Isabelle Delon

2.1k total citations
18 papers, 1.3k citations indexed

About

Isabelle Delon is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Isabelle Delon has authored 18 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Isabelle Delon's work include Developmental Biology and Gene Regulation (7 papers), Cellular Mechanics and Interactions (5 papers) and Genomics and Rare Diseases (3 papers). Isabelle Delon is often cited by papers focused on Developmental Biology and Gene Regulation (7 papers), Cellular Mechanics and Interactions (5 papers) and Genomics and Rare Diseases (3 papers). Isabelle Delon collaborates with scholars based in United Kingdom, France and United States. Isabelle Delon's co-authors include François Payre, Nicholas H. Brown, David L. Stern, Élio Sucena, Jennifer Zanet, Dayalan G. Srinivasan, Alistair P. McGregor, Virginie Courtier‐Orgogozo, Hélène Chanut-Delalande and Pierre Ferrer and has published in prestigious journals such as Nature, Nature Cell Biology and Development.

In The Last Decade

Isabelle Delon

18 papers receiving 1.3k citations

Peers

Isabelle Delon

GENET

CMN

Yoshiaki Kikkawa Japan

Hans H. Epperlein Germany

Brian Biehs United States

Elizabeth H. Chen United States

Makoto Mochii Japan

Jennifer Zanet France

Susan R. Haynes United States

Silke Berger Australia

Akimasa Fukui Japan

Hiroshi Tarui Japan

Yoshiaki Kikkawa Japan

Isabelle Delon

1.1k ×1.5

683 ×1.3

GENET

342 ×1.2

100 ×0.7

CMN

95 ×0.8

Citations per year, relative to Isabelle Delon Isabelle Delon (= 1×) peers Yoshiaki Kikkawa

Countries citing papers authored by Isabelle Delon

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Delon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Delon

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

All Works

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18 of 18 papers shown

French, Courtney E., Helen Dolling, Karyn Mégy, et al.. (2022). Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood. Human Genetics and Genomics Advances. 3(3). 100113–100113. 10 indexed citations

Olszewska, Diana A., Conor Fearon, Terri McVeigh, et al.. (2021). A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene. Neurobiology of Aging. 106. 343.e1–343.e8. 6 indexed citations

Sanchis‐Juan, Alba, Courtney E. French, Isabelle Delon, et al.. (2020). Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data. Genetics in Medicine. 22(5). 945–953. 79 indexed citations

French, Courtney E., Isabelle Delon, Helen Dolling, et al.. (2019). Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children. Intensive Care Medicine. 45(5). 627–636. 149 indexed citations

French, Courtney E., Isabelle Delon, Alba Sanchis‐Juan, et al.. (2018). Whole Genome Sequence Analysis of Intensively Ill Children: A Prospective Study of Parent-Child Trios in the UK. SSRN Electronic Journal. 1 indexed citations

Hague, Jennifer, Isabelle Delon, Kim Brügger, et al.. (2017). Male child with somatic mosaic Osteopathia Striata with Cranial Sclerosis caused by a novel pathogenic AMER1 frameshift mutation. American Journal of Medical Genetics Part A. 173(7). 1931–1935. 5 indexed citations

Hague, Jennifer, Isabelle Delon, Kim Brügger, et al.. (2016). Molecularly proven mosaicism in phenotypically normal parent of a girl with Freeman–Sheldon Syndrome caused by a pathogenic MYH3 mutation. American Journal of Medical Genetics Part A. 170(6). 1608–1612. 9 indexed citations

Taylor, Amy, Isabelle Delon, Kieren Allinson, et al.. (2015). Malignant Peripheral Nerve Sheath Tumor in Cowden Syndrome. Journal of Neuropathology & Experimental Neurology. 74(4). 288–292. 4 indexed citations

Bataillé, Laetitia, Isabelle Delon, Jean Philippe Da Ponte, Nicholas H. Brown, & Krzysztof Jagla. (2010). Downstream of Identity Genes: Muscle-Type-Specific Regulation of the Fusion Process. Developmental Cell. 19(2). 317–328. 41 indexed citations

10.

Delon, Isabelle & Nicholas H. Brown. (2009). The integrin adhesion complex changes its composition and function during morphogenesis of an epithelium. Journal of Cell Science. 122(23). 4363–4374. 56 indexed citations

11.

McGregor, Alistair P., Virginie Courtier‐Orgogozo, Isabelle Delon, et al.. (2007). Morphological evolution through multiple cis-regulatory mutations at a single gene. Nature. 448(7153). 587–590. 234 indexed citations

12.

Delon, Isabelle & Nicholas H. Brown. (2006). Integrins and the actin cytoskeleton. Current Opinion in Cell Biology. 19(1). 43–50. 177 indexed citations

13.

Delon, Isabelle & François Payre. (2004). Evolution of larval morphology in flies: get in shape with shavenbaby. Trends in Genetics. 20(7). 305–313. 32 indexed citations

14.

Sucena, Élio, et al.. (2003). Regulatory evolution of shavenbaby/ovo underlies multiple cases of morphological parallelism. Nature. 424(6951). 935–938. 171 indexed citations

15.

Delon, Isabelle, Hélène Chanut-Delalande, & François Payre. (2003). The Ovo/Shavenbaby transcription factor specifies actin remodelling during epidermal differentiation in Drosophila. Mechanisms of Development. 120(7). 747–758. 74 indexed citations

16.

Polesello, Cédric, Isabelle Delon, Philippe Valenti, Pierre Ferrer, & François Payre. (2002). Dmoesin controls actin-based cell shape and polarity during Drosophila melanogaster oogenesis. Nature Cell Biology. 4(10). 782–789. 116 indexed citations

17.

Cornet, François, et al.. (2000). Functional polarization of the Escherichia coli chromosome terminus: the dif site acts in chromosome dimer resolution only when located between long stretches of opposite polarity. Molecular Microbiology. 36(1). 33–43. 82 indexed citations

18.

Delon, Isabelle, Jining Lü, Maryvonne Mével-Ninio, et al.. (2000). OVO transcription factors function antagonistically in the Drosophila female germline. Development. 127(4). 881–892. 58 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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