Peter M Krawitz

35PUBLICATIONS
444CO-AUTHORS
NeurogeneticsCellular immunologyGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases
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Publications (35)

|Jul 27, 2026
Further characterization of the BRSK2-associated neurodevelopmental disorder.

|Jul 13, 2026
Self-explaining artificial intelligence for the classification of B cell non-Hodgkin lymphoma: A diagnostic decision support study.

|Jul 03, 2026
Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.

|Apr 10, 2026
FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.

Daniel Liedtke, Kristen Rak, Katrina M Schrode

|Apr 08, 2026
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Rocio Rius, Alexander J M Blakes, Yuyang Chen

|Mar 26, 2026
DNA methylation signature and clinical delineation of PACS1-related disorder in 24 unreported individuals.

Quentin Sabbagh, Camille Cenni, Sadegheh Haghshenas

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Frequent Collaborators

10 joint publications

Hannah Klinkhammer

9 joint publications

Tzung-Chien Hsieh

7 joint publications

Alexej Knaus

7 joint publications

Markus Nöthen