Crystal structure of dimethyl (1α,2β,3α,4β,7β,8α,9β,10α) -13-di(methylthio)methylidene-pentacyclo[8.2.1.14,7.0 2,9.03,8]tetradeca-5,11-diene-2,9-dicarboxylate, C 21H24O4S2

by Palmer, C., Russell, R.A., Warrener, R.N., Tiekink, E.R.T.
Published 2014

Cornulin, a marker of late epidermal differentiation, is down-regulated in eczema

by Lieden, A., D'Amato, M., Ekelund, E., Nordenskold, M., Bradley, M., Kuo, I.-C., Huang, C.-H., Chua, K.Y., Kockum, I., Mallbris, L., Wahlgren, C.-F., Stahle, M., Lee, S.P., Palmer, C.N.A., Seng, L.K., Chin, G.Y., Bjorksten, B.
Published 2011

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: The candidate gene association resource (CARe)

by Sobrin, L., Green, T., Sim, X., Jensen, R.A., Shyong Tai, E., Tay, W.T., Wang, J.J., Mitchell, P., Sandholm, N., Liu, Y., Hietala, K., Iyengar, S.K., Brooks, M., Buraczynska, M., van Zuydam, N., Smith, A.V., Gudnason, V., Doney, A.S.F., Morris, A.D., Leese, G.P., Palmer, C.N.A., Swaroop, A., Taylor Jr., H.A., Wilson, J.G., Penman, A., Chen, C.J., Groop, P.-H., Saw, S.-M., Aung, T., Klein, B.E., Rotter, J.I., Siscovick, D.S., Cotch, M.F., Klein, R., Daly, M.J., Wong, T.Y.
Published 2014

A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

by Meng W., Shah K.P., Pollack S., Toppila I., Hebert H.L., McCarthy M.I., Groop L., Ahlqvist E., Lyssenko V., Agardh E., Daniell M., Kaidonis G., Craig J.E., Mitchell P., Liew G., Kifley A., Wang J.J., Christiansen M.W., Jensen R.A., Penman A., Hancock H.A., Chen C.J., Correa A., Kuo J.Z., Li X., Chen Y.-D.I., Rotter J.I., Klein R., Klein B., Wong T.Y., Morris A.D., Doney A.S.F., Colhoun H.M., Price A.L., Burdon K.P., Groop P.-H., Sandholm N., Grassi M.A., Sobrin L., Palmer C.N.A., Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group
Published 2019

Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus

by Strange, A., Bellenguez, C., Sim, X., Luben, R., Hysi, P.G., Ramdas, W.D., van Koolwijk, L.M., Freeman, C., Pirinen, M., Su, Z., Band, G., Pearson, R., Vukcevic, D., Langford, C., Deloukas, P., Hunt, S., Gray, E., Dronov, S., Potter, S.C., Tashakkori-Ghanbaria, A., Edkins, S., Bumpstead, S.J., Blackwell, J.M., Bramon, E., Brown, M.A., Casas, J.P., Corvin, A., Duncanson, A., Jankowski, J.A., Markus, H.S., Mathew, C.G., Palmer, C.N., Plomin, R., Rautanen, A., Sawcer, S.J., Trembath, R.C., Wood, N.W., Barroso, I., Leena Peltonen, L.P., Healey, P., McGuffin, P., Topouzis, F., Klaver, C.C., van Duijn, C.M., Mackey, D.A., Young, T.L., Hammond, C.J., Khaw, K.-T., Wareham, N., Wang, J.J., Wong, T.Y., Foster, P.J., Mitchell, P., Spencer, C.C., Donnelly, P., Viswanathan, A.C.
Published 2014

Genetic Loci for Retinal Arteriolar Microcirculation

by Sim, X., Jensen, R.A., Ikram, M.K., Cotch, M.F., Li, X., MacGregor, S., Xie, J., Smith, A.V., Boerwinkle, E., Mitchell, P., Klein, R., Klein, B.E.K., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., de Jong, P.T.V.M., Hofman, A., Rivadeneira, F., Uitterlinden, A.G., van Duijn, C.M., Aspelund, T., Eiriksdottir, G., Harris, T.B., Jonasson, F., Launer, L.J., Attia, J., Baird, P.N., Harrap, S., Holliday, E.G., Inouye, M., Rochtchina, E., Scott, R.J., Viswanathan, A., Li, G., Smith, N.L., Wiggins, K.L., Kuo, J.Z., Taylor, K.D., Hewitt, A.W., Martin, N.G., Montgomery, G.W., Sun, C., Young, T.L., Mackey, D.A., van Zuydam, N.R., Doney, A.S.F., Palmer, C.N.A., Morris, A.D., Rotter, J.I., Tai, E.S., Gudnason, V., Vingerling, J.R., Siscovick, D.S., Wang, J.J., Wong, T.Y.
Published 2014

New Susceptibility Loci Associated with Kidney Disease in Type 1 Diabetes

by Sandholm N., Salem R.M., McKnight A.J., Brennan E.P., Forsblom C., Isakova T., McKay G.J., Williams W.W., Sadlier D.M., Mäkinen V.-P., Swan E.J., Palmer C., Boright A.P., Ahlqvist E., Deshmukh H.A., Keller B.J., Huang H., Ahola A.J., Fagerholm E., Gordin D., Harjutsalo V., He B., Heikkilä O., Hietala K., Kytö J., Lahermo P., Lehto M., Lithovius R., Österholm A.-M., Parkkonen M., Pitkäniemi J., Rosengård-Bärlund M., Saraheimo M., Sarti C., Söderlund J., Soro-Paavonen A., Syreeni A., Thorn L.M., Tikkanen H., Tolonen N., Tryggvason K., Tuomilehto J., Wadén J., Gill G.V., Prior S., Guiducci C., Mirel D.B., Taylor A., Hosseini S.M., Parving H.-H., Rossing P., Tarnow L., Ladenvall C., Alhenc-Gelas F., Lefebvre P., Rigalleau V., Roussel R., Tregouet D.-A., Maestroni A., Maestroni S., Falhammar H., Gu T., Möllsten A., Cimponeriu D., Ioana M., Mota M., Mota E., Serafinceanu C., Stavarachi M., Hanson R.L., Nelson R.G., Kretzler M., Colhoun H.M., Panduru N.M., Gu H.F., Brismar K., Zerbini G., Hadjadj S., Marre M., Groop L., Lajer M., Bull S.B., Waggott D., Paterson A.D., Savage D.A., Bain S.C., Martin F., Hirschhorn J.N., Godson C., Florez J.C., Groop P.-H., Maxwell A.P., Böger C.A.
Published 2019

The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis

by Fall T., Hägg S., Mägi R., Ploner A., Fischer K., Horikoshi M., Sarin A.-P., Thorleifsson G., Ladenvall C., Kals M., Kuningas M., Draisma H.H.M., Ried J.S., van Zuydam N.R., Huikari V., Mangino M., Sonestedt E., Benyamin B., Nelson C.P., Rivera N.V., Kristiansson K., Shen H.-y., Havulinna A.S., Dehghan A., Donnelly L.A., Kaakinen M., Nuotio M.-L., Robertson N., de Bruijn R.F.A.G., Ikram M.A., Amin N., Balmforth A.J., Braund P.S., Doney A.S.F., Döring A., Elliott P., Esko T., Franco O.H., Gretarsdottir S., Hartikainen A.-L., Heikkilä K., Herzig K.-H., Holm H., Hottenga J.J., Hyppönen E., Illig T., Isaacs A., Isomaa B., Karssen L.C., Kettunen J., Koenig W., Kuulasmaa K., Laatikainen T., Laitinen J., Lindgren C., Lyssenko V., Läärä E., Rayner N.W., Männistö S., Pouta A., Rathmann W., Rivadeneira F., Ruokonen A., Savolainen M.J., Sijbrands E.J.G., Small K.S., Smit J.H., Steinthorsdottir V., Syvänen A.-C., Taanila A., Tobin M.D., Uitterlinden A.G., Willems S.M., Willemsen G., Witteman J., Perola M., Evans A., Ferrières J., Virtamo J., Kee F., Tregouet D.-A., Arveiler D., Amouyel P., Ferrario M.M., Brambilla P., Hall A.S., Heath A.C., Madden P.A.F., Martin N.G., Montgomery G.W., Whitfield J.B., Jula A., Knekt P., Oostra B., van Duijn C.M., Penninx B.W.J.H., Davey Smith G., Kaprio J., Samani N.J., Gieger C., Peters A., Wichmann H.-E., Boomsma D.I., de Geus E.J.C., Tuomi T.M., Power C., Hammond C.J., Spector T.D., Lind L., Orho-Melander M., Palmer C.N.A., Morris A.D., Groop L., Järvelin M.-R., Salomaa V., Vartiainen E., Hofman A., Ripatti S., Metspalu A., Thorsteinsdottir U., Stefansson K., Pedersen N.L., McCarthy M.I., Ingelsson E., Prokopenko I.
Published 2019

Genome-wide association and functional follow-up reveals new loci for kidney function

by Pattaro C., Köttgen A., Teumer A., Garnaas M., Böger C.A., Fuchsberger C., Olden M., Chen M.-H., Tin A., Taliun D., Li M., Gao X., Gorski M., Yang Q., Hundertmark C., Foster M.C., O'Seaghdha C.M., Glazer N., Isaacs A., Liu C.-T., Smith A.V., O'Connell J.R., Struchalin M., Tanaka T., Li G., Johnson A.D., Gierman H.J., Feitosa M., Hwang S.-J., Atkinson E.J., Lohman K., Cornelis M.C., Johansson A., Tönjes A., Dehghan A., Chouraki V., Holliday E.G., Sorice R., Kutalik Z., Lehtimäki T., Esko T., Deshmukh H., Ulivi S., Chu A.Y., Murgia F., Trompet S., Imboden M., Kollerits B., Pistis G., Harris T.B., Launer L.J., Aspelund T., Eiriksdottir G., Mitchell B.D., Boerwinkle E., Schmidt H., Cavalieri M., Rao M., Hu F.B., Demirkan A., Oostra B.A., de Andrade M., Turner S.T., Ding J., Andrews J.S., Freedman B.I., Koenig W., Illig T., Döring A., Wichmann H.-E., Kolcic I., Zemunik T., Boban M., Minelli C., Wheeler H.E., Igl W., Zaboli G., Wild S.H., Wright A.F., Campbell H., Ellinghaus D., Nöthlings U., Jacobs G., Biffar R., Endlich K., Ernst F., Homuth G., Kroemer H.K., Nauck M., Stracke S., Völker U., Völzke H., Kovacs P., Stumvoll M., Mägi R., Hofman A., Uitterlinden A.G., Rivadeneira F., Aulchenko Y.S., Polasek O., Hastie N., Vitart V., Helmer C., Wang J.J., Ruggiero D., Bergmann S., Kähönen M., Viikari J., Nikopensius T., Province M., Ketkar S., Colhoun H., Doney A., Robino A., Giulianini F., Krämer B.K., Portas L., Ford I., Buckley B.M., Adam M., Thun G.-A., Paulweber B., Haun M., Sala C., Metzger M., Mitchell P., Ciullo M., Kim S.K., Vollenweider P., Raitakari O., Metspalu A., Palmer C., Gasparini P., Pirastu M., Jukema J.W., Probst-Hensch N.M., Kronenberg F., Toniolo D., Gudnason V., Shuldiner A.R., Coresh J., Schmidt R., Ferrucci L., Siscovick D.S., van Duijn C.M., Borecki I., Kardia S.L.R., Liu Y., Curhan G.C., Rudan I., Gyllensten U., Wilson J.F., Franke A., Pramstaller P.P., Rettig R., Prokopenko I., Witteman J.C.M., Hayward C., Ridker P., Parsa A., Bochud M., Heid I.M., Goessling W., Chasman D.I., Kao W.H.L., Fox C.S.
Published 2019

Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (Nature Communications, (2020), 11, 1, (2539), 10.1038/s41467-019-12438-5)

by Wang, Qingbo, Pierce-Hoffman, Emma, Cummings, Beryl B., Alföldi, J., Francioli, Laurent C., Gauthier, Laura D., Hill, Andrew J., O’Donnell-Luria, A.H., Armean, Irina M., Banks, E., Bergelson, L., Cibulskis, K., Collins, R.L., Connolly, K.M., Covarrubias, M., Daly, M.J., Donnelly, S., Farjoun, Y., Ferriera, S., Gabriel, S., Gentry, J., Gupta, N., Jeandet, T., Kaplan, D., Laricchia, K.M., Llanwarne, C., Minikel, E.V., Munshi, R., Neale, B.M., Novod, S., Petrillo, N., Poterba, T., Roazen, D., Ruano-Rubio, V., Saltzman, A., Samocha, K.E., Schleicher, M., Seed, C., Solomonson, M., Soto, J., Tiao, G., Tibbetts, K., Tolonen, C., Vittal, C., Wade, G., Wang, A., Ware, J.S., Watts, N.A., Weisburd, B., Whiffin, N., Aguilar Salinas, Carlos A., Ahmad, T., Albert, C.M., Ardissino, D., Atzmon, G., Barnard, J., Beaugerie, L., Benjamin, E.J., Boehnke, M., Bonnycastle, L.L., Bottinger, E.P., Bowden, D.W., Bown, M.J., Chambers, J.C., Chan, J.C., Chasman, D., Cho, J., Chung, M.K., Cohen, B., Correa, A., Dabelea, D., Darbar, D., Duggirala, R., Dupuis, J., Ellinor, P.T., Elosua, R., Erdmann, J., Esko, T., Färkkilä, M., Florez, J., Franke, A., Getz, G., Glaser, B., Glatt, S.J., Goldstein, D., Gonzalez, C., Groop, L., Haiman, C., Hanis, C., Harms, M., Hiltunen, M., Holi, M.M., Hultman, C.M., Kallela, M., Kaprio, J., Kathiresan, S., Kim, B.-J., Kim, Y.J., Kirov, G., Kooner, J., Koskinen, S., Krumholz, H.M., Kugathasan, S., Kwak, S.H., Laakso, M., Lehtimäki, T., Loos, R.J.F., Lubitz, S.A., Ma, R.C.W., Marrugat, J., Mattila, K.M., McCarroll, S., McCarthy, M.I., McGovern, D., McPherson, R., Meigs, J.B., Melander, O., Metspalu, A., Nilsson, P.M., O’Donovan, M.C., Ongur, D., Orozco, L., Owen, M.J., Palmer, C.N.A., Palotie, A., Park, K.S., Pato, C., Pulver, A.E., Rahman, N., Remes, A.M., Rioux, J.D., Ripatti, S., Roden, D.M., Saleheen, D., Salomaa, V., Samani, N.J., Scharf, J., Schunkert, H., Shoemaker, M.B., Sklar, P., Soininen, H., Sokol, H., Spector, T., Sullivan, P.F., Suvisaari, J., Tai, E. Shyong, Teo, Yik Ying, Tiinamaija, T., Tsuang, M., Turner, D., Tusie-Luna, T., Vartiainen, E., Watkins, H., Weersma, R.K., Wessman, M., Wilson, J.G., Xavier, R.J., Vawter, M.P., Karczewski, Konrad J., MacArthur, Daniel G.
Published 2022

Erratum to: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (Nature Communications, (2018), 9, 1, (...

by Iglesias, A.I., Mishra, A., Vitart, V., Bykhovskaya, Y., Höhn, R., Springelkamp, H., Cuellar-Partida, G., Gharahkhani, P., Bailey, J.N.C., Willoughby, C.E., Li, X., Budenz, D.L., Christen, W.G., Fingert, J., Friedman, D.S., Gaasterland, D., Gaasterland, T., Hauser, M.A., Kraft, P., Lee, R.K., Lichter, P.R., Yazar, S., Liu, Y., Loomis, S.J., Moroi, S.E., Pericak-Vance, M.A., Realini, A., Richards, J.E., Schuman, J.S., Scott, W.K., Singh, K., Sit, A.J., Nag, A., Vollrath, D., Weinreb, R.N., Wollstein, G., Zack, D.J., Zhang, K., Uitterlinden, A.G., Vithana, E.N., Foster, P.J., Hysi, P.G., Hewitt, A.W., Khawaja, A.P., Khor, C.C., Pasquale, L.R., Montgomery, G.W., Klaver, C.C.W., Aung, T., Pfeiffer, N., Mackey, D.A., Hammond, C.J., Cheng, C.-Y., Craig, J.E., Polašek, O., Rabinowitz, Y.S., Wiggs, J.L., Burdon, K.P., van Duijn, C.M., MacGregor, S., Siscovick, D., Mitchell, P., Tham, Y.C., Haines, J.L., Kearns, L.S., Hayward, C., Shi, Y., van Leeuwen, E.M., Taylor, K.D., Wang, J.J., Rochtchina, E., Attia, J., Scott, R., Holliday, E.G., Wong, T.Y., Baird, P.N., Xie, J., Inouye, M., Viswanathan, A., Sim, X., Bonnemaijer, P., Rotter, J.I., Martin, N.G., Zeller, T., Mills, R.A., Souzeau, E., Staffieri, S.E., Jonas, J.B., Schmidtmann, I., Boutin, T., Kang, J.H., Lucas, S.E.M., Beutel, M.E., Wilson, J.F., Donnelly, P., Barroso, I., Blackwell, J.M., Bramon, E., Brown, M.A., Casas, J.P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H.S., Mathew, C.G., Palmer, C.N.A., Plomin, R., Rautanen, A., Sawcer, S.J., Trembath, R.C., Wood, N.W., Spencer, C.C.A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Langford, C., Hunt, S.E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S.J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., McCann, O.T., Liddle, J., Potter, S.C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Allingham, R.R., Brilliant, M.H.
Published 2022

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

by Wang, Q., Pierce-Hoffman, E., Cummings, B.B., Alföldi, J., Francioli, L.C., Gauthier, L.D., Hill, A.J., O’Donnell-Luria, A.H., Armean, I.M., Banks, E., Bergelson, L., Cibulskis, K., Collins, R.L., Connolly, K.M., Covarrubias, M., Daly, M.J., Donnelly, S., Farjoun, Y., Ferriera, S., Gabriel, S., Gentry, J., Gupta, N., Jeandet, T., Kaplan, D., Laricchia, K.M., Llanwarne, C., Minikel, E.V., Munshi, R., Neale, B.M., Novod, S., Petrillo, N., Poterba, T., Roazen, D., Ruano-Rubio, V., Saltzman, A., Samocha, K.E., Schleicher, M., Seed, C., Solomonson, M., Soto, J., Tiao, G., Tibbetts, K., Tolonen, C., Vittal, C., Wade, G., Wang, A., Ware, J.S., Watts, N.A., Weisburd, B., Whiffin, N., Aguilar Salinas, C.A., Ahmad, T., Albert, C.M., Ardissino, D., Atzmon, G., Barnard, J., Beaugerie, L., Benjamin, E.J., Boehnke, M., Bonnycastle, L.L., Bottinger, E.P., Bowden, D.W., Bown, M.J., Chambers, J.C., Chan, J.C., Chasman, D., Cho, J., Chung, M.K., Cohen, B., Correa, A., Dabelea, D., Darbar, D., Duggirala, R., Dupuis, J., Ellinor, P.T., Elosua, R., Erdmann, J., Esko, T., Färkkilä, M., Florez, J., Franke, A., Getz, G., Glaser, B., Glatt, S.J., Goldstein, D., Gonzalez, C., Groop, L., Haiman, C., Hanis, C., Harms, M., Hiltunen, M., Holi, M.M., Hultman, C.M., Kallela, M., Kaprio, J., Kathiresan, S., Kim, B.-J., Kim, Y.J., Kirov, G., Kooner, J., Koskinen, S., Krumholz, H.M., Kugathasan, S., Kwak, S.H., Laakso, M., Lehtimäki, T., Loos, R.J.F., Lubitz, S.A., Ma, R.C.W., Marrugat, J., Mattila, K.M., McCarroll, S., McCarthy, M.I., McGovern, D., McPherson, R., Meigs, J.B., Melander, O., Metspalu, A., Nilsson, P.M., O’Donovan, M.C., Ongur, D., Orozco, L., Owen, M.J., Palmer, C.N.A., Palotie, A., Park, K.S., Pato, C., Pulver, A.E., Rahman, N., Remes, A.M., Rioux, J.D., Ripatti, S., Roden, D.M., Saleheen, D., Salomaa, V., Samani, N.J., Scharf, J., Schunkert, H., Shoemaker, M.B., Sklar, P., Soininen, H., Sokol, H., Spector, T., Sullivan, P.F., Suvisaari, J., Tai, E.S., Teo, Y.Y., Tiinamaija, T., Tsuang, M., Turner, D., Tusie-Luna, T., Vartiainen, E., Watkins, H., Weersma, R.K., Wessman, M., Wilson, J.G., Xavier, R.J., Karczewski, K.J., MacArthur, D.G., Genome Aggregation Database Production Team., Genome Aggregation Database Consortium.
Published 2021

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

by Whiffin, N., Karczewski, K.J., Zhang, X., Chothani, S., Smith, M.J., Evans, D.G., Roberts, A.M., Quaife, N.M., Schafer, S., Rackham, O., Alföldi, J., Hultman, C.M., Wang, A., Wang, Q., Watts, N.A., Weisburd, B., Aguilar Salinas, C.A., Ahmad, T., Albert, C.M., Ardissino, D., Atzmon, G., Francioli, L.C., Barnard, J., Kallela, M., Beaugerie, L., Benjamin, E.J., Boehnke, M., Bonnycastle, L.L., Bottinger, E.P., Bowden, D.W., Bown, M.J., Chambers, J.C., McCarroll, S., Chan, J.C., Chasman, D., Kaprio, J., Cho, J., Chung, M.K., Cohen, B., Correa, A., Dabelea, D., Daly, M.J., Darbar, D., McCarthy, M.I., Duggirala, R., Dupuis, J., Ellinor, P.T., Kathiresan, S., Elosua, R., Erdmann, J., Esko, T., Färkkilä, M., Florez, J., Programs in Metabolism and Medical and Population Genetics, Broad Institute., McGovern, D., Department of Medicine, Harvard Medical School, Boston, MA 02115, United States., Franke, A., Getz, G., Glaser, B., Kim, B.-J., Glatt, S.J., Goldstein, D., Gonzalez, C., Groop, L., Haiman, C., McPherson, R., Hanis, C., Harms, M., Hiltunen, M., Kim, Y.J., Kirov, G., Kooner, J., Koskinen, S., O’Donnell-Luria, A.H., Krumholz, H.M., Kugathasan, S., Meigs, J.B., Kwak, S.H., Laakso, M., Lehtimäki, T., Loos, R.J.F., Lubitz, S.A., Ma, R.C.W., Marrugat, J., Mattila, K.M., Melander, O., Metspalu, A., Neale, B.M., Nilsson, P.M., Llanwarne, C., O’Donovan, M.C., Armean, I.M., Ongur, D., Orozco, L., Owen, M.J., Palmer, C.N.A., Palotie, A., Park, K.S., Pato, C., Pulver, A.E., Minikel, E.V., Rahman, N., Remes, A.M., Banks, E., Rioux, J.D., Ripatti, S., Roden, D.M., Saleheen, D., Salomaa, V., Samani, N.J., Scharf, J., Munshi, R., Schunkert, H., Shoemaker, M.B., Sklar, P., Bergelson, L., Soininen, H., Sokol, H., Spector, T., Sullivan, P.F., Suvisaari, J., Tai, E.S., Neale, B.M., Teo, Y.Y., Tiinamaija, T., Tsuang, M., Turner, D., Cibulskis, K., Tusie-Luna, T., Vartiainen, E., Watkins, H., Weersma, R.K., Wessman, M., Novod, S., Wilson, J.G., Xavier, R.J., Cook, S.A., Collins, R.L., Connolly, K.M., Covarrubias, M., Cummings, B., Daly, M.J., Donnelly, S., Farjoun, Y., Petrillo, N., Ferriera, S., Gabriel, S., Gauthier, L.D., Gentry, J., Gupta, N., Jeandet, T., Kaplan, D., Laricchia, K.M., Poterba, T., Roazen, D., Ruano-Rubio, V., Saltzman, A., Holi, M.M., Samocha, K.E., Schleicher, M., Seed, C., Solomonson, M., Soto, J., Tiao, G., Tibbetts, K., Tolonen, C., Vittal, C., Wade, G.
Published 2021

Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans (Nature, (2020), 581, 7809, (434-443), 10.1038/s41586-020-2308-7)

by Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, J., Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, A.H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Aguilar Salinas, C.A., Ahmad, T., Albert, C.M., Ardissino, D., Atzmon, G., Barnard, J., Beaugerie, L., Benjamin, E.J., Boehnke, M., Bonnycastle, L.L., Bottinger, E.P., Bowden, D.W., Bown, M.J., Chambers, J.C., Chan, J.C., Chasman, D., Cho, J., Chung, M.K., Cohen, B., Correa, A., Dabelea, D., Daly, Mark J., Darbar, D., Duggirala, R., Dupuis, J., Ellinor, P.T., Elosua, R., Erdmann, J., Esko, T., Färkkilä, M., Florez, J., Franke, A., Getz, G., Glaser, B., Glatt, S.J., Goldstein, D., Gonzalez, C., Groop, L., Haiman, C., Hanis, C., Harms, M., Hiltunen, M., Holi, M.M., Hultman, C.M., Kallela, M., Kaprio, J., Kathiresan, S., Kim, B.-J., Kim, Y.J., Kirov, G., Kooner, J., Koskinen, S., Krumholz, H.M., Kugathasan, S., Kwak, S.H., Laakso, M., Lehtimäki, T., Loos, R.J.F., Lubitz, S.A., Ma, R.C.W., MacArthur, Daniel G., Marrugat, J., Mattila, K.M., McCarroll, S., McCarthy, M.I., McGovern, D., McPherson, R., Meigs, J.B., Melander, O., Metspalu, A., Neale, Benjamin M., Nilsson, P.M., O’Donovan, M.C., Ongur, D., Orozco, L., Owen, M.J., Palmer, C.N.A., Palotie, A., Park, K.S., Pato, C., Pulver, A.E., Rahman, N., Remes, A.M., Rioux, J.D., Ripatti, S., Roden, D.M., Saleheen, D., Salomaa, V., Samani, N.J., Scharf, J., Schunkert, H., Shoemaker, M.B., Sklar, P., Soininen, H., Sokol, H., Spector, T., Sullivan, P.F., Suvisaari, J., Tai, E.S., Teo, Y.Y., Tiinamaija, T., Tsuang, M., Turner, D., Tusie-Luna, T., Vartiainen, E., Vawter, M.P., Watkins, H., Weersma, R.K., Wessman, M., Wilson, J.G., Xavier, R.J., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G., Genome Aggregation Database Consortium.
Published 2022

Author Correction: Evaluating drug targets through human loss-of-function genetic variation (Nature, (2020), 581, 7809, (459-464), 10.1038/s41586-020-2267-z)

by Minikel, Eric Vallabh, Karczewski, Konrad J., Martin, Hilary C., Cummings, Beryl B., Whiffin, Nicola, Rhodes, Daniel, Alföldi, J., Trembath, Richard C., van Heel, David A., Daly, Mark J., Alföldi, J., Armean, I.M., Banks, E., Bergelson, L., Cibulskis, K., Collins, R.L., Connolly, K.M., Covarrubias, M., Cummings, Beryl B., Daly, Mark J., Donnelly, S., Farjoun, Y., Ferriera, S., Francioli, L., Gabriel, S., Gauthier, L.D., Gentry, J., Gupta, N., Jeandet, T., Kaplan, D., Karczewski, Konrad J., Laricchia, K.M., Llanwarne, C., Minikel, Eric Vallabh, Munshi, R., Neale, B.M., Novod, S., O’Donnell-Luria, A.H., Petrillo, N., Poterba, T., Roazen, D., Ruano-Rubio, V., Saltzman, A., Samocha, K.E., Schleicher, M., Seed, C., Solomonson, M., Soto, J., Tiao, G., Tibbetts, K., Tolonen, C., Vittal, C., Wade, G., Wang, A., Wang, Q., Ware, J.S., Watts, N.A., Weisburd, B., Whiffin, Nicola, Aguilar Salinas, C.A., Ahmad, T., Albert, C.M., Ardissino, D., Atzmon, G., Barnard, J., Beaugerie, L., Benjamin, E.J., Boehnke, M., Bonnycastle, L.L., Bottinger, E.P., Bowden, D.W., Bown, M.J., Chambers, J.C., Chan, J.C., Chasman, D., Cho, J., Chung, M.K., Cohen, B., Correa, A., Dabelea, D., Daly, Mark J., Darbar, D., Duggirala, R., Dupuis, J., Ellinor, P.T., Elosua, R., Erdmann, J., Esko, T., Färkkilä, M., Florez, J., Franke, A., Getz, G., Glaser, B., Glatt, S.J., Goldstein, D., Gonzalez, C., Groop, L., Haiman, C., Hanis, C., Harms, M., Hiltunen, M., Holi, M.M., Hultman, C.M., Kallela, M., Kaprio, J., Kathiresan, S., Kim, B.-J., Kim, Y.J., Kirov, G., Kooner, J., Koskinen, S., Krumholz, H.M., Kugathasan, S., Kwak, S.H., Laakso, M., Lehtimäki, T., Loos, R.J.F., Lubitz, S.A., Ma, R.C.W., MacArthur, Daniel G., Marrugat, J., Mattila, K.M., McCarroll, S., McCarthy, M.I., McGovern, D., McPherson, R., Meigs, J.B., Melander, O., Metspalu, A., Neale, B.M., Nilsson, P.M., O’Donovan, M.C., Ongur, D., Orozco, L., Owen, M.J., Palmer, C.N.A., Palotie, A., Park, K.S., Pato, C., Pulver, A.E., Rahman, N., Remes, A.M., Rioux, J.D., Ripatti, S., Roden, D.M., Saleheen, D., Salomaa, V., Samani, N.J., Scharf, J., Schunkert, H., Shoemaker, M.B., Sklar, P., Soininen, H., Sokol, H., Spector, T., Sullivan, P.F., Suvisaari, J., Tai E Shyong, Yik Ying Teo, Tiinamaija, T., Tsuang, M., Dan Turner, T., Tusie-Luna, T., Vartiainen, E., Vawter, M.P., Watkins, H., Weersma, R.K., Wessman, M., Wilson, J.G., Xavier, R.J., Schreiber, Stuart L., MacArthur, Daniel G., Genome Aggregation Database Production Team., Genome Aggregation Database Consortium.
Published 2022

Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (Nature Communications, (2020), 11, 1, (2523), 10.1038/s41467...

by Whiffin, Nicola, Karczewski, Konrad J., Zhang, Xiaolei, Chothani, Sonia, Smith, Miriam J., Evans, D. Gareth, Roberts, Angharad M., Quaife, Nicholas M., Schafer, Sebastian, Rackham, Owen, Alföldi, J., O’Donnell-Luria, A.H., Francioli, Laurent C., Armean, Irina M., Banks, E., Bergelson, L., Cibulskis, K., Collins, R.L., Connolly, K.M., Covarrubias, M., Cummings, B., Daly, M.J., Donnelly, S., Farjoun, Y., Ferriera, S., Gabriel, S., Gauthier, L.D., Gentry, J., Gupta, N., Jeandet, T., Kaplan, D., Laricchia, K.M., Llanwarne, C., Minikel, E.V., Munshi, R., Neale, B.M., Novod, S., Petrillo, N., Poterba, T., Roazen, D., Ruano-Rubio, V., Saltzman, A., Samocha, K.E., Schleicher, M., Seed, C., Solomonson, M., Soto, J., Tiao, G., Tibbetts, K., Tolonen, C., Vittal, C., Wade, G., Wang, A., Wang, Q., Watts, N.A., Weisburd, B., Aguilar Salinas, Carlos A., Ahmad, T., Albert, C.M., Ardissino, D., Atzmon, G., Barnard, J., Beaugerie, L., Benjamin, E.J., Boehnke, M., Bonnycastle, L.L., Bottinger, E.P., Bowden, D.W., Bown, M.J., Chambers, J.C., Chan, J.C., Chasman, D., Cho, J., Chung, M.K., Cohen, B., Correa, A., Dabelea, D., Daly, M.J., Darbar, D., Duggirala, R., Dupuis, J., Ellinor, P.T., Elosua, R., Erdmann, J., Esko, T., Färkkilä, M., Florez, J., Programs in Metabolism and Medical and Population Genetics, Broad Institute., Department of Medicine, Harvard Medical School, Boston, MA 02115, United States., Franke, A., Getz, G., Glaser, B., Glatt, S.J., Goldstein, D., Gonzalez, C., Groop, L., Haiman, C., Hanis, C., Harms, M., Hiltunen, M., Holi, M.M., Hultman, C.M., Kallela, M., Kaprio, J., Kathiresan, S., Kim, B.-J., Kim, Y.J., Kirov, G., Kooner, J., Koskinen, S., Krumholz, H.M., Kugathasan, S., Kwak, S.H., Laakso, M., Lehtimäki, T., Loos, R.J.F., Lubitz, S.A., Ma, R.C.W., Marrugat, J., Mattila, K.M., McCarroll, S., McCarthy, M.I., McGovern, D., McPherson, R., Meigs, J.B., Melander, O., Metspalu, A., Neale, B.M., Nilsson, P.M., O’Donovan, M.C., Ongur, D., Orozco, L., Owen, M.J., Palmer, C.N.A., Palotie, A., Park, K.S., Pato, C., Pulver, A.E., Rahman, N., Remes, A.M., Rioux, J.D., Ripatti, S., Roden, D.M., Saleheen, D., Salomaa, V., Samani, N.J., Scharf, J., Schunkert, H., Shoemaker, M.B., Sklar, P., Soininen, H., Sokol, H., Spector, T., Sullivan, P.F., Suvisaari, J., Tai, E. Shyong, Teo, Yik Ying, Tiinamaija, T., Tsuang, M., Turner, D., Tusie-Luna, T., Vartiainen, E., Watkins, H., Weersma, R.K., Wessman, M., Wilson, J.G., Xavier, R.J., Vawter, M.P., Cook, Stuart A., Barton, Paul J. R., MacArthur, Daniel G., Ware, James S.
Published 2022

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

by Springelkamp, H, Höhn, R, Mishra, A, Hysi, P.G, Khor, C.-C, Loomis, S.J, Bailey, J.N.C, Gibson, J, Thorleifsson, G, Janssen, S.F, Luo, X, Ramdas, W.D, Vithana, E, Nongpiur, M.E, Montgomery, G.W, Xu, L, Mountain, J.E, Gharahkhani, P, Lu, Y, Amin, N, Karssen, L.C, Sim, K.-S, Van Leeuwen, E.M, Iglesias, A.I, Verhoeven, V.J.M, Hauser, M.A, Loon, S.-C, Despriet, D.D.G, Nag, A, Venturini, C, Sanfilippo, P.G, Schillert, A, Kang, J.H, Landers, J, Jonasson, F, Cree, A.J, Van Koolwijk, L.M.E, Rivadeneira, F, Souzeau, E, Jonsson, V, Menon, G, Mitchell, P, Wang, J.J, Rochtchina, E, Attia, J, Scott, R, Holliday, E.G, Baird, P.N, Xie, J, Inouye, M, Viswanathan, A, Sim, X, Weinreb, R.N, De Jong, P.T.V.M, Oostra, B.A, Uitterlinden, A.G, Hofman, A, Ennis, S, Thorsteinsdottir, U, Burdon, K.P, Allingham, R.R, Brilliant, M.H, Budenz, D.L, Christen, W.G, Fingert, J, Friedman, D.S, Gaasterland, D, Gaasterland, T, Haines, J.L, Kang, J.H, Kraft, P, Lee, R.K, Lichter, P.R, Liu, Y, Moroi, S.E, Pericak-Vance, M.A, Realini, A, Richards, J.E, Schuman, J.S, Scott, W.K, Singh, K, Sit, A.J, Vollrath, D, Wollstein, G, Zack, D.J, Zhang, K, Barroso, I, Blackwell, J.M, Bramon, E, Brown, M.A, Casas, J.P, Corvin, A, Deloukas, P, Duncanson, A, Jankowski, J, Markus, H.S, Mathew, C.G, Palmer, C.N.A, Plomin, R, Rautanen, A, Sawcer, S.J, Trembath, R.C, Viswanathan, A.C, Wood, N.W, Spencer, C.C.A, Band, G, Bellenguez, C, Freeman, C, Hellenthal, G, Giannoulatou, E, Pirinen, M, Pearson, R, Strange, A, Su, Z, Vukcevic, D, Donnelly, P, Langford, C, Hunt, S.E, Edkins, S, Gwilliam, R, Blackburn, H, Bumpstead, S.J, Dronov, S, Gillman, M, Gray, E, Hammond, N, Jayakumar, A, McCann, O.T, Liddle, J, Potter, S.C, Ravindrarajah, R, Ricketts, M, Waller, M, Weston, P, Widaa, S, Whittaker, P, Spector, T.D, Mirshahi, A, Saw, S.-M, Vingerling, J.R, Teo, Y.-Y, Wolfs, R.C.W, Lemij, H.G, Tai, E.-S, Jansonius, N.M, Jonas, J.B, Cheng, C.-Y, Aung, T, Klaver, C.C.W, Craig, J.E, MacGregor, S, MacKey, D.A, Lotery, A.J, Stefansson, K, Bergen, A.A.B, Young, T.L, Wiggs, J.L, Pfeiffer, N, Wong, T.-Y, Pasquale, L.R, Hewitt, A.W, Van Duijn, C.M, Hammond, C.J, Blue Mountains Eye Study-GWAS groupw, NEIGHBORHOOD Consortiumz, Wellcome Trust Case Control Consortium 2 (WTCCC2), Data and Analysis Group, DNA, Genotyping, Data QC and Informatics Group, Publications Committee
Published 2020

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

by Morris, A.P., Voight, B.F., Teslovich, T.M., Ferreira, T., Segrè, A.V., Steinthorsdottir, V., Strawbridge, R.J., Khan, H., Grallert, H., Mahajan, A., Prokopenko, I., Kang, H.M., Dina, C., Esko, T., Fraser, R.M., Kanoni, S., Kumar, A., Lagou, V., Langenberg, C., Luan, J., Lindgren, C.M., Müller-Nurasyid, M., Pechlivanis, S., Rayner, N.W., Scott, L.J., Wiltshire, S., Yengo, L., Kinnunen, L., Rossin, E.J., Raychaudhuri, S., Johnson, A.D., Dimas, A.S., Loos, R.J.F., Vedantam, S., Chen, H., Florez, J.C., Fox, C., Liu, C.-T., Rybin, D., Couper, D.J., Kao, W.H.L., Li, M., Cornelis, M.C., Kraft, P., Sun, Q., Van Dam, R.M., Stringham, H.M., Chines, P.S., Fischer, K., Fontanillas, P., Holmen, O.L., Hunt, S.E., Jackson, A.U., Kong, A., Lawrence, R., Meyer, J., Perry, J.R.B., Platou, C.G.P., Potter, S., Rehnberg, E., Robertson, N., Sivapalaratnam, S., Stančáková, A., Stirrups, K., Thorleifsson, G., Tikkanen, E., Wood, A.R., Almgren, P., Atalay, M., Benediktsson, R., Bonnycastle, L.L., Burtt, N., Carey, J., Charpentier, G., Crenshaw, A.T., Doney, A.S.F., Dorkhan, M., Edkins, S., Emilsson, V., Eury, E., Forsen, T., Gertow, K., Gigante, B., Grant, G.B., Groves, C.J., Guiducci, C., Herder, C., Hreidarsson, A.B., Hui, J., James, A., Jonsson, A., Rathmann, W., Klopp, N., Kravic, J., Krjutškov, K., Langford, C., Leander, K., Lindholm, E., Lobbens, S., MäNnistö, S., Mirza, G., MüHleisen, T.W., Musk, B., Parkin, M., Rallidis, L., Saramies, J., Sennblad, B., Shah, S., Sigursson, G., Silveira, A., Steinbach, G., Thorand, B., Trakalo, J., Veglia, F., Wennauer, R., Winckler, W., Zabaneh, D., Campbell, H., Van Duijn, C., Uitterlinden, A.G., Hofman, A., Sijbrands, E., Abecasis, G.R., Owen, K.R., Zeggini, E., Trip, M.D., Forouhi, N.G., Syvänen, A.-C., Eriksson, J.G., Peltonen, L., Nöthen, M.M., Balkau, B., Palmer, C.N.A., Lyssenko, V., Tuomi, T., Isomaa, B., Hunter, D.J., Qi, L., Shuldiner, A.R., Roden, M., Barroso, I., Wilsgaard, T., Beilby, J., Hovingh, K., Price, J.F., Wilson, J.F., Rauramaa, R., Lakka, T.A., Lind, L., Dedoussis, G., NjøLstad, I., Pedersen, N.L., Khaw, K.-T., Wareham, N.J., Keinanen-Kiukaanniemi, S.M., Saaristo, T.E., Korpi-HyöVäLti, E., Saltevo, J., Laakso, M., Kuusisto, J., Metspalu, A., Collins, F.S., Mohlke, K.L., Bergman, R.N., Tuomilehto, J., Boehm, B.O., Gieger, C., Hveem, K., Cauchi, S., Froguel, P., Baldassarre, D., Tremoli, E., Humphries, S.E., Saleheen, D., Danesh, J., Ingelsson, E., Ripatti, S., Salomaa, V., Erbel, R., JöCkel, K.-H., Moebus, S., Peters, A., Illig, T., Faire, U.D., Hamsten, A., Morris, A.D., Donnelly, P.J., Frayling, T.M., Hattersley, A.T., Boerwinkle, E., Melander, O., Kathiresan, S., Nilsson, P.M., Deloukas, P., Thorsteinsdottir, U., Groop, L.C., Stefansson, K., Hu, F., Pankow, J.S., Dupuis, J., Meigs, J.B., Altshuler, D., Boehnke, M., McCarthy, M.I.
Published 2014

Erratum: Atomic layer deposition of a MoS2 film (Nanoscale (2014) 6 (10584-10588))

by Springelkamp, H, Höhn, R, Mishra, A, Hysi, P.G, Khor, C.-C, Loomis, S.J, Bailey, J.N.C, Gibson, J, Thorleifsson, G, Janssen, S.F, Luo, X, Ramdas, W.D, Vithana, E, Nongpiur, M.E, Montgomery, G.W, Xu, L, Mountain, J.E, Gharahkhani, P, Lu, Y, Amin, N, Karssen, L.C, Sim, K.-S, Van Leeuwen, E.M, Iglesias, A.I, Verhoeven, V.J.M, Hauser, M.A, Loon, S.-C, Despriet, D.D.G, Nag, A, Venturini, C, Sanfilippo, P.G, Schillert, A, Kang, J.H, Landers, J, Jonasson, F, Cree, A.J, Van Koolwijk, L.M.E, Rivadeneira, F, Souzeau, E, Jonsson, V, Menon, G, Mitchell, P, Wang, J.J, Rochtchina, E, Attia, J, Scott, R, Holliday, E.G, Baird, P.N, Xie, J, Inouye, M, Viswanathan, A, Sim, X, Weinreb, R.N, De Jong, P.T.V.M, Oostra, B.A, Uitterlinden, A.G, Hofman, A, Ennis, S, Thorsteinsdottir, U, Burdon, K.P, Allingham, R.R, Brilliant, M.H, Budenz, D.L, Christen, W.G, Fingert, J, Friedman, D.S, Gaasterland, D, Gaasterland, T, Haines, J.L, Kang, J.H, Kraft, P, Lee, R.K, Lichter, P.R, Liu, Y, Moroi, S.E, Pericak-Vance, M.A, Realini, A, Richards, J.E, Schuman, J.S, Scott, W.K, Singh, K, Sit, A.J, Vollrath, D, Wollstein, G, Zack, D.J, Zhang, K, Barroso, I, Blackwell, J.M, Bramon, E, Brown, M.A, Casas, J.P, Corvin, A, Deloukas, P, Duncanson, A, Jankowski, J, Markus, H.S, Mathew, C.G, Palmer, C.N.A, Plomin, R, Rautanen, A, Sawcer, S.J, Trembath, R.C, Viswanathan, A.C, Wood, N.W, Spencer, C.C.A, Band, G, Bellenguez, C, Freeman, C, Hellenthal, G, Giannoulatou, E, Pirinen, M, Pearson, R, Strange, A, Su, Z, Vukcevic, D, Donnelly, P, Langford, C, Hunt, S.E, Edkins, S, Gwilliam, R, Blackburn, H, Bumpstead, S.J, Dronov, S, Gillman, M, Gray, E, Hammond, N, Jayakumar, A, McCann, O.T, Liddle, J, Potter, S.C, Ravindrarajah, R, Ricketts, M, Waller, M, Weston, P, Widaa, S, Whittaker, P, Spector, T.D, Mirshahi, A, Saw, S.-M, Vingerling, J.R, Teo, Y.-Y, Wolfs, R.C.W, Lemij, H.G, Tai, E.-S, Jansonius, N.M, Jonas, J.B, Cheng, C.-Y, Aung, T, Klaver, C.C.W, Craig, J.E, MacGregor, S, MacKey, D.A, Lotery, A.J, Stefansson, K, Bergen, A.A.B, Young, T.L, Wiggs, J.L, Pfeiffer, N, Wong, T.-Y, Pasquale, L.R, Hewitt, A.W, Van Duijn, C.M, Hammond, C.J, Blue Mountains Eye Study-GWAS groupw, NEIGHBORHOOD Consortiumz, Wellcome Trust Case Control Consortium 2 (WTCCC2), Data and Analysis Group, DNA, Genotyping, Data QC and Informatics Group, Publications Committee, Tan, L.K, Liu, B, Teng, J.H, Guo, S, Low, H.Y, Loh, K.P
Published 2020

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis

by Wheeler E., Leong A., Liu C.-T., Hivert M.-F., Strawbridge R.J., Podmore C., Li M., Yao J., Sim X., Hong J., Chu A.Y., Pereira M.A., Peters A., Ridker P.M., Sabanayagam C., Sale M., Saleheen D., Saltevo J., Schwarz P.E.H., Sheu W.H.H., Chang L.-C., Müller-Nurasyid M., Snieder H., Spector T.D., Tabara Y., Tuomilehto J., van Dam R.M., Wilson J.G., Wilson J.F., Wolffenbuttel B.H.R., Chen W.-M., Elks C.E., Nagaraja R., Evans D.S., Fan Q., Giulianini F., Go M.J., Hottenga J.-J., Hu Y., Jackson A.U., Kanoni S., Kim Y.J., Kleber M.E., Nauck M., Ladenvall C., Lecoeur C., Lim S.-H., Lu Y., Mahajan A., Marzi C., Nalls M.A., Navarro P., Nolte I.M., Rose L.M., Pankow J.S., Rybin D.V., Sanna S., Shi Y., Stram D.O., Takeuchi F., Tan S.P., van der Most P.J., Van Vliet-Ostaptchouk J.V., Wong A., Yengo L., Polasek O., Zhao W., Goel A., Martinez Larrad M.T., Radke D., Salo P., Tanaka T., van Iperen E.P.A., Abecasis G., Afaq S., Alizadeh B.Z., Prokopenko I., Bertoni A.G., Bonnefond A., Böttcher Y., Bottinger E.P., Campbell H., Carlson O.D., Chen C.-H., Cho Y.S., Garvey W.T., Gieger C., Ramos P.S., Goodarzi M.O., Grallert H., Hamsten A., Hartman C.A., Herder C., Hsiung C.A., Huang J., Igase M., Isono M., Katsuya T., Rasmussen-Torvik L., Khor C.-C., Kiess W., Kohara K., Kovacs P., Lee J., Lee W.-J., Lehne B., Li H., Liu J., Lobbens S., Rathmann W., Luan J., Lyssenko V., Meitinger T., Miki T., Miljkovic I., Moon S., Mulas A., Müller G., Rich S.S., Zhang W., Robertson N.R., Roden M., Roussel R., Rudan I., Scott R.A., Scott W.R., Sennblad B., Siscovick D.S., Strauch K., Sun L., Wang X., Swertz M., Tajuddin S.M., Taylor K.D., Teo Y.-Y., Tham Y.C., Tönjes A., Wareham N.J., Willemsen G., Wilsgaard T., Hingorani A.D., Chen P., Egan J., Ferrucci L., Hovingh G.K., Jula A., Kivimaki M., Kumari M., Njølstad I., Palmer C.N.A., Serrano Ríos M., Stumvoll M., Maruthur N.M., Watkins H., Aung T., Blüher M., Boehnke M., Boomsma D.I., Bornstein S.R., Chambers J.C., Chasman D.I., Chen Y.-D.I., Chen Y.-T., Porneala B.C., Cheng C.-Y., Cucca F., de Geus E.J.C., Deloukas P., Evans M.K., Fornage M., Friedlander Y., Froguel P., Groop L., Gross M.D., Sharp S.J., Harris T.B., Hayward C., Heng C.-K., Ingelsson E., Kato N., Kim B.-J., Koh W.-P., Kooner J.S., Körner A., Kuh D., Jia Y., Kuusisto J., Laakso M., Lin X., Liu Y., Loos R.J.F., Magnusson P.K.E., März W., McCarthy M.I., Oldehinkel A.J., Ong K.K., Kabagambe E.K., Pedersen N.L.
Published 2020