A citation-based method for searching scientific literature

Tally Lerman-Sagie, Zvi Leibovitz. Can J Neurol Sci 2016
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


A developmental and genetic classification for malformations of cortical development: update 2012.
A James Barkovich, Renzo Guerrini, Ruben I Kuzniecky, Graeme D Jackson, William B Dobyns. Brain 2012
541
23

Lissencephaly: Expanded imaging and clinical classification.
Nataliya Di Donato, Sara Chiari, Ghayda M Mirzaa, Kimberly Aldinger, Elena Parrini, Carissa Olds, A James Barkovich, Renzo Guerrini, William B Dobyns. Am J Med Genet A 2017
51
23

Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly.
Nataliya Di Donato, Andrew E Timms, Kimberly A Aldinger, Ghayda M Mirzaa, James T Bennett, Sarah Collins, Carissa Olds, Davide Mei, Sara Chiari, Gemma Carvill,[...]. Genet Med 2018
52
23

In utero MR imaging in fetuses at high risk of lissencephaly.
Fionn Williams, Paul D Griffiths. Br J Radiol 2017
12
33

Malformations of cortical development: diagnostic accuracy of fetal MR imaging.
Orit A Glenn, Addison A Cuneo, A James Barkovich, Zary Hashemi, Agnes I Bartha, Duan Xu. Radiology 2012
48
23

The genetics of lissencephaly.
Andrew E Fry, Thomas D Cushion, Daniela T Pilz. Am J Med Genet C Semin Med Genet 2014
45
17

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
66
17


Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
64
17

Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes.
Renske Oegema, Thomas D Cushion, Ian G Phelps, Seo-Kyung Chung, Jennifer C Dempsey, Sarah Collins, Jonathan G L Mullins, Tracy Dudding, Harinder Gill, Andrew J Green,[...]. Hum Mol Genet 2015
53
17

The wide spectrum of tubulinopathies: what are the key features for the diagnosis?
Nadia Bahi-Buisson, Karine Poirier, Franck Fourniol, Yoann Saillour, Stéphanie Valence, Nicolas Lebrun, Marie Hully, Catherine Fallet Bianco, Nathalie Boddaert, Caroline Elie,[...]. Brain 2014
161
17

Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.
Catherine Fallet-Bianco, Annie Laquerrière, Karine Poirier, Ferechte Razavi, Fabien Guimiot, Patricia Dias, Laurence Loeuillet, Karine Lascelles, Cherif Beldjord, Nathalie Carion,[...]. Acta Neuropathol Commun 2014
66
17

Mutations in CRADD Result in Reduced Caspase-2-Mediated Neuronal Apoptosis and Cause Megalencephaly with a Rare Lissencephaly Variant.
Nataliya Di Donato, Ying Y Jean, A Murat Maga, Briana D Krewson, Alison B Shupp, Maria I Avrutsky, Achira Roy, Sarah Collins, Carissa Olds, Rebecca A Willert,[...]. Am J Hum Genet 2016
29
11

Genetic Basis of Brain Malformations.
Elena Parrini, Valerio Conti, William B Dobyns, Renzo Guerrini. Mol Syndromol 2016
80
11

Malformations of cortical development: clinical features and genetic causes.
Renzo Guerrini, William B Dobyns. Lancet Neurol 2014
224
11

Post-mortem examination of human fetuses: a comparison of whole-body high-field MRI at 9.4 T with conventional MRI and invasive autopsy.
Sudhin Thayyil, Jon O Cleary, Neil J Sebire, Rosemary J Scott, Kling Chong, Roxanna Gunny, Catherine M Owens, Oystein E Olsen, Amaka C Offiah, Harold G Parks,[...]. Lancet 2009
93
11


Diagnostic imaging of posterior fossa anomalies in the fetus.
Ashley James Robinson, M Ashraf Ederies. Semin Fetal Neonatal Med 2016
19
11

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
35
11

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.
Mitsuhiro Kato, Soma Das, Kristin Petras, Kunio Kitamura, Ken-Ichirou Morohashi, Diane N Abuelo, Mason Barr, Dominique Bonneau, Angela F Brady, Nancy J Carpenter,[...]. Hum Mutat 2004
212
11

Outcome of isolated agenesis of the corpus callosum: A population-based prospective study.
Vincent des Portes, Anne Rolland, Juan Velazquez-Dominguez, Emeline Peyric, Marie-Pierre Cordier, Pascal Gaucherand, Jérôme Massardier, Mona Massoud, Aurore Curie, Anne-Sophie Pellot,[...]. Eur J Paediatr Neurol 2018
23
11

The Management of Myelomeningocele Study: full cohort 30-month pediatric outcomes.
Diana L Farmer, Elizabeth A Thom, John W Brock, Pamela K Burrows, Mark P Johnson, Lori J Howell, Jody A Farrell, Nalin Gupta, N Scott Adzick. Am J Obstet Gynecol 2018
104
11

Neural tube defects.
Nicholas D E Greene, Andrew J Copp. Annu Rev Neurosci 2014
268
11


Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, Eric Rider, Polina Bukshpun, Mari Wakahiro, Susan L Christian, Jean-Baptiste Rivière, Christopher T Sullivan, Jyotsna Sudi,[...]. PLoS Genet 2013
51
11

Developmental disorders of the midbrain and hindbrain.
A James Barkovich. Front Neuroanat 2012
31
11

Agenesis of the corpus callosum: a clinical approach to diagnosis.
Elizabeth Emma Palmer, David Mowat. Am J Med Genet C Semin Med Genet 2014
45
11

Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.
Richard J Leventer, Anna Jansen, Daniela T Pilz, Neil Stoodley, Carla Marini, Francois Dubeau, Jodie Malone, L Anne Mitchell, Simone Mandelstam, Ingrid E Scheffer,[...]. Brain 2010
140
11

Management of children with holoprosencephaly.
Eric B Levey, Elaine Stashinko, Nancy J Clegg, Mauricio R Delgado. Am J Med Genet C Semin Med Genet 2010
49
11

Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
48
11


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
697
11

Prenatal isolated mild ventriculomegaly: outcome in 167 cases.
J Ouahba, D Luton, E Vuillard, C Garel, P Gressens, N Blanc, M Elmaleh, P Evrard, J F Oury. BJOG 2006
103
11

Fetal Brain Anomalies Associated with Ventriculomegaly or Asymmetry: An MRI-Based Study.
E Barzilay, O Bar-Yosef, S Dorembus, R Achiron, E Katorza. AJNR Am J Neuroradiol 2017
19
11

Neurodevelopmental outcomes in children with cerebellar malformations: a systematic review.
Marie-Eve Bolduc, Catherine Limperopoulos. Dev Med Child Neurol 2009
95
11

Neurodevelopmental outcome following prenatal diagnosis of an isolated anomaly of the corpus callosum.
R Mangione, N Fries, P Godard, C Capron, V Mirlesse, D Lacombe, M Duyme. Ultrasound Obstet Gynecol 2011
38
11

Polymicrogyria: a common and heterogeneous malformation of cortical development.
Chloe A Stutterd, Richard J Leventer. Am J Med Genet C Semin Med Genet 2014
53
11

Natural history of fetal isolated ventriculomegaly: Comparison between pre- and post-natal imaging.
Sharon Perlman, Omer Bar-Yosef, Jeffrey-Michael Jacobson, Yinon Gilboa, Estela Derazne, Reuven Achiron, Eldad Katorza. J Matern Fetal Neonatal Med 2018
4
50


Neuroimaging of ventriculomegaly in the fetal period.
V D'Addario, A C Rossi. Semin Fetal Neonatal Med 2012
23
11

Mild ventriculomegaly from fetal consultation to neurodevelopmental assessment: A single center experience and review of the literature.
Barbara Scelsa, Mariangela Rustico, Andrea Righini, Cecilia Parazzini, Marina Antonella Balestriero, Paola Introvini, Luigina Spaccini, Massimo Mastrangelo, Gianluca Lista, Gian Vincenzo Zuccotti,[...]. Eur J Paediatr Neurol 2018
14
14

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
198
11


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
165
11




Developmental outcome of isolated fetal microcephaly.
S Stoler-Poria, D Lev, A Schweiger, T Lerman-Sagie, G Malinger. Ultrasound Obstet Gynecol 2010
30
11

Prenatal diagnosis of cobblestone lissencephaly associated with Walker-Warburg syndrome based on a specific sonographic pattern.
A Lacalm, B Nadaud, M Massoud, A Putoux, P Gaucherand, L Guibaud. Ultrasound Obstet Gynecol 2016
17
11

Congenital Aqueductal Stenosis: Findings at Fetal MRI That Accurately Predict a Postnatal Diagnosis.
K J Heaphy-Henault, C V Guimaraes, A R Mehollin-Ray, C I Cassady, W Zhang, N K Desai, M J Paldino. AJNR Am J Neuroradiol 2018
14
14


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.