D. Héron

1.5k total citations
16 papers, 435 citations indexed

About

D. Héron is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, D. Héron has authored 16 papers receiving a total of 435 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in D. Héron's work include Genetics and Neurodevelopmental Disorders (4 papers), Muscle Physiology and Disorders (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). D. Héron is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Muscle Physiology and Disorders (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). D. Héron collaborates with scholars based in France, Belgium and Martinique. D. Héron's co-authors include Valérie Cormier‐Daire, Stanislas Lyonnet, Arnold Munnich, Laurence Colleaux, Anne Philippe, Richard Redon, Jeanne Amiel, O Raoul, Damien Sanlaville and M Prieur and has published in prestigious journals such as Biological Psychiatry, Journal of Medical Genetics and Orphanet Journal of Rare Diseases.

In The Last Decade

D. Héron

16 papers receiving 419 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D. Héron France	9	272	214	176	38	34	16	435
Elisabeth Gabau Spain	16	463 1.7×	336 1.6×	103 0.6×	42 1.1×	39 1.1×	36	675
Marie‐Christine de Blois France	8	352 1.3×	182 0.9×	96 0.5×	65 1.7×	22 0.6×	10	455
Claude Cancès France	10	310 1.1×	293 1.4×	89 0.5×	24 0.6×	66 1.9×	15	574
Rena Vanzo United States	14	302 1.1×	186 0.9×	74 0.4×	27 0.7×	24 0.7×	25	504
Lars R. Jensen Germany	12	102 0.4×	253 1.2×	42 0.2×	30 0.8×	40 1.2×	32	395
Sailaja Peddada United States	5	394 1.4×	431 2.0×	187 1.1×	29 0.8×	28 0.8×	7	569
Amy Lawson‐Yuen United States	6	223 0.8×	154 0.7×	172 1.0×	13 0.3×	50 1.5×	7	363
Madeleine Fannemel Norway	11	196 0.7×	173 0.8×	58 0.3×	23 0.6×	35 1.0×	18	386
Aia Elise Jønch Denmark	6	306 1.1×	230 1.1×	194 1.1×	7 0.2×	69 2.0×	11	396
David H. Kavanagh United Kingdom	8	179 0.7×	205 1.0×	78 0.4×	8 0.2×	61 1.8×	9	362

Countries citing papers authored by D. Héron

Since Specialization

Citations

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

Fields of papers citing papers by D. Héron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. Héron

This figure shows the co-authorship network connecting the top 25 collaborators of D. Héron. A scholar is included among the top collaborators of D. 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 D. Héron. D. 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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16 of 16 papers shown

Moutton, Sébastien, Ange‐Line Bruel, Mirna Assoum, et al.. (2018). Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid features. Clinical Genetics. 93(6). 1172–1178. 17 indexed citations

Angeard, Nathalie, Aurélia Jacquette, David Cohen, et al.. (2017). Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?. Neuromuscular Disorders. 28(3). 216–221. 18 indexed citations

Vuillaumier‐Barrot, Sandrine, Magali Fasseu, Vassili Valayannopoulos, et al.. (2016). A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity. Orphanet Journal of Rare Diseases. 11(1). 84–84. 39 indexed citations

Jacquette, Aurélia, David Cohen, Marcela Gargiulo, et al.. (2014). Forme infantile de la dystrophie myotonique de type 1 (DM1) et troubles du spectre autistique (TSA) : existe-t-il une comorbidité ?. Neuropsychiatrie de l Enfance et de l Adolescence. 63(2). 91–98. 1 indexed citations

Verloès, Alain, D. Héron, Thierry Billette de Villemeur, et al.. (2012). Stratégie d’exploration d’une déficience intellectuelle inexpliquée. Archives de Pédiatrie. 19(2). 194–207. 6 indexed citations

Joly, Laure, Christel Thauvin‐Robinet, Frédéric Huet, et al.. (2010). Les tests génétiques présymptomatiques chez le mineur : enquête auprès des généticiens français et position du groupe français de génétique prédictive. Archives de Pédiatrie. 17(7). 1000–1007. 4 indexed citations

Gargiulo, Marcela, Nathalie Angeard, Aurélia Jacquette, et al.. (2008). Impact psychologique de la maladie de Duchenne sur l’enfant et l’adolescent, ses parents, sa fratrie. Onze années d’expérience d’une consultation pluridisciplinaire. Neuropsychiatrie de l Enfance et de l Adolescence. 56(2). 73–81. 3 indexed citations

Jacquette, Aurélia, et al.. (2007). Phénotype psychiatrique des maladies neuromusculaires de l’enfant: revue de la littérature. Neuropsychiatrie de l Enfance et de l Adolescence. 56(2). 63–72. 1 indexed citations

Hu, Yanyan, France Leturcq, D. Héron, et al.. (2006). G.P.6 02 Somatic and germinal mosaicism of an out-of-frame deletion in the dystrophin gene in an adult male patient with predominant dilated cardiomyopathy. Neuromuscular Disorders. 16(9-10). 698–698. 1 indexed citations

10.

Nectoux, Juliette, et al.. (2006). Maternal origin of a novel C‐terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome. Clinical Genetics. 70(1). 29–33. 30 indexed citations

11.

Sanlaville, Damien, Richard Redon, O Raoul, et al.. (2006). Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders. Journal of Medical Genetics. 43(11). 843–849. 218 indexed citations

12.

Mikaeloff, Yann, D. Héron, V. Merzoug, et al.. (2003). Neurological Presentation in Pediatric Patients with Congenital Disorders of Glycosylation Type Ia. Neuropediatrics. 34(1). 1–6. 35 indexed citations

13.

Baumann, Barbara & D. Héron. (2001). Syndromes dysmorphiques à la naissance: Que faire?. Archives de Pédiatrie. 8(9). 1000–1005. 1 indexed citations

14.

Leonard, Christiana M., et al.. (1999). Cumulative effect of anatomical risk factors for schizophrenia: an MRI study. Biological Psychiatry. 46(3). 374–382. 39 indexed citations

15.

Héron, D., et al.. (1998). Diffuse leukodystrophy in an infant with cytochrome‐c oxidase deficiency. Journal of Inherited Metabolic Disease. 21(7). 748–752. 14 indexed citations

16.

Héron, D., T Billette de Villemeur, Arnold Munnich, & Stanislas Lyonnet. (1995). Filippi syndrome: a new case with skeletal abnormalities.. Journal of Medical Genetics. 32(8). 659–661. 8 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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