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Marketa Sjögren

Publications

Retrieved from Lund University's publications database

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Publications

Retrieved from Lund University's publications database

2018
- 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, et al.
  (2018) Nature Publishing Group
  Journal article
2017
- 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, et al.
  (2017) Taylor & Francis
  Journal article
- Relationship between selected DNA polymorphisms and coronary artery disease complications
  Marcin Wirtwein, Olle Melander, Marketa Sjögren, Michal Hoffmann, Krzysztof Narkiewicz, et al.
  (2017) Elsevier
  Journal article
2016
- 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, et al.
  (2016) Public Library of Science
  Journal article
- Gene variance in the nicotinic receptor cluster (CHRNA5-CHRNA3-CHRNB4) predicts death from cardiopulmonary disease and cancer in smokers.
  Sara Halldén, Marketa Sjögren, Bo Hedblad, Gunnar Engström, Viktor Hamrefors, et al.
  (2016) Wiley-Blackwell Publishing Ltd
  Journal article
- Genetic vasopressin 1b receptor variance in overweight and diabetes mellitus.
  Sofia Enhörning, Marketa Sjögren, Bo Hedblad, Peter Nilsson, Joachim Struck, et al.
  (2016) Society of the European Journal of Endocrinology
  Journal article
- The Relationship Between Gene Polymorphisms and Dipping Profile in Patients With Coronary Heart Disease
  Marcin Wirtwein, Olle Melander, Marketa Sjögren, Michal Hoffmann, Krzysztof Narkiewicz, et al.
  (2016) Elsevier
  Journal article
2015
- 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, et al.
  (2015) Lippincott Williams & Wilkins
  Journal article
- A genetic risk score for hypertension associates with the risk of ischemic stroke in a Swedish case-control study.
  Cristiano Fava, Marketa Sjögren, Sandra Olsson, Håkan Lövkvist, Katarina Jood, et al.
  (2015) Nature Publishing Group
  Journal article
2014
- ASSOCIATION OF BTG2, CYR61, ZFP36, AND SCD GENE POLYMORPHISMS WITH GRAVES' DISEASE AND OPHTHALMOPATHY.
  Tereza Planck, Bushra Shahida, Marketa Sjögren, Leif Groop, Bengt Hallengren, et al.
  (2014) Mary Ann Liebert, Inc.
  Journal article
- Cardiovascular consequences of a polygenetic component of blood pressure in an urban-based longitudinal study: the Malmö Diet and Cancer.
  Cristiano Fava, Therese Ohlsson, Marketa Sjögren, Angela Tagetti, Peter Almgren, et al.
  (2014) Lippincott Williams & Wilkins
  Journal article
- Ceruloplasmin and atrial fibrillation: evidence of causality from a population-based Mendelian randomization study.
  Samuel Adamsson Eryd, Marketa Sjögren, Gustav Smith, Peter Nilsson, Olle Melander, et al.
  (2014) Wiley-Blackwell Publishing Ltd
  Journal article
- Genetic variation in NEDD4L, an epithelial sodium channel regulator, is associated with cardiovascular disease and cardiovascular death.
  Jonas Dahlberg, Marketa Sjögren, Bo Hedblad, Gunnar Engström, Olle Melander
  (2014) Lippincott Williams & Wilkins
  Journal article
- Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.
  Viktor Hamrefors, Bo Hedblad, George Hindy, Gustav Smith, Peter Almgren, et al.
  (2014) Public Library of Science
  Journal article
- 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, et al.
  (2014) American Heart Association
  Journal article
2013
- Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?
  Håkan Lövkvist, Marketa Sjögren, Peter Höglund, Gunnar Engström, C Jern, et al.
  (2013) Wiley-Blackwell
  Journal article
- Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction.
  Klas Gränsbo, Peter Almgren, Marketa Sjögren, Garrett Smith, Gunnar Engström, et al.
  (2013) Wiley-Blackwell Publishing Ltd
  Journal article
- Genetic Associations with Valvular Calcification and Aortic Stenosis
  George Thanassoulis, Catherine Y. Campbell, David S. Owens, Gustav Smith, Albert V. Smith, et al.
  (2013) Massachusetts Medical Society
  Journal article
- Genetic polymorphisms confer risk of atrial fibrillation in patients with heart failure: a population-based study.
  Gustav Smith, Olle Melander, Marketa Sjögren, Bo Hedblad, Gunnar Engström, et al.
  (2013) Elsevier
  Journal article
- Smoking and obesity associated BDNF gene variance predicts total and cardiovascular mortality in smokers.
  Sara Halldén, Marketa Sjögren, Bo Hedblad, Gunnar Engström, Krzysztof Narkiewicz, et al.
  (2013) BMJ Publishing Group
  Journal article
2012
- A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene.
  Håkan Lövkvist, Sandra Olsson, Peter Höglund, Olle Melander, Christina Jern, et al.
  (2012) Nature Publishing Group
  Journal article
- A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis.
  Viktor Hamrefors, Bo Hedblad, Gunnar Engström, Peter Almgren, Marketa Sjögren, et al.
  (2012) Wiley-Blackwell Publishing Ltd
  Journal article
- Genetic Variation Within the Interleukin-1 Gene Cluster and Ischemic Stroke
  Sandra Olsson, Lukas Holmegaard, Katarina Jood, Marketa Sjögren, Gunnar Engström, et al.
  (2012) American Heart Association
  Journal article
- 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, et al.
  (2012) Nature Publishing Group
  Journal article
- 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, et al.
  (2012) Oxford University Press
  Journal article
- Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
  Viktor Hamrefors, Marketa Sjögren, Peter Almgren, Björn Wahlstrand, Sverre Kjeldsen, et al.
  (2012) Lippincott Williams & Wilkins
  Journal article
- 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, et al.
  (2012) Lippincott Williams & Wilkins
  Journal article
- The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmo Diet and cancer study
  Cristiano Fava, Martina Montagnana, Elisa Danese, Marketa Sjögren, Peter Almgren, et al.
  (2012) BioMed Central
  Journal article
- The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
  Cristiano Fava, Martina Montagnana, Elisa Danese, Marketa Sjögren, Peter Almgren, et al.
  (2012) Elsevier
  Journal article
2011
- A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
  Cristiano Fava, Elisa Danese, Martina Montagnana, Marketa Sjögren, Peter Almgren, et al.
  (2011) Excerpta Medica
  Journal article
- Genetic Variant on Chromosome 12p13 Does Not Show Association to Ischemic Stroke in 3 Swedish Case-Control Studies
  Sandra Olsson, Olle Melander, Katarina Jood, Gustav Smith, Håkan Lövkvist, et al.
  (2011) American Heart Association
  Journal article
- 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, et al.
  (2011) Nature Publishing Group
  Journal article
- Lack of association between genetic variations in the KALRN region and ischemic stroke
  Sandra Olsson, Katarina Jood, Olle Melander, Marketa Sjögren, Bo Norrving, et al.
  (2011) Elsevier
  Journal article
- 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, et al.
  (2011) Lippincott Williams & Wilkins
  Journal article
- Vanin-1 T26I polymorphism, hypertension and cardiovascular events in two large urban-based prospective studies in Swedes.
  Cristiano Fava, Martina Montagnana, E Danese, Marketa Sjögren, Peter Almgren, et al.
  (2011) Elsevier
  Journal article
2010
- Genetic loci influencing kidney function and chronic kidney disease
  John C. Chambers, Weihua Zhang, Graham M. Lord, Pim van der Harst, Debbie A. Lawlor, et al.
  (2010) Nature Publishing Group
  Journal article
- 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, et al.
  (2010) Public Library of Science
  Journal article
- 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, et al.
  (2010) Lippincott Williams & Wilkins
  Conference paper: abstract
- 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, et al.
  (2010) Lippincott Williams & Wilkins
  Conference paper: abstract
2008
- 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, et al.
  (2008) Elsevier
  Journal article
- 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
  Dissertation
- Is there a unifying genetic factor predisposing to the metabolic syndrome?
  Marketa Sjögren, Marju Orho-Melander, Anna Jonsson, Margareta Svensson, Göran Berglund, et al.
  (2008) Springer Verlag
  Conference paper: abstract
- 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, et al.
  (2008) Nature Publishing Group
  Journal article
- The search for putative unifying genetic factors for components of the metabolic syndrome.
  Marketa Sjögren, Valeriya Lyssenko, Anna Jonsson, Göran Berglund, Peter Nilsson, et al.
  (2008) Springer Verlag
  Journal article
2007
- 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, et al.
  (2007) Springer Verlag
  Journal article
- 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, et al.
  (2007) The American Association for the Advancement of Science
  Journal article
- Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
  Valeriya Lyssenko, Roberto Lupi, Piero Marchetti, Silvia Del Guerra, Marju Orho-Melander, et al.
  (2007) The Journal of Clinical Investigation
  Journal article
- Regulation of skeletal muscle PPAR delta mRNA expression in twins
  Emma Nilsson, Pernille Poulsen, Marketa Sjögren, Charlotte Ling, Martin Ridderstråle, et al.
  (2007) The Physiological Society
  Journal article
- Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.
  Jenny Fredriksson, Dragi Anevski, Peter Almgren, Marketa Sjögren, Valeriya Lyssenko, et al.
  (2007) Public Library of Science
  Journal article
2006
- Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals
  Richa Saxena, Lauren Gianniny, Noel P. Burtt, Valeriya Lyssenko, Candace Giuducci, et al.
  (2006) American Diabetes Association Inc.
  Journal article
- The -374 T/A polymorphism in the gene encoding RAGE is associated with diabetic nephropathy and retinopathy in type 1 diabetic patients.
  Eero Lindholm, Ekaterine Bakhtadze, Marketa Sjögren, Corrado Cilio, Elisabet Agardh, et al.
  (2006) Springer Verlag
  Journal article
2005
- Genetic prediction of future type 2 diabetes
  Valeriya Lyssenko, Peter Almgren, Dragi Anevski, Marju Orho-Melander, Marketa Sjögren, et al.
  (2005) Public Library of Science
  Journal article
2004
- Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes
  JC Florez, Marketa Sjögren, N Burtt, Marju Orho-Melander, S Schayer, et al.
  (2004) American Diabetes Association Inc.
  Journal article
2003
- A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
  Florence Demenais, Timo Kanninen, Cecilia Lindgren, Steven Wiltshire, Stéphane Gaget, et al.
  (2003) Oxford University Press
  Journal article

Publications

Retrieved from Lund University's publications database

Conference paper: abstract
- 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, et al.
  (2010) Lippincott Williams & Wilkins, 28 p.341-341
- 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, et al.
  (2010) Lippincott Williams & Wilkins, 28 p.238-238
- Is there a unifying genetic factor predisposing to the metabolic syndrome?
  Marketa Sjögren, Marju Orho-Melander, Anna Jonsson, Margareta Svensson, Göran Berglund, et al.
  (2008) Springer Verlag, 51 p.32-33
Dissertation
- 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, 2008:125
Journal article
- 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, et al.
  (2018) Nature Publishing Group, 9 p.1-11
- Relationship between selected DNA polymorphisms and coronary artery disease complications
  Marcin Wirtwein, Olle Melander, Marketa Sjögren, Michal Hoffmann, Krzysztof Narkiewicz, et al.
  (2017) Elsevier, 228 p.814-820
- 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, et al.
  (2017) Taylor & Francis, 26 p.174-180
- The Relationship Between Gene Polymorphisms and Dipping Profile in Patients With Coronary Heart Disease
  Marcin Wirtwein, Olle Melander, Marketa Sjögren, Michal Hoffmann, Krzysztof Narkiewicz, et al.
  (2016) Elsevier, 29 p.1094-1102
- 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, et al.
  (2016) Public Library of Science, 12
- Gene variance in the nicotinic receptor cluster (CHRNA5-CHRNA3-CHRNB4) predicts death from cardiopulmonary disease and cancer in smokers.
  Sara Halldén, Marketa Sjögren, Bo Hedblad, Gunnar Engström, Viktor Hamrefors, et al.
  (2016) Wiley-Blackwell Publishing Ltd, 279 p.388-398
- Genetic vasopressin 1b receptor variance in overweight and diabetes mellitus.
  Sofia Enhörning, Marketa Sjögren, Bo Hedblad, Peter Nilsson, Joachim Struck, et al.
  (2016) Society of the European Journal of Endocrinology, 174 p.69-75
- 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, et al.
  (2015) Lippincott Williams & Wilkins, 33 Suppl 1 p.3-3
- A genetic risk score for hypertension associates with the risk of ischemic stroke in a Swedish case-control study.
  Cristiano Fava, Marketa Sjögren, Sandra Olsson, Håkan Lövkvist, Katarina Jood, et al.
  (2015) Nature Publishing Group, 23 p.969-974
- 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, et al.
  (2014) American Heart Association, 45 p.2856-2856
- Genetic variation in NEDD4L, an epithelial sodium channel regulator, is associated with cardiovascular disease and cardiovascular death.
  Jonas Dahlberg, Marketa Sjögren, Bo Hedblad, Gunnar Engström, Olle Melander
  (2014) Lippincott Williams & Wilkins, 32 p.294-299
- ASSOCIATION OF BTG2, CYR61, ZFP36, AND SCD GENE POLYMORPHISMS WITH GRAVES' DISEASE AND OPHTHALMOPATHY.
  Tereza Planck, Bushra Shahida, Marketa Sjögren, Leif Groop, Bengt Hallengren, et al.
  (2014) Mary Ann Liebert, Inc., 24 p.1156-1161
- Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.
  Viktor Hamrefors, Bo Hedblad, George Hindy, Gustav Smith, Peter Almgren, et al.
  (2014) Public Library of Science, 9
- Ceruloplasmin and atrial fibrillation: evidence of causality from a population-based Mendelian randomization study.
  Samuel Adamsson Eryd, Marketa Sjögren, Gustav Smith, Peter Nilsson, Olle Melander, et al.
  (2014) Wiley-Blackwell Publishing Ltd, 275 p.164-171
- Cardiovascular consequences of a polygenetic component of blood pressure in an urban-based longitudinal study: the Malmö Diet and Cancer.
  Cristiano Fava, Therese Ohlsson, Marketa Sjögren, Angela Tagetti, Peter Almgren, et al.
  (2014) Lippincott Williams & Wilkins, 32 p.1424-1428
- Genetic polymorphisms confer risk of atrial fibrillation in patients with heart failure: a population-based study.
  Gustav Smith, Olle Melander, Marketa Sjögren, Bo Hedblad, Gunnar Engström, et al.
  (2013) Elsevier, 15 p.250-257
- Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?
  Håkan Lövkvist, Marketa Sjögren, Peter Höglund, Gunnar Engström, C Jern, et al.
  (2013) Wiley-Blackwell, 20 p.1284-1291
- Genetic Associations with Valvular Calcification and Aortic Stenosis
  George Thanassoulis, Catherine Y. Campbell, David S. Owens, Gustav Smith, Albert V. Smith, et al.
  (2013) Massachusetts Medical Society, 368 p.503-512
- Smoking and obesity associated BDNF gene variance predicts total and cardiovascular mortality in smokers.
  Sara Halldén, Marketa Sjögren, Bo Hedblad, Gunnar Engström, Krzysztof Narkiewicz, et al.
  (2013) BMJ Publishing Group, 99 p.949-953
- Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction.
  Klas Gränsbo, Peter Almgren, Marketa Sjögren, Garrett Smith, Gunnar Engström, et al.
  (2013) Wiley-Blackwell Publishing Ltd, 274 p.233-240
- 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, et al.
  (2012) Lippincott Williams & Wilkins
- 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, et al.
  (2012) Nature Publishing Group, 44 p.88-670
- The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmo Diet and cancer study
  Cristiano Fava, Martina Montagnana, Elisa Danese, Marketa Sjögren, Peter Almgren, et al.
  (2012) BioMed Central, 13
- The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
  Cristiano Fava, Martina Montagnana, Elisa Danese, Marketa Sjögren, Peter Almgren, et al.
  (2012) Elsevier, 98 p.31-36
- 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, et al.
  (2012) Oxford University Press, 33 p.2331-2341
- A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis.
  Viktor Hamrefors, Bo Hedblad, Gunnar Engström, Peter Almgren, Marketa Sjögren, et al.
  (2012) Wiley-Blackwell Publishing Ltd, 271 p.271-281
- Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
  Viktor Hamrefors, Marketa Sjögren, Peter Almgren, Björn Wahlstrand, Sverre Kjeldsen, et al.
  (2012) Lippincott Williams & Wilkins, 30 p.1151-1160
- Genetic Variation Within the Interleukin-1 Gene Cluster and Ischemic Stroke
  Sandra Olsson, Lukas Holmegaard, Katarina Jood, Marketa Sjögren, Gunnar Engström, et al.
  (2012) American Heart Association, 43 p.2278-2278
- A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene.
  Håkan Lövkvist, Sandra Olsson, Peter Höglund, Olle Melander, Christina Jern, et al.
  (2012) Nature Publishing Group, 20 p.783-789
- Vanin-1 T26I polymorphism, hypertension and cardiovascular events in two large urban-based prospective studies in Swedes.
  Cristiano Fava, Martina Montagnana, E Danese, Marketa Sjögren, Peter Almgren, et al.
  (2011) Elsevier
- 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, et al.
  (2011) Lippincott Williams & Wilkins, 29 p.484-491
- Genetic Variant on Chromosome 12p13 Does Not Show Association to Ischemic Stroke in 3 Swedish Case-Control Studies
  Sandra Olsson, Olle Melander, Katarina Jood, Gustav Smith, Håkan Lövkvist, et al.
  (2011) American Heart Association, 42 p.214-216
- Lack of association between genetic variations in the KALRN region and ischemic stroke
  Sandra Olsson, Katarina Jood, Olle Melander, Marketa Sjögren, Bo Norrving, et al.
  (2011) Elsevier, 44 p.1018-1020
- A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
  Cristiano Fava, Elisa Danese, Martina Montagnana, Marketa Sjögren, Peter Almgren, et al.
  (2011) Excerpta Medica, 108 p.1432-1437
- 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, et al.
  (2011) Nature Publishing Group, 478 p.103-109
- 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, et al.
  (2010) Public Library of Science, 6
- Genetic loci influencing kidney function and chronic kidney disease
  John C. Chambers, Weihua Zhang, Graham M. Lord, Pim van der Harst, Debbie A. Lawlor, et al.
  (2010) Nature Publishing Group, 42 p.373-375
- 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, et al.
  (2008) Elsevier, 94 p.386-388
- The search for putative unifying genetic factors for components of the metabolic syndrome.
  Marketa Sjögren, Valeriya Lyssenko, Anna Jonsson, Göran Berglund, Peter Nilsson, et al.
  (2008) Springer Verlag, 51 p.2242-2251
- 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, et al.
  (2008) Nature Publishing Group, 40 p.638-645
- 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, et al.
  (2007) Springer Verlag, 50 p.1209-1217
- Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.
  Jenny Fredriksson, Dragi Anevski, Peter Almgren, Marketa Sjögren, Valeriya Lyssenko, et al.
  (2007) Public Library of Science, 2 p.285-285
- Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
  Valeriya Lyssenko, Roberto Lupi, Piero Marchetti, Silvia Del Guerra, Marju Orho-Melander, et al.
  (2007) The Journal of Clinical Investigation, 117 p.2155-2163
- 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, et al.
  (2007) The American Association for the Advancement of Science, 316 p.1331-1336
- Regulation of skeletal muscle PPAR delta mRNA expression in twins
  Emma Nilsson, Pernille Poulsen, Marketa Sjögren, Charlotte Ling, Martin Ridderstråle, et al.
  (2007) The Physiological Society, 584 p.1011-1017
- The -374 T/A polymorphism in the gene encoding RAGE is associated with diabetic nephropathy and retinopathy in type 1 diabetic patients.
  Eero Lindholm, Ekaterine Bakhtadze, Marketa Sjögren, Corrado Cilio, Elisabet Agardh, et al.
  (2006) Springer Verlag, 49 p.2745-2755
- Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals
  Richa Saxena, Lauren Gianniny, Noel P. Burtt, Valeriya Lyssenko, Candace Giuducci, et al.
  (2006) American Diabetes Association Inc., 55 p.2890-2895
- Genetic prediction of future type 2 diabetes
  Valeriya Lyssenko, Peter Almgren, Dragi Anevski, Marju Orho-Melander, Marketa Sjögren, et al.
  (2005) Public Library of Science, 2 p.1299-1308
- Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes
  JC Florez, Marketa Sjögren, N Burtt, Marju Orho-Melander, S Schayer, et al.
  (2004) American Diabetes Association Inc., 53 p.3313-3318
- A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
  Florence Demenais, Timo Kanninen, Cecilia Lindgren, Steven Wiltshire, Stéphane Gaget, et al.
  (2003) Oxford University Press, 12 p.1865-1873

20 October 2016

Marketa Sjögren

E-mail: marketa [dot] sjogren [at] med [dot] lu [dot] se

Assistant researcher

Cardiovascular Research - Hypertension

Telephone number:+46 40 39 12 21

Service point:33

Assistant researcher

EXODIAB: Excellence in Diabetes Research in Sweden

My profile in Lund University research portal

Lund University Diabetes Centre

Exellence of diabetes research in Sweden

Marketa Sjögren

Publications

Publications

Publications