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G. Marenne · SciRah

Researcher profile · Semantic Scholar

G. Marenne

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G. Marenne — researcher profile on SciRah

h-index: 17
Works: 56
Citations: 3,826

Most-cited papers

The UK10K project identifies rare variants in health and disease
Klaudia Walter, Josine L. Min, Jie Huang, L. Crooks +238 more
2015Nature1,070 citations Open access
Semantic Scholar
Rare and low-frequency coding variants alter human adult height
E. Marouli, M. Graff, C. Medina-Gomez, K. Lo +368 more
2017Nature614 citations Open access
Semantic Scholar
Detectable clonal mosaicism and its relationship to aging and cancer
K. Jacobs, M. Yeager, Wei-Yin Zhou, S. Wacholder +185 more
2012Nature Genetics585 citations Open access
Semantic Scholar
The Trans-Ancestral Genomic Architecture of Glycemic Traits
Ji Chen, C. Spracklen, G. Marenne, Arushi Varshney +404 more
2021Nature Genetics465 citations Open access
Semantic Scholar
Mosaic loss of chromosome Y is associated with common variation near TCL1A
Wei-Yin Zhou, M. Machiela, N. Freedman, N. Rothman +34 more
2016Nature Genetics191 citations Open access
Semantic Scholar
Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.
B. Rodríguez-Santiago, N. Malats, N. Rothman, L. Armengol +16 more
2010American Journal of Human Genetics130 citations Open access
Semantic Scholar
Genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
R. Scott, D. Freitag, Li Li, Audrey Y. Chu +135 more
2016Science Translational Medicine111 citations Open access
Semantic Scholar
PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION
A. Justice, T. Karaderi, H. Highland, Kristin L. Young +275 more
2018Nature Genetics94 citations Open access
Semantic Scholar
Genetic Susceptibility to Distinct Bladder Cancer Subphenotypes
L. Guey, M. García-Closas, C. Murta-Nascimento, J. Lloreta +14 more
2009European Urology75 citations Open access
Semantic Scholar
Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription
G. Marenne, A. Hendricks, Aliki Perdikari, R. Bounds +17 more
2020Cell Metabolism73 citations Open access
Semantic Scholar
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, M. G. Closas, L. Pérez-Jurado +11 more
2011Human Mutation72 citations Open access
Semantic Scholar
PFMG2025–integrating genomic medicine into the national healthcare system in France
Caroline Abadie, Aldja Abderrahmane, Ouarda Abdous, Carine Abel +496 more
2025The Lancet Regional Health - Europe61 citations Open access
Semantic Scholar
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
A. Hendricks, E. Bochukova, G. Marenne, J. Keogh +266 more
2017Scientific Reports61 citations Open access
Semantic Scholar
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Valérie Turcot, Ying-Chang Lu, H. Highland, C. Schurmann +396 more
2018Nature Genetics25 citations Open access
Semantic Scholar
Next generation modeling in GWAS: comparing different genetic architectures
Evangelina López de Maturana, N. Ibáñez-Escriche, Óscar González-Recio, G. Marenne +4 more
2014Human Genetics19 citations Open access
Semantic Scholar
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Valérie Turcot, Ying-Chang Lu, H. Highland, C. Schurmann +396 more
2018Nature Genetics17 citations Open access
Semantic Scholar
Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data
G. Marenne, F. Real, N. Rothman, B. Rodríguez-Santiago +7 more
2012BMC Genomics17 citations Open access
Semantic Scholar
Whole Genome Prediction of Bladder Cancer Risk With the Bayesian LASSO
E. L. de Maturana, Stephen J. Chanok, A. Picornell, N. Rothman +12 more
2014Genetic Epidemiology16 citations Open access
Semantic Scholar
End‐Truncated LAMB1 Causes a Hippocampal Memory Defect and a Leukoencephalopathy
C. Aloui, D. Hervé, G. Marenne, Florian Savenier +16 more
2021Annals of Neurology14 citations
Semantic Scholar
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Valérie Turcot, Ying-Chang Lu, H. Highland, C. Schurmann +407 more
2018Nature Genetics12 citations Open access
Semantic Scholar
Reply to ‘Mosaic loss of chromosome Y in leukocytes matters’
Wei-Yin Zhou, M. Machiela, N. Freedman, N. Rothman +34 more
2018Nature Genetics11 citations Open access
Semantic Scholar
Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score
O. Bocher, Thomas E. Ludwig, Marie-Sophie Oglobinsky, G. Marenne +7 more
2021bioRxiv10 citations Open access
Semantic Scholar
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation
N. Ng, Sara M. Willems, Juan Fernandez, Rebecca S. Fine +260 more
2019bioRxiv10 citations Open access
Semantic Scholar
Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants
Hao Wu, Jin-Huan Lin, Xin-Ying Tang, G. Marenne +9 more
2024Human Genomics9 citations Open access
Semantic Scholar
Rare variant association testing for multicategory phenotype
O. Bocher, G. Marenne, Aude Saint Pierre, Thomas E. Ludwig +4 more
2019Genetic Epidemiology9 citations
Semantic Scholar
Genetic aetiology of glycaemic traits: approaches and insights
E. Wheeler, G. Marenne, I. Barroso
2017Human Molecular Genetics9 citations Open access
Semantic Scholar
How local reference panels improve imputation in French populations
A. Herzig, Lourdes Velo-Suárez, Dominique Campion, J. Dartigues +41 more
2024Scientific Reports8 citations Open access
Semantic Scholar
Human genetic structure in Northwest France provides new insights into West European historical demography
Isabel Alves, J. Giemza, Michael G. B. Blum, C. Bernhardsson +48 more
2024Nature Communications7 citations Open access
Semantic Scholar
Genetic population structure across Brittany and the downstream Loire basin provides new insights on the demographic history of Western Europe
Isabel Alves, J. Giemza, M. Blum, C. Bernhardsson +48 more
2022bioRxiv7 citations Open access
Semantic Scholar
RAVAQ: An integrative pipeline from quality control to region‐based rare variant association analysis
G. Marenne, Thomas E. Ludwig, O. Bocher, A. Herzig +3 more
2022Genetic Epidemiology6 citations
Semantic Scholar
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
Sara M. Willems, N. Ng, Juan Fernandez, Rebecca S. Fine +236 more
2023Wellcome Open Research5 citations Open access
Semantic Scholar
Extension of SKAT to multi-category phenotypes through a geometrical interpretation
O. Bocher, G. Marenne, E. Tournier-Lasserve, E. Génin +1 more
2021European Journal of Human Genetics5 citations Open access
Semantic Scholar
Advantage of Using Allele-Specific Copy Numbers When Testing for Association in Regions with Common Copy Number Variants
G. Marenne, S. Chanock, N. Malats, E. Génin
2013PLoS ONE5 citations Open access
Semantic Scholar
Impaired performance of FDR‐based strategies in whole‐genome association studies when SNPs are excluded prior to the analysis
G. Marenne, C. Dalmasso, H. Perdry, E. Génin +1 more
2009Genetic Epidemiology5 citations Open access
Semantic Scholar
PSAP-genomic-regions: a method leveraging population data to prioritize coding and non-coding variants in whole genome sequencing for rare disease diagnosis
Marie-Sophie C. Ogloblinsky, O. Bocher, C. Aloui, A. Leutenegger +8 more
2024bioRxiv2 citations Open access
Semantic Scholar
Moment estimators of relatedness from low-depth whole-genome sequencing data
A. Herzig, M. Ciullo, J. Deleuze, E. Génin +28 more
2022BMC Bioinformatics2 citations Open access
Semantic Scholar
Next generation modeling in GWAS: comparing different genetic architectures
Evangelina López de Maturana, N. Ibáñez-Escriche, Óscar González-Recio, G. Marenne +4 more
2014Human Genetics2 citations Open access
Semantic Scholar
A simple demonstration of a privacy-preserving de-centralised genotype imputation workflow
Alban Letaillandier, David Picard-Druet, Thomas E. Ludwig, G. Marenne +1 more
2025bioRxiv1 citations Open access
Semantic Scholar
Benchmark of computational methods to detect digenism in sequencing data
Marie-Sophie C. Ogloblinsky, D. Conrad, Anaïs Baudot, Elisabeth Tournier-Lasserve +2 more
2025European Journal of Human Genetics1 citations Open access
Semantic Scholar
Identification of rare variants involved in the risk of second cancer following radiotherapy and chemotherapy treatment of pediatric cancers
C. Ducos, F. Brice, F. Rosselli, G. Vu-Bezin +12 more
2023Revue d'épidémiologie et de santé publique1 citations
Semantic Scholar
Exome Sequencing Identifies Multiple Genes and Gene-Sets Contributing to Severe Childhood Obesity
G. Marenne, A. Hendricks, Aliki Perdikari, R. Bounds +17 more
2019Social Science Research Network1 citations
Semantic Scholar
EPS4.02 Porphyromonas, a candidate biomarker for detection of Pseudomonas aeruginosa pulmonary infection in cystic fibrosis
Charles-Antoine Guilloux, G. Marenne, S. Mondot, C. Lamoureux +7 more
2018Journal of Cystic Fibrosis1 citations Open access
Semantic Scholar
Rare Variants Associated With Pediatric Cancer Treatment-Related Second Malignant Neoplasm Risk.
C. Ducos, B. Fresneau, Filippo Rosselli, G. Vu-Bezin +17 more
2025JCO Precision Oncology0 citations
Semantic Scholar
Easy-PSAP: An Integrated Workflow to Prioritize Pathogenic Variants in Sequence Data from a Single Individual
Marie-Sophie C. Ogloblinsky, Marc B Gros-La-Faige, Daniel P. Lewinsohn, M. Nguyen +7 more
2025Human Heredity0 citations Open access
Semantic Scholar
Ravages: An R package for the simulation and analysis of rare variants in multicategory phenotypes
O. Bocher, G. Marenne, E. Genin, H. Perdry
2023Genetic Epidemiology0 citations Open access
Semantic Scholar
47th European Mathematical Genetics Meeting (EMGM) 2019, Dublin, Ireland, April 8-9, 2019
M. Bermingham, R. Walker, R. Marioni, Stewart Morris +22 more
2019Human Heredity0 citations
Semantic Scholar
Universitet Low-frequency variation in TP 53 has large effects on head circumference and intracranial
C. Anderson, R. Anney, Dinu Antony, M. Artigas +158 more
20190 citations
Semantic Scholar
UK 10 K Consortium
S. Al Turki, A. Amuzu, C. Anderson, R. Anney +218 more
20190 citations
Semantic Scholar
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Valérie Turcot, Ying-Chang Lu, H. Highland, C. Schurmann +397 more
2018Nature Genetics0 citations Open access
Semantic Scholar
Utilización conjunta de la información aportada por los diferentes polimorfismos, snps y cnvs, en los estudios de asociación pangenómica: Aplicación al cáncer de vejiga
G. Marenne
20120 citations
Semantic Scholar

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