Joseph Glessner
Overview
Explore the profile of Joseph Glessner including associated specialties, affiliations and a list of published articles.
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Articles
78
Citations
4911
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Recent Articles
1.
Qu H, Qu J, Chang X, Williams N, Mentch F, Snyder J, et al.
Clin Auton Res
. 2025 Feb;
PMID: 39964606
Background: Postural orthostatic tachycardia syndrome (POTS) is a complex disorder with serious health consequences, while its etiology remains largely elusive. Objective: The purpose of this study was to investigate the...
2.
Liu Y, Qu H, Chang X, Mentch F, Qiu H, Nguyen K, et al.
Cancer Commun (Lond)
. 2024 Oct;
44(11):1374-1378.
PMID: 39387321
No abstract available.
3.
Liu Y, Glessner J, Qu H, Chang X, Qiu H, Wang T, et al.
Mol Oncol
. 2024 Aug;
19(3):899-912.
PMID: 39140252
There are two key signatures of pediatric cancers: (a) higher prevalence of germline alterations and (b) heterogeneity in alteration types. Recent population-based assessments have demonstrated that children with birth defects...
4.
Saeidian A, March M, Youssefian L, Watson D, Bhandari E, Wang X, et al.
Genet Med
. 2024 Aug;
26(11):101225.
PMID: 39096151
Purpose: Clinical next-generation sequencing is an effective approach for identifying pathogenic sequence variants that are medically actionable for participants and families but are not associated with the participant's primary diagnosis....
5.
Hernandez Martinez C, Glessner J, Sertori Finoti L, Silva P, Messora M, Coletta R, et al.
Front Cell Infect Microbiol
. 2024 Aug;
14:1369226.
PMID: 39086605
Objective: The study delved into the epigenetic factors associated with periodontal disease in two lineages of mice, namely C57bl/6 and Balb/c. Its primary objective was to elucidate alterations in the...
6.
Mosley J, Shelley J, Dickson A, Zanussi J, Daniel L, Zheng N, et al.
Nat Commun
. 2024 Apr;
15(1):3384.
PMID: 38649760
Polygenic variation unrelated to disease contributes to interindividual variation in baseline white blood cell (WBC) counts, but its clinical significance is uncharacterized. We investigated the clinical consequences of a genetic...
7.
Zhang S, Yang J, Ji D, Meng X, Zhu C, Zheng G, et al.
J Med Genet
. 2024 Mar;
61(7):677-688.
PMID: 38443156
Background: Epigenetics makes substantial contribution to the aetiology of autism spectrum disorder (ASD) and may harbour a unique opportunity to prevent the development of ASD. We aimed to identify novel...
8.
Benfica L, Brito L, do Bem R, Mulim H, Glessner J, Braga L, et al.
BMC Genomics
. 2024 Jan;
25(1):54.
PMID: 38212678
Background: Feeding costs represent the largest expenditures in beef production. Therefore, the animal efficiency in converting feed in high-quality protein for human consumption plays a major role in the environmental...
9.
Chang X, Qu H, Liu Y, Glessner J, Hakonarson H
Biol Psychiatry
. 2023 Oct;
95(9):881-887.
PMID: 37865391
Background: Previous studies have implicated both rare copy number variations (CNVs) and common variants in liability for attention-deficit/hyperactivity disorder (ADHD). However, how common and rare genetic variants jointly contribute to...
10.
Liu Y, Qu H, Chang X, Mentch F, Qiu H, Nguyen K, et al.
Cancer Commun (Lond)
. 2023 Aug;
43(11):1271-1274.
PMID: 37559342
No abstract available.