A citation-based method for searching scientific literature

Annemieke J M H Verkerk, Carol A Mathews, Marijke Joosse, Bert H J Eussen, Peter Heutink, Ben A Oostra. Genomics 2003
Times Cited: 168







List of co-cited articles
1208 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Sequence variants in SLITRK1 are associated with Tourette's syndrome.
Jesse F Abelson, Kenneth Y Kwan, Brian J O'Roak, Danielle Y Baek, Althea A Stillman, Thomas M Morgan, Carol A Mathews, David L Pauls, Mladen-Roko Rasin, Murat Gunel,[...]. Science 2005
658
41

L-histidine decarboxylase and Tourette's syndrome.
A Gulhan Ercan-Sencicek, Althea A Stillman, Ananda K Ghosh, Kaya Bilguvar, Brian J O'Roak, Christopher E Mason, Thomas Abbott, Abha Gupta, Robert A King, David L Pauls,[...]. N Engl J Med 2010
210
36

Familial deletion within NLGN4 associated with autism and Tourette syndrome.
Amy Lawson-Yuen, Juan-Sebastian Saldivar, Steve Sommer, Jonathan Picker. Eur J Hum Genet 2008
192
31

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
31

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
29

Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.
Jose M Belloso, Iben Bache, Miriam Guitart, Maria Rosa Caballin, Christina Halgren, Maria Kirchhoff, Hans-Hilger Ropers, Niels Tommerup, Zeynep Tümer. Eur J Hum Genet 2007
58
46

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.
E Petek, C Windpassinger, J B Vincent, J Cheung, A P Boright, S W Scherer, P M Kroisel, K Wagner. Am J Hum Genet 2001
121
26

Tourette syndrome is associated with recurrent exonic copy number variants.
Senthil K Sundaram, Ahm M Huq, Benjamin J Wilson, Harry T Chugani. Neurology 2010
86
30

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
26

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
24

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
23

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
22

Genome-wide association study of Tourette's syndrome.
J M Scharf, D Yu, C A Mathews, B M Neale, S E Stewart, J A Fagerness, P Evans, E Gamazon, C K Edlund, S K Service,[...]. Mol Psychiatry 2013
116
21

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
20

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
Thomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, A Gulhan Ercan-Sencicek, Young-Shin Kim, Daniel O Fishman, Melanie J Raubeson, Youeun Song, Katsuhito Yasuno, Winson S C Ho,[...]. Biol Psychiatry 2012
121
20

A twin study of Tourette syndrome.
R A Price, K K Kidd, D J Cohen, D L Pauls, J F Leckman. Arch Gen Psychiatry 1985
240
18


Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.
Martin Poot, Vera Beyer, Ira Schwaab, Natalja Damatova, Ruben Van't Slot, Jo Prothero, Sue E Holder, Thomas Haaf. Neurogenetics 2010
96
18

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
18

CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.
Abhishek Nag, Elena G Bochukova, Barbara Kremeyer, Desmond D Campbell, Heike Muller, Ana V Valencia-Duarte, Julio Cardona, Isabel C Rivas, Sandra C Mesa, Mauricio Cuartas,[...]. PLoS One 2013
52
34

Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and mice.
Lissandra Castellan Baldan, Kyle A Williams, Jean-Dominique Gallezot, Vladimir Pogorelov, Maximiliano Rapanelli, Michael Crowley, George M Anderson, Erin Loring, Roxanne Gorczyca, Eileen Billingslea,[...]. Neuron 2014
148
17

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
16

Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development.
Garret R Anderson, Timothy Galfin, Wei Xu, Jason Aoto, Robert C Malenka, Thomas C Südhof. Proc Natl Acad Sci U S A 2012
144
16


The genetics of Tourette syndrome: a review.
Julia A O'Rourke, Jeremiah M Scharf, Dongmei Yu, David L Pauls. J Psychosom Res 2009
108
15

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
15

Shining a light on CNTNAP2: complex functions to complex disorders.
Pedro Rodenas-Cuadrado, Joses Ho, Sonja C Vernes. Eur J Hum Genet 2014
153
15

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Lea K Davis, Dongmei Yu, Clare L Keenan, Eric R Gamazon, Anuar I Konkashbaev, Eske M Derks, Benjamin M Neale, Jian Yang, S Hong Lee, Patrick Evans,[...]. PLoS Genet 2013
159
15

Decreased number of parvalbumin and cholinergic interneurons in the striatum of individuals with Tourette syndrome.
Yuko Kataoka, Paul S A Kalanithi, Heidi Grantz, Michael L Schwartz, Clifford Saper, James F Leckman, Flora M Vaccarino. J Comp Neurol 2010
282
14

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
J Elia, X Gai, H M Xie, J C Perin, E Geiger, J T Glessner, M D'arcy, R deBerardinis, E Frackelton, C Kim,[...]. Mol Psychiatry 2010
366
14

Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.
Chirag Patel, Lisa Cooper-Charles, Dominic J McMullan, Judith M Walker, Val Davison, Jenny Morton. Eur J Hum Genet 2011
52
26

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1.
Anne Gregor, Beate Albrecht, Ingrid Bader, Emilia K Bijlsma, Arif B Ekici, Hartmut Engels, Karl Hackmann, Denise Horn, Juliane Hoyer, Jakub Klapecki,[...]. BMC Med Genet 2011
90
15

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.
I Karagiannidis, R Rizzo, Z Tarnok, T Wolanczyk, J Hebebrand, M M Nöthen, G Lehmkuhl, L Farkas, P Nagy, C Barta,[...]. Mol Psychiatry 2012
39
35

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
14

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
Lauren M McGrath, Dongmei Yu, Christian Marshall, Lea K Davis, Bhooma Thiruvahindrapuram, Bingbin Li, Carolina Cappi, Gloria Gerber, Aaron Wolf, Frederick A Schroeder,[...]. J Am Acad Child Adolesc Psychiatry 2014
77
18

Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome.
H Deng, W D Le, W J Xie, J Jankovic. Acta Neurol Scand 2006
51
25

Altered parvalbumin-positive neuron distribution in basal ganglia of individuals with Tourette syndrome.
Paul S A Kalanithi, Wei Zheng, Yuko Kataoka, Marian DiFiglia, Heidi Grantz, Clifford B Saper, Michael L Schwartz, James F Leckman, Flora M Vaccarino. Proc Natl Acad Sci U S A 2005
337
13

Association of SLITRK1 to Gilles de la Tourette Syndrome.
Debora M Miranda, Karen Wigg, E Mameisia Kabia, Yu Feng, Paul Sandor, Cathy L Barr. Am J Med Genet B Neuropsychiatr Genet 2009
46
28



The genetic basis of Gilles de la Tourette Syndrome.
Peristera Paschou. Neurosci Biobehav Rev 2013
59
22

Relationship of birth weight to the phenotypic expression of Gilles de la Tourette's syndrome in monozygotic twins.
T M Hyde, B A Aaronson, C Randolph, K C Rickler, D R Weinberger. Neurology 1992
134
12

Additional support for the association of SLITRK1 var321 and Tourette syndrome.
B J O'Roak, T M Morgan, D O Fishman, E Saus, P Alonso, M Gratacòs, X Estivill, O Teltsh, Y Kohn, K K Kidd,[...]. Mol Psychiatry 2010
38
31

The genetics of Tourette syndrome.
Hao Deng, Kai Gao, Joseph Jankovic. Nat Rev Neurol 2012
57
21

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families.
Iordanis Karagiannidis, Sandra Dehning, Paul Sandor, Zsanett Tarnok, Renata Rizzo, Tomasz Wolanczyk, Marcos Madruga-Garrido, Johannes Hebebrand, Markus M Nöthen, Gerd Lehmkuhl,[...]. J Med Genet 2013
69
17

Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder.
Alexander Zimprich, Katharina Hatala, Franz Riederer, Elisabeth Stogmann, Harald N Aschauer, Mara Stamenkovic. Psychiatr Genet 2008
37
29

Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder.
Senthil K Sundaram, Ahm M Huq, Zhen Sun, Wu Yu, Lindsey Bennett, Benjamin J Wilson, Michael E Behen, Harry T Chugani. Ann Neurol 2011
36
30

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
11

Tourette syndrome and dopaminergic genes: a family-based association study in the French Canadian founder population.
A Díaz-Anzaldúa, R Joober, J-B Rivière, Y Dion, P Lespérance, F Richer, S Chouinard, G A Rouleau. Mol Psychiatry 2004
55
20

Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome.
Althea A Stillman, Zeljka Krsnik, Jinhao Sun, Mladen-Roko Rasin, Matthew W State, Nenad Sestan, Angeliki Louvi. J Comp Neurol 2009
62
17


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.