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Stacey Gabriel

Showing results (31-40 of 195) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|February 8, 2022
At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan AreaAnn E Woolley, Scott Dryden-Peterson, Andy Kim, et al.
Nature Genetics|July 22, 2011
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarctionJessica Shea, Vineeta Agarwala, Anthony A Philippakis, et al.
BMC Genomics|May 10, 2018
Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platformsMaura Costello, Mark Fleharty, Justin Abreu, et al.
The Journal of Clinical Investigation|November 2, 2012
DGAT1 mutation is linked to a congenital diarrheal disorderJoel T Haas, Harland S Winter, Elaine Lim, et al.
The New England Journal of Medicine|April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's DiseaseJoseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
Open Forum Infectious Diseases|November 16, 2022
At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan AreaAnn E Woolley, Scott Dryden-Peterson, Andy Kim, et al.
American Journal of Human Genetics|March 12, 2013
Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalitiesFarid Radmanesh, Ahmet Okay Caglayan, Jennifer L Silhavy, et al.
Current Protocols in Bioinformatics|November 29, 2014
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipelineGeraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, et al.
Cancer Research|September 3, 2009
Integrative transcriptome analysis reveals common molecular subclasses of human hepatocellular carcinomaYujin Hoshida, Sebastian M B Nijman, Masahiro Kobayashi, et al.
Plos Genetics|February 4, 2015
Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarctionAenne S Thormaehlen, Christian Schuberth, Hong-Hee Won, et al.
Pageof 20

Showing results (31-40 of 195) with videos related to

Sort By:
Pageof 20
Medrxiv : the Preprint Server for Health Sciences|February 8, 2022
At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan AreaAnn E Woolley, Scott Dryden-Peterson, Andy Kim, et al.
Nature Genetics|July 22, 2011
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarctionJessica Shea, Vineeta Agarwala, Anthony A Philippakis, et al.
BMC Genomics|May 10, 2018
Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platformsMaura Costello, Mark Fleharty, Justin Abreu, et al.
The Journal of Clinical Investigation|November 2, 2012
DGAT1 mutation is linked to a congenital diarrheal disorderJoel T Haas, Harland S Winter, Elaine Lim, et al.
The New England Journal of Medicine|April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's DiseaseJoseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
Open Forum Infectious Diseases|November 16, 2022
At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan AreaAnn E Woolley, Scott Dryden-Peterson, Andy Kim, et al.
American Journal of Human Genetics|March 12, 2013
Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalitiesFarid Radmanesh, Ahmet Okay Caglayan, Jennifer L Silhavy, et al.
Current Protocols in Bioinformatics|November 29, 2014
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipelineGeraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, et al.
Cancer Research|September 3, 2009
Integrative transcriptome analysis reveals common molecular subclasses of human hepatocellular carcinomaYujin Hoshida, Sebastian M B Nijman, Masahiro Kobayashi, et al.
Plos Genetics|February 4, 2015
Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarctionAenne S Thormaehlen, Christian Schuberth, Hong-Hee Won, et al.
Pageof 20