Cécile Saint‐Martin

4.1k citations

42 papers · 2.0k indexed · h-index 22

Endocrinology, Diabetes and Metabolism top 2%
- Hyperglycemia and glycemic control in critically ill and hospitalized patients 13
- Diabetes Management and Research 6
- Diabetes Treatment and Management 6
Genetics top 2%
- Diabetes and associated disorders 12
- Myeloproliferative Neoplasms: Diagnosis and Treatment 6
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 5
Surgery top 5%
- Pancreatic function and diabetes 21
Genetics top 5%
- Diabetes and associated disorders 12
- Myeloproliferative Neoplasms: Diagnosis and Treatment 6
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 5
Hematology top 5%

Co-authors: Christine Bellanné‐Chantelot Sian Ellard Kevin Colclough Kara Osbak Nicola L. Beer Anna L. Gloyn José Timsit Sarah E. Flanagan
Cited by: Endocrinology, Diabetes and Metabolism Genetics Surgery
Journals: Blood (4 papers)The Journal of Clinical Endocrinology & Metabolism (2 papers)Neurology (1 paper)
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

The 25 scholars most cited alongside Cécile Saint‐Martin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Cécile Saint‐Martin Line = papers co-authored together Cécile Saint‐Martin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Insulin receptor variants: Extending the traditional Mendelian spectrum Genetics in Medicine ·Delphine Collin‐Chavagnac,Cécile Saint‐Martin,Lotfi Bedidi,Louis Lebreton,Vahid Aslanzadeh,Corinne Vigouroux,Christine Bellanné-Chantelot,Robert K. Semple,Olivier Lascols,Isabelle Jéru	2025	0
2	Molecular mechanism of HNF-1A–mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes JCI Insight ·Laura Kind,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	2024	2
3	Congenital mirror movements are associated with defective polymerisation of RAD51 Journal of Medical Genetics ·Oriane Trouillard,P. Dupaigne,Margaux Dunoyer,Mohamed Doulazmi,Morten Krogh Herlin,Solène Frismand,Audrey Riou,Véronique Legros,Guillaume Chevreux,Xavier Veaute,Didier Busso,Coralie Fouquet,Cécile Saint‐Martin,Aurélie Méneret,Alain Trembleau,Isabelle Dusart,Caroline Dubacq,Emmanuel Roze	2023	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 Human Mutation ·Delphine Bouvet,Amélie Blondel,Jean‐Madeleine de Sainte Agathe,Gwendoline Leroy,Cécile Saint‐Martin,Christine Bellanné‐Chantelot	2023	3
5	Glucocorticoid-Induced Hyperinsulinism in a Preterm Neonate with Inherited ABCC8 Variant Metabolites ·Emmanuelle Motte‐Signoret,Cécile Saint‐Martin,Christine Bellané‐Chantelot,Bernard Portha,Pascal Boileau	2022	1
6	Pregnancy in Women With Monogenic Diabetes due to Pathogenic Variants of the Glucokinase Gene: Lessons and Challenges Frontiers in Endocrinology ·José Timsit,Cécile Ciangura,Danièle Dubois‐Laforgue,Cécile Saint‐Martin,Christine Bellanné‐Chantelot	2022	14
7	Monogenic diabetes in adults: A multi-ancestry study reveals strong disparities in diagnosis rates and clinical presentation Diabetes Research and Clinical Practice ·F. Mifsud,Cécile Saint‐Martin,Danièle Dubois‐Laforgue,D. Bouvet,José Timsit,Christine Bellanné‐Chantelot	2022	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 BMC Medicine ·(unknown),Xavier Donath,Cécile Saint‐Martin,Danièle Dubois‐Laforgue,Ramanan Rajasingham,F. Mifsud,Cécile Ciangura,José Timsit,Christine Bellanné‐Chantelot	2019	44
9	The Common HNF1A Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY 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	2018	19
10	Searching for Maturity-Onset Diabetes of the Young (MODY): When and What for? Canadian Journal of Diabetes ·José Timsit,Cécile Saint‐Martin,Danièle Dubois‐Laforgue,Christine Bellanné‐Chantelot	2016	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 Diabetes & Metabolism ·Christine Bellanné‐Chantelot,Jöel Coste,Cécile Ciangura,Michèle Fonfrède,Cécile Saint‐Martin,C. Bouché,E. Sonnet,René Valéro,D J Levy,Danièle Dubois‐Laforgue,José Timsit	2015	16
12	Strengths and limitations of using¹⁸fluorine-fluorodihydroxyphenylalanine PET/CT for congenital hyperinsulinism 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	2014	1
13	Long term follow up of 93 families with myeloproliferative neoplasms: life expectancy and implications of JAK2V617F in the occurrence of complications Blood Cells Molecules and Diseases ·Sandra Malak,Myriam Labopin,Cécile Saint‐Martin,Christine Bellanné‐Chantelot,A Najman	2012	35
14	Successful treatment of congenital hyperinsulinism with long-acting release octreotide European Journal of Endocrinology ·Kim‐Hanh Le Quan Sang,Jean‐Baptiste Arnoux,Asmaa Mamoune,Cécile Saint‐Martin,Christine Bellanné‐Chantelot,Vassili Valayannopoulos,Anaïs Brassier,Honorine Kayirangwa,Valérie Barbier,Christine Broissand,Jean‐Roch Fabreguettes,Brigitte Charron,Jean‐Christophe Thalabard,Pascale de Lonlay	2011	60
15	Congenital hyperinsulinism: current trends in diagnosis and therapy Orphanet Journal of Rare Diseases ·Jean-Baptiste Arnoux,Virginie Verkarre,Cécile Saint‐Martin,Françoise Montravers,Anaïs Brassier,Vassili Valayannopoulos,Françis Brunelle,Jean-Christophe Fournet,Jean-Jacques Robert,Y. Aigrain,Christine Bellanné‐Chantelot,Pascale de Lonlay	2011	194
16	ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism Journal of Medical Genetics ·Christine Bellanné‐Chantelot,Cécile Saint‐Martin,M.J. Santiago Ribeiro,Chantal Vaury,Virginie Verkarre,Jean‐Baptiste Arnoux,Vassili Valayannopoulos,Sandrine Gobrecht,Christine Sempoux,Jacques Rahier,Jean‐Christophe Fournet,Francis Jaubert,Y. Aigrain,Claire Nihoul‐Feketé,Pascale de Lonlay	2010	90
17	Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome Journal of Medical Genetics ·Christel Depienne,Oriane Trouillard,Isabelle Gourfinkel‐An,Cécile Saint‐Martin,Delphine Bouteiller,Denis Graber,Marie‐Anne Barthez‐Carpentier,Agnès Gautier,Nathalie Villeneuve,Charlotte Dravet,Marie-Odile Livet,Clotilde Rivier-Ringenbach,Claude Adam,Sabrina Dupont,Stéphanie Baulac,Delphine Héron,Rima Nabbout,Eric Leguern	2010	117
18	KATP channel mutations in congenital hyperinsulinism Seminars in Pediatric Surgery ·Cécile Saint‐Martin,Jean‐Baptiste Arnoux,Pascale de Lonlay,Christine Bellanné‐Chantelot	2010	25
19	Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia Human Mutation ·Kara Osbak,Kevin Colclough,Cécile Saint‐Martin,Nicola L. Beer,Christine Bellanné‐Chantelot,Sian Ellard,Anna L. Gloyn	2009	370
20	Parental mosaicism can cause recurrent transmission ofSCN1A mutations associated with severe myoclonic epilepsy of infancy 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	2006	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), Diabetes and associated disorders (12 papers), Diabetes Management and Research (6 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Diabetes Treatment and Management (6 papers) and Genomics and Rare Diseases (5 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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