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

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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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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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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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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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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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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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Common Genetic Variants Explain the Majority of the Correlation Between Height and Intelligence: The Generation Scotland Study von Marioni, Riccardo E., Batty, G. David, Hayward, Caroline, Kerr, Shona M., Campbell, Archie, Hocking, Lynne J., Porteous, David J., Visscher, Peter M., Deary, Ian J.

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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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Functional interaction between Sequestosome-1/p62 and Autophagy-Linked FYVE-containing protein WDFY3 in human osteoclasts von Hocking, Lynne J., Mellis, David J., McCabe, Paul S., Helfrich, Miep H., Rogers, Michael J.

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The functional ACTN3 577X variant increases the risk of falling in older females: results from two large independent cohort studies von Judson, Robert N, Wackerhage, Henning, Hughes, Alun, Mavroeidi, Alexandra, Barr, Rebecca J, Macdonald, Helen M, Ratkevicius, Aivaras, Reid, David M, Hocking, Lynne J

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Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism von Clarke, Toni-Kim, Zeng, Yanni, Navrady, Lauren, Xia, Charley, Haley, Chris, Campbell, Archie, Navarro, Pau, Amador, Carmen, Adams, Mark J., Howard, David M., Soler, Aleix, Hayward, Caroline, Thomson, Pippa A., Smith, Blair H., Padmanabhan, Sandosh, Hocking, Lynne J., Hall, Lynsey S., Porteous, David J., Deary, Ian J., McIntosh, Andrew 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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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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Identification of a Major Locus for Paget's Disease on Chromosome 10p13 in Families of British Descent von Lucas, Gavin JA, Riches, Phillip L, Hocking, Lynne J, Cundy, Tim, Nicholson, Geoff C, Walsh, John P, Ralston, Stuart H

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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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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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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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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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