| Year |
Citation |
Score |
| 2016 |
Laissue P, Lakhal B, Vatin M, Batista F, Burgio G, Mercier E, Santos ED, Buffat C, Sierra-Diaz DC, Renault G, Montagutelli X, Salmon J, Monget P, Veitia RA, Méhats C, ... Fellous M, et al. Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans. Open Biology. 6. PMID 27805902 DOI: 10.1098/Rsob.160109 |
0.325 |
|
| 2016 |
Bramble MS, Goldstein EH, Lipson A, Ngun T, Eskin A, Gosschalk JE, Roach L, Vashist N, Barseghyan H, Lee E, Arboleda VA, Vaiman D, Yuksel Z, Fellous M, Vilain E. A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing. Human Reproduction (Oxford, England). PMID 26911863 DOI: 10.1093/Humrep/Dew025 |
0.733 |
|
| 2016 |
Fauchereau F, Shalev S, Chervinsky E, Fruchter RB, Legois B, Fellous M, Caburet S, Veitia RA. A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency. Clinical Genetics. PMID 26771056 DOI: 10.1111/Cge.12736 |
0.358 |
|
| 2014 |
Caburet S, Arboleda VA, Llano E, Overbeek PA, Barbero JL, Oka K, Harrison W, Vaiman D, Ben-Neriah Z, GarcÃa-Tuñón I, Fellous M, Pendás AM, Veitia RA, Vilain E. Mutant cohesin in premature ovarian failure. The New England Journal of Medicine. 370: 943-9. PMID 24597867 DOI: 10.1056/Nejmoa1309635 |
0.742 |
|
| 2012 |
Fonseca DJ, Ojeda D, Lakhal B, Braham R, Eggers S, Turbitt E, White S, Grover S, Warne G, Zacharin M, Nevin Lam A, Landolsi H, Elghezal H, Saâd A, Restrepo CM, ... Fellous M, et al. CITED2 mutations potentially cause idiopathic premature ovarian failure. Translational Research : the Journal of Laboratory and Clinical Medicine. 160: 384-8. PMID 22709740 DOI: 10.1016/J.Trsl.2012.05.006 |
0.383 |
|
| 2012 |
Caburet S, Zavadakova P, Ben-Neriah Z, Bouhali K, Dipietromaria A, Charon C, Besse C, Laissue P, Chalifa-Caspi V, Christin-Maitre S, Vaiman D, Levi G, Veitia RA, Fellous M. Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure. Plos One. 7: e33412. PMID 22428046 DOI: 10.1371/Journal.Pone.0033412 |
0.401 |
|
| 2011 |
Bouhali K, Dipietromaria A, Fontaine A, Caburet S, Barbieri O, Bellessort B, Fellous M, Veitia RA, Levi G. Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency. Human Molecular Genetics. 20: 2642-50. PMID 21505076 DOI: 10.1093/Hmg/Ddr166 |
0.374 |
|
| 2010 |
Hildebrand MS, Avenarius MR, Fellous M, Zhang Y, Meyer NC, Auer J, Serres C, Kahrizi K, Najmabadi H, Beckmann JS, Smith RJ. Genetic male infertility and mutation of CATSPER ion channels. European Journal of Human Genetics : Ejhg. 18: 1178-84. PMID 20648059 DOI: 10.1038/Ejhg.2010.108 |
0.346 |
|
| 2010 |
Benayoun BA, Caburet S, Dipietromaria A, Georges A, D'Haene B, Pandaranayaka PJ, L'Hôte D, Todeschini AL, Krishnaswamy S, Fellous M, De Baere E, Veitia RA. Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G). Plos One. 5: e8789. PMID 20098707 DOI: 10.1371/Journal.Pone.0008789 |
0.319 |
|
| 2009 |
De Baere E, Fellous M, Veitia RA. The transcription factor FOXL2 in ovarian function and dysfunction. Folia Histochemica Et Cytobiologica / Polish Academy of Sciences, Polish Histochemical and Cytochemical Society. 47: S43-9. PMID 20067892 DOI: 10.2478/V10042-009-0062-7 |
0.336 |
|
| 2009 |
Laissue P, Burgio G, l'Hôte D, Renault G, Marchiol-Fournigault C, Fradelizi D, Fellous M, Serres C, Montagutelli X, Monget P, Vaiman D. Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography. The International Journal of Developmental Biology. 53: 623-9. PMID 19488966 DOI: 10.1387/Ijdb.082613Pl |
0.318 |
|
| 2009 |
Laissue P, Lakhal B, Benayoun BA, Dipietromaria A, Braham R, Elghezal H, Philibert P, Saâd A, Sultan C, Fellous M, Veitia RA. Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2. Journal of Medical Genetics. 46: 455-7. PMID 19429596 DOI: 10.1136/Jmg.2008.065086 |
0.323 |
|
| 2009 |
Wilhelm D, Washburn LL, Truong V, Fellous M, Eicher EM, Koopman P. Antagonism of the testis- and ovary-determining pathways during ovotestis development in mice. Mechanisms of Development. 126: 324-36. PMID 19269320 DOI: 10.1016/J.Mod.2009.02.006 |
0.307 |
|
| 2008 |
Lakhal B, Laissue P, Elghèzal H, Fellous M. [Genetic analysis of premature ovarian failure: role of forkhead and TGF-beta genes]. Gynã©Cologie, Obstã©Trique & Fertilitã©. 36: 862-71. PMID 18692424 DOI: 10.1016/J.Gyobfe.2008.07.002 |
0.3 |
|
| 2008 |
Beysen D, De Jaegere S, Amor D, Bouchard P, Christin-Maitre S, Fellous M, Touraine P, Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, Barel D, Clayton-Smith J, de Ravel T, et al. Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome. Human Mutation. 29: E205-19. PMID 18642388 DOI: 10.1002/Humu.20819 |
0.324 |
|
| 2008 |
Benayoun BA, Caburet S, Dipietromaria A, Bailly-Bechet M, Batista F, Fellous M, Vaiman D, Veitia RA. The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles. Human Molecular Genetics. 17: 3118-27. PMID 18635577 DOI: 10.1093/Hmg/Ddn209 |
0.337 |
|
| 2008 |
Hersmus R, Kalfa N, de Leeuw B, Stoop H, Oosterhuis JW, de Krijger R, Wolffenbuttel KP, Drop SL, Veitia RA, Fellous M, Jaubert F, Looijenga LH. FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD). The Journal of Pathology. 215: 31-8. PMID 18348162 DOI: 10.1002/Path.2335 |
0.354 |
|
| 2008 |
Mandon-Pépin B, Touraine P, Kuttenn F, Derbois C, Rouxel A, Matsuda F, Nicolas A, Cotinot C, Fellous M. Genetic investigation of four meiotic genes in women with premature ovarian failure. European Journal of Endocrinology / European Federation of Endocrine Societies. 158: 107-15. PMID 18166824 DOI: 10.1530/Eje-07-0400 |
0.346 |
|
| 2008 |
Laissue P, Vinci G, Veitia RA, Fellous M. Recent advances in the study of genes involved in non-syndromic premature ovarian failure. Molecular and Cellular Endocrinology. 282: 101-11. PMID 18164539 DOI: 10.1016/J.Mce.2007.11.005 |
0.341 |
|
| 2007 |
Batista F, Vaiman D, Dausset J, Fellous M, Veitia RA. Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics. Proceedings of the National Academy of Sciences of the United States of America. 104: 3330-5. PMID 17360647 DOI: 10.1073/Pnas.0611326104 |
0.501 |
|
| 2006 |
Laissue P, Copelli S, Bergada I, Bergada C, Barrio G, Karaboga S, Wurtz JM, Fellous M, Lalli E, Veitia RA. Partial defects in transcriptional activity of two novel DAX-1 mutations in childhood-onset adrenal hypoplasia congenita. Clinical Endocrinology. 65: 681-6. PMID 17054473 DOI: 10.1111/J.1365-2265.2006.02649.X |
0.34 |
|
| 2006 |
Laissue P, Christin-Maitre S, Touraine P, Kuttenn F, Ritvos O, Aittomaki K, Bourcigaux N, Jacquesson L, Bouchard P, Frydman R, Dewailly D, Reyss AC, Jeffery L, Bachelot A, Massin N, ... Fellous M, et al. Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure. European Journal of Endocrinology / European Federation of Endocrine Societies. 154: 739-44. PMID 16645022 DOI: 10.1530/Eje.1.02135 |
0.34 |
|
| 2005 |
Moumné L, Fellous M, Veitia RA. Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation. Human Molecular Genetics. 14: 3557-64. PMID 16219626 DOI: 10.1093/Hmg/Ddi383 |
0.314 |
|
| 2005 |
Baron D, Batista F, Chaffaux S, Cocquet J, Cotinot C, Cribiu E, De Baere E, De Baeree E, Guiguen Y, Jaubert F, Pailhoux E, Pannetier M, Vaiman D, Vigier B, Veitia R, ... Fellous M, et al. Foxl2 gene and the development of the ovary: a story about goat, mouse, fish and woman. Reproduction, Nutrition, Development. 45: 377-82. PMID 15982462 DOI: 10.1051/Rnd:2005028 |
0.369 |
|
| 2005 |
Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina H, Brooks SS, Christin-Maitre S, Fellous M, Fryns JP, Kim JR, Lapunzina P, Lemyre E, Meire F, et al. Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome. American Journal of Human Genetics. 77: 205-18. PMID 15962237 DOI: 10.1086/432083 |
0.391 |
|
| 2005 |
Bergadá I, Del Rey G, Lapunzina P, Bergadá C, Fellous M, Copelli S. Familial occurrence of the IMAGe association: additional clinical variants and a proposed mode of inheritance. The Journal of Clinical Endocrinology and Metabolism. 90: 3186-90. PMID 15769992 DOI: 10.1210/Jc.2004-1589 |
0.359 |
|
| 2004 |
Baron D, Cocquet J, Xia X, Fellous M, Guiguen Y, Veitia RA. An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation. Journal of Molecular Endocrinology. 33: 705-15. PMID 15591029 DOI: 10.1677/Jme.1.01566 |
0.342 |
|
| 2004 |
Cosseddu GM, Perez-Enciso M, Fellous M, Vaiman D. Interspecific chromosome-wide transcription profiles reveal the existence of mammalian-specific and species-specific chromosome domains. Journal of Molecular Evolution. 59: 317-28. PMID 15553087 DOI: 10.1007/S00239-004-2627-6 |
0.341 |
|
| 2004 |
Thauvin-Robinet C, Faivre L, Cusin V, Khau Van Kien P, Callier P, Parker KL, Fellous M, Borgnon J, Gounot E, Huet F, Sapin E, Mugneret F. Cloacal exstrophy in an infant with 9q34.1-qter deletion resulting from a de novo unbalanced translocation between chromosome 9q and Yq. American Journal of Medical Genetics. Part A. 126: 303-7. PMID 15054847 DOI: 10.1002/Ajmg.A.20596 |
0.343 |
|
| 2003 |
Cocquet J, De Baere E, Gareil M, Pannetier M, Xia X, Fellous M, Veitia RA. Structure, evolution and expression of the FOXL2 transcription unit. Cytogenetic and Genome Research. 101: 206-11. PMID 14684984 DOI: 10.1159/000074338 |
0.346 |
|
| 2003 |
Avidan N, Tamary H, Dgany O, Cattan D, Pariente A, Thulliez M, Borot N, Moati L, Barthelme A, Shalmon L, Krasnov T, Ben-Asher E, Olender T, Khen M, Yaniv I, ... ... Fellous M, et al. CATSPER2, a human autosomal nonsyndromic male infertility gene. European Journal of Human Genetics : Ejhg. 11: 497-502. PMID 12825070 DOI: 10.1038/Sj.Ejhg.5200991 |
0.416 |
|
| 2003 |
Quintana-Murci L, Veitia R, Fellous M, Semino O, Poloni ES. Genetic structure of Mediterranean populations revealed by Y-chromosome haplotype analysis. American Journal of Physical Anthropology. 121: 157-71. PMID 12740959 DOI: 10.1002/Ajpa.10187 |
0.329 |
|
| 2003 |
Flamant S, Pescher P, Lemercier B, Clément-Ziza M, Képès F, Fellous M, Milon G, Marchal G, Besmond C. Characterization of a putative type IV aminophospholipid transporter P-type ATPase. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 21-30. PMID 12532265 DOI: 10.1007/S00335-002-3032-3 |
0.314 |
|
| 2003 |
De Baere E, Beysen D, Oley C, Lorenz B, Cocquet J, De Sutter P, Devriendt K, Dixon M, Fellous M, Fryns JP, Garza A, Jonsrud C, Koivisto PA, Krause A, Leroy BP, et al. FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation. American Journal of Human Genetics. 72: 478-87. PMID 12529855 DOI: 10.1086/346118 |
0.324 |
|
| 2002 |
Vialard F, Cocquet J, Christin-Maitre S, Veitia R, Fellous M. The X chromosome and ovarian function. Cytogenetic and Genome Research. 99: 218-23. PMID 12900567 DOI: 10.1159/000071596 |
0.3 |
|
| 2002 |
Damiani D, Mascolli MA, Almeida MJ, Jaubert F, Fellous M, Dichtchekenian V, Tobo PR, Moreira-Filho CA, Setian N. Persistence of Müllerian remnants in complete androgen insensitivity syndrome. Journal of Pediatric Endocrinology & Metabolism : Jpem. 15: 1553-6. PMID 12503865 DOI: 10.1515/Jpem.2002.15.9.1553 |
0.315 |
|
| 2002 |
Mandon-Pépin B, Derbois C, Matsuda F, Cotinot C, Wolgemuth DJ, Smith K, McElreavey K, Nicolas A, Fellous M. [Human infertility: meiotic genes as potential candidates]. Gynã©Cologie, Obstã©Trique & Fertilitã©. 30: 817-21. PMID 12478991 DOI: 10.1016/S1297-9589(02)00444-7 |
0.398 |
|
| 2002 |
Cocquet J, Pailhoux E, Jaubert F, Servel N, Xia X, Pannetier M, De Baere E, Messiaen L, Cotinot C, Fellous M, Veitia RA. Evolution and expression of FOXL2. Journal of Medical Genetics. 39: 916-21. PMID 12471206 DOI: 10.1136/Jmg.39.12.916 |
0.39 |
|
| 2002 |
Cotinot C, Pailhoux E, Jaubert F, Fellous M. Molecular genetics of sex determination. Seminars in Reproductive Medicine. 20: 157-68. PMID 12428196 DOI: 10.1055/S-2002-35380 |
0.399 |
|
| 2002 |
De Baere E, Lemercier B, Christin-Maitre S, Durval D, Messiaen L, Fellous M, Veitia R. FOXL2 mutation screening in a large panel of POF patients and XX males. Journal of Medical Genetics. 39: e43. PMID 12161610 DOI: 10.1136/Jmg.39.8.E43 |
0.392 |
|
| 2002 |
Vialard F, Ottolenghi C, Gonzales M, Choiset A, Girard S, Siffroi JP, McElreavey K, Vibert-Guigue C, Sebaoun M, Joyé N, Portnoï MF, Jaubert F, Fellous M. Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses. Journal of Medical Genetics. 39: 514-8. PMID 12114486 DOI: 10.1136/Jmg.39.7.514 |
0.406 |
|
| 2002 |
McElreavey K, Krausz C, Patrat C, Fellous M. [Male infertility and microdeletions of the Y chromosome]. Gynã©Cologie, Obstã©Trique & Fertilitã©. 30: 405-12. PMID 12087936 DOI: 10.1016/S1297-9589(02)00340-5 |
0.377 |
|
| 2002 |
Naves R, Lennon AM, Barbieri G, Reyes L, Puga G, Salas L, Deffrennes V, Rosemblatt M, Fellous M, Charron D, Alcaïde-Loridan C, Bono MR. MHC class II-deficient tumor cell lines with a defective expression of the class II transactivator. International Immunology. 14: 481-91. PMID 11978778 DOI: 10.1093/Intimm/14.5.481 |
0.335 |
|
| 2002 |
Jamain S, Betancur C, Quach H, Philippe A, Fellous M, Giros B, Gillberg C, Leboyer M, Bourgeron T. Linkage and association of the glutamate receptor 6 gene with autism. Molecular Psychiatry. 7: 302-10. PMID 11920157 DOI: 10.1038/Sj.Mp.4000979 |
0.32 |
|
| 2002 |
Ottolenghi C, Fellous M, Barbieri M, McElreavey K. Novel paralogy relations among human chromosomes support a link between the phylogeny of doublesex-related genes and the evolution of sex determination. Genomics. 79: 333-43. PMID 11863363 DOI: 10.1006/Geno.2002.6711 |
0.405 |
|
| 2002 |
Jamain S, Quach H, Quintana-Murci L, Betancur C, Philippe A, Gillberg C, Sponheim E, Skjeldal OH, Fellous M, Leboyer M, Bourgeron T. Y chromosome haplogroups in autistic subjects. Molecular Psychiatry. 7: 217-9. PMID 11840316 DOI: 10.1038/Sj.Mp.4000968 |
0.355 |
|
| 2002 |
Morel Y, Rey R, Teinturier C, Nicolino M, Michel-Calemard L, Mowszowicz I, Jaubert F, Fellous M, Chaussain JL, Chatelain P, David M, Nihoul-Fékété C, Forest MG, Josso N. Aetiological diagnosis of male sex ambiguity: a collaborative study. European Journal of Pediatrics. 161: 49-59. PMID 11808880 DOI: 10.1007/S00431-001-0854-Z |
0.345 |
|
| 2001 |
Quintana-Murci L, Fellous M. The Human Y Chromosome: The Biological Role of a "Functional Wasteland" Journal of Biomedicine & Biotechnology. 1: 18-24. PMID 12488622 DOI: 10.1155/S1110724301000080 |
0.311 |
|
| 2001 |
Besmond C, Fellous M. The Human Genome Revolution or Evolution? Journal of Biomedicine & Biotechnology. 1: 96. PMID 12488600 DOI: 10.1155/S1110724301000171 |
0.302 |
|
| 2001 |
Pailhoux E, Vigier B, Vaiman D, Schibler L, Vaiman A, Cribiu E, Nezer C, Georges M, Sundström J, Pelliniemi LJ, Fellous M, Cotinot C. Contribution of domestic animals to the identification of new genes involved in sex determination. The Journal of Experimental Zoology. 290: 700-8. PMID 11748618 DOI: 10.1002/Jez.1120 |
0.421 |
|
| 2001 |
Salas-Cortés L, Jaubert F, Bono MR, Fellous M, Rosemblatt M. Expression of the human SRY protein during development in normal male gonadal and sex-reversed tissues. The Journal of Experimental Zoology. 290: 607-15. PMID 11748609 DOI: 10.1002/Jez.1111 |
0.364 |
|
| 2001 |
Pailhoux E, Vigier B, Chaffaux S, Servel N, Taourit S, Furet JP, Fellous M, Grosclaude F, Cribiu EP, Cotinot C, Vaiman D. A 11.7-kb deletion triggers intersexuality and polledness in goats. Nature Genetics. 29: 453-8. PMID 11726932 DOI: 10.1038/Ng769 |
0.427 |
|
| 2001 |
Jamain S, Girondot M, Leroy P, Clergue M, Quach H, Fellous M, Bourgeron T. Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolution. Genomics. 78: 38-45. PMID 11707071 DOI: 10.1006/Geno.2001.6642 |
0.344 |
|
| 2001 |
De Baere E, Dixon MJ, Small KW, Jabs EW, Leroy BP, Devriendt K, Gillerot Y, Mortier G, Meire F, Van Maldergem L, Courtens W, Hjalgrim H, Huang S, Liebaers I, Van Regemorter N, ... ... Fellous M, et al. Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation. Human Molecular Genetics. 10: 1591-600. PMID 11468277 DOI: 10.1093/Hmg/10.15.1591 |
0.344 |
|
| 2001 |
Veitia RA, Salas-Cortés L, Ottolenghi C, Pailhoux E, Cotinot C, Fellous M. Testis determination in mammals: more questions than answers. Molecular and Cellular Endocrinology. 179: 3-16. PMID 11420125 DOI: 10.1016/S0303-7207(01)00460-9 |
0.397 |
|
| 2001 |
Ottolenghi C, Moreira-Filho C, Mendonça BB, Barbieri M, Fellous M, Berkovitz GD, McElreavey K. Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis. The Journal of Clinical Endocrinology and Metabolism. 86: 2465-9. PMID 11397841 DOI: 10.1210/Jcem.86.6.7539 |
0.397 |
|
| 2001 |
Jamain S, Quach H, Fellous M, Bourgeron T. Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia. Genomics. 74: 36-44. PMID 11374900 DOI: 10.1006/Geno.2001.6535 |
0.317 |
|
| 2001 |
Lennon-Duménil AM, Barbouche MR, Vedrenne J, Prod'Homme T, Béjaoui M, Ghariani S, Charron D, Fellous M, Dellagi K, Alcaïde-Loridan C. Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHC class II deficiency. Journal of Immunology (Baltimore, Md. : 1950). 166: 5681-7. PMID 11313409 DOI: 10.4049/Jimmunol.166.9.5681 |
0.362 |
|
| 2001 |
Nunes M, Blanc I, Maes J, Fellous M, Robert B, McElreavey K. NSPc1, a novel mammalian Polycomb gene, is expressed in neural crest-derived structures of the peripheral nervous system. Mechanisms of Development. 102: 219-22. PMID 11287196 DOI: 10.1016/S0925-4773(01)00288-X |
0.329 |
|
| 2001 |
Quintana-Murci L, Jamain S, Fellous M. [Origin and evolution of mammalian sex chromosomes]. Comptes Rendus De L'Acadã©Mie Des Sciences. Sã©Rie Iii, Sciences De La Vie. 324: 1-11. PMID 11212497 DOI: 10.1016/S0764-4469(00)01278-6 |
0.371 |
|
| 2000 |
Salas-Cortés L, Jaubert F, Nihoul-Feketé C, Brauner R, Rosemblatt M, Fellous M. SRY protein is expressed in ovotestis and streak gonads from human sex-reversal. Cytogenetics and Cell Genetics. 91: 212-6. PMID 11173859 DOI: 10.1159/000056847 |
0.379 |
|
| 2000 |
Siffroi JP, Le Bourhis C, Krausz C, Barbaux S, Quintana-Murci L, Kanafani S, Rouba H, Bujan L, Bourrouillou G, Seifer I, Boucher D, Fellous M, McElreavey K, Dadoune JP. Sex chromosome mosaicism in males carrying Y chromosome long arm deletions. Human Reproduction (Oxford, England). 15: 2559-62. PMID 11098026 DOI: 10.1093/Humrep/15.12.2559 |
0.37 |
|
| 2000 |
Denamur E, Bocquet N, Baudouin V, Da Silva F, Veitia R, Peuchmaur M, Elion J, Gubler MC, Fellous M, Niaudet P, Loirat C. WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis. Kidney International. 57: 1868-72. PMID 10792605 DOI: 10.1046/J.1523-1755.2000.00036.X |
0.323 |
|
| 2000 |
Krausz C, Quintana-Murci L, Fellous M, Siffroi JP, McElreavey K. Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism. Molecular Human Reproduction. 6: 298-302. PMID 10729310 DOI: 10.1093/Molehr/6.4.298 |
0.384 |
|
| 2000 |
Ottolenghi C, Veitia R, Barbieri M, Fellous M, McElreavey K. The human doublesex-related gene, DMRT2, is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript. Genomics. 64: 179-86. PMID 10729224 DOI: 10.1006/Geno.2000.6120 |
0.389 |
|
| 2000 |
Ottolenghi C, Veitia R, Quintana-Murci L, Torchard D, Scapoli L, Souleyreau-Therville N, Beckmann J, Fellous M, McElreavey K. The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain. Genomics. 64: 170-8. PMID 10729223 DOI: 10.1006/Geno.2000.6121 |
0.409 |
|
| 2000 |
Saifi GM, Veitia R, Khodjet El Khil H, Barbaux S, Tilak P, Thomas IM, Fellous M. sY116, a human Y-linked polymorphic STS Journal of Genetics. 79: 17-20. DOI: 10.1007/Bf02715871 |
0.348 |
|
| 1999 |
McElreavey K, Fellous M. Sex determination and the Y chromosome. American Journal of Medical Genetics. 89: 176-85. PMID 10727993 DOI: 10.1002/(Sici)1096-8628(19991229)89:4<176::Aid-Ajmg2>3.0.Co;2-B |
0.379 |
|
| 1999 |
Damiani D, Guedes DR, Fellous M, Barbaux S, McElreavey K, Kalil J, Goldberg AC, Moreira-Filho CA, Barbosa A, Della Manna T, Dichtchekenian V, Setian N. Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments. Journal of Pediatric Endocrinology & Metabolism : Jpem. 12: 827-31. PMID 10614539 DOI: 10.1515/Jpem.1999.12.6.827 |
0.367 |
|
| 1999 |
Alcaïde-Loridan C, Lennon AM, Bono MR, Barbouche R, Dellagi K, Fellous M. Differential expression of MHC class II isotype chains. Microbes and Infection / Institut Pasteur. 1: 929-34. PMID 10614011 DOI: 10.1016/S1286-4579(99)00224-5 |
0.347 |
|
| 1999 |
Krausz C, Quintana-Murci L, Barbaux S, Siffroi JP, Rouba H, Delafontaine D, Souleyreau-Therville N, Arvis G, Antoine JM, Erdei E, Taar JP, Tar A, Jeandidier E, Plessis G, Bourgeron T, ... ... Fellous M, et al. A high frequency of Y chromosome deletions in males with nonidiopathic infertility. The Journal of Clinical Endocrinology and Metabolism. 84: 3606-12. PMID 10523003 DOI: 10.1097/00006254-200003000-00020 |
0.377 |
|
| 1999 |
Barbosa AS, Hadjiathanasiou CG, Theodoridis C, Papathanasiou A, Tar A, Merksz M, Györvári B, Sultan C, Dumas R, Jaubert F, Niaudet P, Moreira-Filho CA, Cotinot C, Fellous M. The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor. Human Mutation. 13: 146-53. PMID 10094551 DOI: 10.1002/(Sici)1098-1004(1999)13:2<146::Aid-Humu7>3.0.Co;2-I |
0.331 |
|
| 1999 |
Vaiman D, Schibler L, Oustry-Vaiman A, Pailhoux E, Goldammer T, Stevanovic M, Furet JP, Schwerin M, Cotinot C, Fellous M, Cribiu EP. High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): the human homologue is contained in a human YAC from HSA3q23. Genomics. 56: 31-9. PMID 10036183 DOI: 10.1006/Geno.1998.5691 |
0.329 |
|
| 1998 |
Veitia R, Laurent A, Quintana-Murci L, Ottolenghi C, Fellous M, Vidaud M, McElreavey K. The INSL4 gene maps close to WI-5527 at 9p24.1-->p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome. Cytogenetics and Cell Genetics. 81: 275-7. PMID 9730618 DOI: 10.1159/000015045 |
0.317 |
|
| 1998 |
Lennon AM, Ottone C, Rosemblatt M, Fellous M, Bono MR, Alcaïde-Loridan C. CIITA B-cell-specific promoter suppression in MHC class II-silenced cell hybrids. Immunogenetics. 48: 283-91. PMID 9716648 DOI: 10.1007/S002510050433 |
0.353 |
|
| 1998 |
Ion R, Telvi L, Chaussain JL, Barbet JP, Nunes M, Safar A, Réthoré MO, Fellous M, McElreavey K. Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene. Human Genetics. 102: 151-6. PMID 9521582 DOI: 10.1007/S004390050669 |
0.382 |
|
| 1997 |
McElreavey K, Fellous M. Sex-determining genes. Trends in Endocrinology and Metabolism: Tem. 8: 342-6. PMID 18406823 DOI: 10.1016/S1043-2760(97)00135-5 |
0.381 |
|
| 1997 |
Bourgeron T, Barbaux S, McElreavey K, Fellous M. [Y chromosome and spermatogenesis]. Contraception, Fertilitã©, Sexualitã© (1992). 25: 620-5. PMID 9410377 |
0.3 |
|
| 1997 |
Barbaux S, Niaudet P, Gubler MC, Grünfeld JP, Jaubert F, Kuttenn F, Fékété CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K. Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Nature Genetics. 17: 467-70. PMID 9398852 DOI: 10.1038/Ng1297-467 |
0.351 |
|
| 1997 |
Veitia RA, Fellous M, McElreavey K. Conservation of Y chromosome-specific sequences immediately 5' to the testis determining gene in primates. Gene. 199: 63-70. PMID 9358040 DOI: 10.1016/S0378-1119(97)00347-8 |
0.41 |
|
| 1997 |
Veitia R, Nunes M, McElreavey K, Fellous M. [Sex determination and differentiation in man: from pathology to genes]. Archives De Pã©Diatrie : Organe Officiel De La Sociã©Te Franã§Aise De Pã©Diatrie. 4: 118s-120s. PMID 9246317 DOI: 10.1016/S0929-693X(97)86476-7 |
0.311 |
|
| 1997 |
Veitia R, Ion A, Barbaux S, Jobling MA, Souleyreau N, Ennis K, Ostrer H, Tosi M, Meo T, Chibani J, Fellous M, McElreavey K. Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype. Human Genetics. 99: 648-52. PMID 9150734 DOI: 10.1007/S004390050422 |
0.397 |
|
| 1997 |
Veitia R, Nunes M, Brauner R, Doco-Fenzy M, Joanny-Flinois O, Jaubert F, Lortat-Jacob S, Fellous M, McElreavey K. Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1. Genomics. 41: 271-4. PMID 9143505 DOI: 10.1006/Geno.1997.4648 |
0.358 |
|
| 1997 |
Seboun E, Barbaux S, Bourgeron T, Nishi S, Agulnik A, Egashira M, Nikkawa N, Bishop C, Fellous M, McElreavey K, Kasahara M, Algonik A. Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene. Genomics. 41: 227-35. PMID 9143498 DOI: 10.1006/Geno.1997.4635 |
0.415 |
|
| 1997 |
Damiani D, Fellous M, McElreavey K, Barbaux S, Barreto ES, Dichtchekenian V, Setian N. True hermaphroditism: clinical aspects and molecular studies in 16 cases. European Journal of Endocrinology / European Federation of Endocrine Societies. 136: 201-4. PMID 9116916 DOI: 10.1530/Eje.0.1360201 |
0.334 |
|
| 1997 |
Tar A, Ion A, Sólyom J, Györvári B, Stephenson C, Barbaux S, Nunes M, Fellous M, McElreavey K. Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13. American Journal of Medical Genetics. 68: 231-5. PMID 9028465 DOI: 10.1002/(Sici)1096-8628(19970120)68:2<231::Aid-Ajmg22>3.0.Co;2-U |
0.373 |
|
| 1997 |
Lennon AM, Ottone C, Rigaud G, Deaven LL, Longmire J, Fellous M, Bono R, Alcaïde-Loridan C. Isolation of a B-cell-specific promoter for the human class II transactivator. Immunogenetics. 45: 266-73. PMID 9002447 DOI: 10.1007/S002510050202 |
0.356 |
|
| 1997 |
Vaiman D, Pailhoux E, Schibler L, Oustry A, Chaffaux S, Cotinot C, Fellous M, Cribiu EP. Genetic mapping of the polled/intersex locus (PIS) in goats Theriogenology. 47: 103-109. DOI: 10.1016/S0093-691X(96)00344-5 |
0.439 |
|
| 1997 |
Veitia R, Nunes M, McElreavey K, Fellous M. Genetic basis of human sex determination: An overview Theriogenology. 47: 83-91. DOI: 10.1016/S0093-691X(96)00342-1 |
0.424 |
|
| 1996 |
Telvi L, Ion A, Carel JC, Desguerre I, Piraud M, Boutin AM, Feingold J, Ponsot G, Fellous M, McElreavey K. A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalities. Journal of Medical Genetics. 33: 767-71. PMID 8880579 DOI: 10.1136/Jmg.33.9.767 |
0.355 |
|
| 1996 |
Vaiman D, Koutita O, Oustry A, Elsen JM, Manfredi E, Fellous M, Cribiu EP. Genetic mapping of the autosomal region involved in XX sex-reversal and horn development in goats. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 133-7. PMID 8835530 DOI: 10.1007/S003359900033 |
0.379 |
|
| 1996 |
McElreavey K, Vilain E, Barbaux S, Fuqua JS, Fechner PY, Souleyreau N, Doco-Fenzy M, Gabriel R, Quereux C, Fellous M, Berkovitz GD. Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination. Proceedings of the National Academy of Sciences of the United States of America. 93: 8590-4. PMID 8710915 DOI: 10.1073/Pnas.93.16.8590 |
0.608 |
|
| 1996 |
Lennon A, Ottone C, Peijnenburg A, Hamon-Benais C, Colland F, Gobin S, van den Elsen P, Fellous M, Bono R, Alcaïde-Loridan C. The RAG cell line defines a new complementation group of MHC class II deficiency. Immunogenetics. 43: 352-9. PMID 8606055 DOI: 10.1007/Bf02199803 |
0.358 |
|
| 1995 |
McElreavey K, Barbaux S, Ion A, Fellous M. The genetic basis of murine and human sex determination: a review. Heredity. 75: 599-611. PMID 8575930 DOI: 10.1038/Hdy.1995.179 |
0.428 |
|
| 1995 |
Barbaux S, Vilain E, Raoul O, Gilgenkrantz S, Jeandidier E, Chadenas D, Souleyreau N, Fellous M, McElreavey K. Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata. Human Molecular Genetics. 4: 1565-8. PMID 8541840 DOI: 10.1093/Hmg/4.9.1565 |
0.592 |
|
| 1995 |
Tar A, Sólyom J, Györvári B, Ion A, Telvi L, Barbaux S, Souleyreau N, Vilain E, Fellous M, McElreavey K. Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion. Human Genetics. 96: 464-8. PMID 7557971 DOI: 10.1007/Bf00191807 |
0.591 |
|
| 1995 |
Gobin SJ, Alcaïde-Loridan C, Bono MR, Ottone C, Chumakov I, Rothstein R, Fellous M. Transfer of yeast artificial chromosomes into mammalian cells and comparative study of their integrity. Gene. 163: 27-33. PMID 7557474 DOI: 10.1016/0378-1119(95)00399-Q |
0.334 |
|
| 1994 |
Pailhoux E, Cribiu EP, Chaffaux S, Darre R, Fellous M, Cotinot C. Molecular analysis of 60,XX pseudohermaphrodite polled goats for the presence of SRY and ZFY genes. Journal of Reproduction and Fertility. 100: 491-6. PMID 8021868 DOI: 10.1530/Jrf.0.1000491 |
0.425 |
|
| 1994 |
Mendonça BB, Barbosa AS, Arnhold IJ, McElreavey K, Fellous M, Moreira-Filho CA. Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene. American Journal of Medical Genetics. 52: 39-43. PMID 7977459 DOI: 10.1002/Ajmg.1320520108 |
0.418 |
|
| 1994 |
Vilain E, Fiblec BL, Morichon-Delvallez N, Brauner R, Dommergues M, Dumez Y, Jaubert F, Boucekkine C, McElreavey K, Vekemans M, Fellous M. SRY-negative XX fetus with complete male phenotype The Lancet. 343: 240-241. PMID 7904700 DOI: 10.1016/S0140-6736(94)91029-4 |
0.544 |
|
| 1994 |
Pierga JY, Giacchetti S, Vilain E, Extra JM, Brice P, Espie M, Maragi JA, Fellous M, Marty M. Dysgerminoma in a pure 45,X Turner syndrome: report of a case and review of the literature. Gynecologic Oncology. 55: 459-64. PMID 7835789 DOI: 10.1006/Gyno.1994.1323 |
0.54 |
|
| 1994 |
Pailhoux E, Popescu PC, Parma P, Boscher J, Legault C, Molteni L, Fellous M, Cotinot C. Genetic analysis of 38XX males with genital ambiguities and true hermaphrodites in pigs. Animal Genetics. 25: 299-305. PMID 7818163 DOI: 10.1111/J.1365-2052.1994.Tb00362.X |
0.364 |
|
| 1993 |
McElreavey K, Vilain E, Abbas N, Herskowitz I, Fellous M. A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development. Proceedings of the National Academy of Sciences of the United States of America. 90: 3368-72. PMID 8475082 DOI: 10.1073/Pnas.90.8.3368 |
0.592 |
|
| 1993 |
Vilain E, Jaubert F, Fellous M, McElreavey K. Pathology of 46,XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor. Differentiation; Research in Biological Diversity. 52: 151-9. PMID 8472885 DOI: 10.1111/J.1432-0436.1993.Tb00625.X |
0.573 |
|
| 1993 |
Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R, Nihoul-Fekete C, Rappaport R, Fellous M. Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome. Comptes Rendus De L'Acadã©Mie Des Sciences. Sã©Rie Iii, Sciences De La Vie. 316: 375-83. PMID 8402263 |
0.551 |
|
| 1993 |
Toublanc JE, Boucekkine C, Abbas N, Barama D, Vilain E, McElreavey K, Toublanc M, Fellous M. Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation. European Journal of Pediatrics. 152: S70-5. PMID 8339747 DOI: 10.1007/Bf02125443 |
0.56 |
|
| 1993 |
McElreavey K, Vilain E, Cotinot C, Payen E, Fellous M. Control of sex determination in animals. European Journal of Biochemistry / Febs. 218: 769-83. PMID 8281929 DOI: 10.1111/j.1432-1033.1993.tb18432.x |
0.45 |
|
| 1993 |
Santachiara Benerecetti AS, Semino O, Passarino G, Torroni A, Brdicka R, Fellous M, Modiano G. The common, Near-Eastern origin of Ashkenazi and Sephardi Jews supported by Y-chromosome similarity. Annals of Human Genetics. 57: 55-64. PMID 8101437 DOI: 10.1111/J.1469-1809.1993.Tb00886.X |
0.351 |
|
| 1993 |
Lobaccaro JM, Leheup B, Boucekkine N, Lumbroso S, Toublanc JE, Fellous M, Sultan C. XX MALES AND AMBIGUOUS GENITALIA: A LINK BETWEEN SRY AND ANDROGEN RECEPTOR (AR) GENE? Pediatric Research. 33: S23-S23. DOI: 10.1203/00006450-199305001-00117 |
0.347 |
|
| 1992 |
McElreavey KD, Vilain E, Boucekkine C, Vidaud M, Jaubert F, Richaud F, Fellous M. XY sex reversal associated with a nonsense mutation in SRY. Genomics. 13: 838-40. PMID 1639410 DOI: 10.1016/0888-7543(92)90164-N |
0.588 |
|
| 1992 |
Vilain E, McElreavey K, Jaubert F, Raymond JP, Richaud F, Fellous M. Familial case with sequence variant in the testis-determining region associated with two sex phenotypes. American Journal of Human Genetics. 50: 1008-11. PMID 1570829 |
0.553 |
|
| 1992 |
Vilain E, McElreavey K, Richaud F, Fellous M. [Isolation of the sex-determining gene in men]. Pathologie-Biologie. 40: 15-7. PMID 1570176 |
0.479 |
|
| 1992 |
Vilain E, Elreavey KM, Richaud F, Fellous M. [Sex genetics]. Presse Mã©Dicale (Paris, France : 1983). 21: 852-6. PMID 1535151 |
0.556 |
|
| 1992 |
McElreavey K, Rappaport R, Vilain E, Abbas N, Richaud F, Lortat-Jacob S, Berger R, LeConiat M, Boucekkine C, Kucheria K, Temtamy S, Nihoul-Fekete C, Brauner R, Fellous M. A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY Human Genetics. 90: 121-125. PMID 1427767 DOI: 10.1007/Bf00210754 |
0.589 |
|
| 1992 |
Velazquez L, Fellous M, Stark GR, Pellegrini S. A protein tyrosine kinase in the interferon alpha/beta signaling pathway. Cell. 70: 313-22. PMID 1386289 DOI: 10.1016/0092-8674(92)90105-L |
0.333 |
|
| 1992 |
Boucekkine C, Toublanc JE, Abbas N, Semrouni M, Vilain E, McElreavey K, Mugneret F, Fellous M. The sole presence of the testis-determining region of the Y chromosome (SRY) in 46,XX patients is associated with phenotypic variability. Hormone Research. 37: 236-40. PMID 1292977 DOI: 10.1159/000182319 |
0.584 |
|
| 1992 |
Amit T, Ish-Shalom S, Glaser B, Youdim MBH, Hochberg Z, Giustina A, Bussi AR, Licini M, Pizzocolo G, Schettino M, Wehrenberg WB, Menis ED, Rin GD, Roiter I, Legovini P, ... ... Fellous M, et al. Subject Index, Vol. 37, 1992 Hormone Research in Paediatrics. 37: 247-248. DOI: 10.1159/000182322 |
0.466 |
|
| 1992 |
Amit T, Ish-Shalom S, Glaser B, Youdim MBH, Hochberg Z, Giustina A, Bussi AR, Licini M, Pizzocolo G, Schettino M, Wehrenberg WB, Menis ED, Rin GD, Roiter I, Legovini P, ... ... Fellous M, et al. Contents, Vol. 37, 1992 Hormone Research in Paediatrics. 37. DOI: 10.1159/000182312 |
0.454 |
|
| 1991 |
Bono MR, Alcaïde-Loridan C, Couillin P, Letouzé B, Grisard MC, Jouin H, Fellous M. Human chromosome 16 encodes a factor involved in induction of class II major histocompatibility antigens by interferon gamma. Proceedings of the National Academy of Sciences of the United States of America. 88: 6077-81. PMID 1906174 DOI: 10.1073/Pnas.88.14.6077 |
0.375 |
|
| 1991 |
Kasahara M, Seboun E, Fellous M, Nadeau JH. Genetic mapping of a male germ cell-expressed gene Tpx-2 to mouse chromosome 17. Immunogenetics. 34: 132-5. PMID 1869307 DOI: 10.1007/Bf00211426 |
0.377 |
|
| 1991 |
Vilain E, McElreavey K, Vidaud M, Richaud F, Fellous M. [The analysis of SRY doesn't explain all the pathology of sex determination]. Annales D'Endocrinologie. 52: 435-6. PMID 1824496 |
0.457 |
|
| 1991 |
Bono MR, Alcaïde-Loridan C, Letouzé B, Jouin H, Gobin SJ, Fellous M. The recombinant human interferon-gamma receptor is fully functional in a human x murine hybrid containing human chromosome 21. Research in Immunology. 142: 765-72. PMID 1665572 DOI: 10.1016/0923-2494(91)90122-Y |
0.385 |
|
| 1990 |
Damiani D, Billerbeck AE, Goldberg AC, Setian N, Fellous M, Kalil J. Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome. Human Genetics. 85: 85-8. PMID 2358305 DOI: 10.1007/Bf00276329 |
0.39 |
|
| 1990 |
Abbas NE, Toublanc JE, Boucekkine C, Toublanc M, Affara NA, Job JC, Fellous M. A possible common origin of "Y-negative" human XX males and XX true hermaphrodites. Human Genetics. 84: 356-60. PMID 2307458 DOI: 10.1007/Bf00196234 |
0.32 |
|
| 1990 |
Torroni A, Semino O, Scozzari R, Sirugo G, Spedini G, Abbas N, Fellous M, Santachiara Benerecetti AS. Y chromosome DNA polymorphisms in human populations: differences between Caucasoids and Africans detected by 49a and 49f probes. Annals of Human Genetics. 54: 287-96. PMID 2285217 DOI: 10.1111/J.1469-1809.1990.Tb00384.X |
0.309 |
|
| 1990 |
Abbas N, Novelli G, Stella NC, Triolo O, Corrado F, Fellous M, Chery M, Gilgenkrantz S, Dallapiccola B. A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1. Human Genetics. 86: 94-8. PMID 2253943 DOI: 10.1007/Bf00205184 |
0.345 |
|
| 1990 |
Berta P, Hawkins JR, Sinclair AH, Taylor A, Griffiths BL, Goodfellow PN, Fellous M. Genetic evidence equating SRY and the testis-determining factor. Nature. 348: 448-50. PMID 2247149 DOI: 10.1038/348448A0 |
0.42 |
|
| 1989 |
Palmer MS, Sinclair AH, Berta P, Ellis NA, Goodfellow PN, Abbas NE, Fellous M. Genetic evidence that ZFY is not the testis-determining factor. Nature. 342: 937-9. PMID 2594087 DOI: 10.1038/342937A0 |
0.426 |
|
| 1989 |
Bono MR, Benech P, Couillin P, Alcaide-Loridan C, Grisard MC, Jouin H, Fischer DG, Fellous M. Characterization of human IFN-gamma response using somatic cell hybrids of hematopoietic and nonhematopoietic origin. Somatic Cell and Molecular Genetics. 15: 513-23. PMID 2556800 DOI: 10.1007/Bf01534912 |
0.36 |
|
| 1988 |
Rosa FM, Fellous M. Regulation of HLA-DR gene by IFN-gamma. Transcriptional and post-transcriptional control. Journal of Immunology (Baltimore, Md. : 1950). 140: 1660-4. PMID 3126233 |
0.498 |
|
| 1987 |
Magenis RE, Casanova M, Fellous M, Olson S, Sheehy R. Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe. Human Genetics. 75: 228-33. PMID 3557449 DOI: 10.1007/Bf00281064 |
0.363 |
|
| 1987 |
Leonard M, Kirszenbaum M, Cotinot C, Chesné P, Heyman Y, Stinnakre MG, Bishop C, Delouis C, Vaiman M, Fellous M. Sexing bovine embryos using Y chromosome specific DNA probe Theriogenology. 27: 248. DOI: 10.1016/0093-691X(87)90125-7 |
0.325 |
|
| 1986 |
Gilgenkrantz S, Droulle P, Seboun E, Casanova M, Schweitzer M, Goosens M, Fellous M. Prenatal identification of a Y-chromosome deletion by Y-specific single copy DNA probes. Prenatal Diagnosis. 6: 307-11. PMID 3748996 DOI: 10.1002/Pd.1970060412 |
0.354 |
|
| 1986 |
Israel A, Kimura A, Fournier A, Fellous M, Kourilsky P. Interferon response sequence potentiates activity of an enhancer in the promoter region of a mouse H-2 gene. Nature. 322: 743-6. PMID 3748155 DOI: 10.1038/322743A0 |
0.324 |
|
| 1986 |
Seboun E, Leroy P, Casanova M, Magenis E, Boucekkine C, Disteche C, Bishop C, Fellous M. A molecular approach to the study of the human Y chromosome and anomalies of sex determination in man. Cold Spring Harbor Symposia On Quantitative Biology. 51: 237-48. PMID 3472720 DOI: 10.1101/Sqb.1986.051.01.029 |
0.345 |
|
| 1986 |
Disteche CM, Casanova M, Saal H, Friedman C, Sybert V, Graham J, Thuline H, Page DC, Fellous M. Small deletions of the short arm of the Y chromosome in 46,XY females. Proceedings of the National Academy of Sciences of the United States of America. 83: 7841-4. PMID 3464001 DOI: 10.1073/Pnas.83.20.7841 |
0.379 |
|
| 1986 |
Billard C, Ferbus D, Kolb JP, Rosa F, Perrot JY, Merlin G, Janiaud P, Raynaud N, Thang MN, Fellous M. Qualitative differences in effects of recombinant alpha-, beta- and gamma-interferons on human peripheral blood leukocytes in vitro. Annales De L'Institut Pasteur. Immunologie. 137: 259-72. PMID 3090926 DOI: 10.1016/S0771-050X(86)80045-6 |
0.522 |
|
| 1986 |
Rosa FM, Cochet MM, Fellous M. Interferon and major histocompatibility complex genes: a model to analyse eukaryotic gene regulation? Interferon. 7: 47-87. PMID 2434435 |
0.461 |
|
| 1986 |
Seboun E, Toublanc JE, Leroy P, Casanova M, Fellous M, Job JC, Canlorbe P. DNA ANALYSIS OF XX MALES WITH GENITAL ABNORMALITIES COMPARED TO "CLASSICAL" XX MALES Pediatric Research. 20: 1183-1183. DOI: 10.1203/00006450-198611000-00059 |
0.321 |
|
| 1986 |
Richard-Mercier N, Bettane-Casanova M, Fellous M, Charniaux-Cotton H. Possible relationship between H-Y antigen and female gonadogenesis in the Colorado potato beetle, Leptinotarsa decemlineata (Coleoptera: Chrysomelidae) International Journal of Invertebrate Reproduction and Development. 10: 243-252. DOI: 10.1080/01688170.1986.10510248 |
0.323 |
|
| 1985 |
Rosa F, Hatat D, Abadie A, Fellous M. Regulation of histocompatibility antigens by interferon. Annales De L'Institut Pasteur. Immunologie. 136: 103-19. PMID 3922280 DOI: 10.1016/S0769-2625(85)80043-X |
0.517 |
|
| 1985 |
Boucekkine C, Nafa D, Casanova-Bettane M, Latron F, Fellous M, Benmiloud M. Evidence of a preferential inactivation of the paternally derived X chromosome in a 46,XX true hermaphrodite. Human Genetics. 69: 91-3. PMID 3855406 DOI: 10.1007/Bf00295538 |
0.313 |
|
| 1985 |
Casanova M, Leroy P, Boucekkine C, Weissenbach J, Bishop C, Fellous M, Purrello M, Fiori G, Siniscalco M. A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distance. Science (New York, N.Y.). 230: 1403-6. PMID 2999986 DOI: 10.1126/Science.2999986 |
0.354 |
|
| 1985 |
Sutherland J, Mannoni P, Rosa F, Huyat D, Turner AR, Fellous M. Induction of the expression of HLA class I antigens on K562 by interferons and sodium butyrate. Human Immunology. 12: 65-73. PMID 2578442 DOI: 10.1016/0198-8859(85)90344-1 |
0.506 |
|
| 1985 |
Fellous M, Cartron JP, Wiels J, Tursz T. A monoclonal antibody against a Burkitt lymphoma associated antigen has an anti-Pk red blood cell specificity. British Journal of Haematology. 60: 559-65. PMID 2410009 DOI: 10.1111/J.1365-2141.1985.Tb07454.X |
0.304 |
|
| 1984 |
Rosa F, Fellous M. The effect of gamma-interferon on MHC antigens. Immunology Today. 5: 261-2. PMID 25290324 DOI: 10.1016/0167-5699(84)90135-X |
0.451 |
|
| 1984 |
Bishop C, Guellaen G, Geldwerth D, Fellous M, Weissenbach J. Extensive sequence homologies between Y and other human chromosomes. Journal of Molecular Biology. 173: 403-17. PMID 6708105 DOI: 10.1016/0022-2836(84)90388-7 |
0.363 |
|
| 1984 |
Guellaen G, Casanova M, Bishop C, Geldwerth D, Andre G, Fellous M, Weissenbach J. Human XX males with Y single-copy DNA fragments. Nature. 307: 172-3. PMID 6537828 DOI: 10.1038/307172A0 |
0.406 |
|
| 1984 |
Layet C, Le Bouteiller PP, N'guyen C, Mercier P, Rosa F, Fellous M, Caillol DH, Jordan BR, Lemonnier FA. Transformation of LMTK- cells with purified HLA class I gene. VI. Serological characterization of HLA-B7 and AW24 molecules. Human Immunology. 11: 31-45. PMID 6207154 DOI: 10.1016/0198-8859(84)90054-5 |
0.545 |
|
| 1984 |
Toublanc JE, Naud C, Fellous M, Bishop C, Casanova M, Job JC, Canlorbe P. Hormonal and DNA studies in XX males Pediatric Research. 18: 1224-1224. DOI: 10.1203/00006450-198411000-00142 |
0.336 |
|
| 1983 |
Rosa F, Berissi H, Weissenbach J, Maroteaux L, Fellous M, Revel M. The beta2-microglobulin mRNA in human Daudi cells has a mutated initiation codon but is still inducible by interferon. The Embo Journal. 2: 239-43. PMID 11894933 DOI: 10.1002/J.1460-2075.1983.Tb01412.X |
0.554 |
|
| 1983 |
Rosa F, Hatat D, Abadie A, Wallach D, Revel M, Fellous M. Differential regulation of HLA-DR mRNAs and cell surface antigens by interferon. The Embo Journal. 2: 1585-9. PMID 11892816 DOI: 10.1002/J.1460-2075.1983.Tb01628.X |
0.547 |
|
| 1983 |
Bishop CE, Guellaen G, Geldwerth D, Voss R, Fellous M, Weissenbach J. Single-copy DNA sequences specific for the human Y chromosome. Nature. 303: 831-2. PMID 6866083 DOI: 10.1038/303831A0 |
0.373 |
|
| 1983 |
Nudelman E, Kannagi R, Hakomori S, Parsons M, Lipinski M, Wiels J, Fellous M, Tursz T. A glycolipid antigen associated with Burkitt lymphoma defined by a monoclonal antibody. Science (New York, N.Y.). 220: 509-11. PMID 6836295 DOI: 10.1126/Science.6836295 |
0.308 |
|
| 1983 |
Bernheim A, Metezeau P, Guellaën G, Fellous M, Goldberg ME, Berger R. Direct hybridization of sorted human chromosomes: localization of the Y chromosome on the flow karyotype. Proceedings of the National Academy of Sciences of the United States of America. 80: 7571-5. PMID 6584872 DOI: 10.1073/Pnas.80.24.7571 |
0.345 |
|
| 1983 |
Rosa F, Le Bouteiller PP, Abadie A, Mishal Z, Lemonnier FA, Bourrel D, Lamotte M, Kalil J, Jordan B, Fellous M. HLA class I genes integrated into murine cells are inducible by interferon. European Journal of Immunology. 13: 495-9. PMID 6190661 DOI: 10.1002/Eji.1830130612 |
0.562 |
|
| 1983 |
Crevat D, Kalil J, Rosa F, Fellous M. [Presence of 2 different epitopes on the human beta 2-microglobulin defined by monoclonal antibodies]. Annales D'Immunologie. 134: 31-41. PMID 6190430 |
0.467 |
|
| 1983 |
Rosa F, Fellous M, Dron M, Tovey M, Revel M. Presence of an abnormal beta 2-microglobulin mRNA in Daudi cells: induction by interferon. Immunogenetics. 17: 125-31. PMID 6186603 DOI: 10.1007/Bf00364752 |
0.54 |
|
| 1983 |
Rosa F, Hatat D, Abadie A, Wallach D, Revel M, Fellous M. Differential regulation of HLA-DR mRNAs and cell surface antigens by interferon. The Embo Journal. 2: 1585-1589. DOI: 10.1002/j.1460-2075.1983.tb01628.x |
0.478 |
|
| 1982 |
Benhaim A, Gangnerau MN, Bettane-Casanova M, Fellous M, Picon R. Effects of H--Y antigen on morphologic and endocrine differentiation of gonads in mammals. Differentiation; Research in Biological Diversity. 22: 53-8. PMID 7201940 DOI: 10.1111/J.1432-0436.1982.Tb01223.X |
0.301 |
|
| 1982 |
Colombani J, Dausset J, Lepage V, Degos L, Kalil J, Fellous M. HLA monoclonal antibody registry: a proposal. Tissue Antigens. 20: 161-71. PMID 6982543 DOI: 10.1111/J.1399-0039.1982.Tb00342.X |
0.465 |
|
| 1982 |
Wallach D, Fellous M, Revel M. Preferential effect of gamma interferon on the synthesis of HLA antigens and their mRNAs in human cells. Nature. 299: 833-6. PMID 6290893 DOI: 10.1038/299833A0 |
0.305 |
|
| 1982 |
Kalil J, Fellous M, Tanigaki N, Rosa F, Pagniez C, Herzog C, Dastot H, Lenoir G. A new Epstein-Barr virus negative Burkitt's lymphoma derived cell-line. I. Analysis of cell surface markers and abnormal expression of HLA antigens. Tissue Antigens. 20: 47-62. PMID 6289490 DOI: 10.1111/J.1399-0039.1982.Tb00328.X |
0.551 |
|
| 1982 |
Wiels J, Lenoir GM, Fellous M, Lipinski M, Salomon JC, Tetaud C, Tursz T. A monoclonal antibody with anti-Burkitt lymphoma specificity. I. Analysis of human haematopoietic and lymphoid cell lines. International Journal of Cancer. Journal International Du Cancer. 29: 653-8. PMID 6286514 DOI: 10.1002/Ijc.2910290609 |
0.312 |
|
| 1982 |
Fellous M, Boué J, Malbrunot C, Wollman E, Sasportes M, Van Cong N, Marcelli A, Rebourcet R, Hubert C, Demenais F, Elston RC, Namboodiri KK, Kaplan EB, Fellous M. A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus. American Journal of Medical Genetics. 12: 465-87. PMID 6214946 DOI: 10.1002/Ajmg.1320120410 |
0.32 |
|
| 1982 |
Rosa F, Fellous M. [Effect of interferon on human cell lines which do not express class I transplantation antigens: K 562 and Daudi. Presence of a pseudo-messenger RNA of beta 2-microglobulin in Daudi cell line]. Comptes Rendus Des Sã©Ances De L'Acadã©Mie Des Sciences. Sã©Rie Iii, Sciences De La Vie. 295: 359-64. PMID 6185189 |
0.484 |
|
| 1982 |
Fellous M, Nir U, Wallach D, Merlin G, Rubinstein M, Revel M. Interferon-dependent induction of mRNA for the major histocompatibility antigens in human fibroblasts and lymphoblastoid cells. Proceedings of the National Academy of Sciences of the United States of America. 79: 3082-6. PMID 6179076 DOI: 10.1073/Pnas.79.10.3082 |
0.346 |
|
| 1981 |
Wiels J, Fellous M, Tursz T. Monoclonal antibody against a Burkitt lymphoma-associated antigen. Proceedings of the National Academy of Sciences of the United States of America. 78: 6485-8. PMID 7031655 DOI: 10.1073/Pnas.78.10.6485 |
0.303 |
|
| 1981 |
Avner P, Bono R, Berger R, Fellous M. Characterization of human teratoma cell lines for their in vitro developmental properties and expression of embryonic and major histocompatibility locus-associated antigens. Journal of Immunogenetics. 8: 151-62. PMID 7014724 DOI: 10.1111/J.1744-313X.1981.Tb00752.X |
0.35 |
|
| 1981 |
Bono R, Cartron JP, Mulet C, Avner P, Fellous M. Selective expression of blood group antigens on human teratocarcinoma cell lines. Revue Franã§Aise De Transfusion Et Immuno-Hã©Matologie. 24: 97-107. PMID 7013006 DOI: 10.1016/S0338-4535(81)80030-X |
0.316 |
|
| 1980 |
Fradelizi D, Gluckman E, Wiels J, Sasportes M, Fellous M, Lepage V, Faille A, Valensi F, Dausset J. Functional study and detection of HLA-D products on fractionated human bone marrow cells. Tissue Antigens. 15: 161-72. PMID 12735316 DOI: 10.1111/J.1399-0039.1980.Tb00900.X |
0.48 |
|
| 1980 |
Zeuthen J, Nørgaard JO, Avner P, Fellous M, Wartiovaara J, Vaheri A, Rosén A, Giovanella BC. Characterization of a human ovarian teratocarcinoma-derived cell line. International Journal of Cancer. Journal International Du Cancer. 25: 19-32. PMID 6931103 DOI: 10.1002/Ijc.2910250104 |
0.319 |
|
| 1979 |
Muramatsu T, Avner P, Fellous M, Gachelin G, Jacob F. Distinctive properties of fucosyl glycopeptides on human teratoma cells. Somatic Cell Genetics. 5: 753-61. PMID 545723 DOI: 10.1007/Bf01542639 |
0.306 |
|
| 1979 |
Rousset JP, Dubois P, Lasserre C, Avilès D, Fellous M, Jami J. Phenotype and surface antigens of mouse teratocarcinoma x fibroblast cell hybrids. Somatic Cell Genetics. 5: 739-52. PMID 545722 DOI: 10.1007/Bf01542638 |
0.302 |
|
| 1979 |
Fellous M, Hors J, Boué J, Dausset J, Jacob F. Are there human analogs of the mouse T locus in central nervous system malformations? Birth Defects Original Article Series. 15: 93-104. PMID 380682 |
0.411 |
|
| 1979 |
Berger R, Bernheim A, Fellous M, Brouet JC. Cytogenetic study of a European Burkitt's lymphoma cell line. Journal of the National Cancer Institute. 62: 1187-92. PMID 286095 DOI: 10.1093/Jnci/62.5.1187 |
0.327 |
|
| 1979 |
Lipinski M, Fridman WH, Tursz T, Vincent C, Pious D, Fellous M. Absence of allogeneic restriction in human T-cell-mediated cytotoxicity to Epstein-Barr virus-infected target cells. Demonstration of an HLA-linked control at the effector level. The Journal of Experimental Medicine. 150: 1310-22. PMID 229186 DOI: 10.1084/Jem.150.6.1310 |
0.318 |
|
| 1979 |
Fellous M, Kamoun M, Gresser I, Bono R. Enhanced expression of HLA antigens and beta 2-microglobulin on interferon-treated human lymphoid cells. European Journal of Immunology. 9: 446-9. PMID 91516 DOI: 10.1002/Eji.1830090606 |
0.335 |
|
| 1979 |
Berger R, Bernheim A, Sasportes M, Hauptmann G, Hors J, Legrand L, Fellous M. Regional mapping of the HLA on the short arm of chromosome 6. Clinical Genetics. 15: 245-51. PMID 84721 DOI: 10.1111/J.1399-0004.1979.Tb00975.X |
0.32 |
|
| 1978 |
Vaiman M, Fellous M, Wiels J, Renard C, Lecointre J, du Mesnil du Buisson F, Dausset J. Presence of SLA and Ia-like antigen on boar spermatozoa. Journal of Immunogenetics. 5: 135-42. PMID 307032 DOI: 10.1111/J.1744-313X.1978.Tb00638.X |
0.479 |
|
| 1978 |
Fellous M, Günther E, Kemler R, Wiels J, Berger R, Guenet JL, Jakob H, Jacob F. Association of the H-Y male antigen with beta2-microglobulin on human lymphoid and differentiated mouse teratocarcinoma cell lines. The Journal of Experimental Medicine. 148: 58-70. PMID 78963 DOI: 10.1084/Jem.148.1.58 |
0.347 |
|
| 1977 |
Hogan B, Fellous M, Avner P, Jacob F. Isolation of a human teratoma cell line which expresses F9 antigen. Nature. 270: 515-8. PMID 593370 DOI: 10.1038/270515A0 |
0.326 |
|
| 1977 |
Kamoun M, Fellous M, Lepage V, Dausset J. The study of human Aa-like specificities using antibody eluates from human lymphoblastoid cell lines. Scandinavian Journal of Immunology. 6: 409-12. PMID 70057 DOI: 10.1111/J.1365-3083.1977.Tb02096.X |
0.508 |
|
| 1977 |
Fellous M, Hors MC, Rebourcet R, Finaz C, Weil D, Heuertz S, Wiels J, Mahouy G, Fridman WH. The expression and relation of HLA, beta2-microglobulin and receptor for marmoset red blood cells on man/mouse and man/Chinese hamster hybrid cells. European Journal of Immunology. 7: 22-6. PMID 66148 DOI: 10.1002/Eji.1830070106 |
0.348 |
|
| 1977 |
Fellous M, Kamoun M, Wiels J, Dausset J, Clements G, Zeuthen J, Klein G. Induction of HLA expression in Daudi cells after cell fusion Immunogenetics. 5: 423-436. DOI: 10.1007/Bf01570501 |
0.516 |
|
| 1976 |
Gachelin G, Fellous M, Guenet JL, Jacob F. Developmental expression of an early embryonic antigen common to mouse spermatozoa and cleavage embryos, and to human spermatozoa: its expression during spermatogenesis. Developmental Biology. 50: 310-20. PMID 946960 DOI: 10.1016/0012-1606(76)90154-8 |
0.344 |
|
| 1976 |
Charmot D, Kamoun M, Crosier P, Sasportes M, Fellous M, Mawas C. Expression on a human cell line (Daudi) lacking both HLA and β2 -microglobulin of HLA-D products and cell-mediated lympholysis targets European Journal of Immunology. 6: 913-916. DOI: 10.1002/Eji.1830061215 |
0.331 |
|
| 1975 |
Dausset J, Degos L, Fellous M, Legrand L. Formal genetics of the HL-A region. Genetics. 79: 251-62. PMID 50252 |
0.455 |
|
| 1974 |
Fellous M, Gerbal A, Tessier C, Frezal J, Dausset J, Salmon C. Studies on the biosynthetic pathway of human P erythrocyte antigens using somatic cells in culture. Vox Sanguinis. 26: 518-36. PMID 4854478 DOI: 10.1111/J.1423-0410.1974.Tb02729.X |
0.426 |
|
| 1974 |
Fellous M, Gachelin G, Buc-Caron MH, Dubois P, Jacob F. Similar location of an early embryonic antigen on mouse and human spermatozoa. Developmental Biology. 41: 331-7. PMID 4615957 DOI: 10.1016/0012-1606(74)90310-8 |
0.317 |
|
| 1973 |
Fellous M, Couillin P, Neauport-Sautes C, Frezal J, Billardon C, Dausset J. Studies of human alloantigens on man-mouse hybrids: possible syntheny between HL-A and P systems. European Journal of Immunology. 3: 543-8. PMID 4588107 DOI: 10.1002/Eji.1830030904 |
0.5 |
|
| 1973 |
Couillin P, Fellous M, Dausset J. [Correlation between the expression of HL-A and P systems antigens in hybrid human x mouse cells and culture media (HATG, Standard, BUDR). Possible linkage of HL-A and P loci with the thymidine kinase locus]. Comptes Rendus Hebdomadaires Des Sã©Ances De L'Acadã©Mie Des Sciences. Sã©Rie D: Sciences Naturelles. 276: 125-8. PMID 4196499 |
0.449 |
|
| 1972 |
Hors-Cayla MC, Fellous M, Picard JY, Trébuchet C, Dausset J, Frézal J. [Linkage between the HL-A histocompatibility system and the thymidine kinase activity in a human-mouse hybrid]. Comptes Rendus Hebdomadaires Des Sã©Ances De L'Acadã©Mie Des Sciences. Sã©Rie D: Sciences Naturelles. 275: 2965-8. PMID 4631962 |
0.41 |
|
| 1971 |
Fellous M, Billardon C, Dausset J, Frézal J. [Probable linkage between the locus "HLA" and"P"]. Comptes Rendus Hebdomadaires Des Sã©Ances De L'Acadã©Mie Des Sciences. Sã©Rie D: Sciences Naturelles. 272: 3356-9. PMID 4997730 |
0.409 |
|
| 1971 |
Sasportes M, Dehay C, Fellous M. Variations of the expression of HL-A antigens on human diploid fibroblasts in vitro. Nature. 233: 332-4. PMID 4940427 DOI: 10.1038/233332A0 |
0.335 |
|
| 1970 |
Fellous M, Dausset J. Probable heploid expression of HL-A antigens on human spermatozoon. Nature. 225: 191-3. PMID 5409969 DOI: 10.1038/225191A0 |
0.495 |
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