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- University of Regensburg (17)
- Medicine (17)
- Lehrstuhl für Humangenetik (17)
- Medicine (17)
B
Berber, Patricia and Bondarenko, Sofiia and Michaelis, Lisa and Weber, Bernhard Heinrich Friedrich (2022) Transient Retention of Photoreceptor Outer Segments in Matrigel-Embedded Retinal Organoids. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (23): 14893. ISSN , 1422-0067
Biasella, Fabiola and Strunz, Tobias and Kiel, Christina and Weber, Bernhard H. F. and Friedrich, Ulrike (2022) Vitronectin and Its Interaction with PAI-1 Suggests a Functional Link to Vascular Changes in AMD Pathobiology. CELLS, 11 (11): 1766. ISSN , 2073-4409
Brandl, Caroline and Grassmann, Felix and Riolfi, Julia and Weber, Bernhard H. F. (2015) Tapping Stem Cells to Target AMD: Challenges and Prospects. MDPI, BASEL.
Brandl, Caroline and Schulz, Heidi L. and Issa, Peter Charbel and Birtel, Johannes and Bergholz, Richard and Lange, Clemens and Dahlke, Claudia and Zobor, Ditta and Weber, Bernhard H. F. and Stoehr, Heidi (2017) Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions. GENES, 8 (7). ISSN 2073-4425
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Cardon, Iseline and Grobecker, Sonja and Kuecuekoktay, Selin and Bader, Stefanie and Jahner, Tatjana and Nothdurfter, Caroline and Koschitzki, Kevin and Berneburg, Mark and Weber, Bernhard H. F. and Stoehr, Heidi and Hoering, Marcus and Liebisch, Gerhard and Braun, Frank and Rothammer-Hampl, Tanja and Riemenschneider, Markus J. and Rupprecht, Rainer and Milenkovic, Vladimir M. and Wetzel, Christian H. (2024) Mitochondrial and Cellular Function in Fibroblasts, Induced Neurons, and Astrocytes Derived from Case Study Patients: Insights into Major Depression as a Mitochondria-Associated Disease. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 25 (2): 963. ISSN 1661-6596, 1422-0067
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Dumont, Martine and Weber-Lassalle, Nana and Joly-Beauparlant, Charles and Ernst, Corinna and Droit, Arnaud and Feng, Bing-Jian and Dubois, Stephane and Collin-Deschesnes, Annie-Claude and Soucy, Penny and Vallee, Maxime and Fournier, Frederic and Lemacon, Audrey and Adank, Muriel A. and Allen, Jamie and Altmueller, Janine and Arnold, Norbert and Ausems, Margreet G. E. M. and Berutti, Riccardo and Bolla, Manjeet K. and Bull, Shelley and Carvalho, Sara and Cornelissen, Sten and Dufault, Michael R. and Dunning, Alison M. and Engel, Christoph and Gehrig, Andrea and Geurts-Giele, Willemina R. R. and Gieger, Christian and Green, Jessica and Hackmann, Karl and Helmy, Mohamed and Hentschel, Julia and Hogervorst, Frans B. L. and Hollestelle, Antoinette and Hooning, Maartje J. and Horvath, Judit and Ikram, M. Arf An and Kaulfuss, Silke and Keeman, Renske and Kuang, Da and Luccarini, Craig and Maier, Wolfgang and Martens, John W. M. and Niederacher, Dieter and Nurnberg, Peter and Ott, Claus-Eric and Peters, Annette and Pharoah, Paul D. P. and Ramirez, Alfredo and Ramser, Juliane and Riedel-Heller, Steffi and Schmidt, Gunnar and Shah, Mitul and Scherer, Martin and Stabler, Antje and Strom, Tim M. and Sutter, Christian and Thiele, Holger and van Asperen, Christi J. and van der Kolk, Lizet and van der Luijt, Rob B. and Volk, Alexander E. and Wagner, Michael and Waisfisz, Quinten and Wang, Qin and Wang-Gohrke, Shan and Weber, Bernhard H. F. and Devilee, Peter and Tavtigian, Sean and Bader, Gary D. and Meindl, Alfons and Goldgar, David E. and Andrulis, Irene L. and Schmutzler, Rita K. and Easton, Douglas F. and Schmidt, Marjanka K. and Hahnen, Eric and Simard, Jacques (2022) Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry. CANCERS, 14 (14): 3363. ISSN , 2072-6694
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Gersch, Julia and Hufendiek, Katerina and Delarocque, Julien and Framme, Carsten and Jacobsen, Christina and Stoehr, Heidi and Kellner, Ulrich and Hufendiek, Karsten (2022) Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (24): 16007. ISSN 1661-6596, 1422-0067
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Hitti-Malin, Rebekkah J. and Panneman, Daan M. and Corradi, Zelia and Boonen, Erica G. M. and Astuti, Galuh and Dhaenens, Claire-Marie and Stoehr, Heidi and Weber, Bernhard H. F. and Sharon, Dror and Banin, Eyal and Karali, Marianthi and Banfi, Sandro and Ben-Yosef, Tamar and Glavac, Damjan and Farrar, G. Jane and Ayuso, Carmen and Liskova, Petra and Dudakova, Lubica and Vajter, Marie and Oldak, Monika and Szaflik, Jacek P. and Matynia, Anna and Gorin, Michael B. and Kaempjaervi, Kati and Bauwens, Miriam and De Baere, Elfride and Hoyng, Carel B. and Li, Catherina H. Z. and Klaver, Caroline C. W. and Inglehearn, Chris F. and Fujinami, Kaoru and Rivolta, Carlo and Allikmets, Rando and Zernant, Jana and Lee, Winston and Podhajcer, Osvaldo L. and Fakin, Ana and Sajovic, Jana and Altalbishi, Alaa and Valeina, Sandra and Taurina, Gita and Vincent, Andrea L. and Roberts, Lisa and Ramesar, Raj and Sartor, Giovanna and Luppi, Elena and Downes, Susan M. and van den Born, L. Ingeborgh and Mclaren, Terri L. and De Roach, John N. and Lamey, Tina M. and Thompson, Jennifer A. and Chen, Fred K. and Tracewska, Anna M. and Kamakari, Smaragda and Sallum, Juliana Maria Ferraz and Bolz, Hanno J. and Kayserili, Huelya and Roosing, Susanne and Cremers, Frans P. M. (2024) Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes. BIOMOLECULES, 14 (3): 367. ISSN , 2218-273X
Hufendiek, Karsten and Hufendiek, Katerina and Jaegle, Herbert and Stoehr, Heidi and Book, Marius and Spital, Georg and Rustambayova, Guenay and Framme, Carsten and Weber, Bernhard H. F. and Renner, Agnes B. and Kellner, Ulrich (2020) Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the BEST1 Gene. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 21 (24): 9353. ISSN 1422-0067
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Kiel, Christina and Berber, Patricia and Karlstetter, Marcus and Aslanidis, Alexander and Strunz, Tobias and Langmann, Thomas and Grassmann, Felix and Weber, Bernhard H. F. (2020) A Circulating MicroRNA Profile in a Laser-Induced Mouse Model of Choroidal Neovascularization. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 21 (8): 2689. ISSN 1422-0067
Kiel, Christina and Strunz, Tobias and Blanton, Susan and Grassmann, Felix and Weber, Bernhard H. F. (2020) Pleiotropic Locus 15q24.1 Reveals a Gender-Specific Association with Neovascular but Not Atrophic Age-Related Macular Degeneration (AMD). CELLS, 9 (10): 2257. ISSN 2073-4409
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Nachtigal, Anna-Lena and Milenkovic, Andrea and Brandl, Caroline and Schulz, Heidi L. and Duerr, Lisa M. J. and Lang, Gabriele E. and Reiff, Charlotte and Herrmann, Philipp and Kellner, Ulrich and Weber, Bernhard H. F. (2020) Mutation-Dependent Pathomechanisms Determine the Phenotype in the Bestrophinopathies. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 21 (5): 1597. ISSN 1422-0067
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Strunz, Tobias and Kellner, Martin and Kiel, Christina and Weber, Bernhard H. F. (2021) Assigning Co-Regulated Human Genes and Regulatory Gene Clusters. CELLS, 10 (9): 2395. ISSN , 2073-4409
Strunz, Tobias and Kiel, Christina and Sauerbeck, Bastian L. and Weber, Bernhard H. F. (2020) Learning from Fifteen Years of Genome-Wide Association Studies in Age-Related Macular Degeneration. CELLS, 9 (10): 2267. ISSN 2073-4409
Strunz, Tobias and Poellmann, Michael and Gamulescu, Maria-Andreea and Tamm, Svenja and Weber, Bernhard H. F. (2022) Genetic Association Analysis of Anti-VEGF Treatment Response in Neovascular Age-Related Macular Degeneration. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (11): 6094. ISSN , 1422-0067
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Todorow, Vanessa and Hintze, Stefan and Kerr, Alastair R. W. and Hehr, Andreas and Schoser, Benedikt and Meinke, Peter (2021) Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 22 (16): 8607. ISSN , 1422-0067
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Wolk, Alyson and Hatipoglu, Dilara and Cutler, Alecia and Ali, Mariya and Bell, Lestella and Qi, Jian Hua and Singh, Rupesh and Batoki, Julia and Karle, Laura and Bonilha, Vera L. and Wessely, Oliver and Stoehr, Heidi and Hascall, Vincent and Anand-Apte, Bela (2020) Role of FGF and Hyaluronan in Choroidal Neovascularization in Sorsby Fundus Dystrophy. CELLS, 9 (3): 608. ISSN 2073-4409

