A citation-based method for searching scientific literature

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, Gemma R Brett, Kirsten Boggs, David Mowat, Edwin P Kirk, Lesley C Adès, Lauren S Akesson, David J Amor, Samantha Ayres, Anne Baxendale, Sarah Borrie, Alessandra Bray, Natasha J Brown, Cheng Yee Chan, Belinda Chong, Corrina Cliffe, Martin B Delatycki, Matthew Edwards, George Elakis, Michael C Fahey, Andrew Fennell, Lindsay Fowles, Lyndon Gallacher, Megan Higgins, Katherine B Howell, Lauren Hunt, Matthew F Hunter, Kristi J Jones, Sarah King, Smitha Kumble, Sarah Lang, Maelle Le Moing, Alan Ma, Dean Phelan, Michael C J Quinn, Anna Richards, Christopher M Richmond, Jessica Riseley, Jonathan Rodgers, Rani Sachdev, Simon Sadedin, Luregn J Schlapbach, Janine Smith, Amanda Springer, Natalie B Tan, Tiong Y Tan, Suzanna L Temple, Christiane Theda, Anand Vasudevan, Susan M White, Alison Yeung, Ying Zhu, Melissa Martyn, Stephanie Best, Tony Roscioli, John Christodoulou, Zornitza Stark. JAMA 2020
Times Cited: 31







List of co-cited articles
85 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
134
45

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
38

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
184
35

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
68
32

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
78
29

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
51
29

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
67
25

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
26
30

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
29
27

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
178
25

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
195
22

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
60
22

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
64
19

Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.
Michelle M Clark, Amber Hildreth, Sergey Batalov, Yan Ding, Shimul Chowdhury, Kelly Watkins, Katarzyna Ellsworth, Brandon Camp, Cyrielle I Kint, Calum Yacoubian,[...]. Sci Transl Med 2019
74
19

Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
102
19

Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019
13
38

RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.
Alison M Elliott, Christèle du Souich, Anna Lehman, Ilaria Guella, Daniel M Evans, Tara Candido, Leah Tooman, Linlea Armstrong, Lorne Clarke, William Gibson,[...]. Eur J Pediatr 2019
19
26

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
49
16

Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.
Laurie D Smith, Laurel K Willig, Stephen F Kingsmore. Cold Spring Harb Perspect Med 2015
54
16

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
11
45

The Novel Coronavirus Originating in Wuhan, China: Challenges for Global Health Governance.
Alexandra L Phelan, Rebecca Katz, Lawrence O Gostin. JAMA 2020
464
12

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
11
36

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
370
12

Targeted gene panel sequencing for the rapid diagnosis of acutely ill infants.
Luca Brunelli, Sabrina M Jenkins, James M Gudgeon, Steven B Bleyl, Christine E Miller, Tatiana Tvrdik, Shale A Dames, Betsy Ostrander, Josue A F Daboub, Brandon A Zielinski,[...]. Mol Genet Genomic Med 2019
11
36

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
35
12

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
25

Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit.
Robert Śmigiel, Mateusz Biela, Krzysztof Szmyd, Michal Błoch, Elżbieta Szmida, Paweł Skiba, Anna Walczak, Piotr Gasperowicz, Joanna Kosińska, Małgorzata Rydzanicz,[...]. J Clin Med 2020
11
36

Clinical utility of 24-h rapid trio-exome sequencing for critically ill infants.
Huijun Wang, Yanyan Qian, Yulan Lu, Qian Qin, Guoping Lu, Guoqiang Cheng, Ping Zhang, Lin Yang, Bingbing Wu, Wenhao Zhou. NPJ Genom Med 2020
7
57


Neonatologists' Attitudes About Diagnostic Whole-Genome Sequencing in the NICU.
Brett Knapp, Carole Decker, John D Lantos. Pediatrics 2019
9
33

Mortality in a neonate with molybdenum cofactor deficiency illustrates the need for a comprehensive rapid precision medicine system.
Stephen F Kingsmore, Nanda Ramchandar, Kiely James, Anna-Kaisa Niemi, Annette Feigenbaum, Yan Ding, Wendy Benson, Charlotte Hobbs, Shareef Nahas, Shimul Chowdhury,[...]. Cold Spring Harb Mol Case Stud 2020
6
50

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
313
9

The Human Phenotype Ontology in 2017.
Sebastian Köhler, Nicole A Vasilevsky, Mark Engelstad, Erin Foster, Julie McMurry, Ségolène Aymé, Gareth Baynam, Susan M Bello, Cornelius F Boerkoel, Kym M Boycott,[...]. Nucleic Acids Res 2017
393
9

Parental experiences of ultrarapid genomic testing for their critically unwell infants and children.
Gemma R Brett, Melissa Martyn, Fiona Lynch, Michelle G de Silva, Samantha Ayres, Lyndon Gallacher, Kirsten Boggs, Anne Baxendale, Sarah Schenscher, Sarah King-Smith,[...]. Genet Med 2020
5
60

Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
Aziz Belkadi, Alexandre Bolze, Yuval Itan, Aurélie Cobat, Quentin B Vincent, Alexander Antipenko, Lei Shang, Bertrand Boisson, Jean-Laurent Casanova, Laurent Abel. Proc Natl Acad Sci U S A 2015
250
9

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
9
33

Clinical utility of 24-h rapid trio-exome sequencing for critically ill infants.
Huijun Wang, Yanyan Qian, Yulan Lu, Qian Qin, Guoping Lu, Guoqiang Cheng, Ping Zhang, Lin Yang, Bingbing Wu, Wenhao Zhou. NPJ Genom Med 2020
10
30

CADD: predicting the deleteriousness of variants throughout the human genome.
Philipp Rentzsch, Daniela Witten, Gregory M Cooper, Jay Shendure, Martin Kircher. Nucleic Acids Res 2019
813
9

Prevention of VTE in nonsurgical patients: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines.
Susan R Kahn, Wendy Lim, Andrew S Dunn, Mary Cushman, Francesco Dentali, Elie A Akl, Deborah J Cook, Alex A Balekian, Russell C Klein, Hoang Le,[...]. Chest 2012
933
6

Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study.
Fei Zhou, Ting Yu, Ronghui Du, Guohui Fan, Ying Liu, Zhibo Liu, Jie Xiang, Yeming Wang, Bin Song, Xiaoying Gu,[...]. Lancet 2020
6

Developing a short-form of the Genetic Counselling Outcome Scale: The Genomics Outcome Scale.
Peter E Grant, Maria Pampaka, Katherine Payne, Angus Clarke, Marion McAllister. Eur J Med Genet 2019
11
18

Genetic Counseling in the Era of Genomics: What's all the Fuss about?
Gemma R Brett, Ella J Wilkins, Emma T Creed, Kirsty West, Anna Jarmolowicz, Giulia M Valente, Yael Prawer, Elly Lynch, Ivan Macciocca. J Genet Couns 2018
5
40

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
13

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.
Holly K Tabor, Jacquie Stock, Tracy Brazg, Margaret J McMillin, Karin M Dent, Joon-Ho Yu, Jay Shendure, Michael J Bamshad. Am J Med Genet A 2012
83
6

Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China.
Chaolin Huang, Yeming Wang, Xingwang Li, Lili Ren, Jianping Zhao, Yi Hu, Li Zhang, Guohui Fan, Jiuyang Xu, Xiaoying Gu,[...]. Lancet 2020
6

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
14

How infants die in the neonatal intensive care unit: trends from 1999 through 2008.
Julie Weiner, Jotishna Sharma, John Lantos, Howard Kilbride. Arch Pediatr Adolesc Med 2011
72
6

Use of whole exome sequencing in the NICU: Case of an extremely low birth weight infant with syndromic features.
Benjamin Kuehne, Eva Heine, Hormos Salimi Dafsari, Raphael Irwin, Raoul Heller, Ursula Bangen, Konrad Brockmeier, Angela Kribs, André Oberthuer, Sebahattin Cirak. Mol Cell Probes 2019
6
33

Integrating Genomics into Healthcare: A Global Responsibility.
Zornitza Stark, Lena Dolman, Teri A Manolio, Brad Ozenberger, Sue L Hill, Mark J Caulfied, Yves Levy, David Glazer, Julia Wilson, Mark Lawler,[...]. Am J Hum Genet 2019
115
6

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
25
8


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.