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

Genetic epidemiology, 2023-09, Vol.47 (6), p.450-460

2023

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PSAP-Genomic-Regions: A Method Leveraging Population Data to Prioritize Coding and Non-Coding Variants in Whole Genome Sequencing for Rare Disease Diagnosis

Genetic epidemiology, 2024-09

2024

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

Genetic epidemiology, 2022-07, Vol.46 (5-6), p.256-265

2022

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Rare variant association testing for multicategory phenotype

Genetic epidemiology, 2019-09, Vol.43 (6), p.646-656

2019

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Evaluation of saliva as a source of accurate whole‐genome and microbiome sequencing data

Genetic epidemiology, 2021-07, Vol.45 (5), p.537-548

2021

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Blood transcriptomic biomarker as a surrogate of ischemic brain gene expression

Annals of clinical and translational neurology, 2019-09, Vol.6 (9), p.1681-1695

2019

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Genetics and postsurgical neuropathic pain: An ancillary study of a multicentre survey

European journal of anaesthesiology, 2019-05, Vol.36 (5), p.342-350

2019

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Genetics and postsurgical neuropathic pain

European journal of anaesthesiology, 2019, Vol.36 (5), p.342-350

2019

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Penetrance estimation of SORL1 loss‐of‐function variants adjusted on APOE genotypes suggest a non‐monogenic inheritance

Alzheimer's & dementia, 2021-12, Vol.17 (S10), p.n/a

2021

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Peroxisomal and mitochondrial status of two murine oligodendrocytic cell lines (158N, 158JP): potential models for the study of peroxisomal disorders associated with dysmyelination processes

Journal of neurochemistry, 2009-10, Vol.111 (1), p.119-131

2009

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Evaluation of saliva as a source of accurate wholegenome and microbiome sequencing data

Genetic epidemiology, 2021-07, Vol.45 (5), p.537-548

2021

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DCTN 4 as a modifier of chronic P seudomonas aeruginosa infection in cystic fibrosis

The clinical respiratory journal, 2016-11, Vol.10 (6), p.777-783

2016

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Regional variation of imputation accuracy in France

Genetic epidemiology, 2021, Vol.45 (7), p.759-760

2021

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The French Exome (FREX) Project: A Population-based Panel of Exomes to Help Filter Out Common Local Variants

Genetic epidemiology, 2017, Vol.41 (7), p.691-691

2017

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Investigation of a Candidate Gene, Environment, and G×E Interaction Using Case‐Control and Case‐Parent Study Designs

Genetic epidemiology, 2001, Vol.21 (S1), p.S843-S848

2001

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Peroxisomal and mitochondrial status of two murine oligodendrocytic cell lines (158N, 158JP): potential models for the study of peroxisomal disorders associated with dysmyelination processes: Peroxisomal and Mitochondrial Status of Two Differentiated Murine Oligodendrocytic Cell Lines (158N, 158JP)

Journal of neurochemistry, 2009-10, Vol.111 (1), p.119-31

2009

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Forkhead pathway in the control of adult neurogenesis

2014

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

PSAP-Genomic-Regions: A Method Leveraging Population Data to Prioritize Coding and Non-Coding Variants in Whole Genome Sequencing for Rare Disease Diagnosis

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

Rare variant association testing for multicategory phenotype

A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet‐Biedl syndrome

Evaluation of saliva as a source of accurate whole‐genome and microbiome sequencing data

Blood transcriptomic biomarker as a surrogate of ischemic brain gene expression

Genetics and postsurgical neuropathic pain: An ancillary study of a multicentre survey

Genetics and postsurgical neuropathic pain

Penetrance estimation of SORL1 loss‐of‐function variants adjusted on APOE genotypes suggest a non‐monogenic inheritance

Peroxisomal and mitochondrial status of two murine oligodendrocytic cell lines (158N, 158JP): potential models for the study of peroxisomal disorders associated with dysmyelination processes

Evaluation of saliva as a source of accurate wholegenome and microbiome sequencing data

Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation

DCTN 4 as a modifier of chronic P seudomonas aeruginosa infection in cystic fibrosis

Regional variation of imputation accuracy in France

The French Exome (FREX) Project: A Population-based Panel of Exomes to Help Filter Out Common Local Variants

Investigation of a Candidate Gene, Environment, and G×E Interaction Using Case‐Control and Case‐Parent Study Designs

CHCHD 10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis

Peroxisomal and mitochondrial status of two murine oligodendrocytic cell lines (158N, 158JP): potential models for the study of peroxisomal disorders associated with dysmyelination processes: Peroxisomal and Mitochondrial Status of Two Differentiated Murine Oligodendrocytic Cell Lines (158N, 158JP)

Forkhead pathway in the control of adult neurogenesis

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