Associated Papers
Comprehensive Analysis of Human Colorectal Cancers Harboring Polymerase Epsilon Mutations.
Gibson LM et al.
International Journal of Molecular Sciences, 2025
40806338 (PubMed )
Supplement: ijms-26-07208-s001.zip › Table_S2.xlsx › Colorectal_CHASM_p-values
Genetic variants in patients with multiple arterial aneurysms.
Körfer D et al.
Langenbeck's Archives of Surgery, 2024
39382597 (PubMed )
Supplement: 423_2024_3488_MOESM2_ESM.xlsx › Supplemental_Table_2
Mapping the serum proteome to neurological diseases using whole genome sequencing.
Png G et al.
Nature Communications, 2021
34857772 (PubMed )
Supplement: 41467_2021_27387_MOESM6_ESM.xlsx › Sheet1
Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
Ferreira MAR et al.
Plos Genetics, 2020
32603359 (PubMed )
Supplement: pgen.1008725.s024.xls › Supp_Table_11
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › Feuil3
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