C. Saint‐Martin

415 total citations
14 papers, 304 citations indexed

About

C. Saint‐Martin is a scholar working on Genetics, Hematology and Surgery. According to data from OpenAlex, C. Saint‐Martin has authored 14 papers receiving a total of 304 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Hematology and 3 papers in Surgery. Recurrent topics in C. Saint‐Martin's work include Hemoglobinopathies and Related Disorders (6 papers), Iron Metabolism and Disorders (5 papers) and Hematological disorders and diagnostics (2 papers). C. Saint‐Martin is often cited by papers focused on Hemoglobinopathies and Related Disorders (6 papers), Iron Metabolism and Disorders (5 papers) and Hematological disorders and diagnostics (2 papers). C. Saint‐Martin collaborates with scholars based in France, Guadeloupe and United States. C. Saint‐Martin's co-authors include Édouard Bingen, Michel Duval, J. Sarfati, E Vilmer, Agnès Carol, Pierre‐Simon Rohrlich, Patricia Mariani, C Berchel, Marc Romana and G. Mérault and has published in prestigious journals such as FEBS Letters, Diabetic Medicine and The Pediatric Infectious Disease Journal.

In The Last Decade

C. Saint‐Martin

14 papers receiving 290 citations

Peers

C. Saint‐Martin

EPIDE

GENET

HEMAT

SURGE

Yosra Ben Youssef Tunisia

Éric Beltan Guadeloupe

J. Sastre Spain

Shinichi Morinaga Japan

H Perrimond France

Kazue Yasuda Japan

Amar Smaïl France

C T Peng Taiwan

Vasiliki Vlacha Greece

Susan Farmand Germany

Yosra Ben Youssef Tunisia

C. Saint‐Martin

109 ×0.8

EPIDE

116 ×1.0

86 ×1.1

GENET

126 ×2.1

HEMAT

44 ×1.0

SURGE

Citations per year, relative to C. Saint‐Martin C. Saint‐Martin (= 1×) peers Yosra Ben Youssef

Countries citing papers authored by C. Saint‐Martin

Since Specialization

Citations

This map shows the geographic impact of C. 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 C. 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 C. Saint‐Martin more than expected).

Fields of papers citing papers by C. Saint‐Martin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. 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 C. Saint‐Martin. The network helps show where C. Saint‐Martin may publish in the future.

Co-authorship network of co-authors of C. Saint‐Martin

This figure shows the co-authorship network connecting the top 25 collaborators of C. Saint‐Martin. A scholar is included among the top collaborators of C. 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 C. Saint‐Martin. C. Saint‐Martin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

Saint‐Martin, C., Qing Zhou, Gregory M. Martin, et al.. (2014). Monoallelic ABCC8 mutations are a common cause of diazoxide‐unresponsive diffuse form of congenital hyperinsulinism. Clinical Genetics. 87(5). 448–454. 19 indexed citations

Atkinson, James B., Anne Sophie Carret, Jean‐Pierre Farmer, et al.. (2011). Treatment-Related Morbidity in Atypical Teratoid/Rhabdoid Tumor: Multifocal Necrotizing Leukoencephalopathy. Pediatric Neurosurgery. 47(1). 7–14. 7 indexed citations

Carette, Claire, Danièle Dubois‐Laforgue, C. Saint‐Martin, et al.. (2010). Familial young‐onset forms of diabetes related to HNF4A and rare HNF1A molecular aetiologies. Diabetic Medicine. 27(12). 1454–1458. 18 indexed citations

Connes, Philippe, et al.. (2006). Does the Pattern of Repeated Sprint Ability Differ between Sickle Cell Trait Carriers and Healthy Subjects?. International Journal of Sports Medicine. 27(12). 937–942. 10 indexed citations

Didier, D, C. Saint‐Martin, Pedro T. Trindade, et al.. (2005). Coarctation of the aorta: pre and postoperative evaluation with MRI and MR angiography; correlation with echocardiography and surgery. International journal of cardiac imaging. 22(3-4). 457–475. 37 indexed citations

Romana, Marc, et al.. (2000). Diverse Genetic Mechanisms Operate to Generate Atypical β^sHaplotypes in the Population of Guadeloupe. Hemoglobin. 24(2). 77–87. 13 indexed citations

Romana, Marc, et al.. (1997). Sickle cell disorder, β-globin gene cluster haplotypes and α-thalassemia in neonates and adults from Guadeloupe. American Journal of Hematology. 55(1). 24–27. 23 indexed citations

Romana, Marc, et al.. (1997). Hemoglobin Sickle-Lepore: An Unusual Case of Sickle Cell Disease. Acta Haematologica. 98(3). 170–171. 2 indexed citations

Romana, Marc, et al.. (1997). Efficiency of prenatal counselling for sickle cell disease in Guadeloupe.. PubMed. 8(1). 25–32. 7 indexed citations

10.

Rohrlich, Pierre‐Simon, J. Sarfati, Patricia Mariani, et al.. (1996). Prospective sandwich enzyme-linked immunosorbent assay for serum galactomannan: early predictive value and clinical use in invasive aspergillosis. The Pediatric Infectious Disease Journal. 15(3). 232–237. 120 indexed citations

11.

Romana, Marc, et al.. (1996). Molecular characterization of β‐thalassemia mutations in Guadeloupe. American Journal of Hematology. 53(4). 228–233. 21 indexed citations

12.

Kalifa, G., et al.. (1995). Sonographic diagnosis and follow-up of diffuse neutropenic colitis: Case report of a child treated for osteogenic sarcoma. Pediatric Radiology. 25(5). 373–374. 13 indexed citations

13.

Bergogne-Bérézin, E, Patricia Mariani‐Kurkdjian, C. Doit, et al.. (1994). [Oropharyngeal flora. Epidemiologic survey of prevalence].. PubMed. 23(30). 1376–80. 4 indexed citations

14.

Mérault, G., C. Saint‐Martin, N. Arous, et al.. (1985). Hemoglobin Roseau‐Pointe a Pitre α₂β₂90 (F6) Glu → Gly: a new hemoglobin variant with slight instability and low oxygen affinity. FEBS Letters. 184(1). 10–13. 10 indexed citations

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.

Explore authors with similar magnitude of impact