A citation-based method for searching scientific literature

Julie Weiner, Jotishna Sharma, John Lantos, Howard Kilbride. Arch Pediatr Adolesc Med 2011
Times Cited: 85







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



Times Cited
  Times     Co-cited
Similarity


Categorizing neonatal deaths: a cross-cultural study in the United States, Canada, and The Netherlands.
A A Eduard Verhagen, Annie Janvier, Steven R Leuthner, B Andrews, J Lagatta, Arend F Bos, William Meadow. J Pediatr 2010
112
32

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
388
28

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
207
24

Death in the neonatal intensive care unit: changing patterns of end of life care over two decades.
D J Wilkinson, J J Fitzsimons, P A Dargaville, N T Campbell, P M Loughnan, P N McDougall, J F Mills. Arch Dis Child Fetal Neonatal Ed 2006
64
31

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
216
20

Deaths in a neonatal intensive care unit: a 10-year perspective.
Cathrine Monrad Hagen, Thor Willy Ruud Hansen. Pediatr Crit Care Med 2004
47
34

End-of-life after birth: death and dying in a neonatal intensive care unit.
Jaideep Singh, John Lantos, William Meadow. Pediatrics 2004
103
17


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
343
16

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
15

A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases.
Neil A Miller, Emily G Farrow, Margaret Gibson, Laurel K Willig, Greyson Twist, Byunggil Yoo, Tyler Marrs, Shane Corder, Lisa Krivohlavek, Adam Walter,[...]. Genome Med 2015
130
15

Neonatal deaths: prospective exploration of the causes and process of end-of-life decisions.
Jonathan Hellmann, Robin Knighton, Shoo K Lee, Prakesh S Shah. Arch Dis Child Fetal Neonatal Ed 2016
43
30

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
96
15

Moral and ethical dilemmas in the special-care nursery.
R S Duff, A G Campbell. N Engl J Med 1973
322
14

Decision making and modes of death in a tertiary neonatal unit.
R Roy, N Aladangady, K Costeloe, V Larcher. Arch Dis Child Fetal Neonatal Ed 2004
62
19

Modes of death in pediatrics: differences in the ethical approach in neonatal and pediatric patients.
Matteo S Fontana, Catherine Farrell, France Gauvin, Jacques Lacroix, Annie Janvier. J Pediatr 2013
63
19

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
85
14



End-of-life decisions in Dutch neonatal intensive care units.
A A Eduard Verhagen, Jozef H H M Dorscheidt, Bernadette Engels, Joep H Hubben, Pieter J Sauer. Arch Pediatr Adolesc Med 2009
49
22

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
171
12

Neonatal end-of-life decision making: Physicians' attitudes and relationship with self-reported practices in 10 European countries.
M Rebagliato, M Cuttini, L Broggin, I Berbik, U de Vonderweid, G Hansen, M Kaminski, L A Kollée, A Kucinskas, S Lenoir,[...]. JAMA 2000
161
11

End-of-life decisions in neonatal intensive care: physicians' self-reported practices in seven European countries. EURONIC Study Group.
M Cuttini, M Nadai, M Kaminski, G Hansen, R de Leeuw, S Lenoir, J Persson, M Rebagliato, M Reid, U de Vonderweid,[...]. Lancet 2000
248
11

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
219
11

Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
107
11

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
58
17

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
60
16


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
61
14

End of life, death and dying in neonatal intensive care units in Latin America.
C A Fajardo, S González, G Zambosco, M J Cancela, L V Forero, M Venegas, H Baquero, L Lemus-Varela, J Kattan, F Wormald,[...]. Acta Paediatr 2012
20
40

Neonatal end-of-life care: a single-center NICU experience in Israel over a decade.
Smadar Eventov-Friedman, Hana Kanevsky, Benjamin Bar-Oz. Pediatrics 2013
22
36

Physician medical decision-making at the end of life in newborns: insight into implementation at 2 Dutch centers.
A A Eduard Verhagen, Mark A H van der Hoeven, R Corine van Meerveld, Pieter J J Sauer. Pediatrics 2007
36
22

Trends in cause-specific mortality at a Canadian outborn NICU.
Charles David Andrew Simpson, Xiang Y Ye, Jonathan Hellmann, Chris Tomlinson. Pediatrics 2010
33
24

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
100
9

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
89
9

The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders.
Vandana Shashi, Allyn McConkie-Rosell, Bruce Rosell, Kelly Schoch, Kasturi Vellore, Marie McDonald, Yong-Hui Jiang, Pingxing Xie, Anna Need, David B Goldstein. Genet Med 2014
163
8

Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration.
Helga Thorvaldsdóttir, James T Robinson, Jill P Mesirov. Brief Bioinform 2013
8

Clinical diagnostics in human genetics with semantic similarity searches in ontologies.
Sebastian Köhler, Marcel H Schulz, Peter Krawitz, Sebastian Bauer, Sandra Dölken, Claus E Ott, Christine Mundlos, Denise Horn, Stefan Mundlos, Peter N Robinson. Am J Hum Genet 2009
267
8

Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study.
P W Yoon, R S Olney, M J Khoury, W M Sappenfield, G F Chavez, D Taylor. Arch Pediatr Adolesc Med 1997
131
8

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
8

Short-term outcome of treatment limitation discussions for newborn infants, a multicentre prospective observational cohort study.
Narendra Aladangady, Chloe Shaw, Katie Gallagher, Elizabeth Stokoe, Neil Marlow. Arch Dis Child Fetal Neonatal Ed 2017
19
36

Etiologies of NICU deaths.
Jack Jacob, Michael Kamitsuka, Reese H Clark, Amy S Kelleher, Alan R Spitzer. Pediatrics 2015
59
11

Causes and circumstances of death in a neonatal unit over 20 years.
Marissa C Michel, Tarah T Colaizy, Jonathan M Klein, Jeffrey L Segar, Edward F Bell. Pediatr Res 2018
12
58

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
109
8

End-of-life decisions in delivery room and neonatal intensive care unit.
Romaine Arlettaz, Dieto Mieth, Hans-Ulrich Bucher, Gabriel Duc, Jean-Claude Fauchère. Acta Paediatr 2005
43
13

Neonatal end-of-life practice in a German perinatal centre.
A Schulz-Baldes, D Huseman, A Loui, J W Dudenhausen, M Obladen. Acta Paediatr 2007
21
28

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
7

Withdrawal of artificial nutrition and hydration in the neonatal intensive care unit: parental perspectives.
Jonathan Hellmann, Constance Williams, Lori Ives-Baine, Prakesh S Shah. Arch Dis Child Fetal Neonatal Ed 2013
27
22


End-of-life choices for African-American and white infants in a neonatal intensive-care unit: a pilot study.
Kathryn L Moseley, Annamaria Church, Bridget Hempel, Harry Yuan, Susan Door Goold, Gary L Freed. J Natl Med Assoc 2004
39
15


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.