His primary areas of investigation include Genetics, Alzheimer's disease, Apolipoprotein E, Genome-wide association study and Allele. Many of his studies involve connections with topics such as Early-onset Alzheimer's disease and Genetics. His Alzheimer's disease research is multidisciplinary, incorporating elements of Biological pathway, Linkage disequilibrium and Allele frequency.
María J. Bullido interconnects Odds ratio, Molecular biology and Genetic association in the investigation of issues within Apolipoprotein E. The concepts of his Genome-wide association study study are interwoven with issues in Gene expression, Case-control study, Neurodegeneration and Genomics. His Single-nucleotide polymorphism research includes elements of Disease susceptibility and Age of onset.
María J. Bullido mainly investigates Genetics, Disease, Apolipoprotein E, Alzheimer's disease and Allele. Genetics is represented through his Single-nucleotide polymorphism, Genotype, Genome-wide association study, Allele frequency and Genetic association research. His studies in Genome-wide association study integrate themes in fields like Case-control study and Genetic predisposition.
His Genetic association research is multidisciplinary, relying on both Odds ratio, PICALM and Age of onset. His Apolipoprotein E research incorporates themes from Immunology and Polymorphism. His Alzheimer's disease study integrates concerns from other disciplines, such as Endocrinology, Pathogenesis, Late onset, Exon and Degenerative disease.
María J. Bullido mostly deals with Disease, Genetics, Genome-wide association study, Dementia and Cell biology. His work deals with themes such as Psychiatry and Genetic association, which intersect with Disease. Genetics is closely attributed to Inbreeding in his work.
His Genome-wide association study study combines topics from a wide range of disciplines, such as Alzheimer's disease and Allele frequency. In his study, which falls under the umbrella issue of Dementia, Bioinformatics, Amyloid and Computational biology is strongly linked to Gene. His biological study spans a wide range of topics, including Oxidative stress and Neurodegeneration.
His primary areas of study are Disease, Genome-wide association study, Dementia, Gene and Genetic association. His Genome-wide association study research incorporates elements of Alzheimer's disease and Allele frequency. The study incorporates disciplines such as Common disease-common variant, Genetic predisposition, Linkage disequilibrium, Case-control study and Minor allele frequency in addition to Alzheimer's disease.
In general Dementia study, his work on Cerebral amyloid angiopathy often relates to the realm of Mechanism, Endophenotype and Causality, thereby connecting several areas of interest. The subject of his Genetic association research is within the realm of Single-nucleotide polymorphism.
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)
Genome-wide association study indentifies variants at CLU and CR1 associated with Alzheimer’s disease
J Lambert;S Heath;G Even;D Campion.
Nature Genetics (2009)
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)
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)
APOE and Alzheimer disease: a major gene with semi-dominant inheritance
E Genin;D Hannequin;D Wallon;K Sleegers.
Molecular Psychiatry (2011)
Microbes and Alzheimer's disease
Ruth F. Itzhaki;Ruth F. Itzhaki;Richard Lathe;Brian J. Balin;Melvyn J. Ball.
Journal of Alzheimer's Disease (2016)
A polymorphism in the regulatory region of APOE associated with risk for Alzheimer's dementia
María Jesus Bullido;María Jesús Artiga;María Recuero;Isabel Sastre.
Nature Genetics (1998)
Allelic polymorphisms in the transcriptional regulatory region of apolipoprotein E gene.
Marı́a J Artiga;Marı́a J Bullido;Isabel Sastre;Marı́a Recuero.
FEBS Letters (1998)
A novel Alzheimer disease locus located near the gene encoding tau protein
G. Jun;C. A. Ibrahim-Verbaas;M. Vronskaya;J-C Lambert;J-C Lambert;J-C Lambert.
Molecular Psychiatry (2016)
Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP
Rita Joao Guerreiro;Miquel Baquero;Rafael Blesa;Mercè Boada.
Neurobiology of Aging (2010)
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: