Prediction of glycosylation sites using random forests von Hamby, Stephen E, Hirst, Jonathan D

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Comparative analysis of genome sequences covering the seven cronobacter species von Joseph, Susan, Desai, Prerak, Ji, Yongmei, Cummings, Craig A, Shih, Rita, Degoricija, Lovorka, Rico, Alain, Brzoska, Pius, Hamby, Stephen E, Masood, Naqash, Hariri, Sumyya, Sonbol, Hana, Chuzhanova, Nadia, McClelland, Michael, Furtado, Manohar R, Forsythe, Stephen J

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Adult height and risk of 50 diseases: a combined epidemiological and genetic analysis von Lai, Florence Y, Nath, Mintu, Hamby, Stephen E, Thompson, John R, Nelson, Christopher P, Samani, Nilesh J

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Prediction of Causal Candidate Genes in Coronary Artery Disease Loci von Brænne, Ingrid, Civelek, Mete, Vilne, Baiba, Di Narzo, Antonio, Johnson, Andrew D, Zhao, Yuqi, Reiz, Benedikt, Codoni, Veronica, Webb, Thomas R, Foroughi Asl, Hassan, Hamby, Stephen E, Zeng, Lingyao, Trégouët, David-Alexandre, Hao, Ke, Topol, Eric J, Schadt, Eric E, Yang, Xia, Samani, Nilesh J, Björkegren, Johan L M, Erdmann, Jeanette, Schunkert, Heribert, Lusis, Aldons J

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Polygenic basis and biomedical consequences of telomere length variation von Codd, Veryan, Wang, Qingning, Allara, Elias, Musicha, Crispin, Kaptoge, Stephen, Stoma, Svetlana, Jiang, Tao, Hamby, Stephen E., Braund, Peter S., Bountziouka, Vasiliki, Budgeon, Charley A., Denniff, Matthew, Swinfield, Chloe, Papakonstantinou, Manolo, Sheth, Shilpi, Nanus, Dominika E., Warner, Sophie C., Wang, Minxian, Khera, Amit V., Eales, James, Ouwehand, Willem H., Thompson, John R., Di Angelantonio, Emanuele, Wood, Angela M., Butterworth, Adam S., Danesh, John N., Nelson, Christopher P., Samani, Nilesh J.

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Novel loss of function mutation in NOTCH1 in a family with bicuspid aortic valve, ventricular septal defect, thoracic aortic aneurysm, and aortic valve stenosis von Debiec, Radoslaw, Hamby, Stephen E., Jones, Peter D., Coolman, Sue, Asiani, Manish, Kharodia, Shireen, Skinner, Gregory J., Samani, Nilesh J., Webb, Tom R., Bolger, Aidan

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In Silico identification of pathogenic strains of Cronobacter from Biochemical data reveals association of inositol fermentation with pathogenicity von Hamby, Stephen E, Joseph, Susan, Forsythe, Stephen J, Chuzhanova, Nadia

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Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation von Adlam, David, Berrandou, Takiy-Eddine, Georges, Adrien, Nelson, Christopher P., Giannoulatou, Eleni, Henry, Joséphine, Ma, Lijiang, Blencowe, Montgomery, Turley, Tamiel N., Yang, Min-Lee, Chopade, Sandesh, Finan, Chris, Braund, Peter S., Sadeg-Sayoud, Ines, Iismaa, Siiri E., Kosel, Matthew L., Zhou, Xiang, Hamby, Stephen E., Cheng, Jenny, Liu, Lu, Tarr, Ingrid, Muller, David W. M., d’Escamard, Valentina, King, Annette, Brunham, Liam R., Baranowska-Clarke, Ania A., Debette, Stéphanie, Amouyel, Philippe, Olin, Jeffrey W., Patil, Snehal, Hesselson, Stephanie E., Junday, Keerat, Kanoni, Stavroula, Aragam, Krishna G., Butterworth, Adam S., Tweet, Marysia S., Gulati, Rajiv, Combaret, Nicolas, Kadian-Dodov, Daniella, Kalman, Jonathan M., Fatkin, Diane, Hingorani, Aroon D., Saw, Jacqueline, Webb, Tom R., Hayes, Sharonne N., Yang, Xia, Ganesh, Santhi K., Olson, Timothy M., Kovacic, Jason C., Graham, Robert M., Samani, Nilesh J., Bouatia-Naji, Nabila

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Contribution of NOTCH1 genetic variants to bicuspid aortic valve and other congenital lesions von Debiec, Radoslaw Marek, Hamby, Stephen E, Jones, Peter D, Safwan, Kassem, Sosin, Michael, Hetherington, Simon Lee, Sprigings, David, Sharman, David, Lee, Kelvin, Salahshouri, Pegah, Wheeldon, Nigel, Chukwuemeka, Andrew, Boutziouka, Vasiliki, Elamin, Mohamed, Coolman, Sue, Asiani, Manish, Kharodia, Shireen, Skinner, Gregory J, Samani, Nilesh J, Webb, Tom R, Bolger, Aidan P

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A meta-analysis of single base-pair substitutions in translational termination codons ('nonstop' mutations) that cause human inherited disease von Hamby, Stephen E, Thomas, Nick S T, Cooper, David N, Chuzhanova, Nadia

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Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia von Georges, Adrien, Albuisson, Juliette, Berrandou, Takiy, Dupré, Délia, Lorthioir, Aurélien, D’Escamard, Valentina, Di Narzo, Antonio F, Kadian-Dodov, Daniella, Olin, Jeffrey W, Warchol-Celinska, Ewa, Prejbisz, Aleksander, Januszewicz, Andrzej, Bruneval, Patrick, Baranowska, Anna A, Webb, Tom R, Hamby, Stephen E, Samani, Nilesh J, Adlam, David, Fendrikova-Mahlay, Natalia, Hazen, Stanley, Wang, Yu, Yang, Min-Lee, Hunker, Kristina, Combaret, Nicolas, Motreff, Pascal, Chédid, Antoine, Fiquet, Béatrice, Plouin, Pierre-François, Mousseaux, Elie, Azarine, Arshid, Amar, Laurence, Azizi, Michel, Gornik, Heather L, Ganesh, Santhi K, Kovacic, Jason C, Jeunemaitre, Xavier, Bouatia-Naji, Nabila

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Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing von Carss, Keren J., Baranowska, Anna A., Armisen, Javier, Webb, Tom R., Hamby, Stephen E., Premawardhana, Diluka, Al-Hussaini, Abtehale, Wood, Alice, Wang, Quanli, Deevi, Sri V. V., Vitsios, Dimitrios, Lewis, Samuel H., Kotecha, Deevia, Bouatia-Naji, Nabila, Hesselson, Stephanie, Iismaa, Siiri E., Tarr, Ingrid, McGrath-Cadell, Lucy, Muller, David W., Dunwoodie, Sally L., Fatkin, Diane, Graham, Robert M., Giannoulatou, Eleni, Samani, Nilesh J., Petrovski, Slavé, Haefliger, Carolina, Adlam, David

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Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing von Tarr, Ingrid, Hesselson, Stephanie, Iismaa, Siiri E., Rath, Emma, Monger, Steven, Troup, Michael, Mishra, Ketan, Wong, Claire M.Y., Hsu, Pei-Chen, Junday, Keerat, Humphreys, David T., Adlam, David, Webb, Tom R., Baranowska-Clarke, Anna A., Hamby, Stephen E., Carss, Keren J., Samani, Nilesh J., Bax, Monique, McGrath-Cadell, Lucy, Kovacic, Jason C., Dunwoodie, Sally L., Fatkin, Diane, Muller, David W.M., Graham, Robert M., Giannoulatou, Eleni

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Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromas von THOMAS, Laura, SPURLOCK, Gill, UPADHYAYA, Meena, EUDALL, Claire, THOMAS, Nick S, MORT, Matthew, HAMBY, Stephen E, CHUZHANOVA, Nadia, BREMS, Hilde, LEGIUS, Eric, COOPER, David N

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Comparative analysis of germline and somatic microlesion mutational spectra in 17 human tumor suppressor genes von Ivanov, Dobril, Hamby, Stephen E., Stenson, Peter D., Phillips, Andrew D., Kehrer-Sawatzki, Hildegard, Cooper, David N., Chuzhanova, Nadia

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Screening in silico predicted remotely acting NF1 gene regulatory elements for mutations in patients with neurofibromatosis type 1 von Hamby, Stephen E, Reviriego, Pablo, Cooper, David N, Upadhyaya, Meena, Chuzhanova, Nadia

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Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing von Tarr, Ingrid, Hesselson, Stephanie, Iismaa, Siiri E., Rath, Emma, Monger, Steven, Troup, Michael, Mishra, Ketan, Wong, Claire M.Y., Hsu, Pei-Chen, Junday, Keerat, Humphreys, David T., Adlam, David, Webb, Tom R., Baranowska-Clarke, Anna A., Hamby, Stephen E., Carss, Keren J., Samani, Nilesh J., Bax, Monique, McGrath-Cadell, Lucy, Kovacic, Jason C., Dunwoodie, Sally L., Fatkin, Diane, Muller, David W.M., Graham, Robert M., Giannoulatou, Eleni

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Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia von Georges, Adrien, Albuisson, Juliette, Berrandou, Takiy, Dupre, Delia, Lorthioir, Aurelien, D'Escamard, Valentina, Di Narzo, Antonio F., Kadian-Dodov, Daniella, Olin, Jeffrey W., Warchol-Celinska, Ewa, Prejbisz, Aleksander, Januszewicz, Andrzej, Bruneval, Patrick, Baranowska, Anna A., Webb, Tom R., Hamby, Stephen E., Samani, Nilesh J., Adlam, David, Fendrikova-Mahlay, Natalia, Hazen, Stanley, Wang, Yu, Yang, Min-Lee, Hunker, Kristina, Combaret, Nicolas, Motreff, Pascal, Chedid, Antoine, Fiquet, Beatrice, Plouin, Pierre-Francois, Mousseaux, Elie, Azarine, Arshid, Amar, Laurence, Azizi, Michel, Gornik, Heather L., Ganesh, Santhi K., Kovacic, Jason C., Jeunemaitre, Xavier, Bouatia-Naji, Nabila

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157 Myeloid expression of trib1 regulates the polarisation state of tissue resident macrophages that has consequences on plasma lipid and metabolic homeostasis von Johnston, Jessica M, Angyal, Adrienn, Hadadi, Eva, Hamby, Stephen E, Bauer, Robert, Ilyas, Zabran, Szili, Daniel, Ariaans, Markus, Wilson, Heather L, Krauss, Ronald M, Rader, Daniel J, Goodall, Alison H, Francis, Sheila E, Kiss-Toth, Endre

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Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease von Webb, Thomas R, Erdmann, Jeanette, Stirrups, Kathleen E, Stitziel, Nathan O, Masca, Nicholas G D, Jansen, Henning, Kanoni, Stavroula, Nelson, Christopher P, Ferrario, Paola G, König, Inke R, Eicher, John D, Johnson, Andrew D, Hamby, Stephen E, Betsholtz, Christer, Ruusalepp, Arno, Franzén, Oscar, Schadt, Eric E, Björkegren, Johan L M, Weeke, Peter E, Auer, Paul L, Schick, Ursula M, Lu, Yingchang, Zhang, He, Dube, Marie-Pierre, Goel, Anuj, Farrall, Martin, Peloso, Gina M, Won, Hong-Hee, Do, Ron, van Iperen, Erik, Kruppa, Jochen, Mahajan, Anubha, Scott, Robert A, Willenborg, Christina, Braund, Peter S, van Capelleveen, Julian C, Doney, Alex S F, Donnelly, Louise A, Asselta, Rosanna, Merlini, Pier A, Duga, Stefano, Marziliano, Nicola, Denny, Josh C, Shaffer, Christian, El-Mokhtari, Nour Eddine, Franke, Andre, Heilmann, Stefanie, Hengstenberg, Christian, Hoffmann, Per, Asselbergs, Folkert W, Wellcome Trust Case Control Consortium

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