Author details

Full Name

Jeffrey W Pennington

Affiliation

ORCID

Career Start Year

2013

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34741438	Evaluating commercially available wireless cardiovascular monitors for measuring and transmitting real-time physiological responses in children with autism.	Autism Research	2022
36214585	Validation of a Computational Phenotype to Identify Acute Brain Dysfunction in Pediatric Sepsis.	Pediatr Crit Care Med	2022
34991135	Prevalence of and Associations With Avascular Necrosis After Pediatric Sepsis: A Single-Center Retrospective Study.	Pediatr Crit Care Med	2022
33166716	Incorporating patient reporting patterns to evaluate spatially targeted TB interventions.	Annals of Epidemiology	2021
33866998	Quantifying geographic heterogeneity in TB incidence and the potential impact of geographically targeted interventions in South and North City Corporations of Dhaka, Bangladesh: a model-based study.	Epidemiology and Infection	2021
34324479	SARS-CoV-2 Infection in Public School District Employees Following a District-Wide Vaccination Program - Philadelphia County, Pennsylvania, March 21-April 23, 2021.	Morbidity and Mortality Weekly Report	2021
31408044	Perspective on the Development of a Large-Scale Clinical Data Repository for Pediatric Hearing Research.	Ear Hear	2020
32032262	Identification of Pediatric Sepsis for Epidemiologic Surveillance Using Electronic Clinical Data.	Pediatr Crit Care Med	2020
29368277	Utilization of the Tablet Application Proband in Pedigree Construction and Assessment.	Journal of Genetic Counseling	2018
29907799	Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss.	Genet Med	2018
30377334	Correction: Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data.	Genet Med	2018
29389922	Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data.	Genet Med	2018
29388940	Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.	Genet Med	2018
29419820	Correction: Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data.	Genet Med	2018
28146330	Using electronic medical record data to report laboratory adverse events.	Br J Haematol	2017
28339689	Genomic decision support needs in pediatric primary care.	J Am Med Inform Assoc	2017
27535360	The biorepository portal toolkit: an honest brokered, modular service oriented software tool set for biospecimen-driven translational research.	BMC Genomics	2016
27183886	Increasing cumulative exposure to volatile anesthetic agents is associated with poorer neurodevelopmental outcomes in children with hypoplastic left heart syndrome.	J Thorac Cardiovasc Surg	2016
27267768	Temporal bone radiology report classification using open source machine learning and natural langue processing libraries.	BMC Med Inform Decis Mak	2016
26187847	Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death.	Hum Genomics	2015
25047600	Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology.	BMC Bioinformatics	2014
24131510	Harvest: an open platform for developing web-based biomedical data discovery and reporting applications.	Journal of the American Medical Informatics Association : JAMIA	2014
24303304	Harvest: a web-based biomedical data discovery and reporting application development platform.		2013