Marie Desgeorges

1.1k total citations
27 papers, 574 citations indexed

About

Marie Desgeorges is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Marie Desgeorges has authored 27 papers receiving a total of 574 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Pulmonary and Respiratory Medicine, 13 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in Marie Desgeorges's work include Cystic Fibrosis Research Advances (25 papers), Congenital Ear and Nasal Anomalies (13 papers) and Neonatal Respiratory Health Research (10 papers). Marie Desgeorges is often cited by papers focused on Cystic Fibrosis Research Advances (25 papers), Congenital Ear and Nasal Anomalies (13 papers) and Neonatal Respiratory Health Research (10 papers). Marie Desgeorges collaborates with scholars based in France, United States and South Africa. Marie Desgeorges's co-authors include Mireille Claustres, Jacques Demaille, Caroline Guittard, Muriel Giansily, H Navratil, P. Costa, Michèle Ramsay, A Goldman, Marie‐Catherine Romey and André Mégarbané and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Human Molecular Genetics and Genomics.

In The Last Decade

Marie Desgeorges

26 papers receiving 559 citations

Peers

Marie Desgeorges
Caroline Guittard France
Angeliki Balassopoulou Greece
Н.В. Петрова Russia
M Keston United Kingdom
V. Faà Italy
Ana Grangeia Portugal
G R Jalali United Kingdom
Susan Marelli Italy
Licia Turolla Italy
JA Goodship United Kingdom
Caroline Guittard France
Marie Desgeorges
Citations per year, relative to Marie Desgeorges Marie Desgeorges (= 1×) peers Caroline Guittard

Countries citing papers authored by Marie Desgeorges

Since Specialization
Citations

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

Fields of papers citing papers by Marie Desgeorges

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie Desgeorges

This figure shows the co-authorship network connecting the top 25 collaborators of Marie Desgeorges. A scholar is included among the top collaborators of Marie Desgeorges 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 Marie Desgeorges. Marie Desgeorges 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.
Munck, À., Virginie Scotet, Mireille Claustres, et al.. (2014). Comprehensive CFTR gene analysis of the French cystic fibrosis screened newborn cohort: implications for diagnosis, genetic counseling, and mutation-specific therapy. Genetics in Medicine. 17(2). 108–116. 33 indexed citations
2.
Guittard, Caroline, et al.. (2007). First functional polymorphism in CFTR promoter that results in decreased transcriptional activity and Sp1/USF binding. Biochemical and Biophysical Research Communications. 361(3). 775–781. 18 indexed citations
3.
4.
Desgeorges, Marie, André Mégarbané, Caroline Guittard, et al.. (1997). Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities. Human Genetics. 100(2). 279–283. 51 indexed citations
5.
Rodier, M., Marie Desgeorges, & Mireille Claustres. (1997). Hypokaliémie d'effort à la chaleur secondaire à une mucoviscidose atypique de révélation tardive. Science & Sports. 12(3). 214–216.
6.
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
7.
Romey, Marie‐Catherine, Sylvie Tuffery‐Giraud, Marie Desgeorges, et al.. (1996). Transcript analysis of CFTR frameshift mutations in lymphocytes using the reverse transcription-polymerase chain reaction technique and the protein truncation test. Human Genetics. 98(3). 328–332. 14 indexed citations
8.
Desgeorges, Marie, A Goldman, Rochelle Thiart, et al.. (1996). First report of CFTR mutations in black cystic fibrosis patients of southern African origin.. Journal of Medical Genetics. 33(9). 802–804. 34 indexed citations
9.
Desgeorges, Marie, Michel Rodier, Michel Piot, Jacques Demaille, & Mireille Claustres. (1995). Four adult patients with the missense mutation L206W and a mild cystic fibrosis phenotype. Human Genetics. 96(6). 717–720. 13 indexed citations
10.
Romey, Marie‐Catherine, et al.. (1995). Novel missense mutation in the first transmembrane segment of the CFTR gene (Q98R) identified in a male adult. Human Mutation. 6(2). 190–191. 9 indexed citations
11.
12.
Desgeorges, Marie, et al.. (1994). A novel splice site mutation in the first exon of the cystic fibrosis transmembrane regulator (CFTR) gene identified in a CBAVD patient. Human Molecular Genetics. 3(2). 369–370. 6 indexed citations
13.
Romey, Marie‐Catherine, et al.. (1994). Homozygosity for a novel missense mutation (1175V) in exon 5 of the CFTR gene in a family of Armenian descent. Human Molecular Genetics. 3(4). 661–662. 4 indexed citations
14.
15.
Claustres, Mireille, et al.. (1993). Analysis of the 27 exons and flanking regions of the cystic fibrosis gene: 40 different mutations account for 91.2% of the mutant alleles in Southern France. Human Molecular Genetics. 2(8). 1209–1213. 80 indexed citations
16.
Claustres, Mireille, et al.. (1992). Analysis of 30 known cystic fibrosis mutations: 10 mutations account for 27% of non-?F508 chromosomes in Southern France. Human Genetics. 90(4). 464–6. 4 indexed citations
17.
Claustres, Mireille, Bernard Gerrard, Marga Belle White, et al.. (1992). A new mutation (1078delT) in exon 7 of the CFTR gene in a southern French adult with cystic fibrosis. Genomics. 13(3). 907–908. 20 indexed citations
18.
Claustres, Mireille, et al.. (1990). Cystic fibrosis typing with DNA probes and screening for ΔF508 deletion in families from Southern France. Human Genetics. 85(4). 398–399. 3 indexed citations
19.
Claustres, Mireille, et al.. (1990). Germinal mosaicism from grand-paternal origin in a family with Duchenne muscular dystrophy. Human Genetics. 86(2). 241–3. 14 indexed citations
20.
Claustres, Mireille, et al.. (1990). Identification of carriers by screening for delta F508 deletion in a multi-generation cystic fibrosis family.. PubMed. 1(3-4). 211–7. 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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