Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.
- Published in:
- Translational Psychiatry, 2017, p. 1, doi. 10.1038/s41398-017-0010-9
- By:
- Publication type:
- Article
Works by Ryan, Niamh M.
Results: 7
1
2
Investigating the dark-side of the genome: a barrier to human disease variant discovery?
- Published in:
- Biological Research, 2023, v. 56, n. 1, p. 1, doi. 10.1186/s40659-023-00455-0
- By:
- Publication type:
- Article
3
BICEP: Bayesian inference for rare genomic variant causality evaluation in pedigrees.
- Published in:
- Briefings in Bioinformatics, 2025, v. 26, n. 1, p. 1, doi. 10.1093/bib/bbae624
- By:
- Publication type:
- Article
4
Converting single nucleotide variants between genome builds: from cautionary tale to solution.
- Published in:
- Briefings in Bioinformatics, 2021, v. 22, n. 5, p. 1, doi. 10.1093/bib/bbab069
- By:
- Publication type:
- Article
5
SuRFing the genomics wave: an R package for prioritizing SNPs by functionality.
- Published in:
- Genome Medicine, 2014, v. 6, n. 10, p. 31, doi. 10.1186/s13073-014-0079-1
- By:
- Publication type:
- Article
6
Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disorders.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-79268-0
- By:
- Publication type:
- Article
7
Whole genome sequencing study of identical twins discordant for psychosis.
- Published in:
- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02982-0
- By:
- Publication type:
- Article