M. Claustres

1.7k total citations · 1 hit paper
18 papers, 1.0k citations indexed

About

M. Claustres is a scholar working on Molecular Biology, Hematology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, M. Claustres has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Hematology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in M. Claustres's work include Cystic Fibrosis Research Advances (4 papers), Hemophilia Treatment and Research (3 papers) and Muscle Physiology and Disorders (2 papers). M. Claustres is often cited by papers focused on Cystic Fibrosis Research Advances (4 papers), Hemophilia Treatment and Research (3 papers) and Muscle Physiology and Disorders (2 papers). M. Claustres collaborates with scholars based in France, Spain and Croatia. M. Claustres's co-authors include Miguel Chillón, Willy Lissens, C. Verlingue, Bernard Mercier, Lluís Bassas, S. Silber, Teresa Casals, Marie‐Catherine Romey, Thierry Soussi and Chikashi Ishioka and has published in prestigious journals such as New England Journal of Medicine, Nature reviews. Cancer and Thrombosis and Haemostasis.

In The Last Decade

M. Claustres

16 papers receiving 974 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

1995 680 citations Miguel Chillón, Teresa Casals et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Claustres France	9	517	308	227	125	115	18	1.0k
P Malet France	15	92 0.2×	336 1.1×	214 0.9×	51 0.4×	119 1.0×	65	768
Tahsin Yakut Türkiye	15	72 0.1×	315 1.0×	191 0.8×	83 0.7×	174 1.5×	78	762
Sevilhan Artan Türkiye	18	75 0.1×	308 1.0×	187 0.8×	156 1.2×	104 0.9×	84	760
Jason D. Engel United States	18	324 0.6×	718 2.3×	130 0.6×	80 0.6×	86 0.7×	39	1.5k
G. Kohnen United Kingdom	15	126 0.2×	288 0.9×	61 0.3×	138 1.1×	491 4.3×	26	1.2k
Hanne Rose Denmark	14	109 0.2×	318 1.0×	480 2.1×	38 0.3×	178 1.5×	30	900
Valentina Fiano Italy	18	206 0.4×	555 1.8×	50 0.2×	112 0.9×	34 0.3×	47	971
Yiming Xing United States	16	500 1.0×	564 1.8×	122 0.5×	33 0.3×	36 0.3×	30	978
Lesa Nelson United States	17	144 0.3×	205 0.7×	247 1.1×	127 1.0×	226 2.0×	31	1.3k
Patricia A. Aronin United States	13	210 0.4×	133 0.4×	38 0.2×	271 2.2×	69 0.6×	25	733

Countries citing papers authored by M. Claustres

Since Specialization

Citations

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

Fields of papers citing papers by M. Claustres

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Claustres

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

All Works

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18 of 18 papers shown

Tapon‐Bretaudière, Jacqueline, et al.. (2012). Lethal factor VII deficiency due to novel mutations in the F7 promoter: Functional analysis reveals disruption of HNF4 binding site. Thrombosis and Haemostasis. 108(8). 277–283. 6 indexed citations

Barat‐Houari, Mouna, Karine Nguyen, Rafaëlle Bernard, et al.. (2009). New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?. European Journal of Human Genetics. 18(5). 533–538. 11 indexed citations

Romey, Marie‐Catherine, et al.. (2008). Direct carrier testing of haemophilia B by SSCP. Clinical & Laboratory Haematology. 16(1). 15–20.

Girodon, E., et al.. (2008). Occurrence of CFTR de novo mutations is not so rare. Journal of Cystic Fibrosis. 7. S6–S6. 4 indexed citations

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

Guittard, Caroline, et al.. (2007). 359 Negative genetic neonatal screening for cystic fibrosis caused by compound heterozygosity for two large CFTR rearrangements. Journal of Cystic Fibrosis. 6. S88–S88. 4 indexed citations

Soussi, Thierry, Chikashi Ishioka, M. Claustres, & Christophe Béroud. (2006). Locus-specific mutation databases: pitfalls and good practice based on the p53 experience. Nature reviews. Cancer. 6(1). 83–90. 102 indexed citations

Guittard, Caroline, B Arnaud, Jacques Demaille, et al.. (2000). BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.. PubMed. 41(6). 1302–8. 78 indexed citations

Griffoin, Jean‐Michel, Corinne Bareil, Sarah Bonnet, et al.. (2000). [Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes].. Journal Français d Ophtalmologie. 23(10). 985–95. 18 indexed citations

10.

Tuffery‐Giraud, Sylvie, et al.. (1999). Point mutations in the dystrophin gene: Evidence for frequent use of cryptic splice sites as a result of splicing defects. Human Mutation. 14(5). 359–368. 43 indexed citations

11.

Girardet, Anne, et al.. (1998). [Retinoblastoma: importance of genetic counseling].. PubMed. 21(4). 295–301. 2 indexed citations

12.

Biron, Christine A., et al.. (1997). Diagnosis strategies in activated protein C resistance: is genotyping still necessary?. Clinical & Laboratory Haematology. 19(1). 67–71. 9 indexed citations

13.

Hamel, Christian, et al.. (1997). An exonic polymorphism (381A/G) in the choroideremia gene.. PubMed. 8(3). 223–5. 1 indexed citations

14.

Claustres, M., Marie Desgeorges, Philippe Le Moine, Núria Morral, & Xavier Estivill. (1996). CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern France. Human Genetics. 98(3). 336–344. 25 indexed citations

15.

Girardet, Anne, M. Claustres, & Franck Pellestor. (1996). Typage génique des spermatozoïdes : application à l'étude du génome. médecine/sciences. 12(12). 1389–1389.

16.

Chillón, Miguel, Teresa Casals, Bernard Mercier, et al.. (1995). Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens. New England Journal of Medicine. 332(22). 1475–1480. 680 indexed citations breakdown →

17.

Aguilar‐Martinez, Patricia, Nelly Fabre, Robert Navarro, et al.. (1993). DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory.. PubMed. 4(4). 311–9. 1 indexed citations

18.

Claustres, M., et al.. (1984). [Ferritin and breast cancer].. PubMed. 32(4). 265–8. 1 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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