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Results: 6

1.

Germline mutations of inhibins in early-onset ovarian epithelial tumors.

Tournier I, Marlin R, Walton K, Charbonnier F, Coutant S, Théry JC, Charbonnier C, Spurrell C, Vezain M, Ippolito L, Bougeard G, Roman H, Tinat J, Sabourin JC, Stoppa-Lyonnet D, Caron O, Bressac-de Paillerets B, Vaur D, King MC, Harrison C, Frebourg T.

Hum Mutat. 2014 Mar;35(3):294-7. doi: 10.1002/humu.22489. Epub 2013 Dec 27.

2.

Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification.

Nicolas G, Pottier C, Maltête D, Coutant S, Rovelet-Lecrux A, Legallic S, Rousseau S, Vaschalde Y, Guyant-Maréchal L, Augustin J, Martinaud O, Defebvre L, Krystkowiak P, Pariente J, Clanet M, Labauge P, Ayrignac X, Lefaucheur R, Le Ber I, Frébourg T, Hannequin D, Campion D.

Neurology. 2013 Jan 8;80(2):181-7. doi: 10.1212/WNL.0b013e31827ccf34. Epub 2012 Dec 19.

PMID:
23255827
3.

EVA: Exome Variation Analyzer, an efficient and versatile tool for filtering strategies in medical genomics.

Coutant S, Cabot C, Lefebvre A, Léonard M, Prieur-Gaston E, Campion D, Lecroq T, Dauchel H.

BMC Bioinformatics. 2012;13 Suppl 14:S9. doi: 10.1186/1471-2105-13-S14-S9. Epub 2012 Sep 7.

4.

High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease.

Pottier C, Hannequin D, Coutant S, Rovelet-Lecrux A, Wallon D, Rousseau S, Legallic S, Paquet C, Bombois S, Pariente J, Thomas-Anterion C, Michon A, Croisile B, Etcharry-Bouyx F, Berr C, Dartigues JF, Amouyel P, Dauchel H, Boutoleau-Bretonnière C, Thauvin C, Frebourg T, Lambert JC, Campion D; PHRC GMAJ Collaborators.

Mol Psychiatry. 2012 Sep;17(9):875-9. doi: 10.1038/mp.2012.15. Epub 2012 Apr 3.

PMID:
22472873
5.

Bistable cell fate specification as a result of stochastic fluctuations and collective spatial cell behaviour.

Stockholm D, Edom-Vovard F, Coutant S, Sanatine P, Yamagata Y, Corre G, Le Guillou L, Neildez-Nguyen TM, Pàldi A.

PLoS One. 2010 Dec 28;5(12):e14441. doi: 10.1371/journal.pone.0014441.

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