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Author Details

Jonathan G Seidman
Harvard Medical School
1973
579
136
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
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
37961405Short-term Pre-operative Methionine Restriction Induces Browning of Perivascular Adipose Tissue and Improves Vein Graft Remodeling in Mice.bioRxiv2023
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
37254794Missense Mutation in Human CHD4 Causes Ventricular Noncompaction by Repressing ADAMTS1.Circ Res2023
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
37961405Short-term Pre-operative Methionine Restriction Induces Browning of Perivascular Adipose Tissue and Improves Vein Graft Remodeling in Mice.bioRxiv2023
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
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
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
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
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
35787042Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model.Proc Natl Acad Sci U S A2022
35536239Population Prevalence of Premature Truncating Variants in Plakophilin-2 and Association With Arrhythmogenic Right Ventricular Cardiomyopathy: A UK Biobank Analysis.Circ Genom Precis Med2022
36577774Mechanism based therapies enable personalised treatment of hypertrophic cardiomyopathy.Sci Rep2022
34272501Genomic frontiers in congenital heart disease.Nat Rev Cardiol2022
35182466Transcription factor protein interactomes reveal genetic determinants in heart disease.Cell2022
35130025Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity.Circ Genom Precis Med2022
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Collaborators

Christine E Seidman
Brigham and Women's Hospital (Y.K.
Co-authored papers 378
Steven R DePalma
Co-authored papers 48
Diane Fatkin
Co-authored papers 23
Hugh Watkins
Co-authored papers 22
Danos C Christodoulou
University of Patras
Co-authored papers 18
Calum A MacRae
Harvard Medical School and Cardiovascular Division, Brigham and Women's Hospital
Co-authored papers 18
Bruce D Gelb
Icahn School of Medicine at Mount Sinai
Co-authored papers 18
Sarah U Morton
Boston Children's Hospital
Co-authored papers 17
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 16
Benoit G Bruneau
Gladstone Institutes of Cardiovascular Disease, Gladstone Institutes
Co-authored papers 15
Elizabeth Goldmuntz
Co-authored papers 15
Martina Brueckner
Co-authored papers 14
Stuart A Cook
Co-authored papers 14
Amy E Roberts
Boston Children's Hospital, Harvard Medical School
Co-authored papers 14
Michael Parfenov
Harvard Medical School, Brigham and Women's Hospital
Co-authored papers 14
William T Pu
Boston Children's Hospital, Harvard Medical School
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Cornelis Murre
University of California
Co-authored papers 13
Alexandre C Pereira
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Jochen D Muehlschlegel
Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 12
Daniel S Herman
University of Pennsylvania
Co-authored papers 12
Raju Kucherlapati
Harvard Medical School
Co-authored papers 12
James S Ware
Co-authored papers 11
Alexander G Bick
Co-authored papers 11
Thomas Quertermous
Co-authored papers 11
George A Porter
Co-authored papers 10
Heidi L Rehm
The Broad Institute of MIT and Harvard
Co-authored papers 10
Richard Kim
Co-authored papers 10
Jane W Newburger
Boston Children's Hospital
Co-authored papers 10
Martin R Pollak
Co-authored papers 10
Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers 9
Release 1.2