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Christopher S Carlson

Showing results (11-20 of 133) with videos related to

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Human Molecular Genetics|April 29, 2006
Direct detection of null alleles in SNP genotyping dataChristopher S Carlson, Joshua D Smith, Ian B Stanaway, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2009
The impact of patents on the development of genome-based clinical diagnostics: an analysis of case studiesBrandon L Pierce, Christopher S Carlson, Patricia C Kuszler, et al.
American Journal of Human Genetics|December 19, 2003
Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibriumChristopher S Carlson, Michael A Eberle, Mark J Rieder, et al.
Immunological Reviews|December 21, 2002
Sequence variation in the human T-cell receptor lociRachel Mackelprang, Christopher S Carlson, Lakshman Subrahmanyan, et al.
Nucleic Acids Research|February 15, 2013
Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA studyChristina T L Chen, Andrew N McDavid, Orsalem J Kahsai, et al.
Human Genetics|March 16, 2007
Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA StudyAlexander P Reiner, Christopher S Carlson, Elad Ziv, et al.
Pharmacogenetics and Genomics|April 27, 2007
Polymorphisms predicted to alter function in prostaglandin E2 synthase and prostaglandin E2 receptorsJeannette Bigler, Justin G Sibert, Elizabeth M Poole, et al.
Science Translational Medicine|July 8, 2011
Deep sequencing of the human TCRγ and TCRβ repertoires suggests that TCRβ rearranges after αβ and γδ T cell commitmentAnna M Sherwood, Cindy Desmarais, Robert J Livingston, et al.
Nature Genetics|March 26, 2003
Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humansChristopher S Carlson, Michael A Eberle, Mark J Rieder, et al.
Human Mutation|October 29, 2002
Cyclooxygenase 1 (COX1) polymorphisms in African-American and Caucasian populationsCornelia M Ulrich, Jeannette Bigler, Justin Sibert, et al.
Pageof 14

Showing results (11-20 of 133) with videos related to

Sort By:
Pageof 14
Human Molecular Genetics|April 29, 2006
Direct detection of null alleles in SNP genotyping dataChristopher S Carlson, Joshua D Smith, Ian B Stanaway, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2009
The impact of patents on the development of genome-based clinical diagnostics: an analysis of case studiesBrandon L Pierce, Christopher S Carlson, Patricia C Kuszler, et al.
American Journal of Human Genetics|December 19, 2003
Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibriumChristopher S Carlson, Michael A Eberle, Mark J Rieder, et al.
Immunological Reviews|December 21, 2002
Sequence variation in the human T-cell receptor lociRachel Mackelprang, Christopher S Carlson, Lakshman Subrahmanyan, et al.
Nucleic Acids Research|February 15, 2013
Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA studyChristina T L Chen, Andrew N McDavid, Orsalem J Kahsai, et al.
Human Genetics|March 16, 2007
Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA StudyAlexander P Reiner, Christopher S Carlson, Elad Ziv, et al.
Pharmacogenetics and Genomics|April 27, 2007
Polymorphisms predicted to alter function in prostaglandin E2 synthase and prostaglandin E2 receptorsJeannette Bigler, Justin G Sibert, Elizabeth M Poole, et al.
Science Translational Medicine|July 8, 2011
Deep sequencing of the human TCRγ and TCRβ repertoires suggests that TCRβ rearranges after αβ and γδ T cell commitmentAnna M Sherwood, Cindy Desmarais, Robert J Livingston, et al.
Nature Genetics|March 26, 2003
Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humansChristopher S Carlson, Michael A Eberle, Mark J Rieder, et al.
Human Mutation|October 29, 2002
Cyclooxygenase 1 (COX1) polymorphisms in African-American and Caucasian populationsCornelia M Ulrich, Jeannette Bigler, Justin Sibert, et al.
Pageof 14