PubRank

Helena Kuivaniemi

Author PubWeight™ 79.12‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet 2008 6.72
2 The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future. Genet Med 2013 4.37
3 Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. Nat Genet 2010 1.79
4 Human spontaneous labor without histologic chorioamnionitis is characterized by an acute inflammation gene expression signature. Am J Obstet Gynecol 2006 1.73
5 Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association. J Vasc Surg 2009 1.72
6 Familial intracranial aneurysms: an analysis of 346 multiplex Finnish families. Stroke 2003 1.65
7 Toll-like receptor-2 and -4 in the chorioamniotic membranes in spontaneous labor at term and in preterm parturition that are associated with chorioamnionitis. Am J Obstet Gynecol 2004 1.49
8 Genome scan for familial abdominal aortic aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13. Circulation 2004 1.44
9 Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy. Invest Ophthalmol Vis Sci 2007 1.43
10 A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes. J Biol Chem 2001 1.42
11 Candidate-gene association study of mothers with pre-eclampsia, and their infants, analyzing 775 SNPs in 190 genes. Hum Hered 2006 1.41
12 Whole genome expression profiling reveals a significant role for immune function in human abdominal aortic aneurysms. BMC Genomics 2007 1.39
13 Klf15 deficiency is a molecular link between heart failure and aortic aneurysm formation. Sci Transl Med 2010 1.35
14 Functionally significant SNP MMP8 promoter haplotypes and preterm premature rupture of membranes (PPROM). Hum Mol Genet 2004 1.35
15 A functional SNP in the promoter of the SERPINH1 gene increases risk of preterm premature rupture of membranes in African Americans. Proc Natl Acad Sci U S A 2006 1.27
16 Regional expression of HOXA4 along the aorta and its potential role in human abdominal aortic aneurysms. BMC Physiol 2011 1.19
17 A polymorphism in the matrix metalloproteinase-9 promoter is associated with increased risk of preterm premature rupture of membranes in African Americans. Mol Hum Reprod 2002 1.17
18 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
19 Bacterial vaginosis, the inflammatory response and the risk of preterm birth: a role for genetic epidemiology in the prevention of preterm birth. Am J Obstet Gynecol 2004 1.13
20 Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function. Am J Med Genet A 2008 1.13
21 Role of matrix metalloproteinase inhibitors in preventing abdominal aortic aneurysm. Ann Vasc Surg 2007 1.12
22 Challenges and opportunities in abdominal aortic aneurysm research. J Vasc Surg 2007 1.12
23 A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm. Hum Mol Genet 2013 1.10
24 MicroRNA expression signature in human abdominal aortic aneurysms. BMC Med Genomics 2012 1.09
25 CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy. Arthritis Rheum 2002 1.08
26 Genetic analysis of polymorphisms in biologically relevant candidate genes in patients with abdominal aortic aneurysms. J Vasc Surg 2005 1.07
27 The role of complement Factor H in age-related macular degeneration: a review. Surv Ophthalmol 2010 1.04
28 Elevated expression of matrix metalloproteinase-13 in abdominal aortic aneurysms. Ann Vasc Surg 2004 1.03
29 Search for intracranial aneurysm susceptibility gene(s) using Finnish families. BMC Med Genet 2002 1.02
30 Macrophage migration inhibitory factor in patients with preterm parturition and microbial invasion of the amniotic cavity. J Matern Fetal Neonatal Med 2005 1.01
31 Genome-wide expression profiling of fetal membranes reveals a deficient expression of proteinase inhibitor 3 in premature rupture of membranes. Am J Obstet Gynecol 2004 1.01
32 Matricellular protein CCN3 mitigates abdominal aortic aneurysm. J Clin Invest 2016 0.96
33 The design, execution, and interpretation of genetic association studies to decipher complex diseases. Am J Obstet Gynecol 2002 0.96
34 Basic research studies to understand aneurysm disease. Drug News Perspect 2008 0.95
35 MMP13 promoter polymorphism is associated with atherosclerosis in the abdominal aorta of young black males. Matrix Biol 2002 0.95
36 Genes and abdominal aortic aneurysm. Ann Vasc Surg 2010 0.95
37 Novel pathways in the pathobiology of human abdominal aortic aneurysms. Pathobiology 2012 0.94
38 The association of genetic variants of matrix metalloproteinases with abdominal aortic aneurysm: a systematic review and meta-analysis. Heart 2013 0.91
39 Novel genetic mechanisms for aortic aneurysms. Curr Atheroscler Rep 2010 0.91
40 Functional genomics and proteomics in term and preterm parturition. J Clin Endocrinol Metab 2002 0.91
41 Molecular basis and genetic predisposition to intracranial aneurysm. Ann Med 2014 0.90
42 Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease. Neurogenetics 2004 0.89
43 Intracranial aneurysms in Finnish families: confirmation of linkage and refinement of the interval to chromosome 19q13.3. Am J Hum Genet 2004 0.89
44 Inhibition of Notch1 signaling reduces abdominal aortic aneurysm in mice by attenuating macrophage-mediated inflammation. Arterioscler Thromb Vasc Biol 2012 0.89
45 Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia. BMC Med Genet 2008 0.89
46 The lifetime prevalence of abdominal aortic aneurysms among siblings of aneurysm patients is eightfold higher than among siblings of spouses: an analysis of 187 aneurysm families in Nova Scotia, Canada. J Vasc Surg 2005 0.88
47 Association of kallikrein gene polymorphisms with intracranial aneurysms. Stroke 2007 0.88
48 The CARD15 2936insC mutation and TLR4 896 A>G polymorphism in African Americans and risk of preterm premature rupture of membranes (PPROM). Mol Hum Reprod 2002 0.88
49 Role of complement cascade in abdominal aortic aneurysms. Arterioscler Thromb Vasc Biol 2011 0.88
50 Genetics of abdominal aortic aneurysm. Curr Opin Cardiol 2013 0.87
51 Fine mapping of the Schnyder's crystalline corneal dystrophy locus. Hum Genet 2004 0.86
52 Integration of expression profiles and genetic mapping data to identify candidate genes in intracranial aneurysm. Physiol Genomics 2007 0.86
53 Identification of novel functional sequence variants in the gene for peptidase inhibitor 3. BMC Med Genet 2006 0.85
54 Gene expression profile of an adenomyoepithelioma of the breast with a reciprocal translocation involving chromosomes 8 and 16. Cancer Genet Cytogenet 2005 0.83
55 Population risk factor estimates for abdominal aortic aneurysm from electronic medical records: a case control study. BMC Cardiovasc Disord 2014 0.83
56 A new mutation in exon 3 of the SCL39A4 gene in a Tunisian family with severe acrodermatitis enteropathica. Nutrition 2006 0.83
57 Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study. BMC Med Genet 2006 0.82
58 A revised allele frequency estimate and haplotype analysis of the DBH deficiency mutation IVS1+2T --> C in African- and European-Americans. Am J Med Genet A 2003 0.82
59 MicroRNA analysis in placentas from patients with preeclampsia: comparison of new and published results. Hypertens Pregnancy 2013 0.82
60 Binding sites for ETS family of transcription factors dominate the promoter regions of differentially expressed genes in abdominal aortic aneurysms. Circ Cardiovasc Genet 2009 0.81
61 Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19. BMC Med Genet 2011 0.79
62 Community-based, nonprofit organization-sponsored ultrasonography screening program for abdominal aortic aneurysms is effective at identifying occult aneurysms. Ann Vasc Surg 2006 0.78
63 Matricellular protein CCN3 mitigates abdominal aortic aneurysm. J Clin Invest 2016 0.77
64 Expression of bone morphogenetic protein 2 in normal spontaneous labor at term, preterm labor, and preterm premature rupture of membranes. Am J Obstet Gynecol 2005 0.77
65 Global expression profiles in human normal and aneurysmal abdominal aorta based on two distinct whole genome microarray platforms. Ann N Y Acad Sci 2006 0.77
66 Highlights of the recent literature on abdominal aortic aneurysm research. Ann Vasc Surg 2006 0.76
67 HLA-DQA is associated with abdominal aortic aneurysms in the Belgian population. Ann N Y Acad Sci 2006 0.76
68 Are there genes for aneurysm in the blueprint of the human genome? Ann Vasc Surg 2004 0.75
69 High-resolution physical map for chromosome 16q12.1-q13, the Blau syndrome locus. BMC Genomics 2002 0.75
70 Aneurysm Outreach Inc., a nonprofit organization, offers community-based, ultrasonography screening for abdominal aortic aneurysms. Ann N Y Acad Sci 2006 0.75