Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study von van Hecke, Oliver, Hocking, Lynne J, Torrance, Nicola, Campbell, Archie, Padmanabhan, Sandosh, Porteous, David J, McIntosh, Andrew M, Burri, Andrea V, Tanaka, Haruka, Williams, Frances M K, Smith, Blair H

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Autophagy: A new player in skeletal maintenance? von Hocking, Lynne J, Whitehouse, Caroline, Helfrich, Miep H

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Bone remodelling at a glance von Crockett, Julie C, Rogers, Michael J, Coxon, Fraser P, Hocking, Lynne J, Helfrich, Miep H

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Predicting the risk of rheumatoid arthritis and its age of onset through modelling genetic risk variants with smoking von Scott, Ian C, Seegobin, Seth D, Steer, Sophia, Tan, Rachael, Forabosco, Paola, Hinks, Anne, Eyre, Stephen, Morgan, Ann W, Wilson, Anthony G, Hocking, Lynne J, Wordsworth, Paul, Barton, Anne, Worthington, Jane, Cope, Andrew P, Lewis, Cathryn M

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Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness von SMITH, Blair H, CAMPBELL, Archie, HOCKING, Lynne J, WISELY, Lucy, FORD, Ian, LINDSAY, Robert S, MORTON, Robin, PALMER, Colin N. A, DOMINICZAK, Anna F, PORTEOUS, David J, MORRIS, Andrew D, LINKSTED, Pamela, FITZPATRICK, Bridie, JACKSON, Cathy, KERR, Shona M, DEARY, Ian J, MACLNTYRE, Donald J, CAMPBELL, Harry, MCGILCHRIST, Mark

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

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Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease von Johnson, Michael R, Shkura, Kirill, Langley, Sarah R, Delahaye-Duriez, Andree, Srivastava, Prashant, Hill, W David, Rackham, Owen J L, Davies, Gail, Harris, Sarah E, Moreno-Moral, Aida, Rotival, Maxime, Speed, Doug, Petrovski, Slavé, Katz, Anaïs, Hayward, Caroline, Porteous, David J, Smith, Blair H, Padmanabhan, Sandosh, Hocking, Lynne J, Starr, John M, Liewald, David C, Visconti, Alessia, Falchi, Mario, Bottolo, Leonardo, Rossetti, Tiziana, Danis, Bénédicte, Mazzuferi, Manuela, Foerch, Patrik, Grote, Alexander, Helmstaedter, Christoph, Becker, Albert J, Kaminski, Rafal M, Deary, Ian J, Petretto, Enrico

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

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Cardiovascular risk factors associated with the metabolic syndrome are more prevalent in people reporting chronic pain: Results from a cross-sectional general population study von Goodson, Nicola J., Smith, Blair H., Hocking, Lynne J., McGilchrist, Mark M., Dominiczak, Anna F., Morris, Andrew, Porteous, David J., Goebel, Andreas

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Molecular genetic contributions to socioeconomic status and intelligence von Marioni, Riccardo E., Davies, Gail, Hayward, Caroline, Liewald, Dave, Kerr, Shona M., Campbell, Archie, Luciano, Michelle, Smith, Blair H., Padmanabhan, Sandosh, Hocking, Lynne J., Hastie, Nicholas D., Wright, Alan F., Porteous, David J., Visscher, Peter M., Deary, Ian J.

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Novel Rheumatoid Arthritis Susceptibility Locus at 22q12 Identified in an Extended UK Genome‐Wide Association Study von Orozco, Gisela, Viatte, Sebastien, Bowes, John, Martin, Paul, Wilson, Anthony G., Morgan, Ann W., Steer, Sophia, Wordsworth, Paul, Hocking, Lynne J., Barton, Anne, Worthington, Jane, Eyre, Stephen

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

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Brief Report: Identification of BACH2 and RAD51B as Rheumatoid Arthritis Susceptibility Loci in a Meta‐Analysis of Genome‐Wide Data von McAllister, Kate, Yarwood, Annie, Bowes, John, Orozco, Gisela, Viatte, Sebastian, Diogo, Dorothée, Hocking, Lynne J., Steer, Sophia, Wordsworth, Paul, Wilson, A. G., Morgan, Ann W., Kremer, Joel M., Pappas, Dimitrios, Gregersen, Peter, Klareskog, Lars, Plenge, Robert, Barton, Anne, Greenberg, Jeffrey, Worthington, Jane, Eyre, Stephen

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Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing von Hocking, Lynne J, Andrews, Claire, Armstrong, Christine, Ansari, Morad, Baty, David, Berg, Jonathan, Bradley, Therese, Clark, Caroline, Diamond, Austin, Doherty, Jill, Lampe, Anne, McGowan, Ruth, Moore, David J, O'Sullivan, Dawn, Purvis, Andrew, Santoyo-Lopez, Javier, Westwood, Paul, Abbott, Michael, Williams, Nicola, Aitman, Timothy J, Miedzybrodzka, Zosia

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Overlapping genetic susceptibility variants between three autoimmune disorders: rheumatoid arthritis, type 1 diabetes and coeliac disease von Eyre, Stephen, Hinks, Anne, Bowes, John, Flynn, Edward, Martin, Paul, Wilson, Anthony G, Morgan, Ann W, Emery, Paul, Steer, Sophia, Hocking, Lynne J, Reid, David M, Harrison, Pille, Wordsworth, Paul, Thomson, Wendy, Worthington, Jane, Barton, Anne

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Study of the common genetic background for rheumatoid arthritis and systemic lupus erythematosus von Orozco, Gisela, Eyre, Steve, Hinks, Anne, Bowes, John, Morgan, Ann W, Wilson, Anthony G, Wordsworth, Paul, Steer, Sophia, Hocking, Lynne, Thomson, Wendy, Worthington, Jane, Barton, Anne

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MICL controls inflammation in rheumatoid arthritis von Redelinghuys, Pierre, Whitehead, Lauren, Augello, Andrea, Drummond, Rebecca A, Levesque, Jean-Michel, Vautier, Simon, Reid, Delyth M, Kerscher, Bernhard, Taylor, Julie A, Nigrovic, Peter A, Wright, John, Murray, Graeme I, Willment, Janet A, Hocking, Lynne J, Fernandes, Maria J G, De Bari, Cosimo, Mcinnes, Iain B, Brown, Gordon D

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A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder von Zeng, Yanni, Navarro, Pau, Fernandez-Pujals, Ana M, Hall, Lynsey S, Clarke, Toni-Kim, Thomson, Pippa A, Smith, Blair H, Hocking, Lynne J, Padmanabhan, Sandosh, Hayward, Caroline, MacIntyre, Donald J, Wray, Naomi R, Deary, Ian J, Porteous, David J, Haley, Chris S, McIntosh, Andrew M

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Genetic variation in the beta2-adrenergic receptor but not catecholamine- O-methyltransferase predisposes to chronic pain: Results from the 1958 British Birth Cohort Study von Hocking, Lynne J., Smith, Blair H., Jones, Gareth T., Reid, David M., Strachan, David P., Macfarlane, Gary J.

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Quantifying the extent to which index event biases influence large genetic association studies von Yaghootkar, Hanieh, Bancks, Michael P, Jones, Sam E, McDaid, Aaron, Beaumont, Robin, Donnelly, Louise, Wood, Andrew R, Campbell, Archie, Tyrrell, Jessica, Hocking, Lynne J, Tuke, Marcus A, Ruth, Katherine S, Pearson, Ewan R, Murray, Anna, Freathy, Rachel M, Munroe, Patricia B, Hayward, Caroline, Palmer, Colin, Weedon, Michael N, Pankow, James S, Frayling, Timothy M, Kutalik, Zoltán

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