Lukasz Sznajder

6PUBLICATIONS
14CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene and molecular therapyInnate immunityNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (6)

|Apr 21, 2025
Autism-related traits in myotonic dystrophy type 1 model mice are due to MBNL sequestration and RNA mis-splicing of autism-risk genes.

Łukasz J Sznajder, Mahreen Khan, Adam Ciesiołka

|Aug 30, 2023
Autistic traits in myotonic dystrophy type 1 due to MBNL inhibition and RNA mis-splicing.

Lukasz Sznajder, Mahreen Khan, Mariam Tadross

|Sep 15, 2020
The sustained expression of Cas9 targeting toxic RNAs reverses disease phenotypes in mouse models of myotonic dystrophy type 1.

Ranjan Batra, David A Nelles, Daniela M Roth

|Apr 26, 2020
Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood.

Łukasz J Sznajder, Marina M Scotti, Jihae Shin

|Jul 21, 2019
Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy.

Łukasz J Sznajder, Maurice S Swanson

|Apr 04, 2018
Intron retention induced by microsatellite expansions as a disease biomarker.

Łukasz J Sznajder, James D Thomas, Ellie M Carrell

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Frequent Collaborators

4 joint publications

Maurice Swanson

2 joint publications

Ryan Yuen

2 joint publications

Christopher Pearson

1 joint publications

Tammy Reid