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  1. 1
    Fetal Physiology and the Transition to Extrauterine Life

    Fetal Physiology and the Transition to Extrauterine Life por Sarah U. Morton, Dara Brodsky

    Publicado em 2016
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  2. 2
    Genomic frontiers in congenital heart disease

    Genomic frontiers in congenital heart disease por Sarah U. Morton, Daniel Quiat, Jonathan G. Seidman, Christine E. Seidman

    Publicado em 2021
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  3. 3
    Thioredoxin is required for S-nitrosation of procaspase-3 and the inhibition of apoptosis in Jurkat cells

    Thioredoxin is required for S-nitrosation of procaspase-3 and the inhibition of apoptosis in Jurkat cells por Douglas A. Mitchell, Sarah U. Morton, Nathaniel B. Fernhoff, Michael A. Marletta

    Publicado em 2007
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  4. 4
    microRNA-138 modulates cardiac patterning during embryonic development

    microRNA-138 modulates cardiac patterning during embryonic development por Sarah U. Morton, Paul Scherz, Kimberly R. Cordes, Kathryn N. Ivey, Didier Y. R. Stainier, Deepak Srivastava

    Publicado em 2008
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  5. 5
    miR-145 and miR-143 regulate smooth muscle cell fate and plasticity

    miR-145 and miR-143 regulate smooth muscle cell fate and plasticity por Kimberly R. Cordes, Neil T. Sheehy, Mark P. White, Emily Berry, Sarah U. Morton, Alecia N. Muth, Ting-Hein Lee, Joseph M. Miano, Kathryn N. Ivey, Deepak Srivastava

    Publicado em 2009
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  6. 6
    miR-126 Regulates Angiogenic Signaling and Vascular Integrity

    miR-126 Regulates Angiogenic Signaling and Vascular Integrity por Jason E. Fish, Massimo Santoro, Sarah U. Morton, Sangho Yu, Ru-Fang Yeh, Joshua D. Wythe, Kathryn N. Ivey, Benoit G. Bruneau, Didier Y. R. Stainier, Deepak Srivastava

    Publicado em 2008
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  7. 7
    <i>AIFM1</i> mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant

    <i>AIFM1</i> mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant por Sarah U. Morton, Sanjay P. Prabhu, Hart G.W. Lidov, Jiahai Shi, Irina Anselm, Catherine A. Brownstein, Matthew N. Bainbridge, Alan H. Beggs, Sara O. Vargas, Pankaj B. Agrawal

    Publicado em 2017
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  8. 8
    Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy

    Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy por André E. Minoche, Claire Horvat, Renée Johnson, Velimir Gayevskiy, Sarah U. Morton, Alexander P. Drew, Kerhan Woo, Aaron L. Statham, Ben Lundie, Richard D. Bagnall, Jodie Ingles, Christopher Semsarian, Jonathan G. Seidman, Christine E. Seidman, Marcel E. Dinger, Mark J. Cowley, Diane Fatkin

    Publicado em 2018
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  9. 9
    Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review

    Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review por Sarah U. Morton, John Christodoulou, Gregory Costain, Francesco Muntoni, Emma Wakeling, Monica H. Wojcik, Courtney E. French, Anna Szuto, James J. Dowling, Ronald D. Cohn, F. Lucy Raymond, Basil T. Darras, David A. Williams, Sebastian Lunke, Zornitza Stark, David H. Rowitch, Pankaj B. Agrawal

    Publicado em 2022
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  10. 10
    Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease

    Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease por Feng Xiao, Xiaoran Zhang, Sarah U. Morton, Seong Won Kim, Youfei Fan, Joshua M. Gorham, Huan Zhang, Paul J. Berkson, Neil Mazumdar, Yangpo Cao, Jian Chen, Jacob Hagen, Xujie Liu, Pingzhu Zhou, Felix Richter, Yufeng Shen, Tarsha Ward, Bruce D. Gelb, Jonathan G. Seidman, Christine E. Seidman, William T. Pu

    Publicado em 2024
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  11. 11
    Paternal-age-related de novo mutations and risk for five disorders

    Paternal-age-related de novo mutations and risk for five disorders por Jacob Taylor, Jean-Christophe Debost, Sarah U. Morton, Emilie M. Wigdor, Henrike Heyne, Dennis Lal, Daniel P. Howrigan, Alex Bloemendal, Janne Tidselbak Larsen, Jack A. Kosmicki, Daniel J. Weiner, Jason Homsy, Jonathan G. Seidman, Christine E. Seidman, Esben Agerbo, John J. McGrath, Preben Bo Mortensen, Liselotte Petersen, Mark J. Daly, Elise Robinson

    Publicado em 2019
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  12. 12
    An ancient founder mutation located between<i>ROBO1</i>and<i>ROBO2</i>is responsible for increased microtia risk in Amerindigenous populations

    An ancient founder mutation located between<i>ROBO1</i>and<i>ROBO2</i>is responsible for increased microtia risk in Amerindigenous populations por Daniel Quiat, Seong Won Kim, Qi Zhang, Sarah U. Morton, Alexandre C. Pereira, Steven R. DePalma, Jon A. L. Willcox, Barbara McDonough, Daniel M. DeLaughter, Joshua M. Gorham, Justin J. Curran, Melissa Tumblin, Yamileth Nicolau, Maria A. Artunduaga, Lourdes Quintanilla‐Dieck, Gabriel Osorno, Luís Serrano, Usama S. Hamdan, Roland D. Eavey, Christine E. Seidman, Jonathan G. Seidman

    Publicado em 2022
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  13. 13
    Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease

    Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease por Sarah U. Morton, Akiko Shimamura, Peter E. Newburger, Alexander R. Opotowsky, Daniel Quiat, Alexandre C. Pereira, Sheng Chih Jin, Michelle Gurvitz, Martina Brueckner, Wendy K. Chung, Yufeng Shen, Daniel Bernstein, Bruce D. Gelb, Anna Giardini, Elizabeth Goldmuntz, Richard W. Kim, Richard P. Lifton, George A. Porter, Deepak Srivastava, Martin Tristani‐Firouzi, Jane W. Newburger, Jonathan G. Seidman, Christine E. Seidman

    Publicado em 2020
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  14. 14
    Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study

    Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study por Emily Griffin, Shannon N. Nees, Sarah U. Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M. Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen King, James F. Cnota, Richard W. Kim, George A. Porter, Martina Brueckner, Christine E. Seidman, Yufeng Shen, Bruce D. Gelb, Elizabeth Goldmuntz, Jane W. Newburger, Amy E. Roberts, Wendy K. Chung

    Publicado em 2023
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  15. 15
    Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery

    Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery por W. Scott Watkins, Edgar J. Hernández, Thomas A. Miller, Nathan R. Blue, Raquel M. Zimmerman, Eric R. Griffiths, Erwin Frise, Daniel Bernstein, Marko T. Boskovski, Martina Brueckner, Wendy K. Chung, J. William Gaynor, Bruce D. Gelb, Elizabeth Goldmuntz, Peter J. Gruber, Jane W. Newburger, Amy E. Roberts, Sarah U. Morton, John E. Mayer, Christine E. Seidman, Jonathan G. Seidman, Yufeng Shen, Michael Wagner, H. Joseph Yost, Mark Yandell, Martin Tristani‐Firouzi

    Publicado em 2025
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  16. 16
    GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm

    GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm por Arun Sharma, Lauren K. Wasson, Jon A. L. Willcox, Sarah U. Morton, Joshua M. Gorham, Daniel M. DeLaughter, Meraj Neyazi, Manuel Schmid, Radhika Agarwal, Min Young Jang, Christopher N. Toepfer, Tarsha Ward, Yuri Kim, Alexandre C. Pereira, Steven R. DePalma, Angela C. Tai, Seong Won Kim, David A. Conner, Daniel Bernstein, Bruce D. Gelb, Wendy K. Chung, Elizabeth Goldmuntz, George A. Porter, Martin Tristani‐Firouzi, Deepak Srivastava, Jonathan G. Seidman, Christine E. Seidman

    Publicado em 2020
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  17. 17
    Author response: GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm

    Author response: GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm por Arun Sharma, Lauren K. Wasson, Jon A. L. Willcox, Sarah U. Morton, Joshua M. Gorham, Daniel M. DeLaughter, Meraj Neyazi, Manuel Schmid, Radhika Agarwal, Min Young Jang, Christopher N. Toepfer, Tarsha Ward, Yuri Kim, Alexandre C. Pereira, Steven R. DePalma, Angela C. Tai, Seong Won Kim, David A. Conner, Daniel Bernstein, Bruce D. Gelb, Wendy K. Chung, Elizabeth Goldmuntz, George A. Porter, Martin Tristani‐Firouzi, Deepak Srivastava, Jonathan G. Seidman, Christine E. Seidman

    Publicado em 2020
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  18. 18
    Transcription factor protein interactomes reveal genetic determinants in heart disease

    Transcription factor protein interactomes reveal genetic determinants in heart disease por Bárbara González‐Terán, Maureen Pittman, Franco Felix, Reuben Thomas, Desmond Richmond-Buccola, Ruth Hüttenhain, Krishna Choudhary, Elisabetta Moroni, Mauro W. Costa, Yu Huang, Arun Padmanabhan, Michael Alexanian, Clara Youngna Lee, Bonnie E.J. Maven, Kaitlen Samse-Knapp, Sarah U. Morton, Michael McGregor, Casey A. Gifford, Jonathan G. Seidman, Christine E. Seidman, Bruce D. Gelb, Giorgio Colombo, Bruce R. Conklin, Brian L. Black, Benoit G. Bruneau, Nevan J. Krogan, Katherine S. Pollard, Deepak Srivastava

    Publicado em 2022
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  19. 19
    Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency

    Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency por Tarsha Ward, Warren Tai, Sarah U. Morton, Francis Impens, Petra Van Damme, Delphi Van Haver, Evy Timmerman, Gabriela Venturini, Kehan Zhang, Min Young Jang, Jon A. L. Willcox, Alireza Haghighi, Bruce D. Gelb, Wendy K. Chung, Elizabeth Goldmuntz, George A. Porter, Richard P. Lifton, Martina Brueckner, H. Joseph Yost, Benoit G. Bruneau, Joshua M. Gorham, Yuri Kim, Alexandre C. Pereira, Jason Homsy, Craig C Benson, Steven R. DePalma, Sylvia Varland, Christopher S. Chen, Thomas Arnesen, Kris Gevaert, Christine E. Seidman, Jonathan G. Seidman

    Publicado em 2021
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  20. 20
    De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease

    De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease por Marko T. Boskovski, Jason Homsy, Meena Nathan, Lynn A. Sleeper, Sarah U. Morton, Kathryn B. Manheimer, Angela C. Tai, Joshua M. Gorham, Matthew Lewis, Michael F. Swartz, George M. Alfieris, Emile Bacha, Mohsen Karimi, David Meyer, Khanh Nguyen, Daniel Bernstein, Angela Romano-Adesman, George A. Porter, Elizabeth Goldmuntz, Wendy K. Chung, Deepak Srivastava, Jonathan R. Kaltman, Martin Tristani‐Firouzi, Richard P. Lifton, Amy E. Roberts, J. William Gaynor, Bruce D. Gelb, Richard Kim, Jonathan G. Seidman, Martina Brueckner, John E. Mayer, Jane W. Newburger, Christine E. Seidman

    Publicado em 2020
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