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Articles September 2020

Longitudinal Changes of Macular Curvature in Patients with Retinitis Pigmentosa

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Monika Meinert; Shinji Ueno; Shiori Komori; Yoshito Koyanagi; Akira Sayo; Sten Andreasson; Taro Kominami; Yasuki Ito; Hiroko Terasaki
TAGS: eye, millon clinical multiaxial inventory, retinitis pigmentosa, shape, spectral domain-optical coherence tomography
Trans. Vis. Sci. Tech.. 2020; 9(10):11. doi: https://doi.org/10.1167/tvst.9.10.11

ARVO Annual Meeting Abstract June 2020

Dark-adapted ffERG can predict changes in composite VFQ score after cataract surgery in AMD

Thomas Forshaw; Hassan Ahmed; Troels Kjær; Sten Andreasson; Torben Sørensen

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):5043. doi:

ARVO Annual Meeting Abstract July 2019

Novel epitopes for anti-bestrophin autoantibodies in vitelliform macular dystrophy

Grazyna Adamus; Sufang Yang; Sten Andreasson; Elisabeth Wittstrom

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):779. doi:

ARVO Annual Meeting Abstract July 2019

Age-related Macular Degeneration: a generalised retinal disorder A prospective study of retinal function using full-field electroretinography

Thomas Forshaw; Sten Andreasson; Torben Lykke Sørensen

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1163. doi:

ARVO Annual Meeting Abstract June 2017

Retinal function improved, assessed with 30-HZ flicker, in patients treated with Aflibercept for neovascular AMD at six months follow-up.

Marion Schroeder; Ivana Huzevkova; Sten Andreasson; Monica Loevestam-Adrian

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):872. doi:

Visual Neuroscience February 2017

The Clinical Phenotype of CNGA3 -Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial

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Ditta Zobor; Annette Werner; Franco Stanzial; Francesco Benedicenti; Günther Rudolph; Ulrich Kellner; Christian Hamel; Sten Andréasson; Gergely Zobor; Torsten Strasser; Bernd Wissinger; Susanne Kohl; Eberhart Zrenner; for the RD-CURE Consortium
TAGS: achromatopsia, genes, vif, phenotype, psychophysics, retinal cone, electroretinography, rod photoreceptors, atrophy, electrophysiology
Invest. Ophthalmol. Vis. Sci.. 2017; 58(2):821-832. doi: https://doi.org/10.1167/iovs.16-20427

Includes: Supplemental Content

Retina November 2016

Increased Plasma cGMP in a Family With Autosomal Recessive Retinitis Pigmentosa Due to Homozygous Mutations in the PDE6A Gene

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Ulrika Kjellström; Patricia Veiga-Crespo; Sten Andréasson; Per Ekström
TAGS: cyclic gmp, family, genes, homozygote, mutation, plasma, retinitis pigmentosa, autosomal recessive inheritance, electroretinography
Invest. Ophthalmol. Vis. Sci.. 2016; 57(14):6048-6057. doi: https://doi.org/10.1167/iovs.16-19861

ARVO Annual Meeting Abstract September 2016

Clinical characterization and genotype-phenotype correlations in PDE6A -related retinitis pigmentosa

Ditta Zobor; Laura Kühlewein; Nicole Weisschuh; Christian P Hamel; Bart Peter Leroy; Sten Andreasson; Ayuso Carmen; Günther Rudolph; Bernd Wissinger; Susanne Kohl; Eberhart Zrenner

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):152. doi:

ARVO Annual Meeting Abstract September 2016

Whole exome screening and identification of novel variants in a cohort of 28 Greek and Swedish families with cone-rod dystrophy.

Nicola Bedoni; Konstantinos Nikopoulos; Pietro Farinelli; Beryl Royer-Bertrand; Sara Balzano; Sten Andreasson; Miltiadis K Tsilimbaris; Chrysanthi Tsika; Stella Blazaki; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):671. doi:

ARVO Annual Meeting Abstract September 2016

Whole exome sequencing reveals CEP78 as a novel disease gene for cone-rod dystrophy

Konstantinos Nikopoulos; Pietro Farinelli; Beryl Royer-Bertrand; Nicola Bedoni; Ulrika Kjellström; Sten Andreasson; Miltiadis K Tsilimbaris; Chrysanthi Tsika; Stella Blazaki; Carlo Rivolta

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

ARVO Annual Meeting Abstract September 2016

Function of the visual pathway in preterm children at school age.

Hanna Maria Akerblom; Sten Andreasson

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3601. doi:

ARVO Annual Meeting Abstract June 2015

Recessive mutations in the polyglutamylase TTLL5, present in photoreceptor cells and spermatozoa, cause cone-rod degeneration and incompletely penetrant male infertility.

Nicola Bedoni; Lonneke Haer-Wigman; Manir Ali; Frans Cremers; Sten Andreasson; Francis L Munier; Carlo Rivolta; TTLL5 European Retinal Disease Consortium Study Group

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2889. doi:

Articles December 2014

Photoreceptor Function in School-Aged Children is Affected by Preterm Birth

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Hanna Åkerblom; Sten Andreasson; Eva Larsson; Gerd Holmström
TAGS: child, photoreceptors, premature birth, rod photoreceptors, school-age child, electroretinography, retinal cone
Trans. Vis. Sci. Tech.. 2014; 3(6):7. doi: https://doi.org/10.1167/tvst.3.6.7

Includes: Supplemental Content

ARVO Annual Meeting Abstract April 2014

Retinal function and morphology in the rabbit eye after intravitreal injection of the TNF alpha inhibitor adalimumab

Anna Cardiakidis Myers; Fredrik K Ghosh; Sten Andreasson; Vesna Ponjavic

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1921. doi:

ARVO Annual Meeting Abstract April 2014

A cross-linked hyaluronic acid hydrogel (Healaflow ®) as a potential vitreous substitute

Henrik Barth; Sven W Crafoord; Cyrille Vinchon; Sten Andreasson; Fredrik K Ghosh

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):2338. doi:

ARVO Annual Meeting Abstract April 2014

Macular function measured with mfERG in prematurely-born children at school-age

Hanna M Akerblom; Gerd Holmstrom; Sten Andreasson

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3504. doi:

Retina September 2013

Angiography and Multifocal Electroretinography Show That Blood Supply to the Pig Retina May Be Both Ipsilateral and Contralateral

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Håkan Morén; Bodil Gesslein; Per Undrén; Sten Andreasson; Malin Malmsjö
TAGS: angiogram, electroretinography, retina, retinal ischemia, vascular flow, vasculature, ophthalmic artery, eye
Invest. Ophthalmol. Vis. Sci.. 2013; 54(9):6112-6117. doi: https://doi.org/10.1167/iovs.13-12376

ARVO Annual Meeting Abstract June 2013

Visual Prognosis and Association Between Geno - and Phenotype in Families with ABCA4 Mutations

Ulrika Kjellstrom; Sten Andreasson

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1327. doi:

ARVO Annual Meeting Abstract June 2013

Cone implicit time as a predictor for visual outcome in Macular Hole Surgery

Sten Andreasson; Sten Kjellstrom; Henrik Barth; Fredrik Ghosh; Department of Ophhalmology Lund University

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5784. doi:

Genetics December 2012

Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease

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Kari Branham; Mohammad Othman; Matthew Brumm; Athanasios J. Karoukis; Pelin Atmaca-Sonmez; Beverly M. Yashar; Sharon B. Schwartz; Niamh B. Stover; Karmen Trzupek; Dianna Wheaton; Barbara Jennings; Maria Laura Ciccarelli; K. Thiran Jayasundera; Richard A. Lewis; David Birch; Jean Bennett; Paul A. Sieving; Sten Andreasson; Jacque L. Duncan; Gerald A. Fishman; Alessandro Iannaccone; Richard G. Weleber; Samuel G. Jacobson; John R. Heckenlively; Anand Swaroop
TAGS: degenerative disorders, mutation, x-linked inheritance, screening, genes
Invest. Ophthalmol. Vis. Sci.. 2012; 53(13):8232-8237. doi: https://doi.org/10.1167/iovs.12-11025

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Longitudinal Changes of Macular Curvature in Patients with Retinitis Pigmentosa

Dark-adapted ffERG can predict changes in composite VFQ score after cataract surgery in AMD

Novel epitopes for anti-bestrophin autoantibodies in vitelliform macular dystrophy

Age-related Macular Degeneration: a generalised retinal disorder A prospective study of retinal function using full-field electroretinography

Retinal function improved, assessed with 30-HZ flicker, in patients treated with Aflibercept for neovascular AMD at six months follow-up.

The Clinical Phenotype of CNGA3 -Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial

Increased Plasma cGMP in a Family With Autosomal Recessive Retinitis Pigmentosa Due to Homozygous Mutations in the PDE6A Gene

Clinical characterization and genotype-phenotype correlations in PDE6A -related retinitis pigmentosa

Whole exome screening and identification of novel variants in a cohort of 28 Greek and Swedish families with cone-rod dystrophy.

Whole exome sequencing reveals CEP78 as a novel disease gene for cone-rod dystrophy

Function of the visual pathway in preterm children at school age.

Recessive mutations in the polyglutamylase TTLL5, present in photoreceptor cells and spermatozoa, cause cone-rod degeneration and incompletely penetrant male infertility.

Photoreceptor Function in School-Aged Children is Affected by Preterm Birth

Retinal function and morphology in the rabbit eye after intravitreal injection of the TNF alpha inhibitor adalimumab

A cross-linked hyaluronic acid hydrogel (Healaflow ®) as a potential vitreous substitute

Macular function measured with mfERG in prematurely-born children at school-age

Angiography and Multifocal Electroretinography Show That Blood Supply to the Pig Retina May Be Both Ipsilateral and Contralateral

Visual Prognosis and Association Between Geno - and Phenotype in Families with ABCA4 Mutations

Cone implicit time as a predictor for visual outcome in Macular Hole Surgery

Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease

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