Mendelian randomization: concepts and scope
RC Richmond, GD Smith - Cold Spring …, 2022 - perspectivesinmedicine.cshlp.org
Mendelian randomization (MR) is a method of studying the causal effects of modifiable
exposures (ie, potential risk factors) on health, social, and economic outcomes using genetic …
exposures (ie, potential risk factors) on health, social, and economic outcomes using genetic …
Genetics of substance use disorders in the era of big data
J Gelernter, R Polimanti - Nature Reviews Genetics, 2021 - nature.com
Substance use disorders (SUDs) are conditions in which the use of legal or illegal
substances, such as nicotine, alcohol or opioids, results in clinical and functional …
substances, such as nicotine, alcohol or opioids, results in clinical and functional …
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Tobacco and alcohol use are leading causes of mortality that influence risk for many
complex diseases and disorders. They are heritable, and etiologically related, behaviors that …
complex diseases and disorders. They are heritable, and etiologically related, behaviors that …
Acetylcholine signaling system in progression of lung cancers
JR Friedman, SD Richbart, JC Merritt, KC Brown… - Pharmacology & …, 2019 - Elsevier
The neurotransmitter acetylcholine (ACh) acts as an autocrine growth factor for human lung
cancer. Several lines of evidence show that lung cancer cells express all of the proteins …
cancer. Several lines of evidence show that lung cancer cells express all of the proteins …
Allosteric modulators of metabotropic glutamate receptors as novel therapeutics for neuropsychiatric disease
DJ Luessen, PJ Conn - Pharmacological Reviews, 2022 - ASPET
Metabotropic glutamate (mGlu) receptors, a family of G-protein-coupled receptors, have
been identified as novel therapeutic targets based on extensive research supporting their …
been identified as novel therapeutic targets based on extensive research supporting their …
Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use
Background Smoking and alcohol use have been associated with common genetic variants
in multiple loci. Rare variants within these loci hold promise in the identification of biological …
in multiple loci. Rare variants within these loci hold promise in the identification of biological …
[HTML][HTML] Identification of susceptibility pathways for the role of chromosome 15q25. 1 in modifying lung cancer risk
Genome-wide association studies (GWAS) identified the chromosome 15q25. 1 locus as a
leading susceptibility region for lung cancer. However, the pathogenic pathways, through …
leading susceptibility region for lung cancer. However, the pathogenic pathways, through …
[HTML][HTML] Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes
M Dannemann, Y Milaneschi, D Yermakovich… - Translational …, 2022 - nature.com
Despite advances in identifying the genetic basis of psychiatric and neurological disorders,
fundamental questions about their evolutionary origins remain elusive. Here, introgressed …
fundamental questions about their evolutionary origins remain elusive. Here, introgressed …
Specific connections of the interpeduncular subnuclei reveal distinct components of the habenulopeduncular pathway
The habenulopeduncular pathway consists of the medial habenula (MHb), its output tract,
the fasciculus retroflexus, and its principal target, the interpeduncular nucleus (IP). Several …
the fasciculus retroflexus, and its principal target, the interpeduncular nucleus (IP). Several …
Evidence for genetic correlations and bidirectional, causal effects between smoking and sleep behaviors
Introduction Cigarette smokers are at increased risk of poor sleep behaviors. However, it is
largely unknown whether these associations are due to shared (genetic) risk factors and/or …
largely unknown whether these associations are due to shared (genetic) risk factors and/or …