Call for Papers: “Morphology is the link between genetics and function”: a tribute to Ewald R. Weibel

od Mühlfeld, Christian, Hsia, Connie C. W., Leikauf, George D., Orgeig, Sandra, Wain, Louise V., Ochs, Matthias
izdano v Am J Physiol Lung Cell Mol Physiol (2021)

Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls

od Artigas, María Soler, Wain, Louise V., Shrine, Nick, McKeever, Tricia M., Sayers, Ian, Hall, Ian P., Tobin, Martin D.
izdano v PLoS One (2017)

Shared genetic etiology between idiopathic pulmonary fibrosis and COVID-19 severity

od Fadista, João, Kraven, Luke M., Karjalainen, Juha, Andrews, Shea J., Geller, Frank, Baillie, J Kenneth, Wain, Louise V., Jenkins, R.Gisli, Feenstra, Bjarke
izdano v EBioMedicine (2021)

The Role of Copy Number Variation in Susceptibility to Amyotrophic Lateral Sclerosis: Genome-Wide Association Study and Comparison with Published Loci

od 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
Izdano 2009

Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function

od 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.
izdano v Wellcome Open Res (2018)

Adjustment for index event bias in genome-wide association studies of subsequent events

od 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.
izdano v Nat Commun (2019)

Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study

od 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
Izdano 2013

The vitamin D binding protein axis modifies disease severity in lymphangioleiomyomatosis

od 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.
izdano v Eur Respir J (2018)

Proportion of Idiopathic Pulmonary Fibrosis Risk Explained by Known Common Genetic Loci in European Populations

od 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.
izdano v Am J Respir Crit Care Med (2021)

Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment

od 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
izdano v Genome Med (2021)

Novel idiopathic pulmonary fibrosis susceptibility variants revealed by deep sequencing

od 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
izdano v ERJ Open Res (2019)

Adaptation of HIV-1 to Its Human Host

od 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.
Izdano 2007

Genome-Wide Gene-by-Smoking Interaction Study of Chronic Obstructive Pulmonary Disease

od 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
izdano v Am J Epidemiol (2020)

Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)

od 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.
Izdano 2014

Copy Number Variation of the Beta-Defensin Genes in Europeans: No Supporting Evidence for Association with Lung Function, Chronic Obstructive Pulmonary Disease or Asthma

od Wain, Louise V., Odenthal-Hesse, Linda, Abujaber, Razan, Sayers, Ian, Beardsmore, Caroline, Gaillard, Erol A., Chappell, Sally, Dogaru, Cristian M., McKeever, Tricia, Guetta-Baranes, Tamar, Kalsheker, Noor, Kuehni, Claudia E., Hall, Ian P., Tobin, Martin D., Hollox, Edward J.
Izdano 2014

Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank

od Fawcett, Katherine A., Song, Kijoung, Qian, Guoqing, Farmaki, Aliki-Eleni, Packer, Richard, John, Catherine, Shrine, Nick, Granell, Raquel, Ring, Sue, Timpson, Nicholas J., Yerges-Armstrong, Laura M., Eastell, Richard, Wain, Louise V., Scott, Robert A., Tobin, Martin D., Hall, Ian P.
izdano v ERJ Open Res (2021)

Age at menarche and lung function: a Mendelian randomization study

od Gill, Dipender, Sheehan, Nuala A., Wielscher, Matthias, Shrine, Nick, Amaral, Andre F. S., Thompson, John R., Granell, Raquel, Leynaert, Bénédicte, Real, Francisco Gómez, Hall, Ian P., Tobin, Martin D., Auvinen, Juha, Ring, Susan M., Jarvelin, Marjo-Riitta, Wain, Louise V., Henderson, John, Jarvis, Deborah, Minelli, Cosetta
izdano v Eur J Epidemiol (2017)

Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia

od Ware, James S., Wain, Louise V., Channavajjhala, Sarath K., Jackson, Victoria E., Edwards, Elizabeth, Lu, Run, Siew, Keith, Jia, Wenjing, Shrine, Nick, Kinnear, Sue, Jalland, Mahli, Henry, Amanda P., Clayton, Jenny, O’Shaughnessy, Kevin M., Tobin, Martin D., Schuster, Victor L., Cook, Stuart, Hall, Ian P., Glover, Mark
izdano v J Clin Invest (2017)

Defining genetic risk factors for scleroderma-associated interstitial lung disease: IRF5 and STAT4 gene variants are associated with scleroderma while STAT4 is protective against s...

od Stock, Carmel J. W., De Lauretis, Angelo, Visca, Dina, Daccord, Cecile, Kokosi, Maria, Kouranos, Vasilis, Margaritopoulos, George, George, Peter M., Molyneaux, Philip L., Nihtyanova, Svetlana, Chua, Felix, Maher, Toby M., Ong, Voon, Abraham, David J., Denton, Christopher P., Wells, Athol U., Wain, Louise V., Renzoni, Elisabetta A.
izdano v Clin Rheumatol (2020)

Chimpanzee Reservoirs of Pandemic and Nonpandemic HIV-1

od Keele, Brandon F., Van Heuverswyn, Fran, Li, Yingying, Bailes, Elizabeth, Takehisa, Jun, Santiago, Mario L., Bibollet-Ruche, Frederic, Chen, Yalu, Wain, Louise V., Liegeois, Florian, Loul, Severin, Ngole, Eitel Mpoudi, Bienvenue, Yanga, Delaporte, Eric, Brookfield, John F. Y., Sharp, Paul M., Shaw, George M., Peeters, Martine, Hahn, Beatrice H.
Izdano 2006