Child Health, Developmental Plasticity, and Epigenetic Programming
Hochberg, Z, Feil, R, Constancia, M, Fraga, M, Junien, C, Carel, J.-C, Boileau, P, Le Bouc, Y, Deal, C. L, Lillycrop, K, Scharfmann, R, Sheppard, A, Skinner, M, Szyf, M, Waterland, R. A, Waxman, D. J, Whitelaw, E, Ong, K, Albertsson-Wikland, K
Published in Endocrine reviews (01.04.2011)
Published in Endocrine reviews (01.04.2011)
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Maternal environment and the reproductive function of the offspring
Dupont, C, Cordier, A.G, Junien, C, Mandon-Pépin, B, Levy, R, Chavatte-Palmer, P
Published in Theriogenology (15.10.2012)
Published in Theriogenology (15.10.2012)
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Placental BDNF/TrkB Signaling System is Modulated by Fetal Growth Disturbances in Rat and Human
Mayeur, S, Silhol, M, Moitrot, E, Barbaux, S, Breton, C, Gabory, A, Vaiman, D, Dutriez-Casteloot, I, Fajardy, I, Vambergue, A, Tapia-Arancibia, L, Bastide, B, Storme, L, Junien, C, Vieau, D, Lesage, J
Published in Placenta (Eastbourne) (01.09.2010)
Published in Placenta (Eastbourne) (01.09.2010)
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Genetics of neonatal hyperinsulinism
Glaser, Benjamin, Thornton, Paul, Otonkoski, Timo, Junien, Claudine
Published in Archives of disease in childhood. Fetal and neonatal edition (01.03.2000)
Published in Archives of disease in childhood. Fetal and neonatal edition (01.03.2000)
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Journal Article
Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome
Diaz-Meyer, N, Day, C D, Khatod, K, Maher, E R, Cooper, W, Reik, W, Junien, C, Graham, G, Algar, E, Der Kaloustian, V M, Higgins, M J
Published in Journal of medical genetics (01.11.2003)
Published in Journal of medical genetics (01.11.2003)
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Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension
Wipff, J., Kahan, A., Hachulla, E., Sibilia, J., Cabane, J., Meyer, O., Mouthon, L., Guillevin, L., Junien, C., Boileau, C., Allanore, Y.
Published in Rheumatology (Oxford, England) (01.04.2007)
Published in Rheumatology (Oxford, England) (01.04.2007)
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Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia
Verkarre, V, Fournet, J C, de Lonlay, P, Gross-Morand, M S, Devillers, M, Rahier, J, Brunelle, F, Robert, J J, Nihoul-Fékété, C, Saudubray, J M, Junien, C
Published in The Journal of clinical investigation (01.10.1998)
Published in The Journal of clinical investigation (01.10.1998)
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Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database
Jeanpierre, C., Denamur, E., Henry, I., Cabanis, M.-O., Luce, S., Cécille, A., Elion, J., Peuchmaur, M., Loirat, C., Niaudet, P., Gubler, M.-C., Junien, C.
Published in American journal of human genetics (01.04.1998)
Published in American journal of human genetics (01.04.1998)
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Journal Article
Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability
SEZNEC, H, LIA-BALDINI, A.-S, DUROS, C, FOUQUET, C, LACROIX, C, HOFMANN-RADVANYI, H, JUNIEN, C, GOURDON, G
Published in Human molecular genetics (01.05.2000)
Published in Human molecular genetics (01.05.2000)
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Journal Article
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy
de Lonlay, P, Fournet, J C, Rahier, J, Gross-Morand, M S, Poggi-Travert, F, Foussier, V, Bonnefont, J P, Brusset, M C, Brunelle, F, Robert, J J, Nihoul-Fékété, C, Saudubray, J M, Junien, C
Published in The Journal of clinical investigation (15.08.1997)
Published in The Journal of clinical investigation (15.08.1997)
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Dietary alleviation of maternal obesity and diabetes: increased resistance to diet-induced obesity transcriptional and epigenetic signatures
Attig, Linda, Vigé, Alexandre, Gabory, Anne, Karimi, Moshen, Beauger, Aurore, Gross, Marie-Sylvie, Athias, Anne, Gallou-Kabani, Catherine, Gambert, Philippe, Ekstrom, Tomas J, Jais, Jean-Philippe, Junien, Claudine
Published in PloS one (2013)
Published in PloS one (2013)
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Journal Article
Defective satellite cells in congenital myotonic dystrophy
FURLING, D, COIFFIER, L, MOULY, V, BARBET, J. P, ST GUILY, J. Lacau, TANEJA, K, GOURDON, G, JUNIEN, C, BUTLER-BROWNE, G. S
Published in Human molecular genetics (15.09.2001)
Published in Human molecular genetics (15.09.2001)
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Journal Article
Congenital hyperinsulinism and mosaic abnormalities of the ploidy
Giurgea, I, Sanlaville, D, Fournet, J-C, Sempoux, C, Bellanné-Chantelot, C, Touati, G, Hubert, L, Groos, M-S, Brunelle, F, Rahier, J, Henquin, J-C, Dunne, M J, Jaubert, F, Robert, J-J, Nihoul-Fékété, C, Vekemans, M, Junien, C, de Lonlay, P
Published in Journal of medical genetics (01.03.2006)
Published in Journal of medical genetics (01.03.2006)
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Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humans
Mayeur, S., Cisse, O., Gabory, A., Barbaux, S., Vaiman, D., Vambergue, A., Fajardy, I., Deloof, S., Junien, C., Laborie, C., Vieau, D., Lesage, J.
Published in Journal of developmental origins of health and disease (01.04.2013)
Published in Journal of developmental origins of health and disease (01.04.2013)
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Uniparental paternal disomy in a genetic cancer-predisposing syndrome
Henry, I, Bonaiti-Pellié, C, Chehensse, V, Beldjord, C, Schwartz, C, Utermann, G, Junien, C
Published in Nature (London) (20.06.1991)
Published in Nature (London) (20.06.1991)
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Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC
Gallou, C., Joly, D., Méjean, A., Staroz, F., Martin, N., Tarlet, G., Orfanelli, M.T., Bouvier, R., Droz, D., Chrétien, Y., Maréchal, J.M., Richard, S., Junien, C., Béroud, C.
Published in Human mutation (1999)
Published in Human mutation (1999)
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