André Chaventré

1.9k total citations
43 papers, 716 citations indexed

About

André Chaventré is a scholar working on Genetics, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, André Chaventré has authored 43 papers receiving a total of 716 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 6 papers in Genetics and 5 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in André Chaventré's work include Hemoglobinopathies and Related Disorders (5 papers), Cystic Fibrosis Research Advances (4 papers) and Thyroid Disorders and Treatments (4 papers). André Chaventré is often cited by papers focused on Hemoglobinopathies and Related Disorders (5 papers), Cystic Fibrosis Research Advances (4 papers) and Thyroid Disorders and Treatments (4 papers). André Chaventré collaborates with scholars based in France, Croatia and Mali. André Chaventré's co-authors include Jacques Élion, Stéphane Bonacorsi, Olivier Clermont, Érick Denamur, Édouard Bingen, Patrick Duriez, Bertrand Picard, Jean‐Jacques Schott, Albert Jacquard and L Degos and has published in prestigious journals such as Nature, The Lancet and Circulation.

In The Last Decade

André Chaventré

40 papers receiving 676 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
André Chaventré France 10 227 142 139 135 118 43 716
Charles E. Cowles United States 13 58 0.3× 208 1.5× 47 0.3× 350 2.6× 38 0.3× 18 882
Peter Corte Australia 12 41 0.2× 42 0.3× 52 0.4× 159 1.2× 332 2.8× 22 856
Michael Seiff United States 7 33 0.1× 153 1.1× 37 0.3× 169 1.3× 58 0.5× 8 508
Jean Tyrrell United States 14 28 0.1× 42 0.3× 39 0.3× 220 1.6× 245 2.1× 20 596
Alejandro Mosquera Spain 10 63 0.3× 55 0.4× 128 0.9× 272 2.0× 14 0.1× 18 620
Nataliya Lutay Sweden 15 188 0.8× 44 0.3× 38 0.3× 234 1.7× 63 0.5× 21 812
Kirill Tsyganov Australia 10 28 0.1× 29 0.2× 40 0.3× 176 1.3× 48 0.4× 16 472
Irina M. Velsko United States 24 45 0.2× 151 1.1× 11 0.1× 471 3.5× 47 0.4× 44 1.6k
Songmin Ying China 13 36 0.2× 30 0.2× 21 0.2× 236 1.7× 72 0.6× 31 691

Countries citing papers authored by André Chaventré

Since Specialization
Citations

This map shows the geographic impact of André Chaventré'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 André Chaventré with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites André Chaventré more than expected).

Fields of papers citing papers by André Chaventré

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by André Chaventré. 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 André Chaventré. The network helps show where André Chaventré may publish in the future.

Co-authorship network of co-authors of André Chaventré

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

All Works

20 of 20 papers shown
1.
Kyndt, Florence, Solena Le Scouarnec, Antoine Legendre, et al.. (2007). [Genetic aspects of valvulopathies].. PubMed. 100(12). 1013–20. 8 indexed citations
2.
Pennarun, Erwan, Toomas Kivisild, Kristiina Tambets, et al.. (2007). An mtDNA perspective of French genetic variation. Annals of Human Biology. 34(1). 68–79. 50 indexed citations
3.
Mechita, Mohcine Bennani, André Chaventré, Amina Barakat, et al.. (2003). Origin of Hb A2′(Hb B2) [δ16(A13)Gly→Arg (GGC→CGC)]. Hemoglobin. 27(2). 105–110. 13 indexed citations
4.
Caignec, Cédric Le, et al.. (2002). Familial Deafness, Congenital Heart Defects, and Posterior Embryotoxon Caused by Cysteine Substitution in the First Epidermal-Growth-Factor–Like Domain of Jagged 1. The American Journal of Human Genetics. 71(1). 180–186. 42 indexed citations
5.
Sanchez‐Mazas, Alicia, R. Bütler, Rosario Calderón, et al.. (2001). A Worldwide Analysis of AG Molecular Diversity Inferred from Serology. Human Biology. 73(5). 637–659. 1 indexed citations
6.
Arnaud, Josiane, et al.. (2001). Selenium Status in an Iodine Deficient Population of the West Ivory Coast.. Journal of PHYSIOLOGICAL ANTHROPOLOGY and Applied Human Science. 20(2). 81–84. 9 indexed citations
7.
Krishnamoorthy, Rajagopal, et al.. (2000). Anthropogenetical analysis of abnormal human alpha-globin gene cluster arrangement on chromosome 16.. PubMed. 24(2). 295–301. 4 indexed citations
8.
Scotet, Virginie, Marc De Braekeleer, Michel Roussey, et al.. (2000). Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis. The Lancet. 356(9232). 789–794. 85 indexed citations
9.
Koffi, Mathurin, et al.. (1999). Stratégies de prise en charge d'une endémie goitreuse en situation de développement. 59(4). 401–410. 1 indexed citations
10.
Braekeleer, Marc De, et al.. (1998). Genetic factors in iodine deficiency disorders: a general review.. PubMed. 22(1). 9–15. 3 indexed citations
11.
Rudan, Igor, Pavao Rudan, André Chaventré, et al.. (1996). Model-bound and Model-free approaches in the holistic analysis of population structure: Example from the Island of Brač, Croatia. HOMO. 49(2). 201–224. 4 indexed citations
12.
Braekeleer, Marc De, André Chaventré, Giorgio Bertorelle, et al.. (1996). Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of Brittany. Human Genetics. 98(2). 223–227. 6 indexed citations
13.
Bellis, Gil, et al.. (1996). Treatment by iodized oil (Lipiodol® UF) of a population in Mali suffering from endemic goiter. Journal of Endocrinological Investigation. 19(1). 1–5. 6 indexed citations
14.
Diallo, Dapa A., et al.. (1994). Haemoglobinopathies C and S in the Dogons.. PubMed. 35(6). 551–4. 3 indexed citations
15.
Ducrocq, Rolande, Mohcine Bennani Mechita, Gil Bellis, et al.. (1994). Hemoglobinopathies in the dogon country: Presence of βs, βc, and δa'genes. American Journal of Hematology. 46(3). 245–247. 7 indexed citations
16.
Chaventré, André, et al.. (1992). Factor Structure of Morphometric Variables Measured on Six Metacarpal Bones.. The Annals of physiological anthropology. 11(1). 3–12. 5 indexed citations
17.
Trabuchet, G, Jacques Élion, Olga Dunda, et al.. (1991). Nucleotide sequence evidence of the unicentric origin of the ?C mutation in Africa. Human Genetics. 87(5). 597–601. 21 indexed citations
18.
Chaventré, André, et al.. (1984). Relationship of lung functions to age, sitting height and body composition in older men and women. Zeitschrift für Morphologie und Anthropologie. 75(1). 97–105. 1 indexed citations
19.
Chaventré, André. (1983). Evolution anthropo-biologique d'une population touarègue : les Kel Kummer et leurs apparentés. Presses Universitaires de France eBooks. 3 indexed citations
20.
Degos, L, et al.. (1974). Selective pressure on HL-A polymorphism. Nature. 249(5452). 62–63. 38 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.

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