CNRGH
Sara Lindström et al.
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Blood 2019, vol. 134, issue 19
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Chris Balak et al.
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation
The American Journal of Human Genetics 2019, vol. 105, issue 3
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Joris Deelen et al.
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Nature Communications 2019, vol. 10, issue 1
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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
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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
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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
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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