CNRGH

Thomas Husson et al.
Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use
Translational Psychiatry 2020, vol. 10, issue 1
doi: 10.1038/s41398-020-0760-7

Kévin Uguen et al.
Genome sequencing in cytogenetics: Comparison of short‐read and linked‐read approaches for germline structural variant detection and characterization
Molecular Genetics & Genomic Medicine 2020, vol. 8, issue 3
doi: 10.1002/mgg3.1114

Gian-Andri Thun et al.
High degree of polyclonality hinders somatic mutation calling in lung brush samples of COPD cases and controls
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-56618-1

Mégane Erblang et al.
The Impact of Genetic Variations in ADORA2A in the Association between Caffeine Consumption and Sleep
Genes 2019, vol. 10, issue 12
doi: 10.3390/genes10121021

Constance Xhaard et al.
Heritability of a resting heart rate in a 20-year follow-up family cohort with GWAS data: Insights from the STANISLAS cohort
European Journal of Preventive Cardiology 2019
doi: 10.1177/2047487319890763

Laetitia Barrault et al.
Expression of miRNAs from the Imprinted DLK1/DIO3 Locus Signals the Osteogenic Potential of Human Pluripotent Stem Cells
Cells 2019, vol. 8, issue 12
doi: 10.3390/cells8121523

Yi Tan et al.
Loss of fragile X mental retardation protein precedes Lewy pathology in Parkinson’s disease
Acta Neuropathologica 2019, vol. 139, issue 2
doi: 10.1007/s00401-019-02099-5

Jacqueline Milet et al.
First genome-wide association study of non-severe malaria in two birth cohorts in Benin
Human Genetics 2019, vol. 138, issue 11-12
doi: 10.1007/s00439-019-02079-5

Rahel T. Florian et al.
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3
Nature Communications 2019, vol. 10, issue 1
doi: 10.1038/s41467-019-12763-9

Joshua C. Bis et al.
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
Molecular Psychiatry 2019
doi: 10.1038/s41380-019-0529-7