M. des Georges

432 total citations
13 papers, 150 citations indexed

About

M. des Georges is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Surgery. According to data from OpenAlex, M. des Georges has authored 13 papers receiving a total of 150 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pulmonary and Respiratory Medicine, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in M. des Georges's work include Cystic Fibrosis Research Advances (6 papers), Neonatal Respiratory Health Research (4 papers) and Prenatal Screening and Diagnostics (2 papers). M. des Georges is often cited by papers focused on Cystic Fibrosis Research Advances (6 papers), Neonatal Respiratory Health Research (4 papers) and Prenatal Screening and Diagnostics (2 papers). M. des Georges collaborates with scholars based in France, Belgium and Réunion. M. des Georges's co-authors include Mireille Claustres, Caroline Guittard, O. Malard, F. Espitalier, Claude Szpirer, S. Swillens, Brigitte Dréno, Gilbert Vassart, Marjolaine Willems and Anne Girardet and has published in prestigious journals such as Thorax, Genomics and Journal of Medical Genetics.

In The Last Decade

M. des Georges

12 papers receiving 148 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. des Georges France	6	86	31	23	22	18	13	150
Phil Bergman Australia	6	31 0.4×	29 0.9×	13 0.6×	8 0.4×	20 1.1×	13	118
M. G. Benetazzo Italy	4	196 2.3×	24 0.8×	11 0.5×	13 0.6×	40 2.2×	4	226
Christine Brunner Austria	8	16 0.2×	20 0.6×	9 0.4×	59 2.7×	51 2.8×	26	143
Nita Patel United States	5	36 0.4×	37 1.2×	8 0.3×	5 0.2×	13 0.7×	9	227
K Tajima Japan	7	72 0.8×	49 1.6×	3 0.1×	13 0.6×	11 0.6×	13	188
Priyanka Ahimaz United States	7	23 0.3×	44 1.4×	10 0.4×	32 1.5×	18 1.0×	14	133
M. De Arce Ireland	7	45 0.5×	36 1.2×	16 0.7×	4 0.2×	25 1.4×	7	181
Amy Shikany United States	10	74 0.9×	115 3.7×	13 0.6×	11 0.5×	45 2.5×	26	255
María Elena Mateos Spain	7	11 0.1×	27 0.9×	24 1.0×	14 0.6×	11 0.6×	16	126
Shiyi Yin United States	10	99 1.2×	135 4.4×	6 0.3×	11 0.5×	16 0.9×	13	234

Countries citing papers authored by M. des Georges

Since Specialization

Citations

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

Fields of papers citing papers by M. des Georges

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. des Georges

This figure shows the co-authorship network connecting the top 25 collaborators of M. des Georges. A scholar is included among the top collaborators of M. des Georges 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. des Georges. M. des Georges 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:

13 of 13 papers shown

Georges, M. des, et al.. (2017). Sinonasal mucosal melanoma: A 44-case study and literature analysis. European Annals of Otorhinolaryngology Head and Neck Diseases. 134(4). 237–242. 27 indexed citations

Girardet, Anne, Marjolaine Willems, Christine Coubes, et al.. (2014). Preimplantation genetic diagnosis for cystic fibrosis: the Montpellier center's 10‐year experience. Clinical Genetics. 87(2). 124–132. 22 indexed citations

Guittard, Caroline, et al.. (2010). Variants in CFTR untranslated regions are associated with congenital bilateral absence of the vas deferens. Journal of Medical Genetics. 48(3). 152–159. 19 indexed citations

Sermet‐Gaudelus, Isabelle, Delphine Roussel, S. Bui, et al.. (2010). Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis. Thorax. 65(6). 539–544. 37 indexed citations

Humbertclaude, Véronique, Sylvie Tuffery‐Giraud, Corinne Bareil, et al.. (2009). Banques de données de mutations : enjeux et perspectives pour les maladies génétiques orphelines. Pathologie Biologie. 58(5). 387–395.

Libioulle, Cécile, et al.. (2009). [Genomics of inflammatory bowel diseases: basis for a new molecular classification and new therapeutic strategies of these diseases].. PubMed. 64 Spec No. 24–8. 1 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

Buys, Nadine, et al.. (2006). Effect of the IGF2-intron3-G3072A mutation on prolificacy in sows.. Proceedings of the 8th World Congress on Genetics Applied to Livestock Production, Belo Horizonte, Minas Gerais, Brazil, 13-18 August, 2006. 6–22. 6 indexed citations

Georges, M. des. (2001). Gène CFTR et infertilité masculine en 2001 Conseil génétique, diagnostic prénatal, diagnostic pré-implantatoire. Andrologie. 11(4). 204–208. 1 indexed citations

10.

Feldmann, D, et al.. (2001). [Genetic testing for cystic fibrosis: evaluation of the Elucigene CF20 kit in blood and buccal cells].. PubMed. 59(3). 277–83. 4 indexed citations

11.

Georges, M. des, Caroline Guittard, & Mireille Claustres. (1998). Les bases moléculaires de la mucoviscidose en France : plus de 300 mutations et 506 génotypes différents sont en cause.. médecine/sciences. 14(12). 1413–1413. 5 indexed citations

12.

Swillens, S., et al.. (1990). Structure, evolution and chromosomal localization of the human pregnancy-specific β1 glycoprotein gene family. Genomics. 6(4). 579–592. 22 indexed citations

13.

Georges, M. des, et al.. (1965). Aspects géographiques de l'élevage dans la zone de montagne du département des Hautes-Alpes. Études rurales. 18(1). 5–36. 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.

Explore authors with similar magnitude of impact