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Claudia B. Volpato

Researcher at University of Lübeck

Publications -  24
Citations -  2708

Claudia B. Volpato is an academic researcher from University of Lübeck. The author has contributed to research in topics: Population & Genetic linkage. The author has an hindex of 13, co-authored 23 publications receiving 2560 citations. Previous affiliations of Claudia B. Volpato include European Academy of Bozen.

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Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Iris M. Heid, +355 more
- 01 Nov 2010 - 
TL;DR: A meta-analysis of genome-wide association studies for WHR adjusted for body mass index provides evidence for multiple loci that modulate body fat distribution independent of overall adiposity and reveal strong gene-by-sex interactions.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Iris M. Heid, +299 more
Journal ArticleDOI

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

Nona Sotoodehnia, +117 more
- 01 Dec 2010 - 
TL;DR: It is demonstrated that SCN10A, a candidate gene at the most significantly associated locus in this study, is expressed in the mouse ventricular conduction system, and treatment with a selective SCN 10A blocker prolongs QRS duration.
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A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

Eleonora Porcu, +93 more
- 07 Feb 2013 - 
TL;DR: A large meta-analysis of genome-wide association studies for serum levels of the highly heritable thyroid function markers TSH and FT4 improves the current knowledge of the regulation of hypothalamic-pituitary-thyroid axis function and the consequences of genetic variation for hypo- or hyperthyroidism.
Journal ArticleDOI

Linkage Analysis Identifies a Novel Locus for Restless Legs Syndrome on Chromosome 2q in a South Tyrolean Population Isolate

TL;DR: The findings reemphasize the genetic heterogeneity of the disorder and strongly support the identification of a novel locus for RLS on chromosome 2q.