Christina Gerth-Kahlert

Scopus Author ID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 24

Top Venues

International journal of molecular sciences

Genes

Klinische Monatsblatter fur Augenheilkunde

Biomedicines

University Hospital of Zurich

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University Hospital of Zurich Aug 01 2015

Switzerland

Head (Leitende Ärztin) of pediatric ophthalmology, oculogenetics, orthoptics (Ophthalmology) Qualification :: Department of Ophthalmology

University Hospital of Zurich Sep 01 2011 - Jul 31 2015

Switzerland

Consultant (Oberärztin) :: Ophthalmology

University of Rostock May 01 2008 - Apr 30 2011

Germany

Consultant (Oberärztin) :: Ophthalmology

Publications

Aylin F Taner, James V M Hanson, Caroline Weber, Dirk Bassler, Daphne L McCulloch, Christina Gerth-Kahlert
Flicker electroretinogram in preterm infants. Eye (London, England) (2024)
Jordi Maggi, Silke Feil, Jiradet Gloggnitzer, Kevin Maggi, Ruxandra Bachmann-Gagescu, Christina Gerth-Kahlert, Samuel Koller, Wolfgang Berger
Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes. International journal of molecular sciences 25 (17) (2024)
Jan Spindler, Samuel Koller, Urs Graf, Wolfgang Berger, Christina Gerth-Kahlert, Frank Blaser
Macular Corneal Dystrophy - Molecular Genetics as the Key in Treatment-Refractory Keratopathy. Klinische Monatsblatter fur Augenheilkunde 241 (4) (2024)
Jordi Maggi, Samuel Koller, Silke Feil, Ruxandra Bachmann-Gagescu, Christina Gerth-Kahlert, Wolfgang Berger
Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient Cohort. International journal of molecular sciences 25 (12) (2024)
Jordi Maggi, Samuel Koller, Silke Feil, Ruxandra Bachmann-Gagescu, Christina Gerth-Kahlert, Wolfgang Berger
Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient Cohort. International journal of molecular sciences 25 (12) (2024)
Jan Spindler, Samuel Koller, Urs Graf, Wolfgang Berger, Christina Gerth-Kahlert, Frank Blaser
Macular Corneal Dystrophy - Molecular Genetics as the Key in Treatment-Refractory Keratopathy. Klinische Monatsblatter fur Augenheilkunde 241 (4) (2024)
Alice M Kitay, James V M Hanson, Nasiq Hasan, Matthew Driban, Jay Chhablani, Daniel Barthelmes, Christina Gerth-Kahlert, Mayss Al-Sheikh
Functional and Morphological Characteristics of the Retina of Patients with Drusen-like Deposits and Systemic Lupus Erythematosus Treated with Hydroxychloroquine: A Retrospective Study. Biomedicines 11 (6) (2023)
Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger
Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 14 (4) (2023)
Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger
Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 14 (4) (2023)
Alice M Kitay, James V M Hanson, Nasiq Hasan, Matthew Driban, Jay Chhablani, Daniel Barthelmes, Christina Gerth-Kahlert, Mayss Al-Sheikh
Functional and Morphological Characteristics of the Retina of Patients with Drusen-like Deposits and Systemic Lupus Erythematosus Treated with Hydroxychloroquine: A Retrospective Study. Biomedicines 11 (6) (2023)
Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger
Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 14 (4) (2023)
Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger
Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 14 (4) (2023)
Flora Delas, Samuel Koller, Silke Feil, Ivanka Dacheva, Christina Gerth-Kahlert, Wolfgang Berger
Novel CRYGC Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract. International journal of molecular sciences 24 (23) (2023)
Fatma Kivrak Pfiffner, Samuel Koller, Anika Ménétrey, Urs Graf, Luzy Bähr, Alessandro Maspoli, Annette Hackenberg, Raimund Kottke, Christina Gerth-Kahlert, Wolfgang Berger
Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment. International journal of molecular sciences 23 (13) (2022)
Lorena Sisera, Sarah Patzelt, Christina Gerth-Kahlert
[Non-Organic Visual Loss in Children and Teenagers]. Klinische Monatsblatter fur Augenheilkunde 239 (4) (2022)
James V M Hanson, Caroline Weber, Oliver A Pfäffli, Dirk Bassler, Daphne L McCulloch, Christina Gerth-Kahlert
Flicker electroretinogram in newborn infants. Documenta ophthalmologica. Advances in ophthalmology 145 (3) (2022)
Laura Gogoll, Katharina Steindl, Pascal Joset, Markus Zweier, Alessandra Baumer, Christina Gerth-Kahlert, Boris Tutschek, Anita Rauch
Confirmation of Ogden syndrome as an X-linked recessive fatal disorder due to a recurrent NAA10 variant and review of the literature. American journal of medical genetics. Part A 185 (8) (2021)
Jennifer Robinson, Manca Tekavčič Pompe, Christina Gerth-Kahlert
Challenges in Patients with Trisomy 21: A Review of Current Knowledge and Recommendations. Journal of ophthalmology 2021 (2021)
Patricia Haug, Samuel Koller, Jordi Maggi, Elena Lang, Silke Feil, Agnès Wlodarczyk, Luzy Bähr, Katharina Steindl, Marianne Rohrbach, Christina Gerth-Kahlert, Wolfgang Berger
Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes. Genes 12 (1) (2021)
Hans-Georg Geiger, Brigitte Simonsz-Toth, Christina Gerth-Kahlert
[Acute Acquired Comitant Esotropia Type 2 - A Retrospective Analysis]. Klinische Monatsblatter fur Augenheilkunde 238 (4) (2021)
Jordi Maggi, Samuel Koller, Luzy Bähr, Silke Feil, Fatma Kivrak Pfiffner, James V M Hanson, Alessandro Maspoli, Christina Gerth-Kahlert, Wolfgang Berger
Long-Range PCR-Based NGS Applications to Diagnose Mendelian Retinal Diseases. International journal of molecular sciences 22 (4) (2021)
Aylin F Taner, Senait Tekle, Torsten Hothorn, Mark Adams, Dirk Bassler, Christina Gerth-Kahlert
Higher incidence of retinopathy of prematurity in extremely preterm infants associated with improved survival rates. Acta paediatrica (Oslo, Norway : 1992) 109 (10) (2020)
Elena Lang, Samuel Koller, David Atac, Oliver A Pfäffli, James V M Hanson, Silke Feil, Luzy Bähr, Angela Bahr, Raimund Kottke, Pascal Joset, Katrin Fasler, Daniel Barthelmes, Katharina Steindl, Daniel Konrad, David-Alexander Wille, Wolfgang Berger, Christina Gerth-Kahlert
Genotype-phenotype spectrum in isolated and syndromic nanophthalmos. Acta ophthalmologica 99 (4) (2020)
Sarah Claudia Ambroz, Marc Töteberg-Harms, James V M Hanson, Jens Funk, Barthelmes Daniel, Christina Gerth-Kahlert
Outcome of Pediatric Cataract Surgeries in a Tertiary Center in Switzerland. Journal of ophthalmology 2018 (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Christina Gerth-Kahlert