Aurélia Jacquette

3.6k citations

23 papers · 498 indexed · h-index 11

Molecular Biology
Cellular and Molecular Neuroscience top 10%
Genetics top 10%
Neurology top 10%
Psychiatry and Mental health

Co-authors: B. Eymard Nathalie Angeard Delphine Héron Marcela Gargiulo H. Radvanyi Thierry Bienvenu David Cohen Jean-Marc Guilé
Topics: Genetic Neurodegenerative Diseases (9 papers)Parkinson's Disease Mechanisms and Treatments (5 papers)Genetics and Neurodevelopmental Disorders (5 papers)
Cited by: Cellular and Molecular Neuroscience Neurology Genetics
Journals: Human Molecular Genetics Epilepsia Developmental Medicine & Child Neurology
Partner nations: France Switzerland Italy

In The Last Decade

Aurélia Jacquette

21 papers receiving 491 citations

Peers

Countries citing papers authored by Aurélia Jacquette

Since Specialization

Citations

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

Fields of papers citing papers by Aurélia Jacquette

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurélia Jacquette

This figure shows the co-authorship network connecting the top 25 collaborators of Aurélia Jacquette. A scholar is included among the top collaborators of Aurélia Jacquette 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 Aurélia Jacquette. Aurélia Jacquette 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	Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder 2019 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),F. Boussion,(unknown),Stéphane Triau,Majida Charif,(unknown),(unknown),(unknown),Alban Ziegler,Céline Bris,A. Laquérrière,Catherine Fallet‐Bianco,Aurélia Jacquette,(unknown),(unknown),Pascal Reynier,Vincent Procaccio,Dominique Bonneau,(unknown)	7
2	Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatment 2017 ·Revue Neurologique ·Boris Dufournet,Karine Nguyen,Perrine Charles,David Grabli,Aurélia Jacquette,Michael Borg,Téodor Danaila,Eugénie Mutez,Sophie Drapier,Olivier Colin,Alexandre Eusébio,N. Philip,J.-P. Azulay	16
3	Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity? 2017 ·Neuromuscular Disorders ·Nathalie Angeard,(unknown),Aurélia Jacquette,David Cohen,Jean Xavier,Marcela Gargiulo,Laurent Servais,B. Eymard,D. Héron	18
4	Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions 2014 ·Molecular Syndromology ·Christèle Dubourg,Frédérique Bonnet‐Brilhault,Annick Toutain,Cyril Mignot,Aurélia Jacquette,Anne Dieux,(unknown),(unknown),Sophie Julia,(unknown),Massimiliano Rossi,S. Odent,Claude Bendavid,Catherine Barthélémy,Alain Verloès,Véronique David	20
5	Forme infantile de la dystrophie myotonique de type 1 (DM1) et troubles du spectre autistique (TSA) : existe-t-il une comorbidité ? 2014 ·Neuropsychiatrie de l Enfance et de l Adolescence ·(unknown),Aurélia Jacquette,David Cohen,Marcela Gargiulo,Laurent Servais,B. Eymard,D. Héron,Nathalie Angeard	1
6	Le conseil génétique dans les maladies neuromusculaires de l'enfant 2014 ·Sandra Whalen,Aurélia Jacquette,Delphine Héron	0
7	Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1 2012 ·Developmental Medicine & Child Neurology ·(unknown),Aurélia Jacquette,David Cohen,Nicolas Bodeau,(unknown),Nathalie Angeard,Jean‐Marie Cuisset,Louis Vallée,B. Eymard,Monique Plaza,Delphine Héron,Jean-Marc Guilé	56
8	Stratégie d’exploration d’une déficience intellectuelle inexpliquée 2012 ·Archives de Pédiatrie ·Alain Verloès,D. Héron,Thierry Billette de Villemeur,(unknown),(unknown),Nadia Bahi‐Buisson,Perrine Charles,Anne Faudet,Aurélia Jacquette,Cyril Mignot,(unknown),Sandrine Passemard,Marlène Rio,Laurence Robel,Christelle Rougeot,Dorothée Ville,Lydie Bürglen,V. des Portes	6
9	Recurrent mutations in the CDKL5 gene: Genotype–phenotype relationships 2012 ·American Journal of Medical Genetics Part A ·Nadia Bahi‐Buisson,Nathalie Villeneuve,(unknown),Aurélia Jacquette,Hélène Maurey,Gert Matthijs,Hilde Van Esch,Andrée Delahaye‐Duriez,Anne Moncla,Mathieu Milh,Flore Zufferey,(unknown),Thierry Bienvenu	45
10	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
11	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
12	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
13	CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery 2009 ·Human Molecular Genetics ·Sara Ricciardi,Charlotte Kilstrup‐Nielsen,Thierry Bienvenu,Aurélia Jacquette,Nicoletta Landsberger,Vania Broccoli	48
14	Psychiatric and cognitive phenotype in children and adolescents with myotonic dystrophy 2009 ·European Child & Adolescent Psychiatry ·(unknown),Aurélia Jacquette,Jean-Marc Guilé,Marie‐Laure Tanguy,Nathalie Angeard,Delphine Héron,Monique Plaza,David Cohen	34
15	Prenatal diagnosis of brachytelephalangic chondrodysplasia punctata: case report 2009 ·Ultrasound in Obstetrics and Gynecology ·(unknown),Marc Dommergues,(unknown),Aurélia Jacquette,(unknown),M. Le Merrer,Hubert Ducou Le Pointe,Cathérine Garel	5
16	Comment explorer une déficience intellectuelle chez l’adulte ? 2009 ·Delphine Héron,Aurélia Jacquette	0
17	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
18	Sleep disorders in childhood-onset myotonic dystrophy type 1 2006 ·Neuromuscular Disorders ·Maria-Antonia Quera Salva,M. Blumen,Aurélia Jacquette,Marie‐Christine Durand,(unknown),(unknown),B. Eymard,Frédéric Lofaso,Delphine Héron	63
19	Exclusion of the dymeclin and PAPSS2 genes in a novel form of spondyloepimetaphyseal dysplasia and mental retardation 2005 ·European Journal of Human Genetics ·David Geneviève,Delphine Héron,Vincent El Ghouzzi,C. Prost‐Squarcioni,Martine Le Merrer,Aurélia Jacquette,Damien Sanlaville,Florence Pinton,Nathalie Villeneuve,G. Kalifa,Arnold Münnich,Valérie Cormier‐Daire	7
20	Compound Heterozygosity for Two New Mutations in the β‐Globin Gene [Codon 9 (+ TA) and Polyadenylation Site (AATAAA→AAAAAA)] Leads to Thalassemia Intermedia in a Tunisian Patient 2004 ·Hemoglobin ·Aurélia Jacquette,Geneviève Roux,(unknown),Michel Goossens,Serge Pissard	10

About Aurélia Jacquette

Aurélia Jacquette is a scholar working on Cellular and Molecular Neuroscience, Neurology and Genetics, having authored 23 papers that have together received 498 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (9 papers), Parkinson's Disease Mechanisms and Treatments (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (231 citations), Neurology (129 citations) and Genetics (191 citations). Aurélia Jacquette has collaborated with scholars based in France, Switzerland and Italy. Frequent co-authors include B. Eymard, Nathalie Angeard, Delphine Héron, Delphine Héron, Marcela Gargiulo, H. Radvanyi, Thierry Bienvenu, David Cohen, Jean-Marc Guilé and Monique Plaza. Their work appears in journals such as Human Molecular Genetics, Epilepsia and Developmental Medicine & Child Neurology.

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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