Author

Sabine Klaassen

Max Delbrück CenterORCID 0000-0001-5925-9912Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alejandro SifrimiD· 1 shared Allan Daly· 1 shared Amilcar Pérez-RiveroliD· 1 shared Amy BakeriD· 1 shared Andres Rico‐Armada· 1 shared Angela Woods· 1 shared Angharad M. RobertsiD· 1 shared Anna WilsdoniD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alejandro SifrimORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 15, 2026

MAP3K7 Loss of Function Causes Dilated Cardiomyopathy

Katherine S. Josephs, Carlos C. Smith-Díaz, Angela Woods…·James S. Ware

This paper shows that loss-of-function variants in MAP3K7 cause dilated cardiomyopathy (DCM), both as part of syndromic disease and as apparently isolated DCM.

DOI 10.64898/2026.09.02.26361780

humanwhole-exome sequencing

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Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedJun 2, 2026

Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome study

Enrique Audain, Anna Wilsdon, Gregor Dombrowsky…·Marc‐Phillip Hitz

This study identifies rare variants and digenic interactions associated with congenital heart disease using a large-scale exome case-control analysis.

5 citations

humanwhole-exome sequencing

𝕏 PostBluesky