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Iuliana Ionita

Showing results (1-10 of 96) with videos related to

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BMC Genetics|June 17, 2006
Optimal two-stage strategy for detecting interacting genes in complex diseasesIuliana Ionita, Michael Man
Human Heredity|January 21, 2006
Multilocus linkage analysis of affected sib pairsIuliana Ionita, Shaw-Hwa Lo
Frontiers in Genetics|May 26, 2015
Integrative analysis of functional genomic annotations and sequencing data to identify rare causal variants via hierarchical modelingMarinela Capanu, Iuliana Ionita-Laza
Genetics|August 16, 2011
Study designs for identification of rare disease variants in complex diseases: the utility of family-based designsIuliana Ionita-Laza, Ruth Ottman
Statistical Applications in Genetics and Molecular Biology|September 4, 2010
On the optimal design of genetic variant discovery studiesIuliana Ionita-Laza, Nan M Laird
Biometrics|June 3, 2015
Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studiesKenneth J McCallum, Iuliana Ionita-Laza
American Journal of Human Genetics|June 15, 2006
Mapping tumor-suppressor genes with multipoint statistics from copy-number-variation dataIuliana Ionita, Raoul-Sam Daruwala, Bud Mishra
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.
Neurology|February 11, 2012
Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAFYuan-Yuan Ho, Iuliana Ionita-Laza, Ruth Ottman
Frontiers in Genetics|December 21, 2020
Cell Type-Specific Annotation and Fine Mapping of Variants Associated With Brain DisordersAbolfazl Doostparast Torshizi, Iuliana Ionita-Laza, Kai Wang
Pageof 10

Showing results (1-10 of 96) with videos related to

Sort By:
Pageof 10
BMC Genetics|June 17, 2006
Optimal two-stage strategy for detecting interacting genes in complex diseasesIuliana Ionita, Michael Man
Human Heredity|January 21, 2006
Multilocus linkage analysis of affected sib pairsIuliana Ionita, Shaw-Hwa Lo
Frontiers in Genetics|May 26, 2015
Integrative analysis of functional genomic annotations and sequencing data to identify rare causal variants via hierarchical modelingMarinela Capanu, Iuliana Ionita-Laza
Genetics|August 16, 2011
Study designs for identification of rare disease variants in complex diseases: the utility of family-based designsIuliana Ionita-Laza, Ruth Ottman
Statistical Applications in Genetics and Molecular Biology|September 4, 2010
On the optimal design of genetic variant discovery studiesIuliana Ionita-Laza, Nan M Laird
Biometrics|June 3, 2015
Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studiesKenneth J McCallum, Iuliana Ionita-Laza
American Journal of Human Genetics|June 15, 2006
Mapping tumor-suppressor genes with multipoint statistics from copy-number-variation dataIuliana Ionita, Raoul-Sam Daruwala, Bud Mishra
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.
Neurology|February 11, 2012
Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAFYuan-Yuan Ho, Iuliana Ionita-Laza, Ruth Ottman
Frontiers in Genetics|December 21, 2020
Cell Type-Specific Annotation and Fine Mapping of Variants Associated With Brain DisordersAbolfazl Doostparast Torshizi, Iuliana Ionita-Laza, Kai Wang
Pageof 10