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

Get your video featured.

Publish with JoVE

Get your video featured.

Publish with JoVE

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

Pageof 6

Frequent Collaborators

Hannah Klinkhammer

Tzung-Chien Hsieh

Alexej Knaus

Markus Nöthen

Shahida Moosa

Tobias Haack

Axel Schmidt

Jean Tori Pantel

Alexander Hustinx

Theresa Brunet

Frequent Collaborators

Hannah Klinkhammer

Tzung-Chien Hsieh

Alexej Knaus

Markus Nöthen