Detalhe da pesquisa
1.
The impact of clinical genome sequencing in a global population with suspected rare genetic disease.
Am J Hum Genet
; 2024 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38843839
2.
Real-world economic evaluation of prospective rapid whole-genome sequencing compared to a matched retrospective cohort of critically ill pediatric patients in the United States.
Pharmacogenomics J
; 22(4): 223-229, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35436997
3.
High-throughput sequencing analysis of a "hit and run" cell and animal model of KSHV tumorigenesis.
PLoS Pathog
; 16(6): e1008589, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32603362
4.
Cost-effectiveness of exome and genome sequencing for children with rare and undiagnosed conditions.
Genet Med
; 24(6): 1349-1361, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396982
5.
A Randomized Pilot Trial Assessing the Role of Human Fibrinogen Concentrate in Decreasing Cryoprecipitate Use and Blood Loss in Infants Undergoing Cardiopulmonary Bypass.
Pediatr Cardiol
; 43(7): 1444-1454, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35305111
6.
Physical Literacy in Elementary Physical Education: A Survey of Fundamental Movement Skill Practice Patterns.
Pediatr Phys Ther
; 34(1): 56-61, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34873120
7.
Pediatric pharmacogenomics: challenges and opportunities: on behalf of the Sanford Children's Genomic Medicine Consortium.
Pharmacogenomics J
; 21(1): 8-19, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32843689
8.
PDGFRA defines the mesenchymal stem cell Kaposi's sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment.
PLoS Pathog
; 15(12): e1008221, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31881074
9.
Liposomal Bupivacaine Infiltration After Median Sternotomy in Pediatric Cardiac Surgery.
J Cardiothorac Vasc Anesth
; 35(6): 1715-1721, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33663978
10.
Perspectives of Pediatric Providers Regarding Clinical Use of Pharmacogenetics.
S D Med
; 74(7): 294-301, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34449988
11.
Evaluating the Humpty Dumpty Fall Scale: An International, Multisite Study.
J Nurs Care Qual
; 35(4): 301-308, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31972778
12.
Cost-effectiveness of exome and genome sequencing for children with rare and undiagnosed conditions.
Genet Med
; 24(11): 2415-2417, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36178484
13.
Response to Grosse and Gudgeon.
Genet Med
; 24(12): 2597-2598, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36166002
14.
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature
; 459(7246): 528-33, 2009 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-19404256
15.
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.
Hum Mol Genet
; 21(15): 3513-23, 2012 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22543975
16.
Viral expression associated with gastrointestinal adenocarcinomas in TCGA high-throughput sequencing data.
Hum Genomics
; 7: 23, 2013 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-24279398
17.
Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting.
Front Pediatr
; 12: 1349519, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38440187
18.
EHR-based Case Identification of Pediatric Long COVID: A Report from the RECOVER EHR Cohort.
medRxiv
; 2024 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38826460
19.
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy.
Eur J Hum Genet
; 2024 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38565639
20.
Feasibility of functional precision medicine for guiding treatment of relapsed or refractory pediatric cancers.
Nat Med
; 30(4): 990-1000, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38605166