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ARVO Annual Meeting Abstract September 2016

A comprehensive molecular analysis of patients with the diagnosis of choroideremia

Christina Zeitz; Barbara Kloeckener-Gruissem; Marie-Elise Lancelot; Aurore Germain; Aline Antonio; Fiona Boyard; Mohaind-Said Saddek; Jose Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):661. doi:

ARVO Annual Meeting Abstract June 2015

A new method to determine efficacies to treat RPGR mutations: Quantification of RPGR transport along the primary cilium in patient-derived cells

Christoph Jüschke; Romain Da Costa; Esther Glaus; Amit Tiwari; Barbara Kloeckener-Gruissem; Wolfgang Berger; John Neidhardt

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2062. doi:

Biochemistry and Molecular Biology August 2014

Lack of Paraoxonase 1 Alters Phospholipid Composition, but Not Morphology and Function of the Mouse Retina

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Jadwiga Oczos; Iryna Sutter; Barbara Kloeckener-Gruissem; Wolfgang Berger; Meliana Riwanto; Katharina Rentsch; Thorsten Hornemann; Arnold von Eckardstein; Christian Grimm
TAGS: phospholipids, mice, retina, morphology, pon1 gene, language morphology
Invest. Ophthalmol. Vis. Sci.. 2014; 55(8):4714-4727. doi: 10.1167/iovs.14-14332

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2013

Identification of the substrate and characterization of transport properties for the cataract associated monocarboxylate transporter MCT12

Barbara Kloeckener-Gruissem; Nancy Philp; Jeannette Abplanalp; Simone Camargo; Daniel Schorderet; Francis Munier; John Neidhardt; François Verrey; Endre Laczko; Wolfgang Berger

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):3683. doi:

ARVO Annual Meeting Abstract June 2013

Paraoxonase-1 (PON1) in retinal physiology and pathophysiology

Jadwiga Oczos; Barbara Kloeckener-Gruissem; Wolfgang Berger; Christian Grimm

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):6081. doi:

ARVO Annual Meeting Abstract March 2012

Long-term Studies On The Anti-VEGF Treatment Success In Age-related Macular Degeneration (amd)

Barbara Kloeckener-Gruissem; Moreno Menghini; Florian Sutter; Johannes Fleischhauer; Malaika Kurz-Levin; Wolfgang Berger; Daniel Barthelmes

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):5168. doi:

Lens August 2011

Juvenile Cataract-Associated Mutation of Solute Carrier SLC16A12 Impairs Trafficking of the Protein to the Plasma Membrane

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John J. Castorino; Shannon M. Gallagher-Colombo; Alex V. Levin; Paul G. FitzGerald; Jessica Polishook; Barbara Kloeckener-Gruissem; Eric Ostertag; Nancy J. Philp
TAGS: mutation, cataract, cell membrane, child, lens, crystalline, lens (device), membrane transport proteins, antibodies, proteins, rats, solutes
Invest. Ophthalmol. Vis. Sci.. 2011; 52(9):6774-6784. doi: 10.1167/iovs.10-6579

Includes: Supplemental Content

Genetics June 2011

Genetic Association with Response to Intravitreal Ranibizumab in Patients with Neovascular AMD

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Barbara Kloeckener-Gruissem; Daniel Barthelmes; Stephan Labs; Christian Schindler; Malaika Kurz-Levin; Stephan Michels; Johannes Fleischhauer; Wolfgang Berger; Florian Sutter; Moreno Menghini
TAGS: genotype, single nucleotide polymorphism, genetics, genetic aspects, exudative age-related macular degeneration, ranibizumab
Invest. Ophthalmol. Vis. Sci.. 2011; 52(7):4694-4702. doi: 10.1167/iovs.10-6080

ARVO Annual Meeting Abstract April 2011

Juvenile Cataract-associated Mutation Of Solute Carrier Slc16a12 Impairs Trafficking Of The Protein To The Plasma Membrane

Nancy J. Philp; Barbara Kloeckener-Gruissem; Alex V. Levin; Paul G. FitzGerald; John J. Castorino

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):3414. doi:

ARVO Annual Meeting Abstract April 2011

Influence of a Loading Phase on Long-term Visual Acuity with Respect to Genetic and Clinical Factors in Patients with Neovascular Age-related Macular Degeneration

Moreno Menghini; Florian K. Sutter; Barbara Kloeckener-Gruissem; Johannes C. Fleischhauer; Malaika M. Kurz; Sandrine A. Zweifel; Stephan Michels; Wolfgang Berger; Daniel Barthelmes

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5243. doi:

ARVO Annual Meeting Abstract April 2011

A Swiss Patient Cohort Reveals Genetic Predisposition Of Known And New Genetic Loci To AMD And To Intravitreal Ranibizumab (lucentis®) Treatment Outcome

Barbara Kloeckener-Gruissem; Moreno Menghini; Daniel Barthelmes; Stephan Labs; Malaika Kurz-Levin; Stephan Michels; Johannes Fleischhauer; Florian Sutter; Wolfgang Berger

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5249. doi:

Biochemistry and Molecular Biology July 2010

Alterations of the 5′Untranslated Region of SLC16A12 Lead to Age-Related Cataract

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Jurian Zuercher; John Neidhardt; Istvan Magyar; Stephan Labs; Anthony T. Moore; Felix C. Tanner; Naushin Waseem; Daniel F. Schorderet; Francis L. Munier; Shomi Bhattacharya; Wolfgang Berger; Barbara Kloeckener-Gruissem
TAGS: alleles, cell culture techniques, mutation, heterogeneity, cataract, dna, single nucleotide polymorphism, cataract, senile, rna
Invest. Ophthalmol. Vis. Sci.. 2010; 51(7):3354-3361. doi: 10.1167/iovs.10-5193

Retina March 2010

Mutation- and Tissue-Specific Alterations of RPGR Transcripts

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Fabian Schmid; Esther Glaus; Frans P. M. Cremers; Barbara Kloeckener-Gruissem; Wolfgang Berger; John Neidhardt
TAGS: mutation, cell lines, dna, complementary, exons, protein isoforms, reverse transcriptase polymerase chain reaction, rna splicing, body tissue, retina
Invest. Ophthalmol. Vis. Sci.. 2010; 51(3):1628-1635. doi: 10.1167/iovs.09-4031

Includes: Supplemental Content

Retina September 2008

Identification and Functional Characterization of a Novel Rhodopsin Mutation Associated with Autosomal Dominant CSNB

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Christina Zeitz; Alecia K. Gross; Dorothee Leifert; Barbara Kloeckener-Gruissem; Suzanne D. McAlear; Johannes Lemke; John Neidhardt; Wolfgang Berger
TAGS: mutation, electroretinography, opsin, rhodopsin, transducin, night blindness, congenital stationary
Invest. Ophthalmol. Vis. Sci.. 2008; 49(9):4105-4114. doi: 10.1167/iovs.08-1717

Retina September 2008

Syndromic Choroideremia: Sublocalization of Phenotypes Associated with Martin-Probst Deafness Mental Retardation Syndrome

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Charlotte M. Poloschek; Barbara Kloeckener-Gruissem; Lutz L. Hansen; Michael Bach; Wolfgang Berger
TAGS: phenotype, choroideremia, dna, family, intellectual disability, syndrome, hearing impairment
Invest. Ophthalmol. Vis. Sci.. 2008; 49(9):4096-4104. doi: 10.1167/iovs.08-2044

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A comprehensive molecular analysis of patients with the diagnosis of choroideremia

A new method to determine efficacies to treat RPGR mutations: Quantification of RPGR transport along the primary cilium in patient-derived cells

Lack of Paraoxonase 1 Alters Phospholipid Composition, but Not Morphology and Function of the Mouse Retina

Identification of the substrate and characterization of transport properties for the cataract associated monocarboxylate transporter MCT12

Paraoxonase-1 (PON1) in retinal physiology and pathophysiology

Long-term Studies On The Anti-VEGF Treatment Success In Age-related Macular Degeneration (amd)

Juvenile Cataract-Associated Mutation of Solute Carrier SLC16A12 Impairs Trafficking of the Protein to the Plasma Membrane

Genetic Association with Response to Intravitreal Ranibizumab in Patients with Neovascular AMD

Juvenile Cataract-associated Mutation Of Solute Carrier Slc16a12 Impairs Trafficking Of The Protein To The Plasma Membrane

Influence of a Loading Phase on Long-term Visual Acuity with Respect to Genetic and Clinical Factors in Patients with Neovascular Age-related Macular Degeneration

A Swiss Patient Cohort Reveals Genetic Predisposition Of Known And New Genetic Loci To AMD And To Intravitreal Ranibizumab (lucentis®) Treatment Outcome

Alterations of the 5′Untranslated Region of SLC16A12 Lead to Age-Related Cataract

Mutation- and Tissue-Specific Alterations of RPGR Transcripts

Identification and Functional Characterization of a Novel Rhodopsin Mutation Associated with Autosomal Dominant CSNB

Syndromic Choroideremia: Sublocalization of Phenotypes Associated with Martin-Probst Deafness Mental Retardation Syndrome

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