Search Results - Victoria N. Parikh

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  1. 1
    Mutational Scanning and Binding Free Energy Computations of the SARS-CoV-2 Spike Complexes with Distinct Groups of Neutralizing Antibodies: Energetic Drivers of Convergent Evolution of Binding Affinity and Immune Escape Hotspots

    Mutational Scanning and Binding Free Energy Computations of the SARS-CoV-2 Spike Complexes with Distinct Groups of Neutralizing Antibodies: Energetic Drivers of Convergent Evolutio... by Mohammed Alshahrani, Victoria N. Parikh, Brian Foley, Nishank Raisinghani, Gennady M. Verkhivker

    Published 2025
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  2. 2
    Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association

    Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association by Kiran Musunuru, Ray E. Hershberger, Sharlene M. Day, N. Jennifer Klinedinst, Andrew P. Landstrom, Victoria N. Parikh, Siddharth K. Prakash, Christopher Semsarian, Amy C. Sturm

    Published 2020
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  3. 3
    Mislocalization of pathogenic RBM20 variants in dilated cardiomyopathy is caused by loss-of-interaction with Transportin-3

    Mislocalization of pathogenic RBM20 variants in dilated cardiomyopathy is caused by loss-of-interaction with Transportin-3 by Julia Kornienko, Marta Rodríguez‐Martínez, Kai Fenzl, Florian Hinze, Daniel Schraivogel, Markus Grosch, Brigit Tunaj, Dominik Lindenhofer, Laura Schraft, Moritz Kueblbeck, Eric D. Smith, Chad Mao, Emily Brown, Anjali Owens, Ardan M. Saguner, Benjamin Meder, Victoria N. Parikh, Michael Gotthardt, Lars M. Steinmetz

    Published 2023
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  4. 4
    MicroRNA-21 Integrates Pathogenic Signaling to Control Pulmonary Hypertension

    MicroRNA-21 Integrates Pathogenic Signaling to Control Pulmonary Hypertension by Victoria N. Parikh, Richard C. Jin, Sabrina Rabello, Natali Gulbahce, Kevin P. White, Andrew Hale, Katherine A. Cottrill, Rahamthulla S. Shaik, Aaron B. Waxman, Yingyi Zhang, Bradley A. Maron, Jochen C. Hartner, Yuko Fujiwara, Stuart H. Orkin, Kathleen J. Haley, Albert‐László Barabási, Joseph Loscalzo, Stephen Y. Chan

    Published 2012
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  5. 5
    Patient-Specific Induced Pluripotent Stem Cells Implicate Intrinsic Impaired Contractility in Hypoplastic Left Heart Syndrome

    Patient-Specific Induced Pluripotent Stem Cells Implicate Intrinsic Impaired Contractility in Hypoplastic Left Heart Syndrome by Sharon L. Paige, Francisco X. Galdos, Soah Lee, Elizabeth T. Chin, Sara Ranjbarvaziri, Dries Feyen, Adrija Darsha, Sidra Xu, Julia Ryan, Aimee Beck, M. Yasir Qureshi, Yifei Miao, Mingxia Gu, Daniel Bernstein, Timothy J. Nelson, Mark Mercola, Marlene Rabinovitch, Euan A. Ashley, Victoria N. Parikh, Sean M. Wu

    Published 2020
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  6. 6
    Allele-Specific Silencing Ameliorates Restrictive Cardiomyopathy Attributable to a Human Myosin Regulatory Light Chain Mutation

    Allele-Specific Silencing Ameliorates Restrictive Cardiomyopathy Attributable to a Human Myosin Regulatory Light Chain Mutation by Kathia Zaleta-Rivera, Alexandra Dainis, Alexandre J. S. Ribeiro, Pablo Cordero, Gabriel Rubio, Ching Shang, Jing Liu, Thomas Finsterbach, Victoria N. Parikh, Shirley Sutton, Kinya Seo, Nikita Sinha, Nikhil Jain, Yong Huang, Roger J. Hajjar, Mark A. Kay, Danuta Szczesna‐Cordary, Beth L. Pruitt, Matthew T. Wheeler, Euan A. Ashley

    Published 2019
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  7. 7
    Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathy

    Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathy by Victor Nauffal, Peter Marstrand, Larry Han, Victoria N. Parikh, Adam S. Helms, Jodie Ingles, Daniel Jacoby, Neal K. Lakdawala, Sunil Kapur, Michelle Michels, Anjali Owens, Euan A. Ashley, Alexandre C. Pereira, Joseph W. Rossano, Sara Saberi, Christopher Semsarian, James S. Ware, Samuel G. Wittekind, Sharlene M. Day, Iacopo Olivotto, Carolyn Y. Ho

    Published 2021
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  8. 8
    Genetic constraint at single amino acid resolution in protein domains improves missense variant prioritisation and gene discovery

    Genetic constraint at single amino acid resolution in protein domains improves missense variant prioritisation and gene discovery by Xiaolei Zhang, Pantazis Theotokis, Nicholas Li, Euan Ashley, Steven D. Colan, Sharlene M. Day, Adam S. Helms, Carolyn Y. Ho, Jodie Ingles, Daniel Jacoby, Neal K. Lakdawala, Michelle Michels, Iacopo Olivotto, Anjali Owens, Victoria N. Parikh, Alexandre C. Pereira, Joseph Rossano, Sara Saberi, Chris Semsarian, Samuel G. Wittekind, Caroline F. Wright, Kaitlin E. Samocha, Nicola Whiffin, James S Ware

    Published 2024
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  9. 9
    Epistasis regulates genetic control of cardiac hypertrophy

    Epistasis regulates genetic control of cardiac hypertrophy by Qianru Wang, Tiffany M. Tang, Michelle Youlton, Chad S. Weldy, Ana Kenney, Omer Ronen, J. Weston Hughes, Elizabeth T. Chin, Shirley Sutton, Abhineet Agarwal, Xiao Li, Merle Behr, Karl Kumbier, Christine S. Moravec, W.H. Wilson Tang, Kenneth B. Margulies, Thomas P. Cappola, Atul J. Butte, Rima Arnaout, James B. Brown, James R. Priest, Victoria N. Parikh, Bin Yu, Euan A. Ashley

    Published 2025
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  10. 10
    Association of Titin Variations With Late-Onset Dilated Cardiomyopathy

    Association of Titin Variations With Late-Onset Dilated Cardiomyopathy by Antonio Cannatà, Marco Merlo, Matteo Dal Ferro, Giulia Barbati, Paolo Manca, Alessia Paldino, Sharon Graw, Marta Gigli, Davide Stolfo, Renée Johnson, Darius Roy, Kevin Tharratt, Daniel I. Bromage, Jean Jirikowic, Antonio Abbate, Allison Goodwin, Krishnasree Rao, Amr Marawan, Gerry Carr‐White, Leema Robert, Victoria N. Parikh, Euan A. Ashley, Theresa A. McDonagh, Neal K. Lakdawala, Diane Fatkin, Matthew R.G. Taylor, Luisa Mestroni, Gianfranco Sinagra

    Published 2022
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  11. 11
    Sex-Specific Clinical and Genetic Factors Associated with Adverse Outcomes in Hypertrophic Cardiomyopathy

    Sex-Specific Clinical and Genetic Factors Associated with Adverse Outcomes in Hypertrophic Cardiomyopathy by Alexandra Butters, Clare Arnott, J. Sweeting, Brian Claggett, Anna Cuomo, Dominic J. Abrams, Euan A. Ashley, Sharlene M. Day, Adam S. Helms, Rachel Lampert, Kim Lin, Michelle Michels, Erin M. Miller, Iacopo Olivotto, Anjali Owens, Victoria N. Parikh, Alexandre C. Pereira, Joseph W. Rossano, Thomas D. Ryan, Sara Saberi, John C. Stendahl, James S. Ware, J. Atherton, Christopher Semsarian, Neal K. Lakdawala, Carolyn Y. Ho, Jodie Ingles

    Published 2023
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  12. 12
    Vascular stiffness mechanoactivates YAP/TAZ-dependent glutaminolysis to drive pulmonary hypertension

    Vascular stiffness mechanoactivates YAP/TAZ-dependent glutaminolysis to drive pulmonary hypertension by Thomas Bertero, William M. Oldham, Katherine A. Cottrill, Sabrina Pisano, Rebecca Vanderpool, Qiujun Yu, Jingsi Zhao, Yi‐Yin Tai, Ying Tang, Ying-Yi Zhang, Sofiya Rehman, Masataka Sugahara, Zhi Wei Qi, John Gorcsan, Sara O. Vargas, Rajan Saggar, Rajeev Saggar, W. Dean Wallace, David J. Ross, Kathleen J. Haley, Aaron B. Waxman, Victoria N. Parikh, Teresa De Marco, Priscilla Y. Hsue, Alison Morris, Marc A. Simon, Karen A. Norris, Cédric Gaggioli, Joseph Loscalzo, Joshua P. Fessel, Stephen Y. Chan

    Published 2016
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  13. 13
    Regional Variation in <i>RBM20</i> Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy

    Regional Variation in <i>RBM20</i> Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy by Victoria N. Parikh, Colleen Caleshu, Chloe M. Reuter, Laura C. Lazzeroni, Jodie Ingles, John Garcia, Kristen McCaleb, Tolulope Adesiyun, Farbod Sedaghat‐Hamedani, Saurabh Kumar, Sharon Graw, Marta Gigli, Davide Stolfo, Matteo Dal Ferro, Alexander Ing, Robert L. Nussbaum, Birgit H. Funke, Matthew T. Wheeler, Ray E. Hershberger, Stuart A. Cook, Lars M. Steinmetz, Neal K. Lakdawala, Matthew R.G. Taylor, Luisa Mestroni, Marco Merlo, Gianfranco Sinagra, Christopher Semsarian, Benjamin Meder, Daniel P. Judge, Euan A. Ashley

    Published 2019
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  14. 14
    A rare splice-site variant in <i>TNNT2</i>: the need for ancestral diversity in genomic reference data sets

    A rare splice-site variant in <i>TNNT2</i>: the need for ancestral diversity in genomic reference data sets by Alexandra Butters, Kate Thomson, Franki Harrington, Natasha Henden, Karen McGuire, Alicia B. Byrne, Samantha J. Bryen, Kathryn A. McGurk, Megan Leask, Michael J. Ackerman, J. Atherton, J. Martijn Bos, Colleen Caleshu, Sharlene M. Day, Kyla Dunn, Ian Hayes, Jyh‐Ming Jimmy Juang, Julie McGaughran, N. Nowak, Victoria N. Parikh, Anne Ronan, Christopher Semsarian, Jil C. Tardiff, Marianne Tiemensma, Tony R. Merriman, James S. Ware, Jonathan R. Skinner, Daniel G. MacArthur, Owen M. Siggs, Richard D. Bagnall, Jodie Ingles

    Published 2025
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  15. 15
    Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants

    Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants by Marta Gigli, Davide Stolfo, Sharon Graw, Marco Merlo, Caterina Gregorio, Suet Nee Chen, Matteo Dal Ferro, Alessia PaldinoMD, Giulia De Angelis, Francesca Brun, Jean Jirikowic, Ernesto Salcedo, Sylvia Turja, Diane Fatkin, Renée Johnson, J. Peter van Tintelen, Anneline S.J.M. te Riele, Arthur A.M. Wilde, Neal K. Lakdawala, Kermshlise Picard, Daniela Miani, Daniele Muser, Giovanni Maria Severini, Hugh Calkins, Cynthia A. James, Brittney Murray, Crystal Tichnell, Victoria N. Parikh, Euan A. Ashley, Chloe M. Reuter, Jiangping Song, Daniel P. Judge, William J. McKenna, Matthew R.G. Taylor, Gianfranco Sinagra, Luisa Mestroni

    Published 2021
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  16. 16
    Clinical Validity of Autosomal Dominant ALPK3 Loss-of-function Variants as a Cause of Hypertrophic Cardiomyopathy

    Clinical Validity of Autosomal Dominant ALPK3 Loss-of-function Variants as a Cause of Hypertrophic Cardiomyopathy by Sophie Hespe, Emma S. Singer, Chloe M. Reuter, Brittney Murray, Elizabeth Jordan, Jessica L. Chowns, Stacey Peters, Megan Mayers, Belinda Gray, Ray E Hershberger, Anjali Owens, Christopher Semsarian, Amber Waddell, Babken Asatryan, Emma Owens, Courtney Thaxton, Mhy-Lanie Adduru, Kailyn Anderson, Emily Brown, Lily Hoffman‐Andrews, F. Stafford, Richard D. Bagnall, Lucas Bronicki, Bert Callewaert, C. Anwar A. Chahal, Cynthia A. James, Olga Jarinova, Andrew P. Landstrom, Elizabeth M. McNally, Laura Muiño Mosquera, Victoria N. Parikh, Roddy Walsh, Bess Wayburn, James S. Ware, Benjamin L. Parker, Enzo R. Porrello, David A. Elliott, James W. McNamara, Jodie Ingles

    Published 2025
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  17. 17
    Impact of SARS‐Cov‐2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry

    Impact of SARS‐Cov‐2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry by Juan R. Gimeno, Iacopo Olivotto, Ana Isabel Enríquez Rodríguez, Carolyn Y. Ho, Adrián Fernández, Alejandro Quiroga, Mari Angeles Espinosa, Cristina Gómez‐González, M. J. López Robledo, Lucas Tojal‐Sierra, Sharlene M. Day, Anjali Owens, Roberto Barriales‐Villa, José M. Larrañaga‐Moreira, José F. Rodríguez‐Palomares, Maribel González‐Del‐Hoyo, Jesús Piqueras‐Flores, Nosheen Reza, О. С. Чумакова, Euan A. Ashley, Victoria N. Parikh, Matthew T. Wheeler, Daniel Jacoby, Alexandre C. Pereira, Sara Saberi, Adam S. Helms, Eduardo Villacorta, María Gallego‐Delgado, Daniel de Castro, Fernándo Domínguez, Tomás Ripoll‐Vera, Esther Zorio, José Carlos Sánchez Martínez, Ana García‐Álvarez, Elena Arbelo, María V. Mogollón, María Eugenia Fuentes‐Cañamero, Elías Grande, Carlos Peña, Lorenzo Monserrat, Neal K. Lakdawala

    Published 2022
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  18. 18
    Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertension

    Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertension by Yi‐Yin Tai, Qiujun Yu, Ying Tang, Wei Sun, Neil J. Kelly, Satoshi Okawa, Jingsi Zhao, Tae‐Hwi Schwantes‐An, Caroline Lacoux, Stéphanie Torrino, Yassmin Al Aaraj, Wadih El Khoury, Vinny Negi, Mingjun Liu, Catherine Corey, Frances Belmonte, Sara O. Vargas, Brian E. Schwartz, B. Venkatesh Bhat, B. Nelson Chau, Jason H. Karnes, Taijyu Satoh, Robert J. Barndt, Haodi Wu, Victoria N. Parikh, Jianrong Wang, Yingze Zhang, Dennis M. McNamara, Gang Li, Gil Speyer, Bing Wang, Sruti Shiva, Brett A. Kaufman, Seungchan Kim, Delphine Gomez, Bernard Mari, Michael H. Cho, Adel Boueiz, Michael W. Pauciulo, Laura Southgate, Richard C. Trembath, Olivier Sitbon, Marc Humbert, Stefan Gräf, Nicholas W. Morrell, Christopher J. Rhodes, Martin R. Wilkins, Mehdi Nouraie, William C. Nichols, Ankit A. Desai, Thomas Bertero, Stephen Y. Chan

    Published 2024
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  19. 19
    A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers

    A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers by Richard Carrick, Alessio Gasperetti, Alexandros Protonotarios, Brittney Murray, Mikaël Laredo, Iris van der Schaaf, Dennis Dooijes, Petros Syrris, Douglas Cannie, Crystal Tichnell, Nisha A. Gilotra, Chiara Cappelletto, Kristen Medo, Ardan M. Saguner, Fırat Duru, Robyn J. Hylind, Dominic Abrams, Neal K. Lakdawala, Julia Cadrin‐Tourigny, Mattia Targetti, Iacopo Olivotto, Maddalena Graziosi, Moniek G.P.J. Cox, Elena Biagini, Jean‐Philippe Charron, Paolo Compagnucci, Michela Casella, Giulio Conte, Claudio Tondo, Momina Yazdani, J Ware, Sanjay Prasad, Leonardo Calò, Eric D. Smith, Adam S. Helms, Sophie Hespe, Jodie Ingles, Harikrishna Tandri, Flavie Ader, Giovanni Peretto, Stacey Peters, Ari Horton, J. Yao, Eric Schulze‐Bahr, Sven Dittman, Eric Carruth, Katelyn Young, Maria Qureshi, Chris Haggerty, Victoria N. Parikh, Matthew Taylor, Luisa Mestroni, Arthur A.M. Wilde, Gianfranco Sinagra, Marco Merlo, Estelle Gandjbakhch, J. Peter van Tintelen, Anneline S.J.M. te Riele, Perry Elliott, Hugh Calkins, Kathérine C. Wu, Cynthia A James

    Published 2024
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  20. 20
    Clinical features and outcomes in carriers of pathogenic desmoplakin variants

    Clinical features and outcomes in carriers of pathogenic desmoplakin variants by Alessio Gasperetti, Richard Carrick, Alexandros Protonotarios, Brittney Murray, Mikaël Laredo, Iris van der Schaaf, Ronald H Lekanne, Petros Syrris, Douglas Cannie, Crystal Tichnell, Chiara Cappelletto, Marta Gigli, Kristen Medo, Ardan M. Saguner, Fırat Duru, Nisha A. Gilotra, Stefan L. Zimmerman, Robyn J. Hylind, Dominic Abrams, Neal K. Lakdawala, Julia Cadrin‐Tourigny, Mattia Targetti, Iacopo Olivotto, Maddalena Graziosi, Moniek G.P.J. Cox, Elena Biagini, Jean‐Philippe Charron, Michela Casella, Claudio Tondo, Momina Yazdani, James S. Ware, Sanjay Prasad Gupta, Leonardo Calò, Eric D. Smith, Adam S. Helms, Sophie Hespe, Jodie Ingles, Harikrishna Tandri, Flavie Ader, Giovanni Peretto, Stacey Peters, Ari Horton, Jess Yao, Sven Dittmann, Eric Schulze‐Bahr, Maria Qureshi, Katelyn Young, Eric Carruth, Chris Haggerty, Victoria N. Parikh, Matthew R.G. Taylor, Luisa Mestroni, Arthur A.M. Wilde, Gianfranco Sinagra, Marco Merlo, Estelle Gandjbakhch, J Peter van Tintelen, Anneline S.J.M. te Riele, Perry Elliott, Hugh Calkins, Cynthia A James

    Published 2024
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