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Single cell whole-genome sequencing of brain cells: age- and cell-type specific mutational profiles

2024 . Capasso, Melania | Aziz, Ahmad

Genomes in clinical care

2024 . Riess, Olaf | Sturm, Marc | Menden, Benita | Liebmann, Alexandra | Demidov, German | Witt, Dennis | Casadei, Nicolas | Admard, Jakob | Schütz , Leon | Ossowski, Stephan | Taylor, Stacie | Schaffer, Sven | Schroeder, Christopher | Dufke, Andreas

High-quality phenotypic and genotypic dataset of barley genebank core collection to unlock untapped genetic diversity

Most Tibetan weedy barleys originated via recombination between Btr1 and Btr2 in domesticated barley

2024 . Gao, Guangqi | Yan, Luxi | Cai, Yu | Guo, Yu | Jiang, Congcong | He, Qiang | Tasnim, Sarah | Feng, Zongyun | Liu, Jun | Zhang, Jing | Komatsuda, Takao | Mascher, Martin | Yang, Ping

Fatal infection caused by a genetically distinct elephant endotheliotropic herpesvirus type 5 in a captive Asian elephant in Germany

2024 . Abdelgawad, Azza | Nascimento, Mariana | Prahl, Adriane | Flügger, Michael | Szentiks, Claudia A. | Holtze, Susanne | Hildebrandt, Thomas B. | Trimpert, Jakob

Variants in mitochondrial disease genes are common causes of inherited peripheral neuropathies

2024 . Ferreira, Tomas | Polavarapu, Kiran | Olimpio, Catarina | Paramonov, Ida | Lochmüller, Hanns | Horvath, Rita

Striated muscle-specific base editing enables correction of mutations causing dilated cardiomyopathy

Metabolic signatures from genebank collections: an underexploited resource for human health?

2023 . Sreenivasulu, Nese | Alseekh, Saleh | Tiozon, Rhowell N Jr | Graner, Andreas | Martin, Cathie | Fernie, Alisdair

The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay

Current status of the analytical validation of next generation sequencing applications for pharmacogenetic profiling

2023 . Huebner, Tatjana | Steffens, Michael | Scholl, Catharina

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