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Malika K Freund

Showing results (1-10 of 9) with videos related to

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Iscience|June 7, 2020
BATMAN: Fast and Accurate Integration of Single-Cell RNA-Seq Datasets via Minimum-Weight MatchingIgor Mandric, Brian L Hill, Malika K Freund, et al.
Nature Genetics|March 31, 2019
Probabilistic fine-mapping of transcriptome-wide association studiesNicholas Mancuso, Malika K Freund, Ruth Johnson, et al.
Genetic Epidemiology|May 16, 2019
Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMIMegan Major, Malika K Freund, Kathryn S Burch, et al.
American Journal of Human Genetics|January 1, 2019
Leveraging Polygenic Functional Enrichment to Improve GWAS PowerGleb Kichaev, Gaurav Bhatia, Po-Ru Loh, et al.
American Journal of Human Genetics|May 23, 2020
Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary DataHuwenbo Shi, Kathryn S Burch, Ruth Johnson, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2020
Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health SystemTimothy S Chang, Yi Ding, Malika K Freund, et al.
Iscience|February 22, 2021
Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factorsTimothy S Chang, Yi Ding, Malika K Freund, et al.
Science Translational Medicine|May 1, 2024
Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency diseaseRuth Johnson, Alexis V Stephens, Rachel Mester, et al.
BMC Genomics|June 25, 2026
Quantitative trait loci mapping of gene expression and chromatin accessibility in primary fibroblasts reveals shared allelic effects between Latin American and European ancestriesToni A Boltz, Merel Bot, Sandra Lapinska, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Iscience|June 7, 2020
BATMAN: Fast and Accurate Integration of Single-Cell RNA-Seq Datasets via Minimum-Weight MatchingIgor Mandric, Brian L Hill, Malika K Freund, et al.
Nature Genetics|March 31, 2019
Probabilistic fine-mapping of transcriptome-wide association studiesNicholas Mancuso, Malika K Freund, Ruth Johnson, et al.
Genetic Epidemiology|May 16, 2019
Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMIMegan Major, Malika K Freund, Kathryn S Burch, et al.
American Journal of Human Genetics|January 1, 2019
Leveraging Polygenic Functional Enrichment to Improve GWAS PowerGleb Kichaev, Gaurav Bhatia, Po-Ru Loh, et al.
American Journal of Human Genetics|May 23, 2020
Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary DataHuwenbo Shi, Kathryn S Burch, Ruth Johnson, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2020
Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health SystemTimothy S Chang, Yi Ding, Malika K Freund, et al.
Iscience|February 22, 2021
Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factorsTimothy S Chang, Yi Ding, Malika K Freund, et al.
Science Translational Medicine|May 1, 2024
Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency diseaseRuth Johnson, Alexis V Stephens, Rachel Mester, et al.
BMC Genomics|June 25, 2026
Quantitative trait loci mapping of gene expression and chromatin accessibility in primary fibroblasts reveals shared allelic effects between Latin American and European ancestriesToni A Boltz, Merel Bot, Sandra Lapinska, et al.
Pageof 1