A citation-based method for searching scientific literature

Lisa-Marie Niestroj, Eduardo Perez-Palma, Daniel P Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus, Peter Nürnberg, Remi Stevelink, Mark J Daly, Aarno Palotie, Dennis Lal. Brain 2020
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


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
64
60

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
236
60

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
110
60


Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasia.
Katja Kobow, Mark Ziemann, Harikrishnan Kaipananickal, Ishant Khurana, Angelika Mühlebner, Martha Feucht, Johannes A Hainfellner, Thomas Czech, Eleonora Aronica, Tom Pieper,[...]. Epilepsia 2019
20
40

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
61
40

DNA methylation-based classification of central nervous system tumours.
David Capper, David T W Jones, Martin Sill, Volker Hovestadt, Daniel Schrimpf, Dominik Sturm, Christian Koelsche, Felix Sahm, Lukas Chavez, David E Reuss,[...]. Nature 2018
720
40

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
119
40

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
239
40

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
106
40

Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy.
Dennis Lal, Katharina Pernhorst, Karl Martin Klein, Philipp Reif, Rossana Tozzi, Mohammad R Toliat, Georg Winterer, Bernd Neubauer, Peter Nürnberg, Felix Rosenow,[...]. Epilepsia 2015
21
40

RNA-Seq: a revolutionary tool for transcriptomics.
Zhong Wang, Mark Gerstein, Michael Snyder. Nat Rev Genet 2009
40

Developmental lineage of cell types in cortical dysplasia with balloon cells.
Phillip Lamparello, Marianna Baybis, John Pollard, Elly M Hol, David D Eisenstat, Eleonora Aronica, Peter B Crino. Brain 2007
75
40

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
963
40

Second-hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA.
Wei Shern Lee, Sarah E M Stephenson, Katherine B Howell, Kate Pope, Greta Gillies, Alison Wray, Wirginia Maixner, Simone A Mandelstam, Samuel F Berkovic, Ingrid E Scheffer,[...]. Ann Clin Transl Neurol 2019
16
40

Precise detection of low-level somatic mutation in resected epilepsy brain tissue.
Nam Suk Sim, Ara Ko, Woo Kyeong Kim, Se Hoon Kim, Ju Seong Kim, Kyu-Won Shim, Eleonora Aronica, Caroline Mijnsbergen, Wim G M Spliet, Hyun Yong Koh,[...]. Acta Neuropathol 2019
34
40

Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.
Elena Boland, Jill Clayton-Smith, Victoria G Woo, Shane McKee, Forbes D C Manson, Livija Medne, Elaine Zackai, Eric A Swanson, David Fitzpatrick, Kathleen J Millen,[...]. Am J Hum Genet 2007
116
20


Astrocytic inclusions in epilepsy: expanding the spectrum of filaminopathies.
Lili-Naz Hazrati, B K Kleinschmidt-DeMasters, Michael H Handler, Mary Lou Smith, Ayako Ochi, Hiroshi Otsubo, James T Rutka, Cristina Go, Shelly Weiss, Cynthia E Hawkins. J Neuropathol Exp Neurol 2008
24
20

The Mendelian disorders of the epigenetic machinery.
Hans Tomas Bjornsson. Genome Res 2015
72
20

Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly.
Diana Alcantara, Andrew E Timms, Karen Gripp, Laura Baker, Kaylee Park, Sarah Collins, Chi Cheng, Fiona Stewart, Sarju G Mehta, Anand Saggar,[...]. Brain 2017
50
20

Cortical Malformations: Lessons in Human Brain Development.
Lakshmi Subramanian, Maria Elisa Calcagnotto, Mercedes F Paredes. Front Cell Neurosci 2020
17
20

Current concepts of polymicrogyria.
A James Barkovich. Neuroradiology 2010
57
20

Definitions and classification of malformations of cortical development: practical guidelines.
Mariasavina Severino, Ana Filipa Geraldo, Norbert Utz, Domenico Tortora, Ivana Pogledic, Wlodzimierz Klonowski, Fabio Triulzi, Filippo Arrigoni, Kshitij Mankad, Richard J Leventer,[...]. Brain 2020
16
20


Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups.
Kristian W Pajtler, Hendrik Witt, Martin Sill, David T W Jones, Volker Hovestadt, Fabian Kratochwil, Khalida Wani, Ruth Tatevossian, Chandanamali Punchihewa, Pascal Johann,[...]. Cancer Cell 2015
481
20

Malformations of cortical development.
Eleonora Aronica, Albert J Becker, Roberto Spreafico. Brain Pathol 2012
68
20

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
133
20


Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
William B Dobyns, Ghayda Mirzaa, Susan L Christian, Kristin Petras, Jessica Roseberry, Gary D Clark, Cynthia J R Curry, Donna McDonald-McGinn, Livija Medne, Elaine Zackai,[...]. Am J Med Genet A 2008
64
20

A novel 11p13 microdeletion encompassing PAX6 in a Chinese Han family with aniridia, ptosis and mental retardation.
Ping Hu, Lulu Meng, Dingyuan Ma, Fengchang Qiao, Yan Wang, Jing Zhou, Long Yi, Zhengfeng Xu. Mol Cytogenet 2015
8
20

Periventricular nodular heterotopia with overlying polymicrogyria.
Gretchen Wieck, Richard J Leventer, Waney M Squier, An Jansen, Eva Andermann, Francois Dubeau, Anna Ramazzotti, Renzo Guerrini, William B Dobyns. Brain 2005
46
20

Cortical malformations.
Roberto Spreafico, Laura Tassi. Handb Clin Neurol 2012
5
20

A New Case with Corpus Callosum Abnormalities, Microcephaly and Seizures Associated with a 2.3-Mb 1q43-q44 Deletion.
Elisabet Lloveras, Anna Canellas, Laura Barranco, Claudia Alves, Marta Vila-Real, Vania Ventura, Daniel Fernández, Begona Mendez, Meritxell Piqué, Margarida Reis-Lima,[...]. Cytogenet Genome Res 2019
3
33

Role of TREK-1 in Health and Disease, Focus on the Central Nervous System.
Alaeddine Djillani, Jean Mazella, Catherine Heurteaux, Marc Borsotto. Front Pharmacol 2019
18
20

The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.
David N Louis, Arie Perry, Guido Reifenberger, Andreas von Deimling, Dominique Figarella-Branger, Webster K Cavenee, Hiroko Ohgaki, Otmar D Wiestler, Paul Kleihues, David W Ellison. Acta Neuropathol 2016
20

Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype.
Subramaniam Ganesh, Antonio V Delgado-Escueta, Toshimitsu Suzuki, Silvana Francheschetti, Concetta Riggio, Giuiliano Avanzini, Adrian Rabinowicz, Saeed Bohlega, Julia Bailey, Maria E Alonso,[...]. Hum Mol Genet 2002
60
20

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
514
20

Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).
Lisa J Strug, Tara Clarke, Theodore Chiang, Minchen Chien, Zeynep Baskurt, Weili Li, Ruslan Dorfman, Bhavna Bali, Elaine Wirrell, Steven L Kugler,[...]. Eur J Hum Genet 2009
130
20

A role of Rnd1 GTPase in dendritic spine formation in hippocampal neurons.
Yukio Ishikawa, Hironori Katoh, Manabu Negishi. J Neurosci 2003
60
20

A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis.
Myriam Vezain, Matthieu Lecuyer, Marina Rubio, Valérie Dupé, Leslie Ratié, Véronique David, Laurent Pasquier, Sylvie Odent, Sophie Coutant, Isabelle Tournier,[...]. Acta Neuropathol Commun 2018
8
20

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.
Christel Depienne, Caroline Nava, Boris Keren, Solveig Heide, Agnès Rastetter, Sandrine Passemard, Sandra Chantot-Bastaraud, Marie-Laure Moutard, Pankaj B Agrawal, Grace VanNoy,[...]. Hum Genet 2017
37
20

Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray.
Yi-an Chen, Mathieu Lemire, Sanaa Choufani, Darci T Butcher, Daria Grafodatskaya, Brent W Zanke, Steven Gallinger, Thomas J Hudson, Rosanna Weksberg. Epigenetics 2013
801
20

Correlation of prenatal events with the development of polymicrogyria.
A J Barkovich, H Rowley, A Bollen. AJNR Am J Neuroradiol 1995
91
20

Type I schizencephaly: CT and neuropathologic findings.
C R Bird, F H Gilles. AJNR Am J Neuroradiol 1987
29
20

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
389
20

deFuse: an algorithm for gene fusion discovery in tumor RNA-Seq data.
Andrew McPherson, Fereydoun Hormozdiari, Abdalnasser Zayed, Ryan Giuliany, Gavin Ha, Mark G F Sun, Malachi Griffith, Alireza Heravi Moussavi, Janine Senz, Nataliya Melnyk,[...]. PLoS Comput Biol 2011
348
20

Polymicrogyria: pathology, fetal origins and mechanisms.
Waney Squier, Anna Jansen. Acta Neuropathol Commun 2014
48
20

Survey of gene amplifications during prostate cancer progression by high-throughout fluorescence in situ hybridization on tissue microarrays.
L Bubendorf, J Kononen, P Koivisto, P Schraml, H Moch, T C Gasser, N Willi, M J Mihatsch, G Sauter, O P Kallioniemi. Cancer Res 1999
461
20

Methylation-based classification of benign and malignant peripheral nerve sheath tumors.
Manuel Röhrich, Christian Koelsche, Daniel Schrimpf, David Capper, Felix Sahm, Annekathrin Kratz, Jana Reuss, Volker Hovestadt, David T W Jones, Melanie Bewerunge-Hudler,[...]. Acta Neuropathol 2016
85
20


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.