Publications
Isabel Alves et al.
Human genetic structure in Northwest France provides new insights into West European historical demography
Nature Communications 2024, vol. 15, issue 1
doi: 10.1038/s41467-024-51087-1
Sarah Meulebrouck et al.
Functional genetics reveals the contribution of delta opioid receptor to type 2 diabetes and beta-cell function
Nature Communications 2024, vol. 15, issue 1
doi: 10.1038/s41467-024-51004-6
Héctor Castillo et al.
Xenopus tropicalis osteoblast-specific open chromatin regions reveal promoters and enhancers involved in human skeletal phenotypes and shed light on early vertebrate evolution
Cells & Development 2024, vol. 179
doi: 10.1016/j.cdev.2024.203924
Claudia Bartoli et al.
The genetic architecture of the adaptive potential of Arabidopsis thaliana in response to Pseudomonas syringae strains isolated from south‐west France
Plant Pathology 2023
doi: 10.1111/ppa.13849
Elise A Lucotte et al.
Investigation of common genetic risk factors between thyroid traits and breast cancer
Human Molecular Genetics 2023, vol. 33, issue 1
doi: 10.1093/hmg/ddad159
Wenwen Gao et al.
Human GLP1R variants affecting GLP1R cell surface expression are associated with impaired glucose control and increased adiposity
Nature Metabolism 2023, vol. 5, issue 10
doi: 10.1038/s42255-023-00889-6
Yann Le Guen et al.
Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes
Proceedings of the National Academy of Sciences 2023, vol. 120, issue 36
doi: 10.1073/pnas.2302720120
Fabrice Ntakirutimana et al.
Genome-wide association analysis identifies natural allelic variants associated with panicle architecture variation in African rice, Oryza glaberrima Steud
G3: Genes, Genomes, Genetics 2023, vol. 13, issue 10
doi: 10.1093/g3journal/jkad174
Monia Zidane et al.
Genetic factors for differentiated thyroid cancer in French Polynesia: new candidate loci
Precision Clinical Medicine 2023, vol. 6, issue 2
doi: 10.1093/pcmedi/pbad015
Jennifer E Huffman et al.
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles
2023
doi: 10.1101/2023.06.07.23291095
Timo Hess et al.
Dissecting the genetic heterogeneity of gastric cancer
eBioMedicine 2023, vol. 92
doi: 10.1016/j.ebiom.2023.104616
et al.
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
JAMA Network Open 2023, vol. 6, issue 5
doi: 10.1001/jamanetworkopen.2023.13734
Adella Karam et al.
WGS Revealed Novel BBS5 Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function Defects
International Journal of Molecular Sciences 2023, vol. 24, issue 10
doi: 10.3390/ijms24108729
Choghag Demirjian et al.
An atypical NLR gene confers bacterial wilt susceptibility in Arabidopsis
Plant Communications 2023, vol. 4, issue 5
doi: 10.1016/j.xplc.2023.100607
Ricardo Cortez Cardoso Penha et al.
Common genetic variations in telomere length genes and lung cancer: a Mendelian randomisation study and its novel application in lung tumour transcriptome
eLife 2023, vol. 12
doi: 10.7554/elife.83118
Daniela Matuozzo et al.
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Genome Medicine 2023, vol. 15, issue 1
doi: 10.1186/s13073-023-01173-8
Lise Folon et al.
Contribution of heterozygous PCSK1 variants to obesity and implications for precision medicine: a case-control study
The Lancet Diabetes & Endocrinology 2023, vol. 11, issue 3
doi: 10.1016/s2213-8587(22)00392-8
Pierre‐Emmanuel Sugier et al.
Investigation of Shared Genetic Risk Factors Between Parkinson’s Disease and Cancers
Movement Disorders 2023, vol. 38, issue 4
doi: 10.1002/mds.29337
Aurélie A G Gabriel et al.
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden
JNCI: Journal of the National Cancer Institute 2022, vol. 114, issue 8
doi: 10.1093/jnci/djac087
M. Guichard et al.
Identification of quantitative trait loci associated with calmness and gentleness in honey bees using whole‐genome sequences
Animal Genetics 2021
doi: 10.1111/age.13070
Elena Gargaun et al.
The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMD
Biomedicines 2021, vol. 9, issue 2
doi: 10.3390/biomedicines9020219
Ozvan Bocher et al.
Extension of SKAT to multi-category phenotypes through a geometrical interpretation
European Journal of Human Genetics 2021 vol.29
doi: 10.1038/s41431-020-00792-8
Réjane Troudet et al.
Gene expression and response prediction to amisulpride in the OPTiMiSE first episode psychoses
Neuropsychopharmacology 2020, vol. 45, issue 10
doi: 10.1038/s41386-020-0703-2
Luca Kleineidam et al.
PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment
Acta Neuropathologica 2020, vol. 139, issue 6
doi: 10.1007/s00401-020-02138-6
Yiyi Ma et al.
Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype
JAMA Neurology 2019, vol. 76, issue 9
doi: 10.1001/jamaneurol.2019.1456