A citation-based method for searching scientific literature

N Hiroi, T Takahashi, A Hishimoto, T Izumi, S Boku, T Hiramoto. Mol Psychiatry 2013
Times Cited: 81







List of co-cited articles
843 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
408
32



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
54
29

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
106
19

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
421
18

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
301
17

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
411
17

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
47
27

Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice.
Go Suzuki, Kathryn M Harper, Takeshi Hiramoto, Takehito Sawamura, MoonSook Lee, Gina Kang, Kenji Tanigaki, Mahalah Buell, Mark A Geyer, William S Trimble,[...]. Hum Mol Genet 2009
53
20

Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain.
Kathryn M Harper, Takeshi Hiramoto, Kenji Tanigaki, Gina Kang, Go Suzuki, William Trimble, Noboru Hiroi. Hum Mol Genet 2012
36
30

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
197
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
120
13

Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
227
12

A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations.
Kim Fejgin, Jacob Nielsen, Michelle R Birknow, Jesper F Bastlund, Vibeke Nielsen, Jes B Lauridsen, Hreinn Stefansson, Stacy Steinberg, Helge B D Sorensen, Troels E Mortensen,[...]. Biol Psychiatry 2014
67
14

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
71
14

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
408
12

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
205
12

Evidence that duplications of 22q11.2 protect against schizophrenia.
E Rees, G Kirov, A Sanders, J T R Walters, K D Chambert, J Shi, J Szatkiewicz, C O'Dushlaine, A L Richards, E K Green,[...]. Mol Psychiatry 2014
85
12

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
50
20

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
89
12

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
195
11

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
385
11

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
428
11

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
62
14

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
36
25

Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.
Alina Guna, Nancy J Butcher, Anne S Bassett. J Neurodev Disord 2015
52
17

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
743
9

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
Guy Horev, Jacob Ellegood, Jason P Lerch, Young-Eun E Son, Lakshmi Muthuswamy, Hannes Vogel, Abba M Krieger, Andreas Buja, R Mark Henkelman, Michael Wigler,[...]. Proc Natl Acad Sci U S A 2011
176
9

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
106
9

A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice.
Noboru Hiroi, Hongwen Zhu, Moonsook Lee, Birgit Funke, Makoto Arai, Masanari Itokawa, Raju Kucherlapati, Bernice Morrow, Takehito Sawamura, Soh Agatsuma. Proc Natl Acad Sci U S A 2005
35
22

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
29
27

Microduplication 22q11.2: a new chromosomal syndrome.
Marie-France Portnoï. Eur J Med Genet 2009
149
8

Neurocognitive growth charting in psychosis spectrum youths.
Ruben C Gur, Monica E Calkins, Theodore D Satterthwaite, Kosha Ruparel, Warren B Bilker, Tyler M Moore, Adam P Savitt, Hakon Hakonarson, Raquel E Gur. JAMA Psychiatry 2014
136
8

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
220
8

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
235
8

Genetic architectures of psychiatric disorders: the emerging picture and its implications.
Patrick F Sullivan, Mark J Daly, Michael O'Donovan. Nat Rev Genet 2012
727
8

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
897
8

TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Tsutomu Ogata, Tetsuya Niihori, Noriko Tanaka, Masahiko Kawai, Takeshi Nagashima, Ryo Funayama, Keiko Nakayama, Shinichi Nakashima, Fumiko Kato, Maki Fukami,[...]. PLoS One 2014
30
23

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
638
8

22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening.
Tara L Wenger, Judith S Miller, Lauren M DePolo, Ashley B de Marchena, Caitlin C Clements, Beverly S Emanuel, Elaine H Zackai, Donna M McDonald-McGinn, Robert T Schultz. Mol Autism 2016
45
15

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
13
53


Clinical features of 78 adults with 22q11 Deletion Syndrome.
Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
288
7

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.
Anne S Bassett, Christian R Marshall, Anath C Lionel, Eva W C Chow, Stephen W Scherer. Hum Mol Genet 2008
128
7

Clinical variability of the 22q11.2 duplication syndrome.
Christian Wentzel, Maria Fernström, Ylva Ohrner, Göran Annerén, Ann-Charlotte Thuresson. Eur J Med Genet 2008
112
7

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
7


Rethinking schizophrenia.
Thomas R Insel. Nature 2010
977
7

Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
Kazutoshi Takahashi, Koji Tanabe, Mari Ohnuki, Megumi Narita, Tomoko Ichisaka, Kiichiro Tomoda, Shinya Yamanaka. Cell 2007
7


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.