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BMC Genetics
|
June 17, 2006
Optimal two-stage strategy for detecting interacting genes in complex diseases
Iuliana Ionita, Michael Man
Human Heredity
|
January 21, 2006
Multilocus linkage analysis of affected sib pairs
Iuliana 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 modeling
Marinela Capanu, Iuliana Ionita-Laza
Genetics
|
August 16, 2011
Study designs for identification of rare disease variants in complex diseases: the utility of family-based designs
Iuliana Ionita-Laza, Ruth Ottman
Statistical Applications in Genetics and Molecular Biology
|
September 4, 2010
On the optimal design of genetic variant discovery studies
Iuliana Ionita-Laza, Nan M Laird
Biometrics
|
June 3, 2015
Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies
Kenneth J McCallum, Iuliana Ionita-Laza
American Journal of Human Genetics
|
June 15, 2006
Mapping tumor-suppressor genes with multipoint statistics from copy-number-variation data
Iuliana 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 datasets
Iuliana Ionita-Laza, Vlad Makarov, , et al.
Neurology
|
February 11, 2012
Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF
Yuan-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 Disorders
Abolfazl Doostparast Torshizi, Iuliana Ionita-Laza, Kai Wang
Page
of 10
Search research articles
Search
Showing results (1-10 of 96) with videos related to
Sort By:
Page
of 10
BMC Genetics
|
June 17, 2006
Optimal two-stage strategy for detecting interacting genes in complex diseases
Iuliana Ionita, Michael Man
Human Heredity
|
January 21, 2006
Multilocus linkage analysis of affected sib pairs
Iuliana 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 modeling
Marinela Capanu, Iuliana Ionita-Laza
Genetics
|
August 16, 2011
Study designs for identification of rare disease variants in complex diseases: the utility of family-based designs
Iuliana Ionita-Laza, Ruth Ottman
Statistical Applications in Genetics and Molecular Biology
|
September 4, 2010
On the optimal design of genetic variant discovery studies
Iuliana Ionita-Laza, Nan M Laird
Biometrics
|
June 3, 2015
Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies
Kenneth J McCallum, Iuliana Ionita-Laza
American Journal of Human Genetics
|
June 15, 2006
Mapping tumor-suppressor genes with multipoint statistics from copy-number-variation data
Iuliana 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 datasets
Iuliana Ionita-Laza, Vlad Makarov, , et al.
Neurology
|
February 11, 2012
Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF
Yuan-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 Disorders
Abolfazl Doostparast Torshizi, Iuliana Ionita-Laza, Kai Wang
Page
of 10