Paper Details

Paper Title

Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in <i>TNNI3</i> and <i>TNNT2</i> That Are Common in Chinese Patients.

Paper Journal Title

Circ Genom Precis Med

Paper Citation Count

Paper Publication Year

2020

Bio Mention

HCM, Hypertrophic Cardiomyopathy, Mutant TNNT2, Patients, R286H, R79C, TNNI3, TNNI3:p.R79C, TNNT2, hypercontractility, hypertrophic cardiomyopathy, iPSC-CMs, induced pluripotent stem cells, induced pluripotent stem cells derived cardiomyocytes, p, p.R286H, p.R79C, patients, thin filament encoding genes

Mesh Descriptor

Author Name	Affiliation
Roddy Walsh	University of Amsterdam
Chiea Chuen Khor	Genome Institute of Singapore (C.C.K.
Charleston W K Chiang	Center for Genetic Epidemiology, University of Southern California (C.W.K.C.).
Charleston W K Chiang	Center for Neurobehavioral Genetics, University of California los angeles
Antonio de Marvao	Cardiovascular Research Center, Royal Brompton Hospital
Antonio de Marvao	National Heart and Lung Institute, Imperial College London
Rachel Buchan	Cardiovascular Research Center, Royal Brompton Hospital
Rachel Buchan	National Heart and Lung Institute, Imperial College London
Paul J R Barton	Cardiovascular Research Center, Royal Brompton Hospital
Paul J R Barton	National Heart and Lung Institute, Imperial College London
Alexandre C Pereira	Harvard Medical School
Alexandre C Pereira	Heart Institute (InCor)-University of Sao Paulo Medical School
Saumya Shekhar Jamuar	Duke-National University of Singapore Medical School (C.W.L.C.
Saumya Shekhar Jamuar	National Heart and Lung Institute, Imperial College London
Saumya Shekhar Jamuar	KK Women's and Children's Hospital
Saumya Shekhar Jamuar
James S Ware	Cardiovascular Research Center, Royal Brompton Hospital
James S Ware	National Heart and Lung Institute, Imperial College London
Jonathan G Seidman	Harvard Medical School
Jonathan G Seidman	Harvard Medical School
Christine E Seidman	Harvard Medical School
Christine E Seidman	Brigham and Women's Hospital, Howard Hughes Medical Institute
Christine E Seidman	Harvard Medical School
Christine E Seidman	Brigham and Women's Hospital, Howard Hughes Medical Institute
Stuart A Cook
Stuart A Cook	Duke-National University of Singapore Medical School (C.W.L.C.
Stuart A Cook	Cardiovascular Research Center, Royal Brompton Hospital
Stuart A Cook	National Heart and Lung Institute, Imperial College London

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

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