A citation-based method for searching scientific literature

Claudio Toma, Amaia Hervás, Bàrbara Torrico, Noemí Balmaña, Marta Salgado, Marta Maristany, Elisabet Vilella, Rafael Martínez-Leal, Ma Inmaculada Planelles, Ivon Cuscó, Miguel del Campo, Luis A Pérez-Jurado, Rafaela Caballero-Andaluz, Yolanda de Diego-Otero, Lucía Pérez-Costillas, Josep A Ramos-Quiroga, Marta Ribasés, Mònica Bayés, Bru Cormand. Psychiatr Genet 2013
Times Cited: 39







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



Times Cited
  Times     Co-cited
Similarity


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
43

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.
Maricela Alarcón, Brett S Abrahams, Jennifer L Stone, Jacqueline A Duvall, Julia V Perederiy, Jamee M Bomar, Jonathan Sebat, Michael Wigler, Christa L Martin, David H Ledbetter,[...]. Am J Hum Genet 2008
559
43

A functional genetic link between distinct developmental language disorders.
Sonja C Vernes, Dianne F Newbury, Brett S Abrahams, Laura Winchester, Jérôme Nicod, Matthias Groszer, Maricela Alarcón, Peter L Oliver, Kay E Davies, Daniel H Geschwind,[...]. N Engl J Med 2008
402
41

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
Dan E Arking, David J Cutler, Camille W Brune, Tanya M Teslovich, Kristen West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin, Edwin H Cook,[...]. Am J Hum Genet 2008
414
41

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.
Kevin A Strauss, Erik G Puffenberger, Matthew J Huentelman, Steven Gottlieb, Seth E Dobrin, Jennifer M Parod, Dietrich A Stephan, D Holmes Morton. N Engl J Med 2006
436
38

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
Betul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, Abha R Gupta, Jesse F Abelson, Thomas M Morgan, Katarzyna Chawarska, Ami Klin, A Gulhan Ercan-Sencicek, Althea A Stillman,[...]. Am J Hum Genet 2008
388
35

A forkhead-domain gene is mutated in a severe speech and language disorder.
C S Lai, S E Fisher, J A Hurst, F Vargha-Khadem, A P Monaco. Nature 2001
33

CNTNAP2 variants affect early language development in the general population.
A J O Whitehouse, D V M Bishop, Q W Ang, C E Pennell, S E Fisher. Genes Brain Behav 2011
115
30

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
791
30

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.
Heather C Whalley, Garret O'Connell, Jessika E Sussmann, Anna Peel, Andrew C Stanfield, Marianna E Hayiou-Thomas, Eve C Johnstone, Stephen M Lawrie, Andrew M McIntosh, Jeremy Hall. Am J Med Genet B Neuropsychiatr Genet 2011
71
28

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.
Ashley A Scott-Van Zeeland, Brett S Abrahams, Ana I Alvarez-Retuerto, Lisa I Sonnenblick, Jeffrey D Rudie, Dara Ghahremani, Jeanette A Mumford, Russell A Poldrack, Mirella Dapretto, Daniel H Geschwind,[...]. Sci Transl Med 2010
179
28

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene.
Weiguo Shu, Julie Y Cho, Yuhui Jiang, Minhua Zhang, Donald Weisz, Gregory A Elder, James Schmeidler, Rita De Gasperi, Miguel A Gama Sosa, Donald Rabidou,[...]. Proc Natl Acad Sci U S A 2005
262
28

Defining the contribution of CNTNAP2 to autism susceptibility.
Srirangan Sampath, Shambu Bhat, Simone Gupta, Ashley O'Connor, Andrew B West, Dan E Arking, Aravinda Chakravarti. PLoS One 2013
25
44

Shining a light on CNTNAP2: complex functions to complex disorders.
Pedro Rodenas-Cuadrado, Joses Ho, Sonja C Vernes. Eur J Hum Genet 2014
153
25

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction.
Ikuko Teramitsu, Lili C Kudo, Sarah E London, Daniel H Geschwind, Stephanie A White. J Neurosci 2004
224
23

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.
Beate Peter, Wendy H Raskind, Mark Matsushita, Mark Lisowski, Tiffany Vu, Virginia W Berninger, Ellen M Wijsman, Zoran Brkanac. J Neurodev Disord 2011
77
23

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1.
Sebastian Poliak, Daniela Salomon, Hadas Elhanany, Helena Sabanay, Brent Kiernan, Larysa Pevny, Colin L Stewart, Xiaorong Xu, Shing-Yan Chiu, Peter Shrager,[...]. J Cell Biol 2003
379
23

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
Matthias Groszer, David A Keays, Robert M J Deacon, Joseph P de Bono, Shweta Prasad-Mulcare, Simone Gaub, Muriel G Baum, Catherine A French, Jérôme Nicod, Julie A Coventry,[...]. Curr Biol 2008
194
23

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
D F Newbury, S Paracchini, T S Scerri, L Winchester, L Addis, Alex J Richardson, J Walter, J F Stein, J B Talcott, A P Monaco. Behav Genet 2011
140
23

Individual common variants exert weak effects on the risk for autism spectrum disorders.
Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, Gillian Baird, Nadia Bolshakova, Sven Bölte, Patrick F Bolton, Thomas Bourgeron,[...]. Hum Mol Genet 2012
239
23


Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
Kay D MacDermot, Elena Bonora, Nuala Sykes, Anne-Marie Coupe, Cecilia S L Lai, Sonja C Vernes, Faraneh Vargha-Khadem, Fiona McKenzie, Robert L Smith, Anthony P Monaco,[...]. Am J Hum Genet 2005
257
20

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
Sonja C Vernes, Peter L Oliver, Elizabeth Spiteri, Helen E Lockstone, Rathi Puliyadi, Jennifer M Taylor, Joses Ho, Cedric Mombereau, Ariel Brewer, Ernesto Lowy,[...]. PLoS Genet 2011
177
20

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.
Elizabeth Spiteri, Genevieve Konopka, Giovanni Coppola, Jamee Bomar, Michael Oldham, Jing Ou, Sonja C Vernes, Simon E Fisher, Bing Ren, Daniel H Geschwind. Am J Hum Genet 2007
176
20

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels.
S Poliak, L Gollan, R Martinez, A Custer, S Einheber, J L Salzer, J S Trimmer, P Shrager, E Peles. Neuron 1999
374
20

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
20

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
Wolfgang Enard, Sabine Gehre, Kurt Hammerschmidt, Sabine M Hölter, Torsten Blass, Mehmet Somel, Martina K Brückner, Christiane Schreiweis, Christine Winter, Reinhard Sohr,[...]. Cell 2009
292
20

Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.
Sebastian Haesler, Christelle Rochefort, Benjamin Georgi, Pawel Licznerski, Pavel Osten, Constance Scharff. PLoS Biol 2007
253
20

FOXP2 is not a major susceptibility gene for autism or specific language impairment.
D F Newbury, E Bonora, J A Lamb, S E Fisher, C S L Lai, G Baird, L Jannoun, V Slonims, C M Stott, M J Merricks,[...]. Am J Hum Genet 2002
151
20

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.
Russell J Ferland, Timothy J Cherry, Patricia O Preware, Edward E Morrisey, Christopher A Walsh. J Comp Neurol 2003
344
20

Genome-wide analyses of human perisylvian cerebral cortical patterning.
B S Abrahams, D Tentler, J V Perederiy, M C Oldham, G Coppola, D H Geschwind. Proc Natl Acad Sci U S A 2007
131
20

FOXP2 as a molecular window into speech and language.
Simon E Fisher, Constance Scharff. Trends Genet 2009
279
17


The role of the FOXP family of transcription factors in ASD.
J Michael Bowers, Genevieve Konopka. Dis Markers 2012
42
17

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.
J I Friedman, T Vrijenhoek, S Markx, I M Janssen, W A van der Vliet, B H W Faas, N V Knoers, W Cahn, R S Kahn, L Edelmann,[...]. Mol Psychiatry 2008
218
17

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
17

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila.
Christiane Zweier, Eiko K de Jong, Markus Zweier, Alfredo Orrico, Lilian B Ousager, Amanda L Collins, Emilia K Bijlsma, Merel A W Oortveld, Arif B Ekici, André Reis,[...]. Am J Hum Genet 2009
241
17

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2.
Geoffrey C Y Tan, Thomas F Doke, John Ashburner, Nicholas W Wood, Richard S J Frackowiak. Neuroimage 2010
81
17

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.
John D Murdoch, Abha R Gupta, Stephan J Sanders, Michael F Walker, John Keaney, Thomas V Fernandez, Michael T Murtha, Samuel Anyanwu, Gordon T Ober, Melanie J Raubeson,[...]. PLoS Genet 2015
40
17


Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case.
Aline L Petrin, Célia M Giacheti, Luciana P Maximino, Dagma V M Abramides, Sthella Zanchetta, Natalia F Rossi, Antônio Richieri-Costa, Jeffrey C Murray. Am J Med Genet A 2010
41
15

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
Fadi F Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, Mathieu Langlois, Gila Foomani, Sylvia Dobrzeniecka, Marie-Odile Krebs, Ridha Joober,[...]. Am J Hum Genet 2010
151
15

Phenotype of FOXP2 haploinsufficiency in a mother and son.
Gregory M Rice, Gordana Raca, Kathy J Jakielski, Jennifer J Laffin, Christina M Iyama-Kurtycz, Sigan L Hartley, Rae E Sprague, Anne T Heintzelman, Lawrence D Shriberg. Am J Med Genet A 2012
45
15

3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination.
Orazio Palumbo, Leonardo D'Agruma, Adelaide Franca Minenna, Pietro Palumbo, Raffaella Stallone, Teresa Palladino, Leopoldo Zelante, Massimo Carella. Gene 2013
31
19

Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.
Lawrence D Shriberg, Kirrie J Ballard, J Bruce Tomblin, Joseph R Duffy, Katharine H Odell, Charles A Williams. J Speech Lang Hear Res 2006
96
15

Knockdown of FoxP2 alters spine density in Area X of the zebra finch.
S B Schulz, S Haesler, C Scharff, C Rochefort. Genes Brain Behav 2010
68
15

What does CNTNAP2 reveal about autism spectrum disorder?
Olga Peñagarikano, Daniel H Geschwind. Trends Mol Med 2012
92
15

Advances in autism genetics: on the threshold of a new neurobiology.
Brett S Abrahams, Daniel H Geschwind. Nat Rev Genet 2008
15

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
15

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
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.