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Dr. Emmanuelle SZENKER-RAVI
Dr. Emmanuelle SZENKER-RAVI
GIS, A*STAR, Singapore
Verified email at gis.a-star.edu.sg
Title
Cited by
Cited by
Year
The double face of the histone variant H3. 3
E Szenker, D Ray-Gallet, G Almouzni
Cell research 21 (3), 421-434, 2011
4432011
RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6
E Szenker-Ravi, U Altunoglu, M Leushacke, C Bosso-Lefèvre, M Khatoo, ...
Nature 557 (7706), 564-569, 2018
1582018
Developmental roles of histone H3 variants and their chaperones
D Filipescu, E Szenker, G Almouzni
Trends in Genetics 29 (11), 630-640, 2013
1492013
HIRA dependent H3.3 deposition is required for transcriptional reprogramming following nuclear transfer to Xenopus oocytes
J Jullien, C Astrand, E Szenker, N Garrett, G Almouzni, JB Gurdon
Epigenetics & chromatin 5, 1-10, 2012
1122012
A developmental requirement for HIRA-dependent H3. 3 deposition revealed at gastrulation in Xenopus
E Szenker, N Lacoste, G Almouzni
Cell reports 1 (6), 730-740, 2012
1092012
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype–phenotype correlation
S Mougou‐Zerelli, S Thomas, E Szenker, S Audollent, N Elkhartoufi, ...
Human mutation 30 (11), 1574-1582, 2009
992009
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
H Hengel, C Bosso-Lefèvre, G Grady, E Szenker-Ravi, H Li, S Pierce, ...
Nature communications 11 (1), 595, 2020
412020
A human pleiotropic multiorgan condition caused by deficient Wnt secretion
G Chai, E Szenker-Ravi, C Chung, Z Li, L Wang, M Khatoo, T Marshall, ...
New England Journal of Medicine 385 (14), 1292-1301, 2021
262021
R-SPONDIN2+ mesenchymal cells form the bud tip progenitor niche during human lung development
RFC Hein, JH Wu, EM Holloway, T Frum, AS Conchola, YH Tsai, A Wu, ...
Developmental cell 57 (13), 1598-1614. e8, 2022
242022
Next‐generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy
H Liu, AG Giguet‐Valard, T Simonet, E Szenker‐Ravi, L Lambert, ...
Human mutation 41 (12), 2167-2178, 2020
232020
R-spondin signalling is essential for the maintenance and differentiation of mouse nephron progenitors
VPI Vidal, F Jian-Motamedi, S Rekima, EP Gregoire, E Szenker-Ravi, ...
Elife 9, e53895, 2020
232020
Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates
E Szenker-Ravi, T Ott, M Khatoo, A Moreau de Bellaing, WX Goh, ...
Nature Genetics 54 (1), 62-72, 2022
222022
Homozygous null TBX4 mutations lead to posterior amelia with pelvic and pulmonary hypoplasia
A Kariminejad, E Szenker-Ravi, C Lekszas, H Tajsharghi, AR Moslemi, ...
The American Journal of Human Genetics 105 (6), 1294-1301, 2019
222019
Properties and functions of histone variants
E Szenker, E Boyarchuk, G Almouzni
Fundamentals of chromatin, 375-426, 2013
122013
A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing
N Nabavizadeh, A Bressin, M Shboul, R Moreno Traspas, PH Chia, ...
EMBO Molecular Medicine 15 (2), e16478, 2023
42023
A GLI3 variant leading to polydactyly in heterozygotes and Pallister‐Hall‐like syndrome in a homozygote
A Kariminejad, S Ghaderi‐Sohi, E Keshavarz, SA Hashemi, E Parsimehr, ...
Clinical genetics 97 (6), 915-919, 2020
42020
Paracrine and autocrine R-spondin signalling is essential for the maintenance and differentiation of renal stem cells
VPI Vidal, E Gregoire, E Szenker-Ravi, M Leushacke, B Reversade, ...
bioRxiv, 859959, 2019
32019
Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6.
E Szenker-Ravi, U Altunoglu, M Leushacke, C Bosso-Lefèvre, M Khatoo, ...
Nature 561 (7722), E7-E7, 2018
12018
Functional analysis of germline VANGL2 variants using rescue assays of vangl2 knockout zebrafish
CJ Derrick, E Szenker-Ravi, A Santos-Ledo, A Alqahtani, A Yusof, L Eley, ...
Human Molecular Genetics 33 (2), 150-169, 2024
2024
Publisher Correction: Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates
E Szenker-Ravi, T Ott, M Khatoo, A Moreau de Bellaing, WX Goh, ...
Nature Genetics 54 (6), 906-906, 2022
2022
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