Medverkande i utredning : Sten Andreasson

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Granse, Lotta A. K. C., Ohnell, Hanna Maria V., Holmström, Gerd, Sundgren, Johanna C., Fahnehjelm, Kristina Teär, Wallin, Agneta, Larsson, Eva, Tsamadou, D, Bjorklund, Lars J., Hellström, Ann, Wallander, Jenny, Hochhard, Karin Sandgren, Andreasson, Sten O. L., Olhager, Elisabeth R., Björk, Jonas och Granse, LAKC, Treating Retinopathy of Prematurity with Dexamethasone Eye Drops : A Difference-in-Differences Study in Sweden Using Register Data, Ophthalmology, 2026, 133 nr 2, s. 248–256, : Elsevier

Gränse, Lotta A.K.C., Öhnell, Hanna Maria V., Holmström, Gerd, Sundgren, Johanna C., Fahnehjelm, Kristina Teär, Wallin, Agneta, Larsson, Eva, Tsamadou, Despoina, Björklund, Lars J., Hellström, Ann, Wallander, Jenny, Sandgren Hochhard, Karin, Andreasson, Sten O.L., Olhager, Elisabeth R. och Björk, Jonas, Treating retinopathy of prematurity with dexamethasone eye drops, Ophthalmology, 2026, 133 nr 2, s. 248–256, : Elsevier

Meinert, Monika, Electrophysiological evaluation and morphology of inherited and acquired retinal diseases, 2025, Lund University, Faculty of Medicine, Lund

Areblom, Maria, Kjellström, Sten, Andréasson, Sten, Öhberg, Anders, Gränse, Lotta och Kjellström, Ulrika, A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing, Genes, 2023, 14 nr 7, : MDPI AG

Panneman, Daan M., Hitti-Malin, Rebekkah J., Holtes, Lara K., de Bruijn, Suzanne E., Reurink, Janine, Boonen, Erica G.M., Khan, Muhammad Imran, Ali, Manir, Andréasson, Sten, De Baere, Elfride, Banfi, Sandro, Bauwens, Miriam, Ben-Yosef, Tamar, Bocquet, Béatrice, De Bruyne, Marieke, Cerda, Berta de la, Coppieters, Frauke, Farinelli, Pietro, Guignard, Thomas, Inglehearn, Chris F., Karali, Marianthi, Kjellström, Ulrika, Koenekoop, Robert, de Koning, Bart, Leroy, Bart P., McKibbin, Martin, Meunier, Isabelle, Nikopoulos, Konstantinos, Nishiguchi, Koji M., Poulter, James A., Rivolta, Carlo, Rodríguez de la Rúa, Enrique, Saunders, Patrick, Simonelli, Francesca, Tatour, Yasmin, Testa, Francesco, Thiadens, Alberta A.H.J., Toomes, Carmel, Tracewska, Anna M., Tran, Hoai Viet, Ushida, Hiroaki, Vaclavik, Veronika, Verhoeven, Virginie J.M., van de Vorst, Maartje, Gilissen, Christian, Hoischen, Alexander, Cremers, Frans P.M. och Roosing, Susanne, Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis, Frontiers in Cell and Developmental Biology, 2023, 11, : Frontiers Media S. A.

Forshaw, Thomas Richard Johansen, Subhi, Yousif, Andréasson, Sten och Sørensen, Torben Lykke, Full-Field Electroretinography Changes Associated with Age-Related Macular Degeneration : A Systematic Review with Meta-Analyses, Ophthalmologica, 2022, 245 nr 3, s. 195–203, : Karger

Kjellström, Ulrika och Andréasson, Sten, A five-year follow-up of ABCA4 carriers showing deterioration of retinal function and increased structural changes, Molecular Vision, 2022, 28, s. 300–316, : Molecular Vision

Schroeder, Marion, Peter, Virginie G., Gränse, Lotta, Andréasson, Sten, Rivolta, Carlo och Kjellström, Ulrika, A novel phenotype associated with the R162W variant in the KCNJ13 gene, Ophthalmic Genetics, 2022, 43 nr 4, s. 500–507, : Taylor & Francis

Solaki, Maria, Baumann, Britta, Reuter, Peggy, Andreasson, Sten, Audo, Isabelle, Ayuso, Carmen, Balousha, Ghassan, Benedicenti, Francesco, Birch, David, Bitoun, Pierre, Blain, Delphine, Bocquet, Beatrice, Branham, Kari, Català-Mora, Jaume, De Baere, Elfride, Dollfus, Helene, Falana, Mohammed, Giorda, Roberto, Golovleva, Irina, Gottlob, Irene, Heckenlively, John R., Jacobson, Samuel G., Jones, Kaylie, Jägle, Herbert, Janecke, Andreas R., Kellner, Ulrich, Liskova, Petra, Lorenz, Birgit, Martorell-Sampol, Loreto, Messias, André, Meunier, Isabelle, Belga Ottoni Porto, Fernanda, Papageorgiou, Eleni, Plomp, Astrid S., de Ravel, Thomy J. L., Reiff, Charlotte M., Renner, Agnes B., Rosenberg, Thomas, Rudolph, Günther, Salati, Roberto, Sener, E. Cumhur, Sieving, Paul A., Stanzial, Franco, Traboulsi, Elias I., Tsang, Stephen H., Varsanyi, Balázs, Weleber, Richard G., Zobor, Ditta, Stingl, Katarina, Wissinger, Bernd och Kohl, Susanne, Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia, Human Mutation, 2022, 43 nr 7, s. 832–858, : John Wiley & Sons

Wissinger, Bernd, Baumann, Britta, Buena-Atienza, Elena, Ravesh, Zeinab, Cideciyan, Artur V., Stingl, Katarina, Audo, Isabelle, Meunier, Isabelle, Bocquet, Beatrice, Traboulsi, Elias I., Hardcastle, Alison J., Gardner, Jessica C., Michaelides, Michel, Branham, Kari E., Rosenberg, Thomas, Andreasson, Sten, Dollfus, Hélène, Birch, David, Vincent, Andrea L., Martorell, Loreto, Mora, Jaume Català, Kellner, Ulrich, Ruther, Klaus, Lorenz, Birgit, Preising, Markus N., Manfredini, Emanuela, Zarate, Yuri A., Vijzelaar, Raymon, Zrenner, Eberhart, Jacobson, Samuel G. och Kohl, Susanne, The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy, Proceedings of the National Academy of Sciences of the United States of America och Proceedings of the National Academy of Sciences, 2022, 119 nr 27 och 119 nr 27, : National Academy of Sciences och : National Academy of Sciences

Öhnell, Hanna Maria, Andreasson, Sten och Gränse, Lotta, Dexamethasone eye-drops for treatment of retinopathy of prematurity, Ophthalmology Retina, 2022, 6 nr 2, s. 181–182, : Elsevier

Kjellström, Ulrika, Martell, Susanne, Brobeck, Cecilia och Andréasson, Sten, Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene, Ophthalmic Genetics, 2021, 42 nr 2, s. 161–169, : Taylor & Francis

Forshaw, Thomas Richard Johansen, Ahmed, Hassan Javed, Kjær, Troels Wesenberg, Andréasson, Sten och Sørensen, Torben Lykke, Full-field Electroretinography in Age-related Macular Degeneration : can retinal electrophysiology predict the subjective visual outcome of cataract surgery?, Acta Ophthalmologica, 2020, 98 nr 7, s. 693–700, : Wiley-Blackwell

Kafantari, Efthymia, Andréasson, Sten, Säll, Torbjörn och Puschmann, Andreas, Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?, Parkinsonism and Related Disorders, 2020, 79, s. 138–140, : Elsevier

Kuehlewein, Laura, Zobor, Ditta, Andreasson, Sten Olof, Ayuso, Carmen, Banfi, Sandro, Bocquet, Beatrice, Bernd, Antje S., Biskup, Saskia, Boon, Camiel J.F., Downes, Susan M., Dominik Fischer, M., Holz, Frank G., Kellner, Ulrich, Leroy, Bart P., Meunier, Isabelle, Nasser, Fadi, Rosenberg, Thomas, Rudolph, Günther, Stingl, Katarina, Thiadens, Alberta A.H.J., Wilhelm, Barbara, Wissinger, Bernd, Zrenner, Eberhart, Kohl, Susanne, Weisschuh, Nicole, Bartz-Schmidt, Karl Ulrich, Bolz, Sylvia, Mühlfriedel, Regine, Neubauer, Jonas, Ochakovski, Alex, Paquet-Durand, Francois, Seeliger, Mathias, Sothilingam, Vithiyanjali, Ueffing, Marius, Wozar, Fabian, Zhour, Ahmad, Biel, Martin, Michalakis, Stylianos, Schön, Christian, Kahle, Nadine, Peters, Tobias, Tsang, Stephen H. och Glöckner, Christian Johannes, Clinical phenotype and course of PDE6A-associated retinitis pigmentosa disease, characterized in preparation for a gene supplementation trial, JAMA Ophthalmology, 2020, 138 nr 12, s. 1241–1250, : American Medical Association

Meinert, Monika, Ueno, Shinji, Komori, Shiori, Koyanagi, Yoshito, Sayo, Akira, Andreasson, Sten, Kominami, Taro, Ito, Yasuki och Terasaki, Hiroko, Longitudinal changes of macular curvature in patients with retinitis pigmentosa, Translational Vision Science and Technology, 2020, 9 nr 10, s. 8, : Association for Research in Vision and Ophthalmology Inc.

Schroeder, Marion Silvia, Evaluation of different macular degenerations. Function, morphology and clinical outcomes., 2020, Lund University, Faculty of Medicine, Lund

Sellman, Anders, Katzman, Per, Andreasson, Sten och Lõndahl, Magnus, Long-term effects of hyperbaric oxygen therapy on visual acuity and retinopathy, Undersea & Hyperbaric Medicine, 2020, 47 nr 3, s. 423–430, : Undersea and Hyperbaric Medical Society

Gorcenco, Sorina, Vaz, Frédéric M., Tracewska-Siemiatkowska, Anna, Tranebjaerg, Lisbeth, Cremers, Frans P. M., Ygland, Emil, Kicsi, Jeno, Rendtorff, Nanna Dahl, Möller, Claes, Kjellström, Ulrika, Andréasson, Sten och Puschmann, Andreas, Oral therapy for riboflavin transporter deficiency : What is the regimen of choice?, Parkinsonism & Related Disorders, 2019, 61, s. 245–247, : Elsevier

Peter, Virginie G., Nikopoulos, Konstantinos, Quinodoz, Mathieu, Granse, Lotta, Farinelli, Pietro, Superti-Furga, Andrea, Andréasson, Sten och Rivolta, Carlo, A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa, Ophthalmic Genetics, 2019, 40 nr 2, s. 177–181, : Taylor & Francis

Sellman, Anders, Retinopathy and Visual Acuity in People with Diabetes Mellitus and Hard-to-Heal Diabetic Foot Ulceration, 2019, Lund University, Faculty of Medicine, Lund

Haugen, Olav H., Andréasson, Sten, Ersland, Lars, Craven, Alexander R. och Hugdahl, Kenneth, Cerebral Functional Magnetic Resonance Imaging and Multifocal Visual Evoked Potentials in a Patient with Unexplained Impairment of Visual Function : A Case Report, Case Reports in Ophthalmology, 2018, 9 nr 2, s. 269–278, : Karger

Gorcenco, Sorina, Komulainen-Ebrahim, Jonna, Nordborg, Karin, Suo-Palosaari, Maria, Andréasson, Sten, Krüger, Johanna, Nilsson, Christer, Kjellström, Ulrika, Rahikkala, Elisa, Turkiewicz, Dominik, Karlberg, Mikael, Nilsson, Lars, Cammenga, Jörg, Tedgård, Ulf, Davidsson, Josef, Uusimaa, Johanna och Puschmann, Andreas, Ataxia-pancytopenia syndrome with SAMD9L mutations, Neurology: Genetics, 2017, 3 nr 5, s. 7, : Lippincott Williams & Wilkins

Kamme, Christina, Mayer, Anja Kathrin, Strom, Tim M., Andréasson, Sten och Weisschuh, Nicole, Genotype and Phenotype in an unusual form of Laurence-Moon-Bardet-Biedl syndrome, Acta Ophthalmologica, 2017, 95 nr 3, s. e250-e252, : Wiley-Blackwell

Molnar, Anna E. C., Andreasson, Sten O., Larsson, Eva K. B., Åkerblom, Hanna M. och Holmström, Gerd E., Reduction of rod and cone function in 6.5-year-old children born extremely preterm, JAMA Ophthalmology, 2017, 135 nr 8, s. 854–861, : American Medical Association