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The trans-ancestral genomic architecture of glycemic traits

 Ji Chen , Cassandra Spracklen , Gaëlle Marenne , Arushi Varshney , Laura Corbin , et al.
Nature Genetics, 2021, 53 (6), pp.840-860. ⟨10.1038/s41588-021-00852-9⟩
Article dans une revue hal-04535845v1
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Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

 Alexandre Belot , Gillian Rice , Sulliman Ommar Omarjee , Quentin Rouchon , Eve Smith , et al.
The Lancet Rheumatology, 2020, 2 (2), pp.e99-e109. ⟨10.1016/S2665-9913(19)30142-0⟩
Article dans une revue hal-02867795v1

Identification of rare variants involved in the risk of second cancer following radiotherapy and chemotherapy treatment of pediatric cancers

 Claire Ducos , Brice Fresneau , Filippo Rosselli , Giao Vu-Bezin , Boris Schwartz , et al.
International Society of Radiation Epidemiology and Dosimetry (ISORED) - 1st meeting, May 2023, Sitges (Barcelona), Spain
Poster de conférence hal-04488114v1

RAVAQ: An integrative pipeline from quality control to region‐based rare variant association analysis

 Gaëlle Marenne , Thomas Ludwig , Ozvan Bocher , Anthony Herzig , Chaker Aloui , et al.
Genetic Epidemiology, 2022, ⟨10.1002/gepi.22450⟩
Article dans une revue hal-03705607v1

The trans-ancestral genomic architecture of glycemic traits

 Ji Chen , Cassandra Spracklen , Gaëlle Marenne , Arushi Varshney , Laura Corbin , et al.
Nature Genetics, 2021, ⟨10.1038/s41588-021-00852-9⟩
Article dans une revue hal-03250310v1
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Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription

 Gaëlle Marenne , Audrey Hendricks , Aliki Perdikari , Rebecca Bounds , Felicity Payne , et al.
Cell Metabolism, 2020, 31 (6), pp.1107-1119.e12. ⟨10.1016/j.cmet.2020.05.007⟩
Article dans une revue inserm-02886314v1

Identification of rare variants involved in the risk of second cancer following radiotherapy and chemotherapy treatment of pediatric cancers

 Claire Ducos , Brice Fresneau , Filippo Rosselli , Giao Vu-Bezin , Boris Schwartz , et al.
17ème conférence francophone d’EPIdémiologie CLINique (EPICLIN), May 2023, NANCY, France
Poster de conférence hal-04488101v1

Ravages: An R package for the simulation and analysis of rare variants in multicategory phenotypes

 Ozvan Bocher , Gaëlle Marenne , Emmanuelle Génin , Hervé Perdry
Genetic Epidemiology, 2023, 47 (6), pp.450-460. ⟨10.1002/gepi.22529⟩
Article dans une revue hal-04188192v1
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Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

 Alexandre Belot , Gillian Rice , Sulliman Ommar Omarjee , Quentin Rouchon , Eve Smith , et al.
The Lancet Rheumatology, 2020, 2 (2), pp.e99-e109. ⟨10.1016/S2665-9913(19)30142-0⟩
Article dans une revue hal-03065973v1
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Assessment of Copy Number Variation using the Illumina Infinium 1M SNP-array: A comparison of methodological approaches in the Spanish Bladder Cancer / EPICURO Study.

 Gaëlle Marenne , Benjamín Rodríguez Santiago , Montserrat García-Closas , Luis Alberto Pérez Jurado , Nathaniel Rothman , et al.
Human Mutation, 2011, 32 (2), pp.240. ⟨10.1002/humu.21398⟩
Article dans une revue hal-00610793v1
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Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data.

 Gaëlle Marenne , Francisco Real , Nathaniel Rothman , Benjamin Rodríguez-Santiago , Luis Pérez-Jurado , et al.
BMC Genomics, 2012, 13 (1), pp.326. ⟨10.1186/1471-2164-13-326⟩
Article dans une revue inserm-00724696v1

Extension of SKAT to multi-category phenotypes through a geometrical interpretation

 Ozvan Bocher , Gaelle Marenne , Elisabeth Tournier-Lasserve , Emmanuelle Génin , Hervé Perdry
European Journal of Human Genetics, 2021, 29 (5), pp.736-744. ⟨10.1038/s41431-020-00792-8⟩
Article dans une revue hal-03700870v1
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