Nicotine withdrawal

I McLaughlin, JA Dani, M De Biasi - The Neuropharmacology of Nicotine …, 2015 - Springer
An aversive abstinence syndrome manifests 4–24 h following cessation of chronic use of
nicotine-containing products. Symptoms peak on approximately the 3rd day and taper off …

Human genetics of addiction: new insights and future directions

DB Hancock, CA Markunas, LJ Bierut… - Current psychiatry …, 2018 - Springer
Abstract Purpose of Review With the advent of the genome-wide association study (GWAS),
our understanding of the genetics of addiction has made significant strides forward. Here …

Coding variants in TREM2 increase risk for Alzheimer's disease

SC Jin, BA Benitez, CM Karch, B Cooper… - Human molecular …, 2014 - academic.oup.com
The triggering receptor expressed on myeloid 2 (TREM2) is an immune phagocytic receptor
expressed on brain microglia known to trigger phagocytosis and regulate the inflammatory …

The genetics of substance dependence

JC Wang, M Kapoor, AM Goate - Annual review of genomics …, 2012 - annualreviews.org
A large segment of the population suffers from addiction to alcohol, smoking, or illicit drugs.
Not only do substance abuse and addiction pose a threat to health, but the consequences of …

Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use

DM Brazel, Y Jiang, JM Hughey, V Turcot, X Zhan… - Biological …, 2019 - Elsevier
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 …

Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis

MB Harms, J Cady, C Zaidman, P Cooper, T Bali… - Neurobiology of …, 2013 - Elsevier
Hexanucleotide repeat expansions in C9ORF72 are a common cause of familial and
apparently sporadic amyotrophic lateral sclerosis (ALS) and frontal temporal dementia …

Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American …

SC Jin, P Pastor, B Cooper, S Cervantes… - Alzheimer's research & …, 2012 - Springer
Abstract Introduction Some familial Alzheimer's disease (AD) cases are caused by rare and
highly-penetrant mutations in APP, PSEN1, and PSEN2. Mutations in GRN and MAPT, two …

The contribution of rare and common variants in 30 genes to risk nicotine dependence

J Yang, S Wang, Z Yang, CA Hodgkinson… - Molecular …, 2015 - nature.com
Genetic and functional studies have revealed that both common and rare variants of several
nicotinic acetylcholine receptor subunits are associated with nicotine dependence (ND). In …

Nicotinic acetylcholine receptors: upregulation, age‐related effects and associations with drug use

WE Melroy‐Greif, JA Stitzel… - Genes, Brain and …, 2016 - Wiley Online Library
Nicotinic acetylcholine receptors are ligand‐gated ion channels that exogenously bind
nicotine. Nicotine produces rewarding effects by interacting with these receptors in the …

Contribution of Variants in CHRNA5/A3/B4 Gene Cluster on Chromosome 15 to Tobacco Smoking: From Genetic Association to Mechanism

L Wen, K Jiang, W Yuan, W Cui, MD Li - Molecular neurobiology, 2016 - Springer
Cigarette smoking is the major cause of preventable death and morbidity throughout the
world. Many compounds are present in tobacco, but nicotine is the primary addictive one …