Patrick Nitschke

7PUBLICATIONS
148CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Child language acquisitionHaematological tumoursGene expression (incl. microarray and other genome-wide approaches)Molecular medicine
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Publications (7)

|Jul 09, 2026
ADAR1 loss-of-function variants altering RNA editing define a new interferon-dependent psoriasis subtype.

|Feb 13, 2025
Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech.

Clothilde Ormieres, Marion Lesieur-Sebellin, Karine Siquier-Pernet

|Apr 24, 2024
Comprehensive Genetic Profiling Reveals Frequent Alterations of Driver Genes on the X Chromosome in Extranodal NK/T-cell Lymphoma.

Yuta Ito, Amira Marouf, Yasunori Kogure

|Jun 18, 2022
Complex regulation of Gephyrin splicing is a determinant of inhibitory postsynaptic diversity.

Raphaël Dos Reis, Etienne Kornobis, Alyssa Pereira

|Dec 01, 2020
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia.

Ekin Ucuncu, Karthyayani Rajamani, Miranda S C Wilson

|Nov 16, 2018
Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome.

Tenzin Gayden, Fernando E Sepulveda, Dong-Anh Khuong-Quang

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Frequent Collaborators

2 joint publications

Tenzin Gayden

2 joint publications

Fernando E Sepulveda

2 joint publications

Dong-Anh Khuong-Quang

2 joint publications

Elvis T Valera