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Stuart Cantsilieris

Showing results (1-10 of 24) with videos related to

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Human Mutation|July 28, 2012
Correlating multiallelic copy number polymorphisms with disease susceptibilityStuart Cantsilieris, Stefan J White
Genomics|November 6, 2012
Molecular methods for genotyping complex copy number polymorphismsStuart Cantsilieris, Paul N Baird, Stefan J White
Recent Patents on DNA & Gene Sequences|June 13, 2009
Recent patents relating to diagnostic advances in age related macular degeneration (AMD)Stuart Cantsilieris, Maria Schache, M Luisa Ashdown, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 9, 2016
Targeted Capture and High-Throughput Sequencing Using Molecular Inversion Probes (MIPs)Stuart Cantsilieris, Holly A Stessman, Jay Shendure, et al.
BMC Genomics|June 3, 2014
Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplicationStuart Cantsilieris, Patrick S Western, Paul N Baird, et al.
Plos One|May 5, 2012
Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degenerationStuart Cantsilieris, Stefan J White, Andrea J Richardson, et al.
Genomics|August 23, 2011
Almost total protection from age-related macular degeneration by haplotypes of the Regulators of Complement ActivationJoseph F Williamson, Craig A McLure, Robyn H Guymer, et al.
Molecular Vision|April 18, 2013
Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degenerationInderjeet Kaur, Stuart Cantsilieris, Saritha Katta, et al.
Journal of Neuroinflammation|April 20, 2016
Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD)Felix Grassmann, Stuart Cantsilieris, Anja-Sabrina Schulz-Kuhnt, et al.
Scientific Reports|October 30, 2019
Rare variants in non-coding regulatory regions of the genome that affect gene expression in systemic lupus erythematosusSarah A Jones, Stuart Cantsilieris, Huapeng Fan, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Human Mutation|July 28, 2012
Correlating multiallelic copy number polymorphisms with disease susceptibilityStuart Cantsilieris, Stefan J White
Genomics|November 6, 2012
Molecular methods for genotyping complex copy number polymorphismsStuart Cantsilieris, Paul N Baird, Stefan J White
Recent Patents on DNA & Gene Sequences|June 13, 2009
Recent patents relating to diagnostic advances in age related macular degeneration (AMD)Stuart Cantsilieris, Maria Schache, M Luisa Ashdown, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 9, 2016
Targeted Capture and High-Throughput Sequencing Using Molecular Inversion Probes (MIPs)Stuart Cantsilieris, Holly A Stessman, Jay Shendure, et al.
BMC Genomics|June 3, 2014
Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplicationStuart Cantsilieris, Patrick S Western, Paul N Baird, et al.
Plos One|May 5, 2012
Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degenerationStuart Cantsilieris, Stefan J White, Andrea J Richardson, et al.
Genomics|August 23, 2011
Almost total protection from age-related macular degeneration by haplotypes of the Regulators of Complement ActivationJoseph F Williamson, Craig A McLure, Robyn H Guymer, et al.
Molecular Vision|April 18, 2013
Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degenerationInderjeet Kaur, Stuart Cantsilieris, Saritha Katta, et al.
Journal of Neuroinflammation|April 20, 2016
Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD)Felix Grassmann, Stuart Cantsilieris, Anja-Sabrina Schulz-Kuhnt, et al.
Scientific Reports|October 30, 2019
Rare variants in non-coding regulatory regions of the genome that affect gene expression in systemic lupus erythematosusSarah A Jones, Stuart Cantsilieris, Huapeng Fan, et al.
Pageof 3