Delphine Trochet

2.8k total citations · 1 hit paper
26 papers, 2.0k citations indexed

About

Delphine Trochet is a scholar working on Endocrine and Autonomic Systems, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Delphine Trochet has authored 26 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Endocrine and Autonomic Systems, 12 papers in Pulmonary and Respiratory Medicine and 9 papers in Molecular Biology. Recurrent topics in Delphine Trochet's work include Neuroscience of respiration and sleep (15 papers), Neonatal Respiratory Health Research (12 papers) and Congenital Diaphragmatic Hernia Studies (7 papers). Delphine Trochet is often cited by papers focused on Neuroscience of respiration and sleep (15 papers), Neonatal Respiratory Health Research (12 papers) and Congenital Diaphragmatic Hernia Studies (7 papers). Delphine Trochet collaborates with scholars based in France, United States and United Kingdom. Delphine Trochet's co-authors include Jeanne Amiel, Stanislas Lyonnet, Arnold Münnich, Loïc de Pontual, Ha Trang, Claude Gaultier, Béatrice Laudier, Jean‐François Brunet, Christo Goridis and Tania Attié‐Bitach and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Delphine Trochet

25 papers receiving 2.0k 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.

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

2003 619 citations Jeanne Amiel, Béatrice Laudier et al. Nature Genetics profile →

Peers

Delphine Trochet

EAS

PRM

SURGE

NEURO

Béatrice Laudier France

Jeff M. Milunsky United States

Lorraine A. Everett United States

U. Schrell Germany

Kristina Törnqvist Sweden

Duncan Morhardt United States

Lucia Ştefăneanu Canada

Manuel E. Velasco United States

Sharon Key United States

Pamela S. Hunt United States

Béatrice Laudier France

Delphine Trochet

614 ×0.5

EAS

425 ×0.5

PRM

559 ×0.9

219 ×0.5

SURGE

105 ×0.3

NEURO

Citations per year, relative to Delphine Trochet Delphine Trochet (= 1×) peers Béatrice Laudier

Countries citing papers authored by Delphine Trochet

Since Specialization

Citations

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

Fields of papers citing papers by Delphine Trochet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Delphine Trochet

This figure shows the co-authorship network connecting the top 25 collaborators of Delphine Trochet. A scholar is included among the top collaborators of Delphine Trochet 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 Trochet. Delphine Trochet 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

Pinzón, Natalia, et al.. (2025). Allele-specific RNAi therapy corrects an extracellular matrix defect in Schuurs-Hoeijmakers syndrome. The American Journal of Human Genetics. 112(10). 2440–2457.

Trochet, Delphine, Bernard Prudhon, Maud Beuvin, et al.. (2022). Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy. Molecular Therapy — Nucleic Acids. 27. 1179–1190. 2 indexed citations

Prudhon, Bernard, et al.. (2022). Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations. Molecular Therapy — Nucleic Acids. 29. 733–748. 6 indexed citations

Trochet, Delphine & Marc Bitoun. (2021). A review of Dynamin 2 involvement in cancers highlights a promising therapeutic target. Journal of Experimental & Clinical Cancer Research. 40(1). 238–238. 27 indexed citations

Szentesi, Péter, Bruno Allard, Delphine Trochet, et al.. (2017). Impaired excitation–contraction coupling in muscle fibres from the dynamin2^R465W mouse model of centronuclear myopathy. The Journal of Physiology. 595(24). 7369–7382. 19 indexed citations

Trochet, Delphine, Bernard Prudhon, Maud Beuvin, et al.. (2017). Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy. EMBO Molecular Medicine. 10(2). 239–253. 43 indexed citations

Trochet, Delphine, Bernard Prudhon, Arnaud Jollet, Stéphanie Lorain, & Marc Bitoun. (2016). Reprogramming the Dynamin 2 mRNA by Spliceosome-mediated RNA Trans-splicing. Molecular Therapy — Nucleic Acids. 5(9). e362–e362. 10 indexed citations

Trochet, Delphine, Ivana Ivković, Michèle Gerbault‐Seureau, et al.. (2015). Telomere regulation during ageing and tumorigenesis of the grey mouse lemur. Biochimie. 113. 100–110. 6 indexed citations

Trochet, Delphine, Bernard Prudhon, Stéphane Vassilopoulos, & Marc Bitoun. (2015). Therapy for Dominant Inherited Diseases by Allele-Specific RNA Interference: Successes and Pitfalls. Current Gene Therapy. 15(5). 503–510. 23 indexed citations

10.

Nagashimada, Mayumi, Hiroshi Ohta, Chong Li, et al.. (2012). Autonomic neurocristopathy-associated mutations in PHOX2B dysregulate Sox10 expression. Journal of Clinical Investigation. 122(9). 3145–3158. 83 indexed citations

11.

Trochet, Delphine, Loïc de Pontual, Christian Straus, et al.. (2007). PHOX2B Germline and Somatic Mutations in Late-Onset Central Hypoventilation Syndrome. American Journal of Respiratory and Critical Care Medicine. 177(8). 906–911. 72 indexed citations

12.

Carré, Aurore, Mireille Castanet, Sylvia Sura‐Trueba, et al.. (2007). Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis. Human Genetics. 122(5). 467–476. 47 indexed citations

13.

Pontual, Loïc de, Anna Pelet, Mathieu Clément‐Ziza, et al.. (2007). Epistatic interactions with a common hypomorphicRET allele in syndromic Hirschsprung disease. Human Mutation. 28(8). 790–796. 57 indexed citations

14.

Lo, Ivan F. M., et al.. (2006). PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome. Chinese Medical Journal. 119(20). 1749–1752. 9 indexed citations

15.

Trochet, Delphine, Louise M. O’Brien, David Gozal, et al.. (2005). PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome. The American Journal of Human Genetics. 76(3). 421–426. 183 indexed citations

16.

Bourdeaut, Franck, Delphine Trochet, Isabelle Janoueix‐Lerosey, et al.. (2005). Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma. Cancer Letters. 228(1-2). 51–58. 57 indexed citations

17.

Trochet, Delphine, Seok Jong Hong, Jinkyu Lim, et al.. (2005). Molecular consequences of PHOX2B missense, frameshift and alanine expansion mutations leading to autonomic dysfunction. Human Molecular Genetics. 14(23). 3697–3708. 114 indexed citations

18.

Trochet, Delphine, Franck Bourdeaut, Isabelle Janoueix‐Lerosey, et al.. (2004). Germline Mutations of the Paired–Like Homeobox 2B (PHOX2B) Gene in Neuroblastoma. The American Journal of Human Genetics. 74(4). 761–764. 235 indexed citations

19.

Trang, Ha, Béatrice Laudier, Delphine Trochet, et al.. (2004). PHOX2B gene mutation in a patient with late‐onset central hypoventilation. Pediatric Pulmonology. 38(4). 349–351. 39 indexed citations

20.

Amiel, Jeanne, Béatrice Laudier, Tania Attié‐Bitach, et al.. (2003). Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nature Genetics. 33(4). 459–461. 619 indexed citations breakdown →

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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