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List of shared articles
Times cited
Cost-effectiveness of genome sequencing for diagnosing patients with undiagnosed rare genetic diseases.
Devin Incerti, Xiang-Ming Xu, Jacquelyn W Chou, Nina Gonzaludo, John W Belmont, Brock E Schroeder. Genet Med 2022
Devin Incerti, Xiang-Ming Xu, Jacquelyn W Chou, Nina Gonzaludo, John W Belmont, Brock E Schroeder. Genet Med 2022
Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases.
Bryce A Schuler, Erica T Nelson, Mary Koziura, Joy D Cogan, Rizwan Hamid, John A Phillips. J Clin Invest 2022
Bryce A Schuler, Erica T Nelson, Mary Koziura, Joy D Cogan, Rizwan Hamid, John A Phillips. J Clin Invest 2022
Best practices for the interpretation and reporting of clinical whole genome sequencing.
Christina A Austin-Tse, Vaidehi Jobanputra, Denise L Perry, David Bick, Ryan J Taft, Eric Venner, Richard A Gibbs, Ted Young, Sarah Barnett, John W Belmont,[...]. NPJ Genom Med 2022
Christina A Austin-Tse, Vaidehi Jobanputra, Denise L Perry, David Bick, Ryan J Taft, Eric Venner, Richard A Gibbs, Ted Young, Sarah Barnett, John W Belmont,[...]. NPJ Genom Med 2022
Cost-effectiveness of exome and genome sequencing for children with rare and undiagnosed conditions.
Tara A Lavelle, Xue Feng, Marlena Keisler, Joshua T Cohen, Peter J Neumann, Daryl Prichard, Brock E Schroeder, Daria Salyakina, Paula S Espinal, Samuel B Weidner,[...]. Genet Med 2022
Tara A Lavelle, Xue Feng, Marlena Keisler, Joshua T Cohen, Peter J Neumann, Daryl Prichard, Brock E Schroeder, Daria Salyakina, Paula S Espinal, Samuel B Weidner,[...]. Genet Med 2022
Emerging technologies for prenatal diagnosis: The application of whole genome and RNA sequencing.
Pengfei Liu, Liesbeth Vossaert. Prenat Diagn 2022
Pengfei Liu, Liesbeth Vossaert. Prenat Diagn 2022
Real-world economic evaluation of prospective rapid whole-genome sequencing compared to a matched retrospective cohort of critically ill pediatric patients in the United States.
Vakaramoko Diaby, Aram Babcock, Yushi Huang, Richard K Moussa, Paula S Espinal, Michelin Janvier, Diana Soler, Apeksha Gupta, Parul Jayakar, Magaly Diaz-Barbosa,[...]. Pharmacogenomics J 2022
Vakaramoko Diaby, Aram Babcock, Yushi Huang, Richard K Moussa, Paula S Espinal, Michelin Janvier, Diana Soler, Apeksha Gupta, Parul Jayakar, Magaly Diaz-Barbosa,[...]. Pharmacogenomics J 2022
Genetic testing for unexplained perinatal disorders.
Thomas Hays, Ronald J Wapner. Curr Opin Pediatr 2021
Thomas Hays, Ronald J Wapner. Curr Opin Pediatr 2021
Application of Full-Spectrum Rapid Clinical Genome Sequencing Improves Diagnostic Rate and Clinical Outcomes in Critically Ill Infants in the China Neonatal Genomes Project.
Bingbing Wu, Wenqing Kang, Yingyuan Wang, Deyi Zhuang, Liping Chen, Long Li, Yajie Su, Xinnian Pan, Qiufen Wei, Zezhong Tang,[...]. Crit Care Med 2021
Bingbing Wu, Wenqing Kang, Yingyuan Wang, Deyi Zhuang, Liping Chen, Long Li, Yajie Su, Xinnian Pan, Qiufen Wei, Zezhong Tang,[...]. Crit Care Med 2021
Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).
Kandamurugu Manickam, Monica R McClain, Laurie A Demmer, Sawona Biswas, Hutton M Kearney, Jennifer Malinowski, Lauren J Massingham, Danny Miller, Timothy W Yu, Fuki M Hisama. Genet Med 2021
Kandamurugu Manickam, Monica R McClain, Laurie A Demmer, Sawona Biswas, Hutton M Kearney, Jennifer Malinowski, Lauren J Massingham, Danny Miller, Timothy W Yu, Fuki M Hisama. Genet Med 2021
The diagnostic trajectory of infants and children with clinical features of genetic disease.
Brock E Schroeder, Nina Gonzaludo, Katie Everson, Kyi-Sin Than, Jeff Sullivan, Ryan J Taft, John W Belmont. NPJ Genom Med 2021
Brock E Schroeder, Nina Gonzaludo, Katie Everson, Kyi-Sin Than, Jeff Sullivan, Ryan J Taft, John W Belmont. NPJ Genom Med 2021
Optimized trio genome sequencing (OTGS) as a first-tier genetic test in critically ill infants: practice in China.
Huijun Wang, Yulan Lu, Xinran Dong, Guoping Lu, Guoqiang Cheng, Yanyan Qian, Qi Ni, Ping Zhang, Lin Yang, Bingbing Wu,[...]. Hum Genet 2020
Huijun Wang, Yulan Lu, Xinran Dong, Guoping Lu, Guoqiang Cheng, Yanyan Qian, Qi Ni, Ping Zhang, Lin Yang, Bingbing Wu,[...]. Hum Genet 2020
Genome-Wide Sequencing for Unexplained Developmental Disabilities or Multiple Congenital Anomalies: A Health Technology Assessment.
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Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature.
Hadley Stevens Smith, J Michael Swint, Seema R Lalani, Jose-Miguel Yamal, Marcia C de Oliveira Otto, Stephan Castellanos, Amy Taylor, Brendan H Lee, Heidi V Russell. Genet Med 2019
Hadley Stevens Smith, J Michael Swint, Seema R Lalani, Jose-Miguel Yamal, Marcia C de Oliveira Otto, Stephan Castellanos, Amy Taylor, Brendan H Lee, Heidi V Russell. Genet Med 2019
Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?
Jan M Friedman, Yvonne Bombard, Martina C Cornel, Conrad V Fernandez, Anne K Junker, Sharon E Plon, Zornitza Stark, Bartha Maria Knoppers. Genet Med 2019
Jan M Friedman, Yvonne Bombard, Martina C Cornel, Conrad V Fernandez, Anne K Junker, Sharon E Plon, Zornitza Stark, Bartha Maria Knoppers. Genet Med 2019
Clinical genome sequencing in an unbiased pediatric cohort.
Isabelle Thiffault, Emily Farrow, Lee Zellmer, Courtney Berrios, Neil Miller, Margaret Gibson, Raymond Caylor, Janda Jenkins, Deb Faller, Sarah Soden,[...]. Genet Med 2019
Isabelle Thiffault, Emily Farrow, Lee Zellmer, Courtney Berrios, Neil Miller, Margaret Gibson, Raymond Caylor, Janda Jenkins, Deb Faller, Sarah Soden,[...]. Genet Med 2019
Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019