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    <title>Berger, K.</title>
    <link>http://repub.eur.nl/res/aut/15395/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease (Article)</title>
      <link>http://repub.eur.nl/res/pub/34243/</link>
      <pubDate>2011-02-01T00:00:00Z</pubDate>
      <description>We performed a meta-analysis of 14 genome-wide association studies of coronary artery disease (CAD) comprising 22,233 individuals with CAD (cases) and 64,762 controls of European descent followed by genotyping of top association signals in 56,682 additional individuals. This analysis identified 13 loci newly associated with CAD at P &lt; 5 - 10'8 and confirmed the association of 10 of 12 previously reported CAD loci. The 13 new loci showed risk allele frequencies ranging from 0.13 to 0.91 and were associated with a 6% to 17% increase in the risk of CAD per allele. Notably, only three of the new loci showed significant association with traditional CAD risk factors and the majority lie in gene regions not previously implicated in the pathogenesis of CAD. Finally, five of the new CAD risk loci appear to have pleiotropic effects, showing strong association with various other human diseases or traits. </description>
    </item> <item>
      <title>CRP gene haplotypes, serum CRP, and cerebral small-vessel disease: The Rotterdam Scan Study and the MEMO Study (Article)</title>
      <link>http://repub.eur.nl/res/pub/35264/</link>
      <pubDate>2007-08-01T00:00:00Z</pubDate>
      <description>BACKGROUND AND PURPOSE - It remains unclear whether C-reactive protein (CRP) is a serum marker for atherothrombotic disease or a causal factor in the pathogenesis of atherosclerosis. We explored the association between CRP gene variations and cerebral small-vessel disease (SVD) in the Rotterdam Scan Study (N=1035) and the MEMO Study (N=268). METHODS - Common haplotypes within the CRP gene were determined by genotype-tagging single-nucleotide polymorphisms. Then their relation with periventricular and subcortical white matter lesions and the prevalence of lacunar brain infarcts was explored by regression analyses. RESULTS - There was no association between CRP haplotypes and measures of cerebral SVD in either study. There was no effect modification of the association between serum CRP levels and measures of SVD by CRP haplotypes. CONCLUSIONS - Our observations suggest that CRP is not causally involved in the pathogenesis of SVD. </description>
    </item> <item>
      <title>The association between blood pressure, hypertension, and cerebral white matter lesions: cardiovascular determinants of dementia study. (Article)</title>
      <link>http://repub.eur.nl/res/pub/13510/</link>
      <pubDate>2004-11-01T00:00:00Z</pubDate>
      <description>Cerebral white matter lesions are frequently observed on magnetic
      resonance imaging (MRI) scans in elderly people and are associated with
      stroke and dementia. Elevated blood pressure is presumed one of the main
      risk factors, although data are almost exclusively derived from
      cross-sectional studies. We assessed in 10 European cohorts the relation
      between concurrently and previously measured blood pressure levels,
      hypertension, its treatment, and severe cerebral white matter lesions. In
      total, 1805 nondemented subjects aged 65 to 75 years were sampled from
      ongoing community-based studies that were initiated 5 to 20 years before
      the MRI. White matter lesions in the periventricular and subcortical
      region were rated separately using semiquantitative measures. We performed
      logistic regression analyses adjusted for potential confounders in 1625
      people with complete data. Concurrently and formerly assessed diastolic
      and systolic blood pressure levels were positively associated with severe
      white matter lesions. Both increases and decreases in diastolic blood
      pressure were associated with more severe periventricular white matter
      lesions. Increase in systolic blood pressure levels was associated with
      more severe periventricular and subcortical white matter lesions. People
      with poorly controlled hypertension had a higher risk of severe white
      matter lesions than those without hypertension, or those with controlled
      or untreated hypertension. Higher blood pressure was associated with an
      increased risk of severe white matter lesions. Successful treatment of
      hypertension may reduce this risk; however, a potential negative effect of
      decreasing diastolic blood pressure level on the occurrence of severe
      periventricular white matter lesions should be taken into account.</description>
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