Search Results - Wain, Louise V.

Call for Papers: “Morphology is the link between genetics and function”: a tribute to Ewald R. Weibel by Mühlfeld, Christian, Hsia, Connie C. W., Leikauf, George D., Orgeig, Sandra, Wain, Louise V., Ochs, Matthias

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Genome-wide gene-air pollution interaction analysis of lung function in 300,000 individuals by Melbourne, Carl A., Mesut Erzurumluoglu, A., Shrine, Nick, Chen, Jing, Tobin, Martin D., Hansell, Anna L., Wain, Louise V.

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Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls by Artigas, María Soler, Wain, Louise V., Shrine, Nick, McKeever, Tricia M., Sayers, Ian, Hall, Ian P., Tobin, Martin D.

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Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank by Fawcett, Katherine A., Demidov, German, Shrine, Nick, Paynton, Megan L., Ossowski, Stephan, Sayers, Ian, Wain, Louise V., Hollox, Edward J.

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Genetic overlap between idiopathic pulmonary fibrosis and COVID−19 by Allen, Richard J, Guillen-Guio, Beatriz, Croot, Emma, Kraven, Luke M, Moss, Samuel, Stewart, Iain, Jenkins, R Gisli, Wain, Louise V

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Shared genetic etiology between idiopathic pulmonary fibrosis and COVID-19 severity by Fadista, João, Kraven, Luke M., Karjalainen, Juha, Andrews, Shea J., Geller, Frank, Baillie, J Kenneth, Wain, Louise V., Jenkins, R.Gisli, Feenstra, Bjarke

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The Role of Copy Number Variation in Susceptibility to Amyotrophic Lateral Sclerosis: Genome-Wide Association Study and Comparison with Published Loci by Wain, Louise V., Pedroso, Inti, Landers, John E., Breen, Gerome, Shaw, Christopher E., Leigh, P. Nigel, Brown, Robert H., Tobin, Martin D., Al-Chalabi, Ammar

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Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function by Adewoye, Adeolu B., Shrine, Nick, Odenthal-Hesse, Linda, Welsh, Samantha, Malarstig, Anders, Jelinsky, Scott, Kilty, Iain, Tobin, Martin D., Hollox, Edward J., Wain, Louise V.

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Adjustment for index event bias in genome-wide association studies of subsequent events by Dudbridge, Frank, Allen, Richard J., Sheehan, Nuala A., Schmidt, A. Floriaan, Lee, James C., Jenkins, R. Gisli, Wain, Louise V., Hingorani, Aroon D., Patel, Riyaz S.

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Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study by Kerr, Shona M, Campbell, Archie, Murphy, Lee, Hayward, Caroline, Jackson, Cathy, Wain, Louise V, Tobin, Martin D, Dominiczak, Anna, Morris, Andrew, Smith, Blair H, Porteous, David J

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The vitamin D binding protein axis modifies disease severity in lymphangioleiomyomatosis by Miller, Suzanne, Coveney, Clare, Johnson, Janice, Farmaki, Aliki-Eleni, Gupta, Nishant, Tobin, Martin D., Wain, Louise V., McCormack, Francis X., Boocock, David J., Johnson, Simon R.

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Proportion of Idiopathic Pulmonary Fibrosis Risk Explained by Known Common Genetic Loci in European Populations by Leavy, Olivia C., Ma, Shwu-Fan, Molyneaux, Philip L., Maher, Toby M., Oldham, Justin M., Flores, Carlos, Noth, Imre, Jenkins, R. Gisli, Dudbridge, Frank, Wain, Louise V., Allen, Richard J.

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Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment by Wielscher, Matthias, Amaral, Andre F. S., van der Plaat, Diana, Wain, Louise V., Sebert, Sylvain, Mosen-Ansorena, David, Auvinen, Juha, Herzig, Karl-Heinz, Dehghan, Abbas, Jarvis, Debbie L., Jarvelin, Marjo-Riitta

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Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis by Allen, Richard J, Stockwell, Amy, Oldham, Justin M, Guillen-Guio, Beatriz, Schwartz, David A, Maher, Toby M, Flores, Carlos, Noth, Imre, Yaspan, Brian L, Jenkins, R Gisli, Wain, Louise V

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Novel idiopathic pulmonary fibrosis susceptibility variants revealed by deep sequencing by Lorenzo-Salazar, Jose M., Ma, Shwu-Fan, Jou, Jonathan, Hou, Pei-Chi, Guillen-Guio, Beatriz, Allen, Richard J., Jenkins, R. Gisli, Wain, Louise V., Oldham, Justin M., Noth, Imre, Flores, Carlos

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Genetic and clinical characteristics of treatment-resistant depression using primary care records in two UK cohorts by Fabbri, Chiara, Hagenaars, Saskia P., John, Catherine, Williams, Alexander T., Shrine, Nick, Moles, Louise, Hanscombe, Ken B., Serretti, Alessandro, Shepherd, David J., Free, Robert C., Wain, Louise V., Tobin, Martin D., Lewis, Cathryn M.

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Adaptation of HIV-1 to Its Human Host by Wain, Louise V., Bailes, Elizabeth, Bibollet-Ruche, Frederic, Decker, Julie M., Keele, Brandon F., Van Heuverswyn, Fran, Li, Yingying, Takehisa, Jun, Ngole, Eitel Mpoudi, Shaw, George M., Peeters, Martine, Hahn, Beatrice H., Sharp, Paul M.

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Genome-Wide Gene-by-Smoking Interaction Study of Chronic Obstructive Pulmonary Disease by Kim, Woori, Prokopenko, Dmitry, Sakornsakolpat, Phuwanat, Hobbs, Brian D, Lutz, Sharon M, Hokanson, John E, Wain, Louise V, Melbourne, Carl A, Shrine, Nick, Tobin, Martin D, Silverman, Edwin K, Cho, Michael H, Beaty, Terri H

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Interaction of Cigarette Smoking and Polygenic Risk Score on Reduced Lung Function by Kim, Woori, Moll, Matthew, Qiao, Dandi, Hobbs, Brian D., Shrine, Nick, Sakornsakolpat, Phuwanat, Tobin, Martin D., Dudbridge, Frank, Wain, Louise V., Ladd-Acosta, Christine, Chatterjee, Nilanjan, Silverman, Edwin K., Cho, Michael H., Beaty, Terri H.

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Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome) by Glover, Mark, Ware, James S., Henry, Amanda, Wolley, Martin, Walsh, Roddy, Wain, Louise V., Xu, Shengxin, Van’t Hoff, William G., Tobin, Martin D., Hall, Ian P., Cook, Stuart, Gordon, Richard D., Stowasser, Michael, O’Shaughnessy, Kevin M.

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