CNRGH

F. Díez-Fuertes et al.
Association of a single nucleotide polymorphism in the ubxn6 gene with long-term non-progression phenotype in HIV-positive individuals
Clinical Microbiology and Infection 2019, vol. 26, issue 1
doi: 10.1016/j.cmi.2019.05.015

Christopher Fitzpatrick et al.
Mitochondrial ncRNA targeting induces cell cycle arrest and tumor growth inhibition of MDA-MB-231 breast cancer cells through reduction of key cell cycle progression factors
Cell Death & Disease 2019, vol. 10, issue 6
doi: 10.1038/s41419-019-1649-3

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

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