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Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.

Roselli C, Yu M, Nauffal V et al.

35245370 PubMed ID
GWAS Study Type
439533 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

RC
Roselli C
YM
Yu M
NV
Nauffal V
GA
Georges A
YQ
Yang Q
LK
Love K
WL
Weng LC
DF
Delling FN
MS
Maurya SR
SM
Schrölkamp M
TJ
Tfelt-Hansen J
HA
Hagège A
JX
Jeunemaitre X
DS
Debette S
AP
Amouyel P
GW
Guan W
MJ
Muehlschlegel JD
BS
Body SC
SS
Shah S
SZ
Samad Z
KS
Kyryachenko S
HC
Haynes C
RM
Rienstra M
LT
Le Tourneau T
PV
Probst V
RR
Roussel R
WH
Wijdh-Den Hamer IJ
SJ
Siland JE
KK
Knowlton KU
JS
Jacques Schott J
LR
Levine RA
BE
Benjamin EJ
VR
Vasan RS
HB
Horne BD
MJ
Muhlestein JB
BG
Benfari G
EM
Enriquez-Sarano M
NA
Natale A
MS
Mohanty S
TC
Trivedi C
SM
Shoemaker MB
YZ
Yoneda ZT
WQ
Wells QS
BM
Baker MT
FE
Farber-Eger E
MH
Michelena HI
LA
Lundby A
NR
Norris RA
SS
Slaugenhaupt SA
DC
Dina C
LS
Lubitz SA
BN
Bouatia-Naji N
EP
Ellinor PT
MD
Milan DJ
Chapter II

Abstract

Summary of the research findings

Aims: Mitral valve prolapse (MVP) is a common valvular heart disease with a prevalence of >2% in the general adult population. Despite this high incidence, there is a limited understanding of the molecular mechanism of this disease, and no medical therapy is available for this disease. We aimed to elucidate the genetic basis of MVP in order to better understand this complex disorder.

4,884 European ancestry cases, 434,649 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

439533
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K., Australia, France, Germany
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

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