Associated Papers
Short tandem repeats significantly contribute to the genetic architecture of metabolic and sensory age-related hearing loss phenotypes.
Ahmed S et al.
Medrxiv : the Preprint Server for Health Sciences, 2026
Large-scale audiometric phenotyping identifies distinct genes and pathways involved in hearing loss subtypes.
Ahmed S et al.
Communications Biology, 2025
41174146 (PubMed )
Supplement: 42003_2025_8778_MOESM6_ESM.pdf
Mendelian non-syndromic and syndromic hearing loss genes contribute to presbycusis.
Cornejo-Sanchez DM et al.
European Journal of Human Genetics : Ejhg, 2025
40055553 (PubMed )
Supplement: 41431_2025_1789_MOESM3_ESM.xlsx › Table_S3
Expanding the prostate cancer cell line repertoire with ACRJ-PC28, an AR-negative neuroendocrine cell line derived from an African-Caribbean patient.
Valentine H et al.
Cancer Research Communications, 2022
36643868 (PubMed )
Supplement: crc-22-0245-s07.xlsx › Variants_All_Exonic.exclude_ncR
Comprehensive Genomic and Transcriptomic Analysis of Three Synchronous Primary Tumours and a Recurrence from a Head and Neck Cancer Patient.
Bresadola L et al.
International Journal of Molecular Sciences, 2021
34299215 (PubMed )
Supplement: ijms-22-07583-s001.zip › SupplementaryTable3.xlsx › germline_mutations
The chronological sequence of somatic mutations in early gastric carcinogenesis inferred from multiregion sequencing of gastric adenomas.
Lim CH et al.
Oncotarget, 2016
27175599 (PubMed )
Supplement: oncotarget-07-39758-s006.xlsx › TableS5
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