Tally Lerman-Sagie, Zvi Leibovitz. Can J Neurol Sci 2016
Times Cited: 17
Times Cited: 17
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
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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
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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
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In utero MR imaging in fetuses at high risk of lissencephaly.
Fionn Williams, Paul D Griffiths. Br J Radiol 2017
Fionn Williams, Paul D Griffiths. Br J Radiol 2017
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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
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The genetics of lissencephaly.
Andrew E Fry, Thomas D Cushion, Daniela T Pilz. Am J Med Genet C Semin Med Genet 2014
Andrew E Fry, Thomas D Cushion, Daniela T Pilz. Am J Med Genet C Semin Med Genet 2014
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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
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
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Contribution of fetal cerebral MRI for diagnosis of structural anomalies.
Laurent Guibaud. Prenat Diagn 2009
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Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
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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
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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
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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
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
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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
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Genetic Basis of Brain Malformations.
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Malformations of cortical development: clinical features and genetic causes.
Renzo Guerrini, William B Dobyns. Lancet Neurol 2014
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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
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Fetal lateral ventricular width: what should be its upper limit? A prospective cohort study and reanalysis of the current and previous data.
Benny Almog, Ronni Gamzu, Reuven Achiron, Ofer Fainaru, Yaron Zalel. J Ultrasound Med 2003
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Diagnostic imaging of posterior fossa anomalies in the fetus.
Ashley James Robinson, M Ashraf Ederies. Semin Fetal Neonatal Med 2016
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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
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
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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
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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
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
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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
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Neurodevelopment after prenatal diagnosis of isolated agenesis of the corpus callosum: an integrative review.
Alexandros Sotiriadis, George Makrydimas. Am J Obstet Gynecol 2012
Alexandros Sotiriadis, George Makrydimas. Am J Obstet Gynecol 2012
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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
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
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Agenesis of the corpus callosum: a clinical approach to diagnosis.
Elizabeth Emma Palmer, David Mowat. Am J Med Genet C Semin Med Genet 2014
Elizabeth Emma Palmer, David Mowat. Am J Med Genet C Semin Med Genet 2014
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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
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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
Eric B Levey, Elaine Stashinko, Nancy J Clegg, Mauricio R Delgado. Am J Med Genet C Semin Med Genet 2010
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Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
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Multiple hits during early embryonic development: digenic diseases and holoprosencephaly.
Jeffrey E Ming, Maximilian Muenke. Am J Hum Genet 2002
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Chromosomal microarray versus karyotyping for prenatal diagnosis.
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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
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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
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Neurodevelopmental outcomes in children with cerebellar malformations: a systematic review.
Marie-Eve Bolduc, Catherine Limperopoulos. Dev Med Child Neurol 2009
Marie-Eve Bolduc, Catherine Limperopoulos. Dev Med Child Neurol 2009
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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
R Mangione, N Fries, P Godard, C Capron, V Mirlesse, D Lacombe, M Duyme. Ultrasound Obstet Gynecol 2011
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Polymicrogyria: a common and heterogeneous malformation of cortical development.
Chloe A Stutterd, Richard J Leventer. Am J Med Genet C Semin Med Genet 2014
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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
Sharon Perlman, Omer Bar-Yosef, Jeffrey-Michael Jacobson, Yinon Gilboa, Estela Derazne, Reuven Achiron, Eldad Katorza. J Matern Fetal Neonatal Med 2018
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The challenge of imaging the fetal central nervous system: an aid to prenatal diagnosis, management and prognosis.
Lyn S Chitty, Gianluigi Pilu. Prenat Diagn 2009
Lyn S Chitty, Gianluigi Pilu. Prenat Diagn 2009
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Neuroimaging of ventriculomegaly in the fetal period.
V D'Addario, A C Rossi. Semin Fetal Neonatal Med 2012
V D'Addario, A C Rossi. Semin Fetal Neonatal Med 2012
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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
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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
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
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Neurodevelopmental outcome in isolated mild fetal ventriculomegaly: systematic review and meta-analysis.
G Pagani, B Thilaganathan, F Prefumo. Ultrasound Obstet Gynecol 2014
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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
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Brain injury in premature infants: a complex amalgam of destructive and developmental disturbances.
Joseph J Volpe. Lancet Neurol 2009
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Sonographic examination of the fetal central nervous system: guidelines for performing the 'basic examination' and the 'fetal neurosonogram'.
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Outcome of fetuses with prenatal diagnosis of isolated severe bilateral ventriculomegaly: systematic review and meta-analysis.
S Carta, A Kaelin Agten, C Belcaro, A Bhide. Ultrasound Obstet Gynecol 2018
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Developmental outcome of isolated fetal microcephaly.
S Stoler-Poria, D Lev, A Schweiger, T Lerman-Sagie, G Malinger. Ultrasound Obstet Gynecol 2010
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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
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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
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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.