Sequencing technologies ??? the next generation, Nature Reviews Genetics, vol.37, issue.1, pp.31-46, 2010. ,
DOI : 10.1038/nrg2626
Disease gene identification strategies for exome sequencing, European Journal of Human Genetics, vol.155, issue.5, pp.490-497, 2012. ,
DOI : 10.1016/j.ajhg.2011.04.005
Fundamentals of cDNA microarray data analysis, Trends in Genetics, vol.19, issue.11, pp.649-659, 2003. ,
DOI : 10.1016/j.tig.2003.09.015
RNA-Seq: a revolutionary tool for transcriptomics, Nature Reviews Genetics, vol.328, issue.1, pp.57-63, 2009. ,
DOI : 10.1038/nrg2484
Genomewide association studies and assessment of the risk of disease, N Engl J Med, vol.363, pp.166-176, 2010. ,
Mapping copy number variation by population-scale genome sequencing, Nature, vol.7, issue.7332, pp.59-65, 2011. ,
DOI : 10.1038/nature09708
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3077050
Comparative interactomics with Funcoup 2.0, Nucleic Acids Research, vol.40, issue.D1, pp.821-828, 2012. ,
DOI : 10.1093/nar/gkr1062
URL : http://doi.org/10.1093/nar/gkr1062
Prioritizing candidate disease genes by network-based boosting of genome-wide association data, Genome Research, vol.21, issue.7, pp.1109-1121, 2011. ,
DOI : 10.1101/gr.118992.110
STRING v9.1: protein-protein interaction networks, with increased coverage and integration, Nucleic Acids Research, vol.41, issue.D1, pp.808-815, 2013. ,
DOI : 10.1093/nar/gks1094
The human gene connectome as a map of short cuts for morbid allele discovery, Proceedings of the National Academy of Sciences, vol.110, issue.14, pp.5558-5563 ,
DOI : 10.1073/pnas.1218167110
T h al e rD S ,S c h u r rE ,Ab e lL,C as a n o vaJ L : Life-threatening infectious diseases of childhood: single-gene inborn errors of immunity, Ann N Y Acad Sci, vol.1214, pp.18-33, 2010. ,
Primary Immunodeficiencies: A Field in Its Infancy, Science, vol.317, issue.5838, pp.617-619, 2007. ,
DOI : 10.1126/science.1142963
How host defense is encoded in the mammalian genome, Mammalian Genome, vol.35, issue.1-2, pp.1-5, 2011. ,
DOI : 10.1007/s00335-010-9312-4
TLR3 Deficiency in Patients with Herpes Simplex Encephalitis, Science, vol.317, issue.5844, pp.31522-1527, 2007. ,
DOI : 10.1126/science.1139522
URL : https://hal.archives-ouvertes.fr/hal-00297308
: The Human Model, Annual Review of Immunology, vol.20, issue.1, pp.581-620, 2002. ,
DOI : 10.1146/annurev.immunol.20.081501.125851
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency, Nature Immunology, vol.7, issue.12, pp.1178-1186, 2012. ,
DOI : 10.1016/j.immuni.2008.05.012
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514453
Exploring Network Structure, Dynamics, and Function Using NetworkX.I nProceedings of the 7th Python in Science Conference, pp.11-15, 2008. ,
Ensembl 2013, Nucleic Acids Research, vol.41, issue.D1, pp.48-55, 2013. ,
DOI : 10.1093/nar/gks1236
URL : http://doi.org/10.1093/nar/gks1236
BioMart Central Portal--unified access to biological data, Nucleic Acids Research, vol.37, issue.Web Server, pp.23-27, 2009. ,
DOI : 10.1093/nar/gkp265
URL : http://doi.org/10.1093/nar/gkp265
Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency, Journal of Clinical Investigation, vol.121, issue.12, pp.4889-4902, 2011. ,
DOI : 10.1172/JCI59259DS1
Human TRAF3 Adaptor Molecule Deficiency Leads to Impaired Toll-like Receptor 3 Response and Susceptibility to Herpes Simplex Encephalitis, Immunity, vol.33, issue.3, pp.400-411, 2010. ,
DOI : 10.1016/j.immuni.2010.08.014
mutations impair TLR3 immunity and underlie herpes simplex encephalitis of childhood, The Journal of Experimental Medicine, vol.5, issue.9, pp.1567-1582, 2012. ,
DOI : 10.1111/j.1600-065X.2008.00698.x
Herpes Simplex Virus Encephalitis in Human UNC-93B Deficiency, Herpes simplex virus encephalitis in human UNC-93B deficiency, pp.308-312, 2006. ,
DOI : 10.1126/science.1128346
Partial IFN-??R2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation, Blood, vol.122, issue.14, pp.2390-2401, 2013. ,
DOI : 10.1182/blood-2013-01-480814
Mycobacterial Disease and Impaired IFN-?? Immunity in Humans with Inherited ISG15 Deficiency, Science, vol.337, issue.6102, pp.1684-1688, 2012. ,
DOI : 10.1126/science.1224026
Dominant-negative STAT1 SH2 domain mutations in unrelated patients with mendelian susceptibility to mycobacterial disease, Human Mutation, vol.226, issue.9, pp.1377-1387, 2012. ,
DOI : 10.1002/humu.22113
Variation Database, Human Mutation, vol.9, issue.2, pp.1329-1339, 2013. ,
DOI : 10.1002/humu.22380
Inherited IL-12p40 Deficiency, Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds, pp.109-122, 2013. ,
DOI : 10.1097/MD.0b013e31828a01f9
URL : http://doi.org/10.1097/md.0b013e31828a01f9
An integrated map of genetic variation from 1,092 human genomes, Nature, vol.491, pp.56-65, 2012. ,