FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Christine Bellanné-Chantelot

Research Profile

Chemicals & Drugs

Physiology

Disorders

Living Beings

Concepts & Ideas

Pedigree

Procedures

DNA Mutational Analysis

Co-author Network

Publications

TOP 3
jean donadieu; Nizar Mahlaoui; Blandine Beaupain; Christine Bellanné-Chantelot
Epidemiology of congenital neutropenia.
Fanny Laffargue; Christine Bellanné-Chantelot; Sylvie Bourthoumieu; Vincent Guigonis; Catherine Yardin
Could FISH on buccal smears become a new method of screening in children suspect of HNF1B anomaly?
Marlène Pasquet; Arnaud Petit; Geneviève Plat; Hélène A Poirel; Naïs Prade; Christian Récher; Pierre Rohrlich; Suzanne Tavitian; Eric Van Den Neste; Françoise Bachelerie; Blandine Beaupain; Christine Bellanné-Chantelot; Jill Corre; jean donadieu; Christophe Ferrand; Thierry Lamy; Olivier Larochelle; Véronique Mansat-De Mas; Marie Ouachée-Chardin; Eric Delabesse
High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Christine Bellanné-Chantelot (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: jean donadieu; Nizar Mahlaoui; Blandine Beaupain; Christine Bellanné-Chantelot
Epidemiology of congenital neutropenia.
Hematology/oncology clinics of North America 2013;27(1):1-17, vii.
2013: Fanny Laffargue; Christine Bellanné-Chantelot; Sylvie Bourthoumieu; Vincent Guigonis; Catherine Yardin
Could FISH on buccal smears become a new method of screening in children suspect of HNF1B anomaly?
European journal of medical genetics 2013;56(2):93-7.
2013: Marlène Pasquet; Arnaud Petit; Geneviève Plat; Hélène A Poirel; Naïs Prade; Christian Récher; Pierre Rohrlich; Suzanne Tavitian; Eric Van Den Neste; Françoise Bachelerie; Blandine Beaupain; Christine Bellanné-Chantelot; Jill Corre; jean donadieu; Christophe Ferrand; Thierry Lamy; Olivier Larochelle; Véronique Mansat-De Mas; Marie Ouachée-Chardin; Eric Delabesse
High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia.
Blood 2013;121(5):822-9.
2012: Olivier Bourron; Beny Charbit; Fatma Chebbi; Marine Halbron; Ahmed Abed; Christine Bellanné-Chantelot; J M Lacorte; Christophe Magnan; Cécile Saint-Martin; Agnès Hartemann
Incretin effect of glucagon-like peptide 1 receptor agonist is preserved in presence of ABCC8/SUR1 mutation in β-cell.
Diabetes care 2012;35(11):e76.
2012: jean donadieu; Odile Fenneteau; Fanny Fouyssac; Virginie Gandemer; Anne Lambilliotte; Thierry Leblanc; Nizar Mahlaoui; Valérie Mialou; Gérard Michel; Alain Morali; Catherine Paillard; Christine Perot; Jacques Schmitz; Nathalie Aladjidi; Sandrine Beaufils; Blandine Beaupain; Florence Bellanger; Christine Bellanné-Chantelot; Yves Bertrand; Patrick Boutard
Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome.
Haematologica 2012;97(9):1312-9.
2012: Veronique Dinand; Sunila Jain; Christine Bellanné-Chantelot; Manorama Bhargava; Satya Prakash Yadav; Anupam Sachdeva
Hepatic hemangioendothelioma in an infant with severe congenital neutropenia.
Journal of pediatric hematology/oncology 2012;34(4):298-300.
2012: Baptiste N Jaeger; Nizar Mahlaoui; Bernard Malissen; Marie Malissen; Emilie Narni-Mancinelli; Diana Ordoñez-Rueda; Eric Vivier; Marc Bajénoff; Vincent Barlogis; Blandine Beaupain; Christine Bellanné-Chantelot; Claire Bernat; Céline Cognet; jean donadieu; Aurore Fenis; Sophie Ugolini
Neutrophil depletion impairs natural killer cell maturation, function, and homeostasis.
The Journal of experimental medicine 2012;209(3):565-80.
2012: Kim-Hanh Le Quan Sang; Asmaa Mamoune; Cécile Saint-Martin; Jean-Christophe Thalabard; Vassili Valayannopoulos; Jean-Baptiste Arnoux; Valérie Barbier; Christine Bellanné-Chantelot; Anais Brassier; Christine Broissand; Brigitte Charron; Jean-Roch Fabreguettes; Honorine Kayirangwa; Pascale de Lonlay
Successful treatment of congenital hyperinsulinism with long-acting release octreotide.
European journal of endocrinology / European Federation of Endocrine Societies 2012;166(2):333-9.
2011: Jean-Claude Henquin; Myriam Nenquin; Claire Nihoul-Fékété; Timo Otonkoski; Christine Bellanné-Chantelot; Pascale de Lonlay; Yves Guiot; Christine Sempoux; Jacques Rahier
In vitro insulin secretion by pancreatic tissue from infants with diazoxide-resistant congenital hyperinsulinism deviates from model predictions.
The Journal of clinical investigation 2011;121(10):3932-42.
2011: Stanislas Faguer; Jean-Philippe Lengelé; Pierre Ronco; Karine Dahan; Stéphane Decramer; Olivier Devuyst; Sandrine Beaufils; Christine Bellanné-Chantelot; Lucie Bessenay; Patrick Calvas; Nicolas Chassaing; Dominique Chauveau
Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood.
Kidney international 2011;80(7):768-76.
2011: Christine Bellanné-Chantelot; Claire Carette; Lucy Chaillous; Danièle Dubois-Laforgue; Jean-François Gautier; Agnès Hartemann; Sandrine Laboureau-Soares; Marie Laloi-Michelin; Etienne Larger; Pierre Lecomte; David Joseph Lévy; Yves Reznik; Jean-Pierre Riveline; Cécile Saint-Martin; Agnès Sola; José Timsit; René Valéro
Clinical characteristics and diagnostic criteria of maturity-onset diabetes of the young (MODY) due to molecular anomalies of the HNF1A gene.
The Journal of clinical endocrinology and metabolism 2011;96(8):E1346-51.
2011: Andrew J Finch; Christine Hilcenko; Nicolas Basse; Lesley F Drynan; Beatriz Goyenechea; Tobias F Menne; Africa González Fernández; Paul Simpson; Clive S D'Santos; Mark J Arends; jean donadieu; Christine Bellanné-Chantelot; Michael Costanzo; Charles Boone; Andrew N McKenzie; Stefan M V Freund; Alan J Warren
Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome.
Genes & development 2011;25(9):917-29.
2011: David Montani; Dermot S O'Callaghan; Caroline O'Connell; Laurent Savale; Gérald Simonneau; Olivier Sitbon; Gérard Zalcman; Hugues Begueret; Christine Bellanné-Chantelot; Emmanuel Bergot; Laurent Bertoletti; Giuseppina Biondi; Florence Coulet; Peter Dorfmuller; Claire Dromer; Mélanie Eyries; Barbara Girerd; Thomas Hugues; Marc Humbert; Xavier Jaïs; Hervé Mal; Charles Marquette; Florent Soubrier
Pulmonary hypertension in patients with neurofibromatosis type I.
Medicine 2011;90(3):201-11.
2011: Sabina I Swierczek; Donghoon Yoon; Christine Bellanné-Chantelot; Soo Jin Kim; Cécile Saint-Martin; Francois Delhommeau; Albert Najman; Josef T Prchal
Extent of hematopoietic involvement by TET2 mutations in JAK2V⁶¹⁷F polycythemia vera.
Haematologica 2011;96(5):775-8.
2011: Philippa D Powell; Christine Bellanné-Chantelot; Sarah E Flanagan; Sian Ellard; Raoul Rooman; Khalid Hussain; Mars Skae; Peter Clayton; Pascale de Lonlay; Mark J Dunne; Karen E Cosgrove
In vitro recovery of ATP-sensitive potassium channels in β-cells from patients with congenital hyperinsulinism of infancy.
Diabetes 2011;60(4):1223-8.
2011: Cécile Saint-Martin; Jean-Baptiste Arnoux; Pascale de Lonlay; Christine Bellanné-Chantelot
KATP channel mutations in congenital hyperinsulinism.
Seminars in pediatric surgery 2011;20(1):18-22.
2011: Jean-Baptiste Arnoux; Christine Bellanné-Chantelot; Anaïs Brassier; Francis Brunelle; Jean-Christophe Fournet; Françoise Montravers; Jean-Jacques Robert; Cécile Saint-Martin; Vassili Valayannopoulos; Virginie Verkarre; Yves Aigrain; Pascale de Lonlay
Congenital hyperinsulinism: current trends in diagnosis and therapy.
Orphanet journal of rare diseases 2011;6():63.
2011: Dunia Ismail; Virpi V Smith; Pascale de Lonlay; Maria-Joao Ribeiro; Jacques Rahier; Oliver Blankenstein; Sarah E Flanagan; Christine Bellanné-Chantelot; Virginie Verkarre; Yves Aigrain; Agostino Pierro; Sian Ellard; Khalid Hussain
Familial focal congenital hyperinsulinism.
The Journal of clinical endocrinology and metabolism 2011;96(1):24-8.
2010: Christine Bellanné-Chantelot; C Saint-Martin; Maria-João Ribeiro; C Vaury; V Verkarre; J-B Arnoux; V Valayannopoulos; S Gobrecht; C Sempoux; J Rahier; J-C Fournet; F Jaubert; Y Aigrain; C Nihoul-Fékété; P de Lonlay
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism.
Journal of medical genetics 2010;47(11):752-9.
2010: Chantal Loirat; Christine Bellanné-Chantelot; Isabelle Husson; Georges Deschênes; Vincent Guigonis; Nadia Chabane
Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010;25(10):3430-3.
2010: Maud Bidet; Christine Bellanné-Chantelot; Marie-Béatrice Galand-Portier; Jean-Louis Golmard; Véronique Tardy; Yves Morel; Séverine Clauin; Christiane Coussieu; Philippe Boudou; Irene Mowzowicz; Anne Bachelot; Philippe Touraine; Frédérique Kuttenn
Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
The Journal of clinical endocrinology and metabolism 2010;95(3):1182-90.
2010: Amélie Bonnefond; Emmanuelle Durand; Olivier Sand; Franck De Graeve; Sophie Gallina; Kanetee Busiah; Stéphane Lobbens; Albane Simon; Christine Bellanné-Chantelot; Louis Létourneau; Raphael Scharfmann; Jérôme Delplanque; Robert Sladek; Michel Polak; Martine Vaxillaire; philippe froguel
Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome.
PloS one 2010;5(10):e13630.
2009: Kara K Osbak; Kevin Colclough; Cecile Saint-Martin; Nicola L Beer; Christine Bellanné-Chantelot; Sian Ellard; Anna L Gloyn
Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.
Human mutation 2009;30(11):1512-26.
2009: Cécile Saint-Martin; Gwendoline Leroy; François Delhommeau; Gérard Panelatti; Sabrina Dupont; Chloé James; Isabelle Plo; Dominique Bordessoule; Christine Chomienne; André Delannoy; Alain Devidas; Martine Gardembas-Pain; Françoise Isnard; Yves Plumelle; Olivier Bernard; William Vainchenker; Albert Najman; Christine Bellanné-Chantelot
Analysis of the ten-eleven translocation 2 (TET2) gene in familial myeloproliferative neoplasms.
Blood 2009;114(8):1628-32.
2009: Julien ZUBER; Christine Bellanné-Chantelot; Claire Carette; Guillaume Canaud; Sandrine Gobrecht; Khaled Gaha; Vincent Mallet; Frank Martinez; Eric Thervet; José Timsit; Christophe Legendre; Danièle Dubois-Laforgue
HNF1B-related diabetes triggered by renal transplantation.
Nature reviews. Nephrology 2009;5(8):480-4.
2009: Agnès Hartemann-Heurtier; A Simon; Christine Bellanné-Chantelot; R Reynaud; H Cavé; M Polak; M Vaxillaire; André Grimaldi
Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetes.
Diabetes & metabolism 2009;35(3):233-5.
2009: Maud Bidet; Christine Bellanné-Chantelot; Marie-Béatrice Galand-Portier; Véronique Tardy; Line Billaud; Kathleen Laborde; Christiane Coussieu; Yves Morel; Christelle Vaury; Jean-Louis Golmard; Aurélie Claustre; Etienne Mornet; Zeina Chakhtoura; Irene Mowszowicz; Anne Bachelot; Philippe Touraine; Frédérique Kuttenn
Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members.
The Journal of clinical endocrinology and metabolism 2009;94(5):1570-8.
2009: Sarah Flanagan; Séverine Clauin; Christine Bellanné-Chantelot; Pascale de Lonlay; Lorna W Harries; Anna L Gloyn; Sian Ellard
Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism.
Human mutation 2009;30(2):170-80.
2009: Kaan Boztug; Giridharan Appaswamy; Angel Ashikov; Alejandro A Schäffer; Ulrich Salzer; Jana Diestelhorst; Manuela Germeshausen; Gudrun Brandes; Jacqueline Lee-Gossler; Fatih Noyan; Anna-Katherina Gatzke; Milen Minkov; Johann Greil; Christian Kratz; Theoni Petropoulou; Isabelle Pellier; Christine Bellanné-Chantelot; Nima Rezaei; Kirsten Mönkemöller; Noha Irani-Hakimeh; Hans Bakker; Rita Gerardy-Schahn; Cornelia Zeidler; Bodo Grimbacher; Karl Welte; Christoph Klein
A syndrome with congenital neutropenia and mutations in G6PC3.
The New England journal of medicine 2009;360(1):32-43.
2008: Delphine Martin; Christine Bellanné-Chantelot; I Deschamps; philippe froguel; Jean-Jacques Robert; Gilberto Velho
Long-term follow-up of oral glucose tolerance test-derived glucose tolerance and insulin secretion and insulin sensitivity indexes in subjects with glucokinase mutations (MODY2).
Diabetes care 2008;31(7):1321-3.
2008: jean donadieu; Blandine Beaupain; Christine Bellanné-Chantelot
[Granulopoeisis and leukemogenesis: lessons from congenital neutropenia].
Médecine sciences : M/S 2008;24(3):284-9.
2008: Christine Bellanné-Chantelot; Claire Carette; Jean-Pierre Riveline; René Valéro; Jean-François Gautier; Etienne Larger; Yves Reznik; Pierre-Henri Ducluzeau; Agnès Sola; Agnès Hartemann-Heurtier; Pierre Lecomte; Lucy Chaillous; Marie Laloi-Michelin; Jean-Marie Wilhem; Pierre Cuny; Françoise Duron; Bruno Guerci; Nathalie Jeandidier; Helen Mosnier-Pudar; Michel Assayag; Danièle Dubois-Laforgue; Gilberto Velho; José Timsit
The type and the position of HNF1A mutation modulate age at diagnosis of diabetes in patients with maturity-onset diabetes of the young (MODY)-3.
Diabetes 2008;57(2):503-8.
2008: Christine Bellanné-Chantelot; P Jego; P Lionne-Huyghe; Micheline Tulliez; Albert Najman
The JAK2(V617F) mutation may be present several years before the occurrence of overt myeloproliferative disorders.
Leukemia 2008;22(2):450-1.
2008: M Mar González-Barroso; Irina Giurgea; Frederic Bouillaud; Andrea Anedda; Christine Bellanné-Chantelot; Laurence Hubert; Yves de Keyzer; Pascale de Lonlay; Daniel Ricquier
Mutations in UCP2 in congenital hyperinsulinism reveal a role for regulation of insulin secretion.
PloS one 2008;3(12):e3850.
2007: Stanislas Faguer; François Bouissou; Philippe Dumazer; Joelle Guitard; Christine Bellanné-Chantelot; Dominique Chauveau
Massively enlarged polycystic kidneys in monozygotic twins with TCF2/HNF-1beta (hepatocyte nuclear factor-1beta) heterozygous whole-gene deletion.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2007;50(6):1023-7.
2007: Maria-João Ribeiro; Nathalie Boddaert; Christine Bellanné-Chantelot; Sandrine Bourgeois; Vassili Valayannopoulos; thierry delzescaux; Francis Jaubert; Claire Nihoul-Fékété; Francis Brunelle; Pascale de Lonlay
The added value of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy: a retrospective study involving 49 children.
European journal of nuclear medicine and molecular imaging 2007;34(12):2120-8.
2007: Nadia Bahi-Buisson; Monika M Eisermann; Sylvie Nivot; Christine Bellanné-Chantelot; Olivier Dulac; Nathalie Bach; Perrine Plouin; Catherine Chiron; Pascale de Lonlay
Infantile spasms as an epileptic feature of DEND syndrome associated with an activating mutation in the potassium adenosine triphosphate (ATP) channel, Kir6.2.
Journal of child neurology 2007;22(9):1147-50.
2007: Daniel C Link; Ghada Kunter; Yumi Kasai; Yu Zhao; Tracie Miner; Michael D McLellan; Rhonda E Ries; Deepak Kapur; Rakesh Nagarajan; David C Dale; Audrey Anna Bolyard; Laurence A Boxer; Karl Welte; Cornelia Zeidler; jean donadieu; Christine Bellanné-Chantelot; James W Vardiman; Michael A Caligiuri; Clara D Bloomfield; John F DiPersio; Michael H Tomasson; Timothy A Graubert; Peter Westervelt; Mark Watson; William D Shannon; Jack Baty; Elaine R Mardis; Richard K Wilson; Timothy J Ley
Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia.
Blood 2007;110(5):1648-55.
2007: Claire Carette; Christelle Vaury; Anne Barthélémy; Séverine Clauin; Jean-Pierre Grünfeld; José Timsit; Christine Bellanné-Chantelot
Exonic duplication of the hepatocyte nuclear factor-1beta gene (transcription factor 2, hepatic) as a cause of maturity onset diabetes of the young type 5.
The Journal of clinical endocrinology and metabolism 2007;92(7):2844-7.
2007: Vassili Valayannopoulos; Martine Vaxillaire; Yves Aigrain; Francis Jaubert; Christine Bellanné-Chantelot; Maria-João Ribeiro; Francis Brunelle; philippe froguel; Jean-Jacques Robert; Michel Polak; Claire Nihoul-Fékété; Pascale de Lonlay
Coexistence in the same family of both focal and diffuse forms of hyperinsulinism.
Diabetes care 2007;30(6):1590-2.
2007: Emmanuelle Jeannot; Karine Poussin; Laurence Chiche; Yannick Bacq; Nathalie Sturm; Jean-Yves Scoazec; Catherine Buffet; Jeanne Tran Van Nhieu; Christine Bellanné-Chantelot; Claudia De Toma; Pierre Laurent-Puig; Paulette Bioulac-Sage; Jessica Zucman-Rossi
Association of CYP1B1 germ line mutations with hepatocyte nuclear factor 1alpha-mutated hepatocellular adenoma.
Cancer research 2007;67(6):2611-6.
2007: Dominique Beckers; Christine Bellanné-Chantelot; Marc Maes
Neonatal cholestatic jaundice as the first symptom of a mutation in the hepatocyte nuclear factor-1beta gene (HNF-1beta).
The Journal of pediatrics 2007;150(3):313-4.
2007: Stéphane Decramer; Olivier Parant; Sandrine Beaufils; Séverine Clauin; Cécile Guillou; Sylvie Kessler; Jacqueline Aziza; Flavio Bandin; Joost P Schanstra; Christine Bellanné-Chantelot
Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys.
Journal of the American Society of Nephrology : JASN 2007;18(3):923-33.
2007: Maria-João Ribeiro; Nathalie Boddaert; thierry delzescaux; Vassili Valayannopoulos; Christine Bellanné-Chantelot; Francis Jaubert; Virginie Verkarre; Claire Nihoul-Fékété; Francis Brunelle; Pascale de Lonlay
Functional imaging of the pancreas: the role of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy.
Endocrine development 2007;12():55-66.
2007: Catherine Diatloff-Zito; A Nicole; G Marcelin; H Labit; Eve Marquis; Christine Bellanné-Chantelot; Jean-Jacques Robert
Genetic and epigenetic defects at the 6q24 imprinted locus in a cohort of 13 patients with transient neonatal diabetes: new hypothesis raised by the finding of a unique case with hemizygotic deletion in the critical region.
Journal of medical genetics 2007;44(1):31-7.
2006: Irina Giurgea; Christine Sempoux; Christine Bellanné-Chantelot; Maria Ribeiro; Laurence Hubert; Nathalie Boddaert; Jean-Marie Saudubray; Jean-Jacques Robert; Francis Brunelle; Jacques Rahier; Francis Jaubert; Claire Nihoul-Fékété; Pascale de Lonlay
The Knudson's two-hit model and timing of somatic mutation may account for the phenotypic diversity of focal congenital hyperinsulinism.
The Journal of clinical endocrinology and metabolism 2006;91(10):4118-23.
2006: Anna L Gloyn; Catherine Diatloff-Zito; Emma L Edghill; Christine Bellanné-Chantelot; Sylvie Nivot; Régis Coutant; Sian Ellard; Andrew T Hattersley; Jean-Jacques Robert
KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features.
European journal of human genetics : EJHG 2006;14(7):824-30.
2006: Christine Bellanné-Chantelot; Isabelle Chaumarel; Myriam Labopin; Florence Bellanger; Véronique Barbu; Claudia De Toma; François Delhommeau; Nicole Casadevall; William Vainchenker; Gilles Thomas; Albert Najman
Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.
Blood 2006;108(1):346-52.
2006: Pascale de Lonlay; Aurore Simon-Carre; Maria-João Ribeiro; Nathalie Boddaert; Irina Giurgea; Kathleen Laborde; Christine Bellanné-Chantelot; Virginie Verkarre; Michel Polak; Jacques Rahier; André Syrota; David J Seidenwurm; Claire Nihoul-Fékété; Jean-Jacques Robert; Francis Brunelle; Francis Jaubert
Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretion.
The Journal of clinical endocrinology and metabolism 2006;91(3):933-40.
2006: Irina Giurgea; D Sanlaville; J-C Fournet; Christine Sempoux; Christine Bellanné-Chantelot; Guy Touati; Laurence Hubert; M-S Groos; Francis Brunelle; Jacques Rahier; J-C Henquin; Mark J Dunne; Francis Jaubert; Jean-Jacques Robert; Claire Nihoul-Fékété; M Vekemans; Claudine Junien; Pascale de Lonlay
Congenital hyperinsulinism and mosaic abnormalities of the ploidy.
Journal of medical genetics 2006;43(3):248-54.
2006: Tim Ulinski; Sandra Lescure; Sandrine Beaufils; Vincent Guigonis; Stéphane Decramer; Denis Morin; Séverine Clauin; Georges Deschênes; François Bouissou; Albert Bensman; Christine Bellanné-Chantelot
Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort.
Journal of the American Society of Nephrology : JASN 2006;17(2):497-503.
2006: Irina Giurgea; Christine Bellanné-Chantelot; Maria Ribeiro; Laurence Hubert; Christine Sempoux; Jean-Jacques Robert; Oliver Blankenstein; Khalid Hussain; Francis Brunelle; Claire Nihoul-Fékété; Jacques Rahier; Francis Jaubert; Pascale de Lonlay
Molecular mechanisms of neonatal hyperinsulinism.
Hormone research 2006;66(6):289-96.
2005: Gaëtan Lebrun; Viorel Vasiliu; Christine Bellanné-Chantelot; Albert Bensman; Tim Ulinski; Yves Chrétien; Jean-Pierre Grünfeld
Cystic kidney disease, chromophobe renal cell carcinoma and TCF2 (HNF1 beta) mutations.
Nature clinical practice. Nephrology 2005;1(2):115-9.
2005: Christine Bellanné-Chantelot; Séverine Clauin; Dominique Chauveau; Philippe Collin; Michèle Daumont; Claire Douillard; Danièle Dubois-Laforgue; Laurent Dusselier; Jean-François Gautier; Michel Jadoul; Marie Laloi-Michelin; Laetitia Jacquesson; Etienne Larger; Jacques Louis; Marc Nicolino; Jean-François Subra; Jean-Marie Wilhem; Jacques Young; Gilberto Velho; José Timsit
Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5.
Diabetes 2005;54(11):3126-32.
2005: Irina Giurgea; Maria-João Ribeiro; Nathalie Boddaert; Guy Touati; Jean-Jacques Robert; J-M Saudubray; Francis Jaubert; Christine Bellanné-Chantelot; Francis Brunelle; Claire Nihoul-Fékété; Pascale de Lonlay
[Congenital hyperinsulinism in newborn and infant].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2005;12(11):1628-35.
2005: Sandra Rebouissou; Viorel Vasiliu; Cristel Thomas; Christine Bellanné-Chantelot; Hung Bui; Yves Chrétien; José Timsit; Christophe Rosty; Pierre Laurent-Puig; Dominique Chauveau; Jessica Zucman-Rossi
Germline hepatocyte nuclear factor 1alpha and 1beta mutations in renal cell carcinomas.
Human molecular genetics 2005;14(5):603-14.
2005: Pascale de Lonlay; Irina Giurgea; Christine Sempoux; Guy Touati; Francis Jaubert; Jacques Rahier; Maria Ribeiro; Francis Brunelle; Claire Nihoul-Fékété; Jean-Jacques Robert; Jean-Marie Saudubray; Charles Stanley; Christine Bellanné-Chantelot
Dominantly inherited hyperinsulinaemic hypoglycaemia.
Journal of inherited metabolic disease 2005;28(3):267-76.
2005: José Timsit; Christine Bellanné-Chantelot; Danièle Dubois-Laforgue; Gilberto Velho
Diagnosis and management of maturity-onset diabetes of the young.
Treatments in endocrinology 2005;4(1):9-18.
2005: jean donadieu; Thierry Leblanc; Brigitte Bader-Meunier; Mohamed Barkaoui; Odile Fenneteau; Yves Bertrand; Micheline Maier-Redelsperger; Marguerite Micheau; Jean Louis Stephan; Noel Phillipe; Pierre Bordigoni; Annie Babin-Boilletot; Philippe Bensaid; Anne-Marie Manel; Etienne Vilmer; Isabelle Thuret; Stephane Blanche; Eliane Gluckman; Alain Fischer; Françoise Mechinaud; Bertrand Joly; Thierry Lamy; Olivier Hermine; Bruno Cassinat; Christine Bellanné-Chantelot; Christine Chomienne
Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group.
Haematologica 2005;90(1):45-53.
2004: N Cheurfa; André F Reis; Danièle Dubois-Laforgue; Christine Bellanné-Chantelot; José Timsit; Gilberto Velho
The Gly482Ser polymorphism in the peroxisome proliferator-activated receptor-gamma coactivator-1 gene is associated with hypertension in type 2 diabetic men.
Diabetologia 2004;47(11):1980-3.
2004: Bruno Cassinat; Christine Bellanné-Chantelot; A Notz-Carrère; Marie-Laurence Menot; Christelle Vaury; Marguerite Micheau; B Bader-Meunier; Yves Perel; Thierry Leblanc; jean donadieu; Christine Chomienne
Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French neutropenia register.
Leukemia 2004;18(9):1553-5.
2004: André F Reis; Danièle Dubois-Laforgue; Christine Bellanné-Chantelot; José Timsit; Gilberto Velho
A polymorphism in the promoter of UCP2 gene modulates lipid levels in patients with type 2 diabetes.
Molecular genetics and metabolism 2004;82(4):339-44.
2004: Christine Bellanné-Chantelot; Séverine Clauin; Thierry Leblanc; Bruno Cassinat; Fernando Rodrigues-Lima; Sandrine Beaufils; Christelle Vaury; Mohamed Barkaoui; Odile Fenneteau; Micheline Maier-Redelsperger; Christine Chomienne; jean donadieu
Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register.
Blood 2004;103(11):4119-25.
2004: Christine Bellanné-Chantelot; Dominique Chauveau; Jean-François Gautier; Danièle Dubois-Laforgue; Séverine Clauin; Sandrine Beaufils; Jean-Marie Wilhelm; Christian Boitard; Laure-Hélène Noël; Gilberto Velho; José Timsit
Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations.
Annals of internal medicine 2004;140(7):510-7.
2004: Pierre-Jean Guillausseau; Danièle Dubois-Laforgue; Pascale Massin; Marie Laloi-Michelin; Christine Bellanné-Chantelot; H Gin; E Bertin; JF Blickle; B Bauduceau; Beatrice Bouhanick; J Cahen-Varsaux; S Casanova; Guillaume Charpentier; P Chedin; C Derrien; A Grimaldi; Bruno Guerci; E Kaloustian; F Lorenzini; A Murat; F Olivier; Michel Paques; Véronique Paquis-Flucklinger; Amélie Tielmans; M Vincenot; Bernard Vialettes; José Timsit
Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD).
Diabetes & metabolism 2004;30(2):181-6.
2004: Irina Giurgea; Kathleen Laborde; Guy Touati; Christine Bellanné-Chantelot; Marie-Cécile Nassogne; Christine Sempoux; Francis Jaubert; Nguyen Khoa; Valérie Chigot; Jacques Rahier; Francis Brunelle; Claire Nihoul-Fékété; Mark J Dunne; Charles Stanley; Jean-Marie Saudubray; Jean-Jacques Robert; Pascale de Lonlay
Acute insulin responses to calcium and tolbutamide do not differentiate focal from diffuse congenital hyperinsulinism.
The Journal of clinical endocrinology and metabolism 2004;89(2):925-9.
2003: Gilberto Velho; Christine Bellanné-Chantelot; José Timsit
[MODY, a model of genotype/phenotype interactions in type 2 diabetes].
Médecine sciences : M/S 2003;19(8-9):854-9.
2003: Ronan Roussel; André F Reis; Danièle Dubois-Laforgue; Christine Bellanné-Chantelot; José Timsit; Gilberto Velho
The N363S polymorphism in the glucocorticoid receptor gene is associated with overweight in subjects with type 2 diabetes mellitus.
Clinical endocrinology 2003;59(2):237-41.
2002: R Barrio; Christine Bellanné-Chantelot; José C Moreno; V Morel; H Calle; M Alonso; C Mustieles
Nine novel mutations in maturity-onset diabetes of the young (MODY) candidate genes in 22 Spanish families.
The Journal of clinical endocrinology and metabolism 2002;87(6):2532-9.
2002: Eve Marquis; Jean-Jacques Robert; C Bouvattier; Christine Bellanné-Chantelot; Claudine Junien; Catherine Diatloff-Zito
Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetes.
Journal of medical genetics 2002;39(5):370-4.
2002: Beatrice Bouhanick; Christine Bellanné-Chantelot; A Salle; G Guilloteau; J M Ebran
Proliferative retinopathy in patients with type 1 diabetes of less than 5 years' duration.
Diabetes & metabolism 2002;28(2):141-4.
2001: WZ Ye; André F Reis; Danièle Dubois-Laforgue; Christine Bellanné-Chantelot; José Timsit; Gilberto Velho
Vitamin D receptor gene polymorphisms are associated with obesity in type 2 diabetic subjects with early age of onset.
European journal of endocrinology / European Federation of Endocrine Societies 2001;145(2):181-6.
2001: WZ Ye; Danièle Dubois-Laforgue; Christine Bellanné-Chantelot; José Timsit; Gilberto Velho
Variations in the vitamin D-binding protein (Gc locus) and risk of type 2 diabetes mellitus in French Caucasians.
Metabolism: clinical and experimental 2001;50(3):366-9.
2000: André F Reis; WZ Ye; Danièle Dubois-Laforgue; Christine Bellanné-Chantelot; José Timsit; Gilberto Velho
Mutations in the insulin promoter factor-1 gene in late-onset type 2 diabetes mellitus.
European journal of endocrinology / European Federation of Endocrine Societies 2000;143(4):511-3.
2000: André F Reis; WZ Ye; Danièle Dubois-Laforgue; Christine Bellanné-Chantelot; José Timsit; Gilberto Velho
Association of a variant in exon 31 of the sulfonylurea receptor 1 (SUR1) gene with type 2 diabetes mellitus in French Caucasians.
Human genetics 2000;107(2):138-44.
2000: A Costa; Mónica Bescós; Gilberto Velho; J Chêvre; J Vidal; Gemma Sesmilo; Christine Bellanné-Chantelot; philippe froguel; Roser Casamitjana; Francisca Rivera-Fillat; Ramon Gomis; Ignacio Conget
Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families.
European journal of endocrinology / European Federation of Endocrine Societies 2000;142(4):380-6.
2000: F Godart; Christine Bellanné-Chantelot; Séverine Clauin; C Gragnoli; Amar Abderrahmani; Hélène Blanché; Philippe Boutin; Jean-Claude Chèvre; philippe froguel; B Bailleul
Identification of seven novel nucleotide variants in the hepatocyte nuclear factor-1alpha (TCF1) promoter region in MODY patients.
Human mutation 2000;15(2):173-80.
1998: Jean-Claude Chèvre; El Habib Hani; Philippe Boutin; Martine Vaxillaire; Hélène Blanché; Nathalie Vionnet; Victor Cavalcanti Pardini; José Timsit; Etienne Larger; Guillaume Charpentier; D Beckers; M Maes; Christine Bellanné-Chantelot; Gilberto Velho; philippe froguel
Mutation screening in 18 Caucasian families suggest the existence of other MODY genes.
Diabetologia 1998;41(9):1017-23.
1997: Hélène Blanché; Patrick Vexiau; Séverine Clauin; I Le Gall; Jean Fiet; E Mornet; Jean Dausset; Christine Bellanné-Chantelot
Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women.
Human genetics 1997;101(1):56-60.
1997: Hélène Blanché; C Valette; Christine Bellanné-Chantelot
Optimization of nonisotopic PCR-single-strand conformation polymorphism analysis.
Clinical chemistry 1997;43(11):2190-2.
1997: Christine Bellanné-Chantelot; Sandrine Beaufils; V Hourdel; Suzanne Lesage; V Morel; N Dessinais; I Le Gall; D Cohen; Jean Dausset
Search for DNA sequence variations using a MutS-based technology.
Mutation research 1997;382(1-2):35-43.
1997: Gilberto Velho; Hélène Blanché; Martine Vaxillaire; Christine Bellanné-Chantelot; Victor Cavalcanti Pardini; José Timsit; Philippe Passa; I Deschamps; Jean-Jacques Robert; Irene T Weber; D Marotta; S J Pilkis; G M Lipkind; G I Bell; philippe froguel
Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.
Diabetologia 1997;40(2):217-24.
1996: Mona NEMANI; Christine Bellanné-Chantelot; D Cohen; H M Cann
Detection of triplet repeat sequences in yeast artificial chromosomes using oligonucleotide probes: application to the SCA1 region in 6p23.
Cytogenetics and cell genetics 1996;72(1):5-8.
1995: Mona NEMANI; Christine Bellanné-Chantelot; D Cohen; H M Cann
Detection by hybridization of trinucleotide repeat sequences in yeast artificial chromosomes.
BioTechniques 1995;19(4):584-7.
1995: I M Chumakov; P Rigault; I Le Gall; Christine Bellanné-Chantelot; A Billault; S Guillou; P Soularue; G Guasconi; E Poullier; I Gros
A YAC contig map of the human genome.
Nature 1995;377(6547 Suppl):175-297.
1992: Christine Bellanné-Chantelot; B Lacroix; P Ougen; A Billault; S Beaufils; S Bertrand; I Georges; F Glibert; I Gros; G Lucotte
Mapping the whole human genome by fingerprinting yeast artificial chromosomes.
Cell 1992;70(6):1059-68.
1991: Christine Bellanné-Chantelot; E Barillot; B Lacroix; D Le Paslier; D Cohen
A test case for physical mapping of human genome by repetitive sequence fingerprints: construction of a physical map of a 420 kb YAC subcloned into cosmids.
Nucleic acids research 1991;19(3):505-10.