Long noncoding RNA NEXN-AS1 mitigates atherosclerosis by regulating the actin-binding protein NEXN von Hu, Yan-Wei, Guo, Feng-Xia, Xu, Yuan-Jun, Li, Pan, Lu, Zhi-Feng, McVey, David G, Zheng, Lei, Wang, Qian, Ye, John H, Kang, Chun-Min, Wu, Shao-Guo, Zhao, Jing-Jing, Ma, Xin, Yang, Zhen, Fang, Fu-Chun, Qiu, Yu-Rong, Xu, Bang-Ming, Xiao, Lei, Wu, Qian, Wu, Li-Mei, Ding, Li, Webb, Tom R, Samani, Nilesh J, Ye, Shu

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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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JCAD Gene at the 10p11 Coronary Artery Disease Locus Regulates Hippo Signaling in Endothelial Cells von Jones, Peter D, Kaiser, Michael A, Ghaderi Najafabadi, Maryam, Koplev, Simon, Zhao, Yuqi, Douglas, Gillian, Kyriakou, Theodosios, Andrews, Sarah, Rajmohan, Rathinasabapathy, Watkins, Hugh, Channon, Keith M, Ye, Shu, Yang, Xia, Björkegren, Johan L.M, Samani, Nilesh J, Webb, Tom R

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Minireview: The Melanocortin 2 Receptor Accessory Proteins von Webb, Tom R, Clark, Adrian J. L

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Active buoyancy adjustment increases dispersal potential in benthic marine animals von Hamel, Jean‐François, Sun, Jiamin, Gianasi, Bruno L., Montgomery, Emaline M., Kenchington, Ellen L., Burel, Benoit, Rowe, Sherrylynn, Winger, Paul D., Mercier, Annie, Webb, Tom

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Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial von Collinge, John, MD, Gorham, Michele, RN, Hudson, Fleur, BA, Kennedy, Angus, MD, Keogh, Geraldine, Pal, Suvankar, MRCP, Rossor, Martin, MD, Rudge, Peter, FRCP, Siddique, Durre, PhD, Spyer, Moira, PhD, Thomas, Dafydd, MD, Walker, Sarah, PhD, Webb, Tom, BSc, Wroe, Steve, MD, Darbyshire, Janet, FRCP

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Effects of Coronary Artery Disease–Associated Variants on Vascular Smooth Muscle Cells von Solomon, Charles U., McVey, David G., Andreadi, Catherine, Gong, Peng, Turner, Lenka, Stanczyk, Paulina J., Khemiri, Sonja, Chamberlain, Julie C., Yang, Wei, Webb, Tom R., Nelson, Christopher P., Samani, Nilesh J., Ye, Shu

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Influence of a Coronary Artery Disease–Associated Genetic Variant on FURIN Expression and Effect of Furin on Macrophage Behavior von Zhao, Guojun, Yang, Wei, Wu, Jingchun, Chen, Bairu, Yang, Xu, Chen, Junhui, McVey, David G, Andreadi, Catherine, Gong, Peng, Webb, Tom R, Samani, Nilesh J, Ye, Shu

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The FES Gene at the 15q26 Coronary-Artery-Disease Locus Inhibits Atherosclerosis von Karamanavi, Elisavet, McVey, David G., van der Laan, Sander W., Stanczyk, Paulina J., Morris, Gavin E., Wang, Yifan, Yang, Wei, Chan, Kenneth, Poston, Robin N., Luo, Jun, Zhou, Xinmiao, Gong, Peng, Jones, Peter D., Cao, Junjun, Kostogrys, Renata B., Webb, Tom R., Pasterkamp, Gerard, Yu, Haojie, Xiao, Qingzhong, Greer, Peter A., Stringer, Emma J., Samani, Nilesh J., Ye, Shu

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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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Individual variation, population‐specific behaviours and stochastic processes shape marine migration phenologies von Freshwater, Cameron, Trudel, Marc, Beacham, Terry D., Gauthier, Stéphane, Johnson, Stewart C., Neville, Chrys‐Ellen, Juanes, Francis, Webb, Tom

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Patterns of bird functional diversity on land-bridge island fragments von Ding, Zhifeng, Feeley, Kenneth J., Wang, Yanping, Pakeman, Robin J., Ding, Ping

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Changes in host–parasitoid food web structure with elevation von Maunsell, Sarah C, Kitching, Roger L, Burwell, Chris J, Morris, Rebecca J, Webb, Tom

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MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family von Chan, Li F, Webb, Tom R, Chung, Teng-Teng, Meimaridou, Eirini, Cooray, Sadani N, Guasti, Leonardo, Chapple, J. Paul, Egertová, Michaela, Elphick, Maurice R, Cheetham, Michael E, Metherell, Louise A, Clark, Adrian J.L

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Coronary Artery Disease–Associated LIPA Coding Variant rs1051338 Reduces Lysosomal Acid Lipase Levels and Activity in Lysosomes von Morris, Gavin E, Braund, Peter S, Moore, Jasbir S, Samani, Nilesh J, Codd, Veryan, Webb, Tom R

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Genetic influence on vascular smooth muscle cell apoptosis von McVey, David G., Andreadi, Catherine, Gong, Peng, Stanczyk, Paulina J., Solomon, Charles U., Turner, Lenka, Yan, Liu, Chen, Runji, Cao, Junjun, Nelson, Christopher P., Thompson, John R., Yu, Haojie, Webb, Tom R., Samani, Nilesh J., Ye, Shu

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Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings von Van Gucht, Ilse, Krebsova, Alice, Diness, Birgitte Rode, Laga, Steven, Adlam, Dave, Kempers, Marlies, Samani, Nilesh J., Webb, Tom R., Baranowska, Ania A., Van Den Heuvel, Lotte, Perik, Melanie, Luyckx, Ilse, Peeters, Nils, Votypka, Pavel, Macek, Milan, Meester, Josephina, Van Laer, Lut, Verstraeten, Aline, Loeys, Bart L.

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HHIPL1, a Gene at the 14q32 Coronary Artery Disease Locus, Positively Regulates Hedgehog Signaling and Promotes Atherosclerosis von Aravani, Dimitra, Morris, Gavin E, Jones, Peter D, Tattersall, Helena K, Karamanavi, Elisavet, Kaiser, Michael A, Kostogrys, Renata B, Ghaderi Najafabadi, Maryam, Andrews, Sarah L, Nath, Mintu, Ye, Shu, Stringer, Emma J, Samani, Nilesh J, Webb, Tom R

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Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23) von WEBB, Tom R, PARFITT, David A, SCHWARZ, Nele, KANUGA, Naheed, MICHAELIDES, Michel, CHEETHAM, Michael E, GORIN, Michael B, HARDCASTLE, Alison J, GARDNER, Jessica C, MARTINEZ, Ariadna, BEVILACQUA, Dalila, DAVIDSON, Alice E, ZITO, Ilaria, THISELTON, Dawn L, RESSA, Jacob H. C, APERGI, Marina

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Do spatial scale and life history affect fish–habitat relationships? von Hale, Robin, Colton, Madhavi A., Peng, Po, Swearer, Stephen E., Webb, Tom

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