Eric N. Anderson

Eric N. Anderson

Emergency Medicine
6801 Breacksville Rd
Independence, OH 44131

Last Updated: 09/26/2026

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Found 37 publications

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder.

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder.

Journal: American journal of human genetics
Published: April 05, 2026

Breaking β-sheets in FUS prion-like domain preserves phase separation and function but prevents aggregation and toxicity.

Breaking β-sheets in FUS prion-like domain preserves phase separation and function but prevents aggregation and toxicity.

Journal: bioRxiv : the preprint server for biology
Published: February 27, 2026

The alternative androgen receptor isoform A mitigates toxicity of polyglutamine-elongated mutant androgen receptor in spinal and bulbar muscular atrophy.

The alternative androgen receptor isoform A mitigates toxicity of polyglutamine-elongated mutant androgen receptor in spinal and bulbar muscular atrophy.

Journal: Journal of advanced research
Published: July 23, 2025

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Journal: medRxiv : the preprint server for health sciences
Published: April 16, 2025

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Journal: American journal of human genetics
Published: April 01, 2025

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder.

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder.

Journal: American journal of human genetics
Published: July 31, 2024

HuD (ELAVL4) gain-of-function impairs neuromuscular junctions and induces apoptosis in in vitro and in vivo models of amyotrophic lateral sclerosis.

HuD (ELAVL4) gain-of-function impairs neuromuscular junctions and induces apoptosis in in vitro and in vivo models of amyotrophic lateral sclerosis.

Journal: bioRxiv : the preprint server for biology
Published: March 11, 2024

CLIP-Seq analysis enables the design of protective ribosomal RNA bait oligonucleotides against C9ORF72 ALS/FTD poly-GR pathophysiology.

CLIP-Seq analysis enables the design of protective ribosomal RNA bait oligonucleotides against C9ORF72 ALS/FTD poly-GR pathophysiology.

Journal: Science advances
Published: November 10, 2023

Small-molecule dissolution of stress granules by redox modulation benefits ALS models.

Small-molecule dissolution of stress granules by redox modulation benefits ALS models.

Journal: Nature chemical biology
Published: August 31, 2023

Loss of function of the ALS-associated NEK1 kinase disrupts microtubule homeostasis and nuclear import.

Loss of function of the ALS-associated NEK1 kinase disrupts microtubule homeostasis and nuclear import.

Journal: Science advances
Published: August 16, 2023

HuD impairs neuromuscular junctions and induces apoptosis in human iPSC and Drosophila ALS models.

HuD impairs neuromuscular junctions and induces apoptosis in human iPSC and Drosophila ALS models.

Journal: Nature communications
Published: August 08, 2023

SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration.

SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration.

Journal: Acta neuropathologica
Published: May 17, 2023
Showing 1-12 of 37

Last Updated: 09/26/2026