Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia

Author:

Molz Barbara,Herbik Anne,Baseler Heidi A.,de Best Pieter B.,Vernon Richard W.,Raz Noa,Gouws Andre D.,Ahmadi Khazar,Lowndes Rebecca,McLean Rebecca J.,Gottlob Irene,Kohl Susanne,Choritz Lars,Maguire John,Kanowski Martin,Käsmann-Kellner Barbara,Wieland Ilse,Banin Eyal,Levin Netta,Hoffmann Michael B.,Morland Antony B.

Funder

Biotechnology and Biological Sciences Research Council

Deutsche Forschungsgemeinschaft

Horizon 2020 Framework Programme

Horizon 2020

H2020 Marie Skłodowska-Curie Actions

Publisher

Elsevier BV

Subject

Cognitive Neuroscience,Neurology (clinical),Neurology,Radiology, Nuclear Medicine and imaging

Reference73 articles.

1. The cone dysfunction syndromes;Aboshiha;Br. J. Ophthalmol.,2016

2. Postretinal structure and function in severe congenital photoreceptor blindness caused by mutations in the GUCY2D gene;Aguirre;Invest. Ophthalmol. Vis. Sci.,2017

3. Patterns of individual variation in visual pathway structure and function in the sighted and blind;Aguirre;PLoS ONE,2016

4. Confound modelling in UK Biobank brain imaging;Alfaro-Almagro;NeuroImage,2021

5. Relationship between cortical thickness and functional activation in the early blind;Anurova;Cerebral Cortex (New York, NY),2015

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1. Update on gene therapies in pediatric ophthalmology;Archives de Pédiatrie;2023-11

2. Achromatopsia—Visual Cortex Stability and Plasticity in the Absence of Functional Cones;Investigative Opthalmology & Visual Science;2023-10-17

3. Vision restoration: Little red booster;Current Biology;2023-09

4. Achromatopsia;Die Ophthalmologie;2023-08-28

5. Seeing color following gene augmentation therapy in achromatopsia;Current Biology;2023-08

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