C. Derbois

发表

Identi fi cation and characterization of two functional variants in the human longevity gene FOXO 3

W. Lieb, L. Christiansen, S. Schreiber, 2018 .

Syddansk Universitet Identification and characterization of two functional variants in the human longevity gene

W. Lieb, L. Christiansen, S. Schreiber, 2017 .

The H2A.J histone variant contributes to Interferon-Stimulated Gene expression in senescence by its weak interaction with H1 and the derepression of repeated DNA sequences

C. Redon, W. Bonner, J. Deleuze, 2020, bioRxiv.

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Nick C Fox, Cory C. Funk, D. G. Clark, 2017, Nature Genetics.

Genetic investigation of four meiotic genes in women with premature ovarian failure.

F. Matsuda, M. Fellous, C. Derbois, 2008, European journal of endocrinology.

Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation

D. Trégouët, M. Germain, P. Amouyel, 2019, Scientific Reports.

Is there still room for additional common susceptibility alleles for venous thromboembolism?

D. Chasman, P. Reitsma, D. Trégouët, 2016, Journal of thrombosis and haemostasis : JTH.

Histone variant H2A.J accumulates in senescent cells and promotes inflammatory gene expression

Michael P. Snyder, Zhihai Ma, B. Benayoun, 2017, Nature Communications.

Syddansk Universitet Immunochip analysis identifies association of the RAD 50 / IL 13 region with human longevity

M. Nöthen, K. Strauch, W. Lieb, 2016 .

University of Southern Denmark Immunochip analysis identifies association of the RAD50/IL13 region with human longevity Flachsbart,

M. Nöthen, K. Strauch, W. Lieb, 2016 .

Immunochip analysis identifies association of the RAD50/IL13 region with human longevity

M. Nöthen, K. Strauch, W. Lieb, 2016, Aging cell.

[Human infertility: meiotic genes as potential candidates].

F. Matsuda, M. Fellous, D. Wolgemuth, 2002, Gynecologie, obstetrique & fertilite.

G6PD and HBB polymorphisms in the Senegalese population: prevalence, correlation with clinical malaria

J. Deleuze, C. Derbois, J. Zagury, 2022, PeerJ.

G6PD and HBB polymorphisms in Senegalese population: prevalence and correlations with clinical malaria

J. Deleuze, C. Derbois, J. Zagury, 2020 .

Genetic Architecture and Dynamics of PfKelch13’s Propeller Domain in Plasmodium Falciparum Clinical Isolates Collected in Senegal.

J. Deleuze, C. Derbois, D. Ménard, 2021 .

Relationship between genetic polymorphisms of cytokines and self-reported sleep complaints and habitual caffeine consumption.

D. Léger, M. Chennaoui, F. Sauvet, 2022, Sleep medicine.

GENETIC POLYMORPHISM OF XRCC1 ANDXRCC3 GENES AND RISK OF CERVICAL CANCER IN SENEGALESE POPULATION

A. Dem, J. Deleuze, C. Derbois, 2020, International Journal of Advanced Research.

PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans

F. Galibert, M. Lathrop, R. Zechner, 2012, Nature Genetics.

Specific TGM1 mutation profiles in bathing suit and self-improving collodion ichthyoses: phenotypic and genotypic data from 9 patients with dynamic phenotypes of autosomal recessive congenital ichthyosis.

C. Derbois, J. Fischer, C. Blanchet‐Bardon, 2012, Archives of dermatology.

PNPLA 1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans

F. Galibert, M. Lathrop, R. Zechner, 2014 .

Systematic analysis of TruSeq, SMARTer and SMARTer Ultra-Low RNA-seq kits for standard, low and ultra-low quantity samples

Robert Olaso, Cyril Dalmasso, Christophe Ambroise, 2019, Scientific Reports.

Glucocorticoids delay RAF-induced senescence promoted by EGR1

J. Cintrat, J. Deleuze, C. Derbois, 2019, Journal of Cell Science.

Comprehensive analysis of RNA-seq kits for standard, low and ultra-low quantity samples

E. Bonnet, C. Ambroise, J. Deleuze, 2019, bioRxiv.

Genetic variants of RNASE3 (ECP) and susceptibility to severe malaria in Senegalese population

J. Deleuze, C. Derbois, R. Olaso, 2018, Malaria Journal.

Genetics and Cognitive Vulnerability to Sleep Deprivation in Healthy Subjects: Interaction of ADORA2A, TNF-α and COMT Polymorphisms

D. Léger, M. Guillard, M. Chennaoui, 2021, Life.

Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation

D. Trégouët, M. Germain, P. Amouyel, 2019, Scientific Reports.

Identification of biological pathways specific to phases preceding rheumatoid arthritis development through gene expression profiling

J. Deleuze, C. Derbois, R. Olaso, 2021, International journal of immunogenetics.

A Missense Mutation in PPP1R15B Causes a Syndrome Including Diabetes, Short Stature, and Microcephaly

A. Hattersley, C. Julier, D. Eizirik, 2015, Diabetes.

Reactive astrocytes promote proteostasis in Huntington’s disease through the JAK2-STAT3 pathway

M. Guillermier, F. Petit, G. Bonvento, 2021, bioRxiv.

The JAK2-STAT3 pathway controls a beneficial proteostasis response of reactive astrocytes in Huntington’s disease

M. Guillermier, F. Petit, G. Bonvento, 2021 .

Juvenile-Onset Diabetes and Congenital Cataract: “Double-Gene” Mutations Mimicking a Syndromic Diabetes Presentation

C. Julier, A. Philippi, C. Derbois, 2017, Genes.

DNAJC3 deficiency induces β-cell mitochondrial apoptosis and causes syndromic young-onset diabetes.

C. Julier, P. Marchetti, D. Eizirik, 2021, European journal of endocrinology.

Genotyping on blood and buccal cells using loop-mediated isothermal amplification in healthy humans

M. Chennaoui, F. Sauvet, A. Boland, 2020, Biotechnology reports.

Genetic variants of RNASE3 (ECP) and susceptibility to severe malaria in Senegalese population

J. Deleuze, C. Derbois, R. Olaso, 2018, Malaria Journal.

Single cell transcriptome sequencing of stimulated and frozen human peripheral blood mononuclear cells

E. Bonnet, J. Deleuze, C. Derbois, 2023, Scientific data.

Nature Genetics Advance Online Publication Pnpla1 Mutations Cause Autosomal Recessive Congenital Ichthyosis in Golden Retriever Dogs and Humans

F. Galibert, M. Lathrop, R. Zechner, 2022 .

Nature Genetics Advance Online Publication Pnpla1 Mutations Cause Autosomal Recessive Congenital Ichthyosis in Golden Retriever Dogs and Humans

F. Galibert, M. Lathrop, R. Zechner, 2022 .

Genetic investigation of four meiotic genes in women with premature ovarian failure.

F. Matsuda, M. Fellous, C. Derbois, 2008, European journal of endocrinology.

Identification and characterization of two functional variants in the human longevity gene FOXO3

W. Lieb, L. Christiansen, P. Rosenstiel, 2017, Nature Communications.