Concentration or representation : the struggle for popular sovereignty

There is a tension in the notion of popular sovereignty, and the notion of democracy associated with it, that is both older than our terms for these notions themselves and more fundamental than the apparently consensual way we tend to use them today. After a review of the competing conceptions of 'the people' that underlie two very different understandings of democracy, this article will defend what might be called a 'neo-Jacobin' commitment to popular sovereignty, understood as the formulation and imposition of a shared political will. A people's egalitarian capacity to concentrate both its collective intelligence and force, from this perspective, takes priority over concerns about how best to represent the full variety of positions and interests that differentiate and divide a community

Le Cri du peuple : journal politique quotidien

08 avril 19141914/04/08 (A26,N22)-1914/04/08

Additional file 6: Figure S1. of An integrative functional genomics framework for effective identification of novel regulatory variants in genome–phenome studies

SNP annotation and enrichment analysis in different types of functional data. Figure S2. A colon-specific TF-target gene regulatory network for inflammatory bowel disease. (PDF 1073 kb

Additional file 1: of Phenome-wide association study identifies marked increased in burden of comorbidities in African Americans with systemic lupus erythematosus

Table S1. Significant codes from the PheWAS of African Americans vs. Caucasians with SLE. Figure S1. Selected SLE disease criteria codes in the PheWAS of African Americans and Cauasians with SLE. Table S2. Selected SLE criteria codes from the PheWAS of African Americans and Caucasians with SLE. Table S3. Selected codes related to renal, cardiovascular disease, and infection from the PheWAS of African American SLE cases compared to matched African American controls. Table S4. Selected codes related to SLE criteria from the PheWAS of African American SLE cases and matched African American controls. Table S5. Selected codes from the PheWAS of Caucasian SLE cases compared to matched Caucasian controls. Table S6. Conditional logistic regression models with SLE cases and matched controls. (DOCX 134 kb

Clinical characteristics and outcomes of systemic loxoscelism.

<p>Clinical characteristics and outcomes of systemic loxoscelism.</p

Significant findings for PheWAS of loxoscelism (adjusted significance level, <i>p</i> < 1.2 x 10⁻⁴).

<p>Significant findings for PheWAS of loxoscelism (adjusted significance level, <i>p</i> < 1.2 x 10⁻⁴).</p

Phenotypes and PheWAS of Individuals with Moderate-Severe Loxoscelism.

<p>(A) Manhattan plot representing the number of individuals with moderate to severe loxoscelism with each phenotype. The most frequent phenotypes validated the loxoscelism definition and included the toxic effect of venom, acquired hemolytic anemia, fever of unknown origin, and rash/skin eruption. (B) PheWAS for moderate-severe loxoscelism. The blue line represents significance level without correction (<i>p</i> = 0.05). The red line is representative of the adjusted significance threshold using the Bonferroni correction for multiple comparisons (<i>p =</i> 1.2 x 10⁻⁴). 29 phenotypes showed a significant correlation (p < 1.2 x 10⁻⁴) with the loxoscelism phenotype when compared to controls.</p

Quisqualis indica L.

原著和名: インドシクンシ科名: シクンシ科 = Combretaceae採集地: 千葉県 千葉市 千葉大学 (下総 千葉市 千葉大学)採集日: 1974/7/6採集者: 萩庭丈壽整理番号: JH007681国立科学博物館整理番号: TNS-VS-95768

Additional file 3: Table S3. of eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

Dataset 1 results at p-value significance of 0.01. (XLSX 67 kb

Additional file 4: Table S4. of eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

Dataset 2 results at p-value significance of 0.01. (XLSX 58 kb