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Jonathan G. Seidman, Ph.D.

Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics
LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart.
Authors: Authors: Alcalai R, Arad M, Wakimoto H, Yadin D, Gorham J, Wang L, Burns E, Maron BJ, Roberts WC, Konno T, Conner DA, Perez-Atayde AR, Seidman JG, Seidman CE.
J Am Heart Assoc
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Contribution of Noncanonical Splice Variants to TTN Truncating Variants Cardiomyopathy.
Authors: Authors: Patel PN, Ito K, Willcox JAL, Haghighi A, Jang MY, Gorham JM, DePalma SR, Lam L, McDonough B, Johnson R, Lakdawala NK, Roberts A, Barton PJR, Cook SA, Fatkin D, Seidman CE, Seidman JG.
Circ Genom Precis Med
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Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation.
Authors: Authors: Agarwal R, Paulo J, Toepfer CN, Ewoldt JK, Sundaram S, Chopra A, Zhang Q, Gorham J, DePalma S, Chen CS, Gygi S, Seidman CE, Seidman JG.
Circ Res
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Genomic frontiers in congenital heart disease.
Authors: Authors: Morton SU, Quiat D, Seidman JG, Seidman CE.
Nat Rev Cardiol
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CalTrack: High-Throughput Automated Calcium Transient Analysis in Cardiomyocytes.
Authors: Authors: Psaras Y, Margara F, Cicconet M, Sparrow AJ, Repetti GG, Schmid M, Steeples V, Wilcox JAL, Bueno-Orovio A, Redwood CS, Watkins HC, Robinson P, Rodriguez B, Seidman JG, Seidman CE, Toepfer CN.
Circ Res
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Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy.
Authors: Authors: Goli R, Li J, Brandimarto J, Levine LD, Riis V, McAfee Q, DePalma S, Haghighi A, Seidman JG, Seidman CE, Jacoby D, Macones G, Judge DP, Rana S, Margulies KB, Cappola TP, Alharethi R, Damp J, Hsich E, Elkayam U, Sheppard R, Alexis JD, Boehmer J, Kamiya C, Gustafsson F, Damm P, Ersbøll AS, Goland S, Hilfiker-Kleiner D, McNamara DM, Arany Z.
Circulation
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Isolation of Nuclei from Mammalian Cells and Tissues for Single-Nucleus Molecular Profiling.
Authors: Authors: Nadelmann ER, Gorham JM, Reichart D, Delaughter DM, Wakimoto H, Lindberg EL, Litvinukova M, Maatz H, Curran JJ, Ischiu Gutierrez D, Hübner N, Seidman CE, Seidman JG.
Curr Protoc
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Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency.
Authors: Authors: Ward T, Tai W, Morton S, Impens F, Van Damme P, Van Haver D, Timmerman E, Venturini G, Zhang K, Jang MY, Willcox JAL, Haghighi A, Gelb BD, Chung WK, Goldmuntz E, Porter GA, Lifton RP, Brueckner M, Yost HJ, Bruneau BG, Gorham J, Kim Y, Pereira A, Homsy J, Benson CC, DePalma SR, Varland S, Chen CS, Arnesen T, Gevaert K, Seidman C, Seidman JG.
Circ Res
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Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease.
Authors: Authors: Morton SU, Shimamura A, Newburger PE, Opotowsky AR, Quiat D, Pereira AC, Jin SC, Gurvitz M, Brueckner M, Chung WK, Shen Y, Bernstein D, Gelb BD, Giardini A, Goldmuntz E, Kim RW, Lifton RP, Porter GA, Srivastava D, Tristani-Firouzi M, Newburger JW, Seidman JG, Seidman CE.
JAMA Cardiol
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Author Correction: poly(UG)-tailed RNAs in genome protection and epigenetic inheritance.
Authors: Authors: Shukla A, Yan J, Pagano DJ, Dodson AE, Fei Y, Gorham J, Seidman JG, Wickens M, Kennedy S.
Nature
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