Génome
Christina Zeitz et al.
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F ‐mediated inherited retinal disorders
Human Mutation 2019, vol. 40, issue 6
doi: 10.1002/humu.23735
Florian Thibord et al.
OPTIMIR, a novel algorithm for integrating available genome-wide genotype data into miRNA sequence alignment analysis
RNA 2019, vol. 25, issue 6
doi: 10.1261/rna.069708.118
Brian W. Kunkle et al.
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Nature Genetics 2019, vol. 51, issue 3
doi: 10.1038/s41588-019-0358-2
Natalia Pinzón et al.
Functional lability of RNA-dependent RNA polymerases in animals
PLOS Genetics 2019, vol. 15, issue 2
doi: 10.1371/journal.pgen.1007915
Sara Frade-Proud’Hon-Clerc et al.
A Novel Rare Missense Variation of the NOD2 Gene: Evidencesof Implication in Crohn’s Disease
International Journal of Molecular Sciences 2019, vol. 20, issue 4
doi: 10.3390/ijms20040835
Xavier Paul Bouteiller et al.
A few north Appalachian populations are the source of European black locust
Ecology and Evolution 2019, vol. 9, issue 5
doi: 10.1002/ece3.4776
Xavière Lornage et al.
ACTN2 mutations cause “Multiple structured Core Disease” (MsCD)
Acta Neuropathologica 2019, vol. 137, issue 3
doi: 10.1007/s00401-019-01963-8
Nicolas Brucato et al.
Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia
Genome Biology and Evolution 2019, vol. 11, issue 3
doi: 10.1093/gbe/evz028
Marie-Joe Karam et al.
Genetic architecture of a plant adaptive trait: QTL mapping of intraspecific variation for tolerance to metal pollution in Arabidopsis halleri
Heredity 2019, vol. 122, issue 6
doi: 10.1038/s41437-019-0184-4
Méyomo G. Wendeu-Foyet et al.
Circadian genes and risk of prostate cancer: Findings from the EPICAP study
International Journal of Cancer 2019, vol. 145, issue 7
doi: 10.1002/ijc.32149