Publications by authors named "Bernhard Weber"

260Publications

Sensorimotor impairment and haptic support in microgravity.

Exp Brain Res 2021 Jan 19. Epub 2021 Jan 19.

German Aerospace Center, Institute of Robotics and Mechatronics, Oberpfaffenhofen, Germany.

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January 2021

Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the Gene.

Int J Mol Sci 2020 Dec 8;21(24). Epub 2020 Dec 8.

Zentrum für Seltene Netzhauterkrankungen, AugenZentrum Siegburg, MVZ Augenärztliches Diagnostik- und Therapiecentrum Siegburg GmbH, Europaplatz 3, 53721 Siegburg, Germany.

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December 2020

Altered Protein Function Caused by AMD-associated Variant rs704 Links Vitronectin to Disease Pathology.

Invest Ophthalmol Vis Sci 2020 Dec;61(14)

Institute of Human Genetics, University of Regensburg, Regensburg, Germany.

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December 2020

Learning from Fifteen Years of Genome-Wide Association Studies in Age-Related Macular Degeneration.

Cells 2020 10 10;9(10). Epub 2020 Oct 10.

Institute of Human Genetics, University of Regensburg, 93053 Regensburg, Germany.

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October 2020

Sensorimotor performance and haptic support in simulated weightlessness.

Exp Brain Res 2020 Oct 7;238(10):2373-2384. Epub 2020 Aug 7.

Institute of Movement and Neurosciences, German Sport University, Cologne, Germany.

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October 2020

Everyday bodily movement is associated with creativity independently from active positive affect: a Bayesian mediation analysis approach.

Sci Rep 2020 07 20;10(1):11985. Epub 2020 Jul 20.

Department of Psychology, Health Psychology Unit, University of Graz, Univ.-Platz 2, 8010, Graz, Austria.

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July 2020

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.

Genet Med 2020 Jul 20;22(7):1235-1246. Epub 2020 Apr 20.

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

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July 2020

Mutation-Dependent Pathomechanisms Determine the Phenotype in the Bestrophinopathies.

Int J Mol Sci 2020 Feb 26;21(5). Epub 2020 Feb 26.

Institute of Human Genetics, University of Regensburg, Franz-Josef-Strauß-Allee 11, 93053 Regensburg, Germany.

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February 2020

Cell-Type-Specific Complement Expression in the Healthy and Diseased Retina.

Cell Rep 2019 11 26;29(9):2835-2848.e4. Epub 2019 Nov 26.

Department of Physiological Genomics, Biomedical Center, Ludwig Maximilians University Munich, Planegg-Martinsried 82152, Germany. Electronic address:

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November 2019