Marketa Sjögren

Associate Researcher
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  1. 2019
  2. 2018
  3. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes

    Gusarova, V., O'Dushlaine, C., Teslovich, T. M., Benotti, P. N., Mirshahi, T., Gottesman, O., Van Hout, C. V., Murray, M. F., Mahajan, A., Nielsen, J. B., Fritsche, L., Wulff, A. B., Gudbjartsson, D. F., Sjögren, M., Emdin, C. A., Scott, R. A., Lee, W-J., Small, A., Kwee, L. C., Dwivedi, O. P. & 61 othersRashmi B Prasad, Bruse, S., Lopez, A. E., Penn, J., Marcketta, A., Leader, J. B., Still, C. D., Kirchner, H. L., Mirshahi, U. L., Wardeh, A. H., Hartle, C. M., Habegger, L., Fetterolf, S. N., Tusie-Luna, T., Morris, A. P., Holm, H., Steinthorsdottir, V., Sulem, P., Thorsteinsdottir, U., Rotter, J. I., Chuang, L-M., Damrauer, S., Birtwell, D., Brummett, C. M., Khera, A. V., Natarajan, P., Marju Orho-Melander, Flannick, J., Lotta, L. A., Willer, C. J., Holmen, O. L., Ritchie, M. D., Ledbetter, D. H., Murphy, A. J., Borecki, I. B., Reid, J. G., Overton, J. D., Ola Hansson, Leif Groop, Shah, S., Kraus, W. E., Rader, D. J., Ida Chen, Y-D., Hveem, K., Wareham, N. J., Kathiresan, S., Olle Melander, Stefansson, K., Nordestgaard, B. G., Tybjaerg-Hansen, A., Abecasis, G. R., Altshuler, D., Florez, J. C., Boehnke, M., McCarthy, M., Yancopoulos, G. D., Carey, D. J., Shuldiner, A. R., Baras, A., Dewey, F. E. & Gromada, J., 2018 Jun 13, In : Nature Communications. 9, p. 1-11 2252.

    Research output: Contribution to journalArticle

  4. 2017
  5. Relationship between selected DNA polymorphisms and coronary artery disease complications

    Wirtwein, M., Olle Melander, Marketa Sjögren, Hoffmann, M., Narkiewicz, K., Gruchala, M. & Sobiczewski, W., 2017 Feb 1, In : International Journal of Cardiology. 228, p. 814-820 7 p.

    Research output: Contribution to journalArticle

  6. Elevated ambulatory systolic-diastolic pressure regression index is genetically determined in hypertensive patients with coronary heart disease

    Wirtwein, M., Olle Melander, Marketa Sjőgren, Hoffmann, M., Narkiewicz, K., Gruchala, M. & Sobiczewski, W., 2017, In : Blood Pressure. 26, 3, p. 174-180 10 p.

    Research output: Contribution to journalArticle

  7. 2016
  8. The Relationship Between Gene Polymorphisms and Dipping Profile in Patients With Coronary Heart Disease

    Wirtwein, M., Olle Melander, Marketa Sjögren, Hoffmann, M., Narkiewicz, K., Gruchala, M. & Sobiczewski, W., 2016 Sep 1, In : American Journal of Hypertension. 29, 9, p. 1094-1102 9 p.

    Research output: Contribution to journalArticle

  9. Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure

    Smith, G., Felix, J. F., Morrison, A. C., Kalogeropoulos, A., Trompet, S., Wilk, J. B., Gidlöf, O., Wang, X., Morley, M., Mendelson, M., Joehanes, R., Ligthart, S., Shan, X., Bis, J. C., Wang, Y. A., Sjögren, M., Ngwa, J., Brandimarto, J., Stott, D. J., Aguilar, D. & 35 othersRice, K. M., Sesso, H. D., Demissie, S., Buckley, B. M., Taylor, K. D., Ford, I., Yao, C., Liu, C., Sotoodehnia, N., van der Harst, P., Stricker, B. H. C., Kritchevsky, S. B., Liu, Y., Gaziano, J. M., Hofman, A., Moravec, C. S., Uitterlinden, A. G., Kellis, M., van Meurs, J. B., Margulies, K. B., Dehghan, A., Levy, D., Björn Olde, Psaty, B. M., Cupples, L. A., Jukema, J. W., Djousse, L., Franco, O. H., Boerwinkle, E., Boyer, L. A., Newton-Cheh, C., Butler, J., Vasan, R. S., Cappola, T. P. & Smith, N. L., 2016 May 1, In : PLoS Genetics. 12, 5, e1006034.

    Research output: Contribution to journalArticle

  10. 2015
  11. 1A.10: ASSOCIATION BETWEEN GENE POLYMORPHISMS AND RISK OF CARDIOVASCULAR EVENTS IN PATIENTS WITH CORONARY HEART DISEASE.

    Wirtwein, M., Jarosz, D., Polonis, K., Hoffman, M., Olle Melander, Marketa Sjögren, Hedner, T., Narkiewicz, K., Gruchala, M. & Sobiczewski, W., 2015, In : Journal of Hypertension. 33 Suppl 1, p. e3

    Research output: Contribution to journalArticle

  12. 2014
  13. Twelve-Single Nucleotide Polymorphism Genetic Risk Score Identifies Individuals at Increased Risk for Future Atrial Fibrillation and Stroke.

    Tada, H., Shiffman, D., Gustav Smith, Marketa Sjögren, Lubitz, S. A., Ellinor, P. T., Louie, J. Z., Catanese, J. J., Gunnar Engström, Devlin, J. J., Kathiresan, S. & Olle Melander, 2014, In : Stroke: a journal of cerebral circulation. 45, 10, p. 2856

    Research output: Contribution to journalArticle

  14. 2013
  15. Genetic Associations with Valvular Calcification and Aortic Stenosis

    Thanassoulis, G., Campbell, C. Y., Owens, D. S., Smith, G., Smith, A. V., Peloso, G. M., Kerr, K. F., Pechlivanis, S., Budoff, M. J., Harris, T. B., Malhotra, R., O'Brien, K. D., Kamstrup, P. R., Nordestgaard, B. G., Tybjaerg-Hansen, A., Allison, M. A., Aspelund, T., Criqui, M. H., Heckbert, S. R., Hwang, S-J. & 19 othersLiu, Y., Marketa Sjögren, Jesper vanderPals, Kaelsch, H., Muehleisen, T. W., Noethen, M. M., Cupples, L. A., Caslake, M., Di Angelantonio, E., Danesh, J., Rotter, J. I., Sigurdsson, S., Wong, Q., Erbel, R., Kathiresan, S., Olle Melander, Gudnason, V., O'Donnell, C. J. & Post, W. S., 2013, In : New England Journal of Medicine. 368, 6, p. 503-512

    Research output: Contribution to journalArticle

  16. Smoking and obesity associated BDNF gene variance predicts total and cardiovascular mortality in smokers.

    Sara Halldén, Marketa Sjögren, Bo Hedblad, Gunnar Engström, Narkiewicz, K., Hoffmann, M., Wahlstrand, B., Hedner, T. & Olle Melander, 2013, In : Heart. 99, 13, p. 949-953

    Research output: Contribution to journalArticle

  17. 2012
  18. Genetic Variation Within the Interleukin-1 Gene Cluster and Ischemic Stroke

    Olsson, S., Holmegaard, L., Jood, K., Marketa Sjögren, Gunnar Engström, Håkan Lövkvist, Blomstrand, C., Bo Norrving, Olle Melander, Arne Lindgren & Jern, C., 2012, In : Stroke: a journal of cerebral circulation. 43, 9, p. 2278

    Research output: Contribution to journalArticle

  19. Meta-analysis identifies six new susceptibility loci for atrial fibrillation

    Ellinor, P. T., Lunetta, K. L., Albert, C. M., Glazer, N. L., Ritchie, M. D., Smith, A. V., Arking, D. E., Mueller-Nurasyid, M., Krijthe, B. P., Lubitz, S. A., Bis, J. C., Chung, M. K., Doerr, M., Ozaki, K., Roberts, J. D., Smith, G., Pfeufer, A., Sinner, M. F., Lohman, K., Ding, J. & 69 othersSmith, N. L., Smith, J. D., Rienstra, M., Rice, K. M., Van Wagoner, D. R., Magnani, J. W., Wakili, R., Clauss, S., Rotter, J. I., Steinbeck, G., Launer, L. J., Davies, R. W., Borkovich, M., Harris, T. B., Lin, H., Voelker, U., Voelzke, H., Milan, D. J., Hofman, A., Boerwinkle, E., Chen, L. Y., Soliman, E. Z., Voight, B. F., Li, G., Chakravarti, A., Kubo, M., Tedrow, U. B., Rose, L. M., Ridker, P. M., Conen, D., Tsunoda, T., Furukawa, T., Sotoodehnia, N., Xu, S., Kamatani, N., Levy, D., Nakamura, Y., Parvez, B., Mahida, S., Furie, K. L., Rosand, J., Muhammad, R., Psaty, B. M., Meitinger, T., Perz, S., Wichmann, H-E., Witteman, J. C. M., Kao, W. H. L., Kathiresan, S., Roden, D. M., Uitterlinden, A. G., Rivadeneira, F., McKnight, B., Marketa Sjögren, Newman, A. B., Liu, Y., Gollob, M. H., Olle Melander, Tanaka, T., Stricker, B. H. C., Felix, S. B., Alonso, A., Darbar, D., Barnard, J., Chasman, D. I., Heckbert, S. R., Benjamin, E. J., Gudnason, V. & Kaeaeb, S., 2012, In : Nature Genetics. 44, 6, p. 670-U88

    Research output: Contribution to journalArticle

  20. Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.

    Fedorowski, A., Franceschini, N., Brody, J., Liu, C., Verwoert, G. C., Boerwinkle, E., Couper, D., Rice, K. M., Rotter, J. I., Raso, F. M., Uitterlinden, A., Hofman, A., Almgren, P., Sjögren, M., Hedblad, B., Larson, M. G., Newton-Cheh, C., Wang, T. J., Rose, K. M., Psaty, B. M. & 3 othersLevy, D., Witteman, J. & Olle Melander, 2012, In : European Heart Journal. 33, 18, p. 2331-2341

    Research output: Contribution to journalArticle

  21. Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.

    Viktor Hamrefors, Marketa Sjögren, Almgren, P., Wahlstrand, B., Kjeldsen, S., Hedner, T. & Olle Melander, 2012, In : Journal of Hypertension. 30, 6, p. 1151-1160

    Research output: Contribution to journalArticle

  22. Prediction of Blood Pressure Changes Over Time and Incidence of Hypertension by a Genetic Risk Score in Swedes.

    Cristiano Fava, Marketa Sjögren, Montagnana, M., Danese, E., Almgren, P., Gunnar Engström, Peter Nilsson, Bo Hedblad, Guidi, G. C., Minuz, P. & Olle Melander, 2012, In : Hypertension.

    Research output: Contribution to journalArticle

  23. The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.

    Cristiano Fava, Montagnana, M., Danese, E., Marketa Sjögren, Almgren, P., Guidi, G. C., Bo Hedblad, Gunnar Engström, Minuz, P. & Olle Melander, 2012, In : Prostaglandins & other Lipid Mediators. 98, 1-2, p. 31-36

    Research output: Contribution to journalArticle

  24. 2011
  25. A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.

    Cristiano Fava, Danese, E., Montagnana, M., Marketa Sjögren, Almgren, P., Guidi, G. C., Bo Hedblad, Gunnar Engström, Lechi, A., Minuz, P. & Olle Melander, 2011, In : American Journal of Cardiology. 108, p. 1432-1437

    Research output: Contribution to journalArticle

  26. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

    Ehret, G. B., Munroe, P. B., Rice, K. M., Bochud, M., Johnson, A. D., Chasman, D. I., Smith, A. V., Tobin, M. D., Verwoert, G. C., Hwang, S-J., Pihur, V., Vollenweider, P., O'Reilly, P. F., Amin, N., Bragg-Gresham, J. L., Teumer, A., Glazer, N. L., Launer, L., Zhao, J. H., Aulchenko, Y. & 326 othersHeath, S., Sober, S., Parsa, A., Luan, J., Arora, P., Dehghan, A., Zhang, F., Lucas, G., Hicks, A. A., Jackson, A. U., Peden, J. F., Tanaka, T., Wild, S. H., Rudan, I., Igl, W., Milaneschi, Y., Parker, A. N., Cristiano Fava, Chambers, J. C., Fox, E. R., Kumari, M., Go, M. J., van der Harst, P., Kao, W. H. L., Marketa Sjögren, Vinay, D. G., Alexander, M., Tabara, Y., Shaw-Hawkins, S., Whincup, P. H., Liu, Y., Shi, G., Kuusisto, J., Tayo, B., Seielstad, M., Sim, X., Khanh-Dung Hoang, N., Lehtimaki, T., Matullo, G., Wu, Y., Gaunt, T. R., Onland-Moret, N. C., Cooper, M. N., Platou, C. G. P., Org, E., Hardy, R., Dahgam, S., Palmen, J., Vitart, V., Braund, P. S., Kuznetsova, T., Uiterwaal, C. S. P. M., Adeyemo, A., Palmas, W., Campbell, H., Ludwig, B., Tomaszewski, M., Tzoulaki, I., Palmer, N. D., Aspelund, T., Garcia, M., Chang, Y-P. C., O'Connell, J. R., Steinle, N. I., Grobbee, D. E., Arking, D. E., Kardia, S. L., Morrison, A. C., Hernandez, D., Najjar, S., McArdle, W. L., Hadley, D., Brown, M. J., Connell, J. M., Hingorani, A. D., Day, I. N. M., Lawlor, D. A., Beilby, J. P., Lawrence, R. W., Clarke, R., Hopewell, J. C., Ongen, H., Dreisbach, A. W., Li, Y., Young, J. H., Bis, J. C., Kahonen, M., Viikari, J., Adair, L. S., Lee, N. R., Chen, M-H., Olden, M., Pattaro, C., Bolton, J. A. H., Koettgen, A., Bergmann, S., Mooser, V., Chaturvedi, N., Frayling, T. M., Islam, M., Jafar, T. H., Erdmann, J., Kulkarni, S. R., Bornstein, S. R., Graessler, J., Groop, L., Voight, B. F., Kettunen, J., Howard, P., Taylor, A., Guarrera, S., Ricceri, F., Emilsson, V., Plump, A., Barroso, I. S., Khaw, K-T., Weder, A. B., Hunt, S. C., Sun, Y. V., Bergman, R. N., Collins, F. S., Bonnycastle, L. L., Scott, L. J., Stringham, H. M., Peltonen, L., Perola, M., Vartiainen, E., Brand, S-M., Staessen, J. A., Wang, T. J., Burton, P. R., Artigas, M. S., Dong, Y., Snieder, H., Wang, X., Zhu, H., Lohman, K. K., Rudock, M. E., Heckbert, S. R., Smith, N. L., Wiggins, K. L., Doumatey, A., Shriner, D., Veldre, G., Viigimaa, M., Kinra, S., Prabhakaran, D., Tripathy, V., Langefeld, C. D., Rosengren, A., Thelle, D. S., Corsi, A. M., Singleton, A., Forrester, T., Hilton, G., McKenzie, C. A., Salako, T., Iwai, N., Kita, Y., Ogihara, T., Ohkubo, T., Okamura, T., Ueshima, H., Umemura, S., Eyheramendy, S., Meitinger, T., Wichmann, H. -E., Cho, Y. S., Kim, H-L., Lee, J-Y., Scott, J., Sehmi, J. S., Zhang, W., Hedblad, B., Peter Nilsson, Smith, G. D., Wong, A., Narisu, N., Stancakova, A., Raffel, L. J., Yao, J., Kathiresan, S., O'Donnell, C. J., Schwartz, S. M., Ikram, M. A., Longstreth, W. T. . J., Mosley, T. H., Seshadri, S., Shrine, N. R. G., Wain, L. V., Morken, M. A., Swift, A. J., Laitinen, J., Prokopenko, I., Zitting, P., Cooper, J. A., Humphries, S. E., Danesh, J., Rasheed, A., Goel, A., Hamsten, A., Watkins, H., Bakker, S. J. L., van Gilst, W. H., Janipalli, C. S., Mani, K. R., Yajnik, C. S., Hofman, A., Mattace-Raso, F. U. S., Oostra, B. A., Demirkan, A., Isaacs, A., Rivadeneira, F., Lakatta, E. G., Orru, M., Scuteri, A., Ala-Korpela, M., Kangas, A. J., Lyytikainen, L-P., Soininen, P., Tukiainen, T., Wurtz, P., Ong, R. T-H., Doerr, M., Kroemer, H. K., Voelker, U., Voelzke, H., Galan, P., Hercberg, S., Lathrop, M., Zelenika, D., Deloukas, P., Mangino, M., Spector, T. D., Zhai, G., Meschia, J. F., Nalls, M. A., Sharma, P., Terzic, J., Kumar, M. V. K., Denniff, M., Zukowska-Szczechowska, E., Wagenknecht, L. E., Fowkes, F. G. R., Charchar, F. J., Schwarz, P. E. H., Hayward, C., Guo, X., Rotimi, C., Bots, M. L., Brand, E., Samani, N. J., Polasek, O., Talmud, P. J., Nyberg, F., Kuh, D., Laan, M., Hveem, K., Palmer, L. J., van der Schouw, Y. T., Casas, J. P., Mohlke, K. L., Vineis, P., Raitakari, O., Ganesh, S. K., Wong, T. Y., Tai, E. S., Cooper, R. S., Laakso, M., Rao, D. C., Harris, T. B., Morris, R. W., Dominiczak, A. F., Kivimaki, M., Marmot, M. G., Miki, T., Saleheen, D., Chandak, G. R., Coresh, J., Navis, G., Salomaa, V., Han, B-G., Zhu, X., Kooner, J. S., Olle Melander, Ridker, P. M., Bandinelli, S., Gyllensten, U. B., Wright, A. F., Wilson, J. F., Ferrucci, L., Farrall, M., Tuomilehto, J., Pramstaller, P. P., Elosua, R., Soranzo, N., Sijbrands, E. J. G., Altshuler, D., Loos, R. J. F., Shuldiner, A. R., Gieger, C., Meneton, P., Uitterlinden, A. G., Wareham, N. J., Gudnason, V., Rotter, J. I., Rettig, R., Uda, M., Strachan, D. P., Witteman, J. C. M., Hartikainen, A-L., Beckmann, J. S., Boerwinkle, E., Vasan, R. S., Boehnke, M., Larson, M. G., Jarvelin, M-R., Psaty, B. M., Abecasis, G. R., Chakravarti, A., Elliott, P., van Duijn, C. M., Newton-Cheh, C., Levy, D., Caulfield, M. J. & Johnson, T., 2011, In : Nature. 478, 7367, p. 103-109

    Research output: Contribution to journalArticle

  27. Lack of association between genetic variations in the KALRN region and ischemic stroke

    Olsson, S., Jood, K., Olle Melander, Marketa Sjögren, Bo Norrving, Nilsson, M., Lindgren, A. & Jern, C., 2011, In : Clinical Biochemistry. 44, 12, p. 1018-1020

    Research output: Contribution to journalArticle

  28. 2010
  29. Genetic loci influencing kidney function and chronic kidney disease

    Chambers, J. C., Zhang, W., Lord, G. M., van der Harst, P., Lawlor, D. A., Sehmi, J. S., Gale, D. P., Wass, M. N., Ahmadi, K. R., Bakker, S. J. L., Beckmann, J., Bilo, H. J. G., Bochud, M., Brown, M. J., Caulfield, M. J., Connell, J. M. C., Cook, H. T., Cotlarciuc, I., Smith, G. D., de Silva, R. & 74 othersDeng, G., Devuyst, O., Dikkeschei, L. D., Dimkovic, N., Dockrell, M., Dominiczak, A., Ebrahim, S., Eggermann, T., Farrall, M., Ferrucci, L., Floege, J., Forouhi, N. G., Gansevoort, R. T., Han, X., Bo Hedblad, van der Heide, J. J. H., Hepkema, B. G., Hernandez-Fuentes, M., Hypponen, E., Johnson, T., de Jong, P. E., Kleefstra, N., Lagou, V., Lapsley, M., Li, Y., Loos, R. J. F., Luan, J., Luttropp, K., Marechal, C., Olle Melander, Munroe, P. B., Nordfors, L., Parsa, A., Peltonen, L., Penninx, B. W., Perucha, E., Pouta, A., Prokopenko, I., Roderick, P. J., Ruokonen, A., Samani, N. J., Sanna, S., Schalling, M., Schlessinger, D., Schlieper, G., Seelen, M. A. J., Shuldiner, A. R., Marketa Sjögren, Smit, J. H., Snieder, H., Soranzo, N., Spector, T. D., Stenvinkel, P., Sternberg, M. J. E., Swaminathan, R., Tanaka, T., Ubink-Veltmaat, L. J., Uda, M., Vollenweider, P., Wallace, C., Waterworth, D., Zerres, K., Waeber, G., Wareham, N. J., Maxwell, P. H., McCarthy, M. I., Jarvelin, M-R., Mooser, V., Abecasis, G. R., Lightstone, L., Scott, J., Navis, G., Elliott, P. & Kooner, J. S., 2010, In : Nature Genetics. 42, 5, p. 373-375

    Research output: Contribution to journalArticle

  30. Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension

    Padmanabhan, S., Melander, O., Johnson, T., Di Blasio, A. M., Lee, W. K., Gentilini, D., Hastie, C. E., Menni, C., Monti, M. C., Delles, C., Laing, S., Corso, B., Navis, G., Kwakernaak, A. J., van der Harst, P., Bochud, M., Maillard, M., Burnier, M., Hedner, T., Kjeldsen, S. & 53 othersWahlstrand, B., Marketa Sjögren, Cristiano Fava, Montagnana, M., Danese, E., Torffvit, O., Bo Hedblad, Snieder, H., Connell, J. M. C., Brown, M., Samani, N. J., Farrall, M., Cesana, G., Mancia, G., Signorini, S., Grassi, G., Eyheramendy, S., Wichmann, H. E., Laan, M., Strachan, D. P., Sever, P., Shields, D. C., Stanton, A., Vollenweider, P., Teumer, A., Voelzke, H., Rettig, R., Newton-Cheh, C., Arora, P., Zhang, F., Soranzo, N., Spector, T. D., Lucas, G., Kathiresan, S., Siscovick, D. S., Luan, J., Loos, R. J. F., Wareham, N. J., Penninx, B. W., Nolte, I. M., McBride, M., Miller, W. H., Nicklin, S. A., Baker, A. H., Graham, D., McDonald, R. A., Pell, J. P., Sattar, N., Welsh, P., Munroe, P., Caulfield, M. J., Zanchetti, A. & Dominiczak, A. F., 2010, In : PLoS Genetics. 6, 10

    Research output: Contribution to journalArticle

  31. Stk39 Is A Candidate Gene For Primary Hypertension Especially In Women: Results From 2 Cohort Studies In Swedes

    Fava, C., Montagnana, M., Danese, E., Marketa Sjögren, Bo Hedblad & Olle Melander, 2010, In : Journal of Hypertension. 28, p. E238-E238

    Research output: Contribution to journalPublished meeting abstract

  32. Vanin-1 I26T Polymorphism And Hypertension In Two Large Urban-Based Prospective Studies In Swedes

    Fava, C., Montagnana, M., Danese, E., Marketa Sjögren, Bo Hedblad & Olle Melander, 2010, In : Journal of Hypertension. 28, p. E341-E341

    Research output: Contribution to journalPublished meeting abstract

  33. 2008
  34. A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population

    Brorsson, C., Bergholdt, R., Marketa Sjögren, Eising, S., Sorensen, K. M., Hougaard, D. M., Marju Orho-Melander, Leif Groop & Pociot, F., 2008, In : Molecular Genetics and Metabolism. 94, 3, p. 386-388

    Research output: Contribution to journalArticle

  35. Genetics of Type 2 Diabetes and Metabolic Syndrome: From Genome Wide Linkage Scan and Candidate Genes to Genome Wide Association Studies

    Marketa Sjögren, 2008, Department of Clinical Sciences, Lund University. 126 p.

    Research output: ThesisDoctoral Thesis (compilation)

  36. Is there a unifying genetic factor predisposing to the metabolic syndrome?

    Marketa Sjögren, Marju Orho-Melander, Jonsson, A., Svensson, M., Berglund, G., Peter Nilsson, Leif Groop & Valeriya Lyssenko, 2008, In : Diabetologia. 51, S1, p. S32-S33

    Research output: Contribution to journalPublished meeting abstract

  37. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

    Zeggini, E., Scott, L. J., Saxena, R., Voight, B. F., Marchini, J. L., Hu, T., de Bakker, P. I. W., Abecasis, G. R., Almgren, P., Andersen, G., Ardlie, K., Bostroem, K. B., Bergman, R. N., Bonnycastle, L. L., Borch-Johnsen, K., Burtt, N. P., Chen, H., Chines, P. S., Daly, M. J., Deodhar, P. & 78 othersDing, C-J., Doney, A. S. F., Duren, W. L., Elliott, K. S., Erdos, M. R., Frayling, T. M., Freathy, R. M., Gianniny, L., Grallert, H., Grarup, N., Groves, C. J., Guiducci, C., Hansen, T., Herder, C., Hitman, G. A., Hughes, T. E., Isomaa, B., Jackson, A. U., Jorgensen, T., Kong, A., Kubalanza, K., Kuruvilla, F. G., Kuusisto, J., Langenberg, C., Lango, H., Lauritzen, T., Li, Y., Lindgren, C. M., Valeriya Lyssenko, Marvelle, A. F., Meisinger, C., Midthjell, K., Mohlke, K. L., Morken, M. A., Morris, A. D., Narisu, N., Nilsson, P., Owen, K. R., Palmer, C. N. A., Payne, F., Perry, J. R. B., Pettersen, E., Platou, C., Prokopenko, I., Qi, L., Qin, L., Rayner, N. W., Rees, M., Roix, J. J., Sandbaek, A., Shields, B., Marketa Sjögren, Steinthorsdottir, V., Stringham, H. M., Swift, A. J., Thorleifsson, G., Thorsteinsdottir, U., Timpson, N. J., Tuomi, T., Tuomilehto, J., Walker, M., Watanabe, R. M., Weedon, M. N., Willer, C. J., Illig, T., Hveem, K., Hu, F. B., Laakso, M., Stefansson, K., Pedersen, O., Wareham, N. J., Barroso, I., Hattersley, A. T., Collins, F. S., Leif Groop, McCarthy, M. I., Boehnke, M. & Altshuler, D., 2008, In : Nature Genetics. 40, 5, p. 638-645

    Research output: Contribution to journalArticle

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  39. Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes

    Florez, J. C., Marketa Sjögren, Agapakis, C. M., Burtt, N. P., Almgren, P., Lindblad, U., Berglund, G., Tuomi, T., Gaudet, D., Daly, M. J., Ardlie, K. G., Hirschhorn, J. N., Altshuler, D. & Leif Groop, 2007, In : Diabetologia. 50, 6, p. 1209-1217

    Research output: Contribution to journalArticle

  40. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

    Saxena, R., Voight, B. F., Lyssenko, V., Burtt, N. P., de Bakker, P. I. W., Chen, H., Roix, J. J., Kathiresan, S., Hirschhorn, J. N., Daly, M. J., Hughes, T. E., Groop, L., Altshuler, D., Almgren, P., Florez, J. C., Meyer, J., Ardlie, K., Bengtsson Boström, K., Isomaa, B., Lettre, G. & 47 othersLindblad, U., Lyon, H. N., Olle Melander, Newton-Cheh, C., Peter Nilsson, Marju Orho-Melander, Lennart Råstam, Speliotes, E. K., Taskinen, M-R., Tuomi, T., Guiducci, C., Berglund, A., Joyce Carlson, Gianniny, L., Hackett, R., Hall, L., Holmkvist, J., Esa Laurila, Marketa Sjögren, Sterner, M., Surti, A., Svensson, M., Svensson, M., Tewhey, R., Blumenstiel, B., Parkin, M., DeFelice, M., Barry, R., Brodeur, W., Camarata, J., Chia, N., Fava, M., Gibbons, J., Handsaker, B., Healy, C., Nguyen, K., Gates, C., Sougnez, C., Gage, D., Nizzari, M., Gabriel, S. B., Chirn, G-W., Ma, Q., Parikh, H., Richardson, D., Ricke, D. & Purcell, S., 2007, In : Science. 316, 5829, p. 1331-1336

    Research output: Contribution to journalArticle

  41. Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.

    Valeriya Lyssenko, Lupi, R., Marchetti, P., Del Guerra, S., Marju Orho-Melander, Almgren, P., Marketa Sjögren, Charlotte Ling, Karl-Fredrik Eriksson, ÅsaLinda Lethagen, Mancarella, R., Berglund, G., Tuomi, T., Peter Nilsson, Del Prato, S. & Leif Groop, 2007, In : Journal of Clinical Investigation. 117, 8, p. 2155-2163

    Research output: Contribution to journalArticle

  42. Regulation of skeletal muscle PPAR delta mRNA expression in twins

    Nilsson, E., Poulsen, P., Marketa Sjögren, Charlotte Ling, Martin Ridderstråle, Leif Groop & Vaag, A., 2007, In : Journal of Physiology. 584, 3, p. 1011-1017

    Research output: Contribution to journalArticle

  43. Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.

    Fredriksson, J., Dragi Anevski, Almgren, P., Marketa Sjögren, Lyssenko, V., Joyce Carlson, Isomaa, B., Taskinen, M-R., Leif Groop & Marju Orho-Melander, 2007, In : PLoS ONE. 2, Mar 14, p. e285-e285

    Research output: Contribution to journalArticle

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