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



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Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
Itaru Kushima, Branko Aleksic, Masahiro Nakatochi, Teppei Shimamura, Takashi Okada, Yota Uno, Mako Morikawa, Kanako Ishizuka, Tomoko Shiino, Hiroki Kimura,[...]. Cell Rep 2018
77
42

Assessing the Cognitive Translational Potential of a Mouse Model of the 22q11.2 Microdeletion Syndrome.
Simon Ro Nilsson, Kim Fejgin, Francois Gastambide, Miriam A Vogt, Brianne A Kent, Vibeke Nielsen, Jacob Nielsen, Peter Gass, Trevor W Robbins, Lisa M Saksida,[...]. Cereb Cortex 2016
17
42

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
42

Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice.
Go Suzuki, Kathryn M Harper, Takeshi Hiramoto, Birgit Funke, MoonSook Lee, Gina Kang, Mahalah Buell, Mark A Geyer, Raju Kucherlapati, Bernice Morrow,[...]. Hum Mol Genet 2009
35
42

Copy number elevation of 22q11.2 genes arrests the developmental maturation of working memory capacity and adult hippocampal neurogenesis.
S Boku, T Izumi, S Abe, T Takahashi, A Nishi, H Nomaru, Y Naka, G Kang, M Nagashima, A Hishimoto,[...]. Mol Psychiatry 2018
11
42

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
386
42

The pattern of cortical dysfunction in a mouse model of a schizophrenia-related microdeletion.
Karine Fénelon, Bin Xu, Cora S Lai, Jun Mukai, Sander Markx, Kimberly L Stark, Pei-Ken Hsu, Wen-Biao Gan, Gerald D Fischbach, Amy B MacDermott,[...]. J Neurosci 2013
70
42

Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model.
Takeshi Hiramoto, Gina Kang, Go Suzuki, Yasushi Satoh, Raju Kucherlapati, Yasuhiro Watanabe, Noboru Hiroi. Hum Mol Genet 2011
53
42

Neurobiological perspective of 22q11.2 deletion syndrome.
Janneke R Zinkstok, Erik Boot, Anne S Bassett, Noboru Hiroi, Nancy J Butcher, Claudia Vingerhoets, Jacob A S Vorstman, Therese A M J van Amelsvoort. Lancet Psychiatry 2019
20
42

Structure and function of neonatal social communication in a genetic mouse model of autism.
T Takahashi, S Okabe, P Ó Broin, A Nishi, K Ye, M V Beckert, T Izumi, A Machida, G Kang, S Abe,[...]. Mol Psychiatry 2016
44
42

Restoring wild-type-like CA1 network dynamics and behavior during adulthood in a mouse model of schizophrenia.
Thomas Marissal, Rodrigo F Salazar, Cristina Bertollini, Sophie Mutel, Mathias De Roo, Ivan Rodriguez, Dominique Müller, Alan Carleton. Nat Neurosci 2018
26
28

Symptom correlates of prepulse inhibition deficits in male schizophrenic patients.
D L Braff, N R Swerdlow, M A Geyer. Am J Psychiatry 1999
280
28

Chromosome engineering in zygotes with CRISPR/Cas9.
Katharina Boroviak, Brendan Doe, Ruby Banerjee, Fengtang Yang, Allan Bradley. Genesis 2016
47
28

Impaired prepulse inhibition of acoustic startle in schizophrenia.
A Parwani, E J Duncan, E Bartlett, S H Madonick, T R Efferen, R Rajan, M Sanfilipo, P B Chappell, S Chakravorty, S Gonzenbach,[...]. Biol Psychiatry 2000
187
28

Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.
Tingwei Guo, Alexander Diacou, Hiroko Nomaru, Donna M McDonald-McGinn, Matthew Hestand, Wolfram Demaerel, Liangtian Zhang, Yingjie Zhao, Francisco Ujueta, Jidong Shan,[...]. Hum Mol Genet 2018
13
28

Post-transcriptional control of DGCR8 expression by the Microprocessor.
Robinson Triboulet, Hao-Ming Chang, Robert J Lapierre, Richard I Gregory. RNA 2009
97
28



Visual scanning of faces in 22q11.2 deletion syndrome: Attention to the mouth or the eyes?
Linda Campbell, Kathryn McCabe, Kate Leadbeater, Ulrich Schall, Carmel Loughland, Dominique Rich. Psychiatry Res 2010
42
28


Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?
Linda E Campbell, Angela F Stevens, Kathryn McCabe, Lynne Cruickshank, Robin G Morris, Declan G M Murphy, Kieran C Murphy. J Neurodev Disord 2011
39
28

Congenital heart disease in mice deficient for the DiGeorge syndrome region.
E A Lindsay, A Botta, V Jurecic, S Carattini-Rivera, Y C Cheah, H M Rosenblatt, A Bradley, A Baldini. Nature 1999
299
28

Specific disruption of thalamic inputs to the auditory cortex in schizophrenia models.
Sungkun Chun, Joby J Westmoreland, Ildar T Bayazitov, Donnie Eddins, Amar K Pani, Richard J Smeyne, Jing Yu, Jay A Blundon, Stanislav S Zakharenko. Science 2014
70
28

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.
R E Gur, J J Yi, D M McDonald-McGinn, S X Tang, M E Calkins, D Whinna, M C Souders, A Savitt, E H Zackai, P J Moberg,[...]. Mol Psychiatry 2014
59
28

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.
C Carlson, H Sirotkin, R Pandita, R Goldberg, J McKie, R Wadey, S R Patanjali, S M Weissman, K Anyane-Yeboa, D Warburton,[...]. Am J Hum Genet 1997
289
28

Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions.
V Shashi, A Veerapandiyan, K Schoch, T Kwapil, M Keshavan, E Ip, S Hooper. J Intellect Disabil Res 2012
52
28

The annual incidence of DiGeorge/velocardiofacial syndrome.
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
257
28

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model.
Kimberly L Stark, Bin Xu, Anindya Bagchi, Wen-Sung Lai, Hui Liu, Ruby Hsu, Xiang Wan, Paul Pavlidis, Alea A Mills, Maria Karayiorgou,[...]. Nat Genet 2008
397
28

Hearing loss in a mouse model of 22q11.2 Deletion Syndrome.
Jennifer C Fuchs, Fhatarah A Zinnamon, Ruth R Taylor, Sarah Ivins, Peter J Scambler, Andrew Forge, Abigail S Tucker, Jennifer F Linden. PLoS One 2013
15
28

Loss-of-function mutation in Mirta22/Emc10 rescues specific schizophrenia-related phenotypes in a mouse model of the 22q11.2 deletion.
Anastasia Diamantopoulou, Ziyi Sun, Jun Mukai, Bin Xu, Karine Fenelon, Maria Karayiorgou, Joseph A Gogos. Proc Natl Acad Sci U S A 2017
16
28

Can Animal Models of Copy Number Variants That Predispose to Schizophrenia Elucidate Underlying Biology?
Annika Forsingdal, Trine Nygaard Jørgensen, Line Olsen, Thomas Werge, Michael Didriksen, Jacob Nielsen. Biol Psychiatry 2019
14
28

Prepulse inhibition of the startle response with chronic schizophrenia: a replication study.
Masatsugu Moriwaki, Taro Kishi, Hidetoshi Takahashi, Ryota Hashimoto, Kunihiro Kawashima, Tomo Okochi, Tsuyoshi Kitajima, Osamu Furukawa, Kiyoshi Fujita, Masatoshi Takeda,[...]. Neurosci Res 2009
36
28

Social cognition in 22q11.2 microdeletion syndrome: relevance to psychosis?
Maria Jalbrzikowski, Chelsea Carter, Damla Senturk, Carolyn Chow, Jessica M Hopkins, Michael F Green, Adriana Galván, Tyrone D Cannon, Carrie E Bearden. Schizophr Res 2012
51
28

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
S Merscher, B Funke, J A Epstein, J Heyer, A Puech, M M Lu, R J Xavier, M B Demay, R G Russell, S Factor,[...]. Cell 2001
650
28

Genotype-phenotype correlation in 22q11.2 deletion syndrome.
Elena Michaelovsky, Amos Frisch, Miri Carmel, Miriam Patya, Omer Zarchi, Tamar Green, Lina Basel-Vanagaite, Abraham Weizman, Doron Gothelf. BMC Med Genet 2012
62
28

Startle gating deficits occur across prepulse intensities in schizophrenic patients.
C Grillon, R Ameli, D S Charney, J Krystal, D Braff. Biol Psychiatry 1992
295
28

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
128
28

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.
N Hiroi, T Takahashi, A Hishimoto, T Izumi, S Boku, T Hiramoto. Mol Psychiatry 2013
76
28

The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
Loyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, Aurélie Pain, Sandra Martin-Brevet, Carina Ferrari, Philippe Conus, Aurélien Macé, Nouchine Hadjikhani, Andres Metspalu,[...]. Biol Psychiatry 2016
49
28

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.
Louise K Hoeffding, Betina B Trabjerg, Line Olsen, Wiktor Mazin, Thomas Sparsø, Anders Vangkilde, Preben B Mortensen, Carsten B Pedersen, Thomas Werge. JAMA Psychiatry 2017
52
28

Psychiatric disorders in children with 16p11.2 deletion and duplication.
Maria Niarchou, Samuel J R A Chawner, Joanne L Doherty, Anne M Maillard, Sébastien Jacquemont, Wendy K Chung, LeeAnne Green-Snyder, Raphael A Bernier, Robin P Goin-Kochel, Ellen Hanson,[...]. Transl Psychiatry 2019
43
28

Reduced adult hippocampal neurogenesis and working memory deficits in the Dgcr8-deficient mouse model of 22q11.2 deletion-associated schizophrenia can be rescued by IGF2.
Yasuo Ouchi, Yuya Banno, Yuko Shimizu, Shouta Ando, Hitoki Hasegawa, Koichi Adachi, Takashi Iwamoto. J Neurosci 2013
103
28

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega,[...]. Prenat Diagn 2015
154
28

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Jacob A S Vorstman, Elemi J Breetvelt, Sasja N Duijff, Stephan Eliez, Maude Schneider, Maria Jalbrzikowski, Marco Armando, Stefano Vicari, Vandana Shashi, Stephen R Hooper,[...]. JAMA Psychiatry 2015
115
28

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.
Richard Paylor, Beate Glaser, Annalisa Mupo, Paris Ataliotis, Corinne Spencer, Angela Sobotka, Chelsey Sparks, Chul-Hee Choi, John Oghalai, Sarah Curran,[...]. Proc Natl Acad Sci U S A 2006
193
28

Cry, baby, cry: Expression of Distress as a Biomarker and Modulator in Autism Spectrum Disorder.
Gianluca Esposito, Noboru Hiroi, Maria Luisa Scattoni. Int J Neuropsychopharmacol 2017
32
28


Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
Santhosh Girirajan, Megan Y Dennis, Carl Baker, Maika Malig, Bradley P Coe, Catarina D Campbell, Kenneth Mark, Tiffany H Vu, Can Alkan, Ze Cheng,[...]. Am J Hum Genet 2013
184
28

Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus.
Ryo Saito, Michinori Koebis, Taku Nagai, Kimiko Shimizu, Jingzhu Liao, Bolati Wulaer, Yuki Sugaya, Kenichiro Nagahama, Naofumi Uesaka, Itaru Kushima,[...]. Transl Psychiatry 2020
10
28


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.