Nature Genetics, 1546-1718

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  1. 2019
  2. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

    Justice, A. E., Paul Franks, North, K. E., Lindgren, C. M. & et al., 2019, In : Nature Genetics. 51, p. 452–469

    Research output: Contribution to journalArticle

  3. Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

    International Consortium for Blood Pressure, Giri, A., Almgren, P., Olle Melander, Hung, A. M. & Edwards, T. L., 2019, In : Nature Genetics. 51, 1, p. 51-62 12 p.

    Research output: Contribution to journalArticle

  4. 2018
  5. Multi-ethnic genome-wide association study for atrial fibrillation

    Roselli, C., Chaffin, M. D., Weng, L. C., Aeschbacher, S., Ahlberg, G., Albert, C. M., Almgren, P., Alonso, A., Anderson, C. D., Aragam, K. G., Arking, D. E., Barnard, J., Bartz, T. M., Benjamin, E. J., Bihlmeyer, N. A., Bis, J. C., Bloom, H. L., Boerwinkle, E., Bottinger, E. B., Brody, J. A. & 33 othersCalkins, H., Campbell, A., Cappola, T. P., Carlquist, J., Chasman, D. I., Chen, L. Y., Chen, Y. D. I., Choi, E. K., Choi, S. H., Christophersen, I. E., Chung, M. K., Cole, J. W., Conen, D., Cook, J., Crijns, H. J., Cutler, M. J., Damrauer, S. M., Daniels, B. R., Darbar, D., Delgado, G., Denny, J. C., Dichgans, M., Dörr, M., Dudink, E. A., Dudley, S. C., Gustafsson, S., Lindgren, C. M., Olle Melander, Peter Nilsson, Marju Orho-Melander, Lubitz, S. A., Lunetta, K. L. & Ellinor, P. T., 2018 Sep, In : Nature Genetics. 50, 9, p. 1225-1233

    Research output: Contribution to journalArticle

  6. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

    NBCS Collaborators, kConFab/AOCS Investigators, Wu, L., Shi, W., Long, J., Guo, X., Michailidou, K., Beesley, J., Bolla, M. K., Shu, X. O., Lu, Y., Cai, Q., Al-Ejeh, F., Rozali, E., Wang, Q., Dennis, J., Li, B., Zeng, C., Feng, H., Gusev, A. & 32 othersBarfield, R. T., Andrulis, I. L., Anton-Culver, H., Arndt, V., Aronson, K. J., Auer, P. L., Barrdahl, M., Baynes, C., Beckmann, M. W., Benitez, J., Bermisheva, M., Blomqvist, C., Bogdanova, N. V., Bojesen, S. E., Brauch, H., Brenner, H., Brinton, L., Per Broberg, Brucker, S. Y., Burwinkel, B., Caldés, T., Canzian, F., Carter, B. D., Castelao, J. E., Chang-Claude, J., Chen, X., Cheng, T. Y. D., Christiansen, H., Clarke, C. L., Collée, M., Humphreys, K. & Håkan Olsson, 2018 Jul, In : Nature Genetics. 50, 7, p. 968-978

    Research output: Contribution to journalArticle

  7. Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer

    Jenny Karlsson, Anders Valind, Linda Holmquist Mengelbier, Bredin, S., Louise Cornmark, Jansson, C., Wali, A., Johan Staaf, Viklund, B., Ingrid Øra, Anna Börjesson, Backman, T., Noémie Braekeveldt, Sandstedt, B., Pal, N., Isaksson, A., Lackner, B. G., Tord Jonson, Daniel Bexell & David Gisselsson, 2018 Jul, In : Nature Genetics. 50, 7, p. 944-950

    Research output: Contribution to journalArticle

  8. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

    Malik, R., Chauhan, G., Traylor, M., Sargurupremraj, M., Okada, Y., Mishra, A., Almgren, P., Olle Melander, Gunnar Engström, Arne Lindgren, Hossein Delavaran, Andreea Ilinca, Bo Norrving & MEGASTROKE Consortium, 2018 Apr, In : Nature Genetics. 50, 4, p. 524-537

    Research output: Contribution to journalArticle

  9. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

    The Million Veteran Program, Evangelou, E., Almgren, P., Olle Melander, Elliott, P. & Caulfield, M. J., 2018, In : Nature Genetics. 50, 10, p. 1412-1425 14 p.

    Research output: Contribution to journalArticle

  10. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    Turcot, V., Lu, Y., Highland, H. M., Schurmann, C., Justice, A. E., Fine, R. S., Paul Franks, Frida Renström & Tibor V Varga, 2018, In : Nature Genetics. 50, 1, p. 26-35 10 p.

    Research output: Contribution to journalArticle

  11. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article

    Mahajan, A., Wessel, J., Willems, S. M., Zhao, W., Robertson, N. R., Chu, A. Y., Jasmina Kravic, Emma Ahlqvist, Anders Rosengren, Leif Groop, Tibor V Varga, Paul Franks, Almgren, P., Olle Melander, Marju Orho-Melander & McCarthy, M. I., 2018, In : Nature Genetics. 50, 4, p. 559-571 13 p.

    Research output: Contribution to journalArticle

  12. 2017
  13. Association analyses based on false discovery rate implicate new loci for coronary artery disease

    Nelson, C. P., Goel, A., Butterworth, A. S., Kanoni, S., Webb, T. R., Marouli, E., Zeng, L., Ntalla, I., Lai, F. Y., Hopewell, J. C., Giannakopoulou, O., Jiang, T., Hamby, S. E., Di Angelantonio, E., Assimes, T. L., Bottinger, E. P., Chambers, J. C., Clarke, R., Palmer, C. N. A., Cubbon, R. M. & 42 othersEllinor, P. T., Ermel, R., Evangelou, E., Paul W. Franks, Grace, C., Gu, D., Hingorani, A. D., Howson, J. M. M., Ingelsson, E., Kastrati, A., Kessler, T., Kyriakou, T., Lehtimäki, T., Lu, X., Lu, Y., März, W., McPherson, R., Metspalu, A., Pujades-Rodriguez, M., Ruusalepp, A., Schadt, E., Schmidt, A. F., Sweeting, M. J., Zalloua, P. A., Alghalayini, K., Keavney, B. D., Kooner, J. S., Loos, R. J. F., Patel, R. S., Rutter, M. K., Tomaszewski, M., Tzoulaki, I., Zeggini, E., Erdmann, J., Dedoussis, G., Björkegren, J. L. M., Schunkert, H., Farrall, M., Danesh, J., Samani, N. J., Watkins, H. & Deloukas, P., 2017 Sep 1, In : Nature Genetics. 49, 9, p. 1385-1391 7 p.

    Research output: Contribution to journalArticle

  14. Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

    McKay, J. D., Hung, R. J., Han, Y., Zong, X., Carreras-Torres, R., Christiani, D. C., Caporaso, N. E., Johansson, M., Xiao, X., Li, Y., Byun, J., Dunning, A., Pooley, K. A., Qian, D. C., Ji, X., Liu, G., Timofeeva, M. N., Bojesen, S. E., Wu, X., Le Marchand, L. & 31 othersAlbanes, D., Bickeböller, H., Aldrich, M. C., Bush, W. S., Tardon, A., Rennert, G., Teare, M. D., Field, J. K., Kiemeney, L. A., Lazarus, P., Haugen, A., Lam, S., Schabath, M. B., Andrew, A. S., Shen, H., Hong, Y-C., Yuan, J-M., Bertazzi, P. A., Pesatori, A. C., Ye, Y., Diao, N., Su, L., Zhang, R., Brhane, Y., Leighl, N., Johansen, J. S., Hans Brunnström, Jonas Manjer, Olle Melander, Song, L. & SpiroMeta Consortium, 2017 Jul, In : Nature Genetics. 49, 7, p. 1126-1132 7 p.

    Research output: Contribution to journalLetter

  15. Functional screen of MSI2 interactors identifies an essential role for SYNCRIP in myeloid leukemia stem cells

    Vu, L. P., Prieto, C., Amin, E. M., Chhangawala, S., Krivtsov, A., Calvo-Vidal, M. N., Chou, T., Chow, A., Minuesa, G., Park, S. M., Barlowe, T. S., Taggart, J., Tivnan, P., Deering, R. P., Chu, L. P., Kwon, J. A., Meydan, C., Perales-Paton, J., Arshi, A., Gönen, M. & 23 othersFamulare, C., Patel, M., Paietta, E., Tallman, M. S., Lu, Y., Glass, J., Garret-Bakelman, F. E., Melnick, A., Levine, R. L., Al-Shahrour, F., Marcus Järås, Hacohen, N., Hwang, A., Garippa, R., Lengner, C. J., Armstrong, S. A., Cerchietti, L., Cowley, G. S., Root, D. E., Doench, J., Leslie, C., Ebert, B. L. & Kharas, M. G., 2017 Jun 1, In : Nature Genetics. 49, 6, p. 866-875 10 p.

    Research output: Contribution to journalArticle

  16. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

    Phelan, C. M., Kuchenbaecker, K. B., Tyrer, J. P., Kar, S. P., Lawrenson, K., Winham, S. J., Dennis, J., Pirie, A., Riggan, M. J., Chornokur, G., Earp, M. A., Lyra, P. C., Lee, J. M., Coetzee, S., Beesley, J., McGuffog, L., Soucy, P., Dicks, E., Lee, A., Barrowdale, D. & 36 othersLecarpentier, J., Leslie, G., Aalfs, C. M., Aben, K. K. H., Adams, M., Adlard, J., Andrulis, I. L., Anton-Culver, H., Antonenkova, N., Aravantinos, G., Arnold, N., Arun, B. K., Arver, B., Azzollini, J., Balmaña, J., Banerjee, S. N., Barjhoux, L., Barkardottir, R. B., Bean, Y., Beckmann, M. W., Beeghly-Fadiel, A., Benitez, J., Bermisheva, M., Bernardini, M. Q., Birrer, M. J., Åke Borg, Per Broberg, Jernetz, M., Päivi Kannisto, Håkan Olsson, HEBON Study, AOCS study group, EMBRACE Study, OPAL study group, KConFab Investigators & GEMO Study Collaborators, 2017 May 1, In : Nature Genetics. 49, 5, p. 680-691 12 p.

    Research output: Contribution to journalArticle

  17. A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers

    Glodzik, D., Morganella, S., Davies, H. R., Simpson, P. T., Li, Y., Zou, X., Diez-Perez, J., Staaf, J., Alexandrov, L. B., Smid, M., Brinkman, A. B., Rye, I. H., Russnes, H., Raine, K., Purdie, C. A., Lakhani, S. R., Thompson, A. M., Birney, E., Stunnenberg, H. G., van de Vijver, M. J. & 10 othersMartens, J. W. M., Børresen-Dale, A-L., Richardson, A. L., Kong, G., Viari, A., Easton, D., Evan, G., Campbell, P. J., Stratton, M. R. & Nik-Zainal, S., 2017 Mar 1, In : Nature Genetics. 49, 3, p. 341-348 8 p.

    Research output: Contribution to journalArticle

  18. Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

    Lotta, L. A., Gulati, P., Day, F. R., Payne, F., Ongen, H., van de Bunt, M., Gaulton, K. J., Eicher, J. D., Sharp, S. J., Luan, J., De Lucia Rolfe, E., Stewart, I. D., Wheeler, E., Willems, S. M., Adams, C., Yaghootkar, H., Sharp, S. J., Forouhi, N. G., Kerrison, N. D., Sims, M. & 32 othersLucarelli, D. M. E., Deloukas, P., McCarthy, M. I., Arriola, L., Balkau, B., Barricarte, A., Boeing, H., Paul W. Franks, Gonzalez, C., Grioni, S., Kaaks, R., Key, T. J., Navarro, C., Peter M. Nilsson, Overvad, K., Palli, D., Panico, S., Quirós, J. R., Rolandsson, O., Sacerdote, C., Salamanca-Fernández, E., Slimani, N., Tjonneland, A., Tumino, R., Spijkerman, A. M. W., van der A, D. L., van der Schouw, Y. T., Riboli, E., Semple, R. K., Stears, A., Cambridge FPLD1 Consortium & EPIC-InterAct Consortium, 2017 Jan 1, In : Nature Genetics. 49, 1, p. 17-26 10 p.

    Research output: Contribution to journalArticle

  19. Exome-wide association study of plasma lipids in >300,000 individuals

    Liu, D. J., Peloso, G. M., Yu, H., Butterworth, A. S., Mahajan, A., Saleheen, D., Paul Franks, Frida Renström, Tibor V Varga, Leif Groop, Olle Melander & Marju Orho-Melander, 2017, In : Nature Genetics. 49, 12, p. 1758-1766 9 p.

    Research output: Contribution to journalArticle

  20. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

    Zhao, W., Rasheed, A., Tikkanen, E., Lee, J-J., Butterworth, A. S., Howson, J. M. M., Marju Orho-Melander & Olle Melander, 2017, In : Nature Genetics. 49, 10, p. 1450-1457 8 p.

    Research output: Contribution to journalArticle

  21. Identification of sequence variants influencing immunoglobulin levels

    Jonsson, S., Sveinbjornsson, G., de Lapuente Portilla, A. L., Swaminathan, B., Plomp, R., Dekkers, G., Ajore, R., Ali, M., Bentlage, A. E. H., Elmér, E., Eyjolfsson, G. I., Gudjonsson, S. A., Gullberg, U., Gylfason, A., Halldorsson, B. V., Hansson, M., Holm, H., Johansson, Å., Johnsson, E., Jonasdottir, A. & 18 othersLudviksson, B. R., Oddsson, A., Olafsson, I., Olafsson, S., Sigurdardottir, O., Sigurdsson, A., Stefansdottir, L., Masson, G., Sulem, P., Wuhrer, M., Anna-Karin Wihlborg, Thorleifsson, G., Gudbjartsson, D. F., Thorsteinsdottir, U., Vidarsson, G., Jonsdottir, I., Björn Nilsson & Stefansson, K., 2017, In : Nature Genetics. 49, 8, p. 1182-1191

    Research output: Contribution to journalArticle

  22. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

    Milne, R. L., Kuchenbaecker, K. B., Michailidou, K., Beesley, J., Kar, S., Lindström, S., Per Broberg, Håkan Olsson & Hans Ehrencrona, 2017, In : Nature Genetics. 49, 12, p. 1767-1778 12 p.

    Research output: Contribution to journalArticle

  23. Lgr6 is a stem cell marker in mouse skin squamous cell carcinoma

    Huang, P. Y., Kandyba, E., Jabouille, A., Jonas Sjölund, Kumar, A., Halliwill, K. D., McCreery, M., DelRosario, R., Kang, H. C., Wong, C. E., Seibler, J., Beuger, V., Pellegrino, M., Sciambi, A., Eastburn, D. J. & Balmain, A., 2017, In : Nature Genetics. 49, 11, p. 1624–1632

    Research output: Contribution to journalArticle

  24. 2016
  25. The genomic landscape of core-binding factor acute myeloid leukemias

    Faber, Z. J., Chen, X., Gedman, A. L., Boggs, K., Cheng, J., Ma, J., Radtke, I., Chao, J-R., Walsh, M. P., Song, G., Andersson, A. K., Dang, J., Dong, L., Liu, Y., Huether, R., Cai, Z., Mulder, H., Wu, G., Edmonson, M., Rusch, M. & 29 othersQu, C., Li, Y., Vadodaria, B., Wang, J., Hedlund, E., Cao, X., Yergeau, D., Nakitandwe, J., Pounds, S. B., Shurtleff, S., Fulton, R. S., Fulton, L. L., Easton, J., Parganas, E., Pui, C-H., Rubnitz, J. E., Ding, L., Mardis, E. R., Wilson, R. K., Gruber, T. A., Mullighan, C. G., Schlenk, R. F., Paschka, P., Döhner, K., Döhner, H., Bullinger, L., Zhang, J., Klco, J. M. & Downing, J. R., 2016 Oct 31, In : Nature Genetics. 48, p. 1551–1556 6 p.

    Research output: Contribution to journalLetter

  26. A reference panel of 64,976 haplotypes for genotype imputation

    McCarthy, S., Das, S., Kretzschmar, W., Delaneau, O., Wood, A. R., Teumer, A., Kang, H. M., Fuchsberger, C., Danecek, P., Sharp, K., Luo, Y., Sidore, C., Kwong, A., Timpson, N., Koskinen, S., Vrieze, S., Scott, L. J., Zhang, H., Mahajan, A., Veldink, J. & 91 othersPeters, U., Pato, C., Van Duijn, C. M., Gillies, C. E., Gandin, I., Mezzavilla, M., Gilly, A., Cocca, M., Traglia, M., Angius, A., Barrett, J. C., Boomsma, D., Branham, K., Breen, G., Brummett, C. M., Busonero, F., Campbell, H., Chan, A., Chen, S., Chew, E., Collins, F. S., Corbin, L. J., Smith, G. D., Dedoussis, G., Dorr, M., Farmaki, A. E., Ferrucci, L., Forer, L., Fraser, R. M., Gabriel, S., Levy, S., Leif Groop, Harrison, T., Hattersley, A., Holmen, O. L., Hveem, K., Kretzler, M., Lee, J. C., McGue, M., Meitinger, T., Melzer, D., Min, J. L., Mohlke, K. L., Vincent, J. B., Nauck, M., Nickerson, D., Palotie, A., Pato, M., Pirastu, N., McInnis, M., Richards, J. B., Sala, C., Salomaa, V., Schlessinger, D., Schoenherr, S., Slagboom, P. E., Small, K., Spector, T., Stambolian, D., Tuke, M., Tuomilehto, J., Van Den Berg, L. H., Van Rheenen, W., Volker, U., Wijmenga, C., Toniolo, D., Zeggini, E., Gasparini, P., Sampson, M. G., Wilson, J. F., Frayling, T., De Bakker, P. I. W., Swertz, M. A., McCarroll, S., Kooperberg, C., Dekker, A., Altshuler, D., Willer, C., Iacono, W., Ripatti, S., Soranzo, N., Walter, K., Swaroop, A., Cucca, F., Anderson, C. A., Myers, R. M., Boehnke, M., McCarthy, M. I., Durbin, R., Abecasis, G. & Marchini, J., 2016 Oct 1, In : Nature Genetics. 48, 10, p. 1279-1283 5 p.

    Research output: Contribution to journalArticle

  27. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

    Ehret, G. B., Ferreira, T., Chasman, D. I., Jackson, A. U., Schmidt, E. M., Johnson, T., Thorleifsson, G., Luan, JA., Donnelly, L. A., Kanoni, S., Petersen, A. K., Pihur, V., Strawbridge, R. J., Shungin, D., Hughes, M. F., Meirelles, O., Kaakinen, M., Bouatia-Naji, N., Kristiansson, K., Shah, S. & 293 othersKleber, M. E., Guo, X., Lyytikäinen, L. P., Cristiano Fava, Eriksson, N., Nolte, I. M., Magnusson, P. K., Salfati, E. L., Rallidis, L. S., Theusch, E., Smith, A. J. P., Folkersen, L., Witkowska, K., Pers, T. H., Joehanes, R., Kim, S. K., Lataniotis, L., Jansen, R., Johnson, A. D., Warren, H., Kim, Y. J., Zhao, W., Wu, Y., Tayo, B. O., Bochud, M., Absher, D., Adair, L. S., Amin, N., Arking, D. E., Axelsson, T., Baldassarre, D., Balkau, B., Bandinelli, S., Barnes, M. R., Barroso, I., Bevan, S., Bis, J. C., Bjornsdottir, G., Boehnke, M., Boerwinkle, E., Bonnycastle, L. L., Boomsma, D. I., Bornstein, S. R., Brown, M. J., Burnier, M., Cabrera, C. P., Chambers, J. C., Chang, I. S., Cheng, C. Y., Chines, P. S., Chung, R. H., Collins, F. S., Connell, J. M., Döring, A., Dallongeville, J., Danesh, J., De Faire, U., Delgado, G., Dominiczak, A. F., Doney, A. S. F., Drenos, F., Edkins, S., Eicher, J. D., Elosua, R., Enroth, S., Erdmann, J., Eriksson, P., Esko, T., Evangelou, E., Evans, A., Fall, T., Farrall, M., Felix, J. F., Ferrières, J., Ferrucci, L., Fornage, M., Forrester, T., Franceschini, N., Franco, O. H., Franco-Cereceda, A., Fraser, R. M., Ganesh, S. K., Gao, H., Gertow, K., Gianfagna, F., Gigante, B., Giulianini, F., Goel, A., Goodall, A. H., Goodarzi, M. O., Gorski, M., Gräßler, J., Groves, C. J., Gudnason, V., Gyllensten, U., Hallmans, G., Hartikainen, A. L., Hassinen, M., Havulinna, A. S., Hayward, C., Hercberg, S., Herzig, K. H., Hicks, A. A., Hingorani, A. D., Hirschhorn, J. N., Hofman, A., Holmen, J., Holmen, O. L., Hottenga, J. J., Howard, P., Hsiung, C. A., Hunt, S. C., Ikram, M. A., Illig, T., Iribarren, C., Jensen, R. A., Kähönen, M., Kang, H. M., Kathiresan, S., Keating, B. J., Khaw, K. T., Kim, Y. K., Kim, E., Kivimaki, M., Klopp, N., Kolovou, G., Komulainen, P., Kooner, J. S., Kosova, G., Krauss, R. M., Kuh, D., Kutalik, Z., Kuusisto, J., Kvaløy, K., Lakka, T. A., Lee, N. R., Lee, I. T., Lee, W. J., Levy, D., Li, X., Liang, K. W., Lin, H., Lin, L., Lindström, J., Lobbens, S., Männistö, S., Müller, G., Müller-Nurasyid, M., Mach, F., Markus, H. S., Marouli, E., McCarthy, M. I., McKenzie, C. A., Meneton, P., Menni, C., Metspalu, A., Mijatovic, V., Moilanen, L., Montasser, M. E., Morris, A. D., Morrison, A. C., Mulas, A., Nagaraja, R., Narisu, N., Nikus, K., O'Donnell, C. J., O'Reilly, P. F., Ong, K. K., Paccaud, F., Palmer, C. D., Parsa, A., Pedersen, N. L., Penninx, B. W., Perola, M., Peters, A., Poulter, N., Pramstaller, P. P., Psaty, B. M., Quertermous, T., Rao, D. C., Rasheed, A., Rayner, N. W., Frida Renström, Rettig, R., Rice, K. M., Roberts, R., Rose, L. M., Rossouw, J., Samani, N. J., Sanna, S., Saramies, J., Schunkert, H., Sebert, S., Sheu, W. H. H., Shin, Y. A., Sim, X., Smit, J. H., Smith, A. V., Sosa, M. X., Spector, T. D., Stančáková, A., Stanton, A. V., Stirrups, K. E., Stringham, H. M., Sundstrom, J., Swift, A. J., Syvänen, A. C., Tai, E. S., Tanaka, T., Tarasov, K. V., Teumer, A., Thorsteinsdottir, U., Tobin, M. D., Tremoli, E., Uitterlinden, A. G., Uusitupa, M., Vaez, A., Vaidya, D., Van Duijn, C. M., Van Iperen, E. P. A., Vasan, R. S., Verwoert, G. C., Virtamo, J., Vitart, V., Voight, B. F., Vollenweider, P., Wagner, A., Wain, L. V., Wareham, N. J., Watkins, H., Weder, A. B., Westra, H. J., Wilks, R., Wilsgaard, T., Wilson, J. F., Wong, T. Y., Yang, T. P., Yao, J., Yengo, L., Zhang, W., Zhao, J. H., Zhu, X., Bovet, P., Cooper, R. S., Mohlke, K. L., Saleheen, D., Lee, J. Y., Elliott, P., Gierman, H. J., Willer, C. J., Franke, L., Hovingh, G. K., Taylor, K. D., Dedoussis, G., Sever, P., Wong, A., Lind, L., Assimes, T. L., Njølstad, I., Schwarz, P. E. H., Langenberg, C., Snieder, H., Caulfield, M. J., Olle Melander, Laakso, M., Saltevo, J., Rauramaa, R., Tuomilehto, J., Ingelsson, E., Lehtimäki, T., Hveem, K., Palmas, W., März, W., Kumari, M., Salomaa, V., Chen, Y. D. I., Rotter, J. I., Froguel, P., Jarvelin, M. R., Lakatta, E. G., Kuulasmaa, K., Paul W. Franks, Hamsten, A., Wichmann, H. E., Palmer, C. N. A., Stefansson, K., Ridker, P. M., Loos, R. J. F., Chakravarti, A., Deloukas, P., Morris, A. P., Newton-Cheh, C. & Munroe, P. B., 2016 Oct 1, In : Nature Genetics. 48, 10, p. 1171-1184 14 p.

    Research output: Contribution to journalArticle

  28. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

    Surendran, P., Drenos, F., Young, R., Warren, H., Cook, J. P., Manning, A. K., Grarup, N., Sim, X., Barnes, D. R., Witkowska, K., Staley, J. R., Tragante, V., Tukiainen, T., Yaghootkar, H., Masca, N., Freitag, D. F., Ferreira, T., Giannakopoulou, O., Tinker, A., Harakalova, M. & 190 othersMihailov, E., Liu, C., Kraja, A. T., Nielsen, S. F., Rasheed, A., Samuel, M., Zhao, W., Bonnycastle, L. L., Jackson, A. U., Narisu, N., Swift, A. J., Southam, L., Marten, J., Huyghe, J. R., Stančáková, A., Cristiano Fava, Therese Ohlsson, Matchan, A., Stirrups, K. E., Bork-Jensen, J., Gjesing, A. P., Kontto, J., Perola, M., Shaw-Hawkins, S., Havulinna, A. S., Zhang, H., Donnelly, L. A., Groves, C. J., Rayner, N. W., Neville, M. J., Robertson, N. R., Yiorkas, A. M., Herzig, K. H., Kajantie, E., Zhang, W., Willems, S. M., Lannfelt, L., Malerba, G., Soranzo, N., Trabetti, E., Verweij, N., Evangelou, E., Moayyeri, A., Vergnaud, A. C., Nelson, C. P., Alaitz Poveda, Tibor V. Varga, Caslake, M., De Craen, A. J. M., Trompet, S., Luan, JA., Scott, R. A., Harris, S. E., Liewald, D. C. M., Marioni, R., Menni, C., Farmaki, A. E., Hallmans, G., Frida Renström, Huffman, J. E., Hassinen, M., Burgess, S., Vasan, R. S., Felix, J. F., Uria-Nickelsen, M., Malarstig, A., Reilly, D. F., Hoek, M., Vogt, T. F., Lin, H., Lieb, W., Traylor, M., Markus, H. S., Highland, H. M., Justice, A. E., Marouli, E., Lindström, J., Uusitupa, M., Komulainen, P., Lakka, T. A., Rauramaa, R., Polasek, O., Rudan, I., Rolandsson, O., Paul W. Franks, Dedoussis, G., Spector, T. D., Jousilahti, P., Männistö, S., Deary, I. J., Starr, J. M., Langenberg, C., Wareham, N. J., Brown, M. J., Dominiczak, A. F., Connell, J. M., Jukema, J. W., Sattar, N., Ford, I., Packard, C. J., Esko, T., Mägi, R., Metspalu, A., De Boer, R. A., Van Der Meer, P., Van Der Harst, P., Gambaro, G., Ingelsson, E., Lind, L., De Bakker, P. I. W., Numans, M. E., Brandslund, I., Christensen, C., Petersen, E. R. B., Korpi-Hyövälti, E., Oksa, H., Chambers, J. C., Kooner, J. S., Blakemore, A. I. F., Franks, S., Jarvelin, M. R., Husemoen, L. L., Linneberg, A., Skaaby, T., Thuesen, B., Karpe, F., Tuomilehto, J., Doney, A. S. F., Morris, A. D., Palmer, C. N. A., Holmen, O. L., Hveem, K., Willer, C. J., Tuomi, T., Leif Groop, Käräjämäki, A., Palotie, A., Ripatti, S., Salomaa, V., Alam, D. S., Majumder, A. A. S., Di Angelantonio, E., Chowdhury, R., McCarthy, M. I., Poulter, N., Stanton, A. V., 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., Olle Melander, Kuusisto, J., Laakso, M., Padmanabhan, S., Porteous, D. J., Hayward, C., Scotland, G., Collins, F. S., Mohlke, K. L., Hansen, T., Pedersen, O., Boehnke, M., Stringham, H. M., Frossard, P., Newton-Cheh, C., Tobin, M. D., Nordestgaard, B. G., Caulfield, M. J., Mahajan, A., Morris, A. P., Tomaszewski, M., Samani, N. J., Saleheen, D., Asselbergs, F. W., Lindgren, C. M., Danesh, J., Wain, L. V., Butterworth, A. S., Howson, J. M. M. & Munroe, P. B., 2016 Oct 1, In : Nature Genetics. 48, 10, p. 1151-1161 11 p.

    Research output: Contribution to journalArticle

  29. Sequencing of the genus Arabidopsis identifies a complex history of nonbifurcating speciation and abundant trans-specific polymorphism

    Novikova, P. Y., Hohmann, N., Nizhynska, V., Tsuchimatsu, T., Ali, J., Muir, G., Guggisberg, A., Paape, T., Schmid, K., Fedorenko, O. M., Holm, S., Säll, T., Schlötterer, C., Marhold, K., Widmer, A., Sese, J., Shimizu, K. K., Weigel, D., Krämer, U., Koch, M. A. & 1 othersNordborg, M., 2016 Sep 1, In : Nature Genetics. 48, 9, p. 1077-1082 6 p.

    Research output: Contribution to journalArticle

  30. Signaling from maize organ primordia via FASCIATED EAR3 regulates stem cell proliferation and yield traits

    Je, B. I., Gruel, J., Lee, Y. K., Bommert, P., Arevalo, E. D., Eveland, A. L., Wu, Q., Goldshmidt, A., Meeley, R., Bartlett, M., Komatsu, M., Sakai, H., Henrik Jönsson & Jackson, D., 2016 Jul 1, In : Nature Genetics. 48, 7, p. 785-791 7 p.

    Research output: Contribution to journalArticle

  31. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

    Dunning, A. M., Michailidou, K., Kuchenbaecker, K. B., Thompson, D., French, J. D., Beesley, J., Healey, C. S., Kar, S., Pooley, K. A., Lopez-Knowles, E., Dicks, E., Barrowdale, D., Sinnott-Armstrong, N. A., Sallari, R. C., Hillman, K. M., Kaufmann, S., Sivakumaran, H., Marjaneh, M. M., Lee, J. S., Hills, M. & 228 othersJarosz, M., Drury, S., Canisius, S., Bolla, M. K., Dennis, J., Wang, Q., Hopper, J. L., Southey, M. C., Broeks, A., Schmidt, M. K., Lophatananon, A., Muir, K., Beckmann, M. W., Fasching, P. A., Dos Santos Silva, G., Peto, J., Sawyer, E. J., Tomlinson, I., Burwinkel, B., Marme, F., Guénel, P., Truong, T., Bojesen, S. E., Flyger, H., González-Neira, A., Perez, J. I. A., Anton-Culver, H., Eunjung, L., Arndt, V., Brenner, H., Meindl, A., Schmutzler, R. K., Brauch, H., Hamann, U., Aittomäki, K., Blomqvist, C., Ito, H., Matsuo, K., Bogdanova, N., Dörk, T., Lindblom, A., Margolin, S., Kosma, V-M., Mannermaa, A., Tseng, C-C., Wu, A. H., Lambrechts, D., Wildiers, H., Chang-Claude, J., Rudolph, A., Peterlongo, P., Radice, P., Olson, J. E., Giles, G. G., Milne, R. L., Haiman, C. A., Henderson, B. E., Goldberg, M. S., Teo, S. H., Yip, C. H., Nord, S., Borresen-Dale, A-L., Kristensen, V., Long, J., Zheng, W., Pylkäs, K., Winqvist, R., Andrulis, I. L., Knight, J. A., Devilee, P., Seynaeve, C., Figueroa, J., Sherman, M. E., Czene, K., Darabi, H., Hollestelle, A., van den Ouweland, A. M. W., Humphreys, K., Gao, Y-T., Shu, X-O., Cox, A., Cross, S. S., Blot, W., Cai, Q., Ghoussaini, M., Perkins, B. J., Shah, M., Choi, J-Y., Kang, D., Lee, S. C., Hartman, M., Kabisch, M., Torres, D., Jakubowska, A., Lubinski, J., Brennan, P., Sangrajrang, S., Ambrosone, C. B., Toland, A. E., Shen, C-Y., Wu, P-E., Orr, N., Swerdlow, A., McGuffog, L., Healey, S., Lee, A., Kapuscinski, M., John, E. M., Terry, M. B., Daly, M. B., Goldgar, D. E., Buys, S. S., Janavicius, R., Tihomirova, L., Tung, N., Dorfling, C. M., van Rensburg, E. J., Neuhausen, S. L., Ejlertsen, B., Hansen, T. V. O., Osorio, A., Benitez, J., Rando, R., Weitzel, J. N., Bonanni, B., Peissel, B., Manoukian, S., Papi, L., Ottini, L., Konstantopoulou, I., Apostolou, P., Garber, J., Rashid, M. U., Frost, D., Izatt, L., Ellis, S., Godwin, A. K., Arnold, N., Niederacher, D., Rhiem, K., Bogdanova-Markov, N., Sagne, C., Stoppa-Lyonnet, D., Damiola, F., Sinilnikova, O. M., Mazoyer, S., Isaacs, C., Claes, K. B. M., De Leeneer, K., de la Hoya, M., Caldes, T., Nevanlinna, H., Khan, S., Mensenkamp, A. R., Hooning, M. J., Rookus, M. A., Kwong, A., Olah, E., Diez, O., Brunet, J., Pujana, M. A., Gronwald, J., Huzarski, T., Barkardottir, R. B., Laframboise, R., Soucy, P., Montagna, M., Agata, S., Teixeira, M. R., Park, S. K., Lindor, N., Couch, F. J., Tischkowitz, M., Foretova, L., Vijai, J., Offit, K., Singer, C. F., Rappaport, C., Phelan, C. M., Greene, M. H., Mai, P. L., Rennert, G., Imyanitov, E. N., Hulick, P. J., Phillips, K-A., Piedmonte, M., Mulligan, A. M., Glendon, G., Bojesen, A., Thomassen, M., Caligo, M. A., Yoon, S-Y., Friedman, E., Laitman, Y., Borg, A., von Wachenfeldt, A., Hans Ehrencrona, Rantala, J., Olopade, O. I., Ganz, P. A., Nussbaum, R. L., Gayther, S. A., Nathanson, K. L., Domchek, S. M., Arun, B. K., Mitchell, G., Karlan, B. Y., Lester, J., Maskarinec, G., Woolcott, C., Scott, C., Stone, J., Apicella, C., Tamimi, R., Luben, R., Khaw, K-T., Helland, Å., Haakensen, V., Dowsett, M., Pharoah, P. D. P., Simard, J., Hall, P., García-Closas, M., Vachon, C., Chenevix-Trench, G., Antoniou, A. C., Easton, D. F. & Edwards, S. L., 2016, In : Nature Genetics.

    Research output: Contribution to journalArticle

  32. Genetic predisposition for beta cell fragility underlies type 1 and type 2 diabetes

    Dooley, J., Tian, L., Schonefeldt, S., Delghingaro-Augusto, V., Garcia-Perez, J. E., Pasciuto, E., Di Marino, D., Carr, E. J., Oskolkov, N., Lyssenko, V., Franckaert, D., Lagou, V., Overbergh, L., Vandenbussche, J., Allemeersch, J., Chabot-Roy, G., Dahlstrom, J. E., Laybutt, D. R., Petrovsky, N., Socha, L. & 9 othersGevaert, K., Jetten, A. M., Lambrechts, D., Linterman, M. A., Goodnow, C. C., Nolan, C. J., Lesage, S., Schlenner, S. M. & Liston, A., 2016, In : Nature Genetics. 48, p. 519-527

    Research output: Contribution to journalArticle

  33. 2015
  34. Identification of six new susceptibility loci for invasive epithelial ovarian cancer

    Kuchenbaecker, K. B., Ramus, S. J., Tyrer, J., Lee, A., Shen, H. C., Beesley, J., Lawrenson, K., McGuffog, L., Healey, S., Lee, J. M., Spindler, T. J., Lin, Y. G., Pejovic, T., Bean, Y., Li, Q., Coetzee, S., Hazelett, D., Miron, A., Southey, M., Terry, M. B. & 31 othersGoldgar, D. E., Buys, S. S., Janavicius, R., Dorfling, C. M., van Rensburg, E. J., Neuhausen, S. L., Ding, Y. C., Hansen, T. V. O., Jønson, L., Gerdes, A-M., Ejlertsen, B., Barrowdale, D., Dennis, J., Benitez, J., Osorio, A., Garcia, M. J., Komenaka, I., Weitzel, J. N., Ganschow, P., Peterlongo, P., Bernard, L., Viel, A., Bonanni, B., Peissel, B., Manoukian, S., Radice, P., Papi, L., Ottini, L., Soller, M., Stenmark-Askmalm, M. & EMBRACE, 2015 Feb, In : Nature Genetics. 47, 2, p. 164-71 8 p.

    Research output: Contribution to journalArticle

  35. A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease

    Nikpay, M., Goel, A., Won, H-H., Hall, L. M., Willenborg, C., Kanoni, S., Saleheen, D., Kyriakou, T., Nelson, C. P., Hopewell, J. C., Webb, T. R., Zeng, L., Dehghan, A., Alver, M., Armasu, S. M., Auro, K., Bjonnes, A., Chasman, D. I., Chen, S., Ford, I. & 131 othersFranceschini, N., Gieger, C., Grace, C., Gustafsson, S., Huang, J., Hwang, S-J., Kim, Y. K., Kleber, M. E., Lau, K. W., Lu, X., Lu, Y., Lyytikainen, L-P., Mihailov, E., Morrison, A. C., Pervjakova, N., Qu, L., Rose, L. M., Salfati, E., Saxena, R., Scholz, M., Smith, A. V., Tikkanen, E., Uitterlinden, A., Yang, X., Zhang, W., Zhao, W., de Andrade, M., de Vries, P. S., van Zuydam, N. R., Anand, S. S., Bertram, L., Beutner, F., Dedoussis, G., Frossard, P., Gauguier, D., Goodall, A. H., Gottesman, O., Haber, M., Han, B-G., Huang, J., Jalilzadeh, S., Kessler, T., Koenig, I. R., Lannfelt, L., Lieb, W., Lind, L., Lindgren, C. M., Lokki, M-L., Magnusson, P. K., Mallick, N. H., Mehra, N., Meitinger, T., Memon, F-R., Morris, A. P., Nieminen, M. S., Pedersen, N. L., Peters, A., Rallidis, L. S., Rasheed, A., Samuel, M., Shah, S. H., Sinisalo, J., Stirrups, K. E., Trompet, S., Wang, L., Zaman, K. S., Ardissino, D., Boerwinkle, E., Borecki, I. B., Bottinger, E. P., Buring, J. E., Chambers, J. C., Collins, R., Cupples, L. A., Danesh, J., Demuth, I., Elosua, R., Epstein, S. E., Esko, T., Feitosa, M. F., Franco, O. H., Franzosi, M. G., Granger, C. B., Gu, D., Gudnason, V., Hall, A. S., Hamsten, A., Harris, T. B., Hazen, S. L., Hengstenberg, C., Hofman, A., Ingelsson, E., Iribarren, C., Jukema, J. W., Karhunen, P. J., Kim, B-J., Kooner, J. S., Kullo, I. J., Lehtimaki, T., Loos, R. J. F., Olle Melander, Metspalu, A., Maerz, W., Palmer, C. N., Perola, M., Quertermous, T., Rader, D. J., Ridker, P. M., Ripatti, S., Roberts, R., Salomaa, V., Sanghera, D. K., Schwartz, S. M., Seedorf, U., Stewart, A. F., Stott, D. J., Thiery, J., Zalloua, P. A., O'Donnell, C. J., Reilly, M. P., Assimes, T. L., Thompson, J. R., Erdmann, J., Clarke, R., Watkins, H., Kathiresan, S., McPherson, R., Deloukas, P., Schunkert, H., Samani, N. J. & Farrall, M., 2015, In : Nature Genetics. 47, 10, p. 1121

    Research output: Contribution to journalArticle

  36. Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists.

    Kohler, A., Kuo, A., Nagy, L. G., Morin, E., Barry, K. W., Buscot, F., Canbäck, B., Choi, C., Cichocki, N., Clum, A., Colpaert, J., Copeland, A., Costa, M. D., Doré, J., Floudas, D., Gay, G., Girlanda, M., Henrissat, B., Herrmann, S., Hess, J. & 32 othersHögberg, N., Tomas Johansson, Khouja, H-R., LaButti, K., Lahrmann, U., Levasseur, A., Lindquist, E. A., Lipzen, A., Marmeisse, R., Martino, E., Murat, C., Ngan, C. Y., Nehls, U., Plett, J. M., Pringle, A., Ohm, R. A., Perotto, S., Peter, M., Riley, R., Rineau, F., Ruytinx, J., Salamov, A., Shah, F., Sun, H., Tarkka, M., Tritt, A., Veneault-Fourrey, C., Zuccaro, A., Anders Tunlid, Grigoriev, I. V., Hibbett, D. S. & Martin, F., 2015, In : Nature Genetics. 47, 4, p. 410-U176

    Research output: Contribution to journalArticle

  37. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.

    Gaulton, K. J., Ferreira, T., Lee, Y., Raimondo, A., Mägi, R., Reschen, M. E., Mahajan, A., Locke, A., William Rayner, N., Robertson, N., Scott, R. A., Prokopenko, I., Scott, L. J., Green, T., Sparso, T., Thuillier, D., Yengo, L., Grallert, H., Wahl, S., Frånberg, M. & 198 othersStrawbridge, R. J., Kestler, H., Chheda, H., Eisele, L., Gustafsson, S., Steinthorsdottir, V., Thorleifsson, G., Qi, L., Karssen, L. C., van Leeuwen, E. M., Willems, S. M., Li, M., Chen, H., Fuchsberger, C., Kwan, P., Ma, C., Linderman, M., Lu, Y., Thomsen, S. K., Rundle, J. K., Beer, N. L., van de Bunt, M., Chalisey, A., Kang, H. M., Voight, B. F., Abecasis, G. R., Almgren, P., Baldassarre, D., Balkau, B., Benediktsson, R., Blüher, M., Boeing, H., Bonnycastle, L. L., Bottinger, E. P., Burtt, N. P., Carey, J., Charpentier, G., Chines, P. S., Cornelis, M. C., Couper, D. J., Crenshaw, A. T., van Dam, R. M., Doney, A. S. F., Mozhgan Dorkhan, Edkins, S., Eriksson, J. G., Esko, T., Eury, E., Fadista, J., Flannick, J., Fontanillas, P., Fox, C., Paul Franks, Gertow, K., Gieger, C., Gigante, B., Gottesman, O., Grant, G. B., Grarup, N., Groves, C. J., Hassinen, M., Have, C. T., Herder, C., Holmen, O. L., Hreidarsson, A. B., Humphries, S. E., Hunter, D. J., Jackson, A. U., Jonsson, A., Jørgensen, M. E., Jørgensen, T., Kao, W-H. L., Kerrison, N. D., Kinnunen, L., Klopp, N., Kong, A., Kovacs, P., Kraft, P., Jasmina Kravic, Langford, C., Leander, K., Liang, L., Lichtner, P., Lindgren, C. M., Eero Lindholm, Linneberg, A., Liu, C-T., Lobbens, S., Luan, J., Valeriya Lyssenko, Männistö, S., McLeod, O., Meyer, J., Mihailov, E., Mirza, G., Mühleisen, T. W., Müller-Nurasyid, M., Navarro, C., Nöthen, M. M., Nikolay Oskolkov, Owen, K. R., Palli, D., Pechlivanis, S., Peltonen, L., Perry, J. R. B., Platou, C. G. P., Roden, M., Ruderfer, D., Rybin, D., van der Schouw, Y. T., Sennblad, B., Sigurðsson, G., Stančáková, A., Steinbach, G., Storm, P., Strauch, K., Stringham, H. M., Sun, Q., Thorand, B., Tikkanen, E., Tonjes, A., Trakalo, J., Tremoli, E., Tuomi, T., Wennauer, R., Wiltshire, S., Wood, A. R., Zeggini, E., Dunham, I., Birney, E., Pasquali, L., Ferrer, J., Loos, R. J. F., Dupuis, J., Florez, J. C., Boerwinkle, E., Pankow, J. S., van Duijn, C., Sijbrands, E., Meigs, J. B., Hu, F. B., Thorsteinsdottir, U., Stefansson, K., Lakka, T. A., Rauramaa, R., Stumvoll, M., Pedersen, N. L., Lind, L., Keinanen-Kiukaanniemi, S. M., Korpi-Hyövälti, E., Saaristo, T. E., Saltevo, J., Kuusisto, J., Laakso, M., Metspalu, A., Erbel, R., Jöcke, K-H., Moebus, S., Ripatti, S., Salomaa, V., Ingelsson, E., Boehm, B. O., Bergman, R. N., Collins, F. S., Mohlke, K. L., Koistinen, H., Tuomilehto, J., Hveem, K., Njølstad, I., Deloukas, P., Donnelly, P. J., Frayling, T. M., Hattersley, A. T., de Faire, U., Hamsten, A., Illig, T., Peters, A., Cauchi, S., Sladek, R., Froguel, P., Hansen, T., Pedersen, O., Morris, A. D., Palmer, C. N. A., Kathiresan, S., Olle Melander, Peter Nilsson, Leif Groop, Barroso, I., Langenberg, C., Wareham, N. J., O'Callaghan, C. A., Gloyn, A. L., Altshuler, D., Boehnke, M., Teslovich, T. M., McCarthy, M. I. & Morris, A. P., 2015, In : Nature Genetics. 47, 12, p. 1415

    Research output: Contribution to journalArticle

  38. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.

    Law, M. H., Bishop, D. T., Lee, J. E., Brossard, M., Martin, N. G., Moses, E. K., Song, F., Barrett, J. H., Kumar, R., Easton, D. F., Pharoah, P. D. P., Swerdlow, A. J., Kypreou, K. P., Taylor, J. C., Harland, M., Randerson-Moor, J., Akslen, L. A., Andresen, P. A., Avril, M-F., Azizi, E. & 55 othersScarrà, G. B., Brown, K. M., Dȩbniak, T., Duffy, D. L., Elder, D. E., Fang, S., Friedman, E., Galan, P., Ghiorzo, P., Gillanders, E. M., Goldstein, A. M., Gruis, N. A., Hansson, J., Helsing, P., Hočevar, M., Höiom, V., Christian Ingvar, Kanetsky, P. A., Chen, W. V., Landi, M. T., Lang, J., Lathrop, G. M., Lubiński, J., Mackie, R. M., Mann, G. J., Molven, A., Montgomery, G. W., Novaković, S., Håkan Olsson, Puig, S., Puig-Butille, J. A., Qureshi, A. A., Radford-Smith, G. L., van der Stoep, N., van Doorn, R., Whiteman, D. C., Craig, J. E., Schadendorf, D., Simms, L. A., Burdon, K. P., Nyholt, D. R., Pooley, K. A., Orr, N., Stratigos, A. J., Cust, A. E., Ward, S. V., Hayward, N. K., Han, J., Schulze, H-J., Dunning, A. M., Bishop, J. A. N., Demenais, F., Amos, C. I., MacGregor, S. & Iles, M. M., 2015, In : Nature Genetics. 47, 9, p. 987

    Research output: Contribution to journalArticle

  39. The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.

    Kajsa Paulsson, Lilljebjörn, H., Biloglav, A., Linda Olsson, Rissler, M., Anders Castor, Barbany, G., Fogelstrand, L., Nordgren, A., Sjögren, H., Thoas Fioretos & Bertil Johansson, 2015, In : Nature Genetics. 47, 6, p. 672-676

    Research output: Contribution to journalArticle

  40. The impact of low-frequency and rare variants on lipid levels.

    Surakka, I., Horikoshi, M., Mägi, R., Sarin, A-P., Mahajan, A., Lagou, V., Marullo, L., Ferreira, T., Miraglio, B., Timonen, S., Kettunen, J., Pirinen, M., Karjalainen, J., Thorleifsson, G., Hägg, S., Hottenga, J-J., Isaacs, A., Ladenvall, C., Beekman, M., Esko, T. & 66 othersRied, J. S., Nelson, C. P., Willenborg, C., Gustafsson, S., Westra, H-J., Blades, M., de Craen, A. J. M., de Geus, E. J., Deelen, J., Grallert, H., Hamsten, A., Havulinna, A. S., Hengstenberg, C., Houwing-Duistermaat, J. J., Hyppönen, E., Karssen, L. C., Lehtimäki, T., Valeriya Lyssenko, Magnusson, P. K. E., Mihailov, E., Müller-Nurasyid, M., Mpindi, J-P., Pedersen, N. L., Penninx, B. W. J. H., Perola, M., Pers, T. H., Peters, A., Rung, J., Smit, J. H., Steinthorsdottir, V., Tobin, M. D., Tsernikova, N., van Leeuwen, E. M., Viikari, J. S., Willems, S. M., Willemsen, G., Schunkert, H., Erdmann, J., Samani, N. J., Kaprio, J., Lind, L., Gieger, C., Metspalu, A., Slagboom, P. E., Leif Groop, van Duijn, C. M., Eriksson, J. G., Jula, A., Salomaa, V., Boomsma, D. I., Power, C., Raitakari, O. T., Ingelsson, E., Järvelin, M-R., Thorsteinsdottir, U., Franke, L., Ikonen, E., Kallioniemi, O., Pietiäinen, V., Lindgren, C. M., Stefansson, K., Palotie, A., McCarthy, M. I., Morris, A. P., Prokopenko, I. & Ripatti, S., 2015, In : Nature Genetics. 47, 6, p. 589-597

    Research output: Contribution to journalArticle

  41. The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias.

    Andersson, A., Ma, J., Wang, J., Chen, X., Gedman, A. L., Dang, J., Nakitandwe, J., Holmfeldt, L., Parker, M., Easton, J., Huether, R., Kriwacki, R., Rusch, M., Wu, G., Li, Y., Mulder, H., Raimondi, S., Pounds, S., Kang, G., Shi, L. & 30 othersBecksfort, J., Gupta, P., Payne-Turner, D., Vadodaria, B., Boggs, K., Yergeau, D., Manne, J., Song, G., Edmonson, M., Nagahawatte, P., Wei, L., Cheng, C., Pei, D., Sutton, R., Venn, N. C., Chetcuti, A., Rush, A., Catchpoole, D., Heldrup, J., Thoas Fioretos, Lu, C., Ding, L., Pui, C-H., Shurtleff, S., Mullighan, C. G., Mardis, E. R., Wilson, R. K., Gruber, T. A., Zhang, J. & Downing, J. R., 2015, In : Nature Genetics. 47, 4, p. 330-U192

    Research output: Contribution to journalArticle

  42. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.

    Kato, N., Loh, M., Takeuchi, F., Verweij, N., Wang, X., Zhang, W., Kelly, T. N., Saleheen, D., Lehne, B., Leach, I. M., Drong, A. W., Abbott, J., Wahl, S., Tan, S-T., Scott, W. R., Campanella, G., Chadeau-Hyam, M., Afzal, U., Ahluwalia, T. S., Bonder, M. J. & 224 othersChen, P., Dehghan, A., Edwards, T. L., Esko, T., Go, M. J., Harris, S. E., Hartiala, J., Kasela, S., Kasturiratne, A., Khor, C-C., Kleber, M. E., Li, H., Mok, Z. Y., Nakatochi, M., Sapari, N. S., Saxena, R., Stewart, A. F. R., Stolk, L., Tabara, Y., Teh, A. L., Wu, Y., Wu, J-Y., Zhang, Y., Aits, I., Da Silva Couto Alves, A., Das, S., Dorajoo, R., Hopewell, J. C., Kim, Y. K., Robert Koivula, Luan, J., Lyytikäinen, L-P., Nguyen, Q. N., Pereira, M. A., Postmus, I., Raitakari, O. T., Bryan, M. S., Scott, R. A., Sorice, R., Tragante, V., Traglia, M., White, J., Yamamoto, K., Zhang, Y., Adair, L. S., Ahmed, A., Akiyama, K., Asif, R., Aung, T., Barroso, I., Bjonnes, A., Braun, T. R., Cai, H., Chang, L-C., Chen, C-H., Cheng, C-Y., Chong, Y-S., Collins, R., Courtney, R., Davies, G., Delgado, G., Do, L. D., Doevendans, P. A., Gansevoort, R. T., Gao, Y-T., Grammer, T. B., Grarup, N., Grewal, J., Gu, D., Wander, G. S., Hartikainen, A-L., Hazen, S. L., He, J., Heng, C-K., Hixson, J. E., Hofman, A., Hsu, C., Huang, W., Husemoen, L. L. N., Hwang, J-Y., Ichihara, S., Igase, M., Isono, M., Justesen, J. M., Katsuya, T., Kibriya, M. G., Kim, Y. J., Kishimoto, M., Koh, W-P., Kohara, K., Kumari, M., Kwek, K., Lee, N. R., Lee, J., Liao, J., Lieb, W., Liewald, D. C. M., Matsubara, T., Matsushita, Y., Meitinger, T., Mihailov, E., Milani, L., Mills, R., Mononen, N., Müller-Nurasyid, M., Nabika, T., Nakashima, E., Ng, H. K., Nikus, K., Nutile, T., Ohkubo, T., Ohnaka, K., Parish, S., Paternoster, L., Peng, H., Peters, A., Pham, S. T., Pinidiyapathirage, M. J., Rahman, M., Rakugi, H., Rolandsson, O., Rozario, M. A., Ruggiero, D., Sala, C. F., Sarju, R., Shimokawa, K., Snieder, H., Sparsø, T., Spiering, W., Starr, J. M., Stott, D. J., Stram, D. O., Sugiyama, T., Szymczak, S., Tang, W. H. W., Tong, L., Trompet, S., Turjanmaa, V., Ueshima, H., Uitterlinden, A. G., Umemura, S., Vaarasmaki, M., van Dam, R. M., van Gilst, W. H., van Veldhuisen, D. J., Viikari, J. S., Waldenberger, M., Wang, Y., Wang, A., Wilson, R., Wong, T-Y., Xiang, Y-B., Yamaguchi, S., Ye, X., Young, R. D., Young, T. L., Yuan, J-M., Zhou, X., Asselbergs, F. W., Ciullo, M., Clarke, R., Deloukas, P., Franke, A., Paul Franks, Franks, S., Friedlander, Y., Gross, M. D., Guo, Z., Hansen, T., Jarvelin, M-R., Jørgensen, T., Jukema, J. W., Kähönen, M., Kajio, H., Kivimaki, M., Lee, J-Y., Lehtimäki, T., Linneberg, A., Miki, T., Pedersen, O., Samani, N. J., Sørensen, T. I. A., Takayanagi, R., Toniolo, D., Ahsan, H., Allayee, H., Chen, Y-T., Danesh, J., Deary, I. J., Franco, O. H., Franke, L., Heijman, B. T., Holbrook, J. D., Isaacs, A., Kim, B-J., Lin, X., Liu, J., März, W., Metspalu, A., Mohlke, K. L., Sanghera, D. K., Shu, X-O., van Meurs, J. B. J., Vithana, E., Wickremasinghe, A. R., Wijmenga, C., Wolffenbuttel, B. H. W., Yokota, M., Zheng, W., Zhu, D., Vineis, P., Kyrtopoulos, S. A., Kleinjans, J. C. S., McCarthy, M. I., Soong, R., Gieger, C., Scott, J., Teo, Y-Y., He, J., Elliott, P., Tai, E. S., van der Harst, P., Kooner, J. S. & Chambers, J. C., 2015, In : Nature Genetics. 47, 11, p. 1282-93

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  43. 2014
  44. Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.

    Flanagan, S. E., Haapaniemi, E., Russell, M. A., Caswell, R., Lango Allen, H., De Franco, E., McDonald, T. J., Rajala, H., Ramelius, A., Barton, J., Heiskanen, K., Heiskanen-Kosma, T., Kajosaari, M., Murphy, N. P., Milenkovic, T., Seppänen, M., Lernmark, Å., Mustjoki, S., Otonkoski, T., Kere, J. & 3 othersMorgan, N. G., Ellard, S. & Hattersley, A. T., 2014, In : Nature Genetics. 46, 8, p. 812-814

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  45. A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.

    Speedy, H. E., Di Bernardo, M. C., Sava, G. P., Dyer, M. J. S., Holroyd, A., Wang, Y., Sunter, N. J., Mansouri, L., Juliusson, G., Smedby, K. E., Roos, G., Jayne, S., Majid, A., Dearden, C., Hall, A. G., Mainou-Fowler, T., Jackson, G. H., Summerfield, G., Harris, R. J., Pettitt, A. R. & 9 othersAllsup, D. J., Bailey, J. R., Pratt, G., Pepper, C., Fegan, C., Rosenquist, R., Catovsky, D., Allan, J. M. & Houlston, R. S., 2014, In : Nature Genetics. 46, 1, p. 56

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  46. Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

    Thompson, B. A., Spurdle, A. B., Plazzer, J-P., Greenblatt, M. S., Akagi, K., Al-Mulla, F., Bapat, B., Bernstein, I., Capellá, G., den Dunnen, J. T., du Sart, D., Fabre, A., Farrell, M. P., Farrington, S. M., Frayling, I. M., Frebourg, T., Goldgar, D. E., Heinen, C. D., Holinski-Feder, E., Kohonen-Corish, M. & 119 othersRobinson, K. L., Leung, S. Y., Martins, A., Moller, P., Morak, M., Nystrom, M., Peltomaki, P., Pineda, M., Qi, M., Ramesar, R., Rasmussen, L., Royer-Pokora, B., Scott, R. J., Sijmons, R., Tavtigian, S. V., Tops, C. M., Weber, T., Wijnen, J., Woods, M. O., Macrae, F., Genuardi, M., Castillejo, A., Sexton, A., Chan, A. K. W., Viel, A., Blanco, A., French, A., Laner, A., Wagner, A., van den Ouweland, A., Mensenkamp, A., Payá, A., Betz, B., Redeker, B., Smith, B., Espenschied, C., Cummings, C., Engel, C., Fornes, C., Valenzuela, C., Alenda, C., Buchanan, D., Barana, D., Konstantinova, D., Cairns, D., Glaser, E., Silva, F., Lalloo, F., Crucianelli, F., Hogervorst, F., Casey, G., Tomlinson, I., Blanco, I., Villar, I. L., Garcia-Planells, J., Bigler, J., Shia, J., Martinez-Lopez, J., Gille, J. J. P., Hopper, J., Potter, J., Soto, J. L., Kantelinen, J., Ellis, K., Mann, K., Varesco, L., Zhang, L., Le Marchand, L., Marafie, M. J., Nordling, M., Tibiletti, M. G., Kahan, M. A., Ligtenberg, M., Clendenning, M., Jenkins, M., Speevak, M., Digweed, M., Kloor, M., Hitchins, M., Myers, M., Aronson, M., Dominguez, M., Kutsche, M., Parsons, M., Walsh, M., Kansikas, M., Zahary, M. N., Pedroni, M., Heider, N., Poplawski, N., Rahner, N., Lindor, N. M., Sala, P., Nan, P., Propping, P., Newcomb, P., Sarin, R., Haile, R., Hofstra, R., Ward, R., Tricarico, R., Bacares, R., Young, S., Chialina, S., Kovalenko, S., Gunawardena, S. R., Moreno, S., Ho, S. L., Yuen, S. T., Thibodeau, S. N., Gallinger, S., Burnett, T., Teitsch, T., Chan, T. L., Smyrk, T., Cranston, T., Psofaki, V., Steinke-Lange, V. & Barbera, V-M., 2014, In : Nature Genetics. 46, p. 107-115

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  47. Defining the role of common variation in the genomic and biological architecture of adult human height.

    Wood, A. R., Esko, T., Yang, J., Vedantam, S., Pers, T. H., Gustafsson, S., Chu, A. Y., Estrada, K., Luan, J., Kutalik, Z., Amin, N., Buchkovich, M. L., Croteau-Chonka, D. C., Day, F. R., Duan, Y., Fall, T., Fehrmann, R., Ferreira, T., Jackson, A. U., Karjalainen, J. & 425 othersLo, K. S., Locke, A. E., Mägi, R., Mihailov, E., Porcu, E., Randall, J. C., Scherag, A., Vinkhuyzen, A. A. E., Westra, H-J., Winkler, T. W., Workalemahu, T., Zhao, J. H., Absher, D., Albrecht, E., Anderson, D., Baron, J., Beekman, M., Demirkan, A., Ehret, G. B., Feenstra, B., Feitosa, M. F., Fischer, K., Fraser, R. M., Goel, A., Gong, J., Justice, A. E., Kanoni, S., Kleber, M. E., Kristiansson, K., Lim, U., Lotay, V., Lui, J. C., Mangino, M., Mateo Leach, I., Medina-Gomez, C., Nalls, M. A., Nyholt, D. R., Palmer, C. D., Pasko, D., Pechlivanis, S., Prokopenko, I., Ried, J. S., Ripke, S., Shungin, D., Stancáková, A., Strawbridge, R. J., Sung, Y. J., Tanaka, T., Teumer, A., Trompet, S., van der Laan, S. W., van Setten, J., Van Vliet-Ostaptchouk, J. V., Wang, Z., Yengo, L., Zhang, W., Afzal, U., Arnlöv, J., Arscott, G. M., Bandinelli, S., Barrett, A., Bellis, C., Bennett, A. J., Berne, C., Blüher, M., Bolton, J. L., Böttcher, Y., Boyd, H. A., Bruinenberg, M., Buckley, B. M., Buyske, S., Caspersen, I. H., Chines, P. S., Clarke, R., Claudi-Boehm, S., Cooper, M., Daw, E. W., De Jong, P. A., Deelen, J., Delgado, G., Denny, J. C., Dhonukshe-Rutten, R., Dimitriou, M., Doney, A. S. F., Dörr, M., Eklund, N., Eury, E., Folkersen, L., Garcia, M. E., Geller, F., Giedraitis, V., Go, A. S., Grallert, H., Grammer, T. B., Gräßler, J., Grönberg, H., de Groot, L. C. P. G. M., Groves, C. J., Haessler, J., Hall, P., Haller, T., Hallmans, G., Hannemann, A., Hartman, C. A., Hassinen, M., Hayward, C., Heard-Costa, N. L., Helmer, Q., Hemani, G., Henders, A. K., Hillege, H. L., Hlatky, M. A., Hoffmann, W., Hoffmann, P., Holmen, O., Houwing-Duistermaat, J. J., Illig, T., Isaacs, A., James, A. L., Jeff, J., Johansen, B., Johansson, A., Jolley, J., Juliusdottir, T., Junttila, J., Kho, A. N., Kinnunen, L., Klopp, N., Kocher, T., Kratzer, W., Lichtner, P., Lind, L., Lindström, J., Lobbens, S., Lorentzon, M., Lu, Y., Lyssenko, V., Magnusson, P. K. E., Mahajan, A., Maillard, M., McArdle, W. L., McKenzie, C. A., McLachlan, S., McLaren, P. J., Menni, C., Merger, S., Milani, L., Moayyeri, A., Monda, K. L., Morken, M. A., Müller, G., Müller-Nurasyid, M., Musk, A. W., Narisu, N., Nauck, M., Nolte, I. M., Nöthen, M. M., Oozageer, L., Pilz, S., Rayner, N. W., Frida Renström, Robertson, N. R., Rose, L. M., Roussel, R., Sanna, S., Scharnagl, H., Scholtens, S., Schumacher, F. R., Schunkert, H., Scott, R. A., Sehmi, J., Seufferlein, T., Shi, J., Silventoinen, K., Smit, J. H., Smith, A. V., Smolonska, J., Stanton, A. V., Stirrups, K., Stott, D. J., Stringham, H. M., Sundström, J., Swertz, M. A., Syvänen, A-C., Tayo, B. O., Thorleifsson, G., Tyrer, J. P., van Dijk, S., van Schoor, N. M., van der Velde, N., van Heemst, D., van Oort, F. V. A., Vermeulen, S. H., Verweij, N., Vonk, J. M., Waite, L. L., Waldenberger, M., Wennauer, R., Wilkens, L. R., Willenborg, C., Wilsgaard, T., Wojczynski, M. K., Wong, A., Wright, A. F., Zhang, Q., Arveiler, D., Bakker, S. J. L., Beilby, J., Bergman, R. N., Bergmann, S., Biffar, R., Blangero, J., Boomsma, D. I., Bornstein, S. R., Bovet, P., Brambilla, P., Brown, M. J., Campbell, H., Caulfield, M. J., Chakravarti, A., Collins, R., Collins, F. S., Crawford, D. C., Cupples, L. A., Danesh, J., de Faire, U., den Ruijter, H. M., Erbel, R., Erdmann, J., Eriksson, J. G., Farrall, M., Ferrannini, E., Ferrières, J., Ford, I., Forouhi, N. G., Forrester, T., Gansevoort, R. T., Gejman, P. V., Gieger, C., Golay, A., Gottesman, O., Gudnason, V., Gyllensten, U., Haas, D. W., Hall, A. S., Harris, T. B., Hattersley, A. T., Heath, A. C., Hengstenberg, C., Hicks, A. A., Hindorff, L. A., Hingorani, A. D., Hofman, A., Hovingh, G. K., Humphries, S. E., Hunt, S. C., Hypponen, E., Jacobs, K. B., Jarvelin, M-R., Jousilahti, P., Jula, A. M., Kaprio, J., Kastelein, J. J. P., Kayser, M., Kee, F., Keinanen-Kiukaanniemi, S. M., Kiemeney, L. A., Kooner, J. S., Kooperberg, C., Koskinen, S., Kovacs, P., Kraja, A. T., Kumari, M., Kuusisto, J., Lakka, T. A., Langenberg, C., Le Marchand, L., Lehtimäki, T., Lupoli, S., Madden, P. A. F., Männistö, S., Manunta, P., Marette, A., Matise, T. C., McKnight, B., Meitinger, T., Moll, F. L., Montgomery, G. W., Morris, A. D., Morris, A. P., Murray, J. C., Nelis, M., Ohlsson, C., Oldehinkel, A. J., Ong, K. K., Ouwehand, W. H., Pasterkamp, G., Peters, A., Pramstaller, P. P., Price, J. F., Qi, L., Raitakari, O. T., Rankinen, T., Rao, D. C., Rice, T. K., Ritchie, M., Rudan, I., Salomaa, V., Samani, N. J., Saramies, J., Sarzynski, M. A., Schwarz, P. E. H., Sebert, S., Sever, P., Shuldiner, A. R., Sinisalo, J., Steinthorsdottir, V., Stolk, R. P., Tardif, J-C., Tönjes, A., Tremblay, A., Tremoli, E., Virtamo, J., Vohl, M-C., Amouyel, P., Asselbergs, F. W., Assimes, T. L., Bochud, M., Boehm, B. O., Boerwinkle, E., Bottinger, E. P., Bouchard, C., Cauchi, S., Chambers, J. C., Chanock, S. J., Cooper, R. S., de Bakker, P. I. W., Dedoussis, G., Ferrucci, L., Paul Franks, Froguel, P., Leif Groop, Haiman, C. A., Hamsten, A., Hayes, M. G., Hui, J., Hunter, D. J., Hveem, K., Jukema, J. W., Kaplan, R. C., Kivimaki, M., Kuh, D., Laakso, M., Liu, Y., Martin, N. G., März, W., Melbye, M., Moebus, S., Munroe, P. B., Njølstad, I., Oostra, B. A., Palmer, C. N. A., Pedersen, N. L., Perola, M., Pérusse, L., Peters, U., Powell, J. E., Power, C., Quertermous, T., Rauramaa, R., Reinmaa, E., Ridker, P. M., Rivadeneira, F., Rotter, J. I., Saaristo, T. E., Saleheen, D., Schlessinger, D., Slagboom, P. E., Snieder, H., Spector, T. D., Strauch, K., Stumvoll, M., Tuomilehto, J., Uusitupa, M., van der Harst, P., Völzke, H., Walker, M., Wareham, N. J., Watkins, H., Wichmann, H-E., Wilson, J. F., Zanen, P., Deloukas, P., Heid, I. M., Lindgren, C. M., Mohlke, K. L., Speliotes, E. K., Thorsteinsdottir, U., Barroso, I., Fox, C. S., North, K. E., Strachan, D. P., Beckmann, J. S., Berndt, S. I., Boehnke, M., Borecki, I. B., McCarthy, M. I., Metspalu, A., Stefansson, K., Uitterlinden, A. G., van Duijn, C. M., Franke, L., Willer, C. J., Price, A. L., Lettre, G., Loos, R. J. F., Weedon, M. N., Ingelsson, E., O'Connell, J. R., Abecasis, G. R., Chasman, D. I., Goddard, M. E., Visscher, P. M., Hirschhorn, J. N. & Frayling, T. M., 2014, In : Nature Genetics. 46, 11, p. 1173-1186

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  48. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

    Arking, D. E., Pulit, S. L., Crotti, L., van der Harst, P., Munroe, P. B., Koopmann, T. T., Sotoodehnia, N., Rossin, E. J., Morley, M., Wang, X., Johnson, A. D., Lundby, A., Gudbjartsson, D. F., Noseworthy, P. A., Eijgelsheim, M., Bradford, Y., Tarasov, K. V., Dörr, M., Müller-Nurasyid, M., Lahtinen, A. M. & 210 othersNolte, I. M., Smith, A. V., Bis, J. C., Isaacs, A., Newhouse, S. J., Evans, D. S., Post, W. S., Waggott, D., Lyytikäinen, L-P., Hicks, A. A., Eisele, L., Ellinghaus, D., Hayward, C., Navarro, P., Ulivi, S., Tanaka, T., Tester, D. J., Chatel, S., Gustafsson, S., Kumari, M., Morris, R. W., Naluai, A. T., Padmanabhan, S., Kluttig, A., Strohmer, B., Panayiotou, A. G., Torres, M., Knoflach, M., Hubacek, J. A., Slowikowski, K., Raychaudhuri, S., Kumar, R. D., Harris, T. B., Launer, L. J., Shuldiner, A. R., Alonso, A., Bader, J. S., Ehret, G., Huang, H., Kao, W. H. L., Strait, J. B., Macfarlane, P. W., Brown, M., Caulfield, M. J., Samani, N. J., Kronenberg, F., Willeit, J., Gustav Smith, Greiser, K. H., Meyer Zu Schwabedissen, H., Werdan, K., Carella, M., Zelante, L., Heckbert, S. R., Psaty, B. M., Rotter, J. I., Kolcic, I., Polašek, O., Wright, A. F., Griffin, M., Daly, M. J., Arnar, D. O., Hólm, H., Thorsteinsdottir, U., Denny, J. C., Roden, D. M., Zuvich, R. L., Emilsson, V., Plump, A. S., Larson, M. G., O'Donnell, C. J., Yin, X., Bobbo, M., D'Adamo, A. P., Iorio, A., Sinagra, G., Carracedo, A., Cummings, S. R., Nalls, M. A., Jula, A., Kontula, K. K., Marjamaa, A., Oikarinen, L., Perola, M., Porthan, K., Erbel, R., Hoffmann, P., Jöckel, K-H., Kälsch, H., Nöthen, M. M., den Hoed, M., Loos, R. J. F., Thelle, D. S., Gieger, C., Meitinger, T., Perz, S., Peters, A., Prucha, H., Sinner, M. F., Waldenberger, M., de Boer, R. A., Franke, L., van der Vleuten, P. A., Beckmann, B. M., Martens, E., Bardai, A., Hofman, N., Wilde, A. A. M., Behr, E. R., Dalageorgou, C., Giudicessi, J. R., Medeiros-Domingo, A., Barc, J., Kyndt, F., Probst, V., Ghidoni, A., Insolia, R., Hamilton, R. M., Scherer, S. W., Brandimarto, J., Margulies, K., Moravec, C. E., Fabiola, NN., Fuchsberger, C., O'Connell, J. R., Lee, W. K., Watt, G. C. M., Campbell, H., Wild, S. H., El Mokhtari, N. E., Frey, N., Asselbergs, F. W., Leach, I. M., Navis, G., van den Berg, M. P., van Veldhuisen, D. J., Kellis, M., Krijthe, B. P., Franco, O. H., Hofman, A., Kors, J. A., Uitterlinden, A. G., Witteman, J. C. M., Kedenko, L., Lamina, C., Oostra, B. A., Abecasis, G. R., Lakatta, E. G., Mulas, A., Orrú, M., Schlessinger, D., Uda, M., Markus, M. R. P., Völker, U., Snieder, H., Spector, T. D., Arnlöv, J., Lind, L., Sundström, J., Syvänen, A-C., Kivimaki, M., Kähönen, M., Mononen, N., Raitakari, O. T., Viikari, J. S., Adamkova, V., Kiechl, S., Brion, M., Nicolaides, A. N., Paulweber, B., Haerting, J., Dominiczak, A. F., Nyberg, F., Whincup, P. H., Hingorani, A. D., Schott, J-J., Bezzina, C. R., Ingelsson, E., Ferrucci, L., Gasparini, P., Wilson, J. F., Rudan, I., Franke, A., Mühleisen, T. W., Pramstaller, P. P., Lehtimäki, T. J., Paterson, A. D., Parsa, A., Liu, Y., van Duijn, C. M., Siscovick, D. S., Gudnason, V., Jamshidi, Y., Salomaa, V., Felix, S. B., Sanna, S., Ritchie, M. D., Stricker, B. H., Stefansson, K., Boyer, L. A., Cappola, T. P., Olsen, J. V., Lage, K., Schwartz, P. J., Kääb, S., Chakravarti, A., Ackerman, M. J., Pfeufer, A., de Bakker, P. I. W. & Newton-Cheh, C., 2014, In : Nature Genetics. 46, 8, p. 826-836

    Research output: Contribution to journalArticle

  49. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

    Mahajan, A., Go, M. J., Zhang, W., Below, J. E., Gaulton, K. J., Ferreira, T., Horikoshi, M., Johnson, A. D., Ng, M. C. Y., Prokopenko, I., Saleheen, D., Wang, X., Zeggini, E., Abecasis, G. R., Adair, L. S., Almgren, P., Atalay, M., Aung, T., Baldassarre, D., Balkau, B. & 312 othersBao, Y., Barnett, A. H., Barroso, I., Basit, A., Been, L. F., Beilby, J., Bell, G. I., Benediktsson, R., Bergman, R. N., Boehm, B. O., Boerwinkle, E., Bonnycastle, L. L., Burtt, N., Cai, Q., Campbell, H., Carey, J., Cauchi, S., Caulfield, M., Chan, J. C. N., Chang, L-C., Chang, T-J., Chang, Y-C., Charpentier, G., Chen, C-H., Chen, H., Chen, Y-T., Chia, K-S., Chidambaram, M., Chines, P. S., Cho, N. H., Cho, Y. M., Chuang, L-M., Collins, F. S., Cornelis, M. C., Couper, D. J., Crenshaw, A. T., van Dam, R. M., Danesh, J., Das, D., de Faire, U., Dedoussis, G., Deloukas, P., Dimas, A. S., Dina, C., Doney, A. S. F., Donnelly, P. J., Mozhgan Dorkhan, van Duijn, C., Dupuis, J., Edkins, S., Elliott, P., Emilsson, V., Erbel, R., Eriksson, J. G., Escobedo, J., Esko, T., Eury, E., Florez, J. C., Fontanillas, P., Forouhi, N. G., Forsen, T., Fox, C., Fraser, R. M., Frayling, T. M., Froguel, P., Frossard, P., Gao, Y., Gertow, K., Gieger, C., Gigante, B., Grallert, H., Grant, G. B., Leif Groop, Groves, C. J., Grundberg, E., Guiducci, C., Hamsten, A., Han, B-G., Hara, K., Hassanali, N., Hattersley, A. T., Hayward, C., Hedman, A. K., Herder, C., Hofman, A., Holmen, O. L., Hovingh, K., Hreidarsson, A. B., Hu, C., Hu, F. B., Hui, J., Humphries, S. E., Hunt, S. E., Hunter, D. J., Hveem, K., Hydrie, Z. I., Ikegami, H., Illig, T., Ingelsson, E., Islam, M., Isomaa, B., Jackson, A. U., Jafar, T., James, A., Jia, W., Joeckel, K-H., Jonsson, A., Jowett, J. B. M., Kadowaki, T., Kang, H. M., Kanoni, S., Kao, W. H. L., Kathiresan, S., Kato, N., Katulanda, P., Keinanen-Kiukaanniemi, S. M., Kelly, A. M., Khan, H., Khaw, K-T., Khor, C-C., Kim, H-L., Kim, S., Kim, Y. J., Kinnunen, L., Klopp, N., Kong, A., Korpi-Hyovalti, E., Kowlessur, S., Kraft, P., Jasmina Kravic, Kristensen, M. M., Krithika, S., Kumar, A., Kumate, J., Kuusisto, J., Kwak, S. H., Laakso, M., Lagou, V., Lakka, T. A., Langenberg, C., Langford, C., Lawrence, R., Leander, K., Lee, J-M., Lee, N. R., Li, M., Li, X., Li, Y., Liang, J., Liju, S., Lim, W-Y., Lind, L., Lindgren, C. M., Eero Lindholm, Liu, C-T., Liu, J. J., Lobbens, S., Long, J., Loos, R. J. F., Lu, W., Luan, J., Valeriya Lyssenko, Ma, R. C. W., Maeda, S., Maegi, R., Mannisto, S., Matthews, D. R., Meigs, J. B., Olle Melander, Metspalu, A., Meyer, J., Mirza, G., Mihailov, E., Moebus, S., Mohan, V., Mohlke, K. L., Morris, A. D., Muehleisen, T. W., Mueller-Nurasyid, M., Musk, B., Nakamura, J., Nakashima, E., Navarro, P., Ng, P-K., Nica, A. C., Peter Nilsson, Njolstad, I., Noethen, M. M., Ohnaka, K., Ong, T. H., Owen, K. R., Palmer, C. N. A., Pankow, J. S., Park, K. S., Parkin, M., Pechlivanis, S., Pedersen, N. L., Peltonen, L., Perry, J. R. B., Peters, A., Pinidiyapathirage, J. M., Platou, C. G. P., Potter, S., Price, J. F., Qi, L., Radha, V., Rallidis, L., Rasheed, A., Rathmann, W., Rauramaa, R., Raychaudhuri, S., Rayner, N. W., Rees, S. D., Rehnberg, E., Ripatti, S., Robertson, N., Roden, M., Rossin, E. J., Rudan, I., Rybin, D., Saaristo, T. E., Salomaa, V., Saltevo, J., Samuel, M., Sanghera, D. K., Saramies, J., Scott, J., Scott, L. J., Scott, R. A., Segre, A. V., Sehmi, J., Sennblad, B., Shah, N., Shah, S., Shera, A. S., Shu, X. O., Shuldiner, A. R., Sigurdsson, G., Sijbrands, E., Silveira, A., Sim, X., Sivapalaratnam, S., Small, K. S., So, W. Y., Stancakova, A., Stefansson, K., Steinbach, G., Steinthorsdottir, V., Stirrups, K., Strawbridge, R. J., Stringham, H. M., Sun, Q., Suo, C., Syvanen, A-C., Takayanagi, R., Takeuchi, F., Tay, W. T., Teslovich, T. M., Thorand, B., Thorleifsson, G., Thorsteinsdottir, U., Tikkanen, E., Trakalo, J., Tremoli, E., Trip, M. D., Tsai, F. J., Tuomi, T., Tuomilehto, J., Uitterlinden, A. G., Valladares-Salgado, A., Vedantam, S., Veglia, F., Voight, B. F., Wang, C., Wareham, N. J., Wennauer, R., Wickremasinghe, A. R., Wilsgaard, T., Wilson, J. F., Wiltshire, S., Winckler, W., Wong, T. Y., Wood, A. R., Wu, J-Y., Wu, Y., Yamamoto, K., Yamauchi, T., Yang, M., Yengo, L., Yokota, M., Young, R., Zabaneh, D., Zhang, F., Zhang, R., Zheng, W., Zimmet, P. Z., Altshuler, D., Bowden, D. W., Cho, Y. S., Cox, N. J., Cruz, M., Hanis, C. L., Kooner, J., Lee, J-Y., Seielstad, M., Teo, Y. Y., Boehnke, M., Parra, E. J., Chambers, J. C., Tai, E. S., McCarthy, M. I. & Morris, A. P., 2014, In : Nature Genetics. 46, 3, p. 234

    Research output: Contribution to journalArticle

  50. GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.

    Karolin Hansén Nord, Lilljebjörn, H., Vezzi, F., Nilsson, J., Magnusson, L., Tayebwa, J., de Jong, D., Bovée, J. V. M. G., Hogendoorn, P. C. W. & Szuhai, K., 2014, In : Nature Genetics. 46, 5, p. 474-477

    Research output: Contribution to journalArticle

  51. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.

    Flannick, J., Thorleifsson, G., Beer, N. L., Jacobs, S. B. R., Grarup, N., Burtt, N. P., Mahajan, A., Fuchsberger, C., Atzmon, G., Benediktsson, R., Blangero, J., Bowden, D. W., Brandslund, I., Brosnan, J., Burslem, F., Chambers, J., Cho, Y. S., Christensen, C., Douglas, D., Duggirala, R. & 60 othersDymek, Z., Farjoun, Y., Fennell, T., Fontanillas, P., Forsén, T., Gabriel, S., Glaser, B., Gudbjartsson, D. F., Hanis, C., Hansen, T., Hreidarsson, A. B., Hveem, K., Ingelsson, E., Isomaa, B., Johansson, S., Jørgensen, T., Jørgensen, M. E., Kathiresan, S., Kong, A., Kooner, J., Jasmina Kravic, Laakso, M., Lee, J-Y., Lind, L., Lindgren, C. M., Linneberg, A., Masson, G., Meitinger, T., Mohlke, K. L., Molven, A., Morris, A. P., Potluri, S., Rauramaa, R., Ribel-Madsen, R., Richard, A-M., Rolph, T., Salomaa, V., Segrè, A. V., Skärstrand, H., Steinthorsdottir, V., Stringham, H. M., Sulem, P., Tai, E. S., Teo, Y. Y., Teslovich, T., Thorsteinsdottir, U., Trimmer, J. K., Tuomi, T., Tuomilehto, J., Vaziri Sani, F., Voight, B. F., Wilson, J. G., Boehnke, M., McCarthy, M. I., Njølstad, P. R., Pedersen, O., Leif Groop, Cox, D. R., Stefansson, K. & Altshuler, D., 2014, In : Nature Genetics. 46, 4, p. 357

    Research output: Contribution to journalArticle

  52. Meta-analysis of gene-level tests for rare variant association.

    Liu, D. J., Peloso, G. M., Zhan, X., Holmen, O. L., Zawistowski, M., Feng, S., Nikpay, M., Auer, P. L., Goel, A., Zhang, H., Peters, U., Farrall, M., Orho-Melander, M., Kooperberg, C., McPherson, R., Watkins, H., Willer, C. J., Hveem, K., Melander, O., Kathiresan, S. & 1 othersAbecasis, G. R., 2014, In : Nature Genetics. 46, 2, p. 200

    Research output: Contribution to journalArticle

  53. Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.

    Styrkarsdottir, U., Thorleifsson, G., Helgadottir, H. T., Bomer, N., Metrustry, S., Bierma-Zeinstra, S., Strijbosch, A. M., Evangelou, E., Hart, D., Beekman, M., Jonasdottir, A., Sigurdsson, A., Eiriksson, F. F., Thorsteinsdottir, M., Frigge, M. L., Kong, A., Gudjonsson, S. A., Magnusson, O. T., Masson, G., Hofman, A. & 16 othersArden, N. K., Ingvarsson, T., Stefan Lohmander, Kloppenburg, M., Rivadeneira, F., Nelissen, R. G. H. H., Spector, T., Uitterlinden, A., Slagboom, P. E., Thorsteinsdottir, U., Jonsdottir, I., Valdes, A. M., Meulenbelt, I., van Meurs, J., Jonsson, H. & Stefansson, K., 2014, In : Nature Genetics. 46, 5, p. 498-502

    Research output: Contribution to journalArticle

  54. 2013
  55. A functional variant in the CFI gene confers a high risk of age-related macular degeneration

    van de Ven, J. P. H., Nilsson, S., Tan, P. L., Buitendijk, G. H. S., Ristau, T., Mohlin, F., Nabuurs, S. B., Schoenmaker-Koller, F. E., Smailhodzic, D., Campochiaro, P. A., Zack, D. J., Duvvari, M. R., Bakker, B., Paun, C. C., Boon, C. J. F., Uitterlinden, A. G., Liakopoulos, S., Klevering, B. J., Fauser, S., Daha, M. R. & 5 othersKatsanis, N., Klaver, C. C. W., Anna Blom, Hoyng, C. B. & den Hollander, A. I., 2013, In : Nature Genetics. 45, 7, p. 813

    Research output: Contribution to journalArticle

  56. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

    Beecham, A. H., Patsopoulos, N. A., Xifara, D. K., Davis, M. F., Kemppinen, A., Cotsapas, C., Shah, T. S., Spencer, C., Booth, D., Goris, A., Oturai, A., Saarela, J., Fontaine, B., Hemmer, B., Martin, C., Zipp, F., D'Alfonso, S., Martinelli-Boneschi, F., Taylor, B., Harbo, H. F. & 173 othersKockum, I., Hillert, J., Olsson, T., Ban, M., Oksenberg, J. R., Hintzen, R., Barcellos, L. F., Agliardi, C., Alfredsson, L., Alizadeh, M., Anderson, C., Andrews, R., Sondergaard, H. B., Baker, A., Band, G., Baranzini, S. E., Barizzone, N., Barrett, J., Bellenguez, C., Bergamaschi, L., Bernardinelli, L., Berthele, A., Biberacher, V., Binder, T. M. C., Blackburn, H., Bomfim, I. L., Brambilla, P., Broadley, S., Brochet, B., Brundin, L., Buck, D., Butzkueven, H., Caillier, S. J., Camu, W., Carpentier, W., Cavalla, P., Celius, E. G., Coman, I., Comi, G., Corrado, L., Cosemans, L., Cournu-Rebeix, I., Cree, B. A. C., Cusi, D., Damotte, V., Defer, G., Delgado, S. R., Deloukas, P., di Sapio, A., Dilthey, A. T., Donnelly, P., Dubois, B., Duddy, M., Edkins, S., Elovaara, I., Esposito, F., Evangelou, N., Fiddes, B., Field, J., Franke, A., Freeman, C., Frohlich, I. Y., Galimberti, D., Gieger, C., Gourraud, P-A., Graetz, C., Graham, A., Grummel, V., Guaschino, C., Hadjixenofontos, A., Hakonarson, H., Halfpenny, C., Hall, G., Hall, P., Hamsten, A., Harley, J., Harrower, T., Hawkins, C., Hellenthal, G., Hillier, C., Hobart, J., Hoshi, M., Hunt, S. E., Jagodic, M., Jelcic, I., Jochim, A., Kendall, B., Kermode, A., Kilpatrick, T., Koivisto, K., Konidari, I., Korn, T., Kronsbein, H., Langford, C., Larsson, M., Lathrop, M., Lebrun-Frenay, C., Lechner-Scott, J., Lee, M. H., Leone, M. A., Leppa, V., Liberatore, G., Lie, B. A., Lill, C. M., Linden, M., Link, J., Luessi, F., Lycke, J., Macciardi, F., Mannisto, S., Manrique, C. P., Martin, R., Martinelli, V., Mason, D., Mazibrada, G., McCabe, C., Mero, I-L., Mescheriakova, J., Moutsianas, L., Myhr, K-M., Nagels, G., Nicholas, R., Petra Nilsson, Piehl, F., Pirinen, M., Price, S. E., Quach, H., Reunanen, M., Robberecht, W., Robertson, N. P., Rodegher, M., Rog, D., Salvetti, M., Schnetz-Boutaud, N. C., Sellebjerg, F., Selter, R. C., Schaefer, C., Shaunak, S., Shen, L., Shields, S., Siffrin, V., Slee, M., Sorensen, P. S., Sorosina, M., Sospedra, M., Spurkland, A., Strange, A., Sundqvist, E., Thijs, V., Thorpe, J., Ticca, A., Tienari, P., van Duijn, C., Visser, E. M., Vucic, S., Westerlind, H., Wiley, J. S., Wilkins, A., Wilson, J. F., Winkelmann, J., Zajicek, J., Zindler, E., Haines, J. L., Pericak-Vance, M. A., Ivinson, A. J., Stewart, G., Hafler, D., Hauser, S. L., Compston, A., McVean, G., De Jager, P., Sawcer, S. J. & McCauley, J. L., 2013, In : Nature Genetics. 45, 11, p. 1353

    Research output: Contribution to journalArticle

  57. Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes

    Flannick, J., Beer, N. L., Bick, A. G., Agarwala, V., Molnes, J., Gupta, N., Burtt, N. P., Florez, J. C., Meigs, J. B., Taylor, H., Lyssenko, V., Irgens, H., Fox, E., Burslem, F., Johansson, S., Brosnan, M. J., Trimmer, J. K., Newton-Cheh, C., Tuomi, T., Molven, A. & 12 othersWilson, J. G., O'Donnell, C. J., Kathiresan, S., Hirschhorn, J. N., Njolstad, P. R., Rolph, T., Seidman, J. G., Gabriel, S., Cox, D. R., Seidman, C. E., Leif Groop & Altshuler, D., 2013, In : Nature Genetics. 45, 11, p. 1380

    Research output: Contribution to journalArticle

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