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Gaelle Marenne
Gaelle Marenne
Inserm UMR1078, Brest, France
Bestätigte E-Mail-Adresse bei inserm.fr
Titel
Zitiert von
Zitiert von
Jahr
Detectable clonal mosaicism and its relationship to aging and cancer
KB Jacobs, M Yeager, W Zhou, S Wacholder, Z Wang, ...
Nature genetics 44 (6), 651-658, 2012
6612012
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
6302017
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ...
Nature communications 6 (1), 8111, 2015
3992015
The trans-ancestral genomic architecture of glycemic traits
J Chen, CN Spracklen, G Marenne, A Varshney, LJ Corbin, J Luan, ...
Nature genetics 53 (6), 840-860, 2021
3632021
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
3182018
Mosaic loss of chromosome Y is associated with common variation near TCL1A
W Zhou, MJ Machiela, ND Freedman, N Rothman, N Malats, C Dagnall, ...
Nature genetics 48 (5), 563-568, 2016
1602016
Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome
B Rodríguez-Santiago, N Malats, N Rothman, L Armengol, ...
The American Journal of Human Genetics 87 (1), 129-138, 2010
1422010
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
RA Scott, DF Freitag, L Li, AY Chu, P Surendran, R Young, N Grarup, ...
Science translational medicine 8 (341), 341ra76-341ra76, 2016
1222016
Whole-genome sequence-based analysis of thyroid function
PN Taylor, E Porcu, S Chew, PJ Campbell, M Traglia, SJ Brown, ...
Nature communications 6 (1), 5681, 2015
1112015
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
AE Justice, T Karaderi, HM Highland, KL Young, M Graff, Y Lu, V Turcot, ...
Nature genetics 51 (3), 452-469, 2019
962019
Genetic susceptibility to distinct bladder cancer subphenotypes
LT Guey, M García-Closas, C Murta-Nascimento, J Lloreta, L Palencia, ...
European urology 57 (2), 283-292, 2010
942010
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
NJ Timpson, K Walter, JL Min, I Tachmazidou, G Malerba, SY Shin, ...
Nature communications 5 (1), 4871, 2014
792014
Assessment of copy number variation using the Illumina Infinium 1M SNP‐array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study
G Marenne, B Rodríguez‐Santiago, MG Closas, L Pérez‐Jurado, ...
Human mutation 32 (2), 240-248, 2011
742011
Rare variant analysis of human and rodent obesity genes in individuals with severe childhood obesity
AE Hendricks, EG Bochukova, G Marenne, JM Keogh, N Atanassova, ...
Scientific reports 7 (1), 4394, 2017
602017
Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia
KM Gorman, E Meyer, D Grozeva, E Spinelli, A McTague, A Sanchis-Juan, ...
The American Journal of Human Genetics 104 (5), 948-956, 2019
582019
Exome sequencing identifies genes and gene sets contributing to severe childhood obesity, linking PHIP variants to repressed POMC transcription
G Marenne, AE Hendricks, A Perdikari, R Bounds, F Payne, JM Keogh, ...
Cell Metabolism 31 (6), 1107-1119. e12, 2020
422020
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts
A Belot, GI Rice, SO Omarjee, Q Rouchon, EMD Smith, M Moreews, ...
The Lancet Rheumatology 2 (2), e99-e109, 2020
402020
Next generation modeling in GWAS: comparing different genetic architectures
E López de Maturana, N Ibáñez-Escriche, Ó González-Recio, G Marenne, ...
Human genetics 133, 1235-1253, 2014
242014
Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array …
G Marenne, FX Real, N Rothman, B Rodríguez-Santiago, L Pérez-Jurado, ...
BMC genomics 13, 1-7, 2012
192012
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (5), 766-767, 2018
162018
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