2023 - Research.com Genetics in United States Leader Award
1995 - Metlife Foundation Award for Medical Research in Alzheimer's Disease
1994 - Potamkin Prize for Research in Pick's, Alzheimer's, and Related Diseases, American Academy of Neurology
1994 - Sedgwick Memorial Medal, American Public Health Association
His primary scientific interests are in Genetics, Genome-wide association study, Alzheimer's disease, Internal medicine and Apolipoprotein E. His Genetics course of study focuses on Autism and Intellectual disability. His Genome-wide association study study incorporates themes from PICALM, Temporal cortex, Linkage disequilibrium and Genetic association.
His studies deal with areas such as Cerebrospinal fluid, Case-control study, Dementia, Age of onset and Degenerative disease as well as Alzheimer's disease. His study in Internal medicine is interdisciplinary in nature, drawing from both Endocrinology, Oncology and Allele frequency. His research in Locus intersects with topics in Allele and Gene mapping.
His main research concerns Genetics, Disease, Alzheimer's disease, Internal medicine and Apolipoprotein E. His work in Genome-wide association study, Gene, Single-nucleotide polymorphism, Allele and Locus is related to Genetics. In his study, Frontotemporal dementia is inextricably linked to Progressive supranuclear palsy, which falls within the broad field of Genome-wide association study.
His Disease research incorporates themes from Computational biology, Neuroscience and Genome. His Alzheimer's disease research is multidisciplinary, relying on both Degenerative disease, Immunology and Age of onset. His biological study spans a wide range of topics, including Endocrinology and Oncology.
Gerard D. Schellenberg mostly deals with Disease, Genetics, Genome-wide association study, Gene and Apolipoprotein E. He combines subjects such as Meta-analysis, Genome, Whole genome sequencing and Computational biology with his study of Disease. Candidate gene is closely connected to Alzheimer's disease in his research, which is encompassed under the umbrella topic of Genetics.
His research investigates the connection between Genome-wide association study and topics such as Genetic association that intersect with problems in Linkage disequilibrium and Endophenotype. His work on Genetic variation, SORL1 and Genotyping as part of general Gene research is often related to High resolution, thus linking different fields of science. The various areas that he examines in his Apolipoprotein E study include Allele and Oncology.
His primary scientific interests are in Genome-wide association study, Genetics, Apolipoprotein E, Gene and Genetic association. His studies deal with areas such as Progressive supranuclear palsy, Temporal cortex, Frontotemporal dementia, Epistasis and Expression quantitative trait loci as well as Genome-wide association study. His Genetics study frequently links to other fields, such as Alzheimer's disease.
His Apolipoprotein E research integrates issues from Allele and Oncology. His study looks at the relationship between Gene and fields such as Dementia, as well as how they intersect with chemical problems. His Genetic association study combines topics in areas such as Chromosome 17, Linkage disequilibrium, Locus and Chromosome 7.
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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)
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
Ephrat Levy-Lahad;Wilma Wasco;Parvoneh Poorkaj;Donna M. Romano.
Science (1995)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney.
Nature (2014)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
Nature (2010)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)
Positional Cloning of the Werner's Syndrome Gene
Chang En Yu;Junko Oshima;Ying Hui Fu;Ellen M. Wijsman.
Science (1996)
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Adam C. Naj;Gyungah Jun;Gary W. Beecham;Li-San Wang.
Nature Genetics (2011)
Patterns and rates of exonic de novo mutations in autism spectrum disorders
Benjamin M. Neale;Yan Kou;Li Liu;Avi Ma'Ayan.
Nature (2012)
Tau is a candidate gene for chromosome 17 frontotemporal dementia.
Parvoneh Poorkaj;Thomas D. Bird;Ellen Wijsman;Ellen Nemens.
Annals of Neurology (1998)
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