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Ellen M Schmidt

Showing results (1-10 of 34) with videos related to

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Current Opinion in Genetics & Development|August 5, 2015
Insights into blood lipids from rare variant discoveryEllen M Schmidt, Cristen J Willer
American Journal of Human Genetics|June 13, 2017
A Fast and Accurate Algorithm to Test for Binary Phenotypes and Its Application to PheWASRounak Dey, Ellen M Schmidt, Goncalo R Abecasis, et al.
Journal of Critical Care|November 22, 2017
Genetic variants and acute kidney injury: A review of the literatureDaniel B Larach, Milo C Engoren, Ellen M Schmidt, et al.
Bioinformatics (Oxford, England)|April 19, 2015
GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approachEllen M Schmidt, Ji Zhang, Wei Zhou, et al.
American Journal of Human Genetics|May 22, 2018
Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics InitiativeLars G Fritsche, Stephen B Gruber, Zhenke Wu, et al.
Plos Genetics|November 11, 2020
LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanksJeffery A Goldstein, Joshua S Weinstock, Lisa A Bastarache, et al.
Nature Neuroscience|January 10, 2019
Publisher Correction: Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Nature Neuroscience|May 13, 2018
Publisher Correction: Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Cell Genomics|February 23, 2023
The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patientsMatthew Zawistowski, Lars G Fritsche, Anita Pandit, et al.
Nature Neuroscience|December 13, 2017
Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Current Opinion in Genetics & Development|August 5, 2015
Insights into blood lipids from rare variant discoveryEllen M Schmidt, Cristen J Willer
American Journal of Human Genetics|June 13, 2017
A Fast and Accurate Algorithm to Test for Binary Phenotypes and Its Application to PheWASRounak Dey, Ellen M Schmidt, Goncalo R Abecasis, et al.
Journal of Critical Care|November 22, 2017
Genetic variants and acute kidney injury: A review of the literatureDaniel B Larach, Milo C Engoren, Ellen M Schmidt, et al.
Bioinformatics (Oxford, England)|April 19, 2015
GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approachEllen M Schmidt, Ji Zhang, Wei Zhou, et al.
American Journal of Human Genetics|May 22, 2018
Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics InitiativeLars G Fritsche, Stephen B Gruber, Zhenke Wu, et al.
Plos Genetics|November 11, 2020
LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanksJeffery A Goldstein, Joshua S Weinstock, Lisa A Bastarache, et al.
Nature Neuroscience|January 10, 2019
Publisher Correction: Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Nature Neuroscience|May 13, 2018
Publisher Correction: Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Cell Genomics|February 23, 2023
The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patientsMatthew Zawistowski, Lars G Fritsche, Anita Pandit, et al.
Nature Neuroscience|December 13, 2017
Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Pageof 4