Delphine Héron

9.4k total citations · 1 hit paper
48 papers, 2.0k citations indexed

About

Delphine Héron is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Delphine Héron has authored 48 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 21 papers in Molecular Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Delphine Héron's work include Genetics and Neurodevelopmental Disorders (21 papers), Genomics and Rare Diseases (13 papers) and Genomic variations and chromosomal abnormalities (13 papers). Delphine Héron is often cited by papers focused on Genetics and Neurodevelopmental Disorders (21 papers), Genomics and Rare Diseases (13 papers) and Genomic variations and chromosomal abnormalities (13 papers). Delphine Héron collaborates with scholars based in France, United States and Belgium. Delphine Héron's co-authors include Ivan Bièche, Éric Pasmant, Michel Vidaud, Ingrid Laurendeau, Dominique Vidaud, Alexandra Afenjar, Nathalie Boddaert, Nadia Bahi‐Buisson, Patricia Marques Pereira and André Hanauer and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and PLoS ONE.

In The Last Decade

Delphine Héron

46 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.

Characterization of a Germ-Line Deletion, Including the Entire INK4/ARF Locus, in a Melanoma-Neural System Tumor Family: Identification of ANRIL , an Antisense Noncoding RNA Whose Expression Coclusters with ARF

2007 500 citations Éric Pasmant, Ingrid Laurendeau et al. Cancer Research profile →

Peers

Delphine Héron

GENET

CMN

PMH

Joseph G. Gleeson United States

Takeshi Mizuguchi Japan

Keiko Shimojima Japan

Francisco Martı́nez Spain

Andreas Tzschach Germany

Alison Condie United Kingdom

Marie Mangelsdorf Australia

Francesca Ariani Italy

Alfredo Brusco Italy

Sulagna C. Saitta United States

Joseph G. Gleeson United States

Delphine Héron

1.3k ×1.1

788 ×0.8

GENET

304 ×0.8

273 ×1.1

CMN

133 ×0.6

PMH

Citations per year, relative to Delphine Héron Delphine Héron (= 1×) peers Joseph G. Gleeson

Countries citing papers authored by Delphine Héron

Since Specialization

Citations

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

Fields of papers citing papers by Delphine Héron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Delphine Héron

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

Amiel, Jeanne, Delphine Héron, & Bertrand Isidor. (2024). Séquençage de l’exome ou du génome et données additionnelles. médecine/sciences. 40(4). 377–380. 1 indexed citations

Valence, Stéphanie, Hélène Maurey, Sarah Weckhuysen, et al.. (2019). Three novel patients with epileptic encephalopathy due to biallelic mutations in the PLCB1 gene. Clinical Genetics. 97(3). 477–482. 11 indexed citations

Masliah‐Planchon, Julien, Delphine Héron, Fabienne Giuliano, et al.. (2018). Does ATRX germline variation predispose to osteosarcoma? Three additional cases of osteosarcoma in two ATR-X syndrome patients. European Journal of Human Genetics. 26(8). 1217–1221. 20 indexed citations

Labalme, Audrey, Marianne Till, Gérald Bussy, et al.. (2018). Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations. Clinical Case Reports. 6(5). 827–834. 3 indexed citations

Vadrot, Nathalie, Patrick Vicart, Ana Ferreiro, et al.. (2017). A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus. PLoS ONE. 12(1). e0169189–e0169189. 20 indexed citations

Bouchghoul, Hanane, D Vauthier, Cécile Cazeneuve, et al.. (2016). Prenatal testing in Huntington disease: after the test, choices recommence. European Journal of Human Genetics. 24(11). 1535–1540. 10 indexed citations

Fraidakis, Matthew J., Claude Jardel, Stéphane Allouche, et al.. (2014). Phenotypic diversity associated with the MT-TV gene m.1644G>A mutation, a matter of quantity. Mitochondrion. 15. 34–39. 9 indexed citations

Jacquette, Aurélia, David Cohen, Nicolas Bodeau, et al.. (2012). Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1. Developmental Medicine & Child Neurology. 54(10). 905–911. 56 indexed citations

Goff, Carine Le, Clémentine Mahaut, Avinash Abhyankar, et al.. (2011). Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome. Nature Genetics. 44(1). 85–88. 117 indexed citations

10.

Afenjar, Alexandra, et al.. (2011). Floating-Harbor Syndrome. Clinical Dysmorphology. 21(1). 11–14. 9 indexed citations

11.

Guen, Tangui Le, Yann Fichou, Juliette Nectoux, et al.. (2010). A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localization. Human Mutation. 32(2). E2026–E2035. 15 indexed citations

12.

Depienne, Christel, Oriane Trouillard, Isabelle Gourfinkel‐An, et al.. (2010). Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome. Journal of Medical Genetics. 47(6). 404–410. 117 indexed citations

13.

Bahi‐Buisson, Nadia, Anna Kamińska, Nathalie Boddaert, et al.. (2008). The three stages of epilepsy in patients with CDKL5 mutations. Epilepsia. 49(6). 1027–1037. 139 indexed citations

14.

Pasmant, Éric, Ingrid Laurendeau, Delphine Héron, et al.. (2007). Characterization of a Germ-Line Deletion, Including the Entire INK4/ARF Locus, in a Melanoma-Neural System Tumor Family: Identification of ANRIL , an Antisense Noncoding RNA Whose Expression Coclusters with ARF. Cancer Research. 67(8). 3963–3969. 500 indexed citations breakdown →

15.

Keren, Boris, Annick Toutain, Delphine Héron, et al.. (2007). Pure proximal deletion of chromosome 21 and kyphosis. European Journal of Medical Genetics. 50(6). 469–474. 4 indexed citations

16.

Verloès, Alain, Dominique Brémond‐Gignac, Bertrand Isidor, et al.. (2006). Blepharophimosis‐mental retardation (BMR) syndromes: A proposed clinical classification of the so‐called Ohdo syndrome, and delineation of two new BMR syndromes, one X‐linked and one autosomal recessive. American Journal of Medical Genetics Part A. 140A(12). 1285–1296. 52 indexed citations

17.

Salva, Maria-Antonia Quera, M. Blumen, Aurélia Jacquette, et al.. (2006). Sleep disorders in childhood-onset myotonic dystrophy type 1. Neuromuscular Disorders. 16(9-10). 564–570. 63 indexed citations

18.

Cohen, David, A. J. C. Wilson, Jean-Marc Guilé, et al.. (2006). Brief Report: Visual-Spatial Deficit in a 16-year-old Girl with Maternally Derived Duplication of Proximal 15q. Journal of Autism and Developmental Disorders. 37(8). 1585–1591. 16 indexed citations

19.

Geneviève, David, Delphine Héron, Vincent El Ghouzzi, et al.. (2005). Exclusion of the dymeclin and PAPSS2 genes in a novel form of spondyloepimetaphyseal dysplasia and mental retardation. European Journal of Human Genetics. 13(5). 541–546. 7 indexed citations

20.

Saugier-Véber, Pascale, Cosette Martin, Nathalie Le Meur, et al.. (1998). Identification of novelL1CAM mutations using fluorescence-assisted mismatch analysis. Human Mutation. 12(4). 259–266. 22 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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