A citation-based method for searching scientific literature

Monica H Wojcik, Dara Brodsky, Jane E Stewart, Jonathan Picker. J Perinatol 2018
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Decreasing use of autopsy for stillbirths and infant deaths: missed opportunity.
Nathalie Auger, Marianne Bilodeau-Bertrand, Julie Poissant, Prakesh S Shah. J Perinatol 2018
7
60

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
40

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
40

Acceptability of a minimally invasive perinatal/paediatric autopsy: healthcare professionals' views and implications for practice.
K Ben-Sasi, L S Chitty, L S Franck, S Thayyil, L Judge-Kronis, A M Taylor, N J Sebire. Prenat Diagn 2013
56
40

Postmortem research: innovations and future directions for the perinatal and paediatric autopsy.
J C Hutchinson, O J Arthurs, N J Sebire. Arch Dis Child Educ Pract Ed 2016
19
40

Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies.
Elizabeth Quinlan-Jones, Jenny Lord, Denise Williams, Sue Hamilton, Tamas Marton, Ruth Y Eberhardt, Gabriele Rinck, Elena Prigmore, Rebecca Keelagher, Dominic J McMullan,[...]. Genet Med 2019
19
20

Mitochondrial citrate synthase crystals: novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations.
Komudi Siriwardena, Nevena Mackay, Valeriy Levandovskiy, Susan Blaser, Julian Raiman, Paul F Kantor, Cameron Ackerley, Brian H Robinson, Andreas Schulze, Jessie M Cameron. Mol Genet Metab 2013
19
20

Mutation in the AGK gene in two siblings with unusual Sengers syndrome.
Sanae Allali, Imen Dorboz, Simon Samaan, Abdelhamid Slama, Charlène Rambaud, Odile Boespflug-Tanguy, Catherine Sarret. Metab Brain Dis 2017
8
20

Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome.
Johannes A Mayr, Tobias B Haack, Elisabeth Graf, Franz A Zimmermann, Thomas Wieland, Birgit Haberberger, Andrea Superti-Furga, Janbernd Kirschner, Beat Steinmann, Matthias R Baumgartner,[...]. Am J Hum Genet 2012
134
20


Acylglycerol Kinase: Mitochondrial Protein Transport Meets Lipid Biosynthesis.
Christoph U Mårtensson, Thomas Becker. Trends Cell Biol 2017
7
20

Mitochondrial DNA maintenance defects.
Ayman W El-Hattab, William J Craigen, Fernando Scaglia. Biochim Biophys Acta Mol Basis Dis 2017
105
20


Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients.
Alireza Haghighi, Tobias B Haack, Mehnaz Atiq, Hassan Mottaghi, Hamidreza Haghighi-Kakhki, Rani A Bashir, Uwe Ahting, René G Feichtinger, Johannes A Mayr, Agnès Rötig,[...]. Orphanet J Rare Dis 2014
47
20

Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria.
Milena Vukotic, Hendrik Nolte, Tim König, Shotaro Saita, Maria Ananjew, Marcus Krüger, Takashi Tatsuta, Thomas Langer. Mol Cell 2017
62
20


Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.
Sarah E Calvo, Alison G Compton, Steven G Hershman, Sze Chern Lim, Daniel S Lieber, Elena J Tucker, Adrienne Laskowski, Caterina Garone, Shangtao Liu, David B Jaffe,[...]. Sci Transl Med 2012
307
20

Confirmation of cause and manner of death via a comprehensive cardiac autopsy including whole exome next-generation sequencing.
Christina G Loporcaro, David J Tester, Joseph J Maleszewski, Teresa Kruisselbrink, Michael J Ackerman. Arch Pathol Lab Med 2014
30
20

Neuroradiologic findings in Sengers syndrome.
M Scott Perry, John T Sladky. Pediatr Neurol 2008
9
20


Identification of a truncation mutation of acylglycerol kinase (AGK) gene in a novel autosomal recessive cataract locus.
Mohammed A Aldahmesh, Arif O Khan, Jawahir Y Mohamed, Mohammed H Alghamdi, Fowzan S Alkuraya. Hum Mutat 2012
48
20

Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction.
David B Beck, Kristina Cusmano-Ozog, Nickie Andescavage, Eyby Leon. Transl Sci Rare Dis 2018
6
20

Biallelic TBCD Mutations Cause Early-Onset Neurodegenerative Encephalopathy.
Noriko Miyake, Ryoko Fukai, Chihiro Ohba, Takahiro Chihara, Masayuki Miura, Hiroshi Shimizu, Akiyoshi Kakita, Eri Imagawa, Masaaki Shiina, Kazuhiro Ogata,[...]. Am J Hum Genet 2016
29
20

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
20

Annual Summary of Vital Statistics: 2013-2014.
Sherry L Murphy, T J Mathews, Joyce A Martin, Cynthia S Minkovitz, Donna M Strobino. Pediatrics 2017
100
20

Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
104
20

Infant and Youth Mortality Trends by Race/Ethnicity and Cause of Death in the United States.
Sahar Q Khan, Amy Berrington de Gonzalez, Ana F Best, Yingxi Chen, Emily A Haozous, Erik J Rodriquez, Susan Spillane, David A Thomas, Diana Withrow, Neal D Freedman,[...]. JAMA Pediatr 2018
28
20

Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy.
Elisabetta Flex, Marcello Niceta, Serena Cecchetti, Isabelle Thiffault, Margaret G Au, Alessandro Capuano, Emanuela Piermarini, Anna A Ivanova, Joshua W Francis, Giovanni Chillemi,[...]. Am J Hum Genet 2016
49
20

Patterns of infant mortality caused by major congenital anomalies.
S W Wen, S Liu, K S Joseph, J Rouleau, A Allen. Teratology 2000
36
20

Infant Mortality, Cause of Death, and Vital Records Reporting in Ohio, United States.
Laura M Seske, Louis J Muglia, Eric S Hall, Kevin E Bove, James M Greenberg. Matern Child Health J 2017
11
20

Modes of Death Within a Children's Hospital.
Amy Trowbridge, Jennifer K Walter, Eric McConathey, Wynne Morrison, Chris Feudtner. Pediatrics 2018
36
20

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
10
20

Variations in mortality rates among Canadian neonatal intensive care units.
Koravangattu Sankaran, Li-Yin Chien, Robin Walker, Mary Seshia, Arne Ohlsson. CMAJ 2002
78
20

De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy.
Monica H Wojcik, Kyoko Okada, Sanjay P Prabhu, Dan W Nowakowski, Keri Ramsey, Chris Balak, Sampath Rangasamy, Catherine A Brownstein, Klaus Schmitz-Abe, Julie S Cohen,[...]. Am J Med Genet A 2018
12
20

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
74
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
23
20

Alternatives to Autopsy for Fetal and Early Neonatal (Perinatal) Deaths: Insights from the Wisconsin Stillbirth Service Program.
Elspeth McPherson, Eirini Nestoridi, Dominique Heinke, Drucilla J Roberts, Ruth Fretts, Mahsa M Yazdy, Angela E Lin. Birth Defects Res 2017
11
20

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
20

Etiologies of NICU deaths.
Jack Jacob, Michael Kamitsuka, Reese H Clark, Amy S Kelleher, Alan R Spitzer. Pediatrics 2015
50
20

CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.
Darci T Butcher, Cheryl Cytrynbaum, Andrei L Turinsky, Michelle T Siu, Michal Inbar-Feigenberg, Roberto Mendoza-Londono, David Chitayat, Susan Walker, Jerry Machado, Oana Caluseriu,[...]. Am J Hum Genet 2017
83
20


The BabySeq project: implementing genomic sequencing in newborns.
Ingrid A Holm, Pankaj B Agrawal, Ozge Ceyhan-Birsoy, Kurt D Christensen, Shawn Fayer, Leslie A Frankel, Casie A Genetti, Joel B Krier, Rebecca C LaMay, Harvey L Levy,[...]. BMC Pediatr 2018
46
20

Mutations in the substrate binding glycine-rich loop of the mitochondrial processing peptidase-α protein (PMPCA) cause a severe mitochondrial disease.
Mugdha Joshi, Irina Anselm, Jiahai Shi, Tejus A Bale, Meghan Towne, Klaus Schmitz-Abe, Laura Crowley, Felix C Giani, Shideh Kazerounian, Kyriacos Markianos,[...]. Cold Spring Harb Mol Case Stud 2016
22
20

Trends in Infant Mortality in the United States, 2005-2014.
T J Mathews, Anne K Driscoll. NCHS Data Brief 2017
34
20

Trends in cause-specific mortality at a Canadian outborn NICU.
Charles David Andrew Simpson, Xiang Y Ye, Jonathan Hellmann, Chris Tomlinson. Pediatrics 2010
30
20

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
20


22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.
Marie-France Portnoï, Fanny Lebas, Nicolas Gruchy, Azarnouche Ardalan, Valérie Biran-Mucignat, Valérie Malan, Lina Finkel, Gilles Roger, Sarah Ducrocq, Francis Gold,[...]. Am J Med Genet A 2005
79
20

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
20

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
20


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.