A citation-based method for searching scientific literature

Hui Pang, Xiaowei Yu, Young Mi Kim, Xianfu Wang, Jeremy K Jinkins, Jianing Yin, Shibo Li, Hongcang Gu. Front Genet 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Stephan Ripke, Colm O'Dushlaine, Kimberly Chambert, Jennifer L Moran, Anna K Kähler, Susanne Akterin, Sarah E Bergen, Ann L Collins, James J Crowley, Menachem Fromer,[...]. Nat Genet 2013
979
100

The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function.
David Warde-Farley, Sylva L Donaldson, Ovi Comes, Khalid Zuberi, Rashad Badrawi, Pauline Chao, Max Franz, Chris Grouios, Farzana Kazi, Christian Tannus Lopes,[...]. Nucleic Acids Res 2010
100

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
G Kirov, A J Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, J Moran, K Chambert, D Toncheva, L Georgieva,[...]. Mol Psychiatry 2012
515
100

A role of Pygopus as an anti-repressor in facilitating Wnt-dependent transcription.
Juliusz Mieszczanek, Marc de la Roche, Mariann Bienz. Proc Natl Acad Sci U S A 2008
31
100



Pregnancy, delivery, and neonatal complications in a population cohort of women with schizophrenia and major affective disorders.
Assen V Jablensky, Vera Morgan, Stephen R Zubrick, Carol Bower, Li-Anne Yellachich. Am J Psychiatry 2005
277
100

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
100

BCL9/9L-β-catenin Signaling is Associated With Poor Outcome in Colorectal Cancer.
Andreas E Moor, Pascale Anderle, Claudio Cantù, Patrick Rodriguez, Norbert Wiedemann, Frédérique Baruthio, Jürgen Deka, Sylvie André, Tomas Valenta, Matthias B Moor,[...]. EBioMedicine 2015
36
100

Common alleles contribute to schizophrenia in CNV carriers.
K E Tansey, E Rees, D E Linden, S Ripke, K D Chambert, J L Moran, S A McCarroll, P Holmans, G Kirov, J Walters,[...]. Mol Psychiatry 2016
47
100

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Michael J Gandal, Jillian R Haney, Neelroop N Parikshak, Virpi Leppa, Gokul Ramaswami, Chris Hartl, Andrew J Schork, Vivek Appadurai, Alfonso Buil, Thomas M Werge,[...]. Science 2018
398
100


Wnt/wingless signaling requires BCL9/legless-mediated recruitment of pygopus to the nuclear beta-catenin-TCF complex.
Thomas Kramps, Oliver Peter, Erich Brunner, Denise Nellen, Barbara Froesch, Sandipan Chatterjee, Maximilien Murone, Stephanie Züllig, Konrad Basler. Cell 2002
442
100


Nuclear localization and dominant-negative suppression by a mutant SKCa3 N-terminal channel fragment identified in a patient with schizophrenia.
M J Miller, H Rauer, H Tomita, H Rauer, J J Gargus, G A Gutman, M D Cahalan, K G Chandy. J Biol Chem 2001
46
100

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
Olafur O Gudmundsson, G Bragi Walters, Andres Ingason, Stefan Johansson, Tetyana Zayats, Lavinia Athanasiu, Ida Elken Sonderby, Omar Gustafsson, Muhammad S Nawaz, Gudbjorn F Jonsson,[...]. Transl Psychiatry 2019
20
100

Association study of polymorphisms between DISC1 and schizophrenia in a Korean population.
Hak-Jae Kim, Hae Jeong Park, Kyung Hee Jung, Ju Yeon Ban, Jehyun Ra, Jong Woo Kim, Jin Kyung Park, Bong-Keun Choe, Sung Vin Yim, Yunhee Kim Kwon,[...]. Neurosci Lett 2008
33
100

Positive association of the human frizzled 3 (FZD3) gene haplotype with schizophrenia in Chinese Han population.
Yanbo Zhang, Xin Yu, Yanbo Yuan, Yansu Ling, Yan Ruan, Tianmei Si, Tianlian Lu, Suping Wu, Xiaohong Gong, Zhongjun Zhu,[...]. Am J Med Genet B Neuropsychiatr Genet 2004
41
100

Neurobehavioral phenotype of autism spectrum disorder associated with germline heterozygous mutations in PTEN.
Robyn M Busch, Siddharth Srivastava, Olivia Hogue, Thomas W Frazier, Patricia Klaas, Antonio Hardan, Julian A Martinez-Agosto, Mustafa Sahin, Charis Eng. Transl Psychiatry 2019
10
100

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
204
100

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
773
100

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
601
100


Common variants in the BCL9 gene conferring risk of schizophrenia.
Junyan Li, Guoquan Zhou, Weidong Ji, Guoyin Feng, Qian Zhao, Jie Liu, Tao Li, You Li, Peng Chen, Zhen Zeng,[...]. Arch Gen Psychiatry 2011
28
100


Wnt-mediated self-renewal of neural stem/progenitor cells.
M Yashar S Kalani, Samuel H Cheshier, Branden J Cord, Simon R Bababeygy, Hannes Vogel, Irving L Weissman, Theo D Palmer, Roel Nusse. Proc Natl Acad Sci U S A 2008
219
100

Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population.
Hiroki Kimura, Satoshi Tanaka, Itaru Kushima, Takayoshi Koide, Masahiro Banno, Tsutomu Kikuchi, Yukako Nakamura, Tomoko Shiino, Akira Yoshimi, Tomoko Oya-Ito,[...]. Sci Rep 2015
4
100


Metabolic Biomarkers of Ageing in C57BL/6J Wild-Type and Flavin-Containing Monooxygenase 5 (FMO5)-Knockout Mice.
Dorsa Varshavi, Flora H Scott, Dorna Varshavi, Sunil Veeravalli, Ian R Phillips, Kirill Veselkov, Nicole Strittmatter, Zoltan Takats, Elizabeth A Shephard, Jeremy R Everett. Front Mol Biosci 2018
6
100

Deficit schizophrenia: association with serum antibodies to cytomegalovirus.
Faith Dickerson, Brian Kirkpatrick, John Boronow, Cassie Stallings, Andrea Origoni, Robert Yolken. Schizophr Bull 2006
50
100

Wnt signaling regulates neuronal differentiation of cortical intermediate progenitors.
Roeben N Munji, Youngshik Choe, Guangnan Li, Julie A Siegenthaler, Samuel J Pleasure. J Neurosci 2011
171
100


Animal models of neuropsychiatric disorders.
Eric J Nestler, Steven E Hyman. Nat Neurosci 2010
100

BCL9 is an essential component of canonical Wnt signaling that mediates the differentiation of myogenic progenitors during muscle regeneration.
Andrew S Brack, Fabienne Murphy-Seiler, Jasmine Hanifi, Jürgen Deka, Sven Eyckerman, Charles Keller, Michel Aguet, Thomas A Rando. Dev Biol 2009
62
100

The role of pro-inflammatory factors in mediating the effects on the fetus of prenatal undernutrition: implications for schizophrenia.
Q Shen, Z Q Li, Y Sun, T Wang, C L Wan, X W Li, X Z Zhao, G Y Feng, Sh Li, D St Clair,[...]. Schizophr Res 2008
32
100

Increased expression of Wnt-1 in schizophrenic brains.
T Miyaoka, H Seno, H Ishino. Schizophr Res 1999
129
100

DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder.
W Hennah, P Thomson, A McQuillin, N Bass, A Loukola, A Anjorin, D Blackwood, D Curtis, I J Deary, S E Harris,[...]. Mol Psychiatry 2009
116
100

Stress in puberty unmasks latent neuropathological consequences of prenatal immune activation in mice.
Sandra Giovanoli, Harald Engler, Andrea Engler, Juliet Richetto, Mareike Voget, Roman Willi, Christine Winter, Marco A Riva, Preben B Mortensen, Joram Feldon,[...]. Science 2013
290
100

Maternal Vitamin D Levels During Pregnancy in Association With Autism Spectrum Disorders (ASD) or Intellectual Disability (ID) in Offspring; Exploring Non-linear Patterns and Demographic Sub-groups.
Gayle C Windham, Michelle Pearl, Victor Poon, Kimberly Berger, Jasmine W Soriano, Darryl Eyles, Kristen Lyall, Martin Kharrazi, Lisa A Croen. Autism Res 2020
3
100

Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series.
Martina Busè, Helenia C Cuttaia, Daniela Palazzo, Marcella V Mazara, Salvatrice A Lauricella, Michela Malacarne, Mauro Pierluigi, Simona Cavani, Maria Piccione. Ital J Pediatr 2017
15
100


Disc1 regulates both β-catenin-mediated and noncanonical Wnt signaling during vertebrate embryogenesis.
Gianluca De Rienzo, Joshua A Bishop, Yingwei Mao, Luyuan Pan, Taylur P Ma, Cecilia B Moens, Li-Huei Tsai, Hazel Sive. FASEB J 2011
31
100

The genetic variability and commonality of neurodevelopmental disease.
Bradley P Coe, Santhosh Girirajan, Evan E Eichler. Am J Med Genet C Semin Med Genet 2012
73
100


1q21.1 Microduplication expression in adults.
Alessia Dolcetti, Candice K Silversides, Christian R Marshall, Anath C Lionel, Dimitri J Stavropoulos, Stephen W Scherer, Anne S Bassett. Genet Med 2013
58
100

Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder.
Deidre R Krupp, Rebecca A Barnard, Yannis Duffourd, Sara A Evans, Ryan M Mulqueen, Raphael Bernier, Jean-Baptiste Rivière, Eric Fombonne, Brian J O'Roak. Am J Hum Genet 2017
75
100

Systematic prioritization and integrative analysis of copy number variations in schizophrenia reveal key schizophrenia susceptibility genes.
Xiongjian Luo, Liang Huang, Leng Han, Zhenwu Luo, Fang Hu, Roger Tieu, Lin Gan. Schizophr Bull 2014
21
100

Association of DISC1 with autism and Asperger syndrome.
H Kilpinen, T Ylisaukko-Oja, W Hennah, O M Palo, T Varilo, R Vanhala, T Nieminen-von Wendt, L von Wendt, T Paunio, L Peltonen. Mol Psychiatry 2008
134
100


Separable neural mechanisms for the pleiotropic association of copy number variants with neuropsychiatric traits.
Jonathan R Reinwald, Alexander Sartorius, Wolfgang Weber-Fahr, Markus Sack, Robert Becker, Michael Didriksen, Tine B Stensbøl, Adam J Schwarz, Andreas Meyer-Lindenberg, Natalia Gass. Transl Psychiatry 2020
3
100


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.