Circulating concentrations of vitamin D in relation to pancreatic cancer risk in European populations by van Duijnhoven, F, Jenab, M, Hveem, K, Bradbury, K

Road traffic noise, air pollution and incident cardiovascular disease: A joint analysis of the HUNT, EPIC-Oxford and UK Biobank cohorts by Cai, Y, Hodgson, S, Blangiardo, M, Gulliver, J, Morley, D, Fecht, D, Vienneau, D, de Hoogh, K, Key, T, Hveem, K, Elliott, P, Hansell, A

A P3G generic access agreement for population genomic studies. by Knoppers, B, Chisholm, R, Kaye, J, Cox, D, Thorogood, A, Burton, P, Brookes, A, Fortier, I, Goodwin, P, Harris, JR, Hveem, K, Kent, A, Little, J, Riegman, P, Ripatti, S, Stolk, R

Road traffic noise, blood pressure and heart rate: pooled analyses of harmonized data from 88,336 participants by Key, T, Zijlema, W, Cai, Y, Doiron, D, Mbatchou, S, Fortier, I, Gulliver, J, de Hoogh, K, Morley, D, Hodgson, S, Elliott, P, Kongsgard, H, Hveem, K, Gaye, A, Burton, P, Hansell, A, Stolk, R, Rosmalen, J, Key, T

Meta-analysis of gene-level tests for rare variant association by Liu, D, Peloso, G, Zhan, X, Holmen, O, Zawistowski, M, Feng, S, Nikpay, M, Auer, P, Goel, A, Zhang, H, Peters, U, Farrall, M, Orho-Melander, M, Kooperberg, C, Mcpherson, R, Watkins, H, Willer, C, Hveem, K, Melander, O, Kathiresan, S, Abecasis, G

Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries by Surakka, I, Wu, K-H, Hornsby, W, Wolford, BN, Shen, F, Zhou, W, Huffman, JE, Pandit, A, Hu, Y, Brumpton, B, Skogholt, AH, Gabrielsen, ME, Walters, RG, Hveem, K, Kooperberg, C, Zöllner, S, Wilson, PWF, Sutton, NR, Daly, MJ, Neale, BM, Willer, CJ

Meta-analysis of gene-level tests for rare variant association. by Liu, D, Peloso, G, Zhan, X, Holmen, O, Zawistowski, M, Feng, S, Nikpay, M, Auer, P, Goel, A, Zhang, H, Peters, U, Farrall, M, Orho-Melander, M, Kooperberg, C, McPherson, R, Watkins, H, Willer, C, Hveem, K, Melander, O, Kathiresan, S, Abecasis, G

Are Requirements to Deposit Data in Research Repositories Compatible With the European Union's General Data Protection Regulation? by Mascalzoni, D, Bentzen, HB, Budin-Ljøsne, I, Bygrave, LA, Bell, J, Dove, ES, Fuchsberger, C, Hveem, K, Mayrhofer, MT, Meraviglia, V, O'Brien, DR, Pattaro, C, Pramstaller, PP, Rakic, V, Rossini, A, Shabani, M, Svantesson, DJB, Tomasi, M, Ursin, L, Wjst, M, Kaye, J

Underlying genetic models of inheritance in established type 2 diabetes associations. by Salanti, G, Southam, L, Altshuler, D, Ardlie, K, Barroso, I, Boehnke, M, Cornelis, M, Frayling, T, Grallert, H, Grarup, N, Groop, L, Hansen, T, Hattersley, A, Hu, F, Hveem, K, Illig, T, Kuusisto, J, Laakso, M, Langenberg, C, Lyssenko, V, McCarthy, M, Morris, A, Morris, A, Palmer, C, Payne, F

Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies. by Fortier, I, Burton, P, Robson, P, Ferretti, V, Little, J, L'Heureux, F, Deschênes, M, Knoppers, B, Doiron, D, Keers, J, Linksted, P, Harris, JR, Lachance, G, Boileau, C, Pedersen, N, Hamilton, C, Hveem, K, Borugian, M, Gallagher, R, McLaughlin, J, Parker, L, Potter, J, Gallacher, J, Kaaks, R, Liu, B

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts by Wang, Y, Namba, S, Lopera, E, Kerminen, S, Tsuo, K, Läll, K, Kanai, M, Zhou, W, Wu, K-H, Favé, M-J, Bhatta, L, Awadalla, P, Brumpton, B, Deelen, P, Hveem, K, Lo Faro, V, Mägi, R, Murakami, Y, Sanna, S, Smoller, JW, Uzunovic, J, Wolford, BN, Willer, C, Gamazon, ER, Cox, NJ, Surakka, I, Okada, Y, Martin, AR, Hirbo, J, Millwood, IY

Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease by Zheng, J, Zhang, Y, Rasheed, H, Walker, V, Sugawara, Y, Li, J, Leng, Y, Elsworth, B, Wootton, RE, Fang, S, Yang, Q, Burgess, S, Haycock, PC, Borges, MC, Cho, Y, Carnegie, R, Howell, A, Robinson, J, Thomas, LF, Brumpton, BM, Hveem, K, Hallan, S, Franceschini, N, Morris, AP, Köttgen, A, Pattaro, C, Wuttke, M, Yamamoto, M, Kashihara, N, Akiyama, M, Kanai, M, Matsuda, K, Kamatani, Y, Okada, Y, Walters, R, Millwood, IY, Chen, Z, Davey Smith, G, Barbour, S, Yu, C, Åsvold, BO, Zhang, H, Gaunt, TR

Biological and clinical insights from genetics of insomnia symptoms by Lane, JM, Jones, SE, Dashti, HS, Wood, AR, Aragam, KG, Van Hees, VT, Strand, LB, Winsvold, B, Wang, H, Bowden, J, Song, Y, Patel, K, Anderson, SG, Beaumont, RN, Bechtold, DA, Cade, B, Haas, M, Kathiresan, S, Little, MA, Luik, A, Loudon, AS, Purcell, S, Richmond, RC, Scheer, FAJL, Schormair, B, Tyrrell, J, Winkelman, JW, Winkelman, J, Hunt All In Sleep, Hveem, K, Zhao, C, Nielsen, JB, Willer, CJ, Redline, S, Spiegelhalder, K, Kyle, S, Ray, DW, Zwart, JA, Brumpton, B, Frayling, TM, Lawlor, DA, Rutter, MK, Weedon, MN, Saxena, R

Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci by Tanskanen, T, van den Berg, L, Välimäki, N, Aavikko, M, Ness-Jensen, E, Hveem, K, Wettergren, Y, Lindskog, E, Tõnisson, N, Metspalu, A, Silander, K, Orlando, G, Law, PJ, Tuupanen, S, Gylfe, AE, Hänninen, UA, Cajuso, T, Kondelin, J, Sarin, AP, Pukkala, E, Jousilahti, P, Salomaa, V, Ripatti, S, Palotie, A, Järvinen, H, Renkonen-Sinisalo, L, Lepistö, A, Böhm, J, Mecklin, JP, Al-Tassan, NA, Palles, C, Martin, L, Barclay, E, Tenesa, A, Farrington, SM, Timofeeva, MN, Meyer, BF, Wakil, SM, Campbell, H, Smith, CG, Idziaszczyk, S, Maughan, TS, Kaplan, R, Kerr, R, Kerr, D, Buchanan, DD, Win, AK, Hopper, J, Jenkins, MA, Newcomb, PA, Gallinger, S, Conti, D, Schumacher, FR, Casey, G, Cheadle, JP, Dunlop, MG, Tomlinson, IP, Houlston, RS, Palin, K, Aaltonen, LA

Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes by Gusarova, V, O'Dushlaine, C, Teslovich, TM, Benotti, PN, Mirshahi, T, Gottesman, O, Van Hout, CV, Murray, MF, Mahajan, A, Nielsen, JB, Fritsche, L, Wulff, AB, Gudbjartsson, DF, Sjögren, M, Emdin, CA, Scott, RA, Lee, W-J, Small, A, Kwee, LC, Dwivedi, OP, Prasad, RB, Bruse, S, Lopez, AE, Penn, J, Marcketta, A, Leader, JB, Still, CD, Kirchner, HL, Mirshahi, UL, Wardeh, AH, Hartle, CM, Habegger, L, Fetterolf, SN, Tusie-Luna, T, Morris, AP, Holm, H, Steinthorsdottir, V, Sulem, P, Thorsteinsdottir, U, Rotter, JI, Chuang, L-M, Damrauer, S, Birtwell, D, Brummett, CM, Khera, AV, Natarajan, P, Orho-Melander, M, Flannick, J, Lotta, LA, Willer, CJ, Holmen, OL, Ritchie, MD, Ledbetter, DH, Murphy, AJ, Borecki, IB, Reid, JG, Overton, JD, Hansson, O, Groop, L, Shah, SH, Kraus, WE, Rader, DJ, Chen, Y-DI, Hveem, K, Wareham, NJ, Kathiresan, S, Melander, O, Stefansson, K, Nordestgaard, BG, Tybjærg-Hansen, A, Abecasis, GR, Altshuler, D, Florez, JC, Boehnke, M, McCarthy, MI, Yancopoulos, GD, Carey, DJ, Shuldiner, AR, Baras, A, Dewey, FE, Gromada, J

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. by Lange, L, Hu, Y, Zhang, H, Xue, C, Schmidt, E, Tang, Z, Bizon, C, Lange, E, Smith, J, Turner, E, Jun, G, Kang, H, Peloso, G, Auer, P, Li, K, Flannick, J, Zhang, J, Fuchsberger, C, Gaulton, K, Lindgren, C, Locke, A, Manning, A, Sim, X, Rivas, M, Holmen, O, Gottesman, O, Lu, Y, Ruderfer, D, Stahl, E, Duan, Q, Li, Y, Durda, P, Jiao, S, Isaacs, A, Hofman, A, Bis, J, Correa, A, Griswold, M, Jakobsdottir, J, Smith, A, Schreiner, P, Feitosa, M, Zhang, Q, Huffman, J, Crosby, J, Wassel, C, Do, R, Franceschini, N, Martin, L, Robinson, J, Assimes, T, Crosslin, DR, Rosenthal, E, Tsai, M, Rieder, M, Farlow, D, Folsom, A, Lumley, T, Fox, E, Carlson, C, Peters, U, Jackson, R, van Duijn, C, Uitterlinden, A, Levy, D, Rotter, J, Taylor, H, Gudnason, V, Siscovick, D, Fornage, M, Borecki, I, Hayward, C, Rudan, I, Chen, Y, Bottinger, E, Loos, R, Sætrom, P, Hveem, K, Boehnke, M, Groop, L, McCarthy, M, Meitinger, T, Ballantyne, C, Gabriel, S, O'Donnell, C, Post, W, North, K, Reiner, A, Boerwinkle, E, Psaty, B, Altshuler, D, Kathiresan, S, Lin, D, Jarvik, G, Cupples, L, Kooperberg, C, Wilson, J, Nickerson, D, Abecasis, G, Rich, S, Tracy, R, Willer, C

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use by Liu, M, Jiang, Y, Wedow, R, Li, Y, Brazel, DM, Chen, F, Datta, G, Davila-Velderrain, J, McGuire, D, Tian, C, Zhan, X, 23Andme Research Team, Hunt All-In Psychiatry, Choquet, H, Docherty, AR, Faul, JD, Foerster, JR, Fritsche, LG, Gabrielsen, ME, Gordon, SD, Haessler, J, Hottenga, J-J, Huang, H, Jang, S-K, Jansen, PR, Ling, Y, Mägi, R, Matoba, N, McMahon, G, Mulas, A, Orrù, V, Palviainen, T, Pandit, A, Reginsson, GW, Skogholt, AH, Smith, JA, Taylor, AE, Turman, C, Willemsen, G, Young, H, Young, KA, Zajac, GJM, Zhao, W, Zhou, W, Bjornsdottir, G, Boardman, JD, Boehnke, M, Boomsma, DI, Chen, C, Cucca, F, Davies, GE, Eaton, CB, Ehringer, MA, Esko, T, Fiorillo, E, Gillespie, NA, Gudbjartsson, DF, Haller, T, Harris, KM, Heath, AC, Hewitt, JK, Hickie, IB, Hokanson, JE, Hopfer, CJ, Hunter, DJ, Iacono, WG, Johnson, EO, Kamatani, Y, Kardia, SLR, Keller, MC, Kellis, M, Kooperberg, C, Kraft, P, Krauter, KS, Laakso, M, Lind, PA, Loukola, A, Lutz, SM, Madden, PAF, Martin, NG, McGue, M, McQueen, MB, Medland, SE, Metspalu, A, Mohlke, KL, Nielsen, JB, Okada, Y, Peters, U, Polderman, TJC, Posthuma, D, Reiner, AP, Rice, JP, Rimm, E, Rose, RJ, Runarsdottir, V, Stallings, MC, Stančáková, A, Stefansson, H, Thai, KK, Tindle, HA, Tyrfingsson, T, Wall, TL, Weir, DR, Weisner, C, Whitfield, JB, Winsvold, BS, Yin, J, Zuccolo, L, Bierut, LJ, Hveem, K, Lee, JJ, Munafò, MR, Saccone, NL, Willer, CJ, Cornelis, MC, David, SP, Hinds, DA, Jorgenson, E, Kaprio, J, Stitzel, JA, Stefansson, K, Thorgeirsson, TE, Abecasis, G, Liu, DJ, Vrieze, S

Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease by Stitziel, N, Stirrups, K, Masca, N, Erdmann, J, Ferrario, P, Koenig, I, Weeke, P, Webb, T, Auer, P, Schick, U, Lu, Y, Zhang, H, Dube, M, Goel, A, Farrall, M, Peloso, G, Won, H, Do, R, van Iperen, E, Kanoni, S, Kruppa, J, Mahajan, A, Scott, R, Willenborg, C, Braund, P, van Capelleveen, J, Doney, A, Donnelly, L, Asselta, R, Merlini, P, Duga, S, Marziliano, N, Denny, J, Shaffer, C, El-Mokhtari, N, Franke, A, Gottesman, O, Heilmann, S, Hengstenberg, C, Hoffmann, P, Holmen, O, Hveem, K, Jansson, J, Joeckel, K, Kessler, T, Kriebel, J, Laugwitz, K, Marouli, E, Martinelli, N, McCarthy, M, Van Zuydam, N, Meisinger, C, Esko, T, Mihailov, E, Escher, SA, Alver, M, Moebus, S, Morris, A, Mueller-Nurasyid, M, Nikpay, M, Olivieri, O, Perreault, L, AlQarawi, A, Robertson, N, Akinsanya, K, Reilly, D, Vogt, T, Yin, W, Asselbergs, F, Kooperberg, C, Jackson, R, Stahl, E, Strauch, K, Varga, T, Waldenberger, M, Zeng, L, Kraja, A, Liu, C, Ehret, G, Newton-Cheh, C, Chasman, D, Chowdhury, R, Ferrario, M, Ford, I, Jukema, J, Kee, F, Kuulasmaa, K, Nordestgaard, BG, Perola, M, Saleheen, D, Sattar, N, Surendran, P, Tregouet, D, Young, R, Howson, J, Butterworth, A, Danesh, J, Ardissino, D, Bottinger, E, Erbel, R, Franks, P, Girelli, D, Hall, A, Hovingh, G, Kastrati, A, Lieb, W, Meitinger, T, Kraus, W, Shah, S, McPherson, R, Orho-Melander, M, Melander, O, Metspalu, A, Palmer, C, Peters, A, Rader, D, Reilly, M, Loos, R, Reiner, A, Roden, D, Tardif, J, Thompson, JR, Wareham, N, Watkins, H, Willer, C, Kathiresan, S, Deloukas, P, Samani, N, Schunkert, H

Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease by Webb, T, Erdmann, J, Stirrups, K, Stitziel, N, Masca, N, Jansen, H, Kanoni, S, Nelson, C, Ferrario, P, König, I, Eicher, J, Johnson, A, Hamby, S, Betsholtz, C, Ruusalepp, A, Franzén, O, Schadt, E, Björkegren, J, Weeke, P, Auer, P, Schick, U, Lu, Y, Zhang, H, Dube, M, Goel, A, Farrall, M, Peloso, G, Won, H, Do, R, van Iperen, E, Kruppa, J, Mahajan, A, Scott, R, Willenborg, C, Braund, P, van Capelleveen, J, Doney, A, Donnelly, L, Asselta, R, Merlini, P, Duga, S, Marziliano, N, Denny, J, Shaffer, C, El-Mokhtari, N, Franke, A, Heilmann, S, Hengstenberg, C, Hoffmann, P, Holmen, O, Hveem, K, Jansson, J, Jöckel, K, Kessler, T, Kriebel, J, Laugwitz, K, Marouli, E, Martinelli, N, McCarthy, M, Van Zuydam, N, Meisinger, C, Esko, T, Mihailov, E, Escher, S, Alver, M, Moebus, S, Morris, A, Virtamo, J, Nikpay, M, Olivieri, O, Provost, S, AlQarawi, A, Robertson, N, Akinsansya, K, Reilly, D, Vogt, T, Yin, W, Asselbergs, F, Kooperberg, C, Jackson, R, Stahl, E, Müller-Nurasyid, M, Strauch, K, Varga, T, Waldenberger, M, Wellcome Trust Case Control Consortium, Zeng, L, Chowdhury, R, Salomaa, V, Ford, I, Jukema, J, Amouyel, P, Kontto, J, MORGAM Investigators, Nordestgaard, B, Ferrières, J, Saleheen, D, Sattar, N, Surendran, P, Wagner, A, Young, R, Howson, J, Butterworth, A, Danesh, J, Ardissino, D, Bottinger, E, Erbel, R, Franks, P, Girelli, D, Hall, A, Hovingh, G, Kastrati, A, Lieb, W, Meitinger, T, Kraus, W, Shah, S, McPherson, R, Orho-Melander, M, Melander, O, Metspalu, A, Palmer, C, Peters, A, Rader, D, Reilly, M, Loos, R, Reiner, A, Roden, D, Tardif, J, Thompson, J, Wareham, N, Watkins, H, Willer, C, Samani, N, Schunkert, H, Deloukas, P, Kathiresan, S, Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension by Surendran, P, Drenos, F, Young, R, Warren, H, Cook, J, Manning, A, Grarup, N, Sim, X, Barnes, D, Witkowska, K, Staley, J, Tragante, V, Tukiainen, T, Yaghootkar, H, Masca, N, Freitag, D, Ferreira, T, Giannakopoulou, O, Tinker, A, Harakalova, M, Mihailov, E, Liu, C, Kraja, A, Nielsen, S, Rasheed, A, Samuel, M, Zhao, W, Bonnycastle, L, Jackson, A, Narisu, N, Swift, A, Southam, L, Marten, J, Huyghe, J, Stančáková, A, Fava, C, Ohlsson, T, Matchan, A, Stirrups, K, Bork-Jensen, J, Gjesing, A, Kontto, J, Perola, M, Shaw-Hawkins, S, Havulinna, A, Zhang, H, Donnelly, L, Groves, C, Rayner, N, Neville, M, Robertson, N, Yiorkas, A, Herzig, K, Kajantie, E, Zhang, W, Willems, S, Lannfelt, L, Malerba, G, Soranzo, N, Trabetti, E, Verweij, N, Evangelou, E, Moayyeri, A, Vergnaud, A, Nelson, C, Poveda, A, Varga, T, Caslake, M, de Craen, A, Trompet, S, Luan, J, Scott, R, Harris, S, Liewald, D, Marioni, R, Menni, C, Farmaki, A, Hallmans, G, Renström, F, Huffman, J, Hassinen, M, Burgess, S, Vasan, R, Felix, J, Uria-Nickelsen, M, Malarstig, A, Reilly, D, Hoek, M, Vogt, T, Lin, H, Lieb, W, Traylor, M, Markus, H, Highland, H, Justice, A, Marouli, E, Lindström, J, Uusitupa, M, Komulainen, P, Lakka, T, Rauramaa, R, Polasek, O, Rudan, I, Rolandsson, O, Franks, P, Dedoussis, G, Spector, T, Jousilahti, P, Männistö, S, Deary, I, Starr, J, Langenberg, C, Wareham, N, Brown, M, Dominiczak, A, Connell, J, Jukema, J, Sattar, N, Ford, I, Packard, C, Esko, T, Mägi, R, Metspalu, A, de Boer, R, van der Meer, P, van der Harst, P, Gambaro, G, Ingelsson, E, Lind, L, de Bakker, P, Numans, M, Brandslund, I, Christensen, C, Petersen, E, Korpi-Hyövälti, E, Oksa, H, Chambers, J, Kooner, J, Blakemore, A, Franks, S, Jarvelin, M, Husemoen, L, Linneberg, A, Skaaby, T, Thuesen, B, Karpe, F, Tuomilehto, J, Doney, A, Morris, A, Palmer, C, Holmen, O, Hveem, K, Willer, C, Tuomi, T, Groop, L, Käräjämäki, A, Palotie, A, Ripatti, S, Salomaa, V, Alam, D, Majumder, A, Di Angelantonio, E, Chowdhury, R, McCarthy, M, Poulter, N, Stanton, A, Sever, P, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrières, J, Kee, F, Kuulasmaa, K, Müller-Nurasyid, M, Veronesi, G, Virtamo, J, Deloukas, P, Elliott, P, Zeggini, E, Kathiresan, S, Melander, O, Kuusisto, J, Laakso, M, Padmanabhan, S, Porteous, D, Hayward, C, Scotland, G, Collins, F, Mohlke, K, Hansen, T, Pedersen, O, Boehnke, M, Stringham, H, Frossard, P, Newton-Cheh, C, Tobin, M, Nordestgaard, B, Caulfield, M, Mahajan, A, Morris, A, Tomaszewski, M, Samani, N, Saleheen, D, Asselbergs, F, Lindgren, C, Danesh, J, Wain, L, Butterworth, A, Howson, J, Munroe, P