A citation-based method for searching scientific literature

Giorgio La Fata, Annette Gärtner, Nuria Domínguez-Iturza, Tom Dresselaers, Julia Dawitz, Rogier B Poorthuis, Michele Averna, Uwe Himmelreich, Rhiannon M Meredith, Tilmann Achsel, Carlos G Dotti, Claudia Bagni. Nat Neurosci 2014
Times Cited: 92







List of co-cited articles
1529 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
Jennifer C Darnell, Sarah J Van Driesche, Chaolin Zhang, Ka Ying Sharon Hung, Aldo Mele, Claire E Fraser, Elizabeth F Stone, Cynthia Chen, John J Fak, Sung Wook Chi,[...]. Cell 2011
31


Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases.
Stephen C Noctor, Verónica Martínez-Cerdeño, Lidija Ivic, Arnold R Kriegstein. Nat Neurosci 2004
20

Circuit level defects in the developing neocortex of Fragile X mice.
J Tiago Gonçalves, James E Anstey, Peyman Golshani, Carlos Portera-Cailliau. Nat Neurosci 2013
185
18

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
16

Altered synaptic plasticity in a mouse model of fragile X mental retardation.
Kimberly M Huber, Sean M Gallagher, Stephen T Warren, Mark F Bear. Proc Natl Acad Sci U S A 2002
978
15

Altered differentiation of neural stem cells in fragile X syndrome.
Maija Castrén, Topi Tervonen, Virve Kärkkäinen, Seppo Heinonen, Eero Castrén, Kim Larsson, Cathy E Bakker, Ben A Oostra, Karl Akerman. Proc Natl Acad Sci U S A 2005
132
15

The mGluR theory of fragile X mental retardation.
Mark F Bear, Kimberly M Huber, Stephen T Warren. Trends Neurosci 2004
14


Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
14

FMRP targets distinct mRNA sequence elements to regulate protein expression.
Manuel Ascano, Neelanjan Mukherjee, Pradeep Bandaru, Jason B Miller, Jeffrey D Nusbaum, David L Corcoran, Christine Langlois, Mathias Munschauer, Scott Dewell, Markus Hafner,[...]. Nature 2012
458
14

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
14

Critical period plasticity is disrupted in the barrel cortex of FMR1 knockout mice.
Emily G Harlow, Sally M Till, Theron A Russell, Lasani S Wijetunge, Peter Kind, Anis Contractor. Neuron 2010
178
14

Neurons derived from radial glial cells establish radial units in neocortex.
S C Noctor, A C Flint, T A Weissman, R S Dammerman, A R Kriegstein. Nature 2001
14

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
631
14

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome.
V Brown, P Jin, S Ceman, J C Darnell, W T O'Donnell, S A Tenenbaum, X Jin, Y Feng, K D Wilkinson, J D Keene,[...]. Cell 2001
864
14

Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
13


Two modes of radial migration in early development of the cerebral cortex.
B Nadarajah, J E Brunstrom, J Grutzendler, R O Wong, A L Pearlman. Nat Neurosci 2001
506
13

Patches of disorganization in the neocortex of children with autism.
Rich Stoner, Maggie L Chow, Maureen P Boyle, Susan M Sunkin, Peter R Mouton, Subhojit Roy, Anthony Wynshaw-Boris, Sophia A Colamarino, Ed S Lein, Eric Courchesne. N Engl J Med 2014
426
13

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
11


Aberrant differentiation of glutamatergic cells in neocortex of mouse model for fragile X syndrome.
Topi A Tervonen, Verna Louhivuori, Xiaohong Sun, Marie-Estelle Hokkanen, Claudius F Kratochwil, Pawel Zebryk, Eero Castrén, Maija L Castrén. Neurobiol Dis 2009
60
18


Dendritic channelopathies contribute to neocortical and sensory hyperexcitability in Fmr1(-/y) mice.
Yu Zhang, Audrey Bonnan, Guillaume Bony, Isabelle Ferezou, Susanna Pietropaolo, Melanie Ginger, Nathalie Sans, Jean Rossier, Ben Oostra, Gwen LeMasson,[...]. Nat Neurosci 2014
122
11

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
581
11

The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes.
Jerzy Wegiel, Izabela Kuchna, Krzysztof Nowicki, Humi Imaki, Jarek Wegiel, Elaine Marchi, Shuang Yong Ma, Abha Chauhan, Ved Chauhan, Teresa Wierzba Bobrowicz,[...]. Acta Neuropathol 2010
369
11

Neuronal subtype specification in the cerebral cortex.
Bradley J Molyneaux, Paola Arlotta, Joao R L Menezes, Jeffrey D Macklis. Nat Rev Neurosci 2007
10

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
10

Rab GTPases-dependent endocytic pathways regulate neuronal migration and maturation through N-cadherin trafficking.
Takeshi Kawauchi, Katsutoshi Sekine, Mima Shikanai, Kaori Chihama, Kenji Tomita, Ken-ichiro Kubo, Kazunori Nakajima, Yo-Ichi Nabeshima, Mikio Hoshino. Neuron 2010
231
10

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Brian J O'Roak, Laura Vives, Wenqing Fu, Jarrett D Egertson, Ian B Stanaway, Ian G Phelps, Gemma Carvill, Akash Kumar, Choli Lee, Katy Ankenman,[...]. Science 2012
839
10


Altered Neuronal and Circuit Excitability in Fragile X Syndrome.
Anis Contractor, Vitaly A Klyachko, Carlos Portera-Cailliau. Neuron 2015
212
10

Pten regulates neuronal arborization and social interaction in mice.
Chang-Hyuk Kwon, Bryan W Luikart, Craig M Powell, Jing Zhou, Sharon A Matheny, Wei Zhang, Yanjiao Li, Suzanne J Baker, Luis F Parada. Neuron 2006
695
10


Dynamic mRNA Transport and Local Translation in Radial Glial Progenitors of the Developing Brain.
Louis-Jan Pilaz, Ashley L Lennox, Jeremy P Rouanet, Debra L Silver. Curr Biol 2016
78
12


Temporally defined neocortical translation and polysome assembly are determined by the RNA-binding protein Hu antigen R.
Matthew L Kraushar, Kevin Thompson, H R Sagara Wijeratne, Barbara Viljetic, Kristina Sakers, Justin W Marson, Dimitris L Kontoyiannis, Steven Buyske, Ronald P Hart, Mladen-Roko Rasin. Proc Natl Acad Sci U S A 2014
60
15

The multipolar stage and disruptions in neuronal migration.
Joseph J LoTurco, Jilin Bai. Trends Neurosci 2006
187
9

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
9


The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP.
Ilaria Napoli, Valentina Mercaldo, Pietro Pilo Boyl, Boris Eleuteri, Francesca Zalfa, Silvia De Rubeis, Daniele Di Marino, Evita Mohr, Marzia Massimi, Mattia Falconi,[...]. Cell 2008
413
9

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
A J Verkerk, M Pieretti, J S Sutcliffe, Y H Fu, D P Kuhl, A Pizzuti, O Reiner, S Richards, M F Victoria, F P Zhang. Cell 1991
9

Mutations causing syndromic autism define an axis of synaptic pathophysiology.
Benjamin D Auerbach, Emily K Osterweil, Mark F Bear. Nature 2011
436
9

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.
Neelroop N Parikshak, Rui Luo, Alice Zhang, Hyejung Won, Jennifer K Lowe, Vijayendran Chandran, Steve Horvath, Daniel H Geschwind. Cell 2013
604
9

Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.
Claudia Bagni, Flora Tassone, Giovanni Neri, Randi Hagerman. J Clin Invest 2012
204
8

The developmental switch in GABA polarity is delayed in fragile X mice.
Qionger He, Toshihiro Nomura, Jian Xu, Anis Contractor. J Neurosci 2014
139
8

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
893
8

Circuit and plasticity defects in the developing somatosensory cortex of FMR1 knock-out mice.
Ingrid Bureau, Gordon M G Shepherd, Karel Svoboda. J Neurosci 2008
153
8

Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex.
Chris Englund, Andy Fink, Charmaine Lau, Diane Pham, Ray A M Daza, Alessandro Bulfone, Tom Kowalczyk, Robert F Hevner. J Neurosci 2005
939
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.