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Meeting Abstract (8)
Journal Articles (6)

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Investigative Ophthalmology & Visual Science (13)
Translational Vision Science & Technology (1)

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ARVO Annual Meeting Abstract (8)
Genetics (3)
Retina (2)
Articles (1)

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Eye Anatomy and Disorders (6)
Retina (5)
Genetics (4)
Imaging (2)
Retinal Imaging (2)
Visual Neuroscience (2)
Glaucoma (1)
Immunology and Microbiology (1)
Translational Research (1)

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electroretinography (3)
mutation (3)
phenotype (3)
autosomal recessive inheritance (2)
cohort studies (2)
eye (2)
family (2)
genes (2)
retina (2)
retinitis pigmentosa (2)

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ARVO Annual Meeting Abstract June 2022

X-linked retinitis pigmentosa caused by a non-canonical splice variant in RPGR

Samuel Koller; Tim Beltramelli; Agnès Wlodarczyk; Silke Feil; Lucy Bähr; Christina Gerth-Kahlert; Moreno Menghini; Wolfgang Berger

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):504 – A0081.

Articles June 2020

Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals CYP1B1 and FOXC1 Variants as Most Frequent Causes

PDF

Elena Lang; Samuel Koller; Luzy Bähr; Marc Töteberg-Harms; David Atac; Françoise Roulez; Angela Bahr; Katharina Steindl; Silke Feil; Wolfgang Berger; Christina Gerth-Kahlert
TAGS: cohort studies, glaucoma, congenital, whole exome sequencing, glaucoma
Trans. Vis. Sci. Tech.. 2020; 9(7):47. https://doi.org/10.1167/tvst.9.7.47

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2019

Higher ROP incidence in extremely preterm infants

Christina Gerth-Kahlert; Aylin Taner; Senait Tekle; Torsten Hothorn; Mark Adams

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):6525.

Genetics July 2019

Genotype–Phenotype Analysis of a Novel Recessive and a Recurrent Dominant SNRNP200 Variant Causing Retinitis Pigmentosa

PDF

Christina Gerth-Kahlert; Samuel Koller; James V. M. Hanson; Luzy Baehr; Amit Tiwari; Fatma Kivrak-Pfiffner; Angela Bahr; Wolfgang Berger
TAGS: family, genotype, phenotype, recurrence, retinitis pigmentosa, missense mutation, mutation, genes, heterozygote, visual acuity
Invest. Ophthalmol. Vis. Sci.. 2019; 60(8):2822-2835. https://doi.org/10.1167/iovs.18-25643

Retina January 2018

Outer Retinal Dysfunction in the Absence of Structural Abnormalities in Multiple Sclerosis

PDF

James V. M. Hanson; Michael Hediger; Praveena Manogaran; Klara Landau; Niels Hagenbuch; Sven Schippling; Christina Gerth-Kahlert
TAGS: electroretinography, eye, multiple sclerosis, pathophysiology, cohort studies, medical history, retina
Invest. Ophthalmol. Vis. Sci.. 2018; 59(1):549-560. https://doi.org/10.1167/iovs.17-22821

Includes: Supplemental Content

Genetics August 2017

C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations

PDF

Christina Gerth-Kahlert; Amit Tiwari; James V. M. Hanson; Vaishnavi Batmanabane; Elias Traboulsi; Mark E. Pennesi; Abdullah A. Al-Qahtani; Byron L. Lam; John Heckenlively; Sandrine A. Zweifel; Ajoy Vincent; Fabienne Fierz; Daniel Barthelmes; Kari Branham; Naheed Khan; Angela Bahr; Luzy Baehr; István Magyar; Samuel Koller; Silvia Azzarello-Burri; Dunja Niedrist; Elise Heon; Wolfgang Berger
TAGS: autosomal recessive inheritance, de novo mutation, genes, mutation, phenotype, retinitis pigmentosa, language morphology, morphology, macular disorders
Invest. Ophthalmol. Vis. Sci.. 2017; 58(10):3840-3850. https://doi.org/10.1167/iovs.17-21597

ARVO Annual Meeting Abstract June 2017

Genotype - phenotype analysis in a family with autosomal dominant retinitis pigmentosa and a mutation in SNRNP200 .

Christina Gerth-Kahlert; Amit Tiwari; Angela Bahr; James V.M. Hanson; Wolfgang Berger

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2767.

Retina February 2017

Senescent Changes and Topography of the Dark-Adapted Multifocal Electroretinogram

PDF

Athanasios Panorgias; Megan Tillman; Erich E. Sutter; Ala Moshiri; Christina Gerth-Kahlert; John S. Werner
TAGS: aging, electroretinography, retina, rod photoreceptors, photopsia
Invest. Ophthalmol. Vis. Sci.. 2017; 58(2):1323-1329. https://doi.org/10.1167/iovs.16-20953

ARVO Annual Meeting Abstract September 2016

Longitudinal study of retinal and optic nerve function in patients with multiple sclerosis – a baseline report

Christina Gerth-Kahlert; Klara Landau; James VM Hanson

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3603.

Genetics May 2016

Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis

PDF

Ajoy Vincent; Judith Ng; Christina Gerth-Kahlert; Erika Tavares; Jason T. Maynes; Thomas Wright; Amit Tiwari; Anupreet Tumber; Shuning Li; James V. M. Hanson; Angela Bahr; Heather MacDonald; Luzy Bähr; Carol Westall; Wolfgang Berger; Frans P. M. Cremers; Anneke I. den Hollander; Elise Héon
TAGS: autosomal recessive inheritance, family, genetics, mutation, phenotype, retinoschisis, eye, relationship - sibling, electroretinography
Invest. Ophthalmol. Vis. Sci.. 2016; 57(6):2637-2646. https://doi.org/10.1167/iovs.15-18281

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2015

Acquired Brown’s Syndrome in children: MRI abnormalities of the superior oblique tendon-trochlea complex

Christina Gerth-Kahlert; Veit Sturm; Werner Wichmann

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):5229.

ARVO Annual Meeting Abstract June 2013

Jalili syndrome: retinal dystrophy and amelogenesis imperfecta: genotype-phenotype analysis in four new cases

Christina Gerth-Kahlert; Britta Seebauer; Sandra Dold; Johannes Fleischhauer; Hubertus van Waes; Wolfgang Berger

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1342.

ARVO Annual Meeting Abstract June 2013

Retinal layer segmentation in a pediatric normal group

Stefan Pelz; Hannes Wildberger; Christina Gerth-Kahlert

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5519.

ARVO Annual Meeting Abstract April 2011

Mutational Analysis In A Large Number Of Patients With Uni- Or Bilateral Anophthalmia

Christina Gerth-Kahlert; Kathy Williamson; Volker Hingst; Rudolf Guthoff; David R. FitzPatrick; Veronica van Heyningen

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):1568.

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