Associated Papers
Genotype-Phenotype Correlation Insights in a Rare Case Presenting with Multiple Osteodysplastic Syndromes.
Yapijakis C et al.
Genes, 2025
Patient with PSEN1 Glu318Gly and Other Possible Disease Risk Mutations, Diagnosed with Early Onset Alzheimer's Disease.
Yang Y et al.
International Journal of Molecular Sciences, 2023
37895139 (PubMed )
Supplement: ijms-24-15461-s001.zip › ijms-2642793-supplementary.pdf
Integrated analysis of whole genome and transcriptome sequencing in a young patient with gastric cancer provides insights for precision therapy.
Hu K et al.
Oncology Letters, 2020
Study on the SFRP4 gene polymorphism and expression in prostate cancer.
Natarajan A et al.
Journal of Genetics, 2020
Frizzled-related proteins 4 (SFRP4) rs1802073G allele predicts the elevated serum lipid levels during acitretin treatment in psoriatic patients from Hunan, China.
Zhou X et al.
Peerj, 2018
Association of Wnt signaling pathway genetic variants in gallbladder cancer susceptibility and survival.
Yadav A et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2016
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A2-A0EM-01A.domain
Genome-wide detection of allelic gene expression in hepatocellular carcinoma cells using a human exome SNP chip.
Park YM et al.
Gene, 2014
Association of common gene variants in the WNT/β-catenin pathway with colon cancer recurrence.
Páez D et al.
The Pharmacogenomics Journal, 2014
Coding regions of INHBA, SFRP4 and HOXA10 are not implicated in familial endometriosis linked to chromosome 7p13-15.
Lin J et al.
Molecular Human Reproduction, 2011
Single nucleotide polymorphisms in Wnt signaling and cell death pathway genes and susceptibility to colorectal cancer.
Frank B et al.
Carcinogenesis, 2010
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