Jeremy W Prokop
Overview
Explore the profile of Jeremy W Prokop including associated specialties, affiliations and a list of published articles.
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Articles
86
Citations
1005
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Recent Articles
1.
Bhargava D, Labadie A, Hanson-Rios-Stutz R, Goodyke A, Moses E, Das A, et al.
Physiol Genomics
. 2025 Mar;
PMID: 40073040
Defining physiology and methods to measure biological mechanisms is essential. Extensive datasets such as RNA sequencing are used with little analysis of the knowledge gained from the various methodologies. Within...
2.
Morris O, Morris M, Jobe S, Bhargava D, Krueger J, Arora S, et al.
Genes (Basel)
. 2025 Jan;
15(12.
PMID: 39766791
Background: Variants within factor VIII (F8) are associated with sex-linked hemophilia A and thrombosis, with gene therapy approaches being available for pathogenic variants. Many variants within F8 remain variants of...
3.
Prokop J, Alberta S, Witteveen-Lane M, Pell S, Farag H, Bhargava D, et al.
Microorganisms
. 2024 Sep;
12(9).
PMID: 39338537
As of 2024, SARS-CoV-2 continues to propagate and drift as an endemic virus, impacting healthcare for years. The largest sequencing initiative for any species was initiated to combat the virus,...
4.
Bejma T, Beidler W, VanSickle E, Prokop J, Brown W, Scheurer-Monaghan A, et al.
Am J Med Genet A
. 2024 Jul;
194(11):e63811.
PMID: 38980148
There are currently multiple disorders of aminoacyl-tRNA synthetases described, including KARS1-related disorder resulting from dysfunctional lysyl-tRNA synthetases. In this report, we describe four novel KARS1 variants in three affected individuals,...
5.
Henderson M, Zieba J, Li X, Campbell D, Williams M, Vogt D, et al.
BioTech (Basel)
. 2024 Jan;
13(1).
PMID: 38247731
Gene therapy holds promise as a life-changing option for individuals with genetic variants that give rise to disease. FDA-approved gene therapies for Spinal Muscular Atrophy (SMA), cerebral adrenoleukodystrophy, β-Thalassemia, hemophilia...
6.
Rudolph H, Stafford A, Hwang H, Kim C, Prokop J, Vogt D
Biology (Basel)
. 2023 Apr;
12(4).
PMID: 37106788
Dysfunction of the WW domain-containing adaptor with coiled-coil, , gene underlies a rare autosomal dominant disorder, DeSanto-Shinawi syndrome (DESSH). DESSH is associated with facial dysmorphia, hypotonia, and cognitive alterations, including...
7.
Koehn O, Lorimer E, Unger B, Harris R, Das A, Suazo K, et al.
J Biol Chem
. 2023 Apr;
299(6):104698.
PMID: 37059183
Identifying events that regulate the prenylation and localization of small GTPases will help define new strategies for therapeutic targeting of these proteins in disorders such as cancer, cardiovascular disease, and...
8.
Cook T, Wilstermann A, Mitchell J, Arnold N, Rajasekaran S, Bupp C, et al.
Biomolecules
. 2023 Feb;
13(2).
PMID: 36830626
Insulin is amongst the human genome's most well-studied genes/proteins due to its connection to metabolic health. Within this article, we review literature and data to build a knowledge base of...
9.
Underwood A, Rasicci D, Hinds D, Mitchell J, Zieba J, Mills J, et al.
Genes (Basel)
. 2023 Jan;
14(1).
PMID: 36672963
The SOX transcription factor family is pivotal in controlling aspects of development. To identify genotype-phenotype relationships of SOX proteins, we performed a non-biased study of SOX using 1890 open-reading frame...
10.
Aniol C, Prokop J, Rajasekaran S, Pageau S, Elizer S, VanSickle E, et al.
BMC Pediatr
. 2023 Jan;
23(1):1.
PMID: 36593444
Noonan Syndrome is caused by variants in a variety of genes found in the RAS/MAPK pathway. As more causative genes for Noonan Syndrome have been identified, more phenotype variability has...