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Scopus Author ID: 35741950300

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Employment (4)

KAUST: THUWAL, SA

2023-10-01 to present | Research Scientist (BESE)
Employment
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

Agency for Science, Technology and Research: Singapore, SG

2021-04 to 2023-09 | Research scientist (Genome Institute of Singapore)
Employment
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

Agency for Science, Technology and Research: Singapore, SG

2013-01 to 2021-04 | Research Fellow (Institute of Medical Biology)
Employment
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

Institut Curie: Paris, Île-de-France, FR

2008-09 to 2012-09 | PhD student
Employment
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

Works (16)

Publisher Correction: Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates

Nature Genetics
2022-06 | Journal article
DOI: 10.1038/s41588-022-01053-8
Contributors: Emmanuelle Szenker-Ravi; Tim Ott; Muznah Khatoo; Anne Moreau de Bellaing; Wei Xuan Goh; Yan Ling Chong; Anja Beckers; Darshini Kannesan; Guillaume Louvel; Priyanka Anujan et al.
Source: check_circle
Crossref

R-SPONDIN2<sup>+</sup> mesenchymal cells form the bud tip progenitor niche during human lung development.

Developmental cell
2022-06-07 | Journal article
DOI: 10.1016/j.devcel.2022.05.010
PMID: 35679862
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates

Nature Genetics
2022-01 | Journal article
DOI: 10.1038/s41588-021-00970-4
Part of ISSN: 1061-4036
Part of ISSN: 1546-1718
Source: Self-asserted source
Emmanuelle SZENKER-RAVI
grade
Preferred source (of 2)‎

A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion.

The New England journal of medicine
2021-09-01 | Journal article
DOI: 10.1056/nejmoa2033911
PMID: 34587386
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

Next-generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy.

Human mutation
2020-11-10 | Journal article
DOI: 10.1002/humu.24132
PMID: 33131162
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

R-spondin signalling is essential for the maintenance and differentiation of mouse nephron progenitors.

eLife
2020-05-01 | Journal article
DOI: 10.7554/elife.53895
PMID: 32324134
PMC: PMC7228766
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

A GLI3 variant leading to polydactyly in heterozygotes and Pallister-Hall-like syndrome in a homozygote.

Clinical genetics
2020-03-10 | Journal article
DOI: 10.1111/cge.13730
PMID: 32112393
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.

Nature communications
2020-01-30 | Journal article
DOI: 10.1038/s41467-020-14360-7
PMID: 32001716
PMC: PMC6992768
Source: Self-asserted source
Emmanuelle SZENKER-RAVI

Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia

American Journal of Human Genetics
2019 | Journal article
DOI: 10.1016/j.ajhg.2019.10.013
EID:

2-s2.0-85075600162
Contributors: Kariminejad, A.; Szenker-Ravi, E.; Lekszas, C.; Tajsharghi, H.; Moslemi, A.-R.; Naert, T.; Tran, H.T.; Ahangari, F.; Rajaei, M.; Nasseri, M. et al.
Source: Self-asserted source
Emmanuelle SZENKER-RAVI via Scopus - Elsevier

RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6

Nature
2018 | Journal article
DOI: 10.1038/s41586-018-0118-y
EID:

2-s2.0-85047253329
Contributors: Szenker-Ravi, E.; Altunoglu, U.; Leushacke, M.; Bosso-Lefèvre, C.; Khatoo, M.; Thi Tran, H.; Naert, T.; Noelanders, R.; Hajamohideen, A.; Beneteau, C. et al.
Source: Self-asserted source
Emmanuelle SZENKER-RAVI via Scopus - Elsevier
grade
Preferred source (of 3)‎

Properties and functions of histone variants

Fundamentals of Chromatin
2014 | Book chapter
Part of DOI: 10.1007/978-1-4614-8624-4_10
EID:

2-s2.0-84928782829
Contributors: Szenker, E.; Boyarchuk, E.; Almouzni, G.
Source: Self-asserted source
Emmanuelle SZENKER-RAVI via Scopus - Elsevier

Developmental roles of histone H3 variants and their chaperones

Trends in Genetics
2013 | Journal article
DOI: 10.1016/j.tig.2013.06.002
EID:

2-s2.0-84886298616
Contributors: Filipescu, D.; Szenker, E.; Almouzni, G.
Source: Self-asserted source
Emmanuelle SZENKER-RAVI via Scopus - Elsevier

A Developmental Requirement for HIRA-Dependent H3.3 Deposition Revealed at Gastrulation in Xenopus

Cell Reports
2012 | Journal article
DOI: 10.1016/j.celrep.2012.05.006
EID:

2-s2.0-84863088107
Contributors: Szenker, E.; Lacoste, N.; Almouzni, G.
Source: Self-asserted source
Emmanuelle SZENKER-RAVI via Scopus - Elsevier

HIRA dependent H3.3 deposition is required for transcriptional reprogramming following nuclear transfer to Xenopus oocytes

Epigenetics and Chromatin
2012 | Journal article
DOI: 10.1186/1756-8935-5-17
EID:

2-s2.0-84867897054
Contributors: Jullien, J.; Astrand, C.; Szenker, E.; Garrett, N.; Almouzni, G.; Gurdon, J.B.
Source: Self-asserted source
Emmanuelle SZENKER-RAVI via Scopus - Elsevier

The double face of the histone variant H3.3

Cell Research
2011 | Journal article
DOI: 10.1038/cr.2011.14
EID:

2-s2.0-79952536146
Contributors: Szenker, E.; Ray-Gallet, D.; Almouzni, G.
Source: Self-asserted source
Emmanuelle SZENKER-RAVI via Scopus - Elsevier

CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation

Human Mutation
2009 | Journal article
DOI: 10.1002/humu.21116
EID:

2-s2.0-70350719356
Contributors: Mougou-Zerelli, S.; Thomas, S.; Szenker, E.; Audollent, S.; Elkhartoufi, N.; Babarit, C.; Romano, S.; Salomon, R.; Amiel, J.; Esculpavit, C. et al.
Source: Self-asserted source
Emmanuelle SZENKER-RAVI via Scopus - Elsevier
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