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Public Health Genomics and Precision Health Knowledge Base (v10.0)
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: Sep 30, 2024
. (Total: 6327 publications)
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Year
Journal
Records 1-10 (of 10 Records)
Query Trace:
Hinton CF[original query]
CDC Grand Rounds: Newborn screening and improved outcomes.
Howell RR , Terry S , Tait VF ,
Olney R
,
Hinton CF
,
Grosse S
,
Eichwald J
,
Cuthbert C
,
Popovic T
,
Glidewell J
.
MMWR Morb Mortal Wkly Rep 2012 61 (21) 390-3
Progress in expanding newborn screening in the United States
Grosse SD
,
Cuthbert C
,
Gaffney M
,
Gaviglio A
,
Hinton CF
,
Kellar-Guenther Y , Kemper AR , McKasson S , Ojodu J ,
Riley C
,
Singh S , Sontag MK ,
Shapira SK
.
Am J Hum Genet 2023 110 (6) 1015-1016
Infants with Congenital Disorders Identified Through Newborn Screening - United States, 2015-2017.
Sontag MK , Yusuf C ,
Grosse SD
,
Edelman S , Miller JI , McKasson S , Kellar-Guenther Y ,
Gaffney M
,
Hinton CF
,
Cuthbert C
,
Singh S , Ojodu J ,
Shapira SK
.
MMWR Morb Mortal Wkly Rep 2020 69 (36) 1265-1268
A framework for assessing outcomes from newborn screening: on the road to measuring its promise.
Hinton CF
,
Homer CJ , Thompson AA , Williams A , Hassell KL , Feuchtbaum L , Berry SA , Comeau AM , Therrell BL , Brower A , Harris KB , Brown C , Monaco J , Ostrander RJ , Zuckerman AE , Kaye C , Dougherty D , Greene C , Green NS .
Mol Genet Metab 2016 118 (4) 221-9
Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen states.
Held PK ,
Shapira SK
,
Hinton CF
,
Jones E ,
Hannon WH
,
Ojodu J .
Mol Genet Metab 2015 116 (3) 133-8
Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings.
Hinton CF
,
Mai CT
,
Nabukera SK , Botto LD , Feuchtbaum L , Romitti PA , Wang Y , Piper KN ,
Olney RS
.
Genet Med 2013 16 (6) 484-90
Improving newborn screening follow-up in pediatric practices: quality improvement innovation network.
Hinton CF
,
Neuspiel DR , Gubernick RS , Geleske T , Healy J , Kemper AR , Lloyd-Puryear MA , Saul RA , Thompson BH , Kaye CI .
Pediatrics 2012 130 (3) e669-75
What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children.
Hinton CF
,
Feuchtbaum L , Kus CA , Kemper AR , Berry SA , Levy-Fisch J , Luedtke J , Kaye C ,
Boyle CA
.
Genet Med 2011 13 (10) 861-865
Birth prevalence rates of newborn screening disorders in relation to screening practices in the United States.
Hertzberg VS ,
Hinton CF
,
Therrell BL ,
Shapira SK
.
J Pediatr 2011 159 (4) 555-60
Ethical implications and practical considerations of ethnically targeted screening for genetic disorders: the case of hemoglobinopathy screening.
Hinton CF
,
Grant AM
,
Grosse SD
.
Ethn Health 2011 16 377-88
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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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