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Million Veteran Program: A mega-biobank to study genetic influences on health and disease
by
Huang, Grant
, Brophy, Mary
, Deen, Jennifer
, Przygodzki, Ronald
, Shannon, Colleen
, Breeling, James
, Anderson, Daniel
, LaFleur, Rene
, Fiore, Louis
, Pyarajan, Saiju
, Muralidhar, Sumitra
, Humphries, Donald
, Guarino, Peter
, Gaziano, John Michael
, Moser, Jennifer
, Concato, John
, Whitbourne, Stacey
, Aslan, Mihaela
, Schaa, Kendra
, O'Leary, Timothy J.
, Hammond, Timothy
in
Arthritis
/ Biological Specimen Banks - organization & administration
/ Biomedical research
/ Cohort studies
/ Consortia
/ Data Collection - methods
/ Electronic Health Records
/ Epidemiology
/ Exome sequencing
/ Female
/ Gastroesophageal reflux
/ Genetic screening
/ Genomes
/ Genomics
/ Genomics - methods
/ Genotype
/ Genotyping
/ Health care
/ Health care delivery
/ Humans
/ Infrastructure
/ Initiatives
/ Internal Medicine
/ Laboratories
/ Longitudinal Studies
/ Male
/ Medical records
/ Medical research
/ Medicine
/ Observational studies
/ Patients
/ Population
/ Research Design
/ Sequence Analysis
/ Studies
/ Surveys and Questionnaires
/ United States
/ Veterans
/ Veterans - statistics & numerical data
/ Whole-genome sequencing
2016
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Million Veteran Program: A mega-biobank to study genetic influences on health and disease
by
Huang, Grant
, Brophy, Mary
, Deen, Jennifer
, Przygodzki, Ronald
, Shannon, Colleen
, Breeling, James
, Anderson, Daniel
, LaFleur, Rene
, Fiore, Louis
, Pyarajan, Saiju
, Muralidhar, Sumitra
, Humphries, Donald
, Guarino, Peter
, Gaziano, John Michael
, Moser, Jennifer
, Concato, John
, Whitbourne, Stacey
, Aslan, Mihaela
, Schaa, Kendra
, O'Leary, Timothy J.
, Hammond, Timothy
in
Arthritis
/ Biological Specimen Banks - organization & administration
/ Biomedical research
/ Cohort studies
/ Consortia
/ Data Collection - methods
/ Electronic Health Records
/ Epidemiology
/ Exome sequencing
/ Female
/ Gastroesophageal reflux
/ Genetic screening
/ Genomes
/ Genomics
/ Genomics - methods
/ Genotype
/ Genotyping
/ Health care
/ Health care delivery
/ Humans
/ Infrastructure
/ Initiatives
/ Internal Medicine
/ Laboratories
/ Longitudinal Studies
/ Male
/ Medical records
/ Medical research
/ Medicine
/ Observational studies
/ Patients
/ Population
/ Research Design
/ Sequence Analysis
/ Studies
/ Surveys and Questionnaires
/ United States
/ Veterans
/ Veterans - statistics & numerical data
/ Whole-genome sequencing
2016
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Do you wish to request the book?
Million Veteran Program: A mega-biobank to study genetic influences on health and disease
by
Huang, Grant
, Brophy, Mary
, Deen, Jennifer
, Przygodzki, Ronald
, Shannon, Colleen
, Breeling, James
, Anderson, Daniel
, LaFleur, Rene
, Fiore, Louis
, Pyarajan, Saiju
, Muralidhar, Sumitra
, Humphries, Donald
, Guarino, Peter
, Gaziano, John Michael
, Moser, Jennifer
, Concato, John
, Whitbourne, Stacey
, Aslan, Mihaela
, Schaa, Kendra
, O'Leary, Timothy J.
, Hammond, Timothy
in
Arthritis
/ Biological Specimen Banks - organization & administration
/ Biomedical research
/ Cohort studies
/ Consortia
/ Data Collection - methods
/ Electronic Health Records
/ Epidemiology
/ Exome sequencing
/ Female
/ Gastroesophageal reflux
/ Genetic screening
/ Genomes
/ Genomics
/ Genomics - methods
/ Genotype
/ Genotyping
/ Health care
/ Health care delivery
/ Humans
/ Infrastructure
/ Initiatives
/ Internal Medicine
/ Laboratories
/ Longitudinal Studies
/ Male
/ Medical records
/ Medical research
/ Medicine
/ Observational studies
/ Patients
/ Population
/ Research Design
/ Sequence Analysis
/ Studies
/ Surveys and Questionnaires
/ United States
/ Veterans
/ Veterans - statistics & numerical data
/ Whole-genome sequencing
2016
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Million Veteran Program: A mega-biobank to study genetic influences on health and disease
Journal Article
Million Veteran Program: A mega-biobank to study genetic influences on health and disease
2016
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Overview
To describe the design and ongoing conduct of the Million Veteran Program (MVP), as an observational cohort study and mega-biobank in the Department of Veterans Affairs (VA) health care system.
Data are being collected from participants using questionnaires, the VA electronic health record, and a blood sample for genomic and other testing. Several ongoing projects are linked to MVP, both as peer-reviewed research studies and as activities to help develop an infrastructure for future, broad-based research uses.
Formal planning for MVP commenced in 2009; the protocol was approved in 2010, and enrollment began in 2011. As of August 3, 2015, and with a steady state of ≈50 recruiting sites nationwide, N = 397,104 veterans have been enrolled. Among N = 199,348 with currently available genotyping data, most participants (as expected) are male (92.0%) between the ages of 50 and 69 years (55.0%). On the basis of self-reported race, white (77.2%) and African American (13.5%) populations are well represented.
By helping to promote the future integration of genetic testing in health care delivery, including clinical decision making, the MVP is designed to contribute to the development of precision medicine.
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