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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: Oct 07, 2024
. (Total: 6342 publications)
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Year
Journal
Records 1-7 (of 7 Records)
Query Trace:
Staercke C[original query]
Biomarker profile in stable Fontan patients.
Saraf A ,
De Staercke C
,
Everitt I , Haouzi A , Ko YA , Jennings S , Kim JH , Rodriguez FH , Kalogeropoulos AP , Quyyumi A , Book W .
Int J Cardiol 2020 305 56-62
VKORC1-1639A allele influences warfarin maintenance dosage among Blacks receiving warfarin anticoagulation: a retrospective cohort study.
Mili FD
,
Allen T ,
Wadell PW
,
Hooper WC
,
Staercke C
,
Bean CJ
,
Lally C , Austin H , Wenger NK .
Future Cardiol 2018 14 (1) 15-26
Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations.
Boylan B
,
Rice AS
,
De Staercke C
,
Eyster ME , Yaish HM , Knoll CM ,
Bean CJ
,
Miller CH
.
J Thromb Haemost 2015 13 (6) 1036-42
Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism.
Lewis DA , Suchindran S ,
Beckman MG
,
Hooper WC
,
Grant AM
,
Heit JA , Manco-Johnson M , Moll S , Philipp CS ,
Kenney K
,
De Staercke C
,
Pyle ME
,
Chi JT , Ortel TL .
Thromb Res 2015 135 (4) 659-65
Evidence for the transmission of parvovirus B19 in patients with bleeding disorders treated with plasma-derived factor concentrates in the era of nucleic acid test screening.
Soucie JM
,
De Staercke C
,
Monahan PE , Recht M , Chitlur MB , Gruppo R , Hooper WC , Kessler C , Kulkarni R , Manco-Johnson MJ , Powell J ,
Pyle M
,
Riske B , Sabio H ,
Trimble S
.
Transfusion 2013 53 (6) 1217-25
New gene variants associated with venous thrombosis - a replication study in United States Whites and Blacks
Austin H ,
De Staercke C
,
Lally C , Bezemer ID , Rosendaal FR ,
Hooper WC
.
J Thromb Haemost 2011 9 (3) 489-95
The lack of association between four point mutations in the promoter region of the toll-like 4 receptor gene and myocardial infarction.
De Staercke Christine, Lally Cathy, Austin Harland, Winston Carla, Dowling Nicole, Williams Byron, Hooper W Craig. Thrombosis research 2006 119(1) 105-10 .
Thrombosis research 2006 119(1) 105-10
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Page last reviewed:
Feb 1, 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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