His scientific interests lie mostly in Genetics, Genome-wide association study, Single-nucleotide polymorphism, Alzheimer's disease and PICALM. His Genetics study integrates concerns from other disciplines, such as Internal medicine and Disease. In general Disease, his work in Disease susceptibility is often linked to CD33 and ABCA7 linking many areas of study.
Vincent Chouraki works mostly in the field of Genome-wide association study, limiting it down to topics relating to Genetic association and, in certain cases, Apolipoprotein E, Age of onset, Heritability, Polymorphism and Cohort. His Alzheimer's disease research incorporates themes from Molecular genetics, Dementia, Case-control study and Late onset. The study of PICALM is intertwined with the study of SORL1 in a number of ways.
Vincent Chouraki spends much of his time researching Genome-wide association study, Genetics, Disease, Genetic association and Internal medicine. His Genome-wide association study research is multidisciplinary, relying on both Alzheimer's disease, Allele frequency, SNP and Locus. Genetics is closely attributed to Apolipoprotein E in his research.
Vincent Chouraki interconnects Meta-analysis, Neuroscience, Polymorphism and Bioinformatics in the investigation of issues within Disease. His Single-nucleotide polymorphism research focuses on subjects like Genetic predisposition, which are linked to Case-control study. As a member of one scientific family, Vincent Chouraki mostly works in the field of PICALM, focusing on SORL1 and, on occasion, Candidate gene, Susceptibility locus and Disease susceptibility.
Vincent Chouraki mainly focuses on Genome-wide association study, Genetics, Dementia, Internal medicine and Disease. His Genome-wide association study research is multidisciplinary, incorporating elements of Apolipoprotein E, Computational biology, Genetic association and Locus. In his research on the topic of Genetic association, PSEN2 is strongly related with Endophenotype.
His research is interdisciplinary, bridging the disciplines of Alzheimer's disease and Genetics. His Dementia research integrates issues from Endocrinology, Cohort study, High-density lipoprotein and Lipoprotein. The study incorporates disciplines such as Meta-analysis, Neuroimaging and Physical medicine and rehabilitation in addition to Disease.
His scientific interests lie mostly in Genome-wide association study, Genetics, Alzheimer's disease, Locus and Allele frequency. His work carried out in the field of Genome-wide association study brings together such families of science as Cohort study, Genetic association, Apolipoprotein E, Risk factor and Comorbidity. His studies in Genetic association integrate themes in fields like Genetic heterogeneity, Clinical psychology and Heritability.
Vincent Chouraki combines subjects such as Dentate gyrus, Hippocampal formation, Subiculum and Episodic memory with his study of Locus. In the subject of general Allele frequency, his work in Minor allele frequency is often linked to TREM2, thereby combining diverse domains of study. His Case-control study research focuses on Linkage disequilibrium and how it connects with Immunology.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj.
Nature Genetics (2013)
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.
Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish.
Nature Genetics (2011)
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
Valentina Escott-Price;Céline Bellenguez;Li-San Wang;Seung-Hoan Choi.
PLOS ONE (2014)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Incidence of Dementia over Three Decades in the Framingham Heart Study
Claudia L. Satizabal;Alexa S. Beiser;Vincent Chouraki;Geneviève Chêne.
The New England Journal of Medicine (2016)
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Rebecca Sims;Sven J. Van Der Lee;Adam C. Naj;Céline Bellenguez;Céline Bellenguez.
Nature Genetics (2017)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Cristian Pattaro;Alexander Teumer;Mathias Gorski;Audrey Y. Chu.
Nature Communications (2016)
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)
G. Davies;N. Armstrong;J. C. Bis;J. Bressler.
A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.
Kuan Lin Huang;Edoardo Marcora;Anna A. Pimenova;Antonio F. Di Narzo.
Nature Neuroscience (2017)
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Joshua C Bis;Charles DeCarli;Albert Vernon Smith;Fedde van der Lijn.
Nature Genetics (2012)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: