Hasil Pencarian - Stephanie M. Ware

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  1. 1
    Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us

    Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us oleh Stephanie M. Ware

    Diterbitkan 2024-01-01
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  2. 2
    The Current Landscape of Genetic Testing in Cardiovascular Malformations: Opportunities and Challenges

    The Current Landscape of Genetic Testing in Cardiovascular Malformations: Opportunities and Challenges oleh Benjamin John Landis, Stephanie M Ware

    Diterbitkan 2016-07-01
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  3. 3
    Septal contributions to olfactory bulb interneuron diversity in the embryonic mouse telencephalon: role of the homeobox gene Gsx2

    Septal contributions to olfactory bulb interneuron diversity in the embryonic mouse telencephalon: role of the homeobox gene Gsx2 oleh Shenyue Qin, Stephanie M. Ware, Ronald R. Waclaw, Kenneth Campbell

    Diterbitkan 2017-08-01
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  4. 4
    Identification of a novel ZIC3 isoform and mutation screening in patients with heterotaxy and congenital heart disease.

    Identification of a novel ZIC3 isoform and mutation screening in patients with heterotaxy and congenital heart disease. oleh James E J Bedard, Allison M Haaning, Stephanie M Ware

    Diterbitkan 2011-01-01
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  5. 5
    Persistent left superior vena cava: an overlooked feature of CHARGE syndrome?

    Persistent left superior vena cava: an overlooked feature of CHARGE syndrome? oleh Paula Goldenberg, Amy Shikany, Ashley Parrott, Stephanie M. Ware, Robert B. Hinton

    Diterbitkan 2015-12-01
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  6. 6
    Targeted capture and massively parallel sequencing in pediatric cardiomyopathy: development of novel diagnostics

    Targeted capture and massively parallel sequencing in pediatric cardiomyopathy: development of novel diagnostics oleh Muhammad Tariq, Thanh-Tam Le, Patrick Putnam, Steven Kindel, Mehdi Keddache, Stephanie M. Ware

    Diterbitkan 2012-05-01
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  7. 7
    Cardiac electrical system involvement in Alström syndrome: uncommon causes of dilated cardiomyopathies

    Cardiac electrical system involvement in Alström syndrome: uncommon causes of dilated cardiomyopathies oleh Richard J. Czosek, Paula Goldenberg, Erin M. Miller, Robert Spicer, Jeffrey A. Towbin, Stephanie M. Ware

    Diterbitkan 2012-01-01
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  8. 8
    Single cell RNA analysis of the left–right organizer transcriptome reveals potential novel heterotaxy genes

    Single cell RNA analysis of the left–right organizer transcriptome reveals potential novel heterotaxy genes oleh Helen M. Bellchambers, Amruta R. Phatak, Mardi J. Nenni, Maria B. Padua, Hongyu Gao, Yunlong Liu, Stephanie M. Ware

    Diterbitkan 2023-07-01
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  9. 9
    Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling

    Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling oleh Margaret E. Armstrong, David D. Weaver, Melissa D. Lah, Gail H. Vance, Benjamin J. Landis, Stephanie M. Ware, Benjamin M. Helm

    Diterbitkan 2018-03-01
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  10. 10
    Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach

    Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach oleh Robert B. Hinton, Kim L. McBride, Steven B. Bleyl, Neil E. Bowles, William L. Border, Vidu Garg, Teresa A. Smolarek, Seema R. Lalani, Stephanie M. Ware

    Diterbitkan 2015-04-01
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  11. 11
    Identification of a common polymorphism in COQ8B acting as a modifier of thoracic aortic aneurysm severity

    Identification of a common polymorphism in COQ8B acting as a modifier of thoracic aortic aneurysm severity oleh Benjamin J. Landis, Dongbing Lai, Dong-Chuan Guo, Joel S. Corvera, Muhammad T. Idrees, Henry W. Stadler, Christian Cuevas, Gavin U. Needler, Courtney E. Vujakovich, Dianna M. Milewicz, Robert B. Hinton, Stephanie M. Ware

    Diterbitkan 2022-01-01
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  12. 12
    Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease

    Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease oleh Benjamin J. Landis, Benjamin M. Helm, Jeremy L. Herrmann, Madeline C. Hoover, Matthew D. Durbin, Lindsey R. Elmore, Manyan Huang, Michael Johansen, Ming Li, Leon F. Przybylowski, Gabrielle C. Geddes, Stephanie M. Ware

    Diterbitkan 2022-10-01
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  13. 13
    A multi-disciplinary, comprehensive approach to management of children with heterotaxy

    A multi-disciplinary, comprehensive approach to management of children with heterotaxy oleh Thomas G. Saba, Gabrielle C. Geddes, Stephanie M. Ware, David N. Schidlow, Pedro J. del Nido, Nathan S. Rubalcava, Samir K. Gadepalli, Terri Stillwell, Anne Griffiths, Laura M. Bennett Murphy, Andrew T. Barber, Margaret W. Leigh, Necia Sabin, Adam J. Shapiro

    Diterbitkan 2022-09-01
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  14. 14
    A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices

    A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices oleh Matthew D. Durbin, Lindsey R. Helvaty, Ming Li, William Border, Sara Fitzgerald-Butt, Vidu Garg, Gabrielle C. Geddes, Benjamin M. Helm, Seema R. Lalani, Kim L. McBride, Alexis McEntire, Dana K. Mitchell, Chaya N. Murali, Stephanie B. Wechsler, Benjamin J. Landis, Stephanie M. Ware

    Diterbitkan 2023-01-01
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  15. 15
    A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease

    A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease oleh Benjamin J. Landis, Lindsey R. Helvaty, Gabrielle C. Geddes, Jiuann‐Huey Ivy Lin, Svetlana A. Yatsenko, Cecilia W. Lo, William L. Border, Stephanie Burns Wechsler, Chaya N. Murali, Mahshid S. Azamian, Seema R. Lalani, Robert B. Hinton, Vidu Garg, Kim L. McBride, Jennelle C. Hodge, Stephanie M. Ware

    Diterbitkan 2023-09-01
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  16. 16
    Progressive Left Ventricular Remodeling for Predicting Mortality in Children With Dilated Cardiomyopathy: The Pediatric Cardiomyopathy Registry

    Progressive Left Ventricular Remodeling for Predicting Mortality in Children With Dilated Cardiomyopathy: The Pediatric Cardiomyopathy Registry oleh Paul F. Kantor, Ling Shi, Steven D. Colan, E. John Orav, James D. Wilkinson, Taye H. Hamza, Steven A. Webber, Charles E. Canter, Jeffrey A. Towbin, Melanie D. Everitt, Elfriede Pahl, Stephanie M. Ware, Paolo G. Rusconi, Jacqueline M. Lamour, John L. Jefferies, Linda J. Addonizio, Steven E. Lipshultz

    Diterbitkan 2024-01-01
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  17. 17
    DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.

    DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia. oleh You Li, Hisato Yagi, Ezenwa Obi Onuoha, Rama Rao Damerla, Richard Francis, Yoshiyuki Furutani, Muhammad Tariq, Stephen M King, Gregory Hendricks, Cheng Cui, Manush Saydmohammed, Dong Min Lee, Maliha Zahid, Iman Sami, Linda Leatherbury, Gregory J Pazour, Stephanie M Ware, Toshio Nakanishi, Elizabeth Goldmuntz, Michael Tsang, Cecilia W Lo

    Diterbitkan 2016-02-01
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  18. 18
    Case Report: An association of left ventricular outflow tract obstruction with 5p deletions

    Case Report: An association of left ventricular outflow tract obstruction with 5p deletions oleh Kira Mascho, Svetlana A. Yatsenko, Cecilia W. Lo, Xinxiu Xu, Jennifer Johnson, Lindsey R. Helvaty, Stephanie Burns Wechsler, Chaya N. Murali, Seema R. Lalani, Vidu Garg, Jennelle C. Hodge, Kim L. McBride, Kim L. McBride, Stephanie M. Ware, Jiuann-Huey Ivy Lin, Jiuann-Huey Ivy Lin, Jiuann-Huey Ivy Lin

    Diterbitkan 2024-10-01
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  19. 19
    Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study

    Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study oleh Stephanie M. Ware, James D. Wilkinson, Muhammad Tariq, Jeffrey A. Schubert, Arthi Sridhar, Steven D. Colan, Ling Shi, Charles E. Canter, Daphne T. Hsu, Steven A. Webber, Debra A. Dodd, Melanie D. Everitt, Paul F. Kantor, Linda J. Addonizio, John L. Jefferies, Joseph W. Rossano, Elfriede Pahl, Paolo Rusconi, Wendy K. Chung, Teresa Lee, Jeffrey A. Towbin, Ashwin K. Lal, Surbhi Bhatnagar, Bruce Aronow, Phillip J. Dexheimer, Lisa J. Martin, Erin M. Miller, Lynn A. Sleeper, Hiedy Razoky, Jason Czachor, Steven E. Lipshultz

    Diterbitkan 2021-05-01
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