Joseph Glessner
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Explore the profile of Joseph Glessner including associated specialties, affiliations and a list of published articles.
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78
Citations
4911
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Recent Articles
11.
Liu Y, Qu H, Chang X, Mentch F, Qiu H, Wang X, et al.
Mol Cancer
. 2023 Aug;
22(1):126.
PMID: 37543594
Children with birth defects (BD) express distinct clinical features that often have various medical consequences, one of which is predisposition to the development of cancers. Identification of the underlying genetic...
12.
Gracia-Diaz C, Perdomo J, Khan M, Disanza B, Cajka G, Lei S, et al.
bioRxiv
. 2023 Jul;
PMID: 37425875
The KOLF2.1J iPSC line was recently proposed as a reference iPSC to promote the standardization of research studies in the stem cell field. Due to overall good performance differentiating to...
13.
Strong A, Qu H, Cullina S, McManus M, Zackai E, Glessner J, et al.
Am J Med Genet A
. 2023 May;
191(8):2156-2163.
PMID: 37227088
Joubert syndrome (JBTS) is a Mendelian disorder of the primary cilium defined by the clinical triad of hypotonia, developmental delay, and a distinct cerebellar malformation called the molar tooth sign....
14.
Qu H, Glessner J, Qu J, Mentch F, Campbell I, Sleiman P, et al.
Metabolomics
. 2022 Dec;
18(12):101.
PMID: 36459297
Background: Previous study has shown that dyslipidemia is common in patients with Sickle cell disease (SCD) and is associated with more serious SCD complications. Methods: This study investigated systematically dyslipidemia...
15.
Liu Y, Qu H, Chang X, Mentch F, Qiu H, Nguyen K, et al.
Biomark Res
. 2022 Nov;
10(1):84.
PMID: 36384586
Background: Children with birth defects (BD) are more likely to develop cancer and the increased risk of cancer persists into adulthood. Prior population-based assessments have demonstrated that even non-chromosomal BDs...
16.
Chang X, March M, Mentch F, Qu H, Liu Y, Glessner J, et al.
J Allergy Clin Immunol
. 2022 Sep;
151(4):1132-1136.
PMID: 36089080
Background: Asthma is a chronic inflammatory disorder with a strong genetic inheritance. Although more than 100 loci were reported through the genome-wide association study of European populations, the genetic underpinning...
17.
Quinlan C, Chang X, March M, Mentch F, Qu H, Liu Y, et al.
Sleep
. 2022 Jul;
47(3).
PMID: 35902206
Study Objectives: To identify genetic susceptibility variants in pediatric obstructive sleep apnea in European American and African American children. Methods: A phenotyping algorithm using electronic medical records was developed to...
18.
Qu H, Glessner J, Qu J, Gilhool S, Mentch F, Campbell I, et al.
iScience
. 2022 Jul;
25(7):104650.
PMID: 35811841
Plasma metabolomics represents a potentially powerful approach to understand the biochemical mechanisms of nutrition and metabolism in asthma. This study aims to acquire knowledge on plasma metabolites in asthma, which...
19.
Liu Y, Qu H, Chang X, Qu J, Mentch F, Nguyen K, et al.
Hum Mol Genet
. 2022 Jun;
31(22):3769-3776.
PMID: 35642741
Mental disorders present a global health concern and have limited treatment options. In today's medical practice, medications such as antidepressants are prescribed not only for depression but also for conditions...
20.
Alexander-Bloch A, Huguet G, Schultz L, Huffnagle N, Jacquemont S, Seidlitz J, et al.
JAMA Psychiatry
. 2022 May;
79(7):699-709.
PMID: 35544191
Importance: Psychiatric and cognitive phenotypes have been associated with a range of specific, rare copy number variants (CNVs). Moreover, IQ is strongly associated with CNV risk scores that model the...