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Public Health Genomics and Precision Health Knowledge Base (v10.0)
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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: Jul 01, 2024
. (Total: 6190 publications)
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Records 1-7 (of 7 Records)
Query Trace:
Familial hypercholesterolemia[original query]
Health equity in the implementation of genomics and precision medicine: A public health imperative.
Khoury MJ
,
Bowen S
,
Dotson WD
,
Drzymalla E
,
Green RF
,
Goldstein R
,
Kolor K
,
Liburd LC
,
Sperling LS
,
Bunnell R
.
Genet Med 2022 24 (8) 1630-1639
Development of an Implementation Framework for Overcoming Underdiagnoses of Familial Hypercholesterolemia in the USA.
Miller DM ,
Gaviglio A
,
Zierhut HA .
Public Health Genomics 2021 24 1-13
Prevalence and Predictors of Cholesterol Screening, Awareness, and Statin Treatment Among US Adults With Familial Hypercholesterolemia or Other Forms of Severe Dyslipidemia (1999-2014).
Bucholz EM , Rodday AM ,
Kolor K
,
Khoury MJ
,
de Ferranti SD .
Circulation 2018 137 (21) 2218-2230
Cascade Screening for Familial Hypercholesterolemia and the Use of Genetic Testing.
Knowles JW , Rader DJ ,
Khoury MJ
.
JAMA 2017 318 (4) 381-382
Reducing the burden of disease and death from familial hypercholesterolemia: a call to action.
Knowles JW , O'Brien EC , Greendale K , Wilemon K , Genest J , Sperling LS , Neal WA , Rader DJ ,
Khoury MJ
.
Am Heart J 2014 168 (6) 807-11
Public health action in genomics is now needed beyond newborn screening.
Bowen MS
,
Kolor K
,
Dotson WD
,
Ned RM
,
Khoury MJ
.
Public Health Genomics 2012 15 (6) 327-34
Cascade Screening for Familial Hypercholesterolemia (FH).
Ned RM
,
Sijbrands EJ .
PLoS Curr 2011 3 Rrn1238
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Page last reviewed:
Feb 1, 2024
Page last updated:
Jul 01, 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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