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1. Discovery of genetic variants of the kinases that activate tenofovir among individuals in the United States, Thailand, and South Africa: HPTN067

Figueroa, Dominique B.; Tillotson, Joseph; Li, Maoji; Piwowar-Manning, Estelle; Hendrix, Craig W.; Holtz, Timothy H.; Bokoch, Kevin; Bekker, Linda-Gail; van Griensven, Frits; Mannheimer, Sharon B.; Hughes, James P.; Grant, Robert M.; Bumpus, Namandje N.
2018
Articles
PhosphorylationAntiviral agentsHuman genetics--VariationBiometryMedicine

2. Effects of Serotonin Transporter Gene Variation on Impulsivity Mediated by Default Mode Network: A Family Study of Depression

Cha, Jiook; Guffanti, Guia; Gingrich, Jay A.; Talati, Ardesheer; Wickramaratne, Priya J.; Weissman, Myrna M.; Posner, Jonathan Eric
2018
Articles
Serotoninergic mechanismsImpulse control disordersBrain--PhysiologyGeneticsHuman genetics--Variation

3. Genetic variants influence on the placenta regulatory landscape

Delahaye, Fabien; Do, Catherine; Kong, Yu; Ashkar, Remi; Salas, Martha; Tycko, Benjamin; Wapner, Ronald J.; Hughes, Francine
2018
Articles
PlacentaHuman genetics--VariationGeneticsDNA--Methylation

4. The generation and phenotypic effect of human genetic mutations

Chen, Chen
2018
Theses
BioinformaticsComputer scienceMutation (Biology)Human genetics--VariationMachine learning

5. Statistical correction of the Winner’s Curse explains replication variability in quantitative trait genome-wide association studies

Palmer, Cameron Douglas; Pe'er, Itshack G.
2017
Articles
DNA replicationGenomes--Data processingHuman genetics--VariationGeneticsStatistics

6. On Identifying Rare Variants for Complex Human Traits

Fan, Ruixue
2015
Theses
Regression analysisGenetics--Statistical methodsGenomics--Data processingHuman genetics--VariationStatisticsBioinformatics

7. Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data

Huang, Jing; Chen, Yong; Swartz, Michael; Ionita-Laza, Iuliana
2014
Articles
Human genetics--VariationBiometryGenetics

8. Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism

Ionita-Laza, Iuliana; Capanu, Marinela; De Rubeis, Silvia; McCallum, Kenneth; Buxbaum, Joseph D.
2014
Articles
Genetic disordersHuman genetics--VariationAutismGeneticsBiometry

9. Small sample properties of rare variant analysis methods

Swartz, Michael; Kim, Taebeom; Niu, Jiangong; Yu, Robert; Shete, Sanjay; Ionita-Laza, Iuliana
2014
Articles
Human genetics--VariationBiometryGenetics

10. New insights into old methods for identifying causal rare variants

Hu, Inchi; Zheng, Tian; Huang, Chien-Hsun; Lo, Shaw-Hwa; Wang, Haitian
2011
Articles
Human genetics--VariationBiometry--Statistical methodsStatistics--MethodologyBiometryStatistics
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