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GWAS Study

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.

Okbay A, Baselmans BM, De Neve JE et al.

27089181 PubMed ID
GWAS Study Type
298420 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

OA
Okbay A
BB
Baselmans BM
DN
De Neve JE
TP
Turley P
NM
Nivard MG
FM
Fontana MA
MS
Meddens SF
LR
Linnér RK
RC
Rietveld CA
DJ
Derringer J
GJ
Gratten J
LJ
Lee JJ
LJ
Liu JZ
DV
de Vlaming R
AT
Ahluwalia TS
BJ
Buchwald J
CA
Cavadino A
FA
Frazier-Wood AC
FN
Furlotte NA
GV
Garfield V
GM
Geisel MH
GJ
Gonzalez JR
HS
Haitjema S
KR
Karlsson R
VD
van der Laan SW
LK
Ladwig KH
LJ
Lahti J
VD
van der Lee SJ
LP
Lind PA
LT
Liu T
ML
Matteson L
ME
Mihailov E
MM
Miller MB
MC
Minica CC
NI
Nolte IM
MD
Mook-Kanamori D
VD
van der Most PJ
OC
Oldmeadow C
QY
Qian Y
RO
Raitakari O
RR
Rawal R
RA
Realo A
RR
Rueedi R
SB
Schmidt B
SA
Smith AV
SE
Stergiakouli E
TT
Tanaka T
TK
Taylor K
TG
Thorleifsson G
WJ
Wedenoja J
WJ
Wellmann J
WH
Westra HJ
WS
Willems SM
ZW
Zhao W
AN
Amin N
BA
Bakshi A
BS
Bergmann S
BG
Bjornsdottir G
BP
Boyle PA
CS
Cherney S
CS
Cox SR
DG
Davies G
DO
Davis OS
DJ
Ding J
DN
Direk N
EP
Eibich P
ER
Emeny RT
FG
Fatemifar G
FJ
Faul JD
FL
Ferrucci L
FA
Forstner AJ
GC
Gieger C
GR
Gupta R
HT
Harris TB
HJ
Harris JM
HE
Holliday EG
HJ
Hottenga JJ
DJ
De Jager PL
KM
Kaakinen MA
KE
Kajantie E
KV
Karhunen V
KI
Kolcic I
KM
Kumari M
LL
Launer LJ
FL
Franke L
LR
Li-Gao R
LD
Liewald DC
KM
Koini M
LA
Loukola A
MP
Marques-Vidal P
MG
Montgomery GW
MM
Mosing MA
PL
Paternoster L
PA
Pattie A
PK
Petrovic KE
PL
Pulkki-Råback L
QL
Quaye L
RK
Räikkönen K
RI
Rudan I
SR
Scott RJ
SJ
Smith JA
SA
Sutin AR
TM
Trzaskowski M
VA
Vinkhuyzen AE
YL
Yu L
ZD
Zabaneh D
AJ
Attia JR
BD
Bennett DA
BK
Berger K
BL
Bertram L
BD
Boomsma DI
SH
Snieder H
CS
Chang SC
CF
Cucca F
DI
Deary IJ
VD
van Duijn CM
EJ
Eriksson JG
BU
Bültmann U
DG
de Geus EJ
GP
Groenen PJ
GV
Gudnason V
HT
Hansen T
HC
Hartman CA
HC
Haworth CM
HC
Hayward C
HA
Heath AC
HD
Hinds DA
HE
Hyppönen E
IW
Iacono WG
JM
Järvelin MR
JK
Jöckel KH
KJ
Kaprio J
KS
Kardia SL
KL
Keltikangas-Järvinen L
KP
Kraft P
KL
Kubzansky LD
LT
Lehtimäki T
MP
Magnusson PK
MN
Martin NG
MM
McGue M
MA
Metspalu A
MM
Mills M
DM
de Mutsert R
OA
Oldehinkel AJ
PG
Pasterkamp G
PN
Pedersen NL
PR
Plomin R
PO
Polasek O
PC
Power C
RS
Rich SS
RF
Rosendaal FR
DR
den Ruijter HM
SD
Schlessinger D
SH
Schmidt H
SR
Svento R
SR
Schmidt R
AB
Alizadeh BZ
ST
Sørensen TI
ST
Spector TD
SJ
Starr JM
SK
Stefansson K
SA
Steptoe A
TA
Terracciano A
TU
Thorsteinsdottir U
TA
Thurik AR
TN
Timpson NJ
TH
Tiemeier H
UA
Uitterlinden AG
VP
Vollenweider P
WG
Wagner GG
WD
Weir DR
YJ
Yang J
CD
Conley DC
SG
Smith GD
HA
Hofman A
JM
Johannesson M
LD
Laibson DI
MS
Medland SE
MM
Meyer MN
PJ
Pickrell JK
ET
Esko T
KR
Krueger RF
BJ
Beauchamp JP
KP
Koellinger PD
BD
Benjamin DJ
BM
Bartels M
CD
Cesarini D
Chapter II

Abstract

Summary of the research findings

Very few genetic variants have been associated with depression and neuroticism, likely because of limitations on sample size in previous studies. Subjective well-being, a phenotype that is genetically correlated with both of these traits, has not yet been studied with genome-wide data. We conducted genome-wide association studies of three phenotypes: subjective well-being (n = 298,420), depressive symptoms (n = 161,460), and neuroticism (n = 170,911). We identify 3 variants associated with subjective well-being, 2 variants associated with depressive symptoms, and 11 variants associated with neuroticism, including 2 inversion polymorphisms. The two loci associated with depressive symptoms replicate in an independent depression sample. Joint analyses that exploit the high genetic correlations between the phenotypes (|ρ^| ≈ 0.8) strengthen the overall credibility of the findings and allow us to identify additional variants. Across our phenotypes, loci regulating expression in central nervous system and adrenal or pancreas tissues are strongly enriched for association.

298,420 Korculan (founder/genetic isolate), Split (founder/genetic isolate), Vis (founder/genetic isolate), Erasmus Rucphen (founder/genetic isolate) and other European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

298420
Total Participants
GWAS
Study Type
Yes
Replicated
368,890 European ancestry individuals
Replication Participants
European
Ancestry
Finland, Sweden, U.S., Australia, Iceland, Italy, Netherlands, Germany, U.K., Croatia, Switzerland, Estonia, Austria, Denmark
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

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