André Reis

39PUBLICATIONS
423CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesHaematological tumoursGene mappingGene expression (incl. microarray and other genome-wide approaches)
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Publications (39)

|Apr 02, 2026
Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Camille Engel, Michaela Rendek, Jessica Assoumani

|Mar 12, 2026
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia.

Cyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli

|Jun 25, 2025
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Camille Engel, Michaela Rendek, Jessica Assoumani

|May 16, 2025
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption.

Caroline Nava, Benjamin Cogne, Amandine Santini

|Mar 28, 2025
A novel human organoid model system reveals requirement of TCF4 for oligodendroglial differentiation.

Federica Furlanetto, Nicole Flegel, Marco Kremp

|Feb 28, 2025
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets.

Nick Dand, Philip E Stuart, John Bowes

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Frequent Collaborators

10 joint publications

Arif Ekici

6 joint publications

Bernt Popp

5 joint publications

Frederic Tran Mau-Them

4 joint publications

Anne-Sophie Denommé-Pichon