Emmanuelle SZENKER-RAVI

Employment

• KAUST Research Scientist
  2023 - Present
• Agency for Science, Technology and Research Research scientist
  2021 - 2023
• Agency for Science, Technology and Research Research Fellow
  2013 - 2021
• Institut Curie PhD student
  2008 - 2012

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (17)

• MMP21 behaves as a fluid flow transported morphogen to impart laterality during development
  2025 DOI: 10.7554/elife.104430.1
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• R-SPONDIN2+ mesenchymal cells form the bud tip progenitor niche during human lung development.
  Developmental cell 2022 DOI: 10.1016/j.devcel.2022.05.010
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• Publisher Correction: Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates
  Emmanuelle Szenker‐Ravi, Tim Ott, Muznah Khatoo +38 more
  Nature Genetics 2022 DOI: 10.1038/s41588-022-01053-8
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• Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates
  Emmanuelle Szenker‐Ravi, Tim Ott, Muznah Khatoo +38 more
  Nature Genetics 2022 DOI: 10.1038/s41588-021-00970-4
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• A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion.
  Guoliang Chai, Emmanuelle Szenker‐Ravi, Changuk Chung +27 more
  The New England journal of medicine 2021 DOI: 10.1056/nejmoa2033911
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• Next-generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy.
  Human mutation 2020 DOI: 10.1002/humu.24132
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• R-spondin signalling is essential for the maintenance and differentiation of mouse nephron progenitors.
  eLife 2020 DOI: 10.7554/elife.53895
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• A GLI3 variant leading to polydactyly in heterozygotes and Pallister-Hall-like syndrome in a homozygote.
  Clinical genetics 2020 DOI: 10.1111/cge.13730
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• Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.
  Nature communications 2020 DOI: 10.1038/s41467-020-14360-7
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• Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia
  American Journal of Human Genetics 2019 DOI: 10.1016/j.ajhg.2019.10.013
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• RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6
  Emmanuelle Szenker‐Ravi, Umut Altunoğlu, Marc Leushacke

  +24 more

  • Célia Bosso-Lefèvre
  • Muznah Khatoo
  • Hong Thi Tran
  • Thomas Naert
  • Rivka Noelanders
  • +19 more
  Nature 2018 DOI: 10.1038/s41586-018-0118-y
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• Properties and functions of histone variants
  Fundamentals of Chromatin 2014 DOI: 10.1007/978-1-4614-8624-4_10
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• Developmental roles of histone H3 variants and their chaperones
  Trends in Genetics 2013 DOI: 10.1016/j.tig.2013.06.002
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• A Developmental Requirement for HIRA-Dependent H3.3 Deposition Revealed at Gastrulation in Xenopus
  Cell Reports 2012 DOI: 10.1016/j.celrep.2012.05.006
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• HIRA dependent H3.3 deposition is required for transcriptional reprogramming following nuclear transfer to Xenopus oocytes
  Epigenetics and Chromatin 2012 DOI: 10.1186/1756-8935-5-17
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• The double face of the histone variant H3.3
  Cell Research 2011 DOI: 10.1038/cr.2011.14
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• CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation
  Human Mutation 2009 DOI: 10.1002/humu.21116
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