary, Ian J., McIntosh, Andrew M.
Publicado 2018

Author Correction: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

por Howard, David M., Adams, Mark J., Shirali, Masoud, Clarke, Toni-Kim, Marioni, Riccardo E., Davies, Gail, Coleman, Jonathan R. I., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Wigmore, Eleanor M., Gibson, Jude, Hagenaars, Saskia P., Lewis, Cathryn M., Ward, Joey, Smith, Daniel J., Sullivan, Patrick F., Haley, Chris S., Breen, Gerome, Deary, Ian J., McIntosh, Andrew M.
Publicado 2021

Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis

por McIntosh, Andrew M., Hall, Lynsey S., Zeng, Yanni, Adams, Mark J., Gibson, Jude, Wigmore, Eleanor, Hagenaars, Saskia P., Davies, Gail, Fernandez-Pujals, Ana Maria, Campbell, Archie I., Clarke, Toni-Kim, Hayward, Caroline, Haley, Chris S., Porteous, David J., Deary, Ian J., Smith, Daniel J., Nicholl, Barbara I., Hinds, David A., Jones, Amy V., Scollen, Serena, Meng, Weihua, Smith, Blair H., Hocking, Lynne J.
Publicado 2016

Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

por Nagy, Reka, Boutin, Thibaud S., Marten, Jonathan, Huffman, Jennifer E., Kerr, Shona M., Campbell, Archie, Evenden, Louise, Gibson, Jude, Amador, Carmen, Howard, David M., Navarro, Pau, Morris, Andrew, Deary, Ian J., Hocking, Lynne J., Padmanabhan, Sandosh, Smith, Blair H., Joshi, Peter, Wilson, James F., Hastie, Nicholas D., Wright, Alan F., McIntosh, Andrew M., Porteous, David J., Haley, Chris S., Vitart, Veronique, Hayward, Caroline
Publicado 2017

Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP

por Wigmore, Eleanor M., Hafferty, Jonathan D., Hall, Lynsey S., Howard, David M., Clarke, Toni-Kim, Fabbri, Chiara, Lewis, Cathryn M., Uher, Rudolf, Navrady, Lauren B., Adams, Mark J., Zeng, Yanni, Campbell, Archie, Gibson, Jude, Thomson, Pippa A., Hayward, Caroline, Smith, Blair H., Hocking, Lynne J., Padmanabhan, Sandosh, Deary, Ian J., Porteous, David J., Mors, Ole, Mattheisen, Manuel, Nicodemus, Kristin K., McIntosh, Andrew M.
Publicado 2019

DNA methylation age of blood predicts all-cause mortality in later life

por Marioni, Riccardo E, Shah, Sonia, McRae, Allan F, Chen, Brian H, Colicino, Elena, Harris, Sarah E, Gibson, Jude, Henders, Anjali K, Redmond, Paul, Cox, Simon R, Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G, Montgomery, Grant W, Feinberg, Andrew P, Fallin, M Daniele, Multhaup, Michael L, Jaffe, Andrew E, Joehanes, Roby, Schwartz, Joel, Just, Allan C, Lunetta, Kathryn L, Murabito, Joanne M, Starr, John M, Horvath, Steve, Baccarelli, Andrea A, Levy, Daniel, Visscher, Peter M, Wray, Naomi R, Deary, Ian J
Publicado 2015

Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach

por Mendelson, Michael M., Marioni, Riccardo E., Joehanes, Roby, Liu, Chunyu, Hedman, Åsa K., Aslibekyan, Stella, Demerath, Ellen W., Guan, Weihua, Zhi, Degui, Yao, Chen, Huan, Tianxiao, Willinger, Christine, Chen, Brian, Courchesne, Paul, Multhaup, Michael, Irvin, Marguerite R., Cohain, Ariella, Schadt, Eric E., Grove, Megan L., Bressler, Jan, North, Kari, Sundström, Johan, Gustafsson, Stefan, Shah, Sonia, McRae, Allan F., Harris, Sarah E., Gibson, Jude, Redmond, Paul, Corley, Janie, Murphy, Lee, Starr, John M., Kleinbrink, Erica, Lipovich, Leonard, Visscher, Peter M., Wray, Naomi R., Krauss, Ronald M., Fallin, Daniele, Feinberg, Andrew, Absher, Devin M., Fornage, Myriam, Pankow, James S., Lind, Lars, Fox, Caroline, Ingelsson, Erik, Arnett, Donna K., Boerwinkle, Eric, Liang, Liming, Levy, Daniel, Deary, Ian J.
Publicado 2017