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Christine Bellanne-Chantelot

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Kevin Colclough; Sarah E Flanagan; Cecile Saint-Martin; Christine Bellanne-Chantelot; Sian Ellard
Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha and 4 alpha in maturity-onset diabetes of the young and hyperinsulinemic hypoglycemia.
Sandra Malak; Albert Najman; Cecile Saint-Martin; Christine Bellanne-Chantelot; Myriam Labopin
Long term follow up of 93 families with myeloproliferative neoplasms: life expectancy and implications of JAK2V617F in the occurrence of complications.
Elena Tudorache; Nadia Tubiana-Rufi; Christine Bellanne-Chantelot; Albert Bensman; Marion Lenoir; Anne-Laure Sellier-Leclerc; Nadia Toubiana; Tim Ulinski
Childhood onset diabetes posttransplant in a girl with TCF2 mutation.

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All Publications

2013: Kevin Colclough; Sarah E Flanagan; Cecile Saint-Martin; Christine Bellanne-Chantelot; Sian Ellard
Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha and 4 alpha in maturity-onset diabetes of the young and hyperinsulinemic hypoglycemia.
Human mutation 2013;34(5):669-85.
2012: Sandra Malak; Albert Najman; Cecile Saint-Martin; Christine Bellanne-Chantelot; Myriam Labopin
Long term follow up of 93 families with myeloproliferative neoplasms: life expectancy and implications of JAK2V617F in the occurrence of complications.
Blood cells, molecules & diseases 2012;49(3-4):170-6.
2012: Elena Tudorache; Nadia Tubiana-Rufi; Christine Bellanne-Chantelot; Albert Bensman; Marion Lenoir; Anne-Laure Sellier-Leclerc; Nadia Toubiana; Tim Ulinski
Childhood onset diabetes posttransplant in a girl with TCF2 mutation.
Pediatric diabetes 2012;13(6):e35-9.
2012: Caroline Poitou; Séverine Beaudreuil; Christine Bellanne-Chantelot; Gérard Benoit; Bernard Charpentier; Séverine Clauin; Hani Damieri; Hélène Francois; Yacine Hammoudi; Hadia Hebibi; Antoine Jacquet; Christian Noel; Antoine Durrbach
Maturity onset diabetes of the young: clinical characteristics and outcome after kidney and pancreas transplantation in MODY3 and RCAD patients: a single center experience.
Transplant international : official journal of the European Society for Organ Transplantation 2012;25(5):564-72.
2008: Denis Pierron; Christophe Rocher; Patricia Amati-Bonneau; Pascal Reynier; Marie-Laure Martin-Négrier; Stéphane Allouche; Cécile Batandier; Benedicte Mousson de Camaret; Catherine Godinot; Agnes Rotig; Delphine Feldmann; Christine Bellanne-Chantelot; Benoit Arveiler; Erwann Pennarun; Rodrigue Rossignol; Marc Crouzet; Pascal Murail; Didier Thoraval; Thierry Letellier
New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation.
BMC medical genetics 2008;9():41.
2007: Heather C Mefford; Séverine Clauin; andrew sharp; Rikke Steensbjerre Møller; Reinhard Ullmann; Raj Kapur; Daniel Pinkel; Gregory Cooper; ventura Mario; Hans-Hilger Ropers; Niels Tommerup; Evan E Eichler; Christine Bellanne-Chantelot
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy.
American journal of human genetics 2007;81(5):1057-69.
2007: Tiina Robins; Christine Bellanne-Chantelot; Michela Barbaro; Sylvie Cabrol; Anna Wedell; Svetlana Lajic
Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia.
Journal of molecular medicine (Berlin, Germany) 2007;85(3):247-55.
2005: Lorna W Harries; Coralie Bingham; Christine Bellanne-Chantelot; Andrew T Hattersley; Sian Ellard
The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay.
Human genetics 2005;118(2):214-24.
2004: Elena Barbacci; Angeliki Chalkiadaki; Christelle Masdeu; Cécile Haumaitre; Ludmilla Lokmane; Chantal Loirat; Sylvie Cloarec; Iannis Talianidis; Christine Bellanne-Chantelot; Silvia Cereghini
HNF1beta/TCF2 mutations impair transactivation potential through altered co-regulator recruitment.
Human molecular genetics 2004;13(24):3139-49.
2004: Yves Reznik; Thong Dao; Regis Coutant; Laurence Chiche; Emmanuelle Jeannot; Séverine Clauin; Pierre Rousselot; Monique Fabre; Frederic Oberti; Armelle Fatome; Jessica Zucman-Rossi; Christine Bellanne-Chantelot
Hepatocyte nuclear factor-1 alpha gene inactivation: cosegregation between liver adenomatosis and diabetes phenotypes in two maturity-onset diabetes of the young (MODY)3 families.
The Journal of clinical endocrinology and metabolism 2004;89(3):1476-80.
2002: Svetlana Lajić; Séverine Clauin; Tiina Robins; Patrick Vexiau; Hélène Blanché; Christine Bellanne-Chantelot; Anna Wedell
Novel mutations in CYP21 detected in individuals with hyperandrogenism.
The Journal of clinical endocrinology and metabolism 2002;87(6):2824-9.