Anne‐Françoise Roux

6.0k citations

90 papers · 3.4k indexed · 1 hit paper · h-index 31

Co-authors: Mireille Claustres Donna Maglott Raymond Dalgleish Jean McGowan‐Jordan Stylianos E. Antonarakis Johan T. den Dunnen Reece K. Hart Peter E.M. Taschner
Topics: Hearing, Cochlea, Tinnitus, Genetics (28 papers)Retinal Development and Disorders (19 papers)RNA and protein synthesis mechanisms (14 papers)
Cited by: Sensory Systems Neurology Molecular Biology
Journals: Journal of Clinical InvestigationSHILAP Revista de lepidopterologíaBrain
Partner nations: France United Kingdom United States

In The Last Decade

Anne‐Françoise Roux

86 papers receiving 3.4k 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.

HGVS Recommendations for the Description of Sequence Variants: 2016 Update

2016 1.0k citations Anne‐Françoise Roux et al. Human Mutation profile →

Peers

Countries citing papers authored by Anne‐Françoise Roux

Since Specialization

Citations

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

Fields of papers citing papers by Anne‐Françoise Roux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne‐Françoise Roux. 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 Anne‐Françoise Roux. The network helps show where Anne‐Françoise Roux may publish in the future.

Co-authorship network of co-authors of Anne‐Françoise Roux

This figure shows the co-authorship network connecting the top 25 collaborators of Anne‐Françoise Roux. A scholar is included among the top collaborators of Anne‐Françoise Roux 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 Anne‐Françoise Roux. Anne‐Françoise Roux 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	The phenotypic spectrum of CEP250 gene variants 2024 ·Ophthalmic Genetics ·(unknown),Claire‐Marie Dhaenens,(unknown),(unknown),Isabelle Audo,A. Lecleire–Collet,(unknown),Sophie Gad,G Lapeyre,Xavier Zanlonghi,Dominique Bonneau,Mélanie Fradin,Guylène Le Meur,Sandrine Marlin,Pierre Blanc,Anne‐Françoise Roux,(unknown),Vincent Michaud	1
2	Identification and in vivo functional investigation of a HOMER2 nonstop variant causing hearing loss 2023 ·European Journal of Human Genetics ·Christel Vaché,Nicolas Cubedo,(unknown),(unknown),David Baux,Valérie Faugère,(unknown),(unknown),Renaud Touraine,Geneviève Lina‐Granade,Mireille Cossée,Anne Bergougnoux,Vasiliki Kalatzis,Mireille Rossel,Anne‐Françoise Roux	1
3	CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 Isoforms 2021 ·International Journal of Molecular Sciences ·(unknown),(unknown),Béatrice Bocquet,Gilles Labesse,Carl Arndt,Sabine Defoort‐Dhellemmes,Xavier Zanlonghi,Dalil Hamroun,D. Denis,Marie‐Christine Picot,(unknown),(unknown),(unknown),Hélèna Huguet,Anne‐Françoise Roux,Vasiliki Kalatzis,Claire‐Marie Dhaenens,Isabelle Meunier	15
4	Mutations in PLS1 , encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss 2019 ·Human Mutation ·Anna Morgan,Daniel C. Koboldt,Elizabeth S. Barrie,(unknown),Gema García‐García,Massimo Mezzavilla,Flavio Faletra,Theresa Mihalic Mosher,Richard K. Wilson,Catherine Blanchet,Kandamurugu Manickam,Anne‐Françoise Roux,Paolo Gasparini,Daniele Dell’Orco,Giorgia Girotto	15
5	Usher syndrome in Denmark: mutation spectrum and some clinical observations 2016 ·Molecular Genetics & Genomic Medicine ·(unknown),Nanna Dahl Rendtorff,Lisbeth Tranebjærg,Karen Grønskov,(unknown),(unknown),Øivind Nilssen,Anne‐Françoise Roux,Thomas Rosenberg,Hanne Jensen,Lisbeth Birk Møller	20
6	Rifle impulse noise affects middle-ear compliance in soldiers wearing protective earplugs 2015 ·International Journal of Audiology ·Agnès Job,(unknown),(unknown),(unknown),Anne‐Françoise Roux,(unknown),Francesco Cardinale,(unknown),Christopher Klein,(unknown)	11
7	Mutation of SLC9A1, encoding the major Na+/H+ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome 2014 ·Human Molecular Genetics ·Claire Guissart,(unknown),Bruno Leheup,Nathalie Drouot,B. Montaut-Verient,Emmanuel Raffo,(unknown),Anne‐Françoise Roux,Mireille Claustres,Larry Fliegel,M. Kœnig	37
8	Functional characterization of G-protein-coupled receptors: A bioinformatics approach 2014 ·Neuroscience ·Luciana Tovo‐Rodrigues,Anne‐Françoise Roux,Mara Helena Hutz,Luís Augusto Rohde,Amina S. Woods	21
9	EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus 2013 ·European Journal of Human Genetics ·(unknown),Lies H. Hoefsloot,Anne‐Françoise Roux,Maria Bitner‐Glindzicz	21
10	Non-USH2A mutations in USH2 patients 2011 ·Human Mutation ·Thomas Besnard,Christel Vaché,David Baux,Lise Larrieu,Caroline Abadie,Catherine Blanchet,Sylvie Odent,Patricia Blanchet,Patrick Calvas,Christian Hamel,Hélène Dollfus,Geneviève Lina‐Granade,James Lespinasse,Albert David,Bertrand Isidor,G Morin,Sue Malcolm,Sylvie Tuffery‐Giraud,Mireille Claustres,Anne‐Françoise Roux	51
11	Missense mutations of conserved glycine residues in fibrillin-1 highlight a potential subtype of cb-EGF-like domains 2009 ·Human Mutation ·Philippe Khau Van Kien,David Baux,Nathalie Pallarès-Ruiz,(unknown),(unknown),Nicolas Chassaing,Patrick Collignon,(unknown),Alain Hovnanian,Dominique Martin‐Coignard,(unknown),(unknown),Anne‐Françoise Roux,Mireille Claustres	11
12	Banques de données de mutations : enjeux et perspectives pour les maladies génétiques orphelines 2009 ·Pathologie Biologie ·Véronique Humbertclaude,Sylvie Tuffery‐Giraud,Corinne Bareil,(unknown),Damien Paulet,François-Olivier Desmet,Dalil Hamroun,David Baux,Anne Girardet,Gwenaëlle Collod‐Béroud,Philippe Khau Van Kien,Anne‐Françoise Roux,M. des Georges,Christophe Béroud,Mireille Claustres	0
13	UMD-USHbases: a comprehensive set of databases to record and analyse pathogenic mutations and unclassified variants in seven Usher syndrome causing genes 2008 ·Human Mutation ·David Baux,Valérie Faugère,Lise Larrieu,(unknown),Dalil Hamroun,Christophe Béroud,Sue Malcolm,Mireille Claustres,Anne‐Françoise Roux	38
14	First molecular screening of deafness in the Altai Republic population 2005 ·BMC Medical Genetics ·Olga L. Posukh,Nathalie Pallarès-Ruiz,(unknown),L. P. Osipova,Mireille Claustres,Anne‐Françoise Roux	54
15	Evaluation of dHPLC for CX26 Mutation Screening in Patients from Southern France with Sensorineural Deafness 2001 ·Genetic Testing ·Nathalie Pallarès-Ruiz,Patricia Blanchet,Michel Mondain,(unknown),Jacques Demaille,Mireille Claustres,Anne‐Françoise Roux	6
16	Restoration of Normal Interleukin‐2 Production by CD4⁺T Cells of Human Immunodeficiency Virus–Infected Patients after 9 Months of Highly Active Antiretroviral Therapy 1999 ·The Journal of Infectious Diseases ·Laurence Weiss,Petronela Ancuța,Pierre‐Marie Girard,Hicham Bouhlal,Anne‐Françoise Roux,(unknown),Michel D. Kazatchkine	42
17	Dinucleotide repeat polymorphism near the RP3 locus in Xp21 (DXS1110) 1993 ·Human Molecular Genetics ·Anne‐Françoise Roux,(unknown),Johanna M. Rommens,Maria A. Musarella	6
18	Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe). 1990 ·Journal of Clinical Investigation ·Laurette Morlé,Anne‐Françoise Roux,Nicole Alloisio,B Pothier,Joëlle Starck,Luc Denoroy,François Morlé,R.-C. Rudigoz,BG Forget,J. Delaunay	36
19	[Identification of pholcodine by paper microelectrophoresis. Differentiation from: codeine, codethyline, morphine]. 1960 ·PubMed ·Anne‐Françoise Roux,(unknown)	2
20	Application of electrophoresis on paper to the identification and control of plant drugs and their pharmaceutical forms. 1956 ·PubMed ·Anne‐Françoise Roux	0

About Anne‐Françoise Roux

Anne‐Françoise Roux is a scholar working on Sensory Systems, Neurology and Ophthalmology, having authored 90 papers that have together received 3.4k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (28 papers), Retinal Development and Disorders (19 papers) and RNA and protein synthesis mechanisms (14 papers). The work is most often cited by research in Sensory Systems (959 citations), Neurology (320 citations) and Molecular Biology (2.2k citations). Anne‐Françoise Roux has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Mireille Claustres, Donna Maglott, Raymond Dalgleish, Jean McGowan‐Jordan, Stylianos E. Antonarakis, Johan T. den Dunnen, Reece K. Hart, Peter E.M. Taschner, Marc S. Greenblatt and Tim D. Smith. Their work appears in journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Brain.

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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