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Natalia obtained a bachelor in Biology and a Master in Bioinformatics from the University of Geneva (Switzerland), and in 2023, she obtained a PhD in Developmental Neuroscience. During her PhD in the lab of Prof. Denis Jabaudon she studied the mechanisms of differential growth rate between brain regions in the mouse. She also contributed to study the temporal plasticity of apical progenitors and the acquisition of neuronal identity during cortical development, mainly using birth-dating techniques and single-cell transcriptomics. After obtaining her PhD, she continued her work in the Jabaudon lab by focusing on the identity acquisition and maturation of piriform cortex neurons using multimodal characterization including single-cell and spatial transcriptomics, morphology and electrophysiological properties.
Natalia is joining the lab in March 2025, she is interested in understanding how cell lineages shape the human CNS during development.
Resources & publications
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Journal (source)Elife
High N-glycan multiplicity is critical for neuronal adhesion and sensitizes t...
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Journal (source)Brain
Biallelic mutations in neurofascin cause neurodevelopmental impairment and pe...
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Journal (source)Brain
De novo mutation screening in childhood-onset cerebellar atrophy identifies g...
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Journal (source)Orphanet J Rare Dis
Utility of whole exome sequencing for the early diagnosis of pediatric-onset ...
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Journal (source)Am. J. Hum. Genet.
Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct,...
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Journal (source)Hum Mutat
Genotype-phenotype correlations in individuals with pathogenic RERE variants.
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Journal (source)Nat Commun
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisph...
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Journal (source)Blood
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative bl...
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Journal (source)Am J Hum Genet
Disruption of POGZ Is Associated with Intellectual Disability and Autism Spec...
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Journal (source)Nat Genet
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and...
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Journal (source)Cell
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neuro...
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Journal (source)Cell
CLP1 founder mutation links tRNA splicing and maturation to cerebellar develo...
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Journal (source)Eur J Hum Genet
Identification of a novel ARL13B variant in a Joubert syndrome-affected patie...
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Journal (source)Nat Commun
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
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Journal (source)Nature Communications
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisph...
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Journal (source)Am J Hum Genet
Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with c...