Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

10.1371/journal.pone.0172995

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Main Authors:	Esslinger U., Garnier S., Korniat A., Proust C., Kararigas G., Müller-Nurasyid M., Empana J.-P., Morley M.P., Perret C., Stark K., Bick A.G., Prasad S.K., Kriebel J., Li J., Tiret L., Strauch K., O'Regan D.P., Marguiles K.B., Seidman J.G., Boutouyrie P., Lacolley P., Jouven X., Hengstenberg C., Komajda M., Hakonarson H., Isnard R., Arbustini E., Grallert H., Cook S.A., Seidman C.E., Regitz-Zagrosek V., Cappola T.P., Charron P., Cambien F., Villard E.
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	2019
Subjects:	ALPK3 gene Article BAG3 gene computer model congestive cardiomyopathy controlled study exome female FHOD3 gene FLNC gene gene gene expression gene function gene identification gene locus gene mapping gene mutation genetic susceptibility genome-wide association study genotype HSPB7 gene human human cell human tissue major clinical study male missense mutation MLIP gene population research single nucleotide polymorphism SLC39A8 gene TTN gene ZBTB17 gene genetic predisposition genetics Cardiomyopathy, Dilated Exome Genetic Predisposition to Disease Humans Mutation, Missense Polymorphism, Single Nucleotide
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/161526
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1615262023-10-31T08:43:26Z Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy Esslinger U. Garnier S. Korniat A. Proust C. Kararigas G. Müller-Nurasyid M. Empana J.-P. Morley M.P. Perret C. Stark K. Bick A.G. Prasad S.K. Kriebel J. Li J. Tiret L. Strauch K. O'Regan D.P. Marguiles K.B. Seidman J.G. Boutouyrie P. Lacolley P. Jouven X. Hengstenberg C. Komajda M. Hakonarson H. Isnard R. Arbustini E. Grallert H. Cook S.A. Seidman C.E. Regitz-Zagrosek V. Cappola T.P. Charron P. Cambien F. Villard E. DUKE-NUS MEDICAL SCHOOL ALPK3 gene Article BAG3 gene computer model congestive cardiomyopathy controlled study exome female FHOD3 gene FLNC gene gene gene expression gene function gene identification gene locus gene mapping gene mutation genetic susceptibility genome-wide association study genotype HSPB7 gene human human cell human tissue major clinical study male missense mutation MLIP gene population research single nucleotide polymorphism SLC39A8 gene TTN gene ZBTB17 gene congestive cardiomyopathy genetic predisposition genetics Cardiomyopathy, Dilated Exome Genetic Predisposition to Disease Humans Mutation, Missense Polymorphism, Single Nucleotide 10.1371/journal.pone.0172995 PLoS ONE 12 3 e0172995 2019-11-06T07:39:52Z 2019-11-06T07:39:52Z 2017 Article Esslinger U., Garnier S., Korniat A., Proust C., Kararigas G., Müller-Nurasyid M., Empana J.-P., Morley M.P., Perret C., Stark K., Bick A.G., Prasad S.K., Kriebel J., Li J., Tiret L., Strauch K., O'Regan D.P., Marguiles K.B., Seidman J.G., Boutouyrie P., Lacolley P., Jouven X., Hengstenberg C., Komajda M., Hakonarson H., Isnard R., Arbustini E., Grallert H., Cook S.A., Seidman C.E., Regitz-Zagrosek V., Cappola T.P., Charron P., Cambien F., Villard E. (2017). Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy. PLoS ONE 12 (3) : e0172995. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0172995 19326203 https://scholarbank.nus.edu.sg/handle/10635/161526 CC0 1.0 Universal http://creativecommons.org/publicdomain/zero/1.0/ Unpaywall 20191101
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	ALPK3 gene Article BAG3 gene computer model congestive cardiomyopathy controlled study exome female FHOD3 gene FLNC gene gene gene expression gene function gene identification gene locus gene mapping gene mutation genetic susceptibility genome-wide association study genotype HSPB7 gene human human cell human tissue major clinical study male missense mutation MLIP gene population research single nucleotide polymorphism SLC39A8 gene TTN gene ZBTB17 gene congestive cardiomyopathy genetic predisposition genetics Cardiomyopathy, Dilated Exome Genetic Predisposition to Disease Humans Mutation, Missense Polymorphism, Single Nucleotide
spellingShingle	ALPK3 gene Article BAG3 gene computer model congestive cardiomyopathy controlled study exome female FHOD3 gene FLNC gene gene gene expression gene function gene identification gene locus gene mapping gene mutation genetic susceptibility genome-wide association study genotype HSPB7 gene human human cell human tissue major clinical study male missense mutation MLIP gene population research single nucleotide polymorphism SLC39A8 gene TTN gene ZBTB17 gene congestive cardiomyopathy genetic predisposition genetics Cardiomyopathy, Dilated Exome Genetic Predisposition to Disease Humans Mutation, Missense Polymorphism, Single Nucleotide Esslinger U. Garnier S. Korniat A. Proust C. Kararigas G. Müller-Nurasyid M. Empana J.-P. Morley M.P. Perret C. Stark K. Bick A.G. Prasad S.K. Kriebel J. Li J. Tiret L. Strauch K. O'Regan D.P. Marguiles K.B. Seidman J.G. Boutouyrie P. Lacolley P. Jouven X. Hengstenberg C. Komajda M. Hakonarson H. Isnard R. Arbustini E. Grallert H. Cook S.A. Seidman C.E. Regitz-Zagrosek V. Cappola T.P. Charron P. Cambien F. Villard E. Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
description	10.1371/journal.pone.0172995
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL Esslinger U. Garnier S. Korniat A. Proust C. Kararigas G. Müller-Nurasyid M. Empana J.-P. Morley M.P. Perret C. Stark K. Bick A.G. Prasad S.K. Kriebel J. Li J. Tiret L. Strauch K. O'Regan D.P. Marguiles K.B. Seidman J.G. Boutouyrie P. Lacolley P. Jouven X. Hengstenberg C. Komajda M. Hakonarson H. Isnard R. Arbustini E. Grallert H. Cook S.A. Seidman C.E. Regitz-Zagrosek V. Cappola T.P. Charron P. Cambien F. Villard E.
format	Article
author	Esslinger U. Garnier S. Korniat A. Proust C. Kararigas G. Müller-Nurasyid M. Empana J.-P. Morley M.P. Perret C. Stark K. Bick A.G. Prasad S.K. Kriebel J. Li J. Tiret L. Strauch K. O'Regan D.P. Marguiles K.B. Seidman J.G. Boutouyrie P. Lacolley P. Jouven X. Hengstenberg C. Komajda M. Hakonarson H. Isnard R. Arbustini E. Grallert H. Cook S.A. Seidman C.E. Regitz-Zagrosek V. Cappola T.P. Charron P. Cambien F. Villard E.
author_sort	Esslinger U.
title	Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
title_short	Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
title_full	Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
title_fullStr	Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
title_full_unstemmed	Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
title_sort	exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
publishDate	2019
url	https://scholarbank.nus.edu.sg/handle/10635/161526
_version_	1781791781270061056

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

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