Delphine Héron

2.9k citations

27 papers · 421 indexed · h-index 11

Co-authors: Marcela Gargiulo Aurélia Jacquette B. Eymard Nathalie Angeard H. Radvanyi Cyril Mignot Christel Depienne Dorothée Ville
Topics: Genetics and Neurodevelopmental Disorders (7 papers)Genetic Neurodegenerative Diseases (6 papers)Genomics and Rare Diseases (4 papers)
Cited by: Cellular and Molecular Neuroscience Genetics Neurology
Journals: Blood Neurology Epilepsia
Partner nations: France United States Germany

In The Last Decade

Delphine Héron

24 papers receiving 416 citations

Peers

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

#	Work	Indexed citations
1	Use of Prenatal Exome Sequencing: Opinion Statement of the French Federation of Human Genetics Working Group 2024 ·Prenatal Diagnosis ·(unknown),Marie‐Bérengère Troadec,Françoise Devillard,(unknown),David Geneviève,François Vialard,Emmanuelle Rial‐Sebbag,Delphine Héron,Tania Attié‐Bitach,Alexandra Benachi,Pascale Saugier-Véber	6
2	Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis 2022 ·Clinical Genetics ·(unknown),Julie Désir,Damien Haye,Pauline Le Tanno,Françoise Devillard,Benjamin Cogné,(unknown),Laura Tecco,Delphine Héron,Claudine Le Vaillant,Madeleine Joubert,Claire Bénéteau	3
3	COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage 2022 ·Prenatal Diagnosis ·Thibault Coste,Catherine Vincent‐Delorme,(unknown),Louise Devisme,A. Gélot,(unknown),Fanny Pelluard,Chaker Aloui,Anne‐Louise Leutenegger,Jean‐Marie Jouannic,Delphine Héron,Douglas B. Gould,Elisabeth Tournier‐Lasserve	11
4	Reproductive choices and intrafamilial communication in neurogenetic diseases with different self-estimated severities 2022 ·Journal of Medical Genetics ·(unknown),Sophie Tézenas du Montcel,Anna Heinzmann,Giulia Coarelli,Delphine Héron,Solveig Heide,(unknown),(unknown),Élodie Petit,Marcela Gargiulo,Alexandra Dürr	6
5	Tremor-like subcortical myoclonus in STXBP1 encephalopathy 2021 ·European Journal of Paediatric Neurology ·(unknown),Diane Doummar,(unknown),Thierry Bienvenu,Perrine Charles,Christel Depienne,Nathalie Dorison,Solveig Heide,Delphine Héron,Christine Ioos,Boris Keren,(unknown),Fanny Mochel,Marie‐Laure Moutard,Claudia Ravelli,Emmanuelle Apartis,Cyril Mignot	4
6	Two Novel Cases of Resistance to Thyroid Hormone Due to THRA Mutation 2020 ·Thyroid ·Albane le Maire,Natacha Bouhours‐Nouet,(unknown),Delphine Mirebeau‐Prunier,Matteo Paloni,(unknown),Delphine Héron,Cyril Mignot,F. Illouz,(unknown),Claire Briet,Patrice Rodien,William Bourguet,Frédéric Flamant,Romain Guyot	19
7	Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutations 2020 ·Developmental Medicine & Child Neurology ·Megan Spencer‐Smith,(unknown),Emmanuelle Lacaze,Christel Depienne,Paul J. Lockhart,Linda J. Richards,Delphine Héron,Richard J. Leventer,Gail Robinson	11
8	DYRK1A mutations in two unrelated patients 2015 ·European Journal of Medical Genetics ·(unknown),Cyril Mignot,Agnès Guët,(unknown),Caroline Nava,Delphine Héron,Boris Keren,Christel Depienne,Valérie Benoît,Isabelle Maystadt,Damien Lederer,Daniel Amsallem,Juliette Piard	24
9	GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia 2015 ·Neurology ·Marie Coutelier,Lydie Bürglen,Emeline Mundwiller,(unknown),Diana Rodriguez,Sandra Chantot‐Bastaraud,Christelle Rougeot,(unknown),Mathieu Milh,Annick Toutain,Delphine Bacq,Vincent Meyer,Alexandra Afenjar,Jean‐François Deleuze,Alexis Brice,Delphine Héron,Giovanni Stévanin,Alexandra Dürr	50
10	Le conseil génétique dans les maladies neuromusculaires de l'enfant 2014 ·Sandra Whalen,Aurélia Jacquette,Delphine Héron	0
11	Deletion of filamin A in two female patients with periventricular nodular heterotopia 2012 ·American Journal of Medical Genetics Part A ·Jodi Warman‐Chardon,Cyril Mignot,Swaroop Aradhya,Boris Keren,Alexandra Afenjar,Anna Kamińska,Chérif Beldjord,Delphine Héron,Kym M. Boycott	6
12	Psychiatric phenotype of juvenile myotonic dystrophy 1 includes internalising disorder, borderline intelligence, visual spatial construction disability and attention deficit disorder 2012 ·Neuropsychiatrie de l Enfance et de l Adolescence ·(unknown),Aurélia Jacquette,Nicolas Bodeau,Nathalie Angeard,(unknown),Jean‐Marie Cuisset,B. Eymard,David Cohen,Delphine Héron,J.-M. Guilé	1
13	STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients 2011 ·Epilepsia ·Cyril Mignot,Marie‐Laure Moutard,Oriane Trouillard,Isabelle Gourfinkel‐An,Aurélia Jacquette,Benoı̂t Arveiler,Fanny Morice‐Picard,Didier Lacombe,Catherine Chiron,Dorothée Ville,Perrine Charles,Eric Leguern,Christel Depienne,Delphine Héron	76
14	A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1) 2011 ·Neuromuscular Disorders ·Nathalie Angeard,Aurélia Jacquette,Marcela Gargiulo,H. Radvanyi,Sylvain Moutier,B. Eymard,Delphine Héron	37
15	Intragenic deletion of UBE3A gene in 2 sisters with Angelman syndrome detected by MLPA 2011 ·American Journal of Medical Genetics Part A ·Juliette Piard,Christel Depienne,Boris Keren,Estelle Fédirko,Oriane Trouillard,Perrine Charles,Delphine Héron	5
16	CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy 2009 ·Epilepsy Research ·Rima Nabbout,Christel Depienne,Mathilde Chipaux,Benôıt Girard,Isabelle Souville,Oriane Trouillard,Olivier Dulac,Jamel Chelly,Alexandra Afenjar,Delphine Héron,Eric Leguern,Chérif Beldjord,Thierry Bienvenu,Nadia Bahi‐Buisson	3
17	Autism, language delay and mental retardation in a patient with 7q11 duplication 2009 ·BMJ Case Reports ·Christel Depienne,Delphine Héron,Catalina Betancur,B Benyahia,Oriane Trouillard,Delphine Bouteiller,Alain Verloès,Eric Leguern,Marion Leboyer,Alexis Brice	5
18	Cognitive profile in childhood myotonic dystrophy type 1: Is there a global impairment? 2007 ·Neuromuscular Disorders ·Nathalie Angeard,Marcela Gargiulo,Aurélia Jacquette,H. Radvanyi,B. Eymard,Delphine Héron	40
19	Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case 2004 ·Prenatal Diagnosis ·Philippe Charron,Delphine Héron,Marcela Gargiulo,Josué Feingold,Jean‐François Oury,Pascale Richard,Michel Komajda	19
20	Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris). 2000 ·Blood ·(unknown),Serge Pissard,Josiane Martin,Delphine Héron,Philippe Labrune,Marie-Odile Livet,M. Mayer,Terri Gelbart,Arthur S. Schneider,Isabelle Max‐Audit,Michel Cohen‐Solal	18

About Delphine Héron

Delphine Héron is a scholar working on Genetics, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 27 papers that have together received 421 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (138 citations), Genetics (157 citations) and Neurology (63 citations). Delphine Héron has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Marcela Gargiulo, Aurélia Jacquette, B. Eymard, Nathalie Angeard, H. Radvanyi, Cyril Mignot, Christel Depienne, Dorothée Ville, Oriane Trouillard and Marie‐Laure Moutard. Their work appears in journals such as Blood, Neurology and Epilepsia.

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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