Marı́a José Barallobre

Institut de Biologia Molecular de Barcelona — Spain

Medicine · Health Sciences

16h-index1.7kcitations32works1.52yr avg
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Research Topics

Down syndrome and intellectual disability research(13), Genetics and Neurodevelopmental Disorders(11), Axon Guidance and Neuronal Signaling(8), Neurogenesis and neuroplasticity mechanisms(6), Autism Spectrum Disorder Research(4)

Publications32 total

STAG2 cohesin cooperates with DREAM to maintain quiescence and suppress tumourigenesis in the urothelium
2025Open Access
Systemic delivery of AAV-GCDH ameliorates HLD-induced phenotype in a glutaric aciduria type I mouse model
Molecular Therapy — Methods & Clinical Development·2024· 3 citedOpen Access
Impaired macroglial development and axonal conductivity contributes to the neuropathology of DYRK1A-related intellectual disability syndrome
Scientific Reports·2022· 9 citedOpen Access
Impaired macroglial development and axonal conductivity contributes to the neuropathology of DYRK1A-related intellectual disability syndrome
Research Square (Research Square)·2022· 1 citedOpen Access
DYRK1A haploinsufficiency affects the development of astroglia and oligodendroglia, and axonal conductivity in the brain
Research Square (Research Square)·2022Open Access
MosaicExplorerJ: Interactive stitching of terabyte-size tiled datasets from lightsheet microscopy
F1000Research·2021· 7 citedOpen Access
MosaicExplorerJ: Interactive stitching of terabyte-size tiled datasets from lightsheet microscopy
F1000Research·2020· 6 citedOpen Access
MosaicExplorerJ F1000Research article extended data
Zenodo (CERN European Organization for Nuclear Research)·2020Open Access
Emb3_2x2_Mosaic_2CAMs_12GB
Zenodo (CERN European Organization for Nuclear Research)·2020Open Access
Emb3_2x2_Mosaic_2CAMs_12GB
Figshare·2020Open Access
MosaicExplorerJ: Interactive stitching of terabyte-size tiled datasets from lightsheet microscopy [version 2; peer review: 2 approved]
Europe PMC (PubMed Central)·2020
Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome
Neurobiology of Disease·2019· 44 citedOpen Access
Impaired development of neocortical circuits contributes to the neurological alterations in <i>DYRK1A</i> haploinsufficiency syndrome
2018· 1 citedOpen Access
DYRK1A Kinase Positively Regulates Angiogenic Responses in Endothelial Cells
Cell Reports·2018· 51 citedOpen Access
DYRK1A-mediated Cyclin D1 Degradation in Neural Stem Cells Contributes to the Neurogenic Cortical Defects in Down Syndrome
EBioMedicine·2015· 83 citedOpen Access
DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson’s disease
Cell Death and Disease·2014· 49 citedOpen Access
Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage
Neurobiology of Disease·2014· 122 citedOpen Access
Upregulation of <i>RCAN1</i> causes Down syndrome-like immune dysfunction
Journal of Medical Genetics·2013· 13 cited
Triplication of DYRK1A causes retinal structural and functional alterations in Down syndrome
Human Molecular Genetics·2013· 52 cited
Corrigendum to “DYRK1A: A master regulatory protein controlling brain growth” [Neurobiology of Disease 46/1 (2012) 190–203]
Neurobiology of Disease·2012· 1 citedOpen Access
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Frequent Co-authors

María L. Arbonés(18), Eduardo Soriano(5), Sònia Najas(5), Jean Maurice Delabar(5), Ariadna Laguna(5), Elisa Balducci(5), Isabel Pijuan(5), Marta Pascual(4), José Antonio del Rı́o(4), Eduardo Fernández(4), Susana de la Luna(4), Sébastien Tosi(4), Lídia Bardia(4), Arrate Muñoz‐Barrutia(4), María Luisa Soto‐Montenegro(4), Julien Colombelli(4), Fayçal Guedj(3), Benoît Souchet(3), Yann Hérault(3), Ignasi Sahún(3)