John R. Gilbert spends much of his time researching Genetics, Single-nucleotide polymorphism, Genome-wide association study, Autism and Alzheimer's disease. Genetics is represented through his Locus, Genetic linkage, Candidate gene, Haplotype and Heritability of autism research. His Single-nucleotide polymorphism research integrates issues from Haplogroup H and Genetic architecture.
His research investigates the connection between Genome-wide association study and topics such as Copy-number variation that intersect with issues in Epigenetics of autism. His Autism study deals with Bioinformatics intersecting with Fragile X syndrome, Intellectual disability, CHD2, Structural variation and GABRA2. The concepts of his Alzheimer's disease study are interwoven with issues in PICALM, Apolipoprotein E, SORL1 and Age of onset.
His scientific interests lie mostly in Genetics, Candidate gene, Single-nucleotide polymorphism, Disease and Genetic linkage. Within one scientific family, he focuses on topics pertaining to Autism under Genetics, and may sometimes address concerns connected to Copy-number variation. His Candidate gene research is multidisciplinary, incorporating elements of Exome sequencing and Chromosome 12.
In his work, Genetically modified mouse, Gene isoform, Cell biology, Endocrinology and Neuroscience is strongly intertwined with Apolipoprotein E, which is a subfield of Single-nucleotide polymorphism. His Genetic linkage study combines topics in areas such as Genetic heterogeneity and Linkage. His biological study spans a wide range of topics, including Genomics and Genetic architecture.
His main research concerns Genetics, Genome-wide association study, Exome sequencing, Disease and Gene. His is involved in several facets of Genetics study, as is seen by his studies on Locus, Gene expression, Genome, Chromosome and Genetic linkage. John R. Gilbert interconnects SNP, Alzheimer's disease, Genetic association and Genomics in the investigation of issues within Genome-wide association study.
His Genetic association research incorporates elements of Autism spectrum disorder and Copy-number variation. John R. Gilbert has included themes like Disease gene, Multiplex, Late onset and Candidate gene in his Exome sequencing study. His work in Disease covers topics such as Immunology which are related to areas like Dementia.
John R. Gilbert mainly investigates Genetics, Genome-wide association study, Genomics, Alzheimer's disease and Gene expression. Locus, Allele, DNA methylation, Genetic architecture and Common disease-common variant are the primary areas of interest in his Genetics study. His research in Locus intersects with topics in Copy-number variation, Meta-analysis, Genotyping, Genetic association and Autism spectrum disorder.
His work in Allele addresses issues such as Apolipoprotein E, which are connected to fields such as Risk factor and White. His study in Genetic architecture is interdisciplinary in nature, drawing from both SNP and Single-nucleotide polymorphism. The study incorporates disciplines such as Minor allele frequency, Allele frequency, Case-control study and Linkage disequilibrium in addition to Common disease-common variant.
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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)
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)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang;Haitao Zhang;Deqiong Ma;Maja Bucan.
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Dalila Pinto;Elsa Delaby;Elsa Delaby;Elsa Delaby;Daniele Merico;Mafalda Barbosa.
American Journal of Human Genetics (2014)
A genome-wide linkage and association scan reveals novel loci for autism
Lauren A. Weiss;Lauren A. Weiss;Dan E. Arking;Mark J. Daly;Mark J. Daly;Aravinda Chakravarti.
Hypothesis: Microtubule Instability and Paired Helical Filament Formation in the Alzheimer Disease Brain Are Related to Apolipoprotein E Genotype
Warren J. Strittmatter;Karl H. Weisgraber;Michel Goedert;Ann M. Saunders.
Experimental Neurology (1994)
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21
Rachel V. Baxter;Kamel Ben Othmane;Julie M. Rochelle;Jason E. Stajich.
Nature Genetics (2002)
SNPing Away at Complex Diseases: Analysis of Single-Nucleotide Polymorphisms around APOE in Alzheimer Disease
Eden R. Martin;Eric H. Lai;John R. Gilbert;Allison R. Rogala.
American Journal of Human Genetics (2000)
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