D Feldmann

1.2k total citations
35 papers, 570 citations indexed

About

D Feldmann is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Sensory Systems. According to data from OpenAlex, D Feldmann has authored 35 papers receiving a total of 570 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pulmonary and Respiratory Medicine, 6 papers in Molecular Biology and 5 papers in Sensory Systems. Recurrent topics in D Feldmann's work include Neonatal Respiratory Health Research (10 papers), Cystic Fibrosis Research Advances (8 papers) and Hearing, Cochlea, Tinnitus, Genetics (5 papers). D Feldmann is often cited by papers focused on Neonatal Respiratory Health Research (10 papers), Cystic Fibrosis Research Advances (8 papers) and Hearing, Cochlea, Tinnitus, Genetics (5 papers). D Feldmann collaborates with scholars based in France, Morocco and Switzerland. D Feldmann's co-authors include Laurence Jonard, Sandrine Marlin, A. Clément, Françoise Denoyelle, R. Couderc, Ralph Epaud, J. de Blic, Florence Flamein, Rola Abou Taam and Isabelle Roux and has published in prestigious journals such as Biochemistry, Journal of the American Society of Nephrology and Clinical Chemistry.

In The Last Decade

D Feldmann

35 papers receiving 545 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D Feldmann France 13 245 160 158 95 74 35 570
Nadia Cerutti Italy 12 36 0.1× 137 0.9× 118 0.7× 39 0.4× 11 0.1× 23 425
Yüksel Olgun Türkiye 12 39 0.2× 126 0.8× 47 0.3× 57 0.6× 59 0.8× 48 340
Min‐Jee Kim South Korea 10 26 0.1× 11 0.1× 78 0.5× 29 0.3× 60 0.8× 43 308
Joanne Grimmer Canada 6 55 0.2× 31 0.2× 281 1.8× 15 0.2× 19 0.3× 11 468
Manfred Kurjak Germany 11 101 0.4× 22 0.1× 109 0.7× 170 1.8× 19 0.3× 21 462
Ann M. Sherry United States 10 103 0.4× 51 0.3× 385 2.4× 130 1.4× 3 0.0× 10 578
Ariel Go United States 8 42 0.2× 29 0.2× 41 0.3× 99 1.0× 20 0.3× 9 293
Ryuji Tamura Japan 11 26 0.1× 31 0.2× 102 0.6× 63 0.7× 12 0.2× 28 361

Countries citing papers authored by D Feldmann

Since Specialization
Citations

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

Fields of papers citing papers by D Feldmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D Feldmann

This figure shows the co-authorship network connecting the top 25 collaborators of D Feldmann. A scholar is included among the top collaborators of D Feldmann 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 D Feldmann. D Feldmann 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.
Sermet‐Gaudelus, Isabelle, et al.. (2010). Recommandations françaises pour la réalisation et l’interprétation du test de la sueur dans le cadre du dépistage néonatal de la mucoviscidose. Archives de Pédiatrie. 17(9). 1349–1358. 18 indexed citations
2.
Thouvenin, Guillaume, Rola Abou Taam, Florence Flamein, et al.. (2010). Characteristics of disorders associated with genetic mutations of surfactant protein C. Archives of Disease in Childhood. 95(6). 449–454. 73 indexed citations
3.
Sbidian, É., D Feldmann, Sylvie Fraitag, et al.. (2010). Germline mosaicism in keratitis–ichthyosis–deafness syndrome: pre‐natal diagnosis in a familial lethal form. Clinical Genetics. 77(6). 587–592. 35 indexed citations
4.
Epaud, Ralph, S. Emond, Aurore Coulomb, et al.. (2010). Surfactant protein C gene (SFTPC) mutation‐associated lung disease: High‐resolution computed tomography (HRCT) findings and its relation to histological analysis. Pediatric Pulmonology. 45(10). 1021–1029. 37 indexed citations
5.
Nguyen‐Khoa, Thao, et al.. (2008). [Sweat testing: review of technical requirements].. PubMed. 66(2). 221–7. 3 indexed citations
6.
Epaud, Ralph, D Feldmann, Loïc Guillot, & A. Clément. (2008). Pathologies respiratoires associées à des anomalies héréditaires du métabolisme du surfactant. Archives de Pédiatrie. 15(10). 1560–1567. 5 indexed citations
7.
Ratbi, Ilham, et al.. (2007). La mutation 35delG du gène de la connexine 26, une cause fréquente des surdités non syndromiques autosomiques récessives au Maroc. Archives de Pédiatrie. 14(5). 450–453. 4 indexed citations
8.
Loundon, Natalie, Isabelle Roux, Isabelle Rouillon, et al.. (2005). Auditory Neuropathy or Endocochlear Hearing Loss?. Otology & Neurotology. 26(4). 748–754. 30 indexed citations
9.
Feldmann, D. (2003). [The French neonatal screening of cystic fibrosis].. PubMed. 60(6). 693–5. 2 indexed citations
10.
Feldmann, D. (2002). Mucoviscidose : un dépistage pour toute la France. Annales de biologie clinique. 60(6). 5 indexed citations
11.
Deschênes, Georges, D Feldmann, & Alain Doucet. (2002). Altérations moléculaires primaires et troubles biologiques secondaires des syndromes de Bartter et de Gitelman. Archives de Pédiatrie. 9(4). 406–416. 5 indexed citations
12.
Feldmann, D, et al.. (2001). A novel nonsense mutation (Q1291X) in exon 20 of CFTR (ABCC7) gene. Human Mutation. 17(4). 356–356. 3 indexed citations
13.
Tredano, Mohammed, Patrick Truffert, F. Capron, et al.. (2000). Déficit constitutionnel en protéine B du surfactant pulmonaire: présentation clinique, diagnostic histologique et moléculaire. Archives de Pédiatrie. 7(6). 641–644. 3 indexed citations
14.
Bienvenu, Thierry, Simon M. Bousquet, Serge Chirón, et al.. (1999). [Different procedures for the isolation of DNA from blood samples].. PubMed. 57(1). 77–84. 5 indexed citations
15.
Feldmann, D, et al.. (1995). Mild course of cystic fibrosis in an adult with the D1152H mutation. Clinical Chemistry. 41(11). 1675–1675. 13 indexed citations
16.
Feldmann, D, Jean‐Michel Rozet, Anna Pelet, et al.. (1992). Site specific screening for point mutations in ornithine transcarbamylase deficiency.. PubMed. 29(7). 471–5. 9 indexed citations
17.
Lamour, Christian, et al.. (1991). [Early tubular involvements in lead poisoning in children].. PubMed. 48(10). 685–9. 4 indexed citations
18.
Feldmann, D, et al.. (1989). [Evaluation of enzymuria as a tracer in nephrotoxicity: results of a multicenter study].. PubMed. 47(6). 340–5. 1 indexed citations
19.
Feldmann, D, et al.. (1982). [Assay of total serum bile acids. Reference values in children].. PubMed. 40(3). 181–5. 3 indexed citations
20.
Wolff, Manfred E., et al.. (1975). Steroidal 21-diazo ketones. Photogenerated corticosteroid receptor labels. Biochemistry. 14(8). 1750–1759. 19 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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