Cécile Saint‐Martin

4.1k citations

42 papers · 2.0k indexed · h-index 22

Surgery top 5%
Genetics top 2%
Molecular Biology top 10%
Endocrinology, Diabetes and Metabolism top 2%
Genetics top 5%

Co-authors: Christine Bellanné‐Chantelot Sian Ellard Kevin Colclough Kara Osbak Nicola L. Beer Anna L. Gloyn José Timsit Sarah E. Flanagan
Topics: Pancreatic function and diabetes (21 papers)Hyperglycemia and glycemic control in critically ill and hospitalized patients (13 papers)Diabetes and associated disorders (12 papers)
Cited by: Endocrinology, Diabetes and Metabolism Genetics Surgery
Journals: Blood The Journal of Clinical Endocrinology & Metabolism Neurology
Partner nations: France United Kingdom United States

In The Last Decade

Cécile Saint‐Martin

39 papers receiving 1.9k citations

Peers

Countries citing papers authored by Cécile Saint‐Martin

Since Specialization

Citations

This map shows the geographic impact of Cécile Saint‐Martin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Cécile Saint‐Martin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cécile Saint‐Martin more than expected).

Fields of papers citing papers by Cécile Saint‐Martin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cécile Saint‐Martin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Cécile Saint‐Martin. The network helps show where Cécile Saint‐Martin may publish in the future.

Co-authorship network of co-authors of Cécile Saint‐Martin

This figure shows the co-authorship network connecting the top 25 collaborators of Cécile Saint‐Martin. A scholar is included among the top collaborators of Cécile Saint‐Martin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Cécile Saint‐Martin. Cécile Saint‐Martin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Insulin receptor variants: Extending the traditional Mendelian spectrum 2025 ·Genetics in Medicine ·(unknown),Cécile Saint‐Martin,(unknown),(unknown),(unknown),(unknown),Christine Bellanné-Chantelot,Robert K. Semple,Olivier Lascols,Isabelle Jéru	0
2	Molecular mechanism of HNF-1A–mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes 2024 ·JCI Insight ·(unknown),Janne Molnes,Erling Tjora,Arne Raasakka,Matti Myllykoski,Kevin Colclough,Cécile Saint‐Martin,Caroline Adelfalk,Petra Dušátková,Štěpánka Průhová,Camilla Valtonen‐André,Christine Bellanné‐Chantelot,Thomas Arnesen,Petri Kursula,Pål R. Njølstad	2
3	Congenital mirror movements are associated with defective polymerisation of RAD51 2023 ·Journal of Medical Genetics ·Oriane Trouillard,P. Dupaigne,(unknown),Mohamed Doulazmi,Morten Krogh Herlin,Solène Frismand,(unknown),(unknown),Guillaume Chevreux,Xavier Veaute,Didier Busso,(unknown),Cécile Saint‐Martin,Aurélie Méneret,Alain Trembleau,Isabelle Dusart,Caroline Dubacq,Emmanuel Roze	1
4	Evaluation in Monogenic Diabetes of the Impact of GCK, HNF1A, and HNF4A Variants on Splicing through the Combined Use of In Silico Tools and Minigene Assays 2023 ·Human Mutation ·(unknown),(unknown),Jean‐Madeleine de Sainte Agathe,(unknown),Cécile Saint‐Martin,Christine Bellanné‐Chantelot	3
5	Glucocorticoid-Induced Hyperinsulinism in a Preterm Neonate with Inherited ABCC8 Variant 2022 ·Metabolites ·Emmanuelle Motte‐Signoret,Cécile Saint‐Martin,Christine Bellané‐Chantelot,Bernard Portha,Pascal Boileau	1
6	Pregnancy in Women With Monogenic Diabetes due to Pathogenic Variants of the Glucokinase Gene: Lessons and Challenges 2022 ·Frontiers in Endocrinology ·José Timsit,Cécile Ciangura,Danièle Dubois‐Laforgue,Cécile Saint‐Martin,Christine Bellanné‐Chantelot	14
7	Monogenic diabetes in adults: A multi-ancestry study reveals strong disparities in diagnosis rates and clinical presentation 2022 ·Diabetes Research and Clinical Practice ·(unknown),Cécile Saint‐Martin,Danièle Dubois‐Laforgue,(unknown),José Timsit,Christine Bellanné‐Chantelot	4
8	Next-generation sequencing identifies monogenic diabetes in 16% of patients with late adolescence/adult-onset diabetes selected on a clinical basis: a cross-sectional analysis 2019 ·BMC Medicine ·(unknown),(unknown),Cécile Saint‐Martin,Danièle Dubois‐Laforgue,(unknown),(unknown),Cécile Ciangura,José Timsit,Christine Bellanné‐Chantelot	44
9	The Common HNF1A Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY 2018 ·Diabetes ·Jonathan M. Locke,Cécile Saint‐Martin,Thomas W. Laver,Kashyap Patel,Andrew R. Wood,Seth A. Sharp,Sian Ellard,Christine Bellanné‐Chantelot,Andrew T. Hattersley,Lorna W. Harries,Michael N. Weedon	19
10	Searching for Maturity-Onset Diabetes of the Young (MODY): When and What for? 2016 ·Canadian Journal of Diabetes ·José Timsit,Cécile Saint‐Martin,Danièle Dubois‐Laforgue,Christine Bellanné‐Chantelot	30
11	High-sensitivity C-reactive protein does not improve the differential diagnosis of HNF1A–MODY and familial young-onset type 2 diabetes: A grey zone analysis 2015 ·Diabetes & Metabolism ·Christine Bellanné‐Chantelot,Jöel Coste,Cécile Ciangura,Michèle Fonfrède,Cécile Saint‐Martin,C. Bouché,E. Sonnet,René Valéro,(unknown),Danièle Dubois‐Laforgue,José Timsit	16
12	Strengths and limitations of using¹⁸fluorine-fluorodihydroxyphenylalanine PET/CT for congenital hyperinsulinism 2014 ·Expert Review of Endocrinology & Metabolism ·Françoise Montravers,Jean‐Baptiste Arnoux,Maria-João Ribeiro,Khaldoun Kerrou,V. Nataf,Louise Galmiche,Y. Aigrain,Christine Bellanné‐Chantelot,Cécile Saint‐Martin,Jessica Ohnona,Soňa Balogová,Virginie Huchet,Laure Michaud,Jean‐Noël Talbot,Pascale de Lonlay	1
13	Long term follow up of 93 families with myeloproliferative neoplasms: life expectancy and implications of JAK2V617F in the occurrence of complications 2012 ·Blood Cells Molecules and Diseases ·Sandra Malak,Myriam Labopin,Cécile Saint‐Martin,Christine Bellanné‐Chantelot,A Najman	35
14	Successful treatment of congenital hyperinsulinism with long-acting release octreotide 2011 ·European Journal of Endocrinology ·Kim‐Hanh Le Quan Sang,Jean‐Baptiste Arnoux,Asmaa Mamoune,Cécile Saint‐Martin,Christine Bellanné‐Chantelot,Vassili Valayannopoulos,Anaïs Brassier,(unknown),Valérie Barbier,Christine Broissand,Jean‐Roch Fabreguettes,Brigitte Charron,Jean‐Christophe Thalabard,Pascale de Lonlay	60
15	Congenital hyperinsulinism: current trends in diagnosis and therapy 2011 ·Orphanet Journal of Rare Diseases ·(unknown),Virginie Verkarre,Cécile Saint‐Martin,Françoise Montravers,Anaïs Brassier,Vassili Valayannopoulos,Françis Brunelle,(unknown),(unknown),Y. Aigrain,Christine Bellanné‐Chantelot,Pascale de Lonlay	194
16	ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism 2010 ·Journal of Medical Genetics ·Christine Bellanné‐Chantelot,Cécile Saint‐Martin,M.J. Santiago Ribeiro,(unknown),Virginie Verkarre,Jean‐Baptiste Arnoux,Vassili Valayannopoulos,(unknown),Christine Sempoux,Jacques Rahier,Jean‐Christophe Fournet,Francis Jaubert,Y. Aigrain,Claire Nihoul‐Feketé,Pascale de Lonlay	90
17	Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome 2010 ·Journal of Medical Genetics ·Christel Depienne,Oriane Trouillard,Isabelle Gourfinkel‐An,Cécile Saint‐Martin,Delphine Bouteiller,Denis Graber,(unknown),Agnès Gautier,Nathalie Villeneuve,Charlotte Dravet,Marie-Odile Livet,(unknown),Claude Adam,Sabrina Dupont,Stéphanie Baulac,Delphine Héron,Rima Nabbout,Eric Leguern	117
18	KATP channel mutations in congenital hyperinsulinism 2010 ·Seminars in Pediatric Surgery ·Cécile Saint‐Martin,Jean‐Baptiste Arnoux,Pascale de Lonlay,Christine Bellanné‐Chantelot	25
19	Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia 2009 ·Human Mutation ·Kara Osbak,Kevin Colclough,Cécile Saint‐Martin,Nicola L. Beer,Christine Bellanné‐Chantelot,Sian Ellard,Anna L. Gloyn	370
20	Parental mosaicism can cause recurrent transmission ofSCN1A mutations associated with severe myoclonic epilepsy of infancy 2006 ·Human Mutation ·Christel Depienne,Alexis Arzimanoglou,Oriane Trouillard,Estelle Fédirko,Stéphanie Baulac,Cécile Saint‐Martin,Merle Ruberg,Charlotte Dravet,Rima Nabbout,Michel Baulac,Isabelle Gourfinkel‐An,Eric Leguern	76

About Cécile Saint‐Martin

Cécile Saint‐Martin is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Genetics, having authored 42 papers that have together received 2.0k indexed citations. Recurring topics across this work include Pancreatic function and diabetes (21 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (13 papers) and Diabetes and associated disorders (12 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (768 citations), Genetics (925 citations) and Surgery (1.0k citations). Cécile Saint‐Martin has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Christine Bellanné‐Chantelot, Sian Ellard, Kevin Colclough, Kara Osbak, Nicola L. Beer, Anna L. Gloyn, José Timsit, Sarah E. Flanagan, Danièle Dubois‐Laforgue and Pascale de Lonlay. Their work appears in journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and Neurology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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