CNRGH

Jaquiéry J et al.
Disentangling the Causes for Faster-X Evolution in Aphids
Genome Biology and Evolution 2018 10(2)
doi: 10.1093/gbe/evy015

Nadjet Belbachir et al.
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome
European Heart Journal 2019, vol. 40, issue 37
doi: 10.1093/eurheartj/ehz308

Angela Bellini et al.
Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma
International Journal of Cancer 2019, vol. 145, issue 10
doi: 10.1002/ijc.32361

Christel Thauvin-Robinet et al.
Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests
European Journal of Human Genetics 2019, vol. 27, issue 8
doi: 10.1038/s41431-019-0384-7

Willem De Ridder et al.
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
Neurology Genetics 2019, vol. 5, issue 2
doi: 10.1212/nxg.0000000000000321

Réjane Troudet et al.
RNA SIGNATURE OF TREATMENT RESPONSE IN FIRST-EPISODE PSYCHOSIS
European Neuropsychopharmacology 2019, vol. 29
doi: 10.1016/j.euroneuro.2017.08.271

Lou Grangeon et al.
Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype
Brain 2019, vol. 142, issue 6
doi: 10.1093/brain/awz095

Emmanuelle Boscher et al.
Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer’s Disease
Journal of Alzheimer's Disease 2019, vol. 68, issue 3
doi: 10.3233/jad-180940

Henri-Corto Stoeklé et al.
Genetic Data, Two-Sided Markets and Dynamic Consent: United States Versus France
Science and Engineering Ethics 2019, vol. 25, issue 5
doi: 10.1007/s11948-019-00085-4

Maëva Veyssiere et al.
A novel nonsense variant in SUPT20H gene associated with Rheumatoid Arthritis identified by Whole Exome Sequencing of multiplex families
PLOS ONE 2019, vol. 14, issue 3
doi: 10.1371/journal.pone.0213387