Recherche
Voici les éléments 1-10 de 19
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 - Encore le « gène du crime » ?
(Éditions EDK, Groupe EDP Sciences, 2015)
A new genetic study focussing on the degree of violence in criminals and using both candidate gene and GWAS approaches finds statistically significant associations of extreme violent behaviour with low activity alleles of ...
Chroniques génomiques - Les pièges de l’amélioration
(EDP Sciences, 2019)
Inactivation of the CCR5 gene by CRISPR editing in human
embryos, as recently attempted in China, was touted as a positive change for the
babies involved since it was expected to ...
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.
Maladie de Crohn et GWAS, d’analyses en méta-analyses : Chroniques génomiques
(Éditions EDK/Groupe EDP Sciences, 2011)
Chroniques génomiques : Du bon usage des exomes
(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 ...