A citation-based method for searching scientific literature

Waney Squier, Anna Jansen. Acta Neuropathol Commun 2014
Times Cited: 56







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



Times Cited
  Times     Co-cited
Similarity


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
33

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
26

The histopathology of polymicrogyria: a series of 71 brain autopsy studies.
Anna C Jansen, Yves Robitaille, Mrinalini Honavar, Nandini Mullatti, Richard J Leventer, Eva Andermann, Frederick Andermann, Waney Squier. Dev Med Child Neurol 2016
22
54

Current concepts of polymicrogyria.
A James Barkovich. Neuroradiology 2010
62
19


Polymicrogyria includes fusion of the molecular layer and decreased neuronal populations but normal cortical laminar organization.
Alexander R Judkins, Daniel Martinez, Pamela Ferreira, William B Dobyns, Jeffrey A Golden. J Neuropathol Exp Neurol 2011
40
25

Genetics of the polymicrogyria syndromes.
A Jansen, E Andermann. J Med Genet 2005
96
17

Malformations of cortical development: clinical features and genetic causes.
Renzo Guerrini, William B Dobyns. Lancet Neurol 2014
224
16

Cerebral cortex expansion and folding: what have we learned?
Virginia Fernández, Cristina Llinares-Benadero, Víctor Borrell. EMBO J 2016
145
16

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
16


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
15

Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.
Xavier Hubert Jaglin, Karine Poirier, Yoann Saillour, Emmanuelle Buhler, Guoling Tian, Nadia Bahi-Buisson, Catherine Fallet-Bianco, Françoise Phan-Dinh-Tuy, Xiang Peng Kong, Pascale Bomont,[...]. Nat Genet 2009
251
14

A role for intermediate radial glia in the tangential expansion of the mammalian cerebral cortex.
Isabel Reillo, Camino de Juan Romero, Miguel Ángel García-Cabezas, Víctor Borrell. Cereb Cortex 2011
375
14

Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies.
Louise Devisme, Céline Bouchet, Marie Gonzalès, Elisabeth Alanio, Anne Bazin, Bettina Bessières, Nicole Bigi, Patricia Blanchet, Dominique Bonneau, Maryse Bonnières,[...]. Brain 2012
97
14

Mechanical model of brain convolutional development.
D P Richman, R M Stewart, J W Hutchinson, V S Caviness. Science 1975
356
12

OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling.
Simone A Fietz, Iva Kelava, Johannes Vogt, Michaela Wilsch-Bräuninger, Denise Stenzel, Jennifer L Fish, Denis Corbeil, Axel Riehn, Wolfgang Distler, Robert Nitsch,[...]. Nat Neurosci 2010
502
12

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
780
12

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
797
12

Integrin αvβ3 and thyroid hormones promote expansion of progenitors in embryonic neocortex.
Denise Stenzel, Michaela Wilsch-Bräuninger, Fong Kuan Wong, Heike Heuer, Wieland B Huttner. Development 2014
72
12

Molecular identity of human outer radial glia during cortical development.
Alex A Pollen, Tomasz J Nowakowski, Jiadong Chen, Hanna Retallack, Carmen Sandoval-Espinosa, Cory R Nicholas, Joe Shuga, Siyuan John Liu, Michael C Oldham, Aaron Diaz,[...]. Cell 2015
409
12

Development and evolution of the human neocortex.
Jan H Lui, David V Hansen, Arnold R Kriegstein. Cell 2011
740
12

Precursor diversity and complexity of lineage relationships in the outer subventricular zone of the primate.
Marion Betizeau, Veronique Cortay, Dorothée Patti, Sabina Pfister, Elodie Gautier, Angèle Bellemin-Ménard, Marielle Afanassieff, Cyril Huissoud, Rodney J Douglas, Henry Kennedy,[...]. Neuron 2013
267
12


Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human.
Michel Kielar, Françoise Phan Dinh Tuy, Sara Bizzotto, Cécile Lebrand, Camino de Juan Romero, Karine Poirier, Renske Oegema, Grazia Maria Mancini, Nadia Bahi-Buisson, Robert Olaso,[...]. Nat Neurosci 2014
78
10

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.
Timothy W Yu, Ganeshwaran H Mochida, David J Tischfield, Sema K Sgaier, Laura Flores-Sarnat, Consolato M Sergi, Meral Topçu, Marie T McDonald, Brenda J Barry, Jillian M Felie,[...]. Nat Genet 2010
205
10

Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division.
Jessica Yingling, Yong Ha Youn, Dawn Darling, Kazuhito Toyo-Oka, Tiziano Pramparo, Shinji Hirotsune, Anthony Wynshaw-Boris. Cell 2008
202
10


Amplification of progenitors in the mammalian telencephalon includes a new radial glial cell type.
Gregor-Alexander Pilz, Atsunori Shitamukai, Isabel Reillo, Emilie Pacary, Julia Schwausch, Ronny Stahl, Jovica Ninkovic, Hugo J Snippert, Hans Clevers, Leanne Godinho,[...]. Nat Commun 2013
135
10

The cell biology of neurogenesis: toward an understanding of the development and evolution of the neocortex.
Elena Taverna, Magdalena Götz, Wieland B Huttner. Annu Rev Cell Dev Biol 2014
389
10

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats.
O Reiner, R Carrozzo, Y Shen, M Wehnert, F Faustinella, W B Dobyns, C T Caskey, D H Ledbetter. Nature 1993
853
10

Cortical gyrification induced by fibroblast growth factor 2 in the mouse brain.
Brian G Rash, Simone Tomasi, H David Lim, Carol Y Suh, Flora M Vaccarino. J Neurosci 2013
63
10

Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal.
Simone A Fietz, Robert Lachmann, Holger Brandl, Martin Kircher, Nikolay Samusik, Roland Schröder, Naharajan Lakshmanaperumal, Ian Henry, Johannes Vogt, Axel Riehn,[...]. Proc Natl Acad Sci U S A 2012
193
10

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
424
10

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
S E Hong, Y Y Shugart, D T Huang, S A Shahwan, P E Grant, J O Hourihane, N D Martin, C A Walsh. Nat Genet 2000
579
10

The outer subventricular zone and primate-specific cortical complexification.
Colette Dehay, Henry Kennedy, Kenneth S Kosik. Neuron 2015
164
10

Gyrification from constrained cortical expansion.
Tuomas Tallinen, Jun Young Chung, John S Biggins, L Mahadevan. Proc Natl Acad Sci U S A 2014
166
10

Gyrification of the cerebral cortex requires FGF signaling in the mammalian brain.
Naoyuki Matsumoto, Yohei Shinmyo, Yoshie Ichikawa, Hiroshi Kawasaki. Elife 2017
45
13

Axons pull on the brain, but tension does not drive cortical folding.
Gang Xu, Andrew K Knutsen, Krikor Dikranian, Christopher D Kroenke, Philip V Bayly, Larry A Taber. J Biomech Eng 2010
146
8

Development of cortical folding during evolution and ontogeny.
Karl Zilles, Nicola Palomero-Gallagher, Katrin Amunts. Trends Neurosci 2013
281
8

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.
E Parrini, A Ramazzotti, W B Dobyns, D Mei, F Moro, P Veggiotti, C Marini, E H Brilstra, B Dalla Bernardina, L Goodwin,[...]. Brain 2006
224
8

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.
Daniel Beltrán-Valero de Bernabé, Sophie Currier, Alice Steinbrecher, Jacopo Celli, Ellen van Beusekom, Bert van der Zwaag, Hülya Kayserili, Luciano Merlini, David Chitayat, William B Dobyns,[...]. Am J Hum Genet 2002
506
8

GPR56 regulates pial basement membrane integrity and cortical lamination.
Shihong Li, Zhaohui Jin, Samir Koirala, Lihong Bu, Lei Xu, Richard O Hynes, Christopher A Walsh, Gabriel Corfas, Xianhua Piao. J Neurosci 2008
164
8

Trnp1 regulates expansion and folding of the mammalian cerebral cortex by control of radial glial fate.
Ronny Stahl, Tessa Walcher, Camino De Juan Romero, Gregor Alexander Pilz, Silvia Cappello, Martin Irmler, José Miguel Sanz-Aquela, Johannes Beckers, Robert Blum, Víctor Borrell,[...]. Cell 2013
172
8

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.
Silvia Cappello, Mary J Gray, Caroline Badouel, Simona Lange, Melanie Einsiedler, Myriam Srour, David Chitayat, Fadi F Hamdan, Zandra A Jenkins, Tim Morgan,[...]. Nat Genet 2013
159
8

Mouse inscuteable induces apical-basal spindle orientation to facilitate intermediate progenitor generation in the developing neocortex.
Maria Pia Postiglione, Christoph Jüschke, Yunli Xie, Gerald A Haas, Christoforos Charalambous, Juergen A Knoblich. Neuron 2011
123
8

Regulation of radial glial survival by signals from the meninges.
Randor Radakovits, Claudia S Barros, Richard Belvindrah, Bruce Patton, Ulrich Müller. J Neurosci 2009
93
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

Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].
Fowzan S Alkuraya, Xuyu Cai, Carina Emery, Ganeshwaran H Mochida, Mohammed S Al-Dosari, Jillian M Felie, R Sean Hill, Brenda J Barry, Jennifer N Partlow, Generoso G Gascon,[...]. Am J Hum Genet 2011
152
8



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.