Papers authored by Christine Seidman
Refreshing results…
2020
Monika Litviňuková,
Carlos Talavera-López 
,
Henrike Maatz,
Daniel Reichart,
Catherine L. Worth ,
Eric L. Lindberg,
Masatoshi Kanda ,
Krzysztof Polanski ,
Matthias Heinig ,
Michael Lee ,
Emily R. Nadelmann,
Kenny Roberts ,
Liz Tuck,
Eirini S. Fasouli,
Daniel M. DeLaughter
and 18 other authors
,
Henrike Maatz,
Daniel Reichart,
Catherine L. Worth ,
Eric L. Lindberg,
Masatoshi Kanda ,
Krzysztof Polanski ,
Matthias Heinig ,
Michael Lee ,
Emily R. Nadelmann,
Kenny Roberts ,
Liz Tuck,
Eirini S. Fasouli,
Daniel M. DeLaughter
and 18 other authors
Cells of the adult human heart
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Akl C. Fahed,
Georges Nemer ,
Fadi F. Bitar ,
Samir Arnaout,
Antoine B. Abchee ,
Manal Batrawi,
Athar Khalil,
Oussama Abou-Hassan ,
Steven R. DePalma ,
Barbara McDonough ,
Mariam T. Arabi,
James S. Ware ,
Jonathan G. Seidman ,
Christine E. Seidman
,
Fadi F. Bitar ,
Samir Arnaout,
Antoine B. Abchee ,
Manal Batrawi,
Athar Khalil,
Oussama Abou-Hassan ,
Steven R. DePalma ,
Barbara McDonough ,
Mariam T. Arabi,
James S. Ware ,
Jonathan G. Seidman ,
Christine E. Seidman
Founder Mutation in N-terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy
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Felix Richter ,
Sarah U. Morton ,
Seong Won Kim,
Alexander Kitaygorodsky,
Lauren K. Wasson ,
Kathleen M. Chen ,
Jian Zhou ,
Hongjian Qi,
Nihir Patel ,
Steven R. DePalma ,
Michael Parfenov,
Jason Homsy,
Joshua M. Gorham,
Kathryn B. Manheimer,
Matthew Velinder
and 20 other authors
,
Sarah U. Morton ,
Seong Won Kim,
Alexander Kitaygorodsky,
Lauren K. Wasson ,
Kathleen M. Chen ,
Jian Zhou ,
Hongjian Qi,
Nihir Patel ,
Steven R. DePalma ,
Michael Parfenov,
Jason Homsy,
Joshua M. Gorham,
Kathryn B. Manheimer,
Matthew Velinder
and 20 other authors
Genomic analyses implicate noncoding de novo variants in congenital heart disease
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2019
W. Scott Watkins,
E. Javier Hernandez,
Sergiusz Wesolowski ,
Brent W. Bisgrove ,
Ryan T. Sunderland,
Edwin Lin,
Gordon Lemmon ,
Bradley L. Demarest ,
Thomas A. Miller,
Daniel Bernstein ,
Martina Brueckner ,
Wendy K. Chung,
Bruce D. Gelb ,
Elizabeth Goldmuntz ,
Jane W. Newburger
and 5 other authors
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,
Brent W. Bisgrove ,
Ryan T. Sunderland,
Edwin Lin,
Gordon Lemmon ,
Bradley L. Demarest ,
Thomas A. Miller,
Daniel Bernstein ,
Martina Brueckner ,
Wendy K. Chung,
Bruce D. Gelb ,
Elizabeth Goldmuntz ,
Jane W. Newburger
and 5 other authors
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Emilie M. Wigdor ,
Jacob L. Taylor,
Daniel J. Weiner,
Jean-Christophe P. G. Debost,
Debost Jp,
Sarah U. Morton ,
Morton Su,
Henrike O. Heyne,
Wigdor Em,
Daniel P. Howrigan,
Heyne Ho,
Dennis Lal,
Janne T. Larsen ,
Alex Bloemendal,
Howrigan Dp
and 15 other authors
,
Jacob L. Taylor,
Daniel J. Weiner,
Jean-Christophe P. G. Debost,
Debost Jp,
Sarah U. Morton ,
Morton Su,
Henrike O. Heyne,
Wigdor Em,
Daniel P. Howrigan,
Heyne Ho,
Dennis Lal,
Janne T. Larsen ,
Alex Bloemendal,
Howrigan Dp
and 15 other authors
Paternal-age-related de novo mutations and risk for five disorders
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Jason D. Roh ,
Ryan Hobson ,
Vinita Chaudhari ,
Pablo Quintero,
Ashish Yeri,
Mark Benson ,
Chunyang Xiao,
Daniel Zlotoff ,
Vassilios Bezzerides,
Nicholas Houstis,
Colin Platt,
Federico Damilano,
Brian R. Lindman,
Sammy Elmariah ,
Michael Biersmith
and 7 other authors
,
Ryan Hobson ,
Vinita Chaudhari ,
Pablo Quintero,
Ashish Yeri,
Mark Benson ,
Chunyang Xiao,
Daniel Zlotoff ,
Vassilios Bezzerides,
Nicholas Houstis,
Colin Platt,
Federico Damilano,
Brian R. Lindman,
Sammy Elmariah ,
Michael Biersmith
and 7 other authors
Activin type II receptor signaling in cardiac aging and heart failure
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Christopher N. Toepfer ,
Hiroko Wakimoto ,
Amanda C. Garfinkel ,
Barbara McDonough ,
Dan Liao,
Jianming Jiang ,
Angela C. Tai,
Joshua M. Gorham ,
Ida G. Lunde ,
Mingyue Lun,
Thomas L. Lynch ,
James W. McNamara ,
Sakthivel Sadayappan,
Charles S. Redwood ,
Hugh C. Watkins
and 2 other authors
,
Hiroko Wakimoto ,
Amanda C. Garfinkel ,
Barbara McDonough ,
Dan Liao,
Jianming Jiang ,
Angela C. Tai,
Joshua M. Gorham ,
Ida G. Lunde ,
Mingyue Lun,
Thomas L. Lynch ,
James W. McNamara ,
Sakthivel Sadayappan,
Charles S. Redwood ,
Hugh C. Watkins
and 2 other authors
Hypertrophic cardiomyopathy mutations in MYBPC3 dysregulate myosin
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2018
Yuxuan Guo ,
Pingzhu Zhou,
Blake D. Jardin ,
Isha Sethi,
Brynn N. Akerberg,
Christopher N. Toepfer ,
Yulan Ai,
Donghui Zhang,
Yifei Li ,
Qing Ma,
Guo-Cheng Yuan ,
Silvia Guatimosim ,
Yongwu Hu,
Nathan J. VanDusen ,
Grigor Varuzhanyan
and 4 other authors
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,
Pingzhu Zhou,
Blake D. Jardin ,
Isha Sethi,
Brynn N. Akerberg,
Christopher N. Toepfer ,
Yulan Ai,
Donghui Zhang,
Yifei Li ,
Qing Ma,
Guo-Cheng Yuan ,
Silvia Guatimosim ,
Yongwu Hu,
Nathan J. VanDusen ,
Grigor Varuzhanyan
and 4 other authors
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Alex C. Y. Chang ,
Andrew C. H. Chang,
Anna Kirillova ,
Koki Sasagawa,
Willis Su,
Gerhard Weber,
Jue Lin,
Vittavat Termglinchan,
Ioannis Karakikes ,
Timon Seeger,
Alexandra M. Dainis,
John T. Hinson,
Jonathan Seidman,
Christine E. Seidman ,
John W. Day
and 3 other authors
,
Andrew C. H. Chang,
Anna Kirillova ,
Koki Sasagawa,
Willis Su,
Gerhard Weber,
Jue Lin,
Vittavat Termglinchan,
Ioannis Karakikes ,
Timon Seeger,
Alexandra M. Dainis,
John T. Hinson,
Jonathan Seidman,
Christine E. Seidman ,
John W. Day
and 3 other authors
Telomere shortening is a hallmark of genetic cardiomyopathies
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