Recherche
Voici les éléments 1-10 de 16
Chroniques génomiques - 23andMe et le mal des transports
(Éditions EDK, Groupe EDP Sciences, 2016)
A Genome Wide Association Study on propensity to motion sickness published by 23andMe gives interesting results, shows validity for self-reported phenotypic information and underlines the value of the model developed by ...
Chroniques génomiques - Couleur de la peau chez l’homme : de nouvelles surprises
(EDP Sciences, 2019)
Careful GWAS analysis of a group of mixed-ancestry Latino-American individuals
reveals the role of a new “light” variant of the MSFD12 gene
which appears to originate in some of the ...
Chroniques génomiques - Les « gènes » de la schizophrénie
(Éditions EDK, Groupe EDP Sciences, 2014)
Very large-scale GWAS analyses confirm the genetic complexity of schizophrenia and provide some new leads to understand the etiology of the condition.
Chroniques génomiques : La séquence… et après ?
(EDK, 2010)
Chroniques génomiques - Une question de pigmentation
(EDP Sciences, 2018)
GWAS analyses for skin colour performed on a series of diverse African groups reveal new loci involved in this phenotype and, surprisingly, the presence within several African populations of the “light” allele of the SLC24A5 ...
Chroniques génomiques - Variants fréquents et rares, caractères multigéniques et héritabilité perdue
(Éditions EDK, Groupe EDP Sciences, 2017)
Recently, a systematic (but limited) search for rare variants implicated in adult height, a highly polygenic trait, has uncovered a number of new variants for which the effect size is inversely correlated with the minor ...
Chroniques génomiques : The sound of silence
(Éditions EDK/Groupe EDP Sciences, 2012)
Chroniques génomiques : Rare is frequent
(Éditions EDK/Groupe EDP Sciences, 2012)
Chroniques génomiques - Balayage du génome et repérage des personnes à risque : Des GWAS aux GPS
(EDP Sciences, 2018)
The accumulation of extensive repositories linking phenotypic and genetic information, together with new computation methods, makes it possible to derive polygenic scores for susceptibility to common diseases that turn out ...