CDC-Authored Genomics and Precision Health Publications Database
Last data update: Jan 13, 2025. (Total: 6490 publications)
| Query Trace: Shapira SK[original query] |
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| 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 |
| 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 |
| A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early Development.
Shapira SK , Tian LH , Aylsworth AS , Elias ER , Hoover-Fong JE , Meeks NJL , Souders MC , Tsai AC , Zackai EH , Alexander AA , Yeargin-Allsopp M , Schieve LA . J Autism Dev Disord 2019 49 (5) 2184-2202 |
| Primary Care Provider Management of Congenital Hypothyroidism Identified Through Newborn Screening.
Rosenthal NA , Bezar E , Mann S , Bachrach LK , Banerjee S , Geffner ME , Gottschalk M , Shapira SK , Hasegawa L , Feuchtbaum L . Ann Thyroid Res 2017 3 (1) 95-101 |
| 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 |
| Expanding diagnostic testing beyond cytogenetics: implications for birth defects research and surveillance
Jackson JM , Druschel CM , Shapira SK . Birth Defects Res A Clin Mol Teratol 2013 97 (11) 726-9 |
| The Study to Explore Early Development (SEED): a multisite epidemiologic study of autism by the Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) network
Schendel DE , Diguiseppi C , Croen LA , Fallin MD , Reed PL , Schieve LA , Wiggins LD , Daniels J , Grether J , Levy SE , Miller L , Newschaffer C , Pinto-Martin J , Robinson C , Windham GC , Alexander A , Aylsworth AS , Bernal P , Bonner JD , Blaskey L , Bradley C , Collins J , Ferretti CJ , Farzadegan H , Giarelli E , Harvey M , Hepburn S , Herr M , Kaparich K , Landa R , Lee LC , Levenseller B , Meyerer S , Rahbar MH , Ratchford A , Reynolds A , Rosenberg S , Rusyniak J , Shapira SK , Smith K , Souders M , Thompson PA , Young L , Yeargin-Allsopp M . J Autism Dev Disord 2012 42 (10) 2121-40 |
| 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 |
| Long-term speech and language developmental issues among children with Duarte galactosemia
Powell KK , Braun KV , Singh RH , Shapira SK , Olney RS , Yeargin-Allsopp M . Genet Med 2009 11 (12) 874-9 |
- Page last reviewed:Feb 1, 2024
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