María Gabriela Otero

Cedars-Sinai Medical Center — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index412citations26works3.22yr avg
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Research Topics

Cellular transport and secretion(5), Mitochondrial Function and Pathology(4), Ubiquitin and proteasome pathways(4), Genetics and Neurodevelopmental Disorders(4), Endoplasmic Reticulum Stress and Disease(3)

Publications26 total

Human iPSC-derived prostate organoids with germline BRCA2 mutation undergo tumorigenic transformations
2025Open Access
Hyperglycemia-induced mitochondrial abnormalities in autonomic neurons via the RAGE axis
Scientific Reports·2025· 6 citedOpen Access
Compound Heterozygous <i>MRPS14</i> Variants Associated With Leigh Syndrome
Annals of Clinical and Translational Neurology·2025· 2 citedOpen Access
Cellular Modeling of CLN6 with IPSC-derived Neurons and Glia
2024· 2 citedOpen Access
Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning
Translational Psychiatry·2024· 6 citedOpen Access
Organ-Chips Enhance the Maturation of Human iPSC-Derived Dopamine Neurons
International Journal of Molecular Sciences·2023· 6 citedOpen Access
Modeling CLN6 with IPSC-derived neurons and glia
Molecular Genetics and Metabolism·2023
A neurodevelopmental disorder associated with an activating<i>de novo</i>missense variant in<i>ARF1</i>
Human Molecular Genetics·2022· 12 citedOpen Access
CRC: A Darwinian model of cellular immunoselection
Elsevier eBooks·2021
Erratum to: Biallelic variants in <i>HPDL</i> cause pure and complicated hereditary spastic paraplegia
Brain·2021· 2 citedOpen Access
Biallelic variants in <i>HPDL</i> cause pure and complicated hereditary spastic paraplegia
Brain·2021· 47 citedOpen Access
Human induced pluripotent stem cell models for CLN6
Molecular Genetics and Metabolism·2021
Kinesin-1-mediated axonal transport of CB1 receptors is required for cannabinoid-dependent axonal growth and guidance
Development·2020· 33 citedOpen Access
Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Genetics in Medicine·2020· 2 citedOpen Access
GATAD2B-associatedneurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-relateddisorder
Genetics in Medicine·2020· 33 citedOpen Access
The NuRD complex and macrocephaly associated neurodevelopmental disorders
American Journal of Medical Genetics Part C Seminars in Medical Genetics·2019· 37 cited
Neuronal <i><scp>KIF</scp>5b</i> deletion induces <i>striatum</i>‐dependent locomotor impairments and defects in membrane presentation of dopamine D2 receptors
Journal of Neurochemistry·2019· 21 citedOpen Access
Modeling rare pediatric neurogenetic disorders with IPSCs
AIMS Cell and Tissue Engineering·2019· 1 citedOpen Access
Novel pathogenic <i><scp>COX</scp>20</i> variants causing dysarthria, ataxia, and sensory neuropathy
Annals of Clinical and Translational Neurology·2018· 26 citedOpen Access
Proteasome stress leads to APP axonal transport defects by promoting its amyloidogenic processing in lysosomes
Journal of Cell Science·2018· 14 citedOpen Access
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Frequent Co-authors

Tyler Mark Pierson(11), Tomás L. Falzone(9), Lucas E. Cromberg(7), John M. Graham(6), Matías Alloatti(5), Trinidad Saez(5), Katheryn Grand(5), Victorio M. Pozo Devoto(4), Juan I. Young(4), Andrew Choi(3), Joel P. Mackay(3), Margaret Au(3), Iván Fernández Bessone(3), Christina Freeman(3), Zachary Myers(3), Yogesh K. Kushwaha(3), Angels Almenar‐Queralt(2), Manuela Wiessner(2), Reza Maroofian(2), Meng-Yuan Ni(2)