Marketa Sjögren

Research Coordinator
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  1. 2020
  2. Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

    Lasse Folkersen, Stefan Gustafsson, Qin Wang, Daniel Hvidberg Hansen, Åsa K Hedman, Andrew Schork, Karen Page, Daria V Zhernakova, Yang Wu, James Peters, Niclas Eriksson, Sarah E Bergen, Thibaud S Boutin, Andrew D Bretherick, Stefan Enroth, Anette Kalnapenkis, Jesper R Gådin, Bianca E Suur, Yan Chen, Ljubica Matic & 32 others, Jeremy D Gale, Julie Lee, Weidong Zhang, Amira Quazi, Mika Ala-Korpela, Seung Hoan Choi, Annique Claringbould, John Danesh, George Davey Smith, Federico de Masi, Sölve Elmståhl, Gunnar Engström, Eric Fauman, Celine Fernandez, Lude Franke, Paul W Franks, Vilmantas Giedraitis, Chris Haley, Anders Hamsten, Andres Ingason, Åsa Johansson, Cecilia M Lindgren, Martin Magnusson, Olle Melander, Peter M Nilsson, Jan Nilsson, Marju Orho-Melander, Marketa Sjögren, Gustav Smith, Jian Yang, Lars Wallentin & SCALLOP Consortium SCALLOP Consortium, 2020 Oct, In: Nature Metabolism. 2, 10, p. 1135-1148 14 p.

    Research output: Contribution to journalArticle

  3. Clinical Evaluation of the Polygenetic Background of Blood Pressure in the Population-Based Setting

    Alice Giontella, Marketa Sjögren, Luca A. Lotta, John D. Overton, Aris Baras, Pietro Minuz, Cristiano Fava & Olle Melander, 2020, In: Hypertension. p. 169-177 9 p.

    Research output: Contribution to journalArticle

  4. Orthostatic hypotension and novel blood pressure associated gene variants in older adults: data from the TILDA Study

    Eamon Laird, Aisling M O'Halloran, Artur Fedorowski, Olle Melander, Ann Hever, Marketa Sjögren, Daniel Carey & Rose Anne Kenny, 2020, In: Journals of Gerontology. Series A: Biological Sciences & Medical Sciences. 75, 11, p. 2074–2080

    Research output: Contribution to journalArticle

  5. 2019
  6. Polygenetic risk for coronary artery disease increases hospitalization burden and mortality

    Marketa Sjögren, Peter Almgren & Olle Melander, 2019 Sep, In: IJC Heart and Vasculature. 24, 100391.

    Research output: Contribution to journalArticle

  7. 2018
  8. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes

    Viktoria Gusarova, Colm O'Dushlaine, Tanya M Teslovich, Peter N Benotti, Tooraj Mirshahi, Omri Gottesman, Cristopher V Van Hout, Michael F Murray, Anubha Mahajan, Jonas B Nielsen, Lars Fritsche, Anders Berg Wulff, Daniel F Gudbjartsson, Marketa Sjögren, Connor A Emdin, Robert A Scott, Wen-Jane Lee, Aeron Small, Lydia C Kwee, Om Prakash Dwivedi & 61 others, Rashmi B Prasad, Shannon Bruse, Alexander E Lopez, John Penn, Anthony Marcketta, Joseph B Leader, Christopher D Still, H Lester Kirchner, Uyenlinh L Mirshahi, Amr H Wardeh, Cassandra M Hartle, Lukas Habegger, Samantha N Fetterolf, Teresa Tusie-Luna, Andrew P Morris, Hilma Holm, Valgerdur Steinthorsdottir, Patrick Sulem, Unnur Thorsteinsdottir, Jerome I Rotter, Lee-Ming Chuang, Scott Damrauer, David Birtwell, Chad M Brummett, Amit V Khera, Pradeep Natarajan, Marju Orho-Melander, Jason Flannick, Luca A. Lotta, Cristen J Willer, Oddgeir L. Holmen, Marylyn D Ritchie, David H. Ledbetter, Andrew J Murphy, Ingrid B Borecki, Jeffrey G. Reid, John D Overton, Ola Hansson, Leif Groop, Svati Shah, William E Kraus, Daniel J Rader, Yii-Der Ida Chen, Kristian Hveem, Nicolas J Wareham, Sekar Kathiresan, Olle Melander, Kari Stefansson, Børge G Nordestgaard, Anne Tybjaerg-Hansen, Goncalo R. Abecasis, David Altshuler, Jose C. Florez, Michael Boehnke, Mark McCarthy, George D Yancopoulos, David J. Carey, Alan R Shuldiner, Aris Baras, Frederick E Dewey & Jesper Gromada, 2018 Jun 13, In: Nature Communications. 9, p. 1-11 2252.

    Research output: Contribution to journalArticle

  9. 2017
  10. Relationship between selected DNA polymorphisms and coronary artery disease complications

    Marcin Wirtwein, Olle Melander, Marketa Sjögren, Michal Hoffmann, Krzysztof Narkiewicz, Marcin Gruchala & Wojciech Sobiczewski, 2017 Feb 1, In: International Journal of Cardiology. 228, p. 814-820 7 p.

    Research output: Contribution to journalArticle

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

    Marcin Wirtwein, Olle Melander, Marketa Sjőgren, Michal Hoffmann, Krzysztof Narkiewicz, Marcin Gruchala & Wojciech Sobiczewski, 2017, In: Blood Pressure. 26, 3, p. 174-180 10 p.

    Research output: Contribution to journalArticle

  12. 2016
  13. The Relationship Between Gene Polymorphisms and Dipping Profile in Patients With Coronary Heart Disease

    Marcin Wirtwein, Olle Melander, Marketa Sjögren, Michal Hoffmann, Krzysztof Narkiewicz, Marcin Gruchala & Wojciech Sobiczewski, 2016 Sep 1, In: American Journal of Hypertension. 29, 9, p. 1094-1102 9 p.

    Research output: Contribution to journalArticle

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

    Gustav Smith, Janine F. Felix, Alanna C. Morrison, Andreas Kalogeropoulos, Stella Trompet, Jemma B. Wilk, Olof Gidlöf, Xinchen Wang, Michael Morley, Michael Mendelson, Roby Joehanes, Symen Ligthart, Xiaoyin Shan, Joshua C. Bis, Ying A. Wang, Marketa Sjögren, Julius Ngwa, Jeffrey Brandimarto, David J. Stott, David Aguilar & 35 others, Kenneth M. Rice, Howard D. Sesso, Serkalem Demissie, Brendan M. Buckley, Kent D. Taylor, Ian Ford, Chen Yao, Chunyu Liu, Nona Sotoodehnia, Pim van der Harst, Bruno H Ch Stricker, Stephen B. Kritchevsky, Yongmei Liu, J. Michael Gaziano, Albert Hofman, Christine S. Moravec, André G. Uitterlinden, Manolis Kellis, Joyce B. van Meurs, Kenneth B. Margulies, Abbas Dehghan, Daniel Levy, Björn Olde, Bruce M. Psaty, L. Adrienne Cupples, J. Wouter Jukema, Luc Djousse, Oscar H. Franco, Eric Boerwinkle, Laurie A. Boyer, Christopher Newton-Cheh, Javed Butler, Ramachandran S. Vasan, Thomas P. Cappola & Nicholas L. Smith, 2016 May 1, In: PLoS Genetics. 12, 5, e1006034.

    Research output: Contribution to journalArticle

  15. 2015
  16. 1A.10: ASSOCIATION BETWEEN GENE POLYMORPHISMS AND RISK OF CARDIOVASCULAR EVENTS IN PATIENTS WITH CORONARY HEART DISEASE.

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

    Research output: Contribution to journalArticle

  17. 2014
  18. Twelve-Single Nucleotide Polymorphism Genetic Risk Score Identifies Individuals at Increased Risk for Future Atrial Fibrillation and Stroke.

    Hayato Tada, Dov Shiffman, Gustav Smith, Marketa Sjögren, Steven A Lubitz, Patrick T Ellinor, Judy Z Louie, Joseph J Catanese, Gunnar Engström, James J Devlin, Sekar Kathiresan & Olle Melander, 2014, In: Stroke: a journal of cerebral circulation. 45, 10, p. 2856

    Research output: Contribution to journalArticle

  19. 2013
  20. Genetic Associations with Valvular Calcification and Aortic Stenosis

    George Thanassoulis, Catherine Y. Campbell, David S. Owens, Gustav Smith, Albert V. Smith, Gina M. Peloso, Kathleen F. Kerr, Sonali Pechlivanis, Matthew J. Budoff, Tamara B. Harris, Rajeev Malhotra, Kevin D. O'Brien, Pia R. Kamstrup, Borge G. Nordestgaard, Anne Tybjaerg-Hansen, Matthew A. Allison, Thor Aspelund, Michael H. Criqui, Susan R. Heckbert, Shih-Jen Hwang & 19 others, Yongmei Liu, Marketa Sjögren, Jesper vanderPals, Hagen Kaelsch, Thomas W. Muehleisen, Markus M. Noethen, L. Adrienne Cupples, Muriel Caslake, Emanuele Di Angelantonio, John Danesh, Jerome I. Rotter, Sigurdur Sigurdsson, Quenna Wong, Raimund Erbel, Sekar Kathiresan, Olle Melander, Vilmundur Gudnason, Christopher J. O'Donnell & Wendy S. Post, 2013, In: New England Journal of Medicine. 368, 6, p. 503-512

    Research output: Contribution to journalArticle

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

    Sara Halldén, Marketa Sjögren, Bo Hedblad, Gunnar Engström, Krzysztof Narkiewicz, Michal Hoffmann, Björn Wahlstrand, Thomas Hedner & Olle Melander, 2013, In: Heart. 99, 13, p. 949-953

    Research output: Contribution to journalArticle

  22. 2012
  23. Genetic Variation Within the Interleukin-1 Gene Cluster and Ischemic Stroke

    Sandra Olsson, Lukas Holmegaard, Katarina Jood, Marketa Sjögren, Gunnar Engström, Håkan Lövkvist, Christian Blomstrand, Bo Norrving, Olle Melander, Arne Lindgren & Christina Jern, 2012, In: Stroke: a journal of cerebral circulation. 43, 9, p. 2278

    Research output: Contribution to journalArticle

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

    Patrick T. Ellinor, Kathryn L. Lunetta, Christine M. Albert, Nicole L. Glazer, Marylyn D. Ritchie, Albert V. Smith, Dan E. Arking, Martina Mueller-Nurasyid, Bouwe P. Krijthe, Steven A. Lubitz, Joshua C. Bis, Mina K. Chung, Marcus Doerr, Kouichi Ozaki, Jason D. Roberts, Gustav Smith, Arne Pfeufer, Moritz F. Sinner, Kurt Lohman, Jingzhong Ding & 69 others, Nicholas L. Smith, Jonathan D. Smith, Michiel Rienstra, Kenneth M. Rice, David R. Van Wagoner, Jared W. Magnani, Reza Wakili, Sebastian Clauss, Jerome I. Rotter, Gerhard Steinbeck, Lenore J. Launer, Robert W. Davies, Matthew Borkovich, Tamara B. Harris, Honghuang Lin, Uwe Voelker, Henry Voelzke, David J. Milan, Albert Hofman, Eric Boerwinkle, Lin Y. Chen, Elsayed Z. Soliman, Benjamin F. Voight, Guo Li, Aravinda Chakravarti, Michiaki Kubo, Usha B. Tedrow, Lynda M. Rose, Paul M. Ridker, David Conen, Tatsuhiko Tsunoda, Tetsushi Furukawa, Nona Sotoodehnia, Siyan Xu, Naoyuki Kamatani, Daniel Levy, Yusuke Nakamura, Babar Parvez, Saagar Mahida, Karen L. Furie, Jonathan Rosand, Raafia Muhammad, Bruce M. Psaty, Thomas Meitinger, Siegfried Perz, H-Erich Wichmann, Jacqueline C. M. Witteman, W. H. Linda Kao, Sekar Kathiresan, Dan M. Roden, Andre G. Uitterlinden, Fernando Rivadeneira, Barbara McKnight, Marketa Sjögren, Anne B. Newman, Yongmei Liu, Michael H. Gollob, Olle Melander, Toshihiro Tanaka, Bruno H. Ch Stricker, Stephan B. Felix, Alvaro Alonso, Dawood Darbar, John Barnard, Daniel I. Chasman, Susan R. Heckbert, Emelia J. Benjamin, Vilmundur Gudnason & Stefan Kaeaeb, 2012, In: Nature Genetics. 44, 6, p. 670-U88

    Research output: Contribution to journalArticle

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

    Artur Fedorowski, Nora Franceschini, Jennifer Brody, Chunyu Liu, Germaine C Verwoert, Eric Boerwinkle, David Couper, Kenneth M Rice, Jerome I Rotter, Francesco Mattace Raso, Andre Uitterlinden, Albert Hofman, Peter Almgren, Marketa Sjögren, Bo Hedblad, Martin G Larson, Christopher Newton-Cheh, Thomas J Wang, Kathryn M Rose, Bruce M Psaty & 3 others, Daniel Levy, Jacqueline Witteman & Olle Melander, 2012, In: European Heart Journal. 33, 18, p. 2331-2341

    Research output: Contribution to journalArticle

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

    Viktor Hamrefors, Marketa Sjögren, Peter Almgren, Björn Wahlstrand, Sverre Kjeldsen, Thomas Hedner & Olle Melander, 2012, In: Journal of Hypertension. 30, 6, p. 1151-1160

    Research output: Contribution to journalArticle

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

    Cristiano Fava, Marketa Sjögren, Martina Montagnana, Elisa Danese, Peter Almgren, Gunnar Engström, Peter Nilsson, Bo Hedblad, Gian Cesare Guidi, Pietro Minuz & Olle Melander, 2012, In: Hypertension.

    Research output: Contribution to journalArticle

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

    Cristiano Fava, Martina Montagnana, Elisa Danese, Marketa Sjögren, Peter Almgren, Gian Cesare Guidi, Bo Hedblad, Gunnar Engström, Pietro Minuz & Olle Melander, 2012, In: Prostaglandins & other Lipid Mediators. 98, 1-2, p. 31-36

    Research output: Contribution to journalArticle

  29. 2011
  30. A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.

    Cristiano Fava, Elisa Danese, Martina Montagnana, Marketa Sjögren, Peter Almgren, Gian Cesare Guidi, Bo Hedblad, Gunnar Engström, Alessandro Lechi, Pietro Minuz & Olle Melander, 2011, In: American Journal of Cardiology. 108, p. 1432-1437

    Research output: Contribution to journalArticle

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

    Georg B. Ehret, Patricia B. Munroe, Kenneth M. Rice, Murielle Bochud, Andrew D. Johnson, Daniel I. Chasman, Albert V. Smith, Martin D. Tobin, Germaine C. Verwoert, Shih-Jen Hwang, Vasyl Pihur, Peter Vollenweider, Paul F. O'Reilly, Najaf Amin, Jennifer L. Bragg-Gresham, Alexander Teumer, Nicole L. Glazer, Lenore Launer, Jing Hua Zhao, Yurii Aulchenko & 326 others, Simon Heath, Siim Sober, Afshin Parsa, Jian'an Luan, Pankaj Arora, Abbas Dehghan, Feng Zhang, Gavin Lucas, Andrew A. Hicks, Anne U. Jackson, John F. Peden, Toshiko Tanaka, Sarah H. Wild, Igor Rudan, Wilmar Igl, Yuri Milaneschi, Alex N. Parker, Cristiano Fava, John C. Chambers, Ervin R. Fox, Meena Kumari, Min Jin Go, Pim van der Harst, Wen Hong Linda Kao, Marketa Sjögren, D. G. Vinay, Myriam Alexander, Yasuharu Tabara, Sue Shaw-Hawkins, Peter H. Whincup, Yongmei Liu, Gang Shi, Johanna Kuusisto, Bamidele Tayo, Mark Seielstad, Xueling Sim, Nguyen Khanh-Dung Hoang, Terho Lehtimaki, Giuseppe Matullo, Ying Wu, Tom R. Gaunt, N. Charlotte Onland-Moret, Matthew N. Cooper, Carl G. P. Platou, Elin Org, Rebecca Hardy, Santosh Dahgam, Jutta Palmen, Veronique Vitart, Peter S. Braund, Tatiana Kuznetsova, Cuno S. P. M. Uiterwaal, Adebowale Adeyemo, Walter Palmas, Harry Campbell, Barbara Ludwig, Maciej Tomaszewski, Ioanna Tzoulaki, Nicholette D. Palmer, Thor Aspelund, Melissa Garcia, Yen-Pei C. Chang, Jeffrey R. O'Connell, Nanette I. Steinle, Diederick E. Grobbee, Dan E. Arking, Sharon L. Kardia, Alanna C. Morrison, Dena Hernandez, Samer Najjar, Wendy L. McArdle, David Hadley, Morris J. Brown, John M. Connell, Aroon D. Hingorani, Ian N. M. Day, Debbie A. Lawlor, John P. Beilby, Robert W. Lawrence, Robert Clarke, Jemma C. Hopewell, Halit Ongen, Albert W. Dreisbach, Yali Li, J. Hunter Young, Joshua C. Bis, Mika Kahonen, Jorma Viikari, Linda S. Adair, Nanette R. Lee, Ming-Huei Chen, Matthias Olden, Cristian Pattaro, Judith A. Hoffman Bolton, Anna Koettgen, Sven Bergmann, Vincent Mooser, Nish Chaturvedi, Timothy M. Frayling, Muhammad Islam, Tazeen H. Jafar, Jeanette Erdmann, Smita R. Kulkarni, Stefan R. Bornstein, Juergen Graessler, Leif Groop, Benjamin F. Voight, Johannes Kettunen, Philip Howard, Andrew Taylor, Simonetta Guarrera, Fulvio Ricceri, Valur Emilsson, Andrew Plump, Ine S. Barroso, Kay-Tee Khaw, Alan B. Weder, Steven C. Hunt, Yan V. Sun, Richard N. Bergman, Francis S. Collins, Lori L. Bonnycastle, Laura J. Scott, Heather M. Stringham, Leena Peltonen, Markus Perola, Erkki Vartiainen, Stefan-Martin Brand, Jan A. Staessen, Thomas J. Wang, Paul R. Burton, Maria Soler Artigas, Yanbin Dong, Harold Snieder, Xiaoling Wang, Haidong Zhu, Kurt K. Lohman, Megan E. Rudock, Susan R. Heckbert, Nicholas L. Smith, Kerri L. Wiggins, Ayo Doumatey, Daniel Shriner, Gudrun Veldre, Margus Viigimaa, Sanjay Kinra, Dorairaj Prabhakaran, Vikal Tripathy, Carl D. Langefeld, Annika Rosengren, Dag S. Thelle, Anna Maria Corsi, Andrew Singleton, Terrence Forrester, Gina Hilton, Colin A. McKenzie, Tunde Salako, Naoharu Iwai, Yoshikuni Kita, Toshio Ogihara, Takayoshi Ohkubo, Tomonori Okamura, Hirotsugu Ueshima, Satoshi Umemura, Susana Eyheramendy, Thomas Meitinger, H. -Erich Wichmann, Yoon Shin Cho, Hyung-Lae Kim, Jong-Young Lee, James Scott, Joban S. Sehmi, Weihua Zhang, Bo Hedblad, Peter Nilsson, George Davey Smith, Andrew Wong, Narisu Narisu, Alena Stancakova, Leslie J. Raffel, Jie Yao, Sekar Kathiresan, Christopher J. O'Donnell, Stephen M. Schwartz, M. Arfan Ikram, W. T., Jr. Longstreth, Thomas H. Mosley, Sudha Seshadri, Nick R. G. Shrine, Louise V. Wain, Mario A. Morken, Amy J. Swift, Jaana Laitinen, Inga Prokopenko, Paavo Zitting, Jackie A. Cooper, Steve E. Humphries, John Danesh, Asif Rasheed, Anuj Goel, Anders Hamsten, Hugh Watkins, Stephan J. L. Bakker, Wiek H. van Gilst, Charles S. Janipalli, K. Radha Mani, Chittaranjan S. Yajnik, Albert Hofman, Francesco U. S. Mattace-Raso, Ben A. Oostra, Ayse Demirkan, Aaron Isaacs, Fernando Rivadeneira, Edward G. Lakatta, Marco Orru, Angelo Scuteri, Mika Ala-Korpela, Antti J. Kangas, Leo-Pekka Lyytikainen, Pasi Soininen, Taru Tukiainen, Peter Wurtz, Rick Twee-Hee Ong, Marcus Doerr, Heyo K. Kroemer, Uwe Voelker, Henry Voelzke, Pilar Galan, Serge Hercberg, Mark Lathrop, Diana Zelenika, Panos Deloukas, Massimo Mangino, Tim D. Spector, Guangju Zhai, James F. Meschia, Michael A. Nalls, Pankaj Sharma, Janos Terzic, M. V. Kranthi Kumar, Matthew Denniff, Ewa Zukowska-Szczechowska, Lynne E. Wagenknecht, F. Gerald R. Fowkes, Fadi J. Charchar, Peter E. H. Schwarz, Caroline Hayward, Xiuqing Guo, Charles Rotimi, Michiel L. Bots, Eva Brand, Nilesh J. Samani, Ozren Polasek, Philippa J. Talmud, Fredrik Nyberg, Diana Kuh, Maris Laan, Kristian Hveem, Lyle J. Palmer, Yvonne T. van der Schouw, Juan P. Casas, Karen L. Mohlke, Paolo Vineis, Olli Raitakari, Santhi K. Ganesh, Tien Y. Wong, E. Shyong Tai, Richard S. Cooper, Markku Laakso, Dabeeru C. Rao, Tamara B. Harris, Richard W. Morris, Anna F. Dominiczak, Mika Kivimaki, Michael G. Marmot, Tetsuro Miki, Danish Saleheen, Giriraj R. Chandak, Josef Coresh, Gerjan Navis, Veikko Salomaa, Bok-Ghee Han, Xiaofeng Zhu, Jaspal S. Kooner, Olle Melander, Paul M. Ridker, Stefania Bandinelli, Ulf B. Gyllensten, Alan F. Wright, James F. Wilson, Luigi Ferrucci, Martin Farrall, Jaakko Tuomilehto, Peter P. Pramstaller, Roberto Elosua, Nicole Soranzo, Eric J. G. Sijbrands, David Altshuler, Ruth J. F. Loos, Alan R. Shuldiner, Christian Gieger, Pierre Meneton, Andre G. Uitterlinden, Nicholas J. Wareham, Vilmundur Gudnason, Jerome I. Rotter, Rainer Rettig, Manuela Uda, David P. Strachan, Jacqueline C. M. Witteman, Anna-Liisa Hartikainen, Jacques S. Beckmann, Eric Boerwinkle, Ramachandran S. Vasan, Michael Boehnke, Martin G. Larson, Marjo-Riitta Jarvelin, Bruce M. Psaty, Goncalo R. Abecasis, Aravinda Chakravarti, Paul Elliott, Cornelia M. van Duijn, Christopher Newton-Cheh, Daniel Levy, Mark J. Caulfield & Toby Johnson, 2011, In: Nature. 478, 7367, p. 103-109

    Research output: Contribution to journalArticle

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

    Sandra Olsson, Katarina Jood, Olle Melander, Marketa Sjögren, Bo Norrving, Michael Nilsson, Arne Lindgren & Christina Jern, 2011, In: Clinical Biochemistry. 44, 12, p. 1018-1020

    Research output: Contribution to journalArticle

  33. Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes.

    Cristiano Fava, Elisa Danese, Martina Montagnana, Marketa Sjögren, Peter Almgren, Gunnar Engström, Peter Nilsson, Bo Hedblad, Gian C Guidi, Pietro Minuz & Olle Melander, 2011, In: Journal of Hypertension. 29, p. 484-491

    Research output: Contribution to journalArticle

  34. 2010
  35. Genetic loci influencing kidney function and chronic kidney disease

    John C. Chambers, Weihua Zhang, Graham M. Lord, Pim van der Harst, Debbie A. Lawlor, Joban S. Sehmi, Daniel P. Gale, Mark N. Wass, Kourosh R. Ahmadi, Stephan J. L. Bakker, Jacqui Beckmann, Henk J. G. Bilo, Murielle Bochud, Morris J. Brown, Mark J. Caulfield, John M. C. Connell, H. Terence Cook, Ioana Cotlarciuc, George Davey Smith, Ranil de Silva & 74 others, Guohong Deng, Olivier Devuyst, Lambert D. Dikkeschei, Nada Dimkovic, Mark Dockrell, Anna Dominiczak, Shah Ebrahim, Thomas Eggermann, Martin Farrall, Luigi Ferrucci, Jurgen Floege, Nita G. Forouhi, Ron T. Gansevoort, Xijin Han, Bo Hedblad, Jaap J. Homan van der Heide, Bouke G. Hepkema, Maria Hernandez-Fuentes, Elina Hypponen, Toby Johnson, Paul E. de Jong, Nanne Kleefstra, Vasiliki Lagou, Marta Lapsley, Yun Li, Ruth J. F. Loos, Jian'an Luan, Karin Luttropp, Celine Marechal, Olle Melander, Patricia B. Munroe, Louise Nordfors, Afshin Parsa, Leena Peltonen, Brenda W. Penninx, Esperanza Perucha, Anneli Pouta, Inga Prokopenko, Paul J. Roderick, Aimo Ruokonen, Nilesh J. Samani, Serena Sanna, Martin Schalling, David Schlessinger, Georg Schlieper, Marc A. J. Seelen, Alan R. Shuldiner, Marketa Sjögren, Johannes H. Smit, Harold Snieder, Nicole Soranzo, Timothy D. Spector, Peter Stenvinkel, Michael J. E. Sternberg, Ramasamyiyer Swaminathan, Toshiko Tanaka, Lielith J. Ubink-Veltmaat, Manuela Uda, Peter Vollenweider, Chris Wallace, Dawn Waterworth, Klaus Zerres, Gerard Waeber, Nicholas J. Wareham, Patrick H. Maxwell, Mark I. McCarthy, Marjo-Riitta Jarvelin, Vincent Mooser, Goncalo R. Abecasis, Liz Lightstone, James Scott, Gerjan Navis, Paul Elliott & Jaspal S. Kooner, 2010, In: Nature Genetics. 42, 5, p. 373-375

    Research output: Contribution to journalArticle

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

    Sandosh Padmanabhan, Olle Melander, Toby Johnson, Anna Maria Di Blasio, Wai K. Lee, Davide Gentilini, Claire E. Hastie, Cristina Menni, Maria Cristina Monti, Christian Delles, Stewart Laing, Barbara Corso, Gerjan Navis, Arjan J. Kwakernaak, Pim van der Harst, Murielle Bochud, Marc Maillard, Michel Burnier, Thomas Hedner, Sverre Kjeldsen & 53 others, Bjorn Wahlstrand, Marketa Sjögren, Cristiano Fava, Martina Montagnana, Elisa Danese, Ole Torffvit, Bo Hedblad, Harold Snieder, John M. C. Connell, Morris Brown, Nilesh J. Samani, Martin Farrall, Giancarlo Cesana, Giuseppe Mancia, Stefano Signorini, Guido Grassi, Susana Eyheramendy, H. Erich Wichmann, Maris Laan, David P. Strachan, Peter Sever, Denis Colm Shields, Alice Stanton, Peter Vollenweider, Alexander Teumer, Henry Voelzke, Rainer Rettig, Christopher Newton-Cheh, Pankaj Arora, Feng Zhang, Nicole Soranzo, Timothy D. Spector, Gavin Lucas, Sekar Kathiresan, David S. Siscovick, Jian'an Luan, Ruth J. F. Loos, Nicholas J. Wareham, Brenda W. Penninx, Ilja M. Nolte, Martin McBride, William H. Miller, Stuart A. Nicklin, Andrew H. Baker, Delyth Graham, Robert A. McDonald, Jill P. Pell, Naveed Sattar, Paul Welsh, Patricia Munroe, Mark J. Caulfield, Alberto Zanchetti & Anna F. Dominiczak, 2010, In: PLoS Genetics. 6, 10

    Research output: Contribution to journalArticle

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

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

    Research output: Contribution to journalPublished meeting abstract

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

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

    Research output: Contribution to journalPublished meeting abstract

  39. 2008
  40. A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population

    Caroline Brorsson, Regine Bergholdt, Marketa Sjögren, Stefanie Eising, Karina Meden Sorensen, David M. Hougaard, Marju Orho-Melander, Leif Groop & Flemming Pociot, 2008, In: Molecular Genetics and Metabolism. 94, 3, p. 386-388

    Research output: Contribution to journalArticle

  41. 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)

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

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

    Research output: Contribution to journalPublished meeting abstract

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

    Eleftheria Zeggini, Laura J. Scott, Richa Saxena, Benjamin F. Voight, Jonathan L. Marchini, Tianle Hu, Paul I. W. de Bakker, Goncalo R. Abecasis, Peter Almgren, Gitte Andersen, Kristin Ardlie, Kristina Bengtsson Bostroem, Richard N. Bergman, Lori L. Bonnycastle, Knut Borch-Johnsen, Noel P. Burtt, Hong Chen, Peter S. Chines, Mark J. Daly, Parimal Deodhar & 78 others, Chia-Jen Ding, Alex S. F. Doney, William L. Duren, Katherine S. Elliott, Michael R. Erdos, Timothy M. Frayling, Rachel M. Freathy, Lauren Gianniny, Harald Grallert, Niels Grarup, Christopher J. Groves, Candace Guiducci, Torben Hansen, Christian Herder, Graham A. Hitman, Thomas E. Hughes, Bo Isomaa, Anne U. Jackson, Torben Jorgensen, Augustine Kong, Kari Kubalanza, Finny G. Kuruvilla, Johanna Kuusisto, Claudia Langenberg, Hana Lango, Torsten Lauritzen, Yun Li, Cecilia M. Lindgren, Valeriya Lyssenko, Amanda F. Marvelle, Christa Meisinger, Kristian Midthjell, Karen L. Mohlke, Mario A. Morken, Andrew D. Morris, Narisu Narisu, Peter Nilsson, Katharine R. Owen, Colin N. A. Palmer, Felicity Payne, John R. B. Perry, Elin Pettersen, Carl Platou, Inga Prokopenko, Lu Qi, Li Qin, Nigel W. Rayner, Matthew Rees, Jeffrey J. Roix, Anelli Sandbaek, Beverley Shields, Marketa Sjögren, Valgerdur Steinthorsdottir, Heather M. Stringham, Amy J. Swift, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Nicholas J. Timpson, Tiinamaija Tuomi, Jaakko Tuomilehto, Mark Walker, Richard M. Watanabe, Michael N. Weedon, Cristen J. Willer, Thomas Illig, Kristian Hveem, Frank B. Hu, Markku Laakso, Kari Stefansson, Oluf Pedersen, Nicholas J. Wareham, Ines Barroso, Andrew T. Hattersley, Francis S. Collins, Leif Groop, Mark I. McCarthy, Michael Boehnke & David Altshuler, 2008, In: Nature Genetics. 40, 5, p. 638-645

    Research output: Contribution to journalArticle

  44. The search for putative unifying genetic factors for components of the metabolic syndrome.

    Marketa Sjögren, Valeriya Lyssenko, Anna Jonsson, Göran Berglund, Peter Nilsson, Leif Groop & Marju Orho-Melander, 2008, In: Diabetologia. 51, p. 2242-2251

    Research output: Contribution to journalArticle

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

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

    Research output: Contribution to journalArticle

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

    Richa Saxena, Benjamin F. Voight, Valeriya Lyssenko, Noel P. Burtt, Paul I. W. de Bakker, Hong Chen, Jeffrey J. Roix, Sekar Kathiresan, Joel N. Hirschhorn, Mark J. Daly, Thomas E. Hughes, Leif Groop, David Altshuler, Peter Almgren, Jose C. Florez, Joanne Meyer, Kristin Ardlie, Kristina Bengtsson Boström, Bo Isomaa, Guillaume Lettre & 47 others, Ulf Lindblad, Helen N. Lyon, Olle Melander, Christopher Newton-Cheh, Peter Nilsson, Marju Orho-Melander, Lennart Råstam, Elizabeth K. Speliotes, Marja-Riitta Taskinen, Tiinamaija Tuomi, Candace Guiducci, Anna Berglund, Joyce Carlson, Lauren Gianniny, Rachel Hackett, Liselotte Hall, Johan Holmkvist, Esa Laurila, Marketa Sjögren, Maria Sterner, Aarti Surti, Margareta Svensson, Malin Svensson, Ryan Tewhey, Brendan Blumenstiel, Melissa Parkin, Matthew DeFelice, Rachel Barry, Wendy Brodeur, Jody Camarata, Nancy Chia, Mary Fava, John Gibbons, Bob Handsaker, Claire Healy, Kieu Nguyen, Casey Gates, Carrie Sougnez, Diane Gage, Marcia Nizzari, Stacey B. Gabriel, Gung-Wei Chirn, Qicheng Ma, Hemang Parikh, Delwood Richardson, Darrell Ricke & Shaun Purcell, 2007, In: Science. 316, 5829, p. 1331-1336

    Research output: Contribution to journalArticle

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