A citation-based method for searching scientific literature

Jagoda Hofman, Michał Hutny, Karolina Sztuba, Justyna Paprocka. Brain Sci 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
50

Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.
Timothy J Edwards, Elliott H Sherr, A James Barkovich, Linda J Richards. Brain 2014
163
50

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
50

Underdevelopment of the Human Hippocampus in Callosal Agenesis: An In Vivo Fetal MRI Study.
V Knezović, G Kasprian, A Štajduhar, E Schwartz, M Weber, G M Gruber, P C Brugger, D Prayer, M Vukšić. AJNR Am J Neuroradiol 2019
8
25

Anatomical subgroup analysis of the MERIDIAN cohort: failed commissuration.
P D Griffiths, K Brackley, M Bradburn, D J A Connolly, M L Gawne-Cain, D I Griffiths, M D Kilby, L Mandefield, C Mooney, S C Robson,[...]. Ultrasound Obstet Gynecol 2017
19
25


Use of MRI in the diagnosis of fetal brain abnormalities in utero (MERIDIAN): a multicentre, prospective cohort study.
Paul D Griffiths, Michael Bradburn, Michael J Campbell, Cindy L Cooper, Ruth Graham, Deborah Jarvis, Mark D Kilby, Gerald Mason, Cara Mooney, Stephen C Robson,[...]. Lancet 2017
124
25

Role of magnetic resonance imaging in fetuses with mild or moderate ventriculomegaly in the era of fetal neurosonography: systematic review and meta-analysis.
D Di Mascio, F G Sileo, A Khalil, G Rizzo, N Persico, R Brunelli, A Giancotti, P B Panici, G Acharya, F D'Antonio. Ultrasound Obstet Gynecol 2019
32
25

ISUOG Practice Guidelines: performance of fetal magnetic resonance imaging.
D Prayer, G Malinger, P C Brugger, C Cassady, L De Catte, B De Keersmaecker, G L Fernandes, P Glanc, L F Gonçalves, G M Gruber,[...]. Ultrasound Obstet Gynecol 2017
70
25


Role of prenatal magnetic resonance imaging in fetuses with isolated agenesis of corpus callosum in the era of fetal neurosonography: A systematic review and meta-analysis.
Filomena Giulia Sileo, Daniele Di Mascio, Giuseppe Rizzo, Massimo Caulo, Lucia Manganaro, Emma Bertucci, Sophie Masmejan, Marco Liberati, Alice D'Amico, Luigi Nappi,[...]. Acta Obstet Gynecol Scand 2021
4
25

Prenatal diagnosis and outcome of partial agenesis and hypoplasia of the corpus callosum.
T Ghi, A Carletti, E Contro, E Cera, P Falco, G Tagliavini, L Michelacci, G Tani, A Youssef, P Bonasoni,[...]. Ultrasound Obstet Gynecol 2010
52
25

How accurate are prenatal tractography results? A postnatal in vivo follow-up study using diffusion tensor imaging.
Jae W Song, Gerlinde M Gruber, Janina M Patsch, Rainer Seidl, Daniela Prayer, Gregor Kasprian. Pediatr Radiol 2018
14
25

Characteristics, associations and outcome of partial agenesis of the corpus callosum in the fetus.
P Volpe, D Paladini, M Resta, A Stanziano, M Salvatore, M Quarantelli, V De Robertis, A L Buonadonna, G Caruso, M Gentile. Ultrasound Obstet Gynecol 2006
84
25

Improved neurodevelopmental prognostication in isolated corpus callosal agenesis: fetal magnetic resonance imaging-based scoring system.
M C Diogo, S Glatter, D Prayer, G M Gruber, D Bettelheim, M Weber, G Dovjak, R Seidl, G Kasprian. Ultrasound Obstet Gynecol 2021
4
25

Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.
Francesco D'Antonio, Giorgio Pagani, Alessandra Familiari, Asma Khalil, Tally-Lerman Sagies, Gustavo Malinger, Zvi Leibovitz, Catherine Garel, Marie Laure Moutard, Gianluigi Pilu,[...]. Pediatrics 2016
63
25

The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.
Erik von Elm, Douglas G Altman, Matthias Egger, Stuart J Pocock, Peter C Gøtzsche, Jan P Vandenbroucke. Lancet 2007
25

Counseling in fetal medicine: agenesis of the corpus callosum.
S Santo, F D'Antonio, T Homfray, P Rich, G Pilu, A Bhide, B Thilaganathan, A T Papageorghiou. Ultrasound Obstet Gynecol 2012
69
25

Multiple imputation using chained equations: Issues and guidance for practice.
Ian R White, Patrick Royston, Angela M Wood. Stat Med 2011
25

Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal ultrasound imaging (part 1): nomenclature, diagnostic accuracy and associated anomalies.
F D'Antonio, A Khalil, C Garel, G Pilu, G Rizzo, T Lerman-Sagie, A Bhide, B Thilaganathan, L Manzoli, A T Papageorghiou. Ultrasound Obstet Gynecol 2016
35
25

Agenesis of the fetal corpus callosum: sonographic signs change with advancing gestational age.
D Paladini, G Pastore, A Cavallaro, M Massaro, C Nappi. Ultrasound Obstet Gynecol 2013
35
25

Fetal midline anomalies: Diagnosis and counselling Part 1: Corpus callosum anomalies.
Martina Leombroni, Asma Khalil, Marco Liberati, Francesco D'Antonio. Eur J Paediatr Neurol 2018
11
25


MRI of the Fetal Brain.
C Weisstanner, G Kasprian, G M Gruber, P C Brugger, D Prayer. Clin Neuroradiol 2015
18
25

ISUOG Practice Guidelines (updated): sonographic examination of the fetal central nervous system. Part 2: performance of targeted neurosonography.
D Paladini, G Malinger, R Birnbaum, A Monteagudo, G Pilu, L J Salomon, I E Timor-Tritsch. Ultrasound Obstet Gynecol 2021
8
25


Prognostic Accuracy of Fetal MRI in Predicting Postnatal Neurodevelopmental Outcome.
M Wilson, K Muir, D Reddy, R Webster, C Kapoor, E Miller. AJNR Am J Neuroradiol 2020
3
33

Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal imaging (part 2): neurodevelopmental outcome.
F D'Antonio, A Khalil, C Garel, G Pilu, G Rizzo, T Lerman-Sagie, A Bhide, B Thilaganathan, L Manzoli, A T Papageorghiou. Ultrasound Obstet Gynecol 2016
34
25




Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation.
Solveig Heide, Myrtille Spentchian, Stéphanie Valence, Julien Buratti, Corinne Mach, Elodie Lejeune, Valérie Olin, Marta Massimello, Daphné Lehalle, Linda Mouthon,[...]. Genet Med 2020
4
25

Accuracy of in-utero MRI to detect fetal brain abnormalities and prognosticate developmental outcome: postnatal follow-up of the MERIDIAN cohort.
Anthony R Hart, Nicholas D Embleton, Michael Bradburn, Daniel J A Connolly, Laura Mandefield, Cara Mooney, Paul D Griffiths. Lancet Child Adolesc Health 2020
7
25

Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome.
Christiane K Bauer, Paolo Calligari, Francesca Clementina Radio, Viviana Caputo, Maria Lisa Dentici, Nadia Falah, Frances High, Francesca Pantaleoni, Sabina Barresi, Andrea Ciolfi,[...]. Am J Hum Genet 2018
43
25

Executive functions in young children with autism.
E M Griffith, B F Pennington, E A Wehner, S J Rogers. Child Dev 1999
194
25

Care for patients with ultra-rare disorders.
Raoul C M Hennekam. Eur J Med Genet 2011
37
25

Childhood absence epilepsy: genes, channels, neurons and networks.
Vincenzo Crunelli, Nathalie Leresche. Nat Rev Neurosci 2002
397
25

Closed-loop optogenetic control of thalamus as a tool for interrupting seizures after cortical injury.
Jeanne T Paz, Thomas J Davidson, Eric S Frechette, Bruno Delord, Isabel Parada, Kathy Peng, Karl Deisseroth, John R Huguenard. Nat Neurosci 2013
312
25


The combination of whole-exome sequencing and copy number variation sequencing enables the diagnosis of rare neurological disorders.
Qingguo Jiao, Haiming Sun, Haoya Zhang, Ran Wang, Suting Li, Dan Sun, Xiu-An Yang, Yan Jin. Clin Genet 2019
16
25



Enhanced tonic GABAA inhibition in typical absence epilepsy.
David W Cope, Giuseppe Di Giovanni, Sarah J Fyson, Gergely Orbán, Adam C Errington, Magor L Lorincz, Timothy M Gould, David A Carter, Vincenzo Crunelli. Nat Med 2009
258
25

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
419
25

WDR26 is a new partner of Axin1 in the canonical Wnt signaling pathway.
Toshiyasu Goto, Junhei Matsuzawa, Shun-Ichiro Iemura, Tohru Natsume, Hiroshi Shibuya. FEBS Lett 2016
16
25

Wnt/β-catenin signaling and disease.
Hans Clevers, Roel Nusse. Cell 2012
25

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
25



Autism in Adulthood: Clinical and Demographic Characteristics of a Cohort of Five Hundred Persons with Autism Analyzed by a Novel Multistep Network Model.
Roberto Keller, Silvia Chieregato, Stefania Bari, Romina Castaldo, Filippo Rutto, Annalisa Chiocchetti, Umberto Dianzani. Brain Sci 2020
6
25


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.