Joshua K Meisner
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Explore the profile of Joshua K Meisner including associated specialties, affiliations and a list of published articles.
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Articles
22
Citations
215
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Recent Articles
1.
Meisner J, Renberg A, Smith E, Tsan Y, Elder B, Bullard A, et al.
Circulation
. 2024 Dec;
PMID: 39633578
Background: Classically, hypertrophic cardiomyopathy (HCM) has been viewed as a single-gene (monogenic) disease caused by pathogenic variants in sarcomere genes. Pathogenic sarcomere variants are individually rare and convey high risk...
2.
Owlett L, Zapanta B, Sandkuhler S, Ames E, Hickey S, MacKenzie S, et al.
Am J Med Genet A
. 2024 Jun;
194(10):e63778.
PMID: 38829177
TANGO2 deficiency disorder (TDD) is a rare, autosomal recessive condition caused by pathogenic variants in TANGO2, a gene residing within the region commonly deleted in 22q11.2 deletion syndrome (22q11.2DS). Although...
3.
Sandkuhler S, Zhang L, Meisner J, Ghaloul-Gonzalez L, Beach C, Harris D, et al.
J Inherit Metab Dis
. 2022 Dec;
46(2):161-162.
PMID: 36550018
No abstract available.
4.
McKissic D, Meisner J, Chen M, Lim H
Pediatr Rev
. 2022 Nov;
43(12):714-716.
PMID: 36450633
No abstract available.
5.
Meisner J, Yu S, Lowery R, Liang W, Schumacher K, Burrows H
Clin Pediatr (Phila)
. 2022 Apr;
61(5-6):428-439.
PMID: 35383471
Under-diagnosis of pediatric hypertension remains pervasive due to difficulty recognizing elevated systolic blood pressures (SBPs). We performed a retrospective review comparing recognition of and response to elevated SBPs ≥95th percentile...
6.
Meisner J, Bradley D, Russell M
Circ Genom Precis Med
. 2021 Aug;
14(5):e003327.
PMID: 34463117
No abstract available.
7.
Meisner J, Koblick S, Walling E, Rabah R, Schumacher K
Cardiol Young
. 2020 Oct;
30(12):1973-1975.
PMID: 33012302
Lymphatic vessel dysplasia is associated with Fontan-associated protein-losing enteropathy. Extra nodal non-Hodgkin lymphomas including mucosa-associated lymphoid tissue (MALT lymphoma) are associated with lymphatic vessel dysplasia. Here, we describe the case...
8.
Meisner J, Ames E, Ahmad A, Si M, Schumacher K, Lim H, et al.
Circ Genom Precis Med
. 2020 Jun;
13(4):e002928.
PMID: 32527145
No abstract available.
9.
Meisner J, Martin D
Am J Med Genet C Semin Med Genet
. 2019 Dec;
184(1):81-89.
PMID: 31833191
CHARGE syndrome is characterized by a pattern of congenital anomalies (Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth, Genital abnormalities, and Ear abnormalities). De novo...
10.
Heuslein J, Murrell K, Leiphart R, Llewellyn R, Meisner J, Price R
Sci Rep
. 2016 Jun;
6:27029.
PMID: 27244251
Arteriogenesis, or the lumenal expansion of pre-existing arterioles in the presence of an upstream occlusion, is a fundamental vascular growth response. Though alterations in shear stress stimulate arteriogenesis, the migration...