Contact information
Research groups
Jacek Szymanski
Postdoctoral Neuroscientist
I have completed my MSc degree at the University of Warsaw, having studied the role of interleukin 6 in the regulation of mouse behaviour at the Nencki Institute of Experimental Biology.
Next, I was awarded a PhD by the University of Valencia, where I researched the genetic and molecular mechanisms underlying neurological disorders with a particular focus on neurodegenerative diseases. As a predoctoral investigator at Centro de Investigación Biomédica en Red Enfermedades Neurodegenerativas (CIBERNED), I was part of a team awarded a grant to study a mutation related to the familial form of Alzheimer’s disease.
I joined the Liliana Minichiello group in February of 2022.
My main interest is understanding the molecular, cellular, and genetic mechanisms governing neurological disorders.
Currently, I study the impact of neurotrophin signalling on the development of neural circuits to comprehend its contribution to cognitive disorders. With the recent establishment of cutting-edge sequencing techniques in the lab, such as RNAseq analysis of single-cell, I wish to identify the sequence of transcriptional and epigenetic changes regulating time-sensitive periods during specific brain circuit development and establish how these are perturbed by the absence of neurotrophin signalling.
I also enjoy supervising students at the laboratory and assisting in general lab management.
Key publications
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NKCC1 Deficiency in Forming Hippocampal Circuits Triggers Neurodevelopmental Disorder: Role of BDNF-TrkB Signalling.
Journal article
Szymanski J. and Minichiello L., (2022), Brain Sci, 12
Recent publications
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Development of a cellular model to study the role of CR1 in Alzheimer's disease
Journal article
Cardona F. et al, (2022), European Journal of Human Genetics
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Evaluation of a novel variant in CR1 in patients with Alzheimer's disease
Journal article
Szymanski J. et al, (2022), European Journal of Human Genetics
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NKCC1 Deficiency in Forming Hippocampal Circuits Triggers Neurodevelopmental Disorder: Role of BDNF-TrkB Signalling.
Journal article
Szymanski J. and Minichiello L., (2022), Brain Sci, 12
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Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome.
Journal article
Vázquez-Costa JF. et al, (2021), Front Mol Neurosci, 14
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Interleukin 6 deficiency affects spontaneous activity of mice in age- and sex-dependent manner.
Journal article
Aniszewska A. et al, (2014), Acta Neurobiol Exp (Wars), 74, 424 - 432