CNRGH

M. Ibrahim-Kosta et al.
Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-40172-x

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

Olivier Fogel et al.
Deregulation of microRNA expression in monocytes and CD4+ T lymphocytes from patients with axial spondyloarthritis
Arthritis Research & Therapy 2019, vol. 21, issue 1
doi: 10.1186/s13075-019-1829-7

Jörg Tost et al.
Immunotherapy-specific miRNA Expression Profiles In Spleenic CD4+ T-cells In A Peanut Sensitized Mouse Model Treated With Oral Or Epicutaneous Immunotherapy
Journal of Allergy and Clinical Immunology 2019, vol. 143, issue 2
doi: 10.1016/j.jaci.2018.12.742

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

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

Claire S Leblond et al.
Both rare and common genetic variants contribute to autism in the Faroe Islands
npj Genomic Medicine 2019, vol. 4, issue 1
doi: 10.1038/s41525-018-0075-2