A citation-based method for searching scientific literature

A James Barkovich, William B Dobyns, Renzo Guerrini. Cold Spring Harb Perspect Med 2015
Times Cited: 59







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



Times Cited
  Times     Co-cited
Similarity


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
35

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
536
32

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
266
28

Malformations of cortical development: clinical features and genetic causes.
Renzo Guerrini, William B Dobyns. Lancet Neurol 2014
220
23

PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia.
Laura A Jansen, Ghayda M Mirzaa, Gisele E Ishak, Brian J O'Roak, Joseph B Hiatt, William H Roden, Sonya A Gunter, Susan L Christian, Sarah Collins, Carissa Adams,[...]. Brain 2015
191
22

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
423
22

Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.
Alissa M D'Gama, Ying Geng, Javier A Couto, Beth Martin, Evan A Boyle, Christopher M LaCoursiere, Amer Hossain, Nicole E Hatem, Brenda J Barry, David J Kwiatkowski,[...]. Ann Neurol 2015
160
20

Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.
Jae Seok Lim, Ramu Gopalappa, Se Hoon Kim, Suresh Ramakrishna, Minji Lee, Woo-Il Kim, Junho Kim, Sang Min Park, Junehawk Lee, Jung-Hwa Oh,[...]. Am J Hum Genet 2017
94
20

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
92
20

Somatic activation of AKT3 causes hemispheric developmental brain malformations.
Annapurna Poduri, Gilad D Evrony, Xuyu Cai, Princess Christina Elhosary, Rameen Beroukhim, Maria K Lehtinen, L Benjamin Hills, Erin L Heinzen, Anthony Hill, R Sean Hill,[...]. Neuron 2012
298
18

Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.
Ghayda M Mirzaa, Catarina D Campbell, Nadia Solovieff, Carleton Goold, Laura A Jansen, Suchithra Menon, Andrew E Timms, Valerio Conti, Jonathan D Biag, Carissa Adams,[...]. JAMA Neurol 2016
138
18

Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutations.
Stéphanie Baulac, Saeko Ishida, Elise Marsan, Catherine Miquel, Arnaud Biraben, Dang Khoa Nguyen, Doug Nordli, Patrick Cossette, Sylvie Nguyen, Virginie Lambrecq,[...]. Ann Neurol 2015
154
18

Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias.
Alissa M D'Gama, Mollie B Woodworth, Amer A Hossain, Sara Bizzotto, Nicole E Hatem, Christopher M LaCoursiere, Imad Najm, Zhong Ying, Edward Yang, A James Barkovich,[...]. Cell Rep 2017
134
18

Somatic Mutations in the MTOR gene cause focal cortical dysplasia type IIb.
Mitsuko Nakashima, Hirotomo Saitsu, Nobuyuki Takei, Jun Tohyama, Mitsuhiro Kato, Hiroki Kitaura, Masaaki Shiina, Hiroshi Shirozu, Hiroshi Masuda, Keisuke Watanabe,[...]. Ann Neurol 2015
114
15

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery.
Ingmar Blumcke, Roberto Spreafico, Gerrit Haaker, Roland Coras, Katja Kobow, Christian G Bien, Margarete Pfäfflin, Christian Elger, Guido Widman, Johannes Schramm,[...]. N Engl J Med 2017
294
15

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Jean-Baptiste Rivière, Ghayda M Mirzaa, Brian J O'Roak, Margaret Beddaoui, Diana Alcantara, Robert L Conway, Judith St-Onge, Jeremy A Schwartzentruber, Karen W Gripp, Sarah M Nikkel,[...]. Nat Genet 2012
446
13

Focal dysplasia of the cerebral cortex in epilepsy.
D C Taylor, M A Falconer, C J Bruton, J A Corsellis. J Neurol Neurosurg Psychiatry 1971
799
13

Malformations of cortical development.
Rahul S Desikan, A James Barkovich. Ann Neurol 2016
54
14

The genomic landscape of tuberous sclerosis complex.
Katie R Martin, Wanding Zhou, Megan J Bowman, Juliann Shih, Kit Sing Au, Kristin E Dittenhafer-Reed, Kellie A Sisson, Julie Koeman, Daniel J Weisenberger, Sandra L Cottingham,[...]. Nat Commun 2017
99
13

The tuberous sclerosis complex.
Peter B Crino, Katherine L Nathanson, Elizabeth Petri Henske. N Engl J Med 2006
13


Dissecting the genetic basis of focal cortical dysplasia: a large cohort study.
Sara Baldassari, Théo Ribierre, Elise Marsan, Homa Adle-Biassette, Sarah Ferrand-Sorbets, Christine Bulteau, Nathalie Dorison, Martine Fohlen, Marc Polivka, Sarah Weckhuysen,[...]. Acta Neuropathol 2019
86
13

Somatic mutation, genomic variation, and neurological disease.
Annapurna Poduri, Gilad D Evrony, Xuyu Cai, Christopher A Walsh. Science 2013
342
11

A developmental and genetic classification for malformations of cortical development.
A J Barkovich, R I Kuzniecky, G D Jackson, R Guerrini, W B Dobyns. Neurology 2005
463
11

Somatic mutations in cerebral cortical malformations.
Saumya S Jamuar, Anh-Thu N Lam, Martin Kircher, Alissa M D'Gama, Jian Wang, Brenda J Barry, Xiaochang Zhang, Robert Sean Hill, Jennifer N Partlow, Aldo Rozzo,[...]. N Engl J Med 2014
207
11

Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study.
Jacqueline A French, John A Lawson, Zuhal Yapici, Hiroko Ikeda, Tilman Polster, Rima Nabbout, Paolo Curatolo, Petrus J de Vries, Dennis J Dlugos, Noah Berkowitz,[...]. Lancet 2016
325
11

Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR.
Richard J Leventer, Thomas Scerri, Ashley P L Marsh, Kate Pope, Greta Gillies, Wirginia Maixner, Duncan MacGregor, A Simon Harvey, Martin B Delatycki, David J Amor,[...]. Neurology 2015
46
15

Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3.
Joe C Sim, Thomas Scerri, Miriam Fanjul-Fernández, Jessica R Riseley, Greta Gillies, Kate Pope, Hanna van Roozendaal, Julian I Heng, Simone A Mandelstam, George McGillivray,[...]. Ann Neurol 2016
79
10

Fetal brain mTOR signaling activation in tuberous sclerosis complex.
Victoria Tsai, Whitney E Parker, Ksenia A Orlova, Marianna Baybis, Anthony W S Chi, Benjamin D Berg, Jacqueline F Birnbaum, Jacqueline Estevez, Kei Okochi, Harvey B Sarnat,[...]. Cereb Cortex 2014
80
10


Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.
Ingrid E Scheffer, Sarah E Heron, Brigid M Regan, Simone Mandelstam, Douglas E Crompton, Bree L Hodgson, Laura Licchetta, Federica Provini, Francesca Bisulli, Lata Vadlamudi,[...]. Ann Neurol 2014
137
10

Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy.
Rikke S Møller, Sarah Weckhuysen, Mathilde Chipaux, Elise Marsan, Valerie Taly, E Martina Bebin, Susan M Hiatt, Jeremy W Prokop, Kevin M Bowling, Davide Mei,[...]. Neurol Genet 2016
67
10

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.
Wei Qin, Jennifer A Chan, Harry V Vinters, Gary W Mathern, David N Franz, Bruce E Taillon, Pascal Bouffard, David J Kwiatkowski. Brain Pathol 2010
81
10

Development of the human cerebral cortex: Boulder Committee revisited.
Irina Bystron, Colin Blakemore, Pasko Rakic. Nat Rev Neurosci 2008
568
10


Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy.
Melodie R Winawer, Nicole G Griffin, Jorge Samanamud, Evan H Baugh, Dinesh Rathakrishnan, Senthilmurugan Ramalingam, David Zagzag, Catherine A Schevon, Patricia Dugan, Manu Hegde,[...]. Ann Neurol 2018
56
10


A classification scheme for malformations of cortical development.
A J Barkovich, R I Kuzniecky, W B Dobyns, G D Jackson, L E Becker, P Evrard. Neuropediatrics 1996
300
8

Genotypically defined lissencephalies show distinct pathologies.
Mark S Forman, Waney Squier, William B Dobyns, Jeffrey A Golden. J Neuropathol Exp Neurol 2005
78
8

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.
J G Gleeson, K M Allen, J W Fox, E D Lamperti, S Berkovic, I Scheffer, E C Cooper, W B Dobyns, S R Minnerath, M E Ross,[...]. Cell 1998
796
8

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.
Karine Poirier, Nicolas Lebrun, Loic Broix, Guoling Tian, Yoann Saillour, Cécile Boscheron, Elena Parrini, Stephanie Valence, Benjamin Saint Pierre, Madison Oger,[...]. Nat Genet 2013
262
8

mTOR signaling in growth control and disease.
Mathieu Laplante, David M Sabatini. Cell 2012
8

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
8

Neurogenic radial glia in the outer subventricular zone of human neocortex.
David V Hansen, Jan H Lui, Philip R L Parker, Arnold R Kriegstein. Nature 2010
774
8

Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5.
Thomas Scerri, Jessica R Riseley, Greta Gillies, Kate Pope, Rosemary Burgess, Simone A Mandelstam, Leanne Dibbens, Chung W Chow, Wirginia Maixner, Anthony Simon Harvey,[...]. Ann Clin Transl Neurol 2015
65
8

The neurology of mTOR.
Jonathan O Lipton, Mustafa Sahin. Neuron 2014
380
8

Mutations in DEPDC5 cause familial focal epilepsy with variable foci.
Leanne M Dibbens, Boukje de Vries, Simona Donatello, Sarah E Heron, Bree L Hodgson, Satyan Chintawar, Douglas E Crompton, James N Hughes, Susannah T Bellows, Karl Martin Klein,[...]. Nat Genet 2013
200
8

Basic mechanisms of epileptogenesis in pediatric cortical dysplasia.
Sara Abdijadid, Gary W Mathern, Michael S Levine, Carlos Cepeda. CNS Neurosci Ther 2015
47
10


On Hypertrophy and Atrophy of the Brain.
J Sims. Med Chir Trans 1835
32
15


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.