Marc Fellous

Affiliations: 
Institut Pasteur, Paris, Paris, France 
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"Marc Fellous"
Mean distance: 20.1 (cluster 57)
 
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Publications

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Laissue P, Lakhal B, Vatin M, et al. (2016) Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans. Open Biology. 6
Bramble MS, Goldstein EH, Lipson A, et al. (2016) A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing. Human Reproduction (Oxford, England)
Fauchereau F, Shalev S, Chervinsky E, et al. (2016) A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency. Clinical Genetics
Caburet S, Arboleda VA, Llano E, et al. (2014) Mutant cohesin in premature ovarian failure. The New England Journal of Medicine. 370: 943-9
Fonseca DJ, Ojeda D, Lakhal B, et al. (2012) CITED2 mutations potentially cause idiopathic premature ovarian failure. Translational Research : the Journal of Laboratory and Clinical Medicine. 160: 384-8
Caburet S, Zavadakova P, Ben-Neriah Z, et al. (2012) 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
Bouhali K, Dipietromaria A, Fontaine A, et al. (2011) 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
Hildebrand MS, Avenarius MR, Fellous M, et al. (2010) Genetic male infertility and mutation of CATSPER ion channels. European Journal of Human Genetics : Ejhg. 18: 1178-84
Benayoun BA, Caburet S, Dipietromaria A, et al. (2010) Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G). Plos One. 5: e8789
De Baere E, Fellous M, Veitia RA. (2009) 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
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