Adam D Kennedy
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Explore the profile of Adam D Kennedy including associated specialties, affiliations and a list of published articles.
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58
Citations
3420
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Recent Articles
1.
Shaath R, Al-Maraghi A, Ali H, AlRayahi J, Kennedy A, DeBalsi K, et al.
Metabolites
. 2024 Mar;
14(3).
PMID: 38535312
Multi-omics approaches, which integrate genomics, transcriptomics, proteomics, and metabolomics, have emerged as powerful tools in the diagnosis of rare diseases. We used untargeted metabolomics and whole-genome sequencing (WGS) to gain...
2.
DeBalsi K, Newman J, Sommerville L, Phillips 3rd J, Hamid R, Cogan J, et al.
Metabolites
. 2023 Mar;
13(3).
PMID: 36984839
We present a case study of a 20-year-old male with an unknown neurodegenerative disease who was referred to the Undiagnosed Diseases Network Vanderbilt Medical Center site. A previous metabolic panel...
3.
Liu N, Xiao J, Gijavanekar C, Pappan K, Glinton K, Shayota B, et al.
JAMA Netw Open
. 2021 Jul;
4(7):e2114155.
PMID: 34251446
Importance: Recent advances in newborn screening (NBS) have improved the diagnosis of inborn errors of metabolism (IEMs); however, many potentially treatable IEMs are not included on NBS panels, nor are...
4.
Kennedy A, Ford L, Wittmann B, Conner J, Wulff J, Mitchell M, et al.
PLoS One
. 2021 Apr;
16(4):e0249797.
PMID: 33831088
Introduction: Analysis of blood for the evaluation of clinically relevant biomarkers requires precise collection and sample handling by phlebotomists and laboratory staff. An important consideration for the clinical application of...
5.
Goodman K, Mitchell M, Evans A, Miller L, Ford L, Wittmann B, et al.
Metabolomics
. 2021 Mar;
17(3):31.
PMID: 33704583
Introduction: Clinical metabolomics has utility as a screen for inborn errors of metabolism (IEM) and variant classification in patients with rare disease. It is important to understand and characterize preanalytical...
6.
Shayota B, Donti T, Xiao J, Gijavanekar C, Kennedy A, Hubert L, et al.
Mol Genet Metab
. 2020 Aug;
131(1-2):147-154.
PMID: 32828637
Inborn errors of metabolism (IEM) involving the non-oxidative pentose phosphate pathway (PPP) include the two relatively rare conditions, transketolase deficiency and transaldolase deficiency, both of which can be difficult to...
7.
Ford L, Kennedy A, Goodman K, Pappan K, Evans A, Miller L, et al.
J Appl Lab Med
. 2020 May;
5(2):342-356.
PMID: 32445384
Background: The application of whole-exome sequencing for the diagnosis of genetic disease has paved the way for systems-based approaches in the clinical laboratory. Here, we describe a clinical metabolomics method...
8.
Kennedy A, Pappan K, Donti T, Delgado M, Shinawi M, Pearson T, et al.
Front Neurosci
. 2020 Feb;
13:1344.
PMID: 32082103
[This corrects the article DOI: 10.3389/fnins.2019.00394.].
9.
Sista R, Ng R, Nuffer M, Basmajian M, Coyne J, Elderbroom J, et al.
Diagnostics (Basel)
. 2020 Jan;
10(1).
PMID: 31906315
"Children are not tiny adults" is an adage commonly used in pediatrics to emphasize the fact that children often have different physiological responses to sickness and trauma compared to adults....
10.
Kennedy A, Pappan K, Donti T, Delgado M, Shinawi M, Pearson T, et al.
Front Neurosci
. 2019 May;
13:394.
PMID: 31133775
Broad-scale untargeted biochemical phenotyping is a technology that supplements widely accepted assays, such as organic acid, amino acid, and acylcarnitine analyses typically utilized for the diagnosis of inborn errors of...