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All papers authored by Gaëlle Marenne

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2023 Ozvan Bocher

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, Gaëlle Marenne

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, Emmanuelle Génin

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, Hervé Perdry

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

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2022 Ozvan Bocher

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, Vincent Plagnol, Thomas E. Ludwig

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, Marie-Sophie Oglobinsky, Gaëlle Marenne

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, Jean-François Deleuze, Suryakant Suryakant, Jacob Odeberg

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, Pierre-Emmanuel Morange

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, David-Alexandre Trégouët

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, Hervé Perdry

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, Emmanuelle Génin

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Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score

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Gaëlle Marenne

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, Thomas E. Ludwig, Ozvan Bocher

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, Anthony F. Herzig

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, Chaker Aloui, Elisabeth Tournier‐Lasserve, Emmanuelle Génin

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

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2021 Ji Chen, Peter J. van der Most, Xiaoshuai Zhang, Hugoline G. de Haan, Erik van den Akker, Jing-Hua Zhao, Wei Zhao, Eco J. C. de Geus, Rob M. van Dam, Diana van Heemst, Astrid van Hylckama Vlieg, Jana V. van Vliet-Ostaptchouk, Ko Willems van Dijk, H. Janaka de Silva, Pim van der Harst and 592 other authors

The trans-ancestral genomic architecture of glycemic traits

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Ozvan Bocher, Gaelle Marenne

ORCID

, Elisabeth Tournier-Lasserve, Emmanuelle Génin, Hervé Perdry

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

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2020 Gaëlle Marenne

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, Audrey E. Hendricks, Aliki Perdikari, Rebecca Bounds, Felicity Payne, Julia M. Keogh, Christopher J. Lelliott, Elana Henning, Saad Pathan, Sofie Ashford, Elena G. Bochukova, Vanisha Mistry, Allan Daly, Caroline Hayward, Nicholas J. Wareham and 6 other authors

Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription

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2019 Ozvan Bocher, Gaëlle Marenne

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, Aude Saint Pierre, Thomas E. Ludwig, Stéphanie Guey, Elisabeth Tournier‐Lasserve, Hervé Perdry, Emmanuelle Génin

Rare variant association testing for multicategory phenotype

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2017 Eleanor Wheeler, Gaëlle Marenne

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, Inês Barroso

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Genetic aetiology of glycaemic traits: approaches and insights

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Audrey E. Hendricks, Margriet van Kogelenberg, Robert A. Scott, Eleftheria Zeggini, Nick J. Wareham, Praveen Surendran, Børge G. Nordestgaard, Dieter Wolke, Sune F. Nielsen, Sofia Papadia, Glenn L. Millhauser, Rafael I. Palomino, Stephen O’Rahilly, Ioanna Tachmazidou, Stephen O'Rahilly and 269 other authors

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity.

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2016 Weiyin Zhou, Mitchell J. Machiela

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, Neal D. Freedman, Nathaniel Rothman, Nuria Malats, Casey Dagnall, Neil Caporaso, Lauren T. Teras, Mia M. Gaudet, Susan M. Gapstur, Victoria L. Stevens, Kevin B. Jacobs, Joshua Sampson, Demetrius Albanes, Stephanie Weinstein and 23 other authors

Mosaic loss of chromosome Y is associated with common variation near TCL1A

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2014 Evangelina López de Maturana, Evangelina López de Maturana, Noelia Ibáñez-Escriche, Oscar González-Recio

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, Gaëlle Marenne

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, Hossein Mehrban, Stephen J. Chanock, Michael E. Goddard, Núria Malats

Next generation modeling in GWAS: comparing different genetic architectures

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E. L. De Maturana, Evangelina López de Maturana, Nathaniel Rothman, Stephen J. Chanok, Jesús Herranz, Adonina Tardón, M. Luz Calle, Antoni C. Picornell

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, Montserrat García-Closas, Debra T. Silverman, Gaëlle Marenne

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, Angela Brand, Francisco X. Real, Alfredo Carrato, Manolis Kogevinas and 2 other authors

Whole genome prediction of bladder cancer risk with the Bayesian LASSO.

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2013 Gaëlle Marenne

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, Stephen J. Chanock, Núria Malats, Emmanuelle Génin

Advantage of Using Allele-Specific Copy Numbers When Testing for Association in Regions with Common Copy Number Variants

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2012 Kevin B. Jacobs, Meredith Yeager, Jacobs Kb, Weiyin Zhou, Sholom Wacholder, Zhaoming Wang, Benjamin Rodriguez-Santiago, Amy Hutchinson, Xiang Deng, Chenwei Liu, Marie-Josephe Horner, Michael Cullen, Caroline G. Epstein, Laurie Burdett, Michael C. Dean and 186 other authors

Detectable clonal mosaicism and its relationship to aging and cancer

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Gaëlle Marenne

ORCID

, Francisco X. Real

ORCID

, Nathaniel Rothman, Benjamin Rodríguez-Santiago, Luis Pérez-Jurado, Manolis Kogevinas, Montse García-Closas, Debra T. Silverman, Stephen J. Chanock, Emmanuelle Génin, Núria Malats

Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data.

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2011 Gaëlle Marenne

ORCID

, Benjamín Rodríguez-Santiago, Montserrat García Closas, Luis Pérez-Jurado, Nathaniel Rothman, Daniel Rico, Guillermo Pita, David G. Pisano, Manolis Kogevinas, Debra T. Silverman, Alfonso Valencia, Francisco X. Real

ORCID

, Stephen J. Chanock, Emmanuelle Génin, Núria Malats

Assessment of Copy Number Variation Using the Illumina Infinium 1M SNP-Array: A Comparison of Methodological Approaches in the Spanish Bladder Cancer/EPICURO Study

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2010 Benjamín Rodríguez-Santiago, Núria Malats, Nathaniel Rothman, Lluís Armengol, Montse Garcia-Closas, Manolis Kogevinas, Olaya Villa, Amy Hutchinson, Julie Earl, Gaëlle Marenne

ORCID

, Kevin Jacobs, Daniel Rico, Adonina Tardón, Alfredo Carrato, Gilles Thomas and 5 other authors

Mosaic Uniparental Disomies and Aneuploidies as Large Structural Variants of the Human Genome

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2009 Lin T. Guey, Montserrat García-Closas, Cristiane Murta-Nascimento, Josep Lloreta, Laia Palencia, Manolis Kogevinas, Nathaniel Rothman, Gemma Vellalta, Malu Luz Calle, Gaëlle Marenne

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, Adonina Tardón, Alfredo Carrato, Reina García Closas, Reina García-Closas, Consol Serra and 4 other authors

Genetic Susceptibility to Distinct Bladder Cancer Subphenotypes

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2008 Gaëlle Marenne

ORCID

, Cyril Dalmasso, Hervé Perdry, Emmanuelle Génin, Philippe Broët

Impaired performance of FDR-based strategies in whole-genome association studies when SNPs are excluded prior to the analysis

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