CNRGH
Elsa Curtit et al.
Prognosis value of a genetic score based on germline genetic variants in a prospective cohort of early triple-negative breast cancer patients.
Journal of Clinical Oncology 2019, vol. 37, issue 15_suppl
doi: 10.1200/jco.2019.37.15_suppl.1529
Marie-Ange Palomares et al.
Systematic analysis of TruSeq, SMARTer and SMARTer Ultra-Low RNA-seq kits for standard, low and ultra-low quantity samples
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-43983-0
Abraham E et al.
Pregnancy exposure to atmospheric pollution and meteorological conditions and placental DNA methylation
Environment International 2018 118
doi: doi./10.1016/j.envint.2018.05.007
Gitte B et al.
miRNA profiling identifies deregulated miRNAs associated with osteosarcoma development and time to metastasis in two large cohorts
Molecular Oncology 2017 12(1)
doi: 10.1002/1878-0261.12154
Gitte B et al.
A Summary of the Biological Processes, Disease-Associated Changes and Clinical Applications of DNA Methylation
Springer New York 2017
doi: 10.1007/978-1-4939-7481-8_1
Anttila V et al.
Analysis of shared heritability in common disorders of the brain
Science 2018 360(6395)
doi: 10.1126/science.aap8757
Assoum M et al.
Further delineation of the clinical spectrum of de novo TRIM8 truncating mutations
American Journal of Medical Genetics Part A 2018 176(11)
doi: 10.1002/ajmg.a.40357
Aubart M et al.
Association of modifiers and other genetic factors explain Marfan syndrome clinical variability
European Journal of Human Genetics 2018 26(12)
doi: 10.1038/s41431-018-0164-9
Ávila-Polo R et al.
Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies
Journal of Neuropathology & Experimental Neurology 2018 77(12)
doi: 10.1093/jnen/nly095
Baudrin LG et al.
Molecular and Computational Methods for the Detection of Microsatellite Instability in Cancer
Frontiers in Oncology 2018 8
doi: 10.3389/fonc.2018.00621