Associated Papers
Multivariate canonical correlation analysis identifies additional genetic variants for chronic kidney disease.
Osborne AJ et al.
Npj Systems Biology and Applications, 2024
38459044 (PubMed )
Supplement: 41540_2024_350_MOESM17_ESM.xlsx › Supplementary_Table_S15
RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis.
Wong S et al.
Embo Molecular Medicine, 2023
37066513 (PubMed )
Supplement: EMMM-15-e17078-s005.xlsx › Compound_Hets
Decoding variants in drug-metabolizing enzymes and transporters in solid tumor patients by whole-exome sequencing.
Aboul-Soud MAM et al.
Saudi Journal of Biological Sciences, 2021
33424349 (PubMed )
Supplement: mmc1.xlsx › Sheet1
Targeted next generation sequencing as a tool for precision medicine.
Gulilat M et al.
Bmc Medical Genomics, 2019
31159795 (PubMed )
Supplement: 12920_2019_527_MOESM1_ESM.xlsx › Table_S6
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Wuttke M et al.
Nature Genetics, 2019
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.
Graham SE et al.
Nature Communications, 2019
31015462 (PubMed )
Supplement: 41467_2019_9861_MOESM1_ESM.pdf
Rare mutations associating with serum creatinine and chronic kidney disease.
Sveinbjornsson G et al.
Human Molecular Genetics, 2014
Select a paper to view details