Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HPK5_het
Association of rs3027178 polymorphism in the circadian clock gene PER1 with susceptibility to Alzheimer's disease and longevity in an Italian population.
Bacalini MG et al.
Geroscience, 2022
34921659 (PubMed )
Supplement: 11357_2021_477_MOESM3_ESM.xlsx › rare_variants_AD
Sacral agenesis: a pilot whole exome sequencing and copy number study.
Porsch RM et al.
Bmc Medical Genetics, 2016
28007035 (PubMed )
Supplement: 12881_2016_359_MOESM2_ESM.xlsx › all_variants
[Mutational landscape of prostate tumors revealed by whole-exome sequencing].
Gilyazova IR et al.
Genetika, 2016
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