Erin L Heinzen

18PUBLICATIONS
99CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Solid tumoursEpigenetics (incl. genome methylation and epigenomics)Autonomic nervous systemGene and molecular therapy
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Publications (18)

|Mar 23, 2026
Disrupted O-GalNAc glycosylation as a mechanism and biomarker of SLC35A2-associated epilepsy.

Robert G Mealer, James J Anderson, Sheridan L Smith

|May 26, 2025
SLC35A2 loss-of-function variants affect glycomic signatures, neuronal fate and network dynamics.

Dulcie Lai, Paulina Sosicka, Damian J Williams

|Feb 17, 2025
RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS.

Avinash V Dharmadhikari, Maria Alba Abad, Sheraz Khan

|Dec 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene.

Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati

|Oct 23, 2023
Post-zygotic rescue of meiotic errors causes brain mosaicism and focal epilepsy.

Katherine E Miller, Adithe C Rivaldi, Noriyuki Shinagawa

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