Whole genome sequencing in support of wellness and health maintenance (Q37666627)

21 August 2017

Whole genome sequencing in support of wellness and health maintenance (English)

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21 August 2017

whole genome sequencing

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11

Atul J Butte

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21 August 2017

Chirag J Patel

1

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21 August 2017

Ambily Sivadas

2

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21 August 2017

Rubina Tabassum

3

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21 August 2017

Thanawadee Preeprem

4

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21 August 2017

Jing Zhao

5

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21 August 2017

Dalia Arafat

6

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21 August 2017

Rong Chen

7

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21 August 2017

Alexander A Morgan

8

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21 August 2017

Gregory S Martin

9

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21 August 2017

Kenneth L Brigham

10

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21 August 2017

Greg Gibson

12

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21 August 2017

language of work or name

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27 June 2013

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21 August 2017

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21 August 2017

5

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21 August 2017

58

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21 August 2017

6

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https://scigraph.springernature.com/pub.10.1186/gm462

21 August 2017

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cites work

Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians

1 reference

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Use of whole exome and genome sequencing in the identification of genetic causes of primary immunodeficiencies

6 September 2017

1 reference

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Comparison of family history and SNPs for predicting risk of complex disease

6 September 2017

1 reference

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Next generation sequencing in the clinical domain: clinical advantages, practical, and ethical challenges

6 September 2017

1 reference

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Sequencing and analysis of a South Asian-Indian personal genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Risk estimation and risk prediction using machine-learning methods.

6 September 2017

1 reference

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Evolution and functional impact of rare coding variation from deep sequencing of human exomes

6 September 2017

1 reference

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Clinical application of exome sequencing in undiagnosed genetic conditions

6 September 2017

1 reference

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Type 2 diabetes risk alleles demonstrate extreme directional differentiation among human populations, compared to other diseases

6 September 2017

1 reference

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

6 September 2017

1 reference

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

6 September 2017

1 reference

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Personal omics profiling reveals dynamic molecular and medical phenotypes

6 September 2017

1 reference

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Exploring concordance and discordance for return of incidental findings from clinical sequencing

6 September 2017

1 reference

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Five years of GWAS discovery

6 September 2017

1 reference

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Phased whole-genome genetic risk in a family quartet using a major allele reference sequence

6 September 2017

1 reference

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Whole exome and whole genome sequencing

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

The reference human genome demonstrates high risk of type 1 diabetes and other disorders.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Predictive health: the imminent revolution in health care

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Hundreds of variants clustered in genomic loci and biological pathways affect human height

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

The characterization of twenty sequenced human genomes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Genomic medicine--an updated primer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Likelihood ratios for genome medicine

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Clinical assessment incorporating a personal genome

6 September 2017

1 reference

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The pursuit of genome-wide association studies: where are we now?

6 September 2017

1 reference

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The genetic interpretation of area under the ROC curve in genomic profiling

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Clinical risk factors, DNA variants, and the development of type 2 diabetes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Genotype score in addition to common risk factors for prediction of type 2 diabetes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Prediction of individual genetic risk of complex disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

General cardiovascular risk profile for use in primary care: the Framingham Heart Study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

The health and cost benefits of work site health-promotion programs

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

The human disease network

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Studies of familial type III hyperlipoproteinemia using as a genetic marker the apoE phenotype E2/2

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Genetic risk prediction in a small cohort of healthy adults in Atlanta

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Integrating comparative effectiveness research programs into predictive health: a unique role for academic health centers

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Overview of the symposium on public health significance of genomics and eco-genetics.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967117

Array-based sequence capture and next-generation sequencing for the identification of primary immunodeficiencies

1 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23806097

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GM462

1 reference

Dimensions Publication ID

21 August 2017

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1 reference

21 August 2017

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