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Author Details

Christine E Seidman
Brigham and Women's Hospital (Y.K.
1975
469
127
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36260083Damaging variants in FOXI3 cause microtia and craniofacial microsomia.Genet Med2023
36260083Damaging variants in FOXI3 cause microtia and craniofacial microsomia.Genet Med2023
38038666The H2Bub1-deposition complex is required for human and mouse cardiogenesis.Development2023
37672268Cardiac Remodeling in Subclinical Hypertrophic Cardiomyopathy: The VANISH Randomized Clinical Trial.JAMA Cardiol2023
37671549DMD-Associated Dilated Cardiomyopathy: Genotypes, Phenotypes, and Phenocopies.Circ Genom Precis Med2023
37572991Effect of pharmacological heart failure drugs and gene therapy on Danon's cardiomyopathy.Biochem Pharmacol2023
37767697Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation.Circ Genom Precis Med2023
36902152Multi-Omics Profiling of Hypertrophic Cardiomyopathy Reveals Altered Mechanisms in Mitochondrial Dynamics and Excitation-Contraction Coupling.Int J Mol Sci2023
36778386Structural variation across 138,134 samples in the TOPMed consortium.Res Sq2023
36709791mTOR signaling inhibition decreases lysosome migration and impairs the success of Trypanosoma cruzi infection and replication in cardiomyocytes.Acta Trop2023
36638792Loss of epigenetic information as a cause of mammalian aging.Cell2023
36814444Cardiomyocyte infection by <i>Trypanosoma cruzi</i> promotes innate immune response and glycolysis activation.Front Cell Infect Microbiol2023
37131696<i>Tbx5</i> maintains atrial identity by regulating an atrial enhancer network.bioRxiv2023
36701153Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease.JAMA Netw Open2023
37254794Missense Mutation in Human CHD4 Causes Ventricular Noncompaction by Repressing ADAMTS1.Circ Res2023
36999957Transforming Growth Factor-β Analysis of the VANISH Trial Cohort.Circ Heart Fail2023
36803080Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study.Circ Genom Precis Med2023
36747810Structural variation across 138,134 samples in the TOPMed consortium.bioRxiv2023
36797483Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice.Nat Med2023
37165897Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease.Circ Genom Precis Med2023
37671549DMD-Associated Dilated Cardiomyopathy: Genotypes, Phenotypes, and Phenocopies.Circ Genom Precis Med2023
37572991Effect of pharmacological heart failure drugs and gene therapy on Danon's cardiomyopathy.Biochem Pharmacol2023
38038666The H2Bub1-deposition complex is required for human and mouse cardiogenesis.Development2023
37767697Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation.Circ Genom Precis Med2023
37672268Cardiac Remodeling in Subclinical Hypertrophic Cardiomyopathy: The VANISH Randomized Clinical Trial.JAMA Cardiol2023
37254794Missense Mutation in Human CHD4 Causes Ventricular Noncompaction by Repressing ADAMTS1.Circ Res2023
37165897Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease.Circ Genom Precis Med2023
37131696<i>Tbx5</i> maintains atrial identity by regulating an atrial enhancer network.bioRxiv2023
36999957Transforming Growth Factor-β Analysis of the VANISH Trial Cohort.Circ Heart Fail2023
36814444Cardiomyocyte infection by <i>Trypanosoma cruzi</i> promotes innate immune response and glycolysis activation.Front Cell Infect Microbiol2023
36747810Structural variation across 138,134 samples in the TOPMed consortium.bioRxiv2023
36778386Structural variation across 138,134 samples in the TOPMed consortium.Res Sq2023
36803080Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study.Circ Genom Precis Med2023
36709791mTOR signaling inhibition decreases lysosome migration and impairs the success of Trypanosoma cruzi infection and replication in cardiomyocytes.Acta Trop2023
36638792Loss of epigenetic information as a cause of mammalian aging.Cell2023
36902152Multi-Omics Profiling of Hypertrophic Cardiomyopathy Reveals Altered Mechanisms in Mitochondrial Dynamics and Excitation-Contraction Coupling.Int J Mol Sci2023
36797483Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice.Nat Med2023
36701153Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease.JAMA Netw Open2023
34272501Genomic frontiers in congenital heart disease.Nat Rev Cardiol2022
35397206Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk.Am J Hum Genet2022
35656974Myocardial Iron Deficiency and Mitochondrial Dysfunction in Advanced Heart Failure in Humans.J Am Heart Assoc2022
35452278Engineering a living cardiac pump on a chip using high-precision fabrication.Sci Adv2022
35584116An ancient founder mutation located between <i>ROBO1</i> and <i>ROBO2</i> is responsible for increased microtia risk in Amerindigenous populations.Proc Natl Acad Sci U S A2022
36286606Multiplexed Single-Nucleus RNA Sequencing Using Lipid-Oligo Barcodes.Curr Protoc2022
36027926Autophagy guided interventions to modify the cardiac phenotype of Danon disease.Biochem Pharmacol2022
36215317Genome-wide association study for Chagas Cardiomyopathy identify a new risk locus on chromosome 18 associated with an immune-related protein and transcriptional signature.PLoS Negl Trop Dis2022
35873155Different Transcriptomic Response to <i>T. cruzi</i> Infection in hiPSC-Derived Cardiomyocytes From Chagas Disease Patients With and Without Chronic Cardiomyopathy.Front Cell Infect Microbiol2022
35926050Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies.Science2022
35358500Genetics of cancer therapy-associated cardiotoxicity.J Mol Cell Cardiol2022
36321451Pathogenesis of Cardiomyopathy Caused by Variants in <i>ALPK3</i>, an Essential Pseudokinase in the Cardiomyocyte Nucleus and Sarcomere.Circulation2022
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Collaborators

Jonathan G Seidman
Harvard Medical School
Co-authored papers 378
Steven R DePalma
Co-authored papers 47
Calum A MacRae
Harvard Medical School and Cardiovascular Division, Brigham and Women's Hospital
Co-authored papers 26
Bruce D Gelb
Icahn School of Medicine at Mount Sinai
Co-authored papers 24
Diane Fatkin
Co-authored papers 23
Hugh Watkins
Co-authored papers 23
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 22
Martina Brueckner
Co-authored papers 19
Elizabeth Goldmuntz
Co-authored papers 19
Sarah U Morton
Boston Children's Hospital
Co-authored papers 19
Amy E Roberts
Boston Children's Hospital, Harvard Medical School
Co-authored papers 18
Alexandre C Pereira
Co-authored papers 18
Benoit G Bruneau
Gladstone Institutes of Cardiovascular Disease, Gladstone Institutes
Co-authored papers 15
Stuart A Cook
Co-authored papers 15
George A Porter
Co-authored papers 14
Heidi L Rehm
The Broad Institute of MIT and Harvard
Co-authored papers 14
Jeffrey A Towbin
University of Tennessee Health Science Center
Co-authored papers 13
Richard Kim
Co-authored papers 13
Jane W Newburger
Boston Children's Hospital
Co-authored papers 13
James S Ware
Co-authored papers 13
Danos C Christodoulou
University of Patras
Co-authored papers 12
Steven D Colan
Boston Children's Hospital, Harvard Medical School
Co-authored papers 11
Alexander G Bick
Co-authored papers 11
Daniel S Herman
University of Pennsylvania
Co-authored papers 11
Richard P Lifton
The Rockefeller University
Co-authored papers 11
William T Pu
Boston Children's Hospital, Harvard Medical School
Co-authored papers 11
Jochen D Muehlschlegel
Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 10
Martin Tristani-Firouzi
Co-authored papers 10
Michael Parfenov
Harvard Medical School, Brigham and Women's Hospital
Co-authored papers 10
Martin R Pollak
Co-authored papers 10
Release 1.2