متابعة
Gaelle Marenne
Gaelle Marenne
Inserm UMR1078, Brest, France
بريد إلكتروني تم التحقق منه على inserm.fr
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
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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مقالات 1–20