A citation-based method for searching scientific literature

Gemma R Brett, Melissa Martyn, Fiona Lynch, Michelle G de Silva, Samantha Ayres, Lyndon Gallacher, Kirsten Boggs, Anne Baxendale, Sarah Schenscher, Sarah King-Smith, Lindsay Fowles, Amanda Springer, Sebastian Lunke, Anand Vasudevan, Emma Krzesinski, Jason Pinner, Sarah A Sandaradura, Christopher Barnett, Chirag Patel, Meredith Wilson, Zornitza Stark. Genet Med 2020
Times Cited: 6







List of co-cited articles
39 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.
Lauge Farnaes, Amber Hildreth, Nathaly M Sweeney, Michelle M Clark, Shimul Chowdhury, Shareef Nahas, Julie A Cakici, Wendy Benson, Robert H Kaplan, Richard Kronick,[...]. NPJ Genom Med 2018
148
83

Meeting the challenges of implementing rapid genomic testing in acute pediatric care.
Zornitza Stark, Sebastian Lunke, Gemma R Brett, Natalie B Tan, Rachel Stapleton, Smitha Kumble, Alison Yeung, Dean G Phelan, Belinda Chong, Miriam Fanjul-Fernandez,[...]. Genet Med 2018
72
83

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.
Stephen F Kingsmore, Julie A Cakici, Michelle M Clark, Mary Gaughran, Michele Feddock, Sergey Batalov, Matthew N Bainbridge, Jeanne Carroll, Sara A Caylor, Christina Clarke,[...]. Am J Hum Genet 2019
79
83

Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges.
Melissa Hill, Jennifer Hammond, Celine Lewis, Rhiannon Mellis, Emma Clement, Lyn S Chitty. Eur J Hum Genet 2020
6
66

Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System.
Sebastian Lunke, Stefanie Eggers, Meredith Wilson, Chirag Patel, Christopher P Barnett, Jason Pinner, Sarah A Sandaradura, Michael F Buckley, Emma I Krzesinski, Michelle G de Silva,[...]. JAMA 2020
41
66

Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children.
Lamia Mestek-Boukhibar, Emma Clement, Wendy D Jones, Suzanne Drury, Louise Ocaka, Andrey Gagunashvili, Polona Le Quesne Stabej, Chiara Bacchelli, Nital Jani, Shamima Rahman,[...]. J Med Genet 2018
53
66

A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants.
Julie A Cakici, David P Dimmock, Sara A Caylor, Mary Gaughran, Christina Clarke, Cynthia Triplett, Michelle M Clark, Stephen F Kingsmore, Cinnamon S Bloss. Am J Hum Genet 2020
16
66

Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
Linyan Meng, Mohan Pammi, Anirudh Saronwala, Pilar Magoulas, Andrew Ray Ghazi, Francesco Vetrini, Jing Zhang, Weimin He, Avinash V Dharmadhikari, Chunjing Qu,[...]. JAMA Pediatr 2017
189
66

Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.
Zornitza Stark, Amy Nisselle, Belinda McClaren, Fiona Lynch, Stephanie Best, Janet C Long, Melissa Martyn, Chirag Patel, Luregn J Schlapbach, Christopher Barnett,[...]. Eur J Hum Genet 2019
16
50

Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children.
Courtney E French, Isabelle Delon, Helen Dolling, Alba Sanchis-Juan, Olga Shamardina, Karyn Mégy, Stephen Abbs, Topun Austin, Sarah Bowdin, Ricardo G Branco,[...]. Intensive Care Med 2019
71
50

Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield.
Cynthia S Gubbels, Grace E VanNoy, Jill A Madden, Deborah Copenheaver, Sandra Yang, Monica H Wojcik, Nina B Gold, Casie A Genetti, Joan Stoler, Richard B Parad,[...]. Genet Med 2020
31
50

Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.
Zornitza Stark, Deborah Schofield, Melissa Martyn, Luke Rynehart, Rupendra Shrestha, Khurshid Alam, Sebastian Lunke, Tiong Y Tan, Clara L Gaff, Susan M White. Genet Med 2019
66
50

Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates.
Samantha Ayres, Lyndon Gallacher, Zornitza Stark, Gemma R Brett. J Genet Couns 2019
12
50

Rapid genome-wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences.
Caitlin E Aldridge, Horacio Osiovich, Harold Hal Siden, Alison M Elliott. J Genet Couns 2021
5
60

Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019
13
50

An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm.
David P Dimmock, Michelle M Clark, Mary Gaughran, Julie A Cakici, Sara A Caylor, Christina Clarke, Michele Feddock, Shimul Chowdhury, Lisa Salz, Cynthia Cheung,[...]. Am J Hum Genet 2020
23
50

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.
Josh E Petrikin, Julie A Cakici, Michelle M Clark, Laurel K Willig, Nathaly M Sweeney, Emily G Farrow, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Lee Zellmer,[...]. NPJ Genom Med 2018
84
50

Fostering implementation of health services research findings into practice: a consolidated framework for advancing implementation science.
Laura J Damschroder, David C Aron, Rosalind E Keith, Susan R Kirsh, Jeffery A Alexander, Julie C Lowery. Implement Sci 2009
33

The current state of implementation science in genomic medicine: opportunities for improvement.
Megan C Roberts, Amy E Kennedy, David A Chambers, Muin J Khoury. Genet Med 2017
70
33

Responsibility, culpability, and parental views on genomic testing for seriously ill children.
Janet Malek, Stacey Pereira, Jill O Robinson, Amanda M Gutierrez, Melody J Slashinski, D Williams Parsons, Sharon E Plon, Amy L McGuire. Genet Med 2019
9
33

Stakeholders' views on the value of outcomes from clinical genetic and genomic interventions.
Maren T Scheuner, Marcia M Russell, Catherine Chanfreau-Coffinier, Jane Peredo, Elizabeth M Yano, Alison B Hamilton, Barbara Lerner, Dawn Provenzale, Sara J Knight, Corrine I Voils. Genet Med 2019
6
33

Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies.
Jill O Robinson, Julia Wynn, Barbara Biesecker, Leslie G Biesecker, Barbara Bernhardt, Kyle B Brothers, Wendy K Chung, Kurt D Christensen, Robert C Green, Amy L McGuire,[...]. Genet Med 2019
25
33

Clinical utility of genomic sequencing: a measurement toolkit.
Robin Z Hayeems, David Dimmock, David Bick, John W Belmont, Robert C Green, Brendan Lanpher, Vaidehi Jobanputra, Roberto Mendoza, Shashi Kulkarni, Megan E Grove,[...]. NPJ Genom Med 2020
9
33

Parents' perceptions of personal utility of exome sequencing results.
Lonna Mollison, Julianne M O'Daniel, Gail E Henderson, Jonathan S Berg, Debra Skinner. Genet Med 2020
14
33

Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.
Allyn McConkie Rosell, Loren D M Pena, Kelly Schoch, Rebecca Spillmann, Jennifer Sullivan, Stephen R Hooper, Yong-Hui Jiang, Nicolas Mathey-Andrews, David B Goldstein, Vandana Shashi. J Genet Couns 2016
49
33

Defining personal utility in genomics: A Delphi study.
J N Kohler, E Turbitt, K L Lewis, B S Wilfond, L Jamal, H L Peay, L G Biesecker, B B Biesecker. Clin Genet 2017
36
33

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
Zornitza Stark, Tiong Y Tan, Belinda Chong, Gemma R Brett, Patrick Yap, Maie Walsh, Alison Yeung, Heidi Peters, Dylan Mordaunt, Shannon Cowie,[...]. Genet Med 2016
203
33

Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
104
33

Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate.
Lauren S Akesson, Adam Bournazos, Andrew Fennell, Emma I Krzesinski, Kenneth Tan, Amanda Springer, Katherine Rose, Ilias Goranitis, David Francis, Crystle Lee,[...]. Hum Mutat 2020
3
66

Benchmarking outcomes in the Neonatal Intensive Care Unit: Cytogenetic and molecular diagnostic rates in a retrospective cohort.
Faheem Malam, Taila Hartley, Meredith K Gillespie, Christine M Armour, Erika Bariciak, Gail E Graham, Sarah M Nikkel, Julie Richer, Sarah L Sawyer, Kym M Boycott,[...]. Am J Med Genet A 2017
14
33

Recommendations for Conduct, Methodological Practices, and Reporting of Cost-effectiveness Analyses: Second Panel on Cost-Effectiveness in Health and Medicine.
Gillian D Sanders, Peter J Neumann, Anirban Basu, Dan W Brock, David Feeny, Murray Krahn, Karen M Kuntz, David O Meltzer, Douglas K Owens, Lisa A Prosser,[...]. JAMA 2016
33

Rapid exome sequencing in PICU patients with new-onset metabolic or neurological disorders.
Abigail S Carey, John P Schacht, Christine Umandap, David Fasel, Chunhua Weng, Joshua Cappell, Wendy K Chung, Steven G Kernie. Pediatr Res 2020
6
33

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
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,[...]. Lancet Respir Med 2015
187
33

Rapid Targeted Genomics in Critically Ill Newborns.
Cleo C van Diemen, Wilhelmina S Kerstjens-Frederikse, Klasien A Bergman, Tom J de Koning, Birgit Sikkema-Raddatz, Joeri K van der Velde, Kristin M Abbott, Johanna C Herkert, Katharina Löhner, Patrick Rump,[...]. Pediatrics 2017
54
33

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.
Sarah E Soden, Carol J Saunders, Laurel K Willig, Emily G Farrow, Laurie D Smith, Josh E Petrikin, Jean-Baptiste LePichon, Neil A Miller, Isabelle Thiffault, Darrell L Dinwiddie,[...]. Sci Transl Med 2014
319
33


Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU.
Erica F Sanford, Michelle M Clark, Lauge Farnaes, Matthew R Williams, James C Perry, Elizabeth G Ingulli, Nathaly M Sweeney, Ami Doshi, Jeffrey J Gold, Benjamin Briggs,[...]. Pediatr Crit Care Med 2019
35
33

Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit.
Emma E Smith, Christèle du Souich, Nick Dragojlovic, Alison M Elliott. J Genet Couns 2019
15
33

Rapid acute care genomics: Challenges and opportunities for genetic counselors.
Fiona Lynch, Amy Nisselle, Clara L Gaff, Belinda McClaren. J Genet Couns 2021
3
66



Preparing for genomic medicine: a real world demonstration of health system change.
Clara L Gaff, Ingrid M Winship, Susan M Forrest, David P Hansen, Julian Clark, Paul M Waring, Mike South, Andrew H Sinclair. NPJ Genom Med 2017
48
16

Australian Genomics: A Federated Model for Integrating Genomics into Healthcare.
Zornitza Stark, Tiffany Boughtwood, Peta Phillips, John Christodoulou, David P Hansen, Jeffrey Braithwaite, Ainsley J Newson, Clara L Gaff, Andrew H Sinclair, Kathryn N North. Am J Hum Genet 2019
36
16

Outcomes for implementation research: conceptual distinctions, measurement challenges, and research agenda.
Enola Proctor, Hiie Silmere, Ramesh Raghavan, Peter Hovmand, Greg Aarons, Alicia Bunger, Richard Griffey, Melissa Hensley. Adm Policy Ment Health 2011
16

Attributes of context relevant to healthcare professionals' use of research evidence in clinical practice: a multi-study analysis.
Janet E Squires, Laura D Aloisio, Jeremy M Grimshaw, Kainat Bashir, Kristin Dorrance, Mary Coughlin, Alison M Hutchinson, Jill Francis, Susan Michie, Anne Sales,[...]. Implement Sci 2019
21
16

Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working Group.
Lori A Orlando, Nina R Sperber, Corrine Voils, Marshall Nichols, Rachel A Myers, R Ryanne Wu, Tejinder Rakhra-Burris, Kenneth D Levy, Mia Levy, Toni I Pollin,[...]. Genet Med 2018
28
16

Methods for designing interventions to change healthcare professionals' behaviour: a systematic review.
Heather L Colquhoun, Janet E Squires, Niina Kolehmainen, Cynthia Fraser, Jeremy M Grimshaw. Implement Sci 2017
87
16

The leadership behaviors needed to implement clinical genomics at scale: a qualitative study.
Stephanie Best, Zornitza Stark, Helen Brown, Janet C Long, Kushani Hewage, Clara Gaff, Jeffrey Braithwaite, Natalie Taylor. Genet Med 2020
3
33

A concept mapping approach to guide and understand dissemination and implementation.
Amy E Green, Danielle L Fettes, Gregory A Aarons. J Behav Health Serv Res 2012
23
16

Implementation of genomics in medical practice to deliver precision medicine for an Asian population.
Yasmin Bylstra, Sonia Davila, Weng Khong Lim, Ryanne Wu, Jing Xian Teo, Sylvia Kam, Tamra Lysaght, Steve Rozen, Bin Tean Teh, Khung Keong Yeo,[...]. NPJ Genom Med 2019
10
16


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.