CNRGH
François Lecoquierre et al.
Confirmation and further delineation of the SMG9‐deficiency syndrome, a rare and severe developmental disorder
American Journal of Medical Genetics Part A 2019, vol. 179, issue 11
doi: 10.1002/ajmg.a.61317
Ana Uzquiano et al.
Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia
Cell Reports 2019, vol. 28, issue 6
doi: 10.1016/j.celrep.2019.06.096
Tiziana La Bella et al.
Adeno-associated virus in the liver: natural history and consequences in tumour development
Gut 2019, vol. 69, issue 4
doi: 10.1136/gutjnl-2019-318281
Cyril Carvalho et al.
Glucocorticoids delay RAF-induced senescence promoted by EGR1
Journal of Cell Science 2019, vol. 132, issue 16
doi: 10.1242/jcs.230748
Morgane Lacour et al.
Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer’s Disease Before 51 Years
Journal of Alzheimer's Disease 2019, vol. 71, issue 1
doi: 10.3233/jad-190193
Stephane Jamain et al.
SU99COMBINING DIFFERENTIAL GENE EXPRESSION ANALYSIS AND GENETIC DATA TO PREDICT TREATMENT RESPONSE IN FIRST-EPISODE PSYCHOSIS
European Neuropsychopharmacology 2019, vol. 29
doi: 10.1016/j.euroneuro.2018.08.463
Kévin Cassinari et al.
A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations
Clinical Chemistry 2019, vol. 65, issue 9
doi: 10.1373/clinchem.2019.304246
Camille Lemattre et al.
Report on three additional patients and genotype–phenotype correlation in SLC25A22-related disorders group
European Journal of Human Genetics 2019, vol. 27, issue 11
doi: 10.1038/s41431-019-0433-2
Florian Thibord et al.
A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process
Journal of Thrombosis and Haemostasis 2019, vol. 17, issue 11
doi: 10.1111/jth.14562
Ruhina S. Laskar et al.
Sex specific associations in genome wide association analysis of renal cell carcinoma
European Journal of Human Genetics 2019, vol. 27, issue 10
doi: 10.1038/s41431-019-0455-9