|Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans|
M Mangino, SJ Hwang, TD Spector, SC Hunt, M Kimura, AL Fitzpatrick, ...
Human molecular genetics 21 (24), 5385-5394, 2012
|Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation|
E Boulanger-Scemama, S El Shamieh, V Démontant, C Condroyer, ...
Orphanet journal of rare diseases 10 (1), 1-20, 2015
|Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)|
M Neuillé, S El Shamieh, E Orhan, C Michiels, A Antonio, ME Lancelot, ...
PloS one 9 (3), e90342, 2014
|Whole-Exome Sequencing Identifies KIZ as a Ciliary Gene Associated with Autosomal-Recessive Rod-Cone Dystrophy|
S El Shamieh, M Neuillé, A Terray, E Orhan, C Condroyer, V Démontant, ...
The American Journal of Human Genetics 94 (4), 625-633, 2014
|A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels|
P Froguel, NC Ndiaye, A Bonnefond, N Bouatia-Naji, A Dechaume, ...
PloS one 7 (3), e32327, 2012
|Genetic biomarkers of hypertension and future challenges integrating epigenomics|
S El Shamieh, S Visvikis-Siest
Clinica chimica acta 414, 259-265, 2012
|Cardiovascular diseases and genome-wide association studies|
NC Ndiaye, MA Nehzad, S El Shamieh, MG Stathopoulou, S Visvikis-Siest
Clinica Chimica Acta 412 (19-20), 1697-1701, 2011
|A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C|
MG Stathopoulou, A Bonnefond, NC Ndiaye, M Azimi-Nezhad, ...
Journal of lipid research 54 (2), 535-541, 2013
|Targeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophy|
S El Shamieh, E Boulanger-Scemama, ME Lancelot, A Antonio, ...
BioMed research international 2015, 2015
|The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel …|
I Audo, K Bujakowska, E Orhan, S El Shamieh, F Sennlaub, ...
Human molecular genetics 23 (2), 491-501, 2014
|Epistatic study reveals two genetic interactions in blood pressure regulation|
NC Ndiaye, S El Shamieh, MG Stathopoulou, G Siest, MY Tsai, ...
BMC medical genetics 14 (1), 2, 2013
|Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levels|
S El Shamieh, B Herbeth, M Azimi-Nezhad, H Benachour, C Masson, ...
Clinica chimica acta 413 (1-2), 34-38, 2012
|Klotho KL-VS genotype is involved in blood pressure regulation|
R Nzietchueng, S El Shamieh, H Benachour, C Labat, B Herbeth, ...
Clinica Chimica Acta 412 (19), 1773-1777, 2011
|The rs3957357C>T SNP in GSTA1 Is Associated with a Higher Risk of Occurrence of Hepatocellular Carcinoma in European Individuals|
H Akhdar, S El Shamieh, O Musso, R Désert, W Joumaa, D Guyader, ...
PLoS One 11 (12), e0167543, 2016
|Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness|
E Orhan, L Prézeau, S El Shamieh, KM Bujakowska, C Michiels, Y Zagar, ...
Investigative ophthalmology & visual science 54 (13), 8041-8050, 2013
|MERTK mutation update in inherited retinal diseases|
I Audo, S Mohand‐Said, E Boulanger‐Scemama, X Zanlonghi, ...
Human mutation 39 (7), 887-913, 2018
|Cone dystrophy in patient with homozygous RP1L1 mutation|
S Kikuchi, S Kameya, K Gocho, S El Shamieh, K Akeo, Y Sugawara, ...
BioMed research international 2015, 2015
|Relationship between catalase haplotype and arterial aging|
V Nivet-Antoine, C Labat, S El Shamieh, X Dulcire, CH Cottart, ...
Atherosclerosis 227 (1), 100-105, 2013
|Functional epistatic interaction between rs6046G> A in F7 and rs5355C> T in SELE modifies systolic blood pressure levels|
S El Shamieh, NC Ndiaye, MG Stathopoulou, HA Murray, C Masson, ...
PloS one 7 (7), e40777, 2012
|Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non‐syndromic rod‐cone dystrophy|
C Méjécase, A Hummel, S Mohand‐Saïd, C Andrieu, S El Shamieh, ...
Clinical genetics 95 (2), 329-333, 2019