Menu
GWAS Study

Genetic diversity fuels gene discovery for tobacco and alcohol use.

Saunders GRB, Wang X, Chen F et al.

36477530 PubMed ID
GWAS Study Type
119589 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SG
Saunders GRB
WX
Wang X
CF
Chen F
JS
Jang SK
LM
Liu M
WC
Wang C
GS
Gao S
JY
Jiang Y
KC
Khunsriraksakul C
OJ
Otto JM
AC
Addison C
AM
Akiyama M
AC
Albert CM
AF
Aliev F
AA
Alonso A
AD
Arnett DK
AA
Ashley-Koch AE
AA
Ashrani AA
BK
Barnes KC
BR
Barr RG
BT
Bartz TM
BD
Becker DM
BL
Bielak LF
BE
Benjamin EJ
BJ
Bis JC
BG
Bjornsdottir G
BJ
Blangero J
BE
Bleecker ER
BJ
Boardman JD
BE
Boerwinkle E
BD
Boomsma DI
BM
Boorgula MP
BD
Bowden DW
BJ
Brody JA
CB
Cade BE
CD
Chasman DI
CS
Chavan S
CY
Chen YI
CZ
Chen Z
CI
Cheng I
CM
Cho MH
CH
Choquet H
CJ
Cole JW
CM
Cornelis MC
CF
Cucca F
CJ
Curran JE
DA
de Andrade M
DD
Dick DM
DA
Docherty AR
DR
Duggirala R
EC
Eaton CB
EM
Ehringer MA
ET
Esko T
FJ
Faul JD
FS
Fernandes Silva L
FE
Fiorillo E
FM
Fornage M
FB
Freedman BI
GM
Gabrielsen ME
GM
Garrett ME
GS
Gharib SA
GC
Gieger C
GN
Gillespie N
GD
Glahn DC
GS
Gordon SD
GC
Gu CC
GD
Gu D
GD
Gudbjartsson DF
GX
Guo X
HJ
Haessler J
HM
Hall ME
HT
Haller T
HK
Harris KM
HJ
He J
HP
Herd P
HJ
Hewitt JK
HI
Hickie I
HB
Hidalgo B
HJ
Hokanson JE
HC
Hopfer C
HJ
Hottenga J
HL
Hou L
HH
Huang H
HY
Hung YJ
HD
Hunter DJ
HK
Hveem K
HS
Hwang SJ
HC
Hwu CM
IW
Iacono W
IM
Irvin MR
JY
Jee YH
JE
Johnson EO
JY
Joo YY
JE
Jorgenson E
JA
Justice AE
KY
Kamatani Y
KR
Kaplan RC
KJ
Kaprio J
KS
Kardia SLR
KM
Keller MC
KT
Kelly TN
KC
Kooperberg C
KT
Korhonen T
KP
Kraft P
KK
Krauter K
KJ
Kuusisto J
LM
Laakso M
LJ
Lasky-Su J
LW
Lee WJ
LJ
Lee JJ
LD
Levy D
LL
Li L
LK
Li K
LY
Li Y
LK
Lin K
LP
Lind PA
LC
Liu C
LD
Lloyd-Jones DM
LS
Lutz SM
MJ
Ma J
MR
Mägi R
MA
Manichaikul A
MN
Martin NG
MR
Mathur R
MN
Matoba N
MP
McArdle PF
MM
McGue M
MM
McQueen MB
MS
Medland SE
MA
Metspalu A
MD
Meyers DA
MI
Millwood IY
MB
Mitchell BD
MK
Mohlke KL
MM
Moll M
MM
Montasser ME
MA
Morrison AC
MA
Mulas A
NJ
Nielsen JB
NK
North KE
OE
Oelsner EC
OY
Okada Y
OV
Orrù V
PN
Palmer ND
PT
Palviainen T
PA
Pandit A
PS
Park SL
PU
Peters U
PA
Peters A
PP
Peyser PA
PT
Polderman TJC
RN
Rafaels N
RS
Redline S
RR
Reed RM
RA
Reiner AP
RJ
Rice JP
RS
Rich SS
RN
Richmond NE
RC
Roan C
RJ
Rotter JI
RM
Rueschman MN
RV
Runarsdottir V
SN
Saccone NL
SD
Schwartz DA
SA
Shadyab AH
SJ
Shi J
SS
Shringarpure SS
SK
Sicinski K
SA
Skogholt AH
SJ
Smith JA
SN
Smith NL
SN
Sotoodehnia N
SM
Stallings MC
SH
Stefansson H
SK
Stefansson K
SJ
Stitzel JA
SX
Sun X
SM
Syed M
TR
Tal-Singer R
TA
Taylor AE
TK
Taylor KD
TM
Telen MJ
TK
Thai KK
TH
Tiwari H
TC
Turman C
TT
Tyrfingsson T
WT
Wall TL
WR
Walters RG
WD
Weir DR
WS
Weiss ST
WW
White WB
WJ
Whitfield JB
WK
Wiggins KL
WG
Willemsen G
WC
Willer CJ
WB
Winsvold BS
XH
Xu H
YL
Yanek LR
YJ
Yin J
YK
Young KL
YK
Young KA
YB
Yu B
ZW
Zhao W
ZW
Zhou W
ZS
Zöllner S
ZL
Zuccolo L
BC
Batini C
BA
Bergen AW
BL
Bierut LJ
DS
David SP
GT
Gagliano Taliun SA
HD
Hancock DB
JB
Jiang B
MM
Munafò MR
TT
Thorgeirsson TE
LD
Liu DJ
VS
Vrieze S
Chapter II

Abstract

Summary of the research findings

Tobacco and alcohol use are heritable behaviours associated with 15% and 5.3% of worldwide deaths, respectively, due largely to broad increased risk for disease and injury1-4. These substances are used across the globe, yet genome-wide association studies have focused largely on individuals of European ancestries5. Here we leveraged global genetic diversity across 3.4 million individuals from four major clines of global ancestry (approximately 21% non-European) to power the discovery and fine-mapping of genomic loci associated with tobacco and alcohol use, to inform function of these loci via ancestry-aware transcriptome-wide association studies, and to evaluate the genetic architecture and predictive power of polygenic risk within and across populations. We found that increases in sample size and genetic diversity improved locus identification and fine-mapping resolution, and that a large majority of the 3,823 associated variants (from 2,143 loci) showed consistent effect sizes across ancestry dimensions. However, polygenic risk scores developed in one ancestry performed poorly in others, highlighting the continued need to increase sample sizes of diverse ancestries to realize any potential benefit of polygenic prediction.

119,589 African ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

119589
Total Participants
GWAS
Study Type
No
Replicated
African unspecified, Hispanic or Latin American, East Asian, European
Ancestry
U.S., China, Japan, Australia
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.