scispace - formally typeset
S

Susan Redline

Researcher at Brigham and Women's Hospital

Publications -  1071
Citations -  97728

Susan Redline is an academic researcher from Brigham and Women's Hospital. The author has contributed to research in topics: Polysomnography & Obstructive sleep apnea. The author has an hindex of 138, co-authored 899 publications receiving 80945 citations. Previous affiliations of Susan Redline include Brown University & University of California, Davis.

Papers
More filters
Journal ArticleDOI

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Margaret A. Taub, +146 more
- 01 Jan 2022 - 
TL;DR: This article reported the first sequencing-based association study for TL across ancestrally-diverse individuals (European, African, Asian and Hispanic/Latino) from the NHLBI Trans-Omics for Precision Medicine (TOPMed) program.
Journal ArticleDOI

Using Linkage Analysis to Identify Quantitative Trait Loci for Sleep Apnea in Relationship to Body Mass Index

TL;DR: To understand the genetics of sleep apnea, the relationship between the apnea hypopnea index (AHI) and body mass index (BMI) is evaluated through linkage analysis to identify genetic loci that may influence AHI and BMI jointly and AHI independent of BMI.
Journal ArticleDOI

OnWARD: Ontology-driven web-based framework for multi-center clinical studies

TL;DR: The initial deployment of OnWARD is demonstrated for a Phase II multi-center clinical trial after a development period of merely three months, and preliminary evaluation results show that OnWARD exceeded expectations of the clinical investigators in efficiency, flexibility and ease in setting up.
Posted ContentDOI

Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

Alexander G. Bick, +122 more
- 27 Sep 2019 - 
TL;DR: Overall, it is observed that germline genetic variation altering hematopoietic stem cell function and the fidelity of DNA-damage repair increase the likelihood of somatic mutations leading to CHIP.