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Christina Zeitz

Research director INSERM, group leader

INSERM

France

Research Interests

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Professors in France Professors in Cell Biology Cell Biology professors in France

Articles (20)

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2025

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Collaborators (17)

Gaël Manes

Chercheur

INSERM

FRANCE

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Isabelle Audo

Professor

Université Pierre et Marie Curie

FRANCE

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Ajoy Vincent

Professor

University of Toronto Faculty of Medicine

CANADA

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Shahad Albadri

Principal Investigator (Chargée de Recherche INSERM)

Institut de la vision

FRANCE

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Fred Chen

University of Western Australia

AUSTRALIA

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Anne Bergougnoux

Assistant Professor

University of Montpellier

FRANCE

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Robin Plevin

University Of Strathclyde

UNITED KINGDOM

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Thierry Leveillard

Directeur de recherche INSERM (DR1)

INSERM

FRANCE

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Serge Picaud

Director of research

INSERM

FRANCE

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Alessio Antropoli

Vita-Salute San Raffaele University

ITALY

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Maurizio Battaglia Parodi

Associate Professor

Università Vita Salute San Raffaele

ITALY

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Stephane Hunot

CNRS Tenured Research Director

Centre National de la Recherche Scientifique (CNRS)

FRANCE

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Stefano Casati

Ricercatori

University of Verona

ITALY

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Guillaume Blot

Université de Montréal

CANADA

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Kinga Bujakowska

Assistant Professor

Harvard University

UNITED STATES

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Jose‐Alain Sahel

Chairman

University of Pittsburgh

UNITED STATES

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Shyamanga Borooah

University of California, San Diego

UNITED STATES

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Christina Zeitz

Research Interests

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Articles (20)

Voretigene neparvovec in RPE65-related inherited retinal dystrophy: the 1-year real-world study LIGHT

LONG-TERM OUTCOMES OF ANTI-VEGF THERAPY FOR MACULAR NEOVASCULARIZATION IN PRPH2-ASSOCIATED RETINOPATHY

PCARE-Associated Retinopathy - Genetics, Clinical Characteristics, and Natural History.

Phenotypic and Genotypic Characterization of RP1L1-Associated Retinopathy.

Identification of IDH3G, encoding the gamma subunit of mitochondrial isocitrate dehydrogenase, as a novel candidate gene for X-linked retinitis pigmentosa.

DRD2 activation inhibits choroidal neovascularization in patients with Parkinson’s disease and age-related macular degeneration

Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study

RDH5 and RLBP1-Associated Inherited Retinal Diseases: Refining the Spectrum of Stationary and Progressive Phenotypes

Extensive Macular Atrophy with Pseudodrusen-like appearance

Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants

Validation of Nanopore long-read sequencing to resolve RPGR ORF15 genotypes in individuals with X-linked retinitis pigmentosa

Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration.

Extensive macular atrophy with pseudodrusen-like appearance (EMAP) clinical characteristics, diagnostic criteria, and insights from allied inherited retinal diseases and age-related macular degeneration.

Differential pathogenetic mechanisms of mutations in helix 2 and helix 6 of rhodopsin

Generation of human induced pluripotent stem cell lines from a subject with UBAP1L-associated retinal dystrophy and CRISPR/cas9-corrected isogenic iPSC lines.

Loss of ON-Pathway Function in Mice Lacking Lrit3 Decreases Recovery From Lens-Induced Myopia.

Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy

The Extraordinary Phenotypic and Genetic Variability of Retinal and Macular Degenerations: The Relevance to Therapeutic Developments

Shedding light on myopia by studying complete congenital stationary night blindness

CRISPR/Cas9: From research to therapeutic application

Collaborators (17)

Gaël Manes

Isabelle Audo

Ajoy Vincent

Shahad Albadri

Fred Chen

Anne Bergougnoux

Robin Plevin

Thierry Leveillard

Serge Picaud

Alessio Antropoli

Maurizio Battaglia Parodi

Stephane Hunot

Stefano Casati

Guillaume Blot

Kinga Bujakowska

Jose‐Alain Sahel

Shyamanga Borooah

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