D. Héron

1.5k citations

26 papers · 1.2k · h-index 15

Impact in

Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research

Papers in

Genetics 13
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 5
- Connective tissue disorders research 3
- Neurogenetic and Muscular Disorders Research 3
Molecular Biology 12
- Muscle Physiology and Disorders 4
- Glycosylation and Glycoproteins Research 2

Co-authors: Valérie Cormier‐Daire (3 shared papers)Arnold Munnich (2 shared papers)Stanislas Lyonnet (2 shared papers)Damien Sanlaville (1 shared paper)Anne Philippe (1 shared paper)Richard Redon (1 shared paper)M Prieur (1 shared paper)Laurence Colleaux (1 shared paper)
Journals: Clinical Genetics (6 papers)Journal of Medical Genetics (3 papers)Neuromuscular Disorders (2 papers)Human Molecular Genetics (2 papers)European Journal of Human Genetics (1 paper)
Partner nations: France United Kingdom United States

In The Last Decade

D. Héron

26 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside D. Héron, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with D. Héron Line = papers co-authored together D. Héron links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders Journal of Medical Genetics ·M-L Jacquemont, Damien Sanlaville, Richard Redon, O Raoul, Valérie Cormier‐Daire, Stanislas Lyonnet, Jeanne Amiel, M Le Merrer	2006	253
2	Mutation update for the CSB / ERCC6 and CSA / ERCC8 genes involved in Cockayne syndrome Human Mutation ·Vincent Laugel, Cécile Dalloz, M. Durand, Florence Sauvanaud, Ulrik Kristensen, M.-C. Vincent, Laurent Pasquier, Sylvie Odent	2009	187
3	Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression Human Molecular Genetics ·Frederic Christopher Daoud, Nathalie Angeard, B. Demerre, I. Martie, Rabah Ben Yaou, France Leturcq, Mireille Cossée, Nathalie Deburgrave	2009	135
4	Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects Human Molecular Genetics ·Annie Laquerrière, Jérôme Maluenda, Adrien Camus, Laura Fontenas, Flora Nolent, Jie Zhou, Nicole Monnier, Philippe Latour	2013	99
5	Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia Journal of Medical Genetics ·Yoann Saillour, Ginevra Zanni, V. des Portes, D. Héron, Guibaud Laurent, M T Iba-Zizen, Jean‐Michel Pédespan, Karine Poirier	2007	69
6	Wiedemann‐Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases Clinical Genetics ·Sarah Baer, Alexandra Afenjar, Thomas Smol, Amélie Piton, Bénédicte Gérard, Yves Alembik, Thierry Bienvenu, Guilaine Boursier	2018	65
7	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 ·Sahar Sabry, Sandrine Vuillaumier‐Barrot, E. Mintet, Magali Fasseu, Vassili Valayannopoulos, D. Héron, Nathalie Dorison, Cyril Mignot	2016	48
8	Cumulative effect of anatomical risk factors for schizophrenia: an MRI study Biological Psychiatry ·Christiana M. Leonard, John M. Kuldau, Joshua I. Breier, Paula A Zuffante, D. Héron, Elise M Lavery, Jennifer Packing, Sharyl Williams	1999	43
9	Neurological Presentation in Pediatric Patients with Congenital Disorders of Glycosylation Type Ia Neuropediatrics ·E. Miossec-Chauvet, Yann Mikaeloff, D. Héron, Valerie Merzoug, Valérie Cormier‐Daire, Pascale de Lonlay, GERT L. MATTHIJS, C. Van Hulle	2003	42
10	Maternal origin of a novel C‐terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome Clinical Genetics ·Juliette Nectoux, D. Héron, Marilyn Tallot, Jamel Chelly, Thierry Bienvenu	2006	33
11	MEF2C mutations are a rare cause of Rett or severe Rett‐like encephalopathies Clinical Genetics ·Laëtitia Lambert, Thierry Bienvenu, Lila Allou, Mylène Valduga, Bernard Échenne, Bertrand Diebold, Cyril Mignot, D. Héron	2012	28
12	MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype Neurogenetics ·Thomas Smol, Florence Petit, Amélie Piton, Boris Keren, Damien Sanlaville, Alexandra Afenjar, Samuel White Baker, Emma C. Bedoukian	2018	27
13	Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity? Neuromuscular Disorders ·Nathalie Angeard, Eleazar Huerta, Aurélia Jacquette, David H. Cohen, Jean Xavier, Marcela Gargiulo, Laurent Servais, B. Eymard	2017	24
14	Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid features Clinical Genetics ·Sébastien Moutton, Ange‐Line Bruel, Mirna Assoum, Martin Chevarin, Elisabeth Sarrazin, Cyril Goizet, A.‐M. Guerrot, Aude Charollais	2018	23
15	Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability Clinical Genetics ·Patrick Callier, Bernard Aral, Nadine Hanna, Sandy Lambert, Hyacintha d’Indy, Clémence Ragon, Muriel Payet, Gwenaëlle Collod‐Béroud	2013	23
16	Diffuse leukodystrophy in an infant with cytochrome‐c oxidase deficiency Journal of Inherited Metabolic Disease ·J‐P. Harpey, D. Héron, Muriel Prudent, Christiane Charpentier, Pierre Rustin, Gérard Ponsot, Valérie Cormier‐Daire	1998	15
17	Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly Clinical Genetics ·Alinoë Lavillaureix, Solveig Heide, Sandra Chantot‐Bastaraud, Isabelle Marey, Boris Keren, R Grigorescu, Jean‐Marie Jouannic, A. Gélot	2017	15
18	Stratégie d’exploration d’une déficience intellectuelle inexpliquée Archives de Pédiatrie ·Alain Verloès, D. Héron, Thierry Billette de Villemeur, A. Afenjar, C. Baumann, Nadia Bahi‐Buisson, Perrine Charles, Anne Faudet	2012	9
19	Filippi syndrome: a new case with skeletal abnormalities. Journal of Medical Genetics ·D. Héron, Th. Billette de Villemeur, Arnold Munnich, Stanislas Lyonnet	1995	8
20	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 ·Marcela Gargiulo, Nathalie Angeard, A. Herson, S. Fosse, Claire Noël, Aurélia Jacquette, B. Eymard, D. Héron	2008	5

About D. Héron

D. Héron is a scholar working on Genetics, Molecular Biology, Genetics, Cellular and Molecular Neuroscience and Developmental Biology, having authored 26 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (5 papers), Muscle Physiology and Disorders (4 papers), Genetic Neurodegenerative Diseases (4 papers), Connective tissue disorders research (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Glycosylation and Glycoproteins Research (2 papers). The work is most often cited by research in Genetics (549 citations), Cognitive Neuroscience (207 citations), Molecular Biology (666 citations), Developmental Neuroscience (27 citations) and Cellular and Molecular Neuroscience (124 citations). D. Héron has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Valérie Cormier‐Daire, Arnold Munnich, Stanislas Lyonnet, Damien Sanlaville, Anne Philippe, Richard Redon, M Prieur, Laurence Colleaux, Jeanne Amiel and O Raoul. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Neuromuscular Disorders, Human Molecular Genetics and European Journal of Human Genetics.

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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