Joan E Bailey-Wilson
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Explore the profile of Joan E Bailey-Wilson including associated specialties, affiliations and a list of published articles.
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185
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6045
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Recent Articles
1.
Li Y, Xiao X, Li J, Han Y, Cheng C, Fernandes G, et al.
Cancer Epidemiol Biomarkers Prev
. 2024 Jan;
33(3):389-399.
PMID: 38180474
Background: Clinical, molecular, and genetic epidemiology studies displayed remarkable differences between ever- and never-smoking lung cancer. Methods: We conducted a stratified multi-population (European, East Asian, and African descent) association study...
2.
Vazzana K, Musolf A, Bailey-Wilson J, Hiraki L, Silverman E, Scott C, et al.
Genes Immun
. 2023 Jul;
24(4):200-206.
PMID: 37488248
Childhood-onset systemic lupus erythematosus (cSLE) patients are unique, with hallmarks of Mendelian disorders (early-onset and severe disease) and thus are an ideal population for genetic investigation of SLE. In this...
3.
Wang S, Chiu C, Wilson A, Bailey-Wilson J, Agron E, Chew E, et al.
Genet Epidemiol
. 2023 Apr;
47(6):409-431.
PMID: 37101379
In genetic studies, many phenotypes have multiple naturally ordered discrete values. The phenotypes can be correlated with each other. If multiple correlated ordinal traits are analyzed simultaneously, the power of...
4.
Simpson C, Kimble D, Chandrasekharappa S, Alqosayer K, Holzinger E, Carrington B, et al.
Mol Genet Genomic Med
. 2023 Apr;
11(8):e2179.
PMID: 37070724
Background: Oral clefts and ectrodactyly are common, heterogeneous birth defects. We performed whole-exome sequencing (WES) analysis in a Syrian family. The proband presented with both orofacial clefting and ectrodactyly but...
5.
Cannon-Albright L, Teerlink C, Stevens J, Facelli J, Carr S, Allen-Brady K, et al.
Int J Cancer
. 2023 Mar;
153(2):364-372.
PMID: 36916144
A unique approach with rare resources was used to identify candidate variants predisposing to familial nonsquamous nonsmall-cell lung cancers (NSNSCLC). We analyzed sequence data from NSNSCLC-affected cousin pairs belonging to...
6.
Musolf A, Haarman A, Luben R, Ong J, Patasova K, Trapero R, et al.
Commun Biol
. 2023 Jan;
6(1):6.
PMID: 36596879
Refractive error, measured here as mean spherical equivalent (SER), is a complex eye condition caused by both genetic and environmental factors. Individuals with strong positive or negative values of SER...
7.
Patasova K, Haarman A, Musolf A, Mahroo O, Rahi J, Falchi M, et al.
PLoS One
. 2022 Sep;
17(9):e0272379.
PMID: 36137074
Purpose: Genetic variants identified through population-based genome-wide studies are generally of high frequency, exerting their action in the central part of the refractive error spectrum. However, the power to identify...
8.
Byun J, Han Y, Li Y, Xia J, Long E, Choi J, et al.
Nat Genet
. 2022 Aug;
54(8):1167-1177.
PMID: 35915169
To identify new susceptibility loci to lung cancer among diverse populations, we performed cross-ancestry genome-wide association studies in European, East Asian and African populations and discovered five loci that have...
9.
Wijesiriwardhana P, Musolf A, Bailey-Wilson J, Wetthasinghe T, Dissanayake V
BMC Res Notes
. 2022 Jun;
15(1):190.
PMID: 35655316
Objective: Although linkage studies have been utilized for the identification of variants associated with cancer in the world, little is known about their role in non BRCA1/2 individuals in the...
10.
Cawley N, Lyons A, Abebe D, Luke R, Yerger J, Telese R, et al.
Int J Mol Sci
. 2022 May;
23(9).
PMID: 35563467
Complex asparagine-linked glycosylation plays key roles in cellular functions, including cellular signaling, protein stability, and immune response. Previously, we characterized the appearance of a complex asparagine-linked glycosylated form of lysosome-associated...