A citation-based method for searching scientific literature

Gloria W C Tam, Louie N van de Lagemaat, Richard Redon, Karen E Strathdee, Mike D R Croning, Mary P Malloy, Walter J Muir, Ben S Pickard, Ian J Deary, Douglas H R Blackwood, Nigel P Carter, Seth G N Grant. Biochem Soc Trans 2010
Times Cited: 102







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



Times Cited
  Times     Co-cited
Similarity


Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
23

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
381
16

A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder.
Bert van der Zwaag, Wouter G Staal, Ron Hochstenbach, Martin Poot, Henk A Spierenburg, Maretha V de Jonge, Nienke E Verbeek, Ruben van 't Slot, Michael A van Es, Frank J Staal,[...]. Am J Med Genet B Neuropsychiatr Genet 2010
69
21

Transcription factor SP4 is a susceptibility gene for bipolar disorder.
Xianjin Zhou, Wei Tang, Tiffany A Greenwood, Shengzhen Guo, Lin He, Mark A Geyer, John R Kelsoe. PLoS One 2009
44
34

Reduced expression of the Sp4 gene in mice causes deficits in sensorimotor gating and memory associated with hippocampal vacuolization.
X Zhou, J M Long, M A Geyer, E Masliah, J R Kelsoe, A Wynshaw-Boris, K R Chien. Mol Psychiatry 2005
62
22

Impaired postnatal development of hippocampal dentate gyrus in Sp4 null mutant mice.
X Zhou, Y Qyang, J R Kelsoe, E Masliah, M A Geyer. Genes Brain Behav 2007
50
28

Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances.
Marianne Doornbos, Birgit Sikkema-Raddatz, Claudia A L Ruijvenkamp, Trijnie Dijkhuizen, Emilia K Bijlsma, Antoinet C J Gijsbers, Yvonne Hilhorst-Hofstee, Roel Hordijk, Krijn T Verbruggen, W S Mieke Kerstjens-Frederikse,[...]. Eur J Med Genet 2009
115
13

The transcription factor SP4 is reduced in postmortem cerebellum of bipolar disorder subjects: control by depolarization and lithium.
Raquel Pinacho, Nuria Villalmanzo, Jasmin Lalonde, Josep Maria Haro, J Javier Meana, Grace Gill, Belén Ramos. Bipolar Disord 2011
36
36


Reduced NMDAR1 expression in the Sp4 hypomorphic mouse may contribute to endophenotypes of human psychiatric disorders.
Xianjin Zhou, Zhiguo Nie, Amanda Roberts, Dongxian Zhang, Jonathan Sebat, Dheeraj Malhotra, John R Kelsoe, Mark A Geyer. Hum Mol Genet 2010
26
46

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
12

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
George Kirov, Detelina Grozeva, Nadine Norton, Dobril Ivanov, Kiran K Mantripragada, Peter Holmans, Nick Craddock, Michael J Owen, Michael C O'Donovan. Hum Mol Genet 2009
305
11


Genome-wide association study of recurrent early-onset major depressive disorder.
J Shi, J B Potash, J A Knowles, M M Weissman, W Coryell, W A Scheftner, W B Lawson, J R DePaulo, P V Gejman, A R Sanders,[...]. Mol Psychiatry 2011
195
11

CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.
Annette Schenck, Barbara Bardoni, Caillin Langmann, Nicholas Harden, Jean Louis Mandel, Angela Giangrande. Neuron 2003
241
11

Case-control association study of the close homologue of L1 (CHL1) gene and schizophrenia in the Chinese population.
Qing-Ying Chen, Qi Chen, Guo-Yin Feng, Klaus Lindpaintner, Yi Chen, Xiaodong Sun, Zhengxiong Chen, Zhensong Gao, Jisheng Tang, Lin He. Schizophr Res 2005
53
20



Transcription factor Sp4 regulates dendritic patterning during cerebellar maturation.
Belén Ramos, Brice Gaudillière, Azad Bonni, Grace Gill. Proc Natl Acad Sci U S A 2007
51
19

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Claire S Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Rastam,[...]. PLoS Genet 2012
263
10

Impairment of sensorimotor gating in mice deficient in the cell adhesion molecule L1 or its close homologue, CHL1.
Andrey Irintchev, Michael Koch, Leila K Needham, Patricia Maness, Melitta Schachner. Brain Res 2004
35
28

p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase.
K Kobayashi, S Kuroda, M Fukata, T Nakamura, T Nagase, N Nomura, Y Matsuura, N Yoshida-Kubomura, A Iwamatsu, K Kaibuchi. J Biol Chem 1998
175
10

Structure and control of the actin regulatory WAVE complex.
Zhucheng Chen, Dominika Borek, Shae B Padrick, Timothy S Gomez, Zoltan Metlagel, Ayman M Ismail, Junko Umetani, Daniel D Billadeau, Zbyszek Otwinowski, Michael K Rosen. Nature 2010
289
10

Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population.
Qian Zhao, Tao Li, XinZhi Zhao, Ke Huang, Ti Wang, ZhiQiang Li, Jue Ji, Zhen Zeng, Zhao Zhang, Kan Li,[...]. Schizophr Bull 2013
38
26

CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation.
Silvia De Rubeis, Emanuela Pasciuto, Ka Wan Li, Esperanza Fernández, Daniele Di Marino, Andrea Buzzi, Linnaea E Ostroff, Eric Klann, Fried J T Zwartkruis, Noboru H Komiyama,[...]. Neuron 2013
152
10



Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies.
Patrick F Sullivan, Kenneth S Kendler, Michael C Neale. Arch Gen Psychiatry 2003
8

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
8

Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.
S I Shyn, J Shi, J B Kraft, J B Potash, J A Knowles, M M Weissman, H A Garriock, J S Yokoyama, P J McGrath, E J Peters,[...]. Mol Psychiatry 2011
191
8


Analysis of Sp transcription factors in the postmortem brain of chronic schizophrenia: a pilot study of relationship to negative symptoms.
Raquel Pinacho, Núria Villalmanzo, Mercedes Roca, Raquel Iniesta, Alfonso Monje, Josep Maria Haro, J Javier Meana, Isidre Ferrer, Grace Gill, Belén Ramos. J Psychiatr Res 2013
29
27

Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice.
Ozlem Bozdagi, Takeshi Sakurai, Nathan Dorr, Marion Pilorge, Nagahide Takahashi, Joseph D Buxbaum. PLoS One 2012
72
11


Modeling a genetic risk for schizophrenia in iPSCs and mice reveals neural stem cell deficits associated with adherens junctions and polarity.
Ki-Jun Yoon, Ha Nam Nguyen, Gianluca Ursini, Fengyu Zhang, Nam-Shik Kim, Zhexing Wen, Georgia Makri, David Nauen, Joo Heon Shin, Youngbin Park,[...]. Cell Stem Cell 2014
159
8

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.
Yuhei Nishimura, Christa L Martin, Araceli Vazquez-Lopez, Sarah J Spence, Ana Isabel Alvarez-Retuerto, Marian Sigman, Corinna Steindler, Sandra Pellegrini, N Carolyn Schanen, Stephen T Warren,[...]. Hum Mol Genet 2007
207
7

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
922
7

CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior.
Suzanna G M Frints, Peter Marynen, Dieter Hartmann, Jean-Pierre Fryns, Jean Steyaert, Melitta Schachner, Bettina Rolf, Katleen Craessaerts, An Snellinx, Karen Hollanders,[...]. Hum Mol Genet 2003
106
7

Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
J H Krystal, L P Karper, J P Seibyl, G K Freeman, R Delaney, J D Bremner, G R Heninger, M B Bowers, D S Charney. Arch Gen Psychiatry 1994
7


Prolonged Ketamine Effects in Sp4 Hypomorphic Mice: Mimicking Phenotypes of Schizophrenia.
Baohu Ji, Xin Wang, Antonio Pinto-Duarte, Minjung Kim, Sorana Caldwell, Jared W Young, Margarita M Behrens, Terrence J Sejnowski, Mark A Geyer, Xianjin Zhou. PLoS One 2013
16
43

Close homolog of L1 and neuropilin 1 mediate guidance of thalamocortical axons at the ventral telencephalon.
Amanda G Wright, Galina P Demyanenko, Ashton Powell, Melitta Schachner, Lilian Enriquez-Barreto, Tracy S Tran, Franck Polleux, Patricia F Maness. J Neurosci 2007
79
8


The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines.
M Pathania, E C Davenport, J Muir, D F Sheehan, G López-Doménech, J T Kittler. Transl Psychiatry 2014
116
7

Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR.
A Oguro-Ando, C Rosensweig, E Herman, Y Nishimura, D Werling, B R Bill, J M Berg, F Gao, G Coppola, B S Abrahams,[...]. Mol Psychiatry 2015
66
10

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag,[...]. Brain 2010
311
6

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study.
Paul Lichtenstein, Benjamin H Yip, Camilla Björk, Yudi Pawitan, Tyrone D Cannon, Patrick F Sullivan, Christina M Hultman. Lancet 2009
6

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Tom Walsh, Jon M McClellan, Shane E McCarthy, Anjené M Addington, Sarah B Pierce, Greg M Cooper, Alex S Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari,[...]. Science 2008
6

Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations.
T Sahoo, S U Peters, N S Madduri, D G Glaze, J R German, L M Bird, R Barbieri-Welge, T J Bichell, A L Beaudet, C A Bacino. J Med Genet 2006
62
9

CHL1 is a selective organizer of the presynaptic machinery chaperoning the SNARE complex.
Aksana Andreyeva, Iryna Leshchyns'ka, Michael Knepper, Christian Betzel, Lars Redecke, Vladimir Sytnyk, Melitta Schachner. PLoS One 2010
38
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.