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Schwitzgebel Valerie
Schwitzgebel Valerie
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Year
Expression of neurogenin3 reveals an islet cell precursor population in the pancreas
VM Schwitzgebel, DW Scheel, JR Conners, J Kalamaras, JE Lee, ...
Development 127 (16), 3533-3542, 2000
8822000
Homeobox gene Nkx6.1 lies downstream of Nkx2.2 in the major pathway of β-cell formation in the pancreas
M Sander, L Sussel, J Conners, D Scheel, J Kalamaras, FD Cruz, ...
Development 127 (24), 5533-5540, 2000
6852000
Perinatal exposure to bisphenol a alters early adipogenesis in the rat
E Somm, VM Schwitzgebel, A Toulotte, CR Cederroth, C Combescure, ...
Environmental health perspectives 117 (10), 1549-1555, 2009
5662009
Prenatal nicotine exposure alters early pancreatic islet and adipose tissue development with consequences on the control of body weight and glucose metabolism later in life
E Somm, VM Schwitzgebel, DM Vauthay, EJ Camm, CY Chen, ...
Endocrinology 149 (12), 6289-6299, 2008
2102008
Agenesis of human pancreas due to decreased half-life of insulin promoter factor 1
VM Schwitzgebel, A Mamin, T Brun, B Ritz-Laser, M Zaiko, A Maret, ...
The Journal of Clinical Endocrinology & Metabolism 88 (9), 4398-4406, 2003
2102003
Normal female infants born of mothers with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
JC Lo, VM Schwitzgebel, JB Tyrrell, PA Fitzgerald, SL Kaplan, FA Conte, ...
The Journal of Clinical Endocrinology & Metabolism 84 (3), 930-936, 1999
1331999
Many faces of monogenic diabetes
VM Schwitzgebel
Journal of diabetes investigation 5 (2), 121-133, 2014
1242014
Programming of the pancreas
VM Schwitzgebel
Molecular and cellular Endocrinology 185 (1-2), 99-108, 2001
972001
Decreased bone turnover in children and adolescents with well controlled type 1 diabetes
ABR Maggio, S Ferrari, M Kraenzlin, LM Marchand, V Schwitzgebel, ...
Journal of Pediatric Endocrinology and Metabolism 23 (7), 697-708, 2010
932010
KLB, encoding β‐Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism
C Xu, A Messina, E Somm, H Miraoui, T Kinnunen, J Acierno Jr, ...
EMBO molecular medicine 9 (10), 1379-1397, 2017
872017
Modeling intrauterine growth retardation in rodents: Impact on pancreas development and glucose homeostasis
VM Schwitzgebel, E Somm, P Klee
Molecular and cellular endocrinology 304 (1-2), 78-83, 2009
812009
Prenatal nicotine exposure and the programming of metabolic and cardiovascular disorders
E Somm, VM Schwitzgebel, DM Vauthay, ML Aubert, PS Hüppi
Molecular and cellular endocrinology 304 (1-2), 69-77, 2009
772009
Inflammatory and prothrombotic states in obese children of European descent
S Stoppa‐Vaucher, MA Dirlewanger, CA Meier, P De Moerloose, G Reber, ...
Obesity 20 (8), 1662-1668, 2012
662012
Hepatic nuclear factor-3 (HNF-3 or Foxa2) regulates glucagon gene transcription by binding to the G1 and G2 promoter elements
BR Gauthier, VM Schwitzgebel, M Zaiko, A Mamin, B Ritz-Laser, ...
Molecular Endocrinology 16 (1), 170-183, 2002
592002
The zinc finger-containing transcription factor Gata-4 is expressed in the developing endocrine pancreas and activates glucagon gene expression
B Ritz-Laser, A Mamin, T Brun, I Avril, VM Schwitzgebel, J Philippe
Molecular Endocrinology 19 (3), 759-770, 2005
562005
Diabetes distress in males and females with type 1 diabetes in adolescence and emerging adulthood
L Lašaitė, R Dobrovolskienė, E Danytė, I Stankutė, ...
Journal of Diabetes and its Complications 30 (8), 1500-1505, 2016
512016
Encephalitis associated with glutamic acid decarboxylase autoantibodies in a child: a treatable condition?
CM Korff, P Parvex, L Cimasoni, A Wilhelm-Bals, CS Hampe, ...
Archives of neurology 68 (8), 1065-1068, 2011
512011
Early metabolic defects in dexamethasone-exposed and undernourished intrauterine growth restricted rats
E Somm, DM Vauthay, A Guérardel, A Toulotte, P Cettour-Rose, P Klee, ...
PloS one 7 (11), e50131, 2012
472012
A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1
M Dirlewanger, D Huser, MC Zennaro, E Girardin, L Schild, ...
American Journal of Physiology-Endocrinology and Metabolism 301 (3), E467-E473, 2011
462011
Severe congenital hyperinsulinism caused by a mutation in the Kir6. 2 subunit of the adenosine triphosphate-sensitive potassium channel impairing trafficking and function
E Marthinet, A Bloc, Y Oka, Y Tanizawa, B Wehrle-Haller, V Bancila, ...
The Journal of Clinical Endocrinology & Metabolism 90 (9), 5401-5406, 2005
422005
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