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Christine Bellanné-Chantelot | Researchclopedia

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Christine Bellanné-Chantelot

Sorbonne Université

15

Works

501

Citations

8

h-index

7

i10-index

Research Topics

Pancreatic function and diabetes Genomics and Rare Diseases Diabetes Treatment and Management

Affiliations

Inserm2015–2017

Université Paris-Saclay2015–2015

Institut Gustave Roussy2015–2015

Sorbonne Université2007–2026

Laboratory of Excellence GR-Ex2017–2017

Top Works

The Type and the Position of <i>HNF1A</i> Mutation Modulate Age at Diagnosis of Diabetes in Patients with Maturity-Onset Diabetes of the Young (MODY)-3

Christine Bellanné-Chantelot,Claire Carette,et al.

2007192 citations

Diabetes Management and Research

Metabolism, Diabetes, and Cancer

Presence of atypical thrombopoietin receptor (MPL) mutations in triple-negative essential thrombocythemia patients

Xénia Cabagnols,Fabrizia Favale,et al.

2015183 citations

Severe chronic primary neutropenia in adults: report on a series of 108 patients

Flore Sicre de Fontbrune,Aline Moignet,et al.

201543 citations

Intellectual disability in patients with MODY due to hepatocyte nuclear factor 1B (HNF1B) molecular defects

Danièle Dubois‐Laforgue,Christine Bellanné-Chantelot,et al.

201627 citations

New pathogenic mechanisms induced by germline erythropoietin receptor mutations in primary erythrocytosis

Florence Pasquier,Caroline Marty,et al.

201719 citations

Identification of biallelic germline variants of SRP68 in a sporadic case with severe congenital neutropenia

Barbara Schmaltz-Panneau,Anne Pagnier,et al.

202016 citations

An update on congenital hyperinsulinism: advances in diagnosis and management

Jean‐Baptiste Arnoux,Cécile Saint‐Martin,et al.

201410 citations

Non-coding cis-regulatory variants in HK1 cause congenital hyperinsulinism with variable disease severity

James T. Bennett,Cécile Saint‐Martin,et al.

20259 citations

Insulin receptor variants: Extending the traditional Mendelian spectrum

Delphine Collin‐Chavagnac,Cécile Saint‐Martin,et al.

20253 citations