Associated Papers
Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz-Jeghers Syndrome.
Khan TN et al.
Human Mutation, 2025
40860288 (PubMed )
Supplement: 5530710.f1.zip › Khan_et_al__Supplementary_Table_3_R3_ES.pdf
Unraveling the function and structure impact of deleterious missense SNPs in the human OX1R receptor by computational analysis.
Farajzadeh-Dehkordi M et al.
Scientific Reports, 2024
38191899 (PubMed )
Supplement: 41598_2023_49809_MOESM5_ESM.xlsx › Table_S2
Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.
Molnár J et al.
Plos One, 2016
26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism
Gender-stratified gene and gene-treatment interactions in smoking cessation.
Lee W et al.
The Pharmacogenomics Journal, 2012
21808284 (PubMed )
Supplement: NIHMS305090-supplement-3.pdf
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