Insomnia is the second most prevalent mental disorder, with no sufficient treatment available. Despite substantial heritability, insight into the associated genes and …
AR Hammerschlag, S Stringer, CA De Leeuw… - Nature …, 2017 - nature.com
Persistent insomnia is among the most frequent complaints in general practice. To identify genetic factors for insomnia complaints, we performed a genome-wide association study …
Insomnia is a worldwide problem with substantial deleterious health effects. Twin studies have shown a heritable basis for various sleep-related traits, including insomnia, but robust …
Excessive daytime sleepiness (EDS) affects 10–20% of the population and is associated with substantial functional deficits. Here, we identify 42 loci for self-reported daytime …
K Watanabe, PR Jansen, JE Savage, P Nandakumar… - Nature …, 2022 - nature.com
Insomnia is a heritable, highly prevalent sleep disorder for which no sufficient treatment currently exists. Previous genome-wide association studies with up to 1.3 million subjects …
This review summarizes current research on the genetics of insomnia, as genetic contributions are thought to be important for insomnia etiology. We begin by providing an …
CORRESPONDENCE of coronary artery disease, HF, and ischemic stroke as a whole, but not AF (Figure). The associations remained in multivariable MR analyses with adjustment for …
HJ Ban, SC Kim, J Seo, HB Kang, JK Choi - PloS one, 2011 - journals.plos.org
Insomnia is reported to chronically affect 10∼ 15% of the adult population. However, very little is known about the genetics and metabolism of insomnia. Here we surveyed 10,038 …