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
The scientist’s investigation covers issues in Genetics, Allele, Locus, Genetic linkage and Genome-wide association study. Her Allele research incorporates themes from Alzheimer's disease, Apolipoprotein E, Immunology and Genotype. Margaret A. Pericak-Vance has researched Apolipoprotein E in several fields, including SORL1 and Risk factor.
Her Locus research focuses on subjects like Chromosome, which are linked to Genetic determinism. Her work investigates the relationship between Genetic linkage and topics such as Amyotrophic lateral sclerosis that intersect with problems in Mutation. Margaret A. Pericak-Vance usually deals with Genome-wide association study and limits it to topics linked to Case-control study and Macular degeneration.
Her primary scientific interests are in Genetics, Disease, Genetic linkage, Gene and Locus. Her work on Alzheimer's disease expands to the thematically related Genetics. Her Alzheimer's disease research is multidisciplinary, incorporating perspectives in Age of onset, Gerontology and Degenerative disease.
The various areas that she examines in her Genetic linkage study include Genetic marker, Chromosome, Gene mapping, Genetic heterogeneity and Linkage. Her Allele study incorporates themes from Apolipoprotein E, Immunology, Genotype and Risk factor. Her studies in Single-nucleotide polymorphism integrate themes in fields like Haplotype and Candidate gene.
Margaret A. Pericak-Vance mainly focuses on Genetics, Disease, Alzheimer's disease, Genome-wide association study and Gene. Her work on Genetics deals in particular with Locus, Allele, Genetic association, Exome sequencing and Single-nucleotide polymorphism. Her Locus research is multidisciplinary, relying on both Minor allele frequency and Genetic linkage.
Her study focuses on the intersection of Allele and fields such as Apolipoprotein E with connections in the field of Genotype, Oncology and Demography. Her biological study spans a wide range of topics, including SORL1, Gerontology and Cohort. Her research integrates issues of Genomics, TREM2, Glaucoma, Open angle glaucoma and Haplotype in her study of Genome-wide association study.
Her main research concerns Genetics, Genome-wide association study, Gene, Alzheimer's disease and Disease. Her is involved in several facets of Genetics study, as is seen by her studies on Locus, Genetic association, Single-nucleotide polymorphism, Allele and Exome sequencing. Margaret A. Pericak-Vance has included themes like Odds ratio and Apolipoprotein E in her Allele study.
Her Genome-wide association study study combines topics in areas such as Allele frequency, Genomics, Meta-analysis and Glaucoma, Open angle glaucoma. Margaret A. Pericak-Vance interconnects Lipid metabolism and Immunology in the investigation of issues within Gene. The study incorporates disciplines such as SORL1, Age of onset and Genetic epidemiology in addition to Alzheimer's disease.
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.
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.
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.
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.
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)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
Profile was last updated on December 6th, 2021.
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