Christine Muti

1.9k total citations
18 papers, 408 citations indexed

About

Christine Muti is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Christine Muti has authored 18 papers receiving a total of 408 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Pulmonary and Respiratory Medicine and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Christine Muti's work include Connective tissue disorders research (8 papers), Aortic Disease and Treatment Approaches (4 papers) and Genetic factors in colorectal cancer (3 papers). Christine Muti is often cited by papers focused on Connective tissue disorders research (8 papers), Aortic Disease and Treatment Approaches (4 papers) and Genetic factors in colorectal cancer (3 papers). Christine Muti collaborates with scholars based in France, Australia and Belgium. Christine Muti's co-authors include Cathérine Boileau, Guillaume Jondeau, Bertrand Chevallier, Jean‐Marie Le Parc, Delphine Détaint, Bertrand Moura, Ariane Boumendil, Brigitte Simon‐Bouy, Bernard Nordlinger and François Radvanyi and has published in prestigious journals such as British Journal of Cancer, International Journal of Cancer and The American Journal of Gastroenterology.

In The Last Decade

Christine Muti

16 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christine Muti France 10 144 134 122 117 100 18 408
Christopher Yanucil United States 9 205 1.4× 128 1.0× 54 0.4× 84 0.7× 47 0.5× 15 627
Jean Jacques Michels France 7 20 0.1× 98 0.7× 152 1.2× 195 1.7× 50 0.5× 11 346
Mairead Casey United States 6 102 0.7× 21 0.2× 144 1.2× 264 2.3× 306 3.1× 7 542
Roger A Hern United Kingdom 7 27 0.2× 250 1.9× 156 1.3× 148 1.3× 32 0.3× 8 491
Brian Czaya United States 9 182 1.3× 109 0.8× 47 0.4× 65 0.6× 44 0.4× 18 588
Mariam Jafri United Kingdom 8 26 0.2× 33 0.2× 64 0.5× 102 0.9× 74 0.7× 15 354
Emma Spurrell United Kingdom 7 37 0.3× 34 0.3× 144 1.2× 184 1.6× 107 1.1× 11 307
Rafael Cabrera Portugal 10 36 0.3× 31 0.2× 61 0.5× 141 1.2× 17 0.2× 26 310
Ragnhild Klepp Norway 8 49 0.3× 38 0.3× 188 1.5× 241 2.1× 63 0.6× 12 309
Lori W. Wilson United States 9 19 0.1× 85 0.6× 68 0.6× 52 0.4× 36 0.4× 15 391

Countries citing papers authored by Christine Muti

Since Specialization
Citations

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

Fields of papers citing papers by Christine Muti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Muti

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

All Works

18 of 18 papers shown
1.
Cholet, Sophie, Bertrand Isidor, Benjamin Cogné, et al.. (2021). MAN1B1-CDG: Three new individuals and associated biochemical profiles. Molecular Genetics and Metabolism Reports. 28. 100775–100775. 9 indexed citations
2.
Taillandier, A., Estelle Colin, Anya Rothenbühler, et al.. (2021). Utility of genetic testing for prenatal presentations of hypophosphatasia. Molecular Genetics and Metabolism. 132(3). 198–203. 4 indexed citations
3.
Mornet, Étienne, et al.. (2020). Hypophosphatasia: a genetic-based nosology and new insights in genotype-phenotype correlation. European Journal of Human Genetics. 29(2). 289–299. 60 indexed citations
4.
Trésallet, Christophe, Antoine Brouquet, Catherine Julié, et al.. (2011). Evaluation of predictive models in daily practice for the identification of patients with Lynch syndrome. International Journal of Cancer. 130(6). 1367–1377. 18 indexed citations
5.
Stheneur, Chantal, Gwenaëlle Collod‐Béroud, Laurence Faivre, et al.. (2009). Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene. European Journal of Human Genetics. 17(9). 1121–1128. 72 indexed citations
6.
Boumendil, Ariane, et al.. (2008). Maternal complication of pregnancy in Marfan syndrome. International Journal of Cardiology. 136(2). 156–161. 65 indexed citations
7.
Julié, Catherine, Christophe Trésallet, Antoine Brouquet, et al.. (2008). Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based ApproachVersusMolecular Screening. The American Journal of Gastroenterology. 103(11). 2825–2835. 89 indexed citations
8.
Moura, Bertrand, Florence Tubach, Cathérine Boileau, et al.. (2006). Densité minérale osseuse et syndrome de Marfan. Étude comparée de 130 patients et comparaison avec une série témoin. Revue du Rhumatisme. 73(12). 1405–1408.
9.
Moura, Bertrand, Florence Tubach, Cathérine Boileau, et al.. (2006). Bone mineral density in Marfan syndrome. A large case-control study. Joint Bone Spine. 73(6). 733–735. 37 indexed citations
10.
Karoui, Mehdi, Christophe Trésallet, C. Julié, et al.. (2004). Loss of heterozygosity on 10q and mutational status of PTEN and BMPR1A in colorectal primary tumours and metastases. British Journal of Cancer. 90(6). 1230–1234. 20 indexed citations
11.
Simon‐Bouy, Brigitte, M Plachot, Ali H. Mokdad, et al.. (2004). Diagnostic prénatal d’une probable chimère humaine après fécondation in vitro. Gynécologie Obstétrique & Fertilité. 32(2). 143–146. 1 indexed citations
12.
Jondeau, Guillaume, Cathérine Boileau, Bertrand Chevallier, et al.. (2003). Le syndrome de Marfan. Sang thrombose vaisseaux. 15(2). 110–115. 1 indexed citations
13.
Simon‐Bouy, Brigitte, M Plachot, Ali H. Mokdad, et al.. (2003). Possible human chimera detected prenatally after in vitro fertilization: a case report. Prenatal Diagnosis. 23(11). 935–937. 10 indexed citations
14.
Jean, M. De Saint, Cathérine Boileau, Bertrand Chevallier, et al.. (2003). Marfan Syndrome Diagnosis by Ophthalmologist. Predictive Value of Ectopia Lentis in a Genotyped Population. Investigative Ophthalmology & Visual Science. 44(13). 813–813. 3 indexed citations
15.
Jondeau, Guillaume, Christine Muti, & Cathérine Boileau. (2003). [Aortic aneurysms excluding Marfan's syndrome].. PubMed. 96(11). 1074–80. 3 indexed citations
16.
Plachot, M, et al.. (2002). Possible human chimera detected prenatally after in vitro fertilization: A case report. Fertility and Sterility. 78. S146–S146. 2 indexed citations
17.
Tubach, Florence, et al.. (2000). Marfan syndrome and fibrillin disorders.. PubMed. 67(5). 401–7. 12 indexed citations
18.
Parc, Jean‐Marie Le, Florence Tubach, Cathérine Boileau, et al.. (2000). Le syndrome de Marfan et les fibrillinopathies. Revue du Rhumatisme. 67(8). 613–620. 2 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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