Brilliant M
No ORCID on file
· 2 papers in corpus
· active 2016-2019
Top journals
Frequent coauthors
- Basile AO 1
- Berry-Kravis E 1
- Baker MW 1
- DaWalt LS 1
- Greenberg J 1
- Hong J 1
- Kuusisto F 1
- Movaghar A 1
- McCarty CA 1
- Mailick MR 1
2019
The impact of the FMR1 premutation on human health is the subject of considerable controversy. A fundamental unanswered question is whether carrying the premutation allele is directly correlated with clinical phenotypes. A challenging probl…
2016
Next-generation sequencing technology has presented an opportunity for rare variant discovery and association of these variants with disease. To address the challenges of rare variant analysis, multiple statistical methods have been develop…