The genetic epidemiology of substance use disorder: A review

EC Prom-Wormley, J Ebejer, DM Dick… - Drug and alcohol …, 2017 - Elsevier
Background Substance use disorder (SUD) remains a significant public health issue. A
greater understanding of how genes and environment interact to regulate phenotypes …

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 …

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

M Liu, Y Jiang, R Wedow, Y Li, DM Brazel, F Chen… - Nature …, 2019 - nature.com
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 …

Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis

S Sigurdsson, KF Alexandersson, P Sulem… - Nature …, 2017 - nature.com
Diverticular disease is characterized by pouches (that is, diverticulae) due to weakness in
the bowel wall, which can become infected and inflamed causing diverticulitis, with …

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence

DB Hancock, Y Guo, GW Reginsson, NC Gaddis… - Molecular …, 2018 - nature.com
Cigarette smoking is a leading cause of preventable mortality worldwide. Nicotine
dependence, which reduces the likelihood of quitting smoking, is a heritable trait with firmly …

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 …

Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

DB Hancock, GW Reginsson, NC Gaddis… - Translational …, 2015 - nature.com
We conducted a 1000 Genomes–imputed genome-wide association study (GWAS) meta-
analysis for nicotine dependence, defined by the Fagerström Test for Nicotine Dependence …

Gene-based burden tests of rare germline variants identify six cancer susceptibility genes

EV Ivarsdottir, J Gudmundsson, V Tragante… - Nature Genetics, 2024 - nature.com
Discovery of cancer risk variants in the sequence of the germline genome can shed light on
carcinogenesis. Here we describe gene burden association analyses, aggregating rare …

The role of pharmacogenetics in smoking

A El‐Boraie, RF Tyndale - Clinical Pharmacology & …, 2021 - Wiley Online Library
Smoking continues to be the leading preventable contributor to death worldwide. Twin
studies have suggested a significant genetic contribution underlying most smoking …

Neuropeptide systems and new treatments for nicotine addiction

AW Bruijnzeel - Psychopharmacology, 2017 - Springer
Rationale The mildly euphoric and cognitive enhancing effects of nicotine play a role in the
initiation of smoking, while dysphoria and anxiety associated with smoking cessation …