Isabelle Meunier

Isabelle Meunier

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Isabelle Meunier

Isabelle Meunier

Publications by authors named "Isabelle Meunier"

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Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.

Genet Med 2020 Apr 20. Epub 2020 Apr 20.

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1038/s41436-020-0787-4DOI Listing
April 2020

Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy.

Stem Cell Res 2019 07 7;38:101478. Epub 2019 Jun 7.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2019.101478DOI Listing
July 2019

Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis.

Stem Cell Res 2019 07 3;38:101476. Epub 2019 Jun 3.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S18735061193010
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http://dx.doi.org/10.1016/j.scr.2019.101476DOI Listing
July 2019

Genome Editing as a Treatment for the Most Prevalent Causative Genes of Autosomal Dominant Retinitis Pigmentosa.

Int J Mol Sci 2019 May 23;20(10). Epub 2019 May 23.

Inserm U1051, Institute for Neurosciences of Montpellier, 80 Avenue Augustin Fliche, 34091 Montpellier, France.

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http://dx.doi.org/10.3390/ijms20102542DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567127PMC
May 2019

Pathogenicity of novel atypical variants leading to choroideremia as determined by functional analyses.

Hum Mutat 2019 01 8;40(1):31-35. Epub 2018 Nov 8.

Laboratoire de Génétique Moléculaire, CHU de Montpellier, Université de Montpellier, Montpellier, France.

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http://dx.doi.org/10.1002/humu.23671DOI Listing
January 2019

Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa.

Stem Cell Res 2018 12 10;33:228-232. Epub 2018 Nov 10.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2018.11.004DOI Listing
December 2018

Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2.

Stem Cell Res 2018 12 16;33:247-250. Epub 2018 Nov 16.

Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S18735061183027
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http://dx.doi.org/10.1016/j.scr.2018.11.007DOI Listing
December 2018

Novel splice-site mutation in TTLL5 causes cone dystrophy in a consanguineous family.

Mol Vis 2017 18;23:131-139. Epub 2017 Mar 18.

Sorbonne Universités, UPMC Univ Paris 06, INSERM U968, CNRS UMR 7210, Institut de la Vision, 17 rue Moreau, Paris, France.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360453PMC
February 2018

LEBER CONGENITAL AMAUROSIS WITH LARGE RETINAL PIGMENT CLUMPS CAUSED BY COMPOUND HETEROZYGOUS MUTATIONS IN KCNJ13.

Retin Cases Brief Rep 2017 Summer;11(3):221-226

*Maladies Sensorielles Génétiques, CHRU, Montpellier, France; †INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France; ‡Université Montpellier, Montpellier, France; §Laboratory of Genetics in Ophthalmology, INSERM UMR 1163, Paris, France; and ¶Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.

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http://dx.doi.org/10.1097/ICB.0000000000000326DOI Listing
January 2018

Cone dystrophy or macular dystrophy associated with novel autosomal dominant mutations.

Mol Vis 2017 3;23:198-209. Epub 2017 Apr 3.

Institut National de la Santé et de la Recherche Médicale, U1051, Institute for Neurosciences of Montpellier, Montpellier, France.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389339PMC
January 2018

RIPK3 interacts with MAVS to regulate type I IFN-mediated immunity to Influenza A virus infection.

PLoS Pathog 2017 Apr 14;13(4):e1006326. Epub 2017 Apr 14.

Department of Medicine, Department of Pathology, Department of Microbiology & Immunology, McGill University Health Centre, McGill International TB Centre, Meakins-Christie Laboratories, McGill University, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1371/journal.ppat.1006326DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406035PMC
April 2017

Unravelling the networks dictating host resistance versus tolerance during pulmonary infections.

Cell Tissue Res 2017 03 6;367(3):525-536. Epub 2017 Feb 6.

Department of Medicine, Department of Microbiology & Immunology, and Department of Pathology, McGill University Health Centre, McGill International TB Centre, Meakins-Christie Laboratories, McGill University, 1001 Decarie Boulevard, Montreal, Quebec, H4A 3J1, Canada.

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http://dx.doi.org/10.1007/s00441-017-2572-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088083PMC
March 2017

Pattern dystrophy in a female carrier of RP2 mutation.

Ophthalmic Genet 2016 12 17;37(4):453-455. Epub 2016 Feb 17.

a Genetics of Sensory Diseases, CHU , Montpellier , France.

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http://dx.doi.org/10.3109/13816810.2015.1081253DOI Listing
December 2016

Martinique Crinkled Retinal Pigment Epitheliopathy: Clinical Stages and Pathophysiologic Insights.

Ophthalmology 2016 10 26;123(10):2196-204. Epub 2016 Jul 26.

Institute for Neurosciences of Montpellier U1051, University of Montpellier - University Hospital, Genetics of Sensory Diseases, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2016.06.028DOI Listing
October 2016

WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity.

Ophthalmology 2016 09 7;123(9):1989-98. Epub 2016 Jul 7.

Maladies Sensorielles Génétiques, CHRU, Montpellier, France; INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France; Université Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2016.05.036DOI Listing
September 2016

Clinical Evaluation and Cone Alterations in Choroideremia.

Ophthalmology 2016 08 15;123(8):1830-1832. Epub 2016 Mar 15.

Genetics of Sensory Diseases, CHU de Montpellier, Montpellier, France; INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France; Université Montpellier, Montpellier, France. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2016.02.025DOI Listing
August 2016

Infection with a Mouse-Adapted Strain of the 2009 Pandemic Virus Causes a Highly Severe Disease Associated with an Impaired T Cell Response.

PLoS One 2015 18;10(9):e0138055. Epub 2015 Sep 18.

Pulmonary Division, Department of Medicine, Faculty of Medicine and Health Sciences, Université de Sherbrooke and Centre de Recherche du CHUS, Sherbrooke, Québec, Canada.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0138055PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575127PMC
June 2016

Inhibition of influenza virus replication by targeting broad host cell pathways.

PLoS One 2014 21;9(10):e110631. Epub 2014 Oct 21.

Department of Medicine, Pulmonary Division, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, Québec, Canada; Centre de Recherche du CHUS, Sherbrooke, Québec, Canada.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0110631PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204995PMC
December 2015

Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopia.

Br J Ophthalmol 2015 Oct 16;99(10):1360-5. Epub 2015 Apr 16.

Maladies Sensorielles Génétiques, CHRU, Montpellier, France INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France Université Montpellier 1, Montpellier, France Université Montpellier 2, Montpellier, France.

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http://dx.doi.org/10.1136/bjophthalmol-2014-306224DOI Listing
October 2015

Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction.

J Neurol Sci 2015 Feb 13;349(1-2):154-60. Epub 2015 Jan 13.

INSERM, U-1051, Institut des Neurosciences, Montpellier, France; CHU Montpellier, Centre of Reference for Genetic Sensory Diseases, Montpellier, France.

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http://dx.doi.org/10.1016/j.jns.2015.01.008DOI Listing
February 2015

Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes.

Ophthalmology 2014 Dec 29;121(12):2406-14. Epub 2014 Jul 29.

Centre de Référence Maladies Sensorielles Génétiques, Hôpital Gui de Chauliac, Montpellier, France; Montpellier University, Montpellier, France; Institute for Neurosciences, INSERM, Montpellier, France.

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http://dx.doi.org/10.1016/j.ophtha.2014.06.028DOI Listing
December 2014

Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations.

Mol Vis 2013 8;19:2487-500. Epub 2013 Dec 8.

INSERM U. 1051, Institute for Neurosciences of Montpellier, Montpellier, France ; Université Montpellier 1, Montpellier, France ; Université Montpellier 2, Montpellier, France.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857159PMC
July 2014

Association of reticular pseudodrusen and early onset drusen.

ISRN Ophthalmol 2013 16;2013:273085. Epub 2013 May 16.

Department of Ophthalmology, Croix-Rousse University Hospital, 103 Grande rue de la Croix Rousse, 69317 Lyon Cedex 04, France.

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https://www.hindawi.com/archive/2013/273085/
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http://dx.doi.org/10.1155/2013/273085DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914185PMC
February 2014

Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1.

JAMA Ophthalmol 2013 Oct;131(10):1314-23

Genetics of Sensory Diseases, Centre Hospitalier Régional Universitaire de Montpellier, Montpellier, France.

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http://dx.doi.org/10.1001/jamaophthalmol.2013.4476DOI Listing
October 2013

Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.

Eur J Ophthalmol 2012 Jul-Aug;22(4):647-53

INSERM 1051, Institute for Neurosciences of Montpellier, Montpellier, France.

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http://dx.doi.org/10.5301/ejo.5000096DOI Listing
October 2012

PB1-F2 modulates early host responses but does not affect the pathogenesis of H1N1 seasonal influenza virus.

J Virol 2012 Apr 8;86(8):4271-8. Epub 2012 Feb 8.

INRS-Institut Armand-Frappier, University of Quebec, Laval, Quebec, Canada.

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http://dx.doi.org/10.1128/JVI.07243-11DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3318652PMC
April 2012

Serological survey of Neospora caninum in small ruminants from Pernambuco State, Brazil.

Rev Bras Parasitol Vet 2011 Jul-Sep;20(3):246-8

Laboratório de Doenças Parasitárias dos Animais Domésticos, Departamento de Medicina Veteriná, Universidade Federal Rural de Pernambuco--UFRPE, Brazil.

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http://www.scielo.br/pdf/rbpv/v20n3/v20n3a13.pdf
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http://dx.doi.org/10.1590/s1984-29612011000300013DOI Listing
February 2012

NS1-mediated delay of type I interferon induction contributes to influenza A virulence in ferrets.

J Gen Virol 2011 Jul 16;92(Pt 7):1635-1644. Epub 2011 Mar 16.

INRS-Institut Armand-Frappier, University of Quebec, Laval, QC H7V 1B7, Canada.

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http://dx.doi.org/10.1099/vir.0.032193-0DOI Listing
July 2011

Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variations.

Ophthalmic Genet 2010 Dec;31(4):200-4

Genetics of Sensory Diseases, Hospital of Montpellier, Montpellier, France.

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http://dx.doi.org/10.3109/13816810.2010.512354DOI Listing
December 2010

Electrophysiological retinal pigment epithelium changes observed with indocyanine green, trypan blue and triamcinolone.

Ophthalmic Res 2010 3;44(1):17-23. Epub 2010 Feb 3.

Ophtalmologie, CHU de Montpellier, Montpellier, France. carl.arndt @ orange.fr

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http://dx.doi.org/10.1159/000279437DOI Listing
October 2010

Influenza pathogenesis: lessons learned from animal studies with H5N1, H1N1 Spanish, and pandemic H1N1 2009 influenza.

Crit Care Med 2010 Apr;38(4 Suppl):e21-9

INRS-Institut Armand-Frappier, University of Quebec, Laval, Canada.

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http://dx.doi.org/10.1097/CCM.0b013e3181c8b4d5DOI Listing
April 2010

Assessment of the efficacy of commercially available and candidate vaccines against a pandemic H1N1 2009 virus.

J Infect Dis 2010 Apr;201(7):1000-6

Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba R3E 3R2, Canada.

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http://dx.doi.org/10.1086/651171DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109664PMC
April 2010

Unilateral retinal pigment epithelium dysgenesis.

Am J Ophthalmol 2009 Dec 5;148(6):914-9.e2. Epub 2009 Sep 5.

Centre Ophthalmologique d'Imagerie et de Laser, Paris, France.

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http://dx.doi.org/10.1016/j.ajo.2009.06.033DOI Listing
December 2009

Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity.

Am J Ophthalmol 2009 Apr 1;147(4):609-20. Epub 2009 Feb 1.

Centre Hospitalier Régional et Universitaire, Centre de Référence Maladies Sensorielles Génétiques, Montpellier, France.

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http://dx.doi.org/10.1016/j.ajo.2008.10.022DOI Listing
April 2009

Study of a novel hypervariable region in hepatitis C virus (HCV) E2 envelope glycoprotein.

Virology 2006 Sep 16;352(2):357-67. Epub 2006 Jun 16.

Unité d'immunopathologie virale, Centre de recherche du CHU mère-enfant Sainte-Justine, Montreal, Quebec, Canada H3T 1C5.

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http://dx.doi.org/10.1016/j.virol.2006.05.015DOI Listing
September 2006

Five-year evolution of basal laminar drusen combined with vitelliform macular detachment.

Arch Ophthalmol 2004 Oct;122(10):1566-7

Centre Ophtalmologique d'Imagerie et de Laser, 15 Rue Antoine Bourdelle, Paris, France 75015.

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http://dx.doi.org/10.1001/archopht.122.10.1566DOI Listing
October 2004

Cu-Ag (111) polymorphism induced by segregation and advacancies.

Phys Rev Lett 2003 Oct 24;91(17):176103. Epub 2003 Oct 24.

LEMHE, UMR 8647 CNRS, Université Paris-Sud, F91405 Orsay CEDEX, France.

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http://dx.doi.org/10.1103/PhysRevLett.91.176103DOI Listing
October 2003