While working in this field, Christopher S. Carlson studies both Alzheimer's disease and Dementia. Christopher S. Carlson combines Dementia and Alzheimer's disease in his studies. He applies his multidisciplinary studies on Internal medicine and Oncology in his research. While working on this project, Christopher S. Carlson studies both Oncology and Internal medicine. He applies his multidisciplinary studies on Genotype and Allele frequency in his research. He performs integrative Allele frequency and Minor allele frequency research in his work. His research on Minor allele frequency often connects related topics like Genotype. His SNP research extends to the thematically linked field of Genetics. The study of SNP is intertwined with the study of Genetics in a number of ways.
While working on this project, Christopher S. Carlson studies both Genetics and Immunology. He incorporates Immunology and Genetics in his studies. While working on this project, Christopher S. Carlson studies both Genotype and Mutation. Christopher S. Carlson conducted interdisciplinary study in his works that combined Mutation and Allele. His multidisciplinary approach integrates Allele and Locus (genetics) in his work. Christopher S. Carlson integrates many fields, such as Locus (genetics) and Genotype, in his works. He applies his multidisciplinary studies on Gene and Genotyping in his research. Borrowing concepts from Genotyping, Christopher S. Carlson weaves in ideas under Single-nucleotide polymorphism. Christopher S. Carlson integrates Genome-wide association study with Genome in his study.
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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)
Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium
Christopher S. Carlson;Michael A. Eberle;Mark J. Rieder;Qian Yi.
American Journal of Human Genetics (2004)
Comprehensive assessment of T-cell receptor β-chain diversity in αβ T cells
Harlan S. Robins;Paulo V. Campregher;Santosh K. Srivastava;Abigail Wacher.
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Rebecca Sims;Sven J. Van Der Lee;Adam C. Naj;Céline Bellenguez;Céline Bellenguez.
Nature Genetics (2017)
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do;Ron Do;Nathan O. Stitziel;Hong Hee Won;Hong Hee Won;Anders Berg Jørgensen.
Using synthetic templates to design an unbiased multiplex PCR assay
Christopher S. Carlson;Ryan O. Emerson;Anna M. Sherwood;Cindy Desmarais.
Nature Communications (2013)
Principles for the post-GWAS functional characterization of cancer risk loci
Matthew L Freedman;Alvaro N A Monteiro;Simon A Gayther;Simon A Gayther;Gerhard A Coetzee.
Nature Genetics (2011)
Genetic analyses of diverse populations improves discovery for complex traits
Genevieve L. Wojcik;Mariaelisa Graff;Katherine K. Nishimura;Ran Tao.
Overlap and Effective Size of the Human CD8+ T Cell Receptor Repertoire
Harlan S. Robins;Santosh K. Srivastava;Paulo V. Campregher;Cameron J. Turtle.
Science Translational Medicine (2010)
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Hou Feng Zheng;Vincenzo Forgetta;Yi Hsiang Hsu;Yi Hsiang Hsu;Karol Estrada.
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