Skip directly to search
Skip directly to A to Z list
Skip directly to navigation
Skip directly to page options
Skip directly to site content
Start of Search Controls
Search Form Controls
Search The CDC
submit
CDC A-Z Index
MENU
CDC A-Z
SEARCH
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
#
Search Form Controls
Search The CDC
submit
CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v8.2)
Note: Javascript is disabled or is not supported by your browser. For this reason, some items on this page will be unavailable. For more information about this message, please visit this page:
About CDC.gov
.
PHGKB
About
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Infectious Diseases PHGKB
HLBS-PopOmics
Rare Diseases PHGKB
Health Equity PHGKB
Family Health History PHGKB
Reproductive and Child Health PHGKB
Pharmacogenomics PHGKB
Neurological Disorders PHGKB
Primary Immune Deficiency Diseases PHGKB
Environmental Health PHGKB
Genomics (A-Z)
Office of Genomics and Precision Public Health
State Public Health Genomics Programs Map
Genomics Precision Health Weekly Scan
(Current Edition)
Advanced Molecular Detection Weekly Clips
(Current Edition)
Non-Genomics Precision Health Weekly Scan
(Current Edition)
CDC-authored Publications Update
COVID-19 Precision Health Weekly Update
(Current Edition)
All Databases
COVID-19 GPH (43139)
CDC/NIH Web Information Database (30786)
CDC-Authored Genomics and Precision Health Publications Database (4179)
Precision Health Database (52264)
Tier-Classified Guidelines Database (509)
State Public Health Genomics Programs Database (319)
Pathogen Advanced Molecular Detection Database (23888)
All of Us Reports and Publications Database (275)
HuGE Navigator
Phenopedia (3416)
Genopedia (16418)
HuGE Literature Finder (169679)
Variant Name Mapper (18583)
Release Note
Contact Us
CDC-Authored Genomics and Precision Health Publications Database|Home|PHGKB
CDC-Authored Genomics and Precision Health Publications Database
Last data update: Jan 26, 2023
. (Total: 4179 publications since 2011)
All
HLBS
RCH
FHH
Equity
Diabetes
Rare
Cancer
COVID-19
ND
PGx
PI
Environmental
dataset
Filtered By:
Select to fine-tune your search
CDC Author
Year
Journal
Records 1-15 (of 15 Records)
Query Trace:
all>>W Craig Hooper[CDC Author]
Evaluation of CDC's Hemophilia Surveillance Program - Universal Data Collection (1998-2011) and Community Counts (2011-2019), United States.
Laura A Schieve
,
Vanessa R Byams
,
Brandi Dupervil
,
Meredith A Oakley
,
Connie H Miller
,
J Michael Soucie
,
Karon Abe
,
Christopher J Bean
, and
W Craig Hooper
Morbidity and mortality weekly report. Surveillance summaries (Washington, D.C. : 2002) 2020 Sep 69(5) 1-18
Similar articles in PubMed
DOI:
10.15585/mmwr.ss6905a1
Origins and organization of the NHLBI State of the Science Workshop: Generating a national blueprint for future research on factor VIII inhibitors.
Denise E Sabatino, Steven W Pipe, Diane J Nugent,
J Michael Soucie
,
W Craig Hooper
, W Keith Hoots, and Donna M DiMichele
Haemophilia : the official journal of the World Federation of Hemophilia 2019 Jul 25(4) 575-580
Similar articles in PubMed
DOI:
10.1111/hae.13737
VKORC1-1639A allele influences warfarin maintenance dosage among Blacks receiving warfarin anticoagulation: a retrospective cohort study.
Fatima Donia Mili
, Tenecia Allen,
Paula Weinstein Wadell
,
W Craig Hooper
,
Christine De Staercke
,
Christopher J Bean
, Cathy Lally, Harland Austin, and Nanette K Wenger
Future cardiology 2018 14(1) 15-26
Similar articles in PubMed
DOI:
10.2217/fca-2017-0025
Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism.
Deborah A Lewis, Sunil Suchindran,
Michele G Beckman
,
W Craig Hooper
,
Althea M Grant
, John A Heit, Marilyn Manco-Johnson, Stephan Moll, Claire S Philipp,
Kristy Kenney
,
Christine De Staercke
,
Meredith E Pyle
, Jen-Tsan Chi, and Thomas L Ortel
Thromb. Res. 2015 Apr 135(4) 659-65
Similar articles in PubMed
DOI:
10.1016/j.thromres.2015.02.003
Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.
Christopher J Bean
,
W Craig Hooper
,
Dorothy Ellingsen
, Michael R Debaun, Jennifer Sonderman, and William J Blot
Public Health Genomics 2014 17(3) 169-72
Similar articles in PubMed
DOI:
10.1159/000360260
Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.
Baijia Jiang, Kathleen A Ryan, Ali Hamedani, Yuching Cheng, Mary J Sparks,
Deborah Koontz
,
Christopher J Bean
,
Margaret Gallagher
,
W Craig Hooper
, Patrick F McArdle, Jeffrey R O'Connell, O Colin Stine, Marcella A Wozniak, Barney J Stern, Braxton D Mitchell, Steven J Kittner, and John W Cole
Stroke 2014 Apr 45(4) 961-7
Similar articles in PubMed
DOI:
10.1161/STROKEAHA.113.004063
Mutation analysis of a cohort of US patients with hemophilia B.
Tengguo Li
,
Connie H Miller
,
Jennifer Driggers
,
Amanda B Payne
,
Dorothy Ellingsen
, and
W Craig Hooper
Am. J. Hematol. 2014 Apr 89(4) 375-9
Similar articles in PubMed
DOI:
10.1002/ajh.23645
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.
Christopher J Bean
,
Sheree L Boulet
,
Genyan Yang
,
Amanda B Payne
,
Nafisa Ghaji
,
Meredith E Pyle
,
W Craig Hooper
, Pallav Bhatnagar, Jeffrey Keefer, Emily A Barron-Casella, James F Casella, and Michael R Debaun
Br. J. Haematol. 2013 Oct 163(2) 268-76
Similar articles in PubMed
DOI:
10.1111/bjh.12507
Relationships between selected gene polymorphisms and blood pressure sensitivity to weight loss in elderly persons with hypertension.
William J Kostis, Javier Cabrera,
W Craig Hooper
, Paul K Whelton, Mark A Espeland, Nora M Cosgrove, Jerry Q Cheng, Yingzi Deng, Christine De Staerck,
Meredith Pyle
, Nisa Maruthur, Ingrid Reyes, Cheryl A M Anderson, Jie Liu, and John B Kostis
Hypertension 2013 Apr 61(4) 857-63
Similar articles in PubMed
DOI:
10.1161/HYPERTENSIONAHA.111.00712
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.
J Michael Soucie
,
Christine De Staercke
,
Paul E Monahan
,
Michael Recht
,
Meera B Chitlur
,
Ralph Gruppo
,
W Craig Hooper
,
Craig Kessler
,
Roshni Kulkarni
,
Marilyn J Manco-Johnson
,
Jerry Powell
,
Meredith Pyle
,
Brenda Riske
,
Hernan Sabio
,
Sean Trimble
, and
Transfusion 2013 Jun 53(6) 1217-25
Similar articles in PubMed
DOI:
10.1111/j.1537-2995.2012.03907.x
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.
Christopher J Bean
,
Sheree L Boulet
,
Dorothy Ellingsen
,
Meredith E Pyle
, Emily A Barron-Casella, James F Casella,
Amanda B Payne
,
Jennifer Driggers
,
Heidi A Trau
,
Genyan Yang
, Kimberly Jones, Solomon F Ofori-Acquah,
W Craig Hooper
, and Michael R Debaun
Blood 2012 Nov 1. 120(18) 3822-8
Similar articles in PubMed
DOI:
10.1182/blood-2011-06-361642
Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks.
Christopher J Bean
,
Sheree L Boulet
,
Dorothy Ellingsen
,
Heidi Trau
,
Nafisa Ghaji
,
W Craig Hooper
, and Harland Austin
Thromb. Res. 2012 Dec 130(6) 942-7
Similar articles in PubMed
DOI:
10.1016/j.thromres.2012.08.300
Family history of myocardial infarction is a risk factor for venous thromboembolism among whites but not among blacks.
Fatima D Mili
,
W Craig Hooper
, Cathy Lally, and Harland Austin
Clin. Appl. Thromb. Hemost. 19(4) 410-7
Similar articles in PubMed
DOI:
10.1177/1076029612448419
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
Jacqueline N Milton, Paola Sebastiani, Nadia Solovieff, Stephen W Hartley, Pallav Bhatnagar, Dan E Arking, Daniel A Dworkis, James F Casella, Emily Barron-Casella,
Christopher J Bean
,
W Craig Hooper
, Michael R Debaun, Melanie E Garrett, Karen Soldano, Marilyn J Telen, Allison Ashley-Koch, Mark T Gladwin, Clinton T Baldwin, Martin H Steinberg, and Elizabeth S Klings
PLoS ONE 2012 7(4) e34741
Similar articles in PubMed
DOI:
10.1371/journal.pone.0034741
The impact of co-morbid conditions on family history of venous thromboembolism in Whites and Blacks.
Fatima D Mili
,
W Craig Hooper
, Cathy Lally, and Harland Austin
Thrombosis research 2011 Apr 127(4) 309-16
Similar articles in PubMed
DOI:
10.1016/j.thromres.2010.12.012
File Formats Help:
How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?
Adobe PDF file
Microsoft PowerPoint file
Microsoft Word file
Microsoft Excel file
Audio/Video file
Apple Quicktime file
RealPlayer file
Text file
Zip Archive file
SAS file
ePub file
Page last reviewed:
Jul 25, 2022
Page last updated:
Jan 26, 2023
Content source:
Office of Genomics and Precision Public Health
,
CDC Office of Science
TOP