Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

Overview of attention for article published in Genome Medicine, August 2023

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In the top 5% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (98th percentile)
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Feinstruktur der Gene: Ursache für Nierenleiden entschlüsselt

Der Tagesspiegel, 28 Aug 2023

Gene sind Teil komplexer biologischer Programme: Berliner Forschende wurden nun davon überrascht, auf welchen Wegen eine…

Team Genetically Decodes Rare Kidney Disease

Laboratory Equipment , 25 Aug 2023

Only use in course of reposrting about this paper or the Genomics platform at Max Delbrück Center.

Rare kidney disease is genetically decoded

Bionity, 25 Aug 2023

Bartter syndrome type 3 is the result of several structural variants in the genome.

News story from Eurasia Review on Wednesday 23 August 2023

Eurasia Review, 23 Aug 2023

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