Łukasz Sznajder

Assistant Professor, Department of Chemistry and Biochemistry
Expertise: Molecular biology and genetics, Neuromuscular and neuropsychiatric disorders, Autism spectrum disorder (ASD), Myotonic dystrophy

Biography

Łukasz Sznajder is an expert in molecular genetics, with particular interest in human hereditary neuropsychiatric and neuromuscular disorders. 

Sznajder is an assistant professor of chemistry and biochemistry within UNLV’s College of Sciences. His long-term goal is to strengthen our understanding of the molecular mechanisms behind neurogenetic disorders caused by repetitive DNA sequences and RNA mis-processing, such as myotonic dystrophy, amyotrophic lateral sclerosis (ALS), and ASD.

For nearly two decades, both in the United States and Poland, he has conducted numerous studies about deciphering disease mechanisms, characterizing mouse models, identifying blood biomarkers, and developing therapeutic approaches for life-threatening human diseases.

Sznajder has 19 peer-reviewed articles in journals such as Nature Neuroscience, Nature Communications, Nature Biomedical Engineering, and PNAS. He's been consistently funded by both federal agencies and non-profit organizations, including the National Institute of General Medical Sciences, Myotonic Dystrophy Foundation, and Muscular Dystrophy Association.

Education

  • Postdoctoral Researcher in Human/Medical Genetics, University of Florida
  • Ph.D. in Molecular Biology, Adam Mickiewicz University (Poland)
  • M.Sc. in Biotechnology, University of Life Sciences (Poland)
  • B.Eng. in Biotechnology, University of Life Sciences (Poland)

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Łukasz Sznajder In The News

K.L.A.S. T.V. 8 News Now
Researchers at the University of Nevada, Las Vegas, have made a significant breakthrough in autism research. The UNLV researchers uncovered a connection to a type of neuromuscular disease called myotonic dystrophy.
Newswise
A recent discovery of a molecular connection between autism and myotonic dystrophy, a type of neuromuscular disease, may provide a breakthrough on how clinicians approach autism spectrum disorder. The new study by an interdisciplinary team of biomedical scientists, published on April 21 in Nature Neuroscience, used myotonic dystrophy as a tool or model to learn more about autism – effectively using one disorder to better understand the other.
Daily Mail
Autism may be caused by a little-known genetic condition, experts say. They've found children with myotonic dystrophy type 1 (DM1) are also 14 times more likely to develop autistic spectrum disorder.
Medical Xpress
Scientists from The Hospital for Sick Children (SickKids) and the University of Las Vegas, Nevada (UNLV) have uncovered a genetic link between autism spectrum disorder (ASD) and a rare genetic condition called myotonic dystrophy type 1 (DM1).

Articles Featuring Łukasz Sznajder

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Campus News | May 1, 2025

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