PubRank

Monika Stoll

Author PubWeight™ 110.89‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011 13.25
2 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 2009 12.19
3 Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet 2012 12.10
4 Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study. Lancet Neurol 2007 2.63
5 Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. J Am Coll Cardiol 2010 2.17
6 Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy. Nat Med 2009 2.08
7 Regulation of transport of the angiotensin AT2 receptor by a novel membrane-associated Golgi protein. Arterioscler Thromb Vasc Biol 2004 1.75
8 Fibrinogen alpha and gamma genes and factor VLeiden in children with thromboembolism: results from 2 family-based association studies. Blood 2009 1.62
9 Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations. Eur J Hum Genet 2003 1.60
10 Systematic association mapping identifies NELL1 as a novel IBD disease gene. PLoS One 2007 1.57
11 A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke. Blood 2012 1.52
12 Inherited thrombophilia in children with venous thromboembolism and the familial risk of thromboembolism: an observational study. Blood 2012 1.51
13 IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis. Am J Hum Genet 2003 1.50
14 Genome-Wide Association Identifies TBX5 as Candidate Gene for Osteochondrosis Providing a Functional Link to Cartilage Perfusion as Initial Factor. Front Genet 2013 1.43
15 Implications of emerging risk factors for therapeutic intervention. Nutr Metab Cardiovasc Dis 2005 1.43
16 The identification of phosducin as a novel candidate gene for hypertension and its role in sympathetic activation. Curr Opin Nephrol Hypertens 2011 1.40
17 Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. J Am Coll Cardiol 2012 1.14
18 Increased afterload induces pathological cardiac hypertrophy: a new in vitro model. Basic Res Cardiol 2012 1.06
19 Genetic kininogen deficiency contributes to aortic aneurysm formation but not to atherosclerosis. Physiol Genomics 2004 1.02
20 Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry. BMC Cardiovasc Disord 2011 1.01
21 A major gene locus links early onset albuminuria with renal interstitial fibrosis in the MWF rat with polygenetic albuminuria. J Am Soc Nephrol 2003 1.01
22 Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations. Eur J Hum Genet 2006 1.00
23 HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy. Genome Res 2008 1.00
24 A common haplotype of the IL-31 gene influencing gene expression is associated with nonatopic eczema. J Allergy Clin Immunol 2007 1.00
25 Genome-wide patterns of standing genetic variation in a marine population of three-spined sticklebacks. Mol Ecol 2012 0.99
26 DNA methylation changes are a late event in acute promyelocytic leukemia and coincide with loss of transcription factor binding. Blood 2012 0.99
27 Phosducin influences sympathetic activity and prevents stress-induced hypertension in humans and mice. J Clin Invest 2009 0.98
28 The functional -374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn's disease. Am J Physiol Gastrointest Liver Physiol 2011 0.98
29 Genetic linkage of albuminuria and renal injury in Dahl salt-sensitive rats on a high-salt diet: comparison with spontaneously hypertensive rats. Physiol Genomics 2004 0.98
30 Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men. Hum Genet 2006 0.98
31 Signal transducer of inflammation gp130 modulates atherosclerosis in mice and man. J Exp Med 2007 0.97
32 The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studies. Hum Genet 2006 0.96
33 Role of discs large homolog 5. World J Gastroenterol 2006 0.93
34 A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy. Eur Heart J 2013 0.92
35 Genetic loci contribute to the progression of vascular and cardiac hypertrophy in salt-sensitive spontaneous hypertension. Arterioscler Thromb Vasc Biol 2003 0.92
36 DLG5 R30Q variant is a female-specific protective factor in pediatric onset Crohn's disease. Am J Gastroenterol 2006 0.91
37 Selective loss of noradrenaline exacerbates early cognitive dysfunction and synaptic deficits in APP/PS1 mice. Biol Psychiatry 2012 0.90
38 Familial elevated factor VIII in children with symptomatic venous thrombosis and post-thrombotic syndrome: results of a multicenter study. Arterioscler Thromb Vasc Biol 2006 0.89
39 Platelet reactivity and clopidogrel resistance are associated with the H2 haplotype of the P2Y12-ADP receptor gene. Int J Cardiol 2008 0.88
40 Susceptibility genes and progression in age-related maculopathy: a study of single eyes. Invest Ophthalmol Vis Sci 2009 0.87
41 CRP gene haplotypes, serum CRP, and cerebral small-vessel disease: the Rotterdam Scan Study and the MEMO Study. Stroke 2007 0.85
42 Gp130-dependent release of acute phase proteins is linked to the activation of innate immune signaling pathways. PLoS One 2011 0.84
43 The contribution of genetic factors to phenotype and progression of drusen in early age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol 2014 0.83
44 Genetic analysis of salt-sensitive hypertension in Dahl rats reveals a link between cardiac fibrosis and high cholesterol. Cardiovasc Res 2008 0.82
45 Development of overt proteinuria in the Munich Wistar Frömter rat is suppressed by replacement of chromosome 6 in a consomic rat strain. J Am Soc Nephrol 2006 0.82
46 Genetics of hemostasis: differential effects of heritability and household components influencing lipid concentrations and clotting factor levels in 282 pediatric stroke families. Environ Health Perspect 2008 0.82
47 Role of reduced ADAMTS13 in arterial ischemic stroke: a pediatric cohort study. Ann Neurol 2012 0.82
48 Genetic variants in the C-reactive protein gene are associated with microangiopathic ischemic stroke. Cerebrovasc Dis 2010 0.82
49 Rat chromosome 19 transfer from SHR ameliorates hypertension, salt-sensitivity, cardiovascular and renal organ damage in salt-sensitive Dahl rats. J Hypertens 2007 0.81
50 Postgwas: advanced GWAS interpretation in R. PLoS One 2013 0.81
51 Promotor polymorphisms of plasminogen activator inhibitor-1 and other thrombophilic genotypes in cerebral venous thrombosis: a case-control study in adults. J Neurol 2012 0.80
52 Genetic variants implicated in telomere length associated with left ventricular function in patients with hypertension and cardiac organ damage. J Mol Med (Berl) 2012 0.80
53 DNA methyltransferase inhibition reverses epigenetically embedded phenotypes in lung cancer preferentially affecting polycomb target genes. Clin Cancer Res 2013 0.80
54 Evolutionary dynamics of co-segregating gene clusters associated with complex diseases. PLoS One 2012 0.79
55 Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis. BMC Genomics 2014 0.79
56 The Crohn's disease susceptibility gene DLG5 as a member of the CARD interaction network. J Mol Med (Berl) 2008 0.79
57 Angiotensin II AT(1)-receptor induces biglycan in neonatal cardiac fibroblasts via autocrine release of TGFbeta in vitro. Cardiovasc Res 2003 0.78
58 LOC387715, smoking and their prognostic impact on visual functional status in age-related macular degeneration-The Muenster Aging and Retina Study (MARS) cohort. Ophthalmic Epidemiol 2008 0.78
59 Association of the protein Z ATG haplotype with symptomatic nonvascular stroke or thromboembolism in white children: a family-based cohort study. Blood 2008 0.76
60 Osteopontin gene variation and cardio/cerebrovascular disease phenotypes. Atherosclerosis 2009 0.76
61 Paradoxical effects on force generation after efficient β1-adrenoceptor knockdown in reconstituted heart tissue. J Pharmacol Exp Ther 2014 0.76
62 Correction: Genomics of Divergence along a Continuum of Parapatric Population Differentiation. PLoS Genet 2015 0.75
63 Inherited risk factors for thrombotic diseases in children: the genome-wide perspective. Semin Thromb Hemost 2011 0.75
64 Induction of C1q expression in glomerular endothelium in a rat model with arterial hypertension and albuminuria. J Hypertens 2007 0.75