Lucia Janickova

University of Fribourg — Switzerland

Biochemistry, Genetics and Molecular Biology · Life Sciences

7h-index303citations13works14.52yr avg
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Research Topics

Sulfur Compounds in Biology(5), Genetics and Neurodevelopmental Disorders(5), Autism Spectrum Disorder Research(3), Mitochondrial Function and Pathology(3), Folate and B Vitamins Research(3)

Publications13 total

Structural basis for a filamentous morpheein model of human cystathionine beta-synthase
2025Open Access
Cyanide overproduction impairs cellular bioenergetics in Down syndrome
Neurotherapeutics·2025· 4 citedOpen Access
Regulation of mammalian cellular metabolism by endogenous cyanide production
Nature Metabolism·2025· 22 citedOpen Access
ER calcium depletion as a key driver for impaired ER-to-mitochondria calcium transfer and mitochondrial dysfunction in Wolfram syndrome
Nature Communications·2024· 40 citedOpen Access
Endogenously produced hydrogen cyanide serves as a novel mammalian gasotransmitter
2024· 1 citedOpen Access
Neurobehavioral dysfunction in a mouse model of Down syndrome: upregulation of cystathionine β-synthase, H2S overproduction, altered protein persulfidation, synaptic dysfunction, endoplasmic reticulum stress, and autophagy
GeroScience·2024· 20 citedOpen Access
ER Calcium Depletion as a Key Driver for Impaired ER-to-Mitochondria Calcium Transfer and Mitochondrial Dysfunction in Wolfram Syndrome
2023· 1 citedOpen Access
Impact of <scp>COVID</scp>‐19 in patients with autoimmune bullous diseases: Report from an international registry
Journal of the European Academy of Dermatology and Venereology·2023Open Access
Overproduction of hydrogen sulfide, generated by cystathionine β-synthase, disrupts brain wave patterns and contributes to neurobehavioral dysfunction in a rat model of down syndrome
Redox Biology·2022· 61 citedOpen Access
Correction to: Absence of parvalbumin increases mitochondria volume and branching of dendrites in inhibitory Pvalb neurons in vivo: a point of convergence of autism spectrum disorder (ASD) risk gene phenotypes
Molecular Autism·2021· 1 citedOpen Access
The Parvalbumin Hypothesis of Autism Spectrum Disorder
Frontiers in Cellular Neuroscience·2020· 111 citedOpen Access
Parvalbumin-Deficiency Accelerates the Age-Dependent ROS Production in Pvalb Neurons in vivo: Link to Neurodevelopmental Disorders
Frontiers in Cellular Neuroscience·2020· 18 citedOpen Access
Absence of parvalbumin increases mitochondria volume and branching of dendrites in inhibitory Pvalb neurons in vivo: a point of convergence of autism spectrum disorder (ASD) risk gene phenotypes
Molecular Autism·2020· 24 citedOpen Access

Frequent Co-authors

Karim Zuhra(5), Csaba Szabó(5), Beat Schwaller(4), Tomáš Majtán(4), Kelly Ascenção(4), Maria Petrosino(3), Moustafa M.R. Khalaf(3), Anna Kieronska‐Rudek(3), Brian A. Logue(3), Miloš R. Filipović(3), Theodora Panagaki(2), Mailis Liiv(2), Annika Vaarmann(2), Vinay Choubey(2), Malle Kuum(2), Zuzana Hodurova(2), Michal Cagalinec(2), Akbar Zeb(2), Miriam A. Hickey(2), Merle Mandel(2)