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1
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel
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Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel

Genetics in medicine, 2018-03, Vol.20 (3), p.351-359 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2018 ;Copyright © 2018 The Author(s) 2018 The Author(s) ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2017.218 ;PMID: 29300372

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2
Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)
Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)
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Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)

Genetics in medicine, 2019-10, Vol.21 (10), p.2406-2409 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2019. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0521-2

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3
MD2 activation by direct AGE interaction drives inflammatory diabetic cardiomyopathy
MD2 activation by direct AGE interaction drives inflammatory diabetic cardiomyopathy
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MD2 activation by direct AGE interaction drives inflammatory diabetic cardiomyopathy

Nature communications, 2020-05, Vol.11 (1), p.2148-2148, Article 2148 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-15978-3 ;PMID: 32358497

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4
Transthyretin V122I (pV142I) cardiac amyloidosis: an age-dependent autosomal dominant cardiomyopathy too common to be overlooked as a cause of significant heart disease in elderly African Americans
Transthyretin V122I (pV142I) cardiac amyloidosis: an age-dependent autosomal dominant cardiomyopathy too common to be overlooked as a cause of significant heart disease in elderly African Americans
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Transthyretin V122I (pV142I) cardiac amyloidosis: an age-dependent autosomal dominant cardiomyopathy too common to be overlooked as a cause of significant heart disease in elderly African Americans

Genetics in medicine, 2017-07, Vol.19 (7), p.733-742 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2017 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2016.200 ;PMID: 28102864

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5
Broken hearts: Iron overload, ferroptosis and cardiomyopathy
Broken hearts: Iron overload, ferroptosis and cardiomyopathy
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Broken hearts: Iron overload, ferroptosis and cardiomyopathy

Cell research, 2019-04, Vol.29 (4), p.263-264 [Peer Reviewed Journal]

2019© IBCB, SIBS, CAS 2019 ;ISSN: 1001-0602 ;EISSN: 1748-7838 ;DOI: 10.1038/s41422-019-0150-y

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6
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
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Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples

Genetics in medicine, 2017-02, Vol.19 (2), p.192-203 [Peer Reviewed Journal]

2017 The Author(s) ;Copyright Nature Publishing Group Feb 2017 ;Copyright © 2017 Official journal of the American College of Medical Genetics and Genomics 2017 Official journal of the American College of Medical Genetics and Genomics ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2016.90 ;PMID: 27532257

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7
Mitochondrial CaMKII causes adverse metabolic reprogramming and dilated cardiomyopathy
Mitochondrial CaMKII causes adverse metabolic reprogramming and dilated cardiomyopathy
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Mitochondrial CaMKII causes adverse metabolic reprogramming and dilated cardiomyopathy

Nature communications, 2020-09, Vol.11 (1), p.4416-4416, Article 4416 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-18165-6 ;PMID: 32887881

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8
PRMT4 promotes ferroptosis to aggravate doxorubicin-induced cardiomyopathy via inhibition of the Nrf2/GPX4 pathway
PRMT4 promotes ferroptosis to aggravate doxorubicin-induced cardiomyopathy via inhibition of the Nrf2/GPX4 pathway
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PRMT4 promotes ferroptosis to aggravate doxorubicin-induced cardiomyopathy via inhibition of the Nrf2/GPX4 pathway

Cell death and differentiation, 2022-10, Vol.29 (10), p.1982-1995 [Peer Reviewed Journal]

2022. The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare. ;The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare 2022. ;The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare 2022 ;ISSN: 1350-9047 ;EISSN: 1476-5403 ;DOI: 10.1038/s41418-022-00990-5 ;PMID: 35383293

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9
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
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Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy

Nature communications, 2020-05, Vol.11 (1), p.2254-2254, Article 2254 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-15823-7 ;PMID: 32382064

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10
METTL14 suppresses pyroptosis and diabetic cardiomyopathy by downregulating TINCR lncRNA
METTL14 suppresses pyroptosis and diabetic cardiomyopathy by downregulating TINCR lncRNA
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METTL14 suppresses pyroptosis and diabetic cardiomyopathy by downregulating TINCR lncRNA

Cell death & disease, 2022-01, Vol.13 (1), p.38-38, Article 38 [Peer Reviewed Journal]

2021. The Author(s). ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2041-4889 ;EISSN: 2041-4889 ;DOI: 10.1038/s41419-021-04484-z ;PMID: 35013106

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11
Integrated analysis of miRNA-mRNA interaction in pediatric dilated cardiomyopathy
Integrated analysis of miRNA-mRNA interaction in pediatric dilated cardiomyopathy
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Integrated analysis of miRNA-mRNA interaction in pediatric dilated cardiomyopathy

Pediatric research, 2022-07, Vol.92 (1), p.98-108 [Peer Reviewed Journal]

2021. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc. ;The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc 2021. ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-021-01548-w ;PMID: 34012027

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12
Silencing long non-coding RNA Kcnq1ot1 alleviates pyroptosis and fibrosis in diabetic cardiomyopathy
Silencing long non-coding RNA Kcnq1ot1 alleviates pyroptosis and fibrosis in diabetic cardiomyopathy
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Silencing long non-coding RNA Kcnq1ot1 alleviates pyroptosis and fibrosis in diabetic cardiomyopathy

Cell death & disease, 2018-09, Vol.9 (10), p.1000-13, Article 1000 [Peer Reviewed Journal]

2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2041-4889 ;EISSN: 2041-4889 ;DOI: 10.1038/s41419-018-1029-4 ;PMID: 30250027

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13
The genetic architecture of Plakophilin 2 cardiomyopathy
The genetic architecture of Plakophilin 2 cardiomyopathy
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The genetic architecture of Plakophilin 2 cardiomyopathy

Genetics in medicine, 2021-10, Vol.23 (10), p.1961-1968 [Peer Reviewed Journal]

2021 The Author(s) ;2021. The Author(s). ;The Author(s) 2021. corrected publication 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021, corrected publication 2021 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-021-01233-7 ;PMID: 34120153

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14
Phospholamban antisense oligonucleotides improve cardiac function in murine cardiomyopathy
Phospholamban antisense oligonucleotides improve cardiac function in murine cardiomyopathy
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Phospholamban antisense oligonucleotides improve cardiac function in murine cardiomyopathy

Nature communications, 2021-08, Vol.12 (1), p.5180-5180, Article 5180 [Peer Reviewed Journal]

2021. The Author(s). ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-25439-0 ;PMID: 34462437

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15
β-Cardiac myosin hypertrophic cardiomyopathy mutations release sequestered heads and increase enzymatic activity
β-Cardiac myosin hypertrophic cardiomyopathy mutations release sequestered heads and increase enzymatic activity
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β-Cardiac myosin hypertrophic cardiomyopathy mutations release sequestered heads and increase enzymatic activity

Nature communications, 2019-06, Vol.10 (1), p.2685-10, Article 2685 [Peer Reviewed Journal]

2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-10555-9 ;PMID: 31213605

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16
Doxorubicin-induced cardiomyopathy associated with inhibition of autophagic degradation process and defects in mitochondrial respiration
Doxorubicin-induced cardiomyopathy associated with inhibition of autophagic degradation process and defects in mitochondrial respiration
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Doxorubicin-induced cardiomyopathy associated with inhibition of autophagic degradation process and defects in mitochondrial respiration

Scientific reports, 2019-02, Vol.9 (1), p.2002, Article 2002 [Peer Reviewed Journal]

This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-018-37862-3 ;PMID: 30765730

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17
Molecular genetics and pathogenesis of cardiomyopathy
Molecular genetics and pathogenesis of cardiomyopathy
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Molecular genetics and pathogenesis of cardiomyopathy

Journal of human genetics, 2016-01, Vol.61 (1), p.41-50 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jan 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2015.83 ;PMID: 26178429

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18
Disorganization of intercalated discs in dilated cardiomyopathy
Disorganization of intercalated discs in dilated cardiomyopathy
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Disorganization of intercalated discs in dilated cardiomyopathy

Scientific reports, 2021-06, Vol.11 (1), p.11852-11852, Article 11852 [Peer Reviewed Journal]

The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-90502-1 ;PMID: 34088908

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19
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing
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The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing

Genetics in medicine, 2014-08, Vol.16 (8), p.601-608 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2014. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2013.204 ;PMID: 24503780

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20
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
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Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2018-09, Vol.20 (9), p.899-909 [Peer Reviewed Journal]

Copyright Nature Publishing Group Sep 2018 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-018-0039-z ;PMID: 29904160

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