Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Iris te Paske, Stephan Ossowski et al.|European Journal of Human Genetics|2021Cited by 104
Twist exome capture allows for lower average sequence coverage in clinical exome sequencingBurcu Yaldız, Erdi Küçük, Juliet E. Hampstead et al.|Human Genomics|2023Cited by 33
Solving unsolved rare neurological diseases—a Solve-RD viewpointMarc Sturm, Dagmar Timmann, Jennifer Reichbauer et al.|European Journal of Human Genetics|2021Cited by 16
An interconnected data infrastructure to support large-scale rare disease researchLennart Johansson, Matthis Synofzik, Steven Laurie et al.|GigaScience|2024Cited by 9
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Nienke van Os, Kornelia Ellwanger et al.|European Journal of Human Genetics|2021Cited by 1