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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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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: Sep 16, 2024
. (Total: 6309 publications)
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Year
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Records 1-23 (of 23 Records)
Query Trace:
Bean C [original query]
Regional Consortia : A Framework for Public Health Laboratory Collaboration and Service Sharing.
Ned-Sykes RM
,
Pentella M , Kurimski L , Zanto S , Matt Charles E , Bean C , Gibson D , Breckenridge K , Su B ,
Ridderhof J
.
Public Health Rep 2021 137 (2) 333549211002774
Genetic causes of haemophilia in women and girls.
Miller CH
,
Bean CJ
.
Haemophilia 2020 27 (2) e164-e179
Evaluation of CDC's Hemophilia Surveillance Program - Universal Data Collection (1998-2011) and Community Counts (2011-2019), United States.
Schieve LA
,
Byams VR
,
Dupervil B
,
Oakley MA
,
Miller CH
,
Soucie JM
,
Abe K
,
Bean CJ
,
Hooper WC
.
MMWR Surveill Summ 2020 69 (5) 1-18
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.
Jenkins MM
,
Almli LM
,
Pangilinan F , Chong JX , Blue EE ,
Shapira SK
,
White J , McGoldrick D , Smith JD , Mullikin JC , Bean CJ , Nembhard WN , Lou XY , Shaw GM , Romitti PA , Keppler-Noreuil K , Yazdy MM , Kay DM , Carter TC , Olshan AF , Moore KJ , Nascone-Yoder N , Finnell RH , Lupo PJ , Feldkamp ML , Nickerson DA , Bamshad MJ , Brody LC ,
Reefhuis J
.
Birth Defects Res 2019 111 (20) 1618-1632
Large Outbreak of Hepatitis C Virus Associated With Drug Diversion by a Healthcare Technician.
Alroy-Preis S , Daly ER , Adamski C , Dionne-Odom J , Talbot EA , Gao F , Cavallo SJ , Hansen K , Mahoney JC , Metcalf E , Loring C , Bean C ,
Drobeniuc J
,
Xia GL
,
Kamili S
,
Montero JT .
Clin Infect Dis 2018 67 (6) 845-853
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
Genome-wide association study to identify variants associated with vaso-occlusive pain in sickle cell anemia.
Chaturvedi S , Bhatnagar P ,
Bean CJ
,
Steinberg MH , Milton JN , Casella JF , Barron-Casella E , Arking DE , DeBaun MR .
Blood 2017 130 (5) 686-688
Genome-wide siRNA Screening at Biosafety Level 4 Reveals a Crucial Role for Fibrillarin in Henipavirus Infection.
Deffrasnes C , Marsh GA , Foo CH , Rootes CL , Gould CM , Grusovin J , Monaghan P ,
Lo MK
,
Tompkins SM , Adams TE , Lowenthal JW , Simpson KJ , Stewart CR , Bean AG , Wang LF .
PLoS Pathog 2016 12 (3) e1005478
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
Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.
Bean CJ
,
Hooper WC
,
Ellingsen D
,
Debaun MR , Sonderman J , Blot WJ .
Public Health Genomics 2014 17 (3) 169-72
Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.
Jiang B , Ryan KA , Hamedani A , Cheng Y , Sparks MJ ,
Koontz D
,
Bean CJ
,
Gallagher M
,
Hooper WC
,
McArdle PF , O'Connell JR , Stine OC , Wozniak MA , Stern BJ , Mitchell BD , Kittner SJ , Cole JW .
Stroke 2014 45 (4) 961-7
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.
Bean CJ
,
Boulet SL
,
Yang G
,
Payne AB
,
Ghaji N
,
Pyle ME
,
Hooper WC
,
Bhatnagar P , Keefer J , Barron-Casella EA , Casella JF , Debaun MR .
Br J Haematol 2013 163 (2) 268-76
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.
Hollis ND , Allen EG , Oliver TR , Tinker SW , Druschel C , Hobbs CA ,
O'Leary LA
,
Romitti PA , Royle MH , Torfs CP , Freeman SB , Sherman SL , Bean LJ .
Am J Med Genet A 2013 161 (3) 438-44
Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia
Thangarajh M ,
Yang G
,
Fuchs D , Ponisio MR , McKinstry RC , Jaju A , Noetzel MJ , Casella JF , Barron-Casella E ,
Hooper WC
,
Boulet SL
,
Bean CJ
,
Pyle ME
,
Payne AB
,
Driggers J
,
Trau HA
,
Vendt BA , Rodeghier M , Debaun MR .
Br J Haematol 2012 159 (3) 352-9
Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans
Bae HT , Baldwin CT , Sebastiani P , Telen MJ , Ashley-Koch A , Garrett M ,
Hooper WC
,
Bean CJ
,
Debaun MR , Arking DE , Bhatnagar P , Casella JF , Keefer JR , Barron-Casella E , Gordeuk V , Kato GJ , Minniti C , Taylor J , Campbell A , Luchtman-Jones L , Hoppe C , Gladwin MT , Zhang Y , Steinberg MH .
Blood 2012 120 (9) 1961-2
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.
Bean CJ
,
Boulet SL
,
Ellingsen D
,
Pyle ME
,
Barron-Casella EA , Casella JF ,
Payne AB
,
Driggers J
,
Trau HA
,
Yang G
,
Jones K , Ofori-Acquah SF ,
Hooper WC
,
Debaun MR .
Blood 2012 120 (18) 3822-8
Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks.
Bean CJ
,
Boulet SL
,
Ellingsen D
,
Trau H
,
Ghaji N
,
Hooper WC
,
Austin H .
Thromb Res 2012 130 (6) 942-7
Utility of multiplex ligation-dependent probe amplification (MLPA) for hemophilia mutation screening.
Payne A
,
Bean C
,
Hooper W
,
Miller C
.
J Thromb Haemost 2012 10 (9) 1951-4
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
Milton JN , Sebastiani P , Solovieff N , Hartley SW , Bhatnagar P , Arking DE , Dworkis DA , Casella JF , Barron-Casella E ,
Bean CJ
,
Hooper WC
,
Debaun MR , Garrett ME , Soldano K , Telen MJ , Ashley-Koch A , Gladwin MT , Baldwin CT , Steinberg MH , Klings ES .
PLoS One 2012 7 (4) e34741
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.
Bean LJH , Allen EG , Tinker SW , Hollis ND , Locke AE , Druschel C , Hobbs CA ,
O'Leary L
,
Romitti PA , Royle MH , Torfs CP , Dooley KJ , Freeman SB , Sherman SL .
Birth Defects Res A Clin Mol Teratol 2011 91 (10) 885-93
Blood gene expression profiling detects silica exposure and toxicity.
Sellamuthu R
,
Umbright C
,
Roberts JR
,
Chapman R
,
Young SH
,
Richardson D
,
Leonard H
,
McKinney W
,
Chen B
,
Frazer D
,
Li S
,
Kashon M
,
Joseph P
.
Toxicol Sci 2011 122 (2) 253-64
Inhalation exposure of gas-metal arc stainless steel welding fume increased atherosclerotic lesions in apolipoprotein E knockout mice.
Erdely A
,
Hulderman T
,
Salmen-Muniz R
,
Liston A
,
Zeidler-Erdely PC
,
Chen BT
,
Stone S
,
Frazer DG
,
Antonini JM
,
Simeonova PP
.
Toxicol Lett 2011 204 (1) 12-6
Highly pathogenic (H5N1) avian influenza induces an inflammatory T helper type 1 cytokine response in the chicken
Karpala AJ , Bingham J , Schat KA ,
Chen LM
,
Donis RO
,
Lowenthal JW , Bean AG .
J Interferon Cytokine Res 2011 31 (4) 393-400
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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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