CNRGH
Nicolas Brucato et al.
Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia
Genome Biology and Evolution 2019, vol. 11, issue 3
doi: 10.1093/gbe/evz028
Méyomo G. Wendeu-Foyet et al.
Circadian genes and risk of prostate cancer: Findings from the EPICAP study
International Journal of Cancer 2019, vol. 145, issue 7
doi: 10.1002/ijc.32149
Claire S Leblond et al.
Both rare and common genetic variants contribute to autism in the Faroe Islands
npj Genomic Medicine 2019, vol. 4, issue 1
doi: 10.1038/s41525-018-0075-2
Sara Lindström et al.
A large‐scale exome array analysis of venous thromboembolism
Genetic Epidemiology 2019, vol. 43, issue 4
doi: 10.1002/gepi.22187
Cécile Desjobert et al.
Demethylation by low-dose 5-aza-2′-deoxycytidine impairs 3D melanoma invasion partially through miR-199a-3p expression revealing the role of this miR in melanoma
Clinical Epigenetics 2019, vol. 11, issue 1
doi: 10.1186/s13148-018-0600-2
Laura Gouder et al.
Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-018-36993-x
Mattias Johansson et al.
The influence of obesity-related factors in the etiology of renal cell carcinoma—A mendelian randomization study
PLOS Medicine 2019, vol. 16, issue 1
doi: 10.1371/journal.pmed.1002724
Pau Erola et al.
Learning Differential Module Networks Across Multiple Experimental Conditions
Methods in Molecular Biology 2018
doi: 10.1007/978-1-4939-8882-2_13
Nadine AME van der Beek et al.
A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1
European Journal of Human Genetics 2018, vol. 27, issue 3
doi: 10.1038/s41431-018-0250-z
Nadine AME van der Beek et al.
A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1
European Journal of Human Genetics 2018, vol. 27, issue 3
doi: 10.1038/s41431-018-0250-z