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Marketa Sjögren

Publications

Retrieved from Lund University's publications database

Latest

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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 Communications
  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) Blood Pressure
  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) International Journal of Cardiology
  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) PLoS Genetics
  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) Journal of Internal Medicine1989-01-01+01:00
  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) European Journal of Endocrinology1994-01-01+01:00
  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) American Journal of Hypertension
  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) Journal of Hypertension
  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) European Journal of Human Genetics
  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) Thyroid
  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) Journal of Hypertension
  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) Journal of Internal Medicine1989-01-01+01:00
  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) Journal of Hypertension
  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) PLoS ONE
  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) Stroke: a journal of cerebral circulation
  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) European Journal of Neurology
  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) Journal of Internal Medicine1989-01-01+01:00
  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) New England Journal of Medicine
  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) European Journal of Heart Failure
  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) Heart
  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) European Journal of Human Genetics
  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) Journal of Internal Medicine1989-01-01+01:00
  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) Stroke: a journal of cerebral circulation
  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 Genetics
  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) European Heart Journal
  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) Journal of Hypertension
  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) Hypertension
  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) BMC Medical Genetics
  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) Prostaglandins & other Lipid Mediators
  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) American Journal of Cardiology
  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) Stroke: a journal of cerebral circulation
  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
  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) Clinical Biochemistry
  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) Journal of Hypertension
  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) Nutrition Metabolism and Cardiovascular Diseases
  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 Genetics
  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) PLoS Genetics
  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) Journal of Hypertension
  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) Journal of Hypertension
  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) Molecular Genetics and Metabolism
  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) Lund University Faculty of Medicine Doctoral Dissertation Series
  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) Diabetologia
  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 Genetics
  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) Diabetologia
  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) Diabetologia
  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) 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) 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) Journal of Physiology
  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) PLoS ONE
  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) Diabetes
  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) Diabetologia
  Journal article
2005
- Genetic prediction of future type 2 diabetes
  Valeriya Lyssenko, Peter Almgren, Dragi Anevski, Marju Orho-Melander, Marketa Sjögren, et al.
  (2005) PLoS Medicine
  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) Diabetes
  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) Human Molecular Genetics
  Journal article

Publications

Retrieved from Lund University's publications database

Conference paper: abstract
- 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) Journal of Hypertension, 28 p.238-238
- 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) Journal of Hypertension, 28 p.341-341
- 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) Diabetologia, 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) Lund University Faculty of Medicine Doctoral Dissertation Series, 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 Communications, 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) International Journal of Cardiology, 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) Blood Pressure, 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) American Journal of Hypertension, 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) PLoS Genetics, 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) Journal of Internal Medicine1989-01-01+01:00, 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) European Journal of Endocrinology1994-01-01+01:00, 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) Journal of Hypertension, 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) European Journal of Human Genetics, 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) Stroke: a journal of cerebral circulation, 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) Journal of Hypertension, 32 p.294-299
- 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) Journal of Hypertension, 32 p.1424-1428
- 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) Thyroid, 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) PLoS ONE, 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) Journal of Internal Medicine1989-01-01+01:00, 275 p.164-171
- 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) European Journal of Heart Failure, 15 p.250-257
- Genetic Associations with Valvular Calcification and Aortic Stenosis
  George Thanassoulis, Catherine Y. Campbell, David S. Owens, Gustav Smith, Albert V. Smith, et al.
  (2013) New England Journal of Medicine, 368 p.503-512
- Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?
  Håkan Lövkvist, Marketa Sjögren, Peter Höglund, Gunnar Engström, C Jern, et al.
  (2013) European Journal of Neurology, 20 p.1284-1291
- 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) Journal of Internal Medicine1989-01-01+01:00, 274 p.233-240
- 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) Heart, 99 p.949-953
- 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) Hypertension
- 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 Genetics, 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) BMC Medical Genetics, 13
- Genetic Variation Within the Interleukin-1 Gene Cluster and Ischemic Stroke
  Sandra Olsson, Lukas Holmegaard, Katarina Jood, Marketa Sjögren, Gunnar Engström, et al.
  (2012) Stroke: a journal of cerebral circulation, 43 p.2278-2278
- 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) European Heart Journal, 33 p.2331-2341
- 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) European Journal of Human Genetics, 20 p.783-789
- Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
  Viktor Hamrefors, Marketa Sjögren, Peter Almgren, Björn Wahlstrand, Sverre Kjeldsen, et al.
  (2012) Journal of Hypertension, 30 p.1151-1160
- 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) Journal of Internal Medicine1989-01-01+01:00, 271 p.271-281
- 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) Prostaglandins & other Lipid Mediators, 98 p.31-36
- 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) Nutrition Metabolism and Cardiovascular Diseases
- 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) Stroke: a journal of cerebral circulation, 42 p.214-216
- 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) Journal of Hypertension, 29 p.484-491
- 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) Clinical Biochemistry, 44 p.1018-1020
- 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, 478 p.103-109
- 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) American Journal of Cardiology, 108 p.1432-1437
- 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) PLoS Genetics, 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 Genetics, 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) Molecular Genetics and Metabolism, 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) Diabetologia, 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 Genetics, 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) Diabetologia, 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) PLoS ONE, 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) Journal of Clinical Investigation, 117 p.2155-2163
- Regulation of skeletal muscle PPAR delta mRNA expression in twins
  Emma Nilsson, Pernille Poulsen, Marketa Sjögren, Charlotte Ling, Martin Ridderstråle, et al.
  (2007) Journal of Physiology, 584 p.1011-1017
- 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) Science, 316 p.1331-1336
- 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) Diabetes, 55 p.2890-2895
- 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) Diabetologia, 49 p.2745-2755
- Genetic prediction of future type 2 diabetes
  Valeriya Lyssenko, Peter Almgren, Dragi Anevski, Marju Orho-Melander, Marketa Sjögren, et al.
  (2005) PLoS Medicine, 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) Diabetes, 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) Human Molecular Genetics, 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

Excellence of diabetes research in Sweden

Marketa Sjögren

Publications

Publications

Publications