Delphine Feldmann

3.7k total citations
27 papers, 1.3k citations indexed

About

Delphine Feldmann is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Sensory Systems. According to data from OpenAlex, Delphine Feldmann has authored 27 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Pulmonary and Respiratory Medicine and 4 papers in Sensory Systems. Recurrent topics in Delphine Feldmann's work include Neonatal Respiratory Health Research (7 papers), Cystic Fibrosis Research Advances (7 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Delphine Feldmann is often cited by papers focused on Neonatal Respiratory Health Research (7 papers), Cystic Fibrosis Research Advances (7 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Delphine Feldmann collaborates with scholars based in France, Germany and Netherlands. Delphine Feldmann's co-authors include Friedhelm Hildebrandt, Corinne Antignac, Martin Vollmer, Martin Konrad, Nine V.A.M. Knoers, Lisa M. Guay‐Woodford, Sandrine Marlin, Henny H. Lemmink, Lambertus P. van den Heuvel and Rémy Couderc and has published in prestigious journals such as Nature Genetics, Hepatology and Biochemical and Biophysical Research Communications.

In The Last Decade

Delphine Feldmann

25 papers receiving 1.3k citations

Peers

Delphine Feldmann

PRM

NEPHR

Ferry F.J. Kersten Netherlands

Qiusheng Tong United States

Lynne H. Liu United States

Amy J. Pace United States

Sunita Trivedi United States

Kotaro Oshio Japan

Srisaila Basavappa United States

Simon Bulley United States

Jonathan Neumann United States

Lama Al‐Qusairi United States

Ferry F.J. Kersten Netherlands

Delphine Feldmann

811 ×0.9

126 ×0.3

PRM

416 ×1.6

315 ×1.6

172 ×1.1

NEPHR

Citations per year, relative to Delphine Feldmann Delphine Feldmann (= 1×) peers Ferry F.J. Kersten

Countries citing papers authored by Delphine Feldmann

Since Specialization

Citations

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

Fields of papers citing papers by Delphine Feldmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Delphine Feldmann

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

All Works

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20 of 20 papers shown

Bouyacoub, Yosra, Lilia Romdhane, Rym Kéfi, et al.. (2013). Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss. Gene. 525(1). 1–4. 27 indexed citations

Cortés, Nicolás Gutiérrez, Elodie Dumon, Étienne Hébert-Chatelain, et al.. (2012). Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss. Human Mutation. 33(4). 681–689. 32 indexed citations

René, Céline, Damien Paulet, Emmanuelle Girodon, et al.. (2010). p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study. European Journal of Human Genetics. 19(1). 36–42. 5 indexed citations

Guillot, Loïc, Aurore Carré, Gabor Szinnai, et al.. (2009). NKX2-1mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in “Brain-Lung-Thyroid Syndrome”. Human Mutation. 31(2). E1146–E1162. 80 indexed citations

Taam, Rola Abou, Francis Jaubert, S. Emond, et al.. (2009). Familial interstitial disease with I73T mutation: A mid‐ and long‐term study. Pediatric Pulmonology. 44(2). 167–175. 53 indexed citations

Pierron, Denis, Christophe Rocher, Pascal Reynier, et al.. (2008). New evidence of a mitochondrial genetic background paradox: Impact of the J haplogroup on the A3243G mutation. BMC Medical Genetics. 9(1). 41–41. 24 indexed citations

Feldmann, Delphine, Cédric Le Maréchal, Laurence Jonard, et al.. (2008). A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss. European Journal of Medical Genetics. 52(4). 195–200. 38 indexed citations

Jonard, Laurence, Delphine Feldmann, Martine Sinico, et al.. (2007). A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E. European Journal of Medical Genetics. 51(1). 35–43. 49 indexed citations

Feldmann, Delphine, Françoise Denoyelle, Natalie Loundon, et al.. (2003). Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene. European Journal of Human Genetics. 12(4). 279–284. 40 indexed citations

10.

Feldmann, Delphine, Rémy Couderc, Marie‐Pierre Audrézet, et al.. (2003). CFTR genotypes in patients with normal or borderline sweat chloride levels. Human Mutation. 22(4). 340–340. 59 indexed citations

11.

Houdayer, Claude, Thierry Billette de Villemeur, Michel Bahuau, et al.. (2002). Simple Fluorescent PCR Assay for Discriminating FRAXA Fully Mutated Females from Normal Homozygotes. Genetic Testing. 6(2). 135–139. 7 indexed citations

12.

Chapiro, Élise, Delphine Feldmann, Françoise Denoyelle, et al.. (2002). Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor. European Journal of Human Genetics. 10(12). 851–856. 47 indexed citations

13.

Birkenhäger, Ralf, Edgar A. Otto, Martin Vollmer, et al.. (2001). Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nature Genetics. 29(3). 310–314. 377 indexed citations

14.

Konrad, Martin, Martin Vollmer, Henny H. Lemmink, et al.. (2000). Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome. Journal of the American Society of Nephrology. 11(8). 1449–1459. 221 indexed citations

15.

Feldmann, Delphine, et al.. (2000). A new case of alpha-1-antitrypsin frameshift mutation (1123insT) causing severe deficiency and emphysema. Human Mutation. 16(5). 447–447.

16.

Feldmann, Delphine, et al.. (2000). Genotype Analysis and Phenotypic Manifestations of Children With Intermediate Sweat Chloride Test Results. CHEST Journal. 118(6). 1591–1597. 24 indexed citations

17.

Vollmer, Martin, Nikola Jeck, Henny H. Lemmink, et al.. (2000). Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31. Nephrology Dialysis Transplantation. 15(7). 970–974. 18 indexed citations

18.

Houdayer, Claude, Alban Le Monnier, Marion Gérard, et al.. (1999). Improved Fluorescent PCR-Based Assay for Sizing CGG Repeats at the FRAXA Locus. Clinical Chemistry and Laboratory Medicine (CCLM). 37(4). 397–402. 18 indexed citations

19.

Vargas‐Poussou, Rosa, Delphine Feldmann, Martin Vollmer, et al.. (1998). Novel Molecular Variants of the Na-K-2Cl Cotransporter Gene Are Responsible for Antenatal Bartter Syndrome. The American Journal of Human Genetics. 62(6). 1332–1340. 119 indexed citations

20.

Feldmann, Delphine, et al.. (1998). Identification of three novel mutations in the CFTR gene, R117P, ΔD192, and 3121-1G→A in four French patients. Human Mutation. 11(S1). S78–S80. 3 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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