← Evidence map

ArticleF1000Research2018

Using regulatory genomics data to interpret the function of disease variants and prioritise genes from expression studies.

Enrico FerreroPubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

3 papers cite it

2018
2019
2020
2021
2022
2023
2024
this paperpooled itcites it
Full record →Abstract, authors, funding and every citing paper · PMID 29568492