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Technologie(s) : GWAS
36 résultats
Page 1 sur 2

Myriam Rahmouni et al.
Deep analysis of the major histocompatibility complex genetic associations using covariate analysis and haploblocks unravels new mechanisms for the molecular etiology of Elite Control in AIDS
BMC Immunology 2025, vol. 26, issue 1
doi: 10.1186/s12865-024-00680-6

Chloé Morin et al.
Intricate ribosome composition and translational reprogramming in epithelial–mesenchymal transition
Proceedings of the National Academy of Sciences 2024, vol. 121, issue 50
doi: 10.1073/pnas.2408114121

Julie Le Borgne et al.
X‐chromosome-wide association study for Alzheimer’s disease
Molecular Psychiatry 2024
doi: 10.1038/s41380-024-02838-5

Kimberley Burrows et al.
A framework for conducting GWAS using repeated measures data with an application to childhood BMI
Nature Communications 2024, vol. 15, issue 1
doi: 10.1038/s41467-024-53687-3

Simon Rio et al.
Genome-wide association for agro-morphological traits in a triploid banana population with large chromosome rearrangements
Horticulture Research 2024, vol. 12, issue 2
doi: 10.1093/hr/uhae307

Simon Rio et al.
Genome-wide association for agro-morphological traits in a triploid banana population with large chromosome rearrangements
Horticulture Research 2024, vol. 12, issue 2
doi: 10.1093/hr/uhae307

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

Emily K. Hasser et al.
Genome-wide investigation of exogenous female hormones, genetic variation, and venous thromboembolism risk
Journal of Thrombosis and Haemostasis 2024, vol. 22, issue 8
doi: 10.1016/j.jtha.2024.05.011

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

Chaker Aloui et al.
An AluYa5 Insertion in the 3′UTR of COL4A1 and Cerebral Small Vessel Disease
JAMA Network Open 2024, vol. 7, issue 4
doi: 10.1001/jamanetworkopen.2024.7034

Camille Pubert et al.
A cluster of putative resistance genes is associated with a dominant resistance to sunflower broomrape
Theoretical and Applied Genetics 2024, vol. 137, issue 5
doi: 10.1007/s00122-024-04594-0

Hasnaa Talimi et al.
A comparative genomics approach reveals a local genetic signature of Leishmania tropica in Morocco
Microbial Genomics 2024, vol. 10, issue 4
doi: 10.1099/mgen.0.001230

Sarah TEBEKA et al.
Genome-wide association study of early-onset and late-onset postpartum depression: the IGEDEPP prospective study
European Psychiatry 2024
doi: 10.1192/j.eurpsy.2024.26

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

36 résultats
Page 1 sur 2