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Vlad Makarov

Showing results (1-10 of 7) with videos related to

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American Journal of Human Genetics|May 15, 2012
Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasetsIuliana Ionita-Laza, Vlad Makarov, , et al.
American Journal of Human Genetics|May 21, 2013
Sequence kernel association tests for the combined effect of rare and common variantsIuliana Ionita-Laza, Seunggeun Lee, Vlad Makarov, et al.
American Journal of Human Genetics|December 6, 2011
Finding disease variants in Mendelian disorders by using sequence data: methods and applicationsIuliana Ionita-Laza, Vlad Makarov, Seungtai Yoon, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 18, 2013
Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autismIuliana Ionita-Laza, Bin Xu, Vlad Makarov, et al.
Genome Medicine|December 19, 2022
Spatiotemporal evolution of the clear cell renal cell carcinoma microenvironment links intra-tumoral heterogeneity to immune escapeMahdi Golkaram, Fengshen Kuo, Sounak Gupta, et al.
JCI Insight|May 30, 2023
The MIF promoter SNP rs755622 is associated with immune activation in glioblastomaTyler J Alban, Matthew M Grabowski, Balint Otvos, et al.
Science (New York, N.Y.)|March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaTom Walsh, Jon M McClellan, Shane E McCarthy, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Human Genetics|May 15, 2012
Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasetsIuliana Ionita-Laza, Vlad Makarov, , et al.
American Journal of Human Genetics|May 21, 2013
Sequence kernel association tests for the combined effect of rare and common variantsIuliana Ionita-Laza, Seunggeun Lee, Vlad Makarov, et al.
American Journal of Human Genetics|December 6, 2011
Finding disease variants in Mendelian disorders by using sequence data: methods and applicationsIuliana Ionita-Laza, Vlad Makarov, Seungtai Yoon, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 18, 2013
Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autismIuliana Ionita-Laza, Bin Xu, Vlad Makarov, et al.
Genome Medicine|December 19, 2022
Spatiotemporal evolution of the clear cell renal cell carcinoma microenvironment links intra-tumoral heterogeneity to immune escapeMahdi Golkaram, Fengshen Kuo, Sounak Gupta, et al.
JCI Insight|May 30, 2023
The MIF promoter SNP rs755622 is associated with immune activation in glioblastomaTyler J Alban, Matthew M Grabowski, Balint Otvos, et al.
Science (New York, N.Y.)|March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaTom Walsh, Jon M McClellan, Shane E McCarthy, et al.
Pageof 1