Research
Print page Print page
Switch language
Rigshospitalet - a part of Copenhagen University Hospital

Nature Genetics, 1061-4036

Journal

  1. 2020
  2. Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing

    PCAWG-Structural Variation Working Group, 5 Feb 2020, In : Nature Genetics.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer

    PCAWG-Structural Variation Working Group, 5 Feb 2020, In : Nature Genetics.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition

    PCAWG-Structural Variation Working Group, 5 Feb 2020, In : Nature Genetics.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

    GEMO Study Collaborators, Jan 2020, In : Nature Genetics. 52, 1, p. 56-73 18 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. 2019
  7. Published

    The genetic evolution of metastatic uveal melanoma

    Shain, A. H., Bagger, M. M., Yu, R., Chang, D., Liu, S., Vemula, S., Weier, J. F., Wadt, K., Heegaard, S., Bastian, B. C. & Kiilgaard, J. F., Jul 2019, In : Nature Genetics. 51, 7, p. 1123-1130 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    A catalog of genetic loci associated with kidney function from analyses of a million individuals

    LifeLines Cohort study, 1 Jun 2019, In : Nature Genetics. 51, 6, p. 957-972 16 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Osteogenesis depends on commissioning of a network of stem cell transcription factors that act as repressors of adipogenesis

    Rauch, A., Haakonsson, A. K., Madsen, J. G. S., Larsen, M., Forss, I., Madsen, M. R., Van Hauwaert, E. L., Wiwie, C., Jespersen, N. Z., Tencerova, M., Nielsen, R., Larsen, B. D., Röttger, R., Baumbach, J., Scheele, C., Kassem, M. & Mandrup, S., Apr 2019, In : Nature Genetics. 51, 4, p. 716-727 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

    CHD Exome+ Consortium, 1 Mar 2019, In : Nature Genetics. 51, 3, p. 452-469 18 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (Nature Genetics, (2018), 50, 7, (928-936), 10.1038/s41588-018-0142-8)

    Schumacher, F. R., Olama, A. A. A., Berndt, S. I., Benlloch, S., Ahmed, M., Saunders, E. J., Dadaev, T., Leongamornlert, D., Anokian, E., Cieza-Borrella, C., Goh, C., Brook, M. N., Sheng, X., Fachal, L., Dennis, J., Tyrer, J., Muir, K., Lophatananon, A., Stevens, V. L., Gapstur, S. M., Carter, B. D., Tangen, C. M., Goodman, P. J., Thompson, I. M., Batra, J., Chambers, S., Moya, L., Clements, J., Horvath, L., Tilley, W., Risbridger, G. P., Gronberg, H., Aly, M., Nordström, T., Pharoah, P., Pashayan, N., Schleutker, J., Tammela, T. L. J., Sipeky, C., Auvinen, A., Albanes, D., Weinstein, S., Wolk, A., Håkansson, N., Nordestgaard, B. G., Nielsen, S. F., Weischer, M., Bisbjerg, R., Røder, M. A., Iversen, P. & Profile Study, Feb 2019, In : Nature Genetics. 51, 2, p. 363 1 p.

    Research output: Contribution to journalComment/debateResearchpeer-review

  12. 2018
  13. Published

    De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation

    Basilicata, M. F., Bruel, A-L., Semplicio, G., Valsecchi, C. I. K., Aktaş, T., Duffourd, Y., Rumpf, T., Morton, J., Bache, I., Szymanski, W. G., Gilissen, C., Vanakker, O., Õunap, K., Mittler, G., van der Burgt, I., El Chehadeh, S., Cho, M. T., Pfundt, R., Tan, T. Y., Kirchhoff, M., Menten, B., Vergult, S., Lindstrom, K., Reis, A., Johnson, D. S., Fryer, A., McKay, V., Fisher, R. B., Thauvin-Robinet, C., Francis, D., Roscioli, T., Pajusalu, S., Radtke, K., Ganesh, J., Brunner, H. G., Wilson, M., Faivre, L., Kalscheuer, V. M., Thevenon, J., Akhtar, A. & DDD Study, Oct 2018, In : Nature Genetics. 50, 10, p. 1442-1451 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

    Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

    Profile Study, 11 Jun 2018, In : Nature Genetics. 50, p. 928-36

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

    Wray, N. R., Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E. M., Abdellaoui, A., Adams, M. J., Agerbo, E., Air, T. M., Andlauer, T. M. F., Bacanu, S-A., Bækvad-Hansen, M., Beekman, A. F. T., Bigdeli, T. B., Binder, E. B., Blackwood, D. R. H., Bryois, J., Buttenschøn, H. N., Bybjerg-Grauholm, J., Cai, N., Castelao, E., Christensen, J. H., Clarke, T-K., Coleman, J. I. R., Colodro-Conde, L., Couvy-Duchesne, B., Craddock, N., Crawford, G. E., Crowley, C. A., Dashti, H. S., Davies, G., Deary, I. J., Degenhardt, F., Derks, E. M., Direk, N., Dolan, C. V., Dunn, E. C., Eley, T. C., Eriksson, N., Escott-Price, V., Kiadeh, F. H. F., Finucane, H. K., Forstner, A. J., Frank, J., Hansen, T. F., Krogh, J., Thompson, W., Weinsheimer, S. M., Nordentoft, M., Werge, T. & eQTLGen, May 2018, In : Nature Genetics. 50, 5, p. 668-681 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. Published

    Publisher Correction: 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., Bradfield, J. P., Esko, T., Giri, A., Graff, M., Guo, X., Hendricks, A. E., Karaderi, T., Lempradl, A., Locke, A. E., Mahajan, A., Marouli, E., Sivapalaratnam, S., Young, K. L., Alfred, T., Feitosa, M. F., Masca, N. G. D., Manning, A. K., Medina-Gomez, C., Mudgal, P., Ng, M. C. Y., Reiner, A. P., Vedantam, S., Willems, S. M., Winkler, T. W., Abecasis, G., Bang, L. E., Benn, M., Bork-Jensen, J., Friedrich, N., Frikke-Schmidt, R., Hansen, T., Jensen, G. B., Jørgensen, M. E., Jørgensen, T., Kamstrup, P. R., Linneberg, A., Nielsen, S. F., Nordestgaard, B. G., Pers, T. H., Petersen, E. R. B., Thuesen, B. H., Tybjaerg-Hansen, A., Varbo, A., Vestergaard, H. & CHD Exome+ Consortium, May 2018, In : Nature Genetics. 50, 5, p. 765-766 2 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published

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

    Mahajan, A., Wessel, J., Willems, S. M., Zhao, W., Robertson, N. R., Chu, A. Y., Gan, W., Kitajima, H., Taliun, D., Rayner, N. W., Guo, X., Lu, Y., Li, M., Jensen, R. A., Hu, Y., Huo, S., Lohman, K. K., Zhang, W., Cook, J. P., Prins, B. P., Flannick, J., Grarup, N., Trubetskoy, V. V., Kravic, J., Kim, Y. J., Rybin, D. V., Yaghootkar, H., Müller-Nurasyid, M., Meidtner, K., Li-Gao, R., Varga, T. V., Marten, J., Li, J., Smith, A. V., An, P., Ligthart, S., Gustafsson, S., Malerba, G., Afzal, S., Bang, L. B., Bork-Jensen, J., Tybjærg-Hansen, A., Jørgensen, M. E., Jørgensen, T., Linneberg, A., Nielsen, S. F., Rode, L., Varbo, A., Rosengren, A. H., Nordestgaard, B. G. & ExomeBP Consortium, Apr 2018, In : Nature Genetics. 50, 4, p. 559-571 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. Published

    Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes

    Grarup, N., Moltke, I., Andersen, M. K., Dalby, M., Vitting-Seerup, K., Kern, T., Mahendran, Y., Jørsboe, E., Larsen, C. V. L., Dahl-Petersen, I. K., Gilly, A., Suveges, D., Dedoussis, G., Zeggini, E., Pedersen, O., Andersson, R., Bjerregaard, P., Jørgensen, M. E., Albrechtsen, A. & Hansen, T., Jan 2018, In : Nature Genetics. 50, p. 172-174 2 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. Published

    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., Bradfield, J. P., Esko, T., Giri, A., Graff, M., Guo, X., Hendricks, A. E., Karaderi, T., Lempradl, A., Locke, A. E., Mahajan, A., Marouli, E., Sivapalaratnam, S., Young, K. L., Alfred, T., Feitosa, M. F., Masca, N. G. D., Manning, A. K., Medina-Gomez, C., Mudgal, P., Ng, M. C. Y., Reiner, A. P., Vedantam, S., Willems, S. M., Winkler, T. W., Abecasis, G., Aben, K. K., Alam, D. S., Alharthi, S. E., Bang, L. E., Benn, M., Bork-Jensen, J., Frikke-Schmidt, R., Jensen, G. B., Jørgensen, M. E., Jørgensen, T., Kamstrup, P. R., Linneberg, A., Nielsen, S. F., Nordestgaard, B. G., Pers, T. H., Thuesen, B. H., Tybjaerg-Hansen, A., Varbo, A., Vestergaard, H. & CHD Exome+ Consortium, Jan 2018, In : Nature Genetics. 50, 1, p. 26-41 16 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  20. Published

    Multi-ethnic genome-wide association study for atrial fibrillation

    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., Calkins, 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., Esa, N., Olesen, M. S., Refsgaard, L., Svendsen, J. H., Weeke, P. E. & Roselli, Caroline, 2018, In : Nature Genetics. 50, p. 1225-38

    Research output: Contribution to journalLetterResearchpeer-review

  21. 2017
  22. Published

    Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease

    Lu, X., Peloso, G. M., Liu, D. J., Wu, Y., Zhang, H., Zhou, W., Li, J., Tang, C. S-M., Dorajoo, R., Li, H., Long, J., Guo, X., Xu, M., Spracklen, C. N., Chen, Y., Liu, X., Zhang, Y., Khor, C. C., Liu, J., Sun, L., Wang, L., Gao, Y-T., Hu, Y., Yu, K., Wang, Y., Cheung, C. Y. Y., Wang, F., Huang, J., Fan, Q., Cai, Q., Chen, S., Shi, J., Yang, X., Zhao, W., Sheu, W. H-H., Cherny, S. S., He, M., Feranil, A. B., Adair, L. S., Gordon-Larsen, P., Du, S., Varma, R., Chen, Y-D. I., Shu, X-O., Lam, K. S. L., Wong, T. Y., Ganesh, S. K., Mo, Z., Hveem, K., Nielsen, J. B. & GLGC Consortium, Dec 2017, In : Nature Genetics. 49, 12, p. 1722-1730 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. Published

    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., Hui, S., Lemaçon, A., Soucy, P., Dennis, J., Jiang, X., Rostamianfar, A., Finucane, H., Bolla, M. K., McGuffog, L., Wang, Q., Aalfs, C. M., Adams, M., Adlard, J., Agata, S., Ahmed, S., Ahsan, H., Aittomäki, K., Al-Ejeh, F., Allen, J., Ambrosone, C. B., Amos, C. I., Andrulis, I. L., Anton-Culver, H., Antonenkova, N. N., Arndt, V., Arnold, N., Aronson, K. J., Auber, B., Auer, P. L., Ausems, M. G. E. M., Azzollini, J., Bacot, F., Balmaña, J., Barile, M., Barjhoux, L., Barkardottir, R. B., Bojesen, S. E., Ejlertsen, B., Flyger, H., Gerdes, A-M., Hansen, T. V. O., Lænkholm, A-V., Nielsen, S. F., Nordestgaard, B. G. & ABCTB Investigators, Dec 2017, In : Nature Genetics. 49, 12, p. 1767-1778 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    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., Assimes, T. L., Chowdhury, R., Orho-Melander, M., Damrauer, S., Small, A., Asma, S., Imamura, M., Yamauch, T., Chambers, J. C., Chen, P., Sapkota, B. R., Shah, N., Jabeen, S., Surendran, P., Lu, Y., Zhang, W., Imran, A., Abbas, S., Majeed, F., Trindade, K., Qamar, N., Mallick, N. H., Yaqoob, Z., Saghir, T., Rizvi, S. N. H., Memon, A., Rasheed, S. Z., Memon, F-U-R., Mehmood, K., Ahmed, N., Qureshi, I. H., Tanveer-Us-Salam, Iqbal, W., Malik, U., Mehra, N., Kuo, J. Z., Sheu, W. H-H., Guo, X., Nielsen, S. F., Nordestgaard, B. G., Tybjaerg-Hansen, A., Benn, M., Frikke-Schmidt, R., Kamstrup, P. R. & CHD Exome+ Consortium, Oct 2017, In : Nature Genetics. 49, 10, p. 1450-1457 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

    Howson, J. M. M., Zhao, W., Barnes, D. R., Ho, W-K., Young, R., Paul, D. S., Waite, L. L., Freitag, D. F., Fauman, E. B., Salfati, E. L., Sun, B. B., Eicher, J. D., Johnson, A. D., Sheu, W. H. H., Nielsen, S. F., Lin, W-Y., Surendran, P., Malarstig, A., Wilk, J. B., Tybjærg-Hansen, A., Rasmussen, K. L., Kamstrup, P. R., Deloukas, P., Erdmann, J., Kathiresan, S., Samani, N. J., Schunkert, H., Watkins, H., Do, R., Rader, D. J., Johnson, J. A., Hazen, S. L., Quyyumi, A. A., Spertus, J. A., Pepine, C. J., Franceschini, N., Justice, A., Reiner, A. P., Buyske, S., Hindorff, L. A., Carty, C. L., North, K. E., Kooperberg, C., Boerwinkle, E., Young, K., Graff, M., Peters, U., Absher, D., Hsiung, C. A., Nordestgaard, B. G. & CARDIoGRAMplusC4D, Jul 2017, In : Nature Genetics. 49, 7, p. 1113-1119 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. Published

    Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

    Aung, T., Ozaki, M., Lee, M. C., Schlötzer-Schrehardt, U., Thorleifsson, G., Mizoguchi, T., Igo, R. P., Haripriya, A., Williams, S. E., Astakhov, Y. S., Orr, A. C., Burdon, K. P., Nakano, S., Mori, K., Abu-Amero, K., Hauser, M., Li, Z., Prakadeeswari, G., Bailey, J. N. C., Cherecheanu, A. P., Kang, J. H., Nelson, S., Hayashi, K., Manabe, S-I., Kazama, S., Zarnowski, T., Inoue, K., Irkec, M., Coca-Prados, M., Sugiyama, K., Järvelä, I., Schlottmann, P., Lerner, S. F., Lamari, H., Nilgün, Y., Bikbov, M., Park, K. H., Cha, S. C., Yamashiro, K., Zenteno, J. C., Jonas, J. B., Kumar, R. S., Perera, S. A., Chan, A. S. Y., Kobakhidze, N., George, R., Vijaya, L., Do, T., Edward, D. P., de Juan Marcos, L., Pakravan, M., Moghimi, S., Ideta, R., Bach-Holm, D., Kappelgaard, P., Wirostko, B., Thomas, S., Gaston, D., Bedard, K., Greer, W. L., Yang, Z., Chen, X., Huang, L., Sang, J., Jia, H., Jia, L., Qiao, C., Zhang, H., Liu, X., Zhao, B., Wang, Y-X., Xu, L., Leruez, S., Reynier, P., Chichua, G., Tabagari, S., Uebe, S., Zenkel, M., Berner, D., Mossböck, G., Weisschuh, N., Hoja, U., Welge-Luessen, U-C., Mardin, C., Founti, P., Chatzikyriakidou, A., Pappas, T., Anastasopoulos, E., Lambropoulos, A., Ghosh, A., Shetty, R., Porporato, N., Saravanan, V., Venkatesh, R., Shivkumar, C., Kalpana, N., Sarangapani, S., Kanavi, M. R., Beni, A. N., Yazdani, S., Lashay, A., Naderifar, H., Khatibi, N., Fea, A., Lavia, C., Dallorto, L., Rolle, T., Frezzotti, P., Paoli, D., Salvi, E., Manunta, P., Mori, Y., Miyata, K., Higashide, T., Chihara, E., Ishiko, S., Yoshida, A., Yanagi, M., Kiuchi, Y., Ohashi, T., Sakurai, T., Sugimoto, T., Chuman, H., Aihara, M., Inatani, M., Miyake, M., Gotoh, N., Matsuda, F., Yoshimura, N., Ikeda, Y., Ueno, M., Sotozono, C., Jeoung, J. W., Sagong, M., Park, K. H., Ahn, J., Cruz-Aguilar, M., Ezzouhairi, S. M., Rafei, A., Chong, Y. F., Ng, X. Y., Goh, S. R., Chen, Y., Yong, V. H. K., Khan, M. I., Olawoye, O. O., Ashaye, A. O., Ugbede, I., Onakoya, A., Kizor-Akaraiwe, N., Teekhasaenee, C., Suwan, Y., Supakontanasan, W., Okeke, S., Uche, N. J., Asimadu, I., Ayub, H., Akhtar, F., Kosior-Jarecka, E., Lukasik, U., Lischinsky, I., Castro, V., Grossmann, R. P., Megevand, G. S., Roy, S., Dervan, E., Silke, E., Rao, A., Sahay, P., Fornero, P., Cuello, O., Sivori, D., Zompa, T., Mills, R. A., Souzeau, E., Mitchell, P., Wang, J. J., Hewitt, A. W., Coote, M., Crowston, J. G., Astakhov, S. Y., Akopov, E. L., Emelyanov, A., Vysochinskaya, V., Kazakbaeva, G., Fayzrakhmanov, R., Al-Obeidan, S. A., Owaidhah, O., Aljasim, L. A., Chowbay, B., Foo, J. N., Soh, R. Q., Sim, K. S., Xie, Z., Cheong, A. W. O., Mok, S. Q., Soo, H. M., Chen, X. Y., Peh, S. Q., Heng, K. K., Husain, R., Ho, S-L., Hillmer, A. M., Cheng, C-Y., Escudero-Domínguez, F. A., González-Sarmiento, R., Martinon-Torres, F., Salas, A., Pathanapitoon, K., Hansapinyo, L., Wanichwecharugruang, B., Kitnarong, N., Sakuntabhai, A., Nguyn, H. X., Nguyn, G. T. T., Nguyn, T. V., Zenz, W., Binder, A., Klobassa, D. S., Hibberd, M. L., Davila, S., Herms, S., Nöthen, M. M., Moebus, S., Rautenbach, R. M., Ziskind, A., Carmichael, T. R., Ramsay, M., Álvarez, L., García, M., González-Iglesias, H., Rodríguez-Calvo, P. P., Fernández-Vega Cueto, L., Oguz, Ç., Tamcelik, N., Atalay, E., Batu, B., Aktas, D., Kasım, B., Wilson, M. R., Coleman, A. L., Challa, P., Herndon, L., Kuchtey, R. W., Kuchtey, J., Curtin, K., Chaya, C. J., Crandall, A., Zangwill, L. M., Wong, T. Y., Nakano, M., Kinoshita, S., den Hollander, A. I., Vesti, E., Fingert, J. H., Lee, R. K., Sit, A. J., Shingleton, B. J., Wang, N., Cusi, D., Qamar, R., Kraft, P., Pericak-Vance, M. A., Raychaudhuri, S., Heegaard, S., Kivelä, T., Reis, A., Kruse, F. E., Weinreb, R. N., Pasquale, L. R., Haines, J. L., Thorsteinsdottir, U., Jonasson, F., Allingham, R. R., Milea, D., Ritch, R., Kubota, T., Tashiro, K., Vithana, E. N., Micheal, S., Topouzis, F., Craig, J. E., Dubina, M., Sundaresan, P., Stefansson, K., Wiggs, J. L., Pasutto, F. & Khor, C. C., Jul 2017, In : Nature Genetics. 49, 7, p. 993-1004 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  27. Published

    Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

    Weiner, D. J., Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A., Grove, J., Samocha, K. E., Goldstein, J. I., Okbay, A., Bybjerg-Grauholm, J., Werge, T., Hougaard, D. M., Taylor, J., Skuse, D., Devlin, B., Anney, R., Sanders, S. J., Bishop, S., Mortensen, P. B., Børglum, A. D., Smith, G. D., Daly, M. J., Robinson, E. B., iPSYCH-Broad Autism Group & Hansen, T. F., Jul 2017, In : Nature Genetics. 49, 7, p. 978-985 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  28. Published

    Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor

    Wang, Z., McGlynn, K. A., Rajpert-De Meyts, E., Bishop, D. T., Chung, C. C., Dalgaard, M. D., Greene, M. H., Gupta, R., Grotmol, T., Haugen, T. B., Karlsson, R., Litchfield, K., Mitra, N., Nielsen, K., Pyle, L. C., Schwartz, S. M., Thorsson, V., Vardhanabhuti, S., Wiklund, F., Turnbull, C., Chanock, S. J., Kanetsky, P. A., Nathanson, K. L. & Testicular Cancer Consortium, 12 Jun 2017, In : Nature Genetics. 49, 7, p. 1141–1147 doi:10.1038/ng.3879.

    Research output: Contribution to journalJournal articleResearchpeer-review

  29. Published

    Adiposity amplifies the genetic risk of fatty liver disease conferred by multiple loci

    Stender, S., Kozlitina, J., Nordestgaard, B. G., Tybjærg-Hansen, A., Hobbs, H. H. & Cohen, J. C., Jun 2017, In : Nature Genetics. 49, 6, p. 842-847 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  30. Published

    Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

    Melin, B. S., Barnholtz-Sloan, J. S., Wrensch, M. R., Johansen, C., Il'yasova, D., Kinnersley, B., Ostrom, Q. T., Labreche, K., Chen, Y., Armstrong, G., Liu, Y., Eckel-Passow, J. E., Decker, P. A., Labussière, M., Idbaih, A., Hoang-Xuan, K., Di Stefano, A-L., Mokhtari, K., Delattre, J-Y., Broderick, P., Galan, P., Gousias, K., Schramm, J., Schoemaker, M. J., Fleming, S. J., Herms, S., Heilmann, S., Nöthen, M. M., Wichmann, H-E., Schreiber, S., Swerdlow, A., Lathrop, M., Simon, M., Sanson, M., Andersson, U., Rajaraman, P., Chanock, S., Linet, M., Wang, Z., Yeager, M., Wiencke, J. K., Hansen, H., McCoy, L., Rice, T., Kosel, M. L., Sicotte, H., Amos, C. I., Bernstein, J. L., Davis, F., Lachance, D. & GliomaScan Consortium, May 2017, In : Nature Genetics. 49, 5, p. 789-794 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  31. Published

    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., Lecarpentier, 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., Ejlertsen, B., Gerdes, A-M., Hansen, T. V. O., Høgdall, C. K., Høgdall, E., Jensen, A., Kjaer, S. K., Lundvall, L., Nedergaard, L. & AOCS study group, May 2017, In : Nature Genetics. 49, 5, p. 680-691 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  32. Published

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

    Charge Diabetes Working Group, The EPIC-InterAct Consortium, EPIC-CVD Consortium, GOLD Consortium & VA Million Veteran Program, 2017, In : Nature Genetics. 49, 12, p. 1758-1766

    Research output: Contribution to journalJournal articleResearchpeer-review

  33. 2016
  34. Published

    Pan-cancer analysis of somatic copy-number alterations implicates IRS4 and IGF2 in enhancer hijacking

    Weischenfeldt, J., Dubash, T., Drainas, A. P., Mardin, B. R., Chen, Y., Stütz, A. M., Waszak, S. M., Bosco, G., Halvorsen, A. R., Raeder, B., Efthymiopoulos, T., Erkek, S., Siegl, C., Brenner, H., Brustugun, O. T., Dieter, S. M., Northcott, P. A., Petersen, I., Pfister, S. M., Schneider, M., Solberg, S. K., Thunissen, E., Weichert, W., Zichner, T., Thomas, R., Peifer, M., Helland, A., Ball, C. R., Jechlinger, M., Sotillo, R., Glimm, H. & Korbel, J. O., 21 Nov 2016, In : Nature Genetics. 49, 1, p. 65-74

    Research output: Contribution to journalJournal articleResearchpeer-review

  35. Published

    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., Mihailov, 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., Fava, C., Ohlsson, T., Matchan, A., Stirrups, K. E., Bork-Jensen, J., Gjesing, A. P., Kontto, J., Perola, M., Shaw-Hawkins, S., Havulinna, A. S., Husemoen, L. L., Linneberg, A., Skaaby, T., Thuesen, B., Nordestgaard, B. G. & CHARGE-Heart Failure Consortium, Oct 2016, In : Nature Genetics. 48, 10, p. 1151-61 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  36. Published

    Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

    Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T., Pers, T. H., Farh, K-H., Cuenca-Leon, E., Muona, M., Furlotte, N. A., Kurth, T., Ingason, A., McMahon, G., Ligthart, L., Terwindt, G. M., Kallela, M., Freilinger, T. M., Ran, C., Gordon, S. G., Stam, A. H., Steinberg, S., Borck, G., Koiranen, M., Quaye, L., Adams, H. H. H., Lehtimäki, T., Sarin, A-P., Wedenoja, J., Hinds, D. A., Buring, J. E., Schürks, M., Ridker, P. M., Hrafnsdottir, M. G., Stefansson, H., Ring, S. M., Hottenga, J-J., Penninx, B. W. J. H., Färkkilä, M., Artto, V., Kaunisto, M., Vepsäläinen, S., Malik, R., Heath, A. C., Madden, P. A. F., Martin, N. G., Esserlind, A-L., Christensen, A. F., Hansen, T. F., Werge, T., Olesen, J. & International Headache Genetics Consortium, 28 Sep 2016, In : Nature Genetics. 48, 10, p. 1296

    Research output: Contribution to journalJournal articleResearchpeer-review

  37. Published

    Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

    Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T., Pers, T. H., Farh, K-H., Cuenca-Leon, E., Muona, M., Furlotte, N. A., Kurth, T., Ingason, A., McMahon, G., Ligthart, L., Terwindt, G. M., Kallela, M., Freilinger, T. M., Ran, C., Gordon, S. G., Stam, A. H., Steinberg, S., Borck, G., Koiranen, M., Quaye, L., Adams, H. H. H., Lehtimäki, T., Sarin, A-P., Wedenoja, J., Hinds, D. A., Buring, J. E., Schürks, M., Ridker, P. M., Hrafnsdottir, M. G., Stefansson, H., Ring, S. M., Hottenga, J-J., Penninx, B. W. J. H., Färkkilä, M., Artto, V., Kaunisto, M., Vepsäläinen, S., Malik, R., Heath, A. C., Madden, P. A. F., Martin, N. G., Esserlind, A-L., Christensen, A. F., Hansen, T. F., Werge, T., Olesen, J. & International Headache Genetics Consortium, Aug 2016, In : Nature Genetics. 48, 8, p. 856-66 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  38. Published

    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., Moradi Marjaneh, M., Lee, J. S., Hills, M., Jarosz, 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, I., 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., Ejlertsen, B., Hansen, T. V. O., Bojesen, S. E. & EMBRACE, Apr 2016, In : Nature Genetics. 48, 4, p. 374-86 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  39. Published

    NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity

    Moriyama, T., Nishii, R., Perez-Andreu, V., Yang, W., Klussmann, F. A., Zhao, X., Lin, T-N., Hoshitsuki, K., Nersting, J., Kihira, K., Hofmann, U., Komada, Y., Kato, M., McCorkle, R., Li, L., Koh, K., Najera, C. R., Kham, S. K-Y., Isobe, T., Chen, Z., Chiew, E. K-H., Bhojwani, D., Jeffries, C., Lu, Y., Schwab, M., Inaba, H., Pui, C-H., Relling, M. V., Manabe, A., Hori, H., Schmiegelow, K., Yeoh, A. E. J., Evans, W. E. & Yang, J. J., 15 Feb 2016, In : Nature Genetics. 48, 4, p. 367-73

    Research output: Contribution to journalJournal articleResearchpeer-review

  40. Published

    Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer

    Bolton, K. L., Tyrer, J., Song, H., Ramus, S. J., Notaridou, M., Jones, C., Sher, T., Gentry-Maharaj, A., Wozniak, E., Tsai, Y-Y., Weidhaas, J., Paik, D., Van Den Berg, D. J., Stram, D. O., Pearce, C. L., Wu, A. H., Brewster, W., Anton-Culver, H., Ziogas, A., Narod, S. A., Levine, D. A., Kaye, S. B., Brown, R., Paul, J., Flanagan, J., Sieh, W., McGuire, V., Whittemore, A. S., Campbell, I., Gore, M. E., Lissowska, J., Yang, H. P., Medrek, K., Gronwald, J., Lubinski, J., Jakubowska, A., Le, N. D., Cook, L. S., Kelemen, L. E., Brooks-Wilson, A., Massuger, L. F. A. G., Kiemeney, L. A., Aben, K. K. H., van Altena, A. M., Houlston, R., Tomlinson, I., Palmieri, R. T., Kjær, S. K., Høgdall, E. V. S., Hogdall, C. & Australian Ovarian Cancer Study Group, Jan 2016, In : Nature Genetics. 48, 1, p. 101

    Research output: Contribution to journalJournal articleResearchpeer-review

  41. 2015
  42. Published

    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., Strawbridge, 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., Jørgensen, M. E., Jørgensen, T., Linneberg, A. & DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium, Dec 2015, In : Nature Genetics. 47, 12, p. 1415-25 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  43. Published

    Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

    Waage, J., Bønnelykke, K., Thyssen, J. P., Kreiner-Møller, E., Bisgaard, H., EArly Genetics and Lifecourse Epidemiology (EAGLE) Eczema Consortium (Ried JS, Li J, Zuo XB, Zheng XD, Yin XY, Sun LD, McAleer MA, O'Regan GM, Fahy CM, Campbell LE, Macek M, Kurek M, Hu D, Eng C, Postma DS, Feenstra B, Geller F, Hottenga JJ, Middeldorp CM, Hysi P, Bataille V, Spector T, Tiesler CM, Thiering E, Pahukasahasram B, Yang JJ, Imboden M, Huntsman S, Vilor-Tejedor N, Relton CL, Myhre R, Nystad W, Custovic A, Weiss ST, Meyers DA, Söderhäll C, Melén E, Ober C, Raby BA, Simpson A, Jacobsson B, Holloway JW, Bisgaard H, Sunyer J, Probst-Hensch NM, Williams LK, Godfrey KM, Wang CA, Boomsma DI, Melbye M, Koppelman GH, Jarvis D, McLean WH, Irvine AD, Zhang XJ, Hakonarson H, Gieger C, Burchard EG, Martin NG, Duijts L, Linneberg A, Jarvelin MR, Nöthen MM, Lau S, Hübner N, Lee YA, Tamari M, Hinds DA, Glass D, Brown SJ, Heinrich J, Evans DM, Weidinger S, members) & Linneberg, A., Dec 2015, In : Nature Genetics. 47, 12, p. 1449-56 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  44. Published

    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., Mateo Leach, I., 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., Chen, 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., Husemoen, L. L. N., Sparsø, T., Hansen, T., Jørgensen, T., Linneberg, A., Sørensen, T. I. A. & BIOS-consortium, Nov 2015, In : Nature Genetics. 47, 11, p. 1282-93 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  45. Published

    Class II HLA interactions modulate genetic risk for multiple sclerosis

    Oturai, A., Søndergaard, H. B. & International Multiple Sclerosis Genetics Consortium, Oct 2015, In : Nature Genetics. 47, 10, p. 1107-13 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  46. Published

    Genome-wide significant risk associations for mucinous ovarian carcinoma

    Kelemen, L. E., Lawrenson, K., Tyrer, J., Li, Q., Lee, J. M., Seo, J-H., Phelan, C. M., Beesley, J., Chen, X., Spindler, T. J., Aben, K. K. H., Anton-Culver, H., Antonenkova, N., Australian Cancer Study & Kjær, S., Aug 2015, In : Nature Genetics. 47, 8, p. 888-97 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  47. Published

    Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

    Taylor, J. C., Martin, H. C., Lise, S., Broxholme, J., Cazier, J-B., Rimmer, A., Kanapin, A., Lunter, G., Fiddy, S., Allan, C., Aricescu, A. R., Attar, M., Babbs, C., Becq, J., Beeson, D., Bento, C., Bignell, P., Blair, E., Buckle, V. J., Bull, K., Cais, O., Cario, H., Chapel, H., Copley, R. R., Cornall, R., Craft, J., Dahan, K., Davenport, E. E., Dendrou, C., Devuyst, O., Fenwick, A. L., Flint, J., Fugger, L., Gilbert, R. D., Goriely, A., Green, A., Greger, I. H., Grocock, R., Gruszczyk, A. V., Hastings, R., Hatton, E., Higgs, D., Hill, A., Holmes, C., Howard, M., Hughes, L., Humburg, P., Johnson, D., Karpe, F., Kingsbury, Z., Kini, U., Knight, J. C., Krohn, J., Lamble, S., Langman, C., Lonie, L., Luck, J., McCarthy, D., McGowan, S. J., McMullin, M. F., Miller, K. A., Murray, L., Németh, A. H., Nesbit, M. A., Nutt, D., Ormondroyd, E., Oturai, A. B., Pagnamenta, A., Patel, S. Y., Percy, M., Petousi, N., Piazza, P., Piret, S. E., Polanco-Echeverry, G., Popitsch, N., Powrie, F., Pugh, C., Quek, L., Robbins, P. A., Robson, K., Russo, A., Sahgal, N., van Schouwenburg, P. A., Schuh, A., Silverman, E., Simmons, A., Sørensen, P. S., Sweeney, E., Taylor, J. E., Thakker, R. V., Tomlinson, I., Trebes, A., Twigg, S. R. F., Uhlig, H. H., Vyas, P., Vyse, T., Wall, S. A., Watkins, H., Whyte, M., Witty, L., Wright, B., Yau, C., Buck, D., Humphray, S., Ratcliffe, P. J., Bell, J. I., Wilkie, A. O. M., Bentley, D., Donnelly, P. & McVean, G., 18 May 2015, In : Nature Genetics. 47, 7, p. 717-26

    Research output: Contribution to journalJournal articleResearchpeer-review

  48. Published

    A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

    Aung, T., Ozaki, M., Mizoguchi, T., Allingham, R. R., Li, Z., Haripriya, A., Nakano, S., Uebe, S., Harder, J. M., Chan, A. S. Y., Lee, M. C., Burdon, K. P., Astakhov, Y. S., Abu-Amero, K. K., Zenteno, J. C., Nilgün, Y., Zarnowski, T., Pakravan, M., Safieh, L. A., Jia, L., Wang, Y. X., Williams, S., Paoli, D., Schlottmann, P. G., Huang, L., Sim, K. S., Foo, J. N., Nakano, M., Ikeda, Y., Kumar, R., Ueno, M., Manabe, S., Hayashi, K., Kazama, S., Ideta, R., Mori, Y., Miyata, K., Sugiyama, K., Higashide, T., Chihara, E., Inoue, K., Ishiko, S., Yoshida, A., Yanagi, M., Kiuchi, Y., Aihara, M., Ohashi, T., Sakurai, T., Heegaard, S., Blue Mountains Eye Study GWAS Team & Heegaard, S., Apr 2015, In : Nature Genetics. 47, 4, p. 387-92 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  49. Published

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

    Andersson, A. K., 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., Becksfort, J., Gupta, P. K., 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., Fioretos, T., Lu, C., Ding, L., Pui, C-H., Shurtleff, S., Mullighan, C. G., Mardis, E. R., Wilson, J. R., Gruber, T. A., Zhang, J., Downing, J. R. & St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project, Apr 2015, In : Nature Genetics. 47, 4, p. 330-7 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  50. Published

    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., Goldgar, 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., Jensen, A., Kjaer, S. K., Hogdall, E., Hogdall, C., Lundvall, L., Nedergaard, L. & EMBRACE, Feb 2015, In : Nature Genetics. 47, 2, p. 164-71 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  51. Published

    Convergent evolution and adaptation of Pseudomonas aeruginosa within patients with cystic fibrosis

    Marvig, R. L., Sommer, L. M., Molin, S. & Johansen, H. K., Jan 2015, In : Nature Genetics. 47, 1, p. 57-64 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  52. 2014
  53. Published

    A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

    Al Olama, A. A., Kote-Jarai, Z., Berndt, S. I., Conti, D. V., Schumacher, F., Han, Y., Benlloch, S., Hazelett, D. J., Wang, Z., Saunders, E., Leongamornlert, D., Lindstrom, S., Jugurnauth-Little, S., Dadaev, T., Tymrakiewicz, M., Stram, D. O., Rand, K., Wan, P., Stram, A., Sheng, X., Pooler, L. C., Park, K., Xia, L., Tyrer, J., Kolonel, L. N., Le Marchand, L., Hoover, R. N., Machiela, M. J., Yeager, M., Burdette, L., Chung, C. C., Hutchinson, A., Yu, K., Goh, C., Ahmed, M., Govindasami, K., Guy, M., Tammela, T. L. J., Auvinen, A., Wahlfors, T., Schleutker, J., Visakorpi, T., Leinonen, K. A., Xu, J., Weischer, M., Nordestgaard, B. G., Nielsen, S. F., Klarskov, P., Røder, M. A., Iversen, P. & The Breast and Prostate Cancer Cohort Consortium (BPC3), 14 Sep 2014, In : Nature Genetics. 46, 10, p. 1103-9 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  54. Published

    Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease

    Kozlitina, J., Smagris, E., Stender, S., Nordestgaard, B. G., Zhou, H. H., Tybjærg-Hansen, A., Vogt, T. F., Hobbs, H. H. & Cohen, J. C., Apr 2014, In : Nature Genetics. 46, 4, p. 352-6 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  55. Published

    Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability

    Tatton-Brown, K., Seal, S., Ruark, E., Harmer, J., Ramsay, E., Del Vecchio Duarte, S., Zachariou, A., Hanks, S., O'Brien, E., Aksglaede, L., Baralle, D., Dabir, T., Gener, B., Goudie, D., Homfray, T., Kumar, A., Pilz, D. T., Selicorni, A., Temple, I. K., Van Maldergem, L., Yachelevich, N., van Montfort, R., Rahman, N. & Childhood Overgrowth Consortium, Apr 2014, In : Nature Genetics. 46, 4, p. 385-8 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  56. Published

    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. A., Duggirala, R., Dymek, 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., Kravic, J., 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., Boehnke, M., McCarthy, M. I., Njølstad, P. R., Pedersen, O., Groop, L., Cox, D. R., Stefansson, K. & Altshuler, D., 2 Mar 2014, In : Nature Genetics. 46, 4, p. 357-63

    Research output: Contribution to journalJournal articleResearchpeer-review

  57. 2013
  58. Published

    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., Kockum, 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., Søndergaard, 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., Blackburn, H., Bomfim, I. L., Brambilla, P., Broadley, S., Sellebjerg, F., Sorensen, P. S. & International Multiple Sclerosis Genetics Consortium (IMSGC), Nov 2013, In : Nature Genetics. 45, 11, p. 1353-60 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

Previous 1 2 Next

ID: 82863