A citation-based method for searching scientific literature

Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
Times Cited: 323







List of co-cited articles
1099 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
452
29

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
427
26

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
497
20

Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia.
Torfi Sigurdsson, Kimberly L Stark, Maria Karayiorgou, Joseph A Gogos, Joshua A Gordon. Nature 2010
459
18


Age-Dependent Specific Changes in Area CA2 of the Hippocampus and Social Memory Deficit in a Mouse Model of the 22q11.2 Deletion Syndrome.
Rebecca A Piskorowski, Kaoutsar Nasrallah, Anastasia Diamantopoulou, Jun Mukai, Sami I Hassan, Steven A Siegelbaum, Joseph A Gogos, Vivien Chevaleyre. Neuron 2016
87
17

Molecular substrates of altered axonal growth and brain connectivity in a mouse model of schizophrenia.
Jun Mukai, Makoto Tamura, Karine Fénelon, Andrew M Rosen, Timothy J Spellman, Rujun Kang, Amy B MacDermott, Maria Karayiorgou, Joshua A Gordon, Joseph A Gogos. Neuron 2015
100
14

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
754
14

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
509
14

The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.
Rachel K Jonas, Caroline A Montojo, Carrie E Bearden. Biol Psychiatry 2014
118
13

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
133
11

Schizophrenia and 22q11.2 deletion syndrome.
Anne S Bassett, Eva W C Chow. Curr Psychiatry Rep 2008
147
11

The schizophrenia phenotype in 22q11 deletion syndrome.
Anne S Bassett, Eva W C Chow, Philip AbdelMalik, Mirona Gheorghiu, Janice Husted, Rosanna Weksberg. Am J Psychiatry 2003
225
11


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
80
12

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
10

Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex.
Karine Fénelon, Jun Mukai, Bin Xu, Pei-Ken Hsu, Liam J Drew, Maria Karayiorgou, Gerald D Fischbach, Amy B Macdermott, Joseph A Gogos. Proc Natl Acad Sci U S A 2011
143
10

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice.
Marta Paterlini, Stanislav S Zakharenko, Wen-Sung Lai, Jie Qin, Hui Zhang, Jun Mukai, Koen G C Westphal, Berend Olivier, David Sulzer, Paul Pavlidis,[...]. Nat Neurosci 2005
189
10

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
137
10

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.
Daqiang Sun, Christopher R K Ching, Amy Lin, Jennifer K Forsyth, Leila Kushan, Ariana Vajdi, Maria Jalbrzikowski, Laura Hansen, Julio E Villalon-Reina, Xiaoping Qu,[...]. Mol Psychiatry 2020
72
13


Derepression of a neuronal inhibitor due to miRNA dysregulation in a schizophrenia-related microdeletion.
Bin Xu, Pei-Ken Hsu, Kimberly L Stark, Maria Karayiorgou, Joseph A Gogos. Cell 2013
106
9

The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.
Liam J Drew, Gregg W Crabtree, Sander Markx, Kimberly L Stark, Florence Chaverneff, Bin Xu, Jun Mukai, Karine Fenelon, Pei-Ken Hsu, Joseph A Gogos,[...]. Int J Dev Neurosci 2011
91
9

The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.
C E Bearden, M F Woodin, P P Wang, E Moss, D McDonald-McGinn, E Zackai, B Emannuel, T D Cannon. J Clin Exp Neuropsychol 2001
174
9

Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan,[...]. J Pediatr 2011
329
9

Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.
Jun Mukai, Alefiya Dhilla, Liam J Drew, Kimberly L Stark, Luxiang Cao, Amy B MacDermott, Maria Karayiorgou, Joseph A Gogos. Nat Neurosci 2008
187
9

Prodromal assessment with the structured interview for prodromal syndromes and the scale of prodromal symptoms: predictive validity, interrater reliability, and training to reliability.
Tandy J Miller, Thomas H McGlashan, Joanna L Rosen, Kristen Cadenhead, Tyrone Cannon, Joseph Ventura, William McFarlane, Diana O Perkins, Godfrey D Pearlson, Scott W Woods. Schizophr Bull 2003
8

Altered auditory processing in frontal and left temporal cortex in 22q11.2 deletion syndrome: a group at high genetic risk for schizophrenia.
Tonia A Rihs, Miralena I Tomescu, Juliane Britz, Vincent Rochas, Anna Custo, Maude Schneider, Martin Debbané, Stephan Eliez, Christoph M Michel. Psychiatry Res 2013
37
21

Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice.
Michael Didriksen, Kim Fejgin, Simon R O Nilsson, Michelle R Birknow, Hannah M Grayton, Peter H Larsen, Jes B Lauridsen, Vibeke Nielsen, Pau Celada, Noemi Santana,[...]. J Psychiatry Neurosci 2017
39
20

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
76
10



COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.
Doron Gothelf, Stephan Eliez, Tracy Thompson, Christine Hinard, Lauren Penniman, Carl Feinstein, Hower Kwon, Shuting Jin, Booil Jo, Stylianos E Antonarakis,[...]. Nat Neurosci 2005
258
8

Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia.
Lily Van, Erik Boot, Anne S Bassett. Curr Opin Psychiatry 2017
51
15

A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014
954
8

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.
T H Shaikh, H Kurahashi, S C Saitta, A M O'Hare, P Hu, B A Roe, D A Driscoll, D M McDonald-McGinn, E H Zackai, M L Budarf,[...]. Hum Mol Genet 2000
383
8

Age-dependent microRNA control of synaptic plasticity in 22q11 deletion syndrome and schizophrenia.
Laurie R Earls, R Gaines Fricke, Jing Yu, Raymond B Berry, Lisa T Baldwin, Stanislav S Zakharenko. J Neurosci 2012
78
10

Altered Cortical Ensembles in Mouse Models of Schizophrenia.
Jordan P Hamm, Darcy S Peterka, Joseph A Gogos, Rafael Yuste. Neuron 2017
96
8

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
675
8

Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.
Daniel W Meechan, Thomas M Maynard, Eric S Tucker, Alejandra Fernandez, Beverly A Karpinski, Lawrence A Rothblat, Anthony-S LaMantia. Prog Neurobiol 2015
54
14

Long-Lasting Rescue of Network and Cognitive Dysfunction in a Genetic Schizophrenia Model.
Arghya Mukherjee, Fernando Carvalho, Stephan Eliez, Pico Caroni. Cell 2019
62
12

Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion.
J Ellegood, S Markx, J P Lerch, P E Steadman, C Genç, F Provenzano, S A Kushner, R M Henkelman, M Karayiorgou, J A Gogos. Mol Psychiatry 2014
39
17

Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome).
Giles M Tan, Danilo Arnone, Andrew M McIntosh, Klaus P Ebmeier. Schizophr Res 2009
51
13

Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome.
Tamar Green, Doron Gothelf, Bronwyn Glaser, Martin Debbane, Amos Frisch, Moshe Kotler, Abraham Weizman, Stephan Eliez. J Am Acad Child Adolesc Psychiatry 2009
203
7

The hippocampal CA2 region is essential for social memory.
Frederick L Hitti, Steven A Siegelbaum. Nature 2014
466
7

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
513
7

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
56
12

Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome.
Laurie R Earls, Ildar T Bayazitov, Robert G Fricke, Raymond B Berry, Elizabeth Illingworth, Guy Mittleman, Stanislav S Zakharenko. J Neurosci 2010
52
13

Abnormal neural oscillations and synchrony in schizophrenia.
Peter J Uhlhaas, Wolf Singer. Nat Rev Neurosci 2010
7

Cognitive ability is associated with altered medial frontal cortical circuits in the LgDel mouse model of 22q11.2DS.
D W Meechan, H L H Rutz, M S Fralish, T M Maynard, L A Rothblat, A-S LaMantia. Cereb Cortex 2015
33
21


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.