1997 - Metlife Foundation Award for Medical Research in Alzheimer's Disease
1995 - Potamkin Prize for Research in Pick's, Alzheimer's, and Related Diseases, American Academy of Neurology
1995 - Sedgwick Memorial Medal, American Public Health Association
His primary areas of study are Alzheimer's disease, Amyloid precursor protein, Genetics, Genetically modified mouse and Internal medicine. His Alzheimer's disease research incorporates themes from Mutation, Immunology, Epigenomics, Differentially methylated regions and Degenerative disease. The study incorporates disciplines such as Molecular biology, Amyloid beta and Neuroscience in addition to Amyloid precursor protein.
His Genetics research focuses on subjects like Late onset, which are linked to Human genetics and Molecular genetics. In his study, Mutant and Senile plaques is inextricably linked to Presenilin, which falls within the broad field of Genetically modified mouse. In his work, Amyloid is strongly intertwined with Endocrinology, which is a subfield of Internal medicine.
Steven G. Younkin focuses on Genetics, Disease, Internal medicine, Alzheimer's disease and Genome-wide association study. His study brings together the fields of Apolipoprotein E and Genetics. His biological study deals with issues like Endocrinology, which deal with fields such as Amyloid precursor protein.
His Amyloid precursor protein study incorporates themes from Molecular biology and Presenilin. As a part of the same scientific family, he mostly works in the field of Alzheimer's disease, focusing on Amyloid and, on occasion, Biochemistry, Genetically modified mouse and Amyloid beta. His Genome-wide association study research includes elements of Temporal cortex, Case-control study, PICALM, Genetic association and Candidate gene.
Steven G. Younkin spends much of his time researching Genetics, Disease, Genome-wide association study, Alzheimer's disease and Single-nucleotide polymorphism. His Genetics study frequently involves adjacent topics like Case-control study. The subject of his Disease research is within the realm of Internal medicine.
His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology and Pathology. Steven G. Younkin combines subjects such as Progressive supranuclear palsy, Temporal cortex, Endophenotype, Cerebral amyloid angiopathy and Apolipoprotein E with his study of Genome-wide association study. His Alzheimer's disease research incorporates themes from Biological pathway, Transcriptome, Dementia and Oncology.
His scientific interests lie mostly in Genetics, Alzheimer's disease, Genome-wide association study, Single-nucleotide polymorphism and Disease. Steven G. Younkin undertakes multidisciplinary studies into Genetics and TREM2 in his work. His research investigates the connection between Alzheimer's disease and topics such as Dementia that intersect with issues in Lower risk.
His work in Genome-wide association study addresses issues such as Genetic association, which are connected to fields such as Haplotype. His research investigates the link between Single-nucleotide polymorphism and topics such as Apolipoprotein E that cross with problems in Cell biology and Allele. The Internal medicine study combines topics in areas such as PICALM and Endophenotype.
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.
Correlative Memory Deficits, Aβ Elevation, and Amyloid Plaques in Transgenic Mice
Karen Hsiao;Paul Chapman;Steven Nilsen;Chris Eckman.
Science (1996)
Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease.
D. Scheuner;C. Eckman;C. Eckman;M. Jensen;X. Song.
Nature Medicine (1996)
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 identifies variants at CLU and PICALM associated with Alzheimer's disease
Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims.
Nature Genetics (2009)
TREM2 Variants in Alzheimer's Disease
Rita Guerreiro;Rita Guerreiro;Aleksandra Wojtas;Jose Bras;Minerva Carrasquillo.
The New England Journal of Medicine (2013)
An increased percentage of long amyloid beta protein secreted by familial amyloid beta protein precursor (beta APP717) mutants
Nobuhiro Suzuki;Tobun T. Cheung;Xiao Dan Cai;Asano Odaka.
Science (1994)
Familial Alzheimer's Disease–Linked Presenilin 1 Variants Elevate Aβ1–42/1–40 Ratio In Vitro and In Vivo
David R. Borchelt;Gopal Thinakaran;Christopher B. Eckman;Christopher B. Eckman;Michael K. Lee.
Neuron (1996)
Increased amyloid-β42(43) in brains of mice expressing mutant presenilin 1
Karen Duff;Karen Duff;Chris Eckman;Cindy Zehr;Cindy Zehr;Xin Yu.
Nature (1996)
Production of the Alzheimer amyloid β protein by normal proteolytic processing
Mikio Shoji;Todd E. Golde;Jorge Ghiso;Tobun T. Cheung.
Science (1992)
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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