A citation-based method for searching scientific literature

Monica H Wojcik, Talia S Schwartz, Katri E Thiele, Heather Paterson, Rachel Stadelmaier, Thomas E Mullen, Grace E VanNoy, Casie A Genetti, Jill A Madden, Cynthia S Gubbels, Timothy W Yu, Wen-Hann Tan, Pankaj B Agrawal. J Perinatol 2019
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


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
46

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
46

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
166
38

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
134
38

Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
104
38

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
38

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
38

Death Certification Errors and the Effect on Mortality Statistics.
Lauri McGivern, Leanne Shulman, Jan K Carney, Steven Shapiro, Elizabeth Bundock. Public Health Rep 2017
61
38

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.
Ozge Ceyhan-Birsoy, Jaclyn B Murry, Kalotina Machini, Matthew S Lebo, Timothy W Yu, Shawn Fayer, Casie A Genetti, Talia S Schwartz, Pankaj B Agrawal, Richard B Parad,[...]. Am J Hum Genet 2019
61
30

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
30

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
17
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
84
30

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
30

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
81
30

Accuracy of Death Certificates and Assessment of Factors for Misclassification of Underlying Cause of Death.
Makiko Naka Mieno, Noriko Tanaka, Tomio Arai, Takuya Kawahara, Aya Kuchiba, Shizukiyo Ishikawa, Motoji Sawabe. J Epidemiol 2016
70
30

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
23

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
23
23

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
23

Molecular autopsy in maternal-fetal medicine.
Hanan E Shamseldin, Wesam Kurdi, Fatima Almusafri, Maha Alnemer, Alya Alkaff, Zeneb Babay, Amal Alhashem, Maha Tulbah, Nada Alsahan, Rubina Khan,[...]. Genet Med 2018
47
23

Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges.
Neeta L Vora, Bradford Powell, Alicia Brandt, Natasha Strande, Emily Hardisty, Kelly Gilmore, Ann Katherine M Foreman, Kirk Wilhelmsen, Chris Bizon, Jason Reilly,[...]. Genet Med 2017
86
23

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
819
23

Genetic aetiology of early infant deaths in a neonatal intensive care unit.
Lin Yang, Xu Liu, Zixiu Li, Peng Zhang, Bingbing Wu, Huijun Wang, Liyuan Hu, Guoqiang Cheng, Laishuan Wang, Wenhao Zhou. J Med Genet 2020
10
30

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
375
23

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
23

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
23

Application of Whole Genome Sequencing Technology in the Investigation of Genetic Causes of Fetal, Perinatal, and Early Infant Death.
Jane E Armes, Mark Williams, Gareth Price, Tristan Wallis, Renee Gallagher, Admire Matsika, Christopher Joy, Melanie Galea, Glenn Gardener, Rick Leach,[...]. Pediatr Dev Pathol 2018
11
27

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
24
15

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.
Michelle M Clark, Zornitza Stark, Lauge Farnaes, Tiong Y Tan, Susan M White, David Dimmock, Stephen F Kingsmore. NPJ Genom Med 2018
174
15

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
15

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
664
15

Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data.
Breidge Boyle, Marie-Claude Addor, Larraitz Arriola, Ingeborg Barisic, Fabrizio Bianchi, Melinda Csáky-Szunyogh, Hermien E K de Walle, Carlos Matias Dias, Elizabeth Draper, Miriam Gatt,[...]. Arch Dis Child Fetal Neonatal Ed 2018
53
15

The National Birth Defects Prevention Study: A review of the methods.
Jennita Reefhuis, Suzanne M Gilboa, Marlene Anderka, Marilyn L Browne, Marcia L Feldkamp, Charlotte A Hobbs, Mary M Jenkins, Peter H Langlois, Kimberly B Newsome, Andrew F Olshan,[...]. Birth Defects Res A Clin Mol Teratol 2015
131
15

Using ICD-9 codes to establish prevalence of malformations in newborn infants.
Lewis B Holmes, Marie-Noel Westgate. Birth Defects Res A Clin Mol Teratol 2012
24
15

Lacosamide for SCN2A-related intractable neonatal and infantile seizures.
Hadar Flor-Hirsch, Eli Heyman, Ayelet Livneh, Orit Reish, Nathan Watemberg, Ita Litmanovits, Anat Ben Sason Lilli, Dorit Lev, Tally Lerman Sagie, Haim Bassan. Epileptic Disord 2018
10
20

Rapid whole-genome sequencing identifies a novel AIRE variant associated with autoimmune polyendocrine syndrome type 1.
Erica Sanford, Kelly Watkins, Shareef Nahas, Michael Gottschalk, Nicole G Coufal, Lauge Farnaes, David Dimmock, Stephen F Kingsmore. Cold Spring Harb Mol Case Stud 2018
9
22

Alcohol consumption among low-income pregnant Latinas.
Christina D Chambers, Suzanne Hughes, Susan B Meltzer, Dennis Wahlgren, Nada Kassem, Sarah Larson, Edward P Riley, Melbourne F Hovell. Alcohol Clin Exp Res 2005
36
15

Prenatally diagnosed 17q12 microdeletion syndrome with a novel association with congenital diaphragmatic hernia.
Nancy W Hendrix, Michele Clemens, Timothy P Canavan, Urvashi Surti, Aleksandar Rajkovic. Fetal Diagn Ther 2012
24
15

Osteopetrosis: genetics, treatment and new insights into osteoclast function.
Cristina Sobacchi, Ansgar Schulz, Fraser P Coxon, Anna Villa, Miep H Helfrich. Nat Rev Endocrinol 2013
277
15

A child with terminal 14q deletion syndrome: consideration of genotype-phenotype correlations.
Kamilla Schlade-Bartusiak, Holly Ardinger, Diane W Cox. Am J Med Genet A 2009
19
15

Health Advantages and Disparities in Preterm Birth Among Immigrants Despite Disparate Sociodemographic, Behavioral, and Maternal Risk Factors in San Diego, California.
Maria Rosario G Araneta, Rebecca J Baer, Louis J Muglia, Kelli K Ryckman, Julie Ryu, Dean E Sidelinger, Laura L Jeliffe-Powlowski, Christina D Chambers. Matern Child Health J 2020
3
66

An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian study.
Karina A Issekutz, John M Graham, Chitra Prasad, Isabel M Smith, Kim D Blake. Am J Med Genet A 2005
150
15

A novel SOX9 nonsense mutation, q401x, in a case of campomelic dysplasia with XY sex reversal.
R Stoeva, L Grozdanova, G Scherer, M Krasteva, E Bausch, T Krastev, A Linev, M Stefanova. Genet Couns 2011
7
28

Mortality in the United States, 2017.
Sherry L Murphy, Jiaquan Xu, Kenneth D Kochanek, Elizabeth Arias. NCHS Data Brief 2018
167
15

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
15

Carnitine-acylcarnitine translocase deficiency: Two neonatal cases with common splicing mutation and in vitro bezafibrate response.
Nithiwat Vatanavicharn, Kenji Yamada, Yuka Aoyama, Toshiyuki Fukao, Narumon Densupsoontorn, Pipop Jirapinyo, Achara Sathienkijkanchai, Seiji Yamaguchi, Pornswan Wasant. Brain Dev 2015
18
15

Ketogenic diet as a successful early treatment modality for SCN2A mutation.
Dilsad Turkdogan, Gulten Thomas, Birsen Demirel. Brain Dev 2019
8
25

Novel Factor XIII variant identified through whole-genome sequencing in a child with intracranial hemorrhage.
Benjamin Briggs, Kiely N James, Shimul Chowdhury, Courtney Thornburg, Lauge Farnaes, David Dimmock, Stephen F Kingsmore. Cold Spring Harb Mol Case Stud 2018
8
25

Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation.
Nina Eide Hasselberg, Trine Fink Haland, Jørg Saberniak, Pål Haugar Brekke, Knut Erik Berge, Trond Paul Leren, Thor Edvardsen, Kristina Hermann Haugaa. Eur Heart J 2018
93
15

Ketogenic diet in pyruvate dehydrogenase complex deficiency: short- and long-term outcomes.
Kalliopi Sofou, Maria Dahlin, Tove Hallböök, Marie Lindefeldt, Gerd Viggedal, Niklas Darin. J Inherit Metab Dis 2017
59
15

Rapid whole-genome sequencing identifies a novel homozygous NPC1 variant associated with Niemann-Pick type C1 disease in a 7-week-old male with cholestasis.
Amber Hildreth, Kristen Wigby, Shimul Chowdhury, Shareef Nahas, Jaime Barea, Paulina Ordonez, Sergey Batalov, David Dimmock, Stephen Kingsmore. Cold Spring Harb Mol Case Stud 2017
13
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.