Sabrina Mechaussier

Employment

• Institut Pasteur Post Doctoral Researcher
  2021 - Present
• Imagine Institute for Genetic Diseases PhD student
  2017 - 2021
• Imagine Institute for Genetic Diseases Master 2 Internship
  2016 - 2017
• Imagine Institute for Genetic Diseases Master 1 Internship
  2016 - 2016

Education

• Institut Pasteur Company tutor training: how to integrate, train and build loyalty?
  2023 - 2023
• Institut Pasteur Specific training to design and perform surgical procedures on rodents
  2022 - 2022
• Imagine Institute for Genetic Diseases Teaching Paris-Diderot Training L2 level students
  2019 - 2019
• École Nationale Vétérinaire d'Alfort Animal Experimentation Training - General and Rodents/Rabbits Specialization Modules
  2018 - 2018

Projects & Funding

Projects & funding information is unavailable.

Publications (10)

• Single-cell spatially resolved transcriptomic characterization of the developing mouse cochlea
  2026 DOI: 10.64898/2026.01.21.700589
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• Deciphering Auditory Hyperexcitability in Otogl Mutant Mice Unravels an Auditory Neuropathy Mechanism
  Advanced Science 2025 DOI: 10.1002/advs.202410776
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• Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules
  Daniel O Dodd, Sabrina Méchaussier, Patricia Levy Yeyati +80 more
  Science 2024 DOI: 10.1126/science.adf5489
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• Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies
  Proceedings of the National Academy of Sciences 2023 DOI: 10.1073/pnas.2221744120
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• TUBB4B variants specifically impact ciliary function, causing a ciliopathic spectrum
  2022 DOI: 10.1101/2022.10.19.22280748
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• Caractérisation des bases moléculaires et physiopathologiques des cécités rétiniennes héréditaires de l'enfant et validation fonctionnelle de nouveaux gènes impliqués
  2021 DOI: 10.70675/0f27736cz66dbz4ffdza4b0z9d16ba94c4b8
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• Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement
  The American Journal of Human Genetics 2020 DOI: 10.1016/j.ajhg.2020.08.004
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• Heimler Syndrome
  Advances in Experimental Medicine and Biology 2020 DOI: 10.1007/978-3-030-60204-8_7
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• Genetic Deciphering of Early-Onset and Severe Retinal Dystrophy Associated with Sensorineural Hearing Loss
  Retinal Degenerative Diseases 2019 DOI: 10.1007/978-3-030-27378-1_38
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• Mutations in TUBB4B Cause a Distinctive Sensorineural Disease
  The American Journal of Human Genetics 2017 DOI: 10.1016/j.ajhg.2017.10.010
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