| Year |
Citation |
Score |
| 2020 |
Frade-Barros AF, Ianni BM, Cabantous S, Pissetti CW, Saba B, Lin-Wang HT, Buck P, Marin-Neto JA, Schmidt A, Dias F, Hirata MH, Sampaio M, Fragata A, Pereira AC, Donadi E, ... ... Chevillard C, et al. Polymorphisms in Genes Affecting Interferon-γ Production and Th1 T Cell Differentiation Are Associated With Progression to Chagas Disease Cardiomyopathy. Frontiers in Immunology. 11: 1386. PMID 32733459 DOI: 10.3389/Fimmu.2020.01386 |
0.428 |
|
| 2019 |
Santos A, Chevillard C, Gonfinetti N, Bertonha F, Moreira-Filho C, Kalil J, Cunha-Neto E, Silva ME. 1696-P: PBMC of Recent-Onset Patients with Type 1 Diabetes Present a Differential Gene Expression Profile Diabetes. 68. DOI: 10.2337/Db19-1696-P |
0.34 |
|
| 2018 |
Chevillard C, Nunes JPS, Frade AF, Almeida RR, Pandey RP, Nascimento MS, Kalil J, Cunha-Neto E. Disease Tolerance and Pathogen Resistance Genes May Underlie Persistence and Differential Progression to Chagas Disease Cardiomyopathy. Frontiers in Immunology. 9: 2791. PMID 30559742 DOI: 10.3389/Fimmu.2018.02791 |
0.382 |
|
| 2018 |
Silva MC, Davoli-Ferreira M, Medina TS, Sesti-Costa R, Silva GK, Lopes CD, Cardozo LE, Gava FN, Lyroni K, Dias FC, Frade AF, Baron M, Nakaya HI, Figueiredo F, Alves-Filho JC, ... ... Chevillard C, et al. Canonical PI3Kγ signaling in myeloid cells restricts Trypanosoma cruzi infection and dampens chagasic myocarditis. Nature Communications. 9: 1513. PMID 29666415 DOI: 10.1038/S41467-018-03986-3 |
0.314 |
|
| 2017 |
Ferreira LRP, Ferreira FM, Laugier L, Cabantous S, Navarro IC, da Silva Cândido D, Rigaud VC, Real JM, Pereira GV, Pereira IR, Ruivo L, Pandey RP, Savoia M, Kalil J, Lannes-Vieira J, ... ... Chevillard C, et al. Integration of miRNA and gene expression profiles suggest a role for miRNAs in the pathobiological processes of acute Trypanosoma cruzi infection. Scientific Reports. 7: 17990. PMID 29269773 DOI: 10.1038/S41598-017-18080-9 |
0.336 |
|
| 2017 |
Medina TS, Oliveira GG, Silva MC, David BA, Silva GK, Fonseca DM, Sesti-Costa R, Frade AF, Baron MA, Ianni B, Pereira AC, Chevillard C, Cunha-Neto E, Marin-Neto JA, Silva JS. Ebi3 Prevents Trypanosoma cruzi-Induced Myocarditis by Dampening IFN-γ-Driven Inflammation. Frontiers in Immunology. 8: 1213. PMID 29033934 DOI: 10.3389/Fimmu.2017.01213 |
0.365 |
|
| 2017 |
Laugier L, Frade AF, Ferreira FM, Baron MA, Teixeira PC, Cabantous S, Ferreira LRP, Louis L, Rigaud VOC, Gaiotto FA, Bacal F, Pomerantzeff P, Bocchi E, Kalil J, Santos RHB, ... ... Chevillard C, et al. Whole genome Cardiac DNA methylation fingerprint and gene expression analysis provide new insights in the pathogenesis of Chronic Chagas disease Cardiomyopathy. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. PMID 28575239 DOI: 10.1093/Cid/Cix506 |
0.355 |
|
| 2016 |
Frade AF, Laugier L, Ferreira LR, Baron MA, Benvenuti LA, Teixeira PC, Navarro IC, Cabantous S, Ferreira FM, Cândido DD, Gaiotto FA, Bacal F, Pomerantzeff P, Santos RH, Kalil J, ... ... Chevillard C, et al. The MIAT long non-coding RNA is over-expressed in chronic Chagas disease cardiomyopathy. The Journal of Infectious Diseases. PMID 26951817 DOI: 10.1093/Infdis/Jiw095 |
0.314 |
|
| 2015 |
Nogueira LG, Frade AF, Ianni BM, Laugier L, Pissetti CW, Cabantous S, Baron M, Peixoto Gde L, Borges Ade M, Donadi E, Marin-Neto JA, Schmidt A, Dias F, Saba B, Wang HT, ... ... Chevillard C, et al. Functional IL18 polymorphism and susceptibility to Chronic Chagas Disease. Cytokine. 73: 79-83. PMID 25743241 DOI: 10.1016/J.Cyto.2015.01.037 |
0.375 |
|
| 2014 |
Cunha-Neto E, Chevillard C. Chagas disease cardiomyopathy: immunopathology and genetics. Mediators of Inflammation. 2014: 683230. PMID 25210230 DOI: 10.1155/2014/683230 |
0.347 |
|
| 2013 |
Frade AF, Teixeira PC, Ianni BM, Pissetti CW, Saba B, Wang LH, Kuramoto A, Nogueira LG, Buck P, Dias F, Giniaux H, Llored A, Alves S, Schmidt A, Donadi E, ... ... Chevillard C, et al. Polymorphism in the alpha cardiac muscle actin 1 gene is associated to susceptibility to chronic inflammatory cardiomyopathy. Plos One. 8: e83446. PMID 24367596 DOI: 10.1371/Journal.Pone.0083446 |
0.448 |
|
| 2013 |
Frade AF, Pissetti CW, Ianni BM, Saba B, Lin-Wang HT, Nogueira LG, de Melo Borges A, Buck P, Dias F, Baron M, Ferreira LR, Schmidt A, Marin-Neto JA, Hirata M, Sampaio M, ... ... Chevillard C, et al. Genetic susceptibility to Chagas disease cardiomyopathy: involvement of several genes of the innate immunity and chemokine-dependent migration pathways. Bmc Infectious Diseases. 13: 587. PMID 24330528 DOI: 10.1186/1471-2334-13-587 |
0.408 |
|
| 2010 |
Isnard A, Kouriba B, Doumbo O, Chevillard C. Association of rs7719175, located in the IL13 gene promoter, with Schistosoma haematobium infection levels and identification of a susceptibility haplotype. Genes and Immunity. 12: 31-9. PMID 20861864 DOI: 10.1038/Gene.2010.43 |
0.388 |
|
| 2010 |
Granel B, Argiro L, Hachulla E, Fajardy I, Weiller PJ, Durand JM, Frances Y, Dombey AM, Marquet S, Lesavre N, Disdier P, Bernard F, Hatron PY, Chevillard C. Association between a CTGF gene polymorphism and systemic sclerosis in a French population. The Journal of Rheumatology. 37: 351-8. PMID 20032097 DOI: 10.3899/Jrheum.090290 |
0.387 |
|
| 2009 |
Dessein A, Chevillard C, Arnaud V, Hou X, Hamdoun AA, Dessein H, He H, Abdelmaboud SA, Luo X, Li J, Varoquaux A, Mergani A, Abdelwahed M, Zhou J, Monis A, et al. Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes. The Journal of Experimental Medicine. 206: 2321-8. PMID 19822645 DOI: 10.1084/Jem.20090383 |
0.402 |
|
| 2008 |
Isnard A, Chevillard C. Recent advances in the characterization of genetic factors involved in human susceptibility to infection by schistosomiasis. Current Genomics. 9: 290-300. PMID 19471606 DOI: 10.2174/138920208785133262 |
0.364 |
|
| 2008 |
Salhi A, Rodrigues V, Santoro F, Dessein H, Romano A, Castellano LR, Sertorio M, Rafati S, Chevillard C, Prata A, Alcaïs A, Argiro L, Dessein A. Immunological and genetic evidence for a crucial role of IL-10 in cutaneous lesions in humans infected with Leishmania braziliensis. Journal of Immunology (Baltimore, Md. : 1950). 180: 6139-48. PMID 18424735 DOI: 10.4049/Jimmunol.180.9.6139 |
0.321 |
|
| 2008 |
Marquet S, Doumbo O, Cabantous S, Poudiougou B, Argiro L, Safeukui I, Konate S, Sissoko S, Chevereau E, Traore A, Keita MM, Chevillard C, Abel L, Dessein AJ. A functional promoter variant in IL12B predisposes to cerebral malaria. Human Molecular Genetics. 17: 2190-5. PMID 18413324 DOI: 10.1093/Hmg/Ddn118 |
0.388 |
|
| 2008 |
He H, Isnard A, Kouriba B, Cabantous S, Dessein A, Doumbo O, Chevillard C. A STAT6 gene polymorphism is associated with high infection levels in urinary schistosomiasis. Genes and Immunity. 9: 195-206. PMID 18273035 DOI: 10.1038/Gene.2008.2 |
0.423 |
|
| 2007 |
Retter I, Chevillard C, Scharfe M, Conrad A, Hafner M, Im TH, Ludewig M, Nordsiek G, Severitt S, Thies S, Mauhar A, Blöcker H, Müller W, Riblet R. Sequence and characterization of the Ig heavy chain constant and partial variable region of the mouse strain 129S1. Journal of Immunology (Baltimore, Md. : 1950). 179: 2419-27. PMID 17675503 DOI: 10.4049/Jimmunol.179.4.2419 |
0.328 |
|
| 2006 |
Bucheton B, Argiro L, Chevillard C, Marquet S, Kheir MM, Mergani A, El-Safi SH, Dessein AJ. Identification of a novel G245R polymorphism in the IL-2 receptor beta membrane proximal domain associated with human visceral leishmaniasis. Genes and Immunity. 8: 79-83. PMID 17108990 DOI: 10.1038/Sj.Gene.6364355 |
0.365 |
|
| 2006 |
Granel B, Chevillard C, Allanore Y, Arnaud V, Cabantous S, Marquet S, Weiller PJ, Durand JM, Harlé JR, Grange C, Frances Y, Berbis P, Gaudart J, de Micco P, Kahan A, et al. Evaluation of interleukin 13 polymorphisms in systemic sclerosis. Immunogenetics. 58: 693-9. PMID 16832637 DOI: 10.1007/S00251-006-0135-0 |
0.338 |
|
| 2005 |
Kouriba B, Chevillard C, Bream JH, Argiro L, Dessein H, Arnaud V, Sangare L, Dabo A, Beavogui AH, Arama C, Traoré HA, Doumbo O, Dessein A. Analysis of the 5q31-q33 locus shows an association between IL13-1055C/T IL-13-591A/G polymorphisms and Schistosoma haematobium infections Journal of Immunology. 174: 6274-6281. PMID 15879126 DOI: 10.4049/Jimmunol.174.10.6274 |
0.374 |
|
| 2005 |
Machev N, Saut N, Longepied G, Terriou P, Navarro A, Levy N, Guichaoua M, Metzler-Guillemain C, Collignon P, Frances AM, Belougne J, Clemente E, Chiaroni J, Chevillard C, Durand C, et al. Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility. Journal of Medical Genetics. 41: 814-25. PMID 15520406 DOI: 10.1136/Jmg.2004.022111 |
0.391 |
|
| 2004 |
Dessein A, Kouriba B, Eboumbou C, Dessein H, Argiro L, Marquet S, Elwali NE, Rodrigues V, Li Y, Doumbo O, Chevillard C. Interleukin-13 in the skin and interferon-gamma in the liver are key players in immune protection in human schistosomiasis. Immunological Reviews. 201: 180-90. PMID 15361241 DOI: 10.1111/J.0105-2896.2004.00195.X |
0.361 |
|
| 2003 |
Chevillard C, Moukoko CE, Elwali NE, Bream JH, Kouriba B, Argiro L, Rahoud S, Mergani A, Henri S, Gaudart J, Mohamed-Ali Q, Young HA, Dessein AJ. IFN-gamma polymorphisms (IFN-gamma +2109 and IFN-gamma +3810) are associated with severe hepatic fibrosis in human hepatic schistosomiasis (Schistosoma mansoni). Journal of Immunology (Baltimore, Md. : 1950). 171: 5596-601. PMID 14607968 DOI: 10.4049/Jimmunol.171.10.5596 |
0.395 |
|
| 2003 |
Moukoko CE, El Wali N, Saeed OK, Mohamed-Ali Q, Gaudart J, Dessein AJ, Chevillard C. No evidence for a major effect of tumor necrosis factor alpha gene polymorphisms in periportal fibrosis caused by Schistosoma mansoni infection. Infection and Immunity. 71: 5456-60. PMID 14500462 DOI: 10.1128/Iai.71.10.5456-5460.2003 |
0.323 |
|
| 2003 |
Bucheton B, Abel L, Kheir MM, Mirgani A, El-Safi SH, Chevillard C, Dessein A. Genetic control of visceral leishmaniasis in a Sudanese population: candidate gene testing indicates a linkage to the NRAMP1 region. Genes and Immunity. 4: 104-9. PMID 12618857 DOI: 10.1038/Sj.Gene.6363927 |
0.423 |
|
| 2002 |
Zhou J, Ashouian N, Delepine M, Matsuda F, Chevillard C, Riblet R, Schildkraut CL, Birshtein BK. The origin of a developmentally regulated Igh replicon is located near the border of regulatory domains for Igh replication and expression. Proceedings of the National Academy of Sciences of the United States of America. 99: 13693-8. PMID 12370427 DOI: 10.1073/Pnas.212392399 |
0.347 |
|
| 2002 |
Henri S, Chevillard C, Mergani A, Paris P, Gaudart J, Camilla C, Dessein H, Montero F, Elwali NE, Saeed OK, Magzoub M, Dessein AJ. Cytokine regulation of periportal fibrosis in humans infected with Schistosoma mansoni: IFN-gamma is associated with protection against fibrosis and TNF-alpha with aggravation of disease. Journal of Immunology (Baltimore, Md. : 1950). 169: 929-36. PMID 12097398 DOI: 10.4049/Jimmunol.169.2.929 |
0.324 |
|
| 2002 |
Chevillard C, Ozaki J, Herring CD, Riblet R. A three-megabase yeast artificial chromosome contig spanning the C57BL mouse Igh locus. Journal of Immunology (Baltimore, Md. : 1950). 168: 5659-66. PMID 12023364 DOI: 10.4049/Jimmunol.168.11.5659 |
0.388 |
|
| 2002 |
Henri S, Stefani F, Parzy D, Eboumbou C, Dessein A, Chevillard C. Description of three new polymorphisms in the intronic and 3'UTR regions of the human interferon gamma gene. Genes and Immunity. 3: 1-4. PMID 11857052 DOI: 10.1038/Sj.Gene.6363809 |
0.384 |
|
| 2002 |
Chevillard C, Henri S, Stefani F, Parzy D, Dessein A. Two new polymorphisms in the human interferon gamma (IFN-gamma) promoter. European Journal of Immunogenetics. 29: 53-56. PMID 11841489 DOI: 10.1046/J.0960-7420.2001.00281.X |
0.303 |
|
| 2001 |
Villard L, Lévy N, Xiang F, Kpebe A, Labelle V, Chevillard C, Zhang Z, Schwartz CE, Tardieu M, Chelly J, Anvret M, Fontès M. Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease. Journal of Medical Genetics. 38: 435-42. PMID 11432961 DOI: 10.1136/Jmg.38.7.435 |
0.492 |
|
| 2001 |
Williams GS, Martinez A, Montalbano A, Tang A, Mauhar A, Ogwaro KM, Merz D, Chevillard C, Riblet R, Feeney AJ. Unequal VH gene rearrangement frequency within the large VH7183 gene family is not due to recombination signal sequence variation, and mapping of the genes shows a bias of rearrangement based on chromosomal location. Journal of Immunology (Baltimore, Md. : 1950). 167: 257-63. PMID 11418657 DOI: 10.4049/Jimmunol.167.1.257 |
0.375 |
|
| 1999 |
Ermakova OV, Nguyen LH, Little RD, Chevillard C, Riblet R, Ashouian N, Birshtein BK, Schildkraut CL. Evidence that a single replication fork proceeds from early to late replicating domains in the IgH locus in a non-B cell line. Molecular Cell. 3: 321-30. PMID 10198634 DOI: 10.1016/S1097-2765(00)80459-1 |
0.332 |
|
| 1997 |
Michaelson JS, Ermakova O, Birshtein BK, Ashouian N, Chevillard C, Riblet R, Schildkraut CL. Regulation of the replication of the murine immunoglobulin heavy chain gene locus: evaluation of the role of the 3' regulatory region. Molecular and Cellular Biology. 17: 6167-74. PMID 9315677 DOI: 10.1128/Mcb.17.10.6167 |
0.354 |
|
| 1995 |
Cudrey C, Chevillard C, Paslier DL, Vignal A, Passage E, Fontes M. Assignment of microsatellite sequences to the region duplicated in CMT1A (17p12): a useful tool for diagnosis. Journal of Medical Genetics. 32: 231-233. PMID 7783177 DOI: 10.1136/Jmg.32.3.231 |
0.608 |
|
| 1993 |
Chevillard C, Attali B, Lesage F, Fontes M, Barhanin J, Lazdunski M, Mattei MG. Localization of a potassium channel gene (KCNE1) to 21q22.1-q22.2 by in situ hybridization and somatic cell hybridization. Genomics. 15: 243-5. PMID 8432548 DOI: 10.1006/Geno.1993.1051 |
0.592 |
|
| 1993 |
Chevillard C, Reik W, Dermott MM, Fontes M, Mattei MG, Singh PB. Chromosomal localization of human homologs of the Drosophila heterochromatin protein 1 (HP1) gene Mammalian Genome. 4: 124-126. PMID 8431637 DOI: 10.1007/Bf00290438 |
0.602 |
|
| 1993 |
Chevillard C, Le Paslier D, Passage E, Ougen P, Billault A, Boyer S, Mazan S, Bachellerie JP, Vignal A, Cohen D. Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndrome. Human Molecular Genetics. 2: 1235-43. PMID 8401506 DOI: 10.1093/Hmg/2.8.1235 |
0.41 |
|
| Show low-probability matches. |