A citation-based method for searching scientific literature

Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Sarah E Soden, Julie A Cakici, Suzanne M Herd, Greyson Twist, Aaron Noll, Mitchell Creed, Patria M Alba, Shannon L Carpenter, Mark A Clements, Ryan T Fischer, J Allyson Hays, Howard Kilbride, Ryan J McDonough, Jamie L Rosterman, Sarah L Tsai, Lee Zellmer, Emily G Farrow, Stephen F Kingsmore. Lancet Respir Med 2015
Times Cited: 207



Anath C Lionel, Gregory Costain, Nasim Monfared, Susan Walker, Miriam S Reuter, S Mohsen Hosseini, Bhooma Thiruvahindrapuram, Daniele Merico, Rebekah Jobling, Thomas Nalpathamkalam, Giovanna Pellecchia, Wilson W L Sung, Zhuozhi Wang, Peter Bikangaga, Cyrus Boelman, Melissa T Carter, Dawn Cordeiro, Cheryl Cytrynbaum, Sharon D Dell, Priya Dhir, James J Dowling, Elise Heon, Stacy Hewson, Linda Hiraki, Michal Inbar-Feigenberg, Regan Klatt, Jonathan Kronick, Ronald M Laxer, Christoph Licht, Heather MacDonald, Saadet Mercimek-Andrews, Roberto Mendoza-Londono, Tino Piscione, Rayfel Schneider, Andreas Schulze, Earl Silverman, Komudi Siriwardena, O Carter Snead, Neal Sondheimer, Joanne Sutherland, Ajoy Vincent, Jonathan D Wasserman, Rosanna Weksberg, Cheryl Shuman, Chris Carew, Michael J Szego, Robin Z Hayeems, Raveen Basran, Dimitri J Stavropoulos, Peter N Ray, Sarah Bowdin, M Stephen Meyn, Ronald D Cohn, Stephen W Scherer, Christian R Marshall. Genet Med 2018
Times Cited: 228




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
1

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
0

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
0

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
1


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
0

Genetic testing for unexplained perinatal disorders.
Thomas Hays, Ronald J Wapner. Curr Opin Pediatr 2021
1

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
4

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
38

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
2

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
25


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
52

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
30

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
23

Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019
17