Allan Bayat

40PUBLICATIONS
245CO-AUTHORS
Infant and child healthCharacterisation of biological macromoleculesNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (40)

|Jul 22, 2026
Abnormal ClC-3/TMEM9-mediated endosomal ion transport in CLCN3-associated neurodevelopmental disease.

|Jun 02, 2026
Add-on treatment with vinpocetine reduces seizure frequency and improves comorbidities in patients with loss-of-function γ-aminobutyric acid type A receptor variants.

|Mar 26, 2026
DNA methylation signature and clinical delineation of PACS1-related disorder in 24 unreported individuals.

Quentin Sabbagh, Camille Cenni, Sadegheh Haghshenas

|Jan 13, 2026
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans.

Claudia M Bonardi, Rikke S Møller, Nuria Ruiz-Reig

|Oct 12, 2025
The LMSz method - an automatable scalable approach to constructing gene-specific growth charts in rare disorders.

Karen J Low, Julia Foreman, Rachel J Hobson

|Sep 17, 2025
PIGC-related encephalopathy: Lessons learned from 18 new probands.

Allan Bayat, Maria Carla Borroto, Smrithi Salian

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Frequent Collaborators

12 joint publications

Rikke Steensbjerre Møller

8 joint publications

Elena Gardella

7 joint publications

Gaetan Lesca

5 joint publications

Ángel Aledo-Serrano