Stephanie M Ware

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 18

Top Topics

Left Ventricular

Clinical Practice

Top Venues

Journal of the American Heart Association

Scientific reports

Journal of genetic counseling

This page only lists publications with an associated author ORCID identifier.

Publications

Stephanie M Ware
Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us. Journal of the American Heart Association 13 (2) (2024)
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 Lynn Jefferies, Linda J Addonizio, Steven E Lipshultz, null null
Progressive Left Ventricular Remodeling for Predicting Mortality in Children With Dilated Cardiomyopathy: The Pediatric Cardiomyopathy Registry. Journal of the American Heart Association (2024)
Stephanie M Ware
Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us. Journal of the American Heart Association 13 (2) (2024)
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 Lynn Jefferies, Linda J Addonizio, Steven E Lipshultz, null null
Progressive Left Ventricular Remodeling for Predicting Mortality in Children With Dilated Cardiomyopathy: The Pediatric Cardiomyopathy Registry. Journal of the American Heart Association 13 (2) (2024)
Stephanie M Ware
Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us. Journal of the American Heart Association 13 (2) (2024)
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 Lynn Jefferies, Linda J Addonizio, Steven E Lipshultz, null null
Progressive Left Ventricular Remodeling for Predicting Mortality in Children With Dilated Cardiomyopathy: The Pediatric Cardiomyopathy Registry. Journal of the American Heart Association 13 (2) (2024)
Stephanie M Ware
Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us. Journal of the American Heart Association 13 (2) (2024)
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 Lynn Jefferies, Linda J Addonizio, Steven E Lipshultz, null null
Progressive Left Ventricular Remodeling for Predicting Mortality in Children With Dilated Cardiomyopathy: The Pediatric Cardiomyopathy Registry. Journal of the American Heart Association 13 (2) (2024)
Stephanie M Ware
Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us. Journal of the American Heart Association (2024)
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 Lynn Jefferies, Linda J Addonizio, Steven E Lipshultz, null null
Progressive Left Ventricular Remodeling for Predicting Mortality in Children With Dilated Cardiomyopathy: The Pediatric Cardiomyopathy Registry. Journal of the American Heart Association 13 (2) (2024)
Helen M Bellchambers, Amruta R Phatak, Mardi J Nenni, Maria B Padua, Hongyu Gao, Yunlong Liu, Stephanie M Ware
Single cell RNA analysis of the left-right organizer transcriptome reveals potential novel heterotaxy genes. Scientific reports 13 (1) (2023)
Helen M Bellchambers, Amruta R Phatak, Mardi J Nenni, Maria B Padua, Hongyu Gao, Yunlong Liu, Stephanie M Ware
Single cell RNA analysis of the left-right organizer transcriptome reveals potential novel heterotaxy genes. Scientific reports 13 (1) (2023)
Benjamin J Landis, Lindsey R Helvaty, Gabrielle C Geddes, Jiuann-Huey Ivy Lin, Svetlana A Yatsenko, Cecelia 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
A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease. Journal of the American Heart Association (2023)
Sean P Reuter, Mark H Soonpaa, Dorothy Field, Ed Simpson, Michael Rubart, Han Kyu Lee, Arthi Sridhar, Stephanie M Ware, Nick Green, Xiaochun Li, Susan Ofner, Douglas A Marchuk, Kai C Wollert, Loren J Field
Cardiac Troponin I-interacting Kinase Impacts Cardiomyocyte S-phase Activity But Not Cardiomyocyte Proliferation. Circulation (2022)
Allison F Rickman, Sara M Fitzgerald-Butt, Katherine G Spoonamore, Stephanie M Ware, Benjamin M Helm
A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America. Journal of genetic counseling (2022)
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
Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease. Journal of the American Heart Association 11 (19) (2022)
Hannah E Ison, Stephanie M Ware, Tae-Hwi Schwantes-An, Samantha Freeze, Lindsey Elmore, Katherine G Spoonamore
The impact of cardiovascular genetic counseling on patient empowerment. Journal of genetic counseling 28 (3) (2019)
Jeffrey Schubert, Muhammad Tariq, Gabrielle Geddes, Steven Kindel, Erin M Miller, Stephanie M Ware
Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy. Human mutation 39 (12) (2018)