A citation-based method for searching scientific literature

Jack Jacob, Michael Kamitsuka, Reese H Clark, Amy S Kelleher, Alan R Spitzer. Pediatrics 2015
Times Cited: 50







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



Times Cited
  Times     Co-cited
Similarity


Causes and timing of death in extremely premature infants from 2000 through 2011.
Ravi M Patel, Sarah Kandefer, Michele C Walsh, Edward F Bell, Waldemar A Carlo, Abbot R Laptook, Pablo J Sánchez, Seetha Shankaran, Krisa P Van Meurs, M Bethany Ball,[...]. N Engl J Med 2015
344
16

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
185
16

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
182
16

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
14

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
200
14

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
371
12

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
56
12

Trends in cause-specific mortality at a Canadian outborn NICU.
Charles David Andrew Simpson, Xiang Y Ye, Jonathan Hellmann, Chris Tomlinson. Pediatrics 2010
28
17

Necrotizing enterocolitis.
Josef Neu, W Allan Walker. N Engl J Med 2011
10

Association of Red Blood Cell Transfusion, Anemia, and Necrotizing Enterocolitis in Very Low-Birth-Weight Infants.
Ravi M Patel, Andrea Knezevic, Neeta Shenvi, Michael Hinkes, Sarah Keene, John D Roback, Kirk A Easley, Cassandra D Josephson. JAMA 2016
132
10


Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions.
Tiong Yang Tan, Oliver James Dillon, Zornitza Stark, Deborah Schofield, Khurshid Alam, Rupendra Shrestha, Belinda Chong, Dean Phelan, Gemma R Brett, Emma Creed,[...]. JAMA Pediatr 2017
141
10

Contribution of genetic disorders to neonatal mortality in a regional intensive care setting.
S M Hudome, R S Kirby, J W Senner, C Cunniff. Am J Perinatol 1994
24
20

Genetic disorders and mortality in infancy and early childhood: delayed diagnoses and missed opportunities.
Monica H Wojcik, Talia S Schwartz, Inbar Yamin, Heather L Edward, Casie A Genetti, Meghan C Towne, Pankaj B Agrawal. Genet Med 2018
22
22

Intestinal dysbiosis in preterm infants preceding necrotizing enterocolitis: a systematic review and meta-analysis.
Mohan Pammi, Julia Cope, Phillip I Tarr, Barbara B Warner, Ardythe L Morrow, Volker Mai, Katherine E Gregory, J Simon Kroll, Valerie McMurtry, Michael J Ferris,[...]. Microbiome 2017
214
10

Neonatal outcomes of extremely preterm infants from the NICHD Neonatal Research Network.
Barbara J Stoll, Nellie I Hansen, Edward F Bell, Seetha Shankaran, Abbot R Laptook, Michele C Walsh, Ellen C Hale, Nancy S Newman, Kurt Schibler, Waldemar A Carlo,[...]. Pediatrics 2010
8

Variations in mortality rates among Canadian neonatal intensive care units.
Koravangattu Sankaran, Li-Yin Chien, Robin Walker, Mary Seshia, Arne Ohlsson. CMAJ 2002
78
8

Diagnosis and cause of death in a neonatal intensive care unit--how important is autopsy?
Sandra Costa, Manuela Rodrigues, Maria José Centeno, Angelina Martins, Ana Vilan, Otília Brandão, Hercília Guimarães. J Matern Fetal Neonatal Med 2011
10
40

Trends in Care Practices, Morbidity, and Mortality of Extremely Preterm Neonates, 1993-2012.
Barbara J Stoll, Nellie I Hansen, Edward F Bell, Michele C Walsh, Waldemar A Carlo, Seetha Shankaran, Abbot R Laptook, Pablo J Sánchez, Krisa P Van Meurs, Myra Wyckoff,[...]. JAMA 2015
8

Randomized trial of liberal versus restrictive guidelines for red blood cell transfusion in preterm infants.
Edward F Bell, Ronald G Strauss, John A Widness, Larry T Mahoney, Donald M Mock, Victoria J Seward, Gretchen A Cress, Karen J Johnson, Irma J Kromer, M Bridget Zimmerman. Pediatrics 2005
266
8

The Premature Infants in Need of Transfusion (PINT) study: a randomized, controlled trial of a restrictive (low) versus liberal (high) transfusion threshold for extremely low birth weight infants.
Haresh Kirpalani, Robin K Whyte, Chad Andersen, Elizabeth V Asztalos, Nancy Heddle, Morris A Blajchman, Abraham Peliowski, Angel Rios, Meena LaCorte, Robert Connelly,[...]. J Pediatr 2006
291
8


Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
103
8

Trends in Infant Mortality in the United States, 2005-2014.
T J Mathews, Anne K Driscoll. NCHS Data Brief 2017
35
11

Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.
Hussein Daoud, Stephanie M Luco, Rui Li, Eric Bareke, Chandree Beaulieu, Olga Jarinova, Nancy Carson, Sarah M Nikkel, Gail E Graham, Julie Richer,[...]. CMAJ 2016
51
8

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
317
8

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
8

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
27
14


Prolonged duration of initial empirical antibiotic treatment is associated with increased rates of necrotizing enterocolitis and death for extremely low birth weight infants.
C Michael Cotten, Sarah Taylor, Barbara Stoll, Ronald N Goldberg, Nellie I Hansen, Pablo J Sánchez, Namasivayam Ambalavanan, Daniel K Benjamin. Pediatrics 2009
505
6

Mortality of necrotizing enterocolitis expressed by birth weight categories.
Shimae Cross Fitzgibbons, Yiming Ching, David Yu, Joe Carpenter, Michael Kenny, Christopher Weldon, Craig Lillehei, Clarissa Valim, Jeffrey D Horbar, Tom Jaksic. J Pediatr Surg 2009
311
6

Survival and morbidity of preterm children born at 22 through 34 weeks' gestation in France in 2011: results of the EPIPAGE-2 cohort study.
Pierre-Yves Ancel, François Goffinet, Pierre Kuhn, Bruno Langer, Jacqueline Matis, Xavier Hernandorena, Pierre Chabanier, Laurence Joly-Pedespan, Bénédicte Lecomte, Françoise Vendittelli,[...]. JAMA Pediatr 2015
332
6

Between-hospital variation in treatment and outcomes in extremely preterm infants.
Matthew A Rysavy, Lei Li, Edward F Bell, Abhik Das, Susan R Hintz, Barbara J Stoll, Betty R Vohr, Waldemar A Carlo, Seetha Shankaran, Michele C Walsh,[...]. N Engl J Med 2015
319
6

Infant Mortality Statistics From the 2013 Period Linked Birth/Infant Death Data Set.
T J Matthews, Marian F MacDorman, Marie E Thoma. Natl Vital Stat Rep 2015
318
6

Short term outcomes after extreme preterm birth in England: comparison of two birth cohorts in 1995 and 2006 (the EPICure studies).
Kate L Costeloe, Enid M Hennessy, Sadia Haider, Fiona Stacey, Neil Marlow, Elizabeth S Draper. BMJ 2012
443
6


Effect of fresh red blood cell transfusions on clinical outcomes in premature, very low-birth-weight infants: the ARIPI randomized trial.
Dean A Fergusson, Paul Hébert, Debora L Hogan, Louise LeBel, Nicole Rouvinez-Bouali, John A Smyth, Koravangattu Sankaran, Alan Tinmouth, Morris A Blajchman, Lajos Kovacs,[...]. JAMA 2012
265
6



Temporal changes in blood product usage in preterm neonates born at less than 30 weeks' gestation in Canada.
Amy K Keir, Junmin Yang, Adele Harrison, Ermelinda Pelausa, Prakesh S Shah. Transfusion 2015
36
8

Red blood cell transfusion-related necrotizing enterocolitis in very-low-birthweight infants: a near-infrared spectroscopy investigation.
Terri Marin, James Moore, Niki Kosmetatos, John D Roback, Paul Weiss, Melinda Higgins, Linda McCauley, Ora L Strickland, Cassandra D Josephson. Transfusion 2013
41
7


Necrotizing enterocolitis: new insights into pathogenesis and mechanisms.
Diego F Niño, Chhinder P Sodhi, David J Hackam. Nat Rev Gastroenterol Hepatol 2016
188
6

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
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
21

Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement.
Zornitza Stark, Deborah Schofield, Khurshid Alam, William Wilson, Nessie Mupfeki, Ivan Macciocca, Rupendra Shrestha, Susan M White, Clara Gaff. Genet Med 2017
115
6

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
6

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
129
6



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.