Marketa Sjögren
Research coordinator
Publications
Displaying of publications. Sorted by year, then title.
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, et al.
(2020) Nature Metabolism, 2 p.1135-1148
Journal articleOrthostatic 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, et al.
(2020) Journals of Gerontology. Series A: Biological Sciences & Medical Sciences, 75 p.2074-2080
Journal articleClinical 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, et al.
(2020) Hypertension , p.169-177
Journal articlePolygenetic risk for coronary artery disease increases hospitalization burden and mortality
Marketa Sjögren, Peter Almgren, Olle Melander
(2019) IJC Heart and Vasculature, 24
Journal articleGenetic 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
Journal articleRelationship 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
Journal articleElevated 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
Journal articleThe 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
Journal articleDiscovery 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
Journal articleGenetic 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 Endocrinology, 174 p.69-75
Journal articleGene 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 Medicine, 279 p.388-398
Journal articleGenetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Pattaro C., C. Fava, B. Hedblad, O. Melander, P. Nilsson, et al.
(2016) Nature Communications, 7
Journal articleA 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
Journal article1A.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
Journal articleSmoking 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
Journal articleASSOCIATION 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
Journal articleCeruloplasmin 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 Medicine, 275 p.164-171
Journal articleTwelve-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
Journal articleGenetic 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
Journal articleCardiovascular 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
Journal articleGenetic 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
Journal articleGenetic 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
Journal articleAre 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
Journal articleSmoking 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
Journal articleChromosome 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 Medicine, 274 p.233-240
Journal articlePrediction 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 articleThe 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
Journal articleMeta-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
Journal articleGenetic 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
Journal articleA 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
Journal articleThe 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
Journal articleA 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 Medicine, 271 p.271-281
Journal articlePharmacogenetic 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
Journal articleOrthostatic 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
Journal articleVanin-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 articleGenetic 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
Journal articleA 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
Journal articleGenetic 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
Journal articleLack 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
Journal articleSerine/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
Journal articleGenetic 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
Journal articleStk39 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
Conference paper: abstractGenome-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
Journal articleVanin-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
Conference paper: abstractMeta-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
Journal articleA 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
Journal articleThe 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
Journal articleIs 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
Conference paper: abstractGenetics 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
DissertationMechanisms 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
Journal articleGenome-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
Journal articleRegulation 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
Journal articleVariation 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
Journal articleAssociation 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
Journal articleThe -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
Journal articleCommon 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
Journal articleGenetic 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
Journal articleAssociation 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
Journal articleA 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
Journal articleLentivirus gene transfer in murine hematopoietic progenitor cells is compromised by a delay in proviral integration and results in transduction mosaicism and heterogeneous gene expression in progeny cells
H Mikkola, N B Woods, M Sjögren, Hildur Helgadottir, I Hamaguchi, et al.
(2000) Journal of Virology, 74 p.8-11911
Journal article