Jared M Evans
Overview
Explore the profile of Jared M Evans including associated specialties, affiliations and a list of published articles.
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36
Citations
1055
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Recent Articles
1.
Turley T, Theis J, Evans J, Fogarty Z, Gulati R, Hayes S, et al.
J Cardiovasc Dev Dis
. 2023 Sep;
10(9).
PMID: 37754822
Rare familial spontaneous coronary artery dissection (SCAD) kindreds implicate genetic disease predisposition and provide a unique opportunity for candidate gene discovery. Whole-genome sequencing was performed in fifteen probands with non-syndromic...
2.
Walton N, Hafen B, Graceffo S, Sutherland N, Emmerson M, Palmquist R, et al.
J Pers Med
. 2022 Dec;
12(11).
PMID: 36579594
The clinical use of genomic analysis has expanded rapidly resulting in an increased availability and utility of genomic information in clinical care. We have developed an infrastructure utilizing informatics tools...
3.
Theis J, Hu J, Sundsbak R, Evans J, Bamlet W, Qureshi M, et al.
Circ Genom Precis Med
. 2020 Dec;
14(1):e003126.
PMID: 33325730
Background: Hypoplastic left heart syndrome (HLHS) with risk of poor outcome has been linked to variants, implicating overlap in genetic etiologies of structural and myopathic heart disease. Methods: Whole genome...
4.
Theis J, Vogler G, Missinato M, Li X, Nielsen T, Zeng X, et al.
Elife
. 2020 Oct;
9.
PMID: 33006316
Congenital heart diseases (CHDs), including hypoplastic left heart syndrome (HLHS), are genetically complex and poorly understood. Here, a multidisciplinary platform was established to functionally evaluate novel CHD gene candidates, based...
5.
Kargaran P, Evans J, Bodbin S, Smith J, Nelson T, Denning C, et al.
J Clin Med
. 2020 Jul;
9(8).
PMID: 32718021
Hypertrophic cardiomyopathy (HCM) is a prevalent and untreatable cardiovascular disease with a highly complex clinical and genetic causation. HCM patients bearing similar sarcomeric mutations display variable clinical outcomes, implying the...
6.
Turley T, Theis J, Sundsbak R, Evans J, OByrne M, Gulati R, et al.
Circ Genom Precis Med
. 2019 Mar;
12(4):e002437.
PMID: 30888838
Background: Spontaneous coronary artery dissection (SCAD) is an uncommon idiopathic disorder predominantly affecting young, otherwise healthy women. Rare familial cases reveal a genetic predisposition to disease. The aim of this...
7.
Takahashi P, Jenkins G, Welkie B, McDonnell S, Evans J, Cerhan J, et al.
Appl Clin Genet
. 2018 Dec;
11:121-127.
PMID: 30498369
Purpose: In aging adults, mitochondrial dysfunction may be an important contributor. We evaluated the association between mitochondrial DNA (mtDNA) copy number, which is a biomarker for mitochondrial function, and self-rated...
8.
Tester D, Wong L, Chanana P, Gray B, Jaye A, Evans J, et al.
J Pediatr
. 2018 Oct;
203:423-428.e11.
PMID: 30268395
Objective: To determine whether a monogenic basis explains sudden infant death syndrome (SIDS) using an exome-wide focus. Study Design: A cohort of 427 unrelated cases of SIDS (257 male; average...
9.
Gray B, Tester D, Wong L, Chanana P, Jaye A, Evans J, et al.
Genet Med
. 2018 Aug;
21(3):641-649.
PMID: 30139991
Purpose: Sudden infant death syndrome (SIDS) is the commonest cause of sudden death of an infant; however, the genetic basis remains poorly understood. We aimed to identify noncardiac genes underpinning...
10.
Wu C, Evans J, Huang S, Mahoney D, Dukek B, Taylor W, et al.
BMC Genomics
. 2018 May;
19(1):401.
PMID: 29801434
Background: MicroRNA (miRNA) profiling is an important step in studying biological associations and identifying marker candidates. miRNA exists in isoforms, called isomiRs, which may exhibit distinct properties. With conventional profiling...