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Peter M Krawitz

34PUBLICATIONS
419CO-AUTHORS
Cellular immunologyGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases
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Journal

Publications (34)

Sort by Publication Date:
|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.

|May 18, 2026
Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

|Apr 10, 2026
<i>FRMPD4</i>, 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

9 joint publications

Hannah Klinkhammer

8 joint publications

Tzung-Chien Hsieh

7 joint publications

Alexej Knaus

7 joint publications

Markus Nöthen

6 joint publications

Shahida Moosa

5 joint publications

Tobias Haack

5 joint publications

Axel Schmidt

5 joint publications

Jean Tori Pantel

5 joint publications

Alexander Hustinx

4 joint publications

Theresa Brunet

Frequent Collaborators

9 joint publications

Hannah Klinkhammer

8 joint publications

Tzung-Chien Hsieh

7 joint publications

Alexej Knaus

7 joint publications

Markus Nöthen