A James Barkovich, William B Dobyns, Renzo Guerrini. Cold Spring Harb Perspect Med 2015
Times Cited: 59
Times Cited: 59
Times Cited
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The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission.
Ingmar Blümcke, Maria Thom, Eleonora Aronica, Dawna D Armstrong, Harry V Vinters, Andre Palmini, Thomas S Jacques, Giuliano Avanzini, A James Barkovich, Giorgio Battaglia,[...]. Epilepsia 2011
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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
A James Barkovich, Renzo Guerrini, Ruben I Kuzniecky, Graeme D Jackson, William B Dobyns. Brain 2012
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Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy.
Jae Seok Lim, Woo-il Kim, Hoon-Chul Kang, Se Hoon Kim, Ah Hyung Park, Eun Kyung Park, Young-Wook Cho, Sangwoo Kim, Ho Min Kim, Jeong A Kim,[...]. Nat Med 2015
Jae Seok Lim, Woo-il Kim, Hoon-Chul Kang, Se Hoon Kim, Ah Hyung Park, Eun Kyung Park, Young-Wook Cho, Sangwoo Kim, Ho Min Kim, Jeong A Kim,[...]. Nat Med 2015
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Malformations of cortical development: clinical features and genetic causes.
Renzo Guerrini, William B Dobyns. Lancet Neurol 2014
Renzo Guerrini, William B Dobyns. Lancet Neurol 2014
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PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia.
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De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly.
Jeong Ho Lee, My Huynh, Jennifer L Silhavy, Sangwoo Kim, Tracy Dixon-Salazar, Andrew Heiberg, Eric Scott, Vineet Bafna, Kiley J Hill, Adrienne Collazo,[...]. Nat Genet 2012
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Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.
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Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.
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Second-hit mosaic mutation in mTORC1 repressor DEPDC5 causes focal cortical dysplasia-associated epilepsy.
Théo Ribierre, Charlotte Deleuze, Alexandre Bacq, Sara Baldassari, Elise Marsan, Mathilde Chipaux, Giuseppe Muraca, Delphine Roussel, Vincent Navarro, Eric Leguern,[...]. J Clin Invest 2018
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Somatic activation of AKT3 causes hemispheric developmental brain malformations.
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Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.
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Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutations.
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Somatic Mutations in the MTOR gene cause focal cortical dysplasia type IIb.
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De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
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Focal dysplasia of the cerebral cortex in epilepsy.
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Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR.
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Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3.
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Fetal brain mTOR signaling activation in tuberous sclerosis complex.
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Ruben Kuzniecky. Curr Opin Neurol 2015
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Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.
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Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy.
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Analysis of TSC cortical tubers by deep sequencing of TSC1, TSC2 and KRAS demonstrates that small second-hit mutations in these genes are rare events.
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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.