2023 - Research.com Genetics in United States Leader Award
2022 - Research.com Best Female Scientist Award
2022 - Research.com Best Scientist Award
2011 - Fellow of the American Association for the Advancement of Science (AAAS)
2003 - Member of the National Academy of Medicine (NAM)
2001 - Grand Prix scientifique de la Fondation Louis D., Institut de France
Margaret A. Pericak-Vance spends much of her time researching Genetics, Allele, Genome-wide association study, Locus and Genetic linkage. Her Genetics study frequently links to related topics such as Autism. Her Allele research includes themes of Multiple sclerosis, Immunology, Apolipoprotein E and Genotype.
Her Genome-wide association study study also includes
Her main research concerns Genetics, Disease, Genetic linkage, Gene and Allele. Her Locus, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Haplotype investigations are all subjects of Genetics research. Margaret A. Pericak-Vance has researched Disease in several fields, including Oncology and Bioinformatics.
Her Genetic linkage research is multidisciplinary, incorporating elements of Genetic marker, Chromosome, Gene mapping, Genetic heterogeneity and Linkage. She works mostly in the field of Allele, limiting it down to topics relating to Apolipoprotein E and, in certain cases, Alzheimer's disease. Her Alzheimer's disease study integrates concerns from other disciplines, such as Age of onset and Degenerative disease.
Genetics, Disease, Genome-wide association study, Alzheimer's disease and Gene are her primary areas of study. Her study in Genetics focuses on Locus, Allele, Exome sequencing, Genetic association and Single-nucleotide polymorphism. Her Locus study frequently intersects with other fields, such as Genetic linkage.
Her work in Allele covers topics such as Apolipoprotein E which are related to areas like Oncology and Demography. Her study looks at the relationship between Disease and fields such as Gerontology, as well as how they intersect with chemical problems. The Genome-wide association study study combines topics in areas such as Genomics, Glaucoma, Open angle glaucoma, Minor allele frequency and Haplotype.
Her primary scientific interests are in Genetics, Genome-wide association study, Gene, Allele and Disease. Her research is interdisciplinary, bridging the disciplines of Alzheimer's disease and Genetics. Her studies in Genome-wide association study integrate themes in fields like Linkage disequilibrium, Allele frequency, Genomics and Glaucoma, Open angle glaucoma.
Her Gene research integrates issues from Multiple sclerosis and Cancer research. Her studies deal with areas such as Odds ratio, Apolipoprotein E and Immunology as well as Allele. Within one scientific family, Margaret A. Pericak-Vance focuses on topics pertaining to Genetic variation under Disease, and may sometimes address concerns connected to Candidate gene.
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.
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
E. H. Corder;A. M. Saunders;W. J. Strittmatter;D. E. Schmechel.
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.
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.
Warren J. Strittmatter;Ann M. Saunders;Donald Schmechel;Margaret Pericak-Vance.
Proceedings of the National Academy of Sciences of the United States of America (1993)
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
R. Sherrington;E. I. Rogaev;Y. Liang;E. A. Rogaeva.
Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis
Lindsay A. Farrer;L. Adrienne Cupples;Jonathan L. Haines;Bradley T Hyman.
Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease.
A. M. Saunders;W. J. Strittmatter;D. Schmechel;P. H. St. George-Hyslop.
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)
Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium.
L A Farrer;L A Cupples;J L Haines;B Hyman.
Complement factor H variant increases the risk of age-related macular degeneration.
Jonathan L. Haines;Michael A. Hauser;Silke Schmidt;William K. Scott.
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
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: