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Eric Banks

Showing results (31-40 of 54) with videos related to

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The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Cell Genomics|February 24, 2022
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-spaceMichael C Schatz, Anthony A Philippakis, Enis Afgan, et al.
Cell Stem Cell|December 19, 2012
A TALEN genome-editing system for generating human stem cell-based disease modelsQiurong Ding, Youn-Kyoung Lee, Esperance A K Schaefer, et al.
Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Nature|January 28, 2014
A polygenic burden of rare disruptive mutations in schizophreniaShaun M Purcell, Jennifer L Moran, Menachem Fromer, et al.
Annual Review of Biomedical Data Science|August 10, 2023
The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical ResearchKelsey R Mayo, Melissa A Basford, Robert J Carroll, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Science (New York, N.Y.)|May 9, 2015
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.
Nature|January 15, 2024
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomesSiwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Nature|December 6, 2023
A genomic mutational constraint map using variation in 76,156 human genomesSiwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Cell Genomics|February 24, 2022
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-spaceMichael C Schatz, Anthony A Philippakis, Enis Afgan, et al.
Cell Stem Cell|December 19, 2012
A TALEN genome-editing system for generating human stem cell-based disease modelsQiurong Ding, Youn-Kyoung Lee, Esperance A K Schaefer, et al.
Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Nature|January 28, 2014
A polygenic burden of rare disruptive mutations in schizophreniaShaun M Purcell, Jennifer L Moran, Menachem Fromer, et al.
Annual Review of Biomedical Data Science|August 10, 2023
The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical ResearchKelsey R Mayo, Melissa A Basford, Robert J Carroll, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Science (New York, N.Y.)|May 9, 2015
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.
Nature|January 15, 2024
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomesSiwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Nature|December 6, 2023
A genomic mutational constraint map using variation in 76,156 human genomesSiwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Pageof 6