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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
PHGKB Weekly Horizon Scan
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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
CDC-Authored Genomics and Precision Health Publications Database
Last data update: Apr 22, 2024
. (Total: 5878 publications)
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Records 1-14 (of 14 Records)
Query Trace:
Wulf A[original query]
From public health genomics to precision public health: a 20-year journey.
Khoury MJ
,
Bowen MS
,
Clyne M
,
Dotson WD
,
Gwinn ML
,
Green RF
,
Kolor K
,
Rodriguez JL
,
Wulf A
,
Yu W
.
Genet Med 2017 20 (6) 574-582
A knowledge base for tracking the impact of genomics on population health.
Yu W
,
Gwinn M
,
Dotson WD
,
Green RF
,
Clyne M ,
Wulf A
,
Bowen S
,
Kolor K
,
Khoury MJ
.
Genet Med 2016 18 (12) 1312-1314
A systematic review of cancer GWAS and candidate gene meta-analyses reveals limited overlap but similar effect sizes.
Chang CQ ,
Yesupriya A
,
Rowell JL , Pimentel CB , Clyne M , Gwinn M ,
Khoury MJ
,
Wulf A
,
Schully SD .
Eur J Hum Genet 2014 22 (3) 402-8
Horizon scanning for translational genomic research beyond bench to bedside.
Clyne M , Schully SD ,
Dotson WD
,
Douglas MP
,
Gwinn M
,
Kolor K
,
Wulf A
,
Bowen MS
,
Khoury MJ
.
Genet Med 2014 16 (7) 535-8
Prioritizing genomic applications for action by level of evidence: a horizon-scanning method.
Dotson WD
,
Douglas MP
,
Kolor K
,
Stewart AC
,
Bowen MS
,
Gwinn M
,
Wulf A
,
Anders HM
,
Chang CQ , Clyne M , Lam TK , Schully SD , Marrone M , Feero WG ,
Khoury MJ
.
Clin Pharmacol Ther 2013 95 (4) 394-402
Cancer GAMAdb: database of cancer genetic associations from meta-analyses and genome-wide association studies.
Schully SD ,
Yu W
,
McCallum V , Benedicto CB , Dong LM ,
Wulf A
,
Clyne M
,
Khoury MJ
.
Eur J Hum Genet 2011 19 (8) 928-30
GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies.
Yu W
,
Yesupriya A
,
Wulf A
,
Hindorff LA ,
Dowling N
,
Khoury MJ
,
Gwinn M
.
Eur J Hum Genet 2011 19 (10) 1095-9
Horizon scanning for new genomic tests.
Gwinn M
,
Grossniklaus DA
,
Yu W
,
Melillo S
,
Wulf A
,
Flome J
,
Dotson WD
,
Khoury MJ
.
Genet Med 2011 13 (2) 161-5
The need for genetic variant naming standards in published abstracts of human genetic association studies.
Yu W
,
Ned R
,
Wulf A
,
Liu T
,
Khoury MJ
,
Gwinn M
.
BMC Res Notes 2009 2 56
Gene Prospector: an evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases.
Yu Wei, Wulf Anja, Liu Tiebin, Khoury Muin J, Gwinn Marta. BMC bioinformatics 2008 9528 .
BMC bioinformatics 2008 9528
HuGE Watch: tracking trends and patterns of published studies of genetic association and human genome epidemiology in near-real time.
Yu Wei, Wulf Anja, Yesupriya Ajay, Clyne Melinda, Khoury Muin Joseph, Gwinn Marta. European journal of human genetics : EJHG 2008 16(9) 1155-8 .
European journal of human genetics : EJHG 2008 16(9) 1155-8
GAPscreener: an automatic tool for screening human genetic association literature in PubMed using the support vector machine technique.
Yu Wei, Clyne Melinda, Dolan Siobhan M, Yesupriya Ajay, Wulf Anja, Liu Tiebin, Khoury Muin J, Gwinn Marta. BMC bioinformatics 2008 9205 .
BMC bioinformatics 2008 9205
An open source infrastructure for managing knowledge and finding potential collaborators in a domain-specific subset of PubMed, with an example from human genome epidemiology.
Yu Wei, Yesupriya Ajay, Wulf Anja, Qu Junfeng, Khoury Muin J, Gwinn Marta. BMC bioinformatics 2007 8436 .
BMC bioinformatics 2007 8436
An automatic method to generate domain-specific investigator networks using PubMed abstracts.
Yu Wei, Yesupriya Ajay, Wulf Anja, Qu Junfeng, Gwinn Marta, Khoury Muin J. BMC medical informatics and decision making 2007 717 .
BMC medical informatics and decision making 2007 717
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 22, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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