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Author Details
Full Name
Jingxiong Xu
Affiliation
Lunenfeld-Tanenbaum Research Institute
ORCID
Career Start Year
2014
Papers
13
H Index
7
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36889065
Toker Cell Hyperplasia in the Nipple-Areolar Complex of Transmasculine Individuals.
Mod Pathol
2023
37738239
Large-scale whole exome sequencing studies identify two genes,CTSL and APOE, associated with lung cancer.
PLoS Genet
2023
35977396
Intake of mother's milk by very-low-birth-weight infants and variation in DNA methylation of genes involved in neurodevelopment at 5.5 years of age.
Am J Clin Nutr
2022
32277476
A Bayes factor approach with informative prior for rare genetic variant analysis from next generation sequencing data.
Biometrics
2021
34937578
DNA methylation mediates the association between breastfeeding and early-life growth trajectories.
Clin Epigenetics
2021
30646839
sim1000G: a user-friendly genetic variant simulator in R for unrelated individuals and family-based designs.
BMC Bioinformatics
2019
28544645
Germline INDELs and CNVs in a cohort of colorectal cancer patients: their characteristics, associations with relapse-free survival time, and potential time-varying effects on the risk of relapse.
Cancer Med
2017
28376164
Germline Mutations in the Kallikrein 6 Region and Predisposition for Aggressive Prostate Cancer.
J Natl Cancer Inst
2017
27333071
Maternal Whole Blood Gene Expression at 18 and 28 Weeks of Gestation Associated with Spontaneous Preterm Birth in Asymptomatic Women.
PLoS One
2016
27334288
No associations of a set of SNPs in the Vascular Endothelial Growth Factor (VEGF) and Matrix Metalloproteinase (MMP) genes with survival of colorectal cancer patients.
Cancer Med
2016
25866641
A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes.
Biomark Res
2015
26064972
A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer.
Biomed Res Int
2015
24691024
Investigation of genetic variants, birthweight and hypothalamic-pituitary-adrenal axis function suggests a genetic variant in the SERPINA6 gene is associated with corticosteroid binding globulin in the western Australia pregnancy cohort (Raine) study.
PLoS One
2014
1 - 13 of 13
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