Sarah Weckhuysen

25PUBLICATIONS
238CO-AUTHORS
NeonatologyGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Genomics
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Publications (25)

|Aug 18, 2026
Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

|Jan 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Sebastian Ortiz, Leonardo Affronte, Chiara Bagliani

|Jan 07, 2026
Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.

Johannes R Lemke, Andrea Eoli, Ilona Krey

|Oct 14, 2025
GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.

Johannes R Lemke, Andrea Eoli, Ilona Krey

|Jul 06, 2025
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes.

Cristina T Vicente, Tejasvi Niranjan, Elise Coopman

|Jun 05, 2025
The genetic and phenotypic spectrum of GABRB1-related disorders.

Charissa Millevert, Anthony Sze Hon Kan, Moritz Hanke

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Frequent Collaborators

8 joint publications

Rikke Steensbjerre Møller

5 joint publications

Johannes R Lemke

4 joint publications

Matthias De Wachter

4 joint publications

Ingo Helbig