2023 - Research.com Genetics in United States Leader Award
2022 - Research.com Best Female Scientist Award
2016 - Member of the National Academy of Medicine (NAM)
2012 - Fellow of the American Association for the Advancement of Science (AAAS)
1994 - Metlife Foundation Award for Medical Research in Alzheimer's Disease
1993 - Potamkin Prize for Research in Pick's, Alzheimer's, and Related Diseases, American Academy of Neurology
1993 - Sedgwick Memorial Medal, American Public Health Association
Her primary areas of investigation include Genetics, Alzheimer's disease, Genome-wide association study, Single-nucleotide polymorphism and Disease. Her study in Alcohol dependence extends to Genetics with its themes. Her Alzheimer's disease study integrates concerns from other disciplines, such as Apolipoprotein E, Dementia and Case-control study.
Her Genome-wide association study study combines topics in areas such as Late onset, Linkage disequilibrium, Minor allele frequency, Allele frequency and Cognitive decline. Her Single-nucleotide polymorphism research is multidisciplinary, relying on both Nicotine, Haplotype and Candidate gene. The concepts of her Disease study are interwoven with issues in Biomarker, Neuroscience, Gerontology and Bioinformatics.
Her main research concerns Genetics, Disease, Alzheimer's disease, Genome-wide association study and Gene. Her study looks at the relationship between Genetics and fields such as Alcohol dependence, as well as how they intersect with chemical problems. Her Disease research incorporates elements of Biomarker, Neuroscience, Immunology and Bioinformatics.
Her Alzheimer's disease research includes themes of Apolipoprotein E and Dementia. Alison Goate usually deals with Locus and limits it to topics linked to Genetic linkage and Linkage. Alison Goate has included themes like Haplotype and Candidate gene in her Single-nucleotide polymorphism study.
Alison Goate focuses on Disease, Genome-wide association study, Genetics, Gene and Internal medicine. Her Disease research is multidisciplinary, incorporating perspectives in Cognition and Computational biology. Her work deals with themes such as Alcohol dependence, Genetic association, Locus and Alcohol use disorder, which intersect with Genome-wide association study.
Her Genetics study frequently draws connections between adjacent fields such as Meta-analysis. Her Gene research is multidisciplinary, incorporating elements of Innate immune system and Microglia. The Alzheimer's disease study combines topics in areas such as Neuroscience and Neurodegeneration.
Her main research concerns Genome-wide association study, Genetics, Disease, Gene and Internal medicine. Her Genome-wide association study research includes elements of Gene expression profiling, Transcriptome, Genetic association, Locus and Genetic architecture. Her study connects Meta-analysis and Genetics.
Amyloid and Tau protein is closely connected to Atrophy in her research, which is encompassed under the umbrella topic of Disease. Her work on Alzheimer's disease as part of general Internal medicine research is frequently linked to African descent, thereby connecting diverse disciplines of science. Her Clinical Dementia Rating study in the realm of Alzheimer's disease connects with subjects such as Dysdiadochokinesia.
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.
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.
Alison Goate;Marie-Christine Chartier-Harlin;Mike Mullan;Jeremy Brown.
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
M. Hutton;C. L. Lendon;P. Rizzu;M. Baker.
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)
Clinical and Biomarker Changes in Dominantly Inherited Alzheimer’s Disease
Randall J. Bateman;Chengjie Xiong;Tammie L.S. Benzinger;Anne M. Fagan.
The New England Journal of Medicine (2012)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims.
Nature Genetics (2009)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (Nature Genetics (2009) 41 (1088-1093))
D Harold;R Abraham;P Hollingworth;R Sims.
Nature Genetics (2013)
A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain.
Bart De Strooper;Wim Annaert;Philippe Cupers;Paul Saftig.
TREM2 Variants in Alzheimer's Disease
Rita Guerreiro;Rita Guerreiro;Aleksandra Wojtas;Jose Bras;Minerva Carrasquillo.
The New England Journal of Medicine (2013)
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Javier Simón-Sánchez;Claudia Schulte;Jose M Bras;Jose M Bras;Manu Sharma.
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)
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