A citation-based method for searching scientific literature

Marta Paterlini, Stanislav S Zakharenko, Wen-Sung Lai, Jie Qin, Hui Zhang, Jun Mukai, Koen G C Westphal, Berend Olivier, David Sulzer, Paul Pavlidis, Steven A Siegelbaum, Maria Karayiorgou, Joseph A Gogos. Nat Neurosci 2005
Times Cited: 182







List of co-cited articles
1406 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
34

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
33

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Grégory Raux, Emilie Bumsel, Bernadette Hecketsweiler, Therese van Amelsvoort, Janneke Zinkstok, Sylvie Manouvrier-Hanu, Carole Fantini, Georges-Marie M Brévière, Gabriella Di Rosa, Giuseppina Pustorino,[...]. Hum Mol Genet 2007
109
30

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele.
Jacob A S Vorstman, Bruce I Turetsky, Monique E J Sijmens-Morcus, Monique G de Sain, Bert Dorland, Mirjam Sprong, Eric F Rappaport, Frits A Beemer, Beverly S Emanuel, René S Kahn,[...]. Neuropsychopharmacology 2009
68
42

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice.
J A Gogos, M Santha, Z Takacs, K D Beck, V Luine, L R Lucas, J V Nadler, M Karayiorgou. Nat Genet 1999
199
28

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
254
25

Hyperprolinemia is a risk factor for schizoaffective disorder.
H Jacquet, C Demily, E Houy, B Hecketsweiler, J Bou, G Raux, J Lerond, G Allio, S Haouzir, A Tillaux,[...]. Mol Psychiatry 2005
74
32

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
24

Functional consequences of PRODH missense mutations.
Hans-Ulrich Bender, Shlomo Almashanu, Gary Steel, Chien-An Hu, Wei-Wen Lin, Alecia Willis, Ann Pulver, David Valle. Am J Hum Genet 2005
100
23

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia.
Jun Mukai, Hui Liu, Rachel A Burt, Dionne E Swor, Wen-Sung Lai, Maria Karayiorgou, Joseph A Gogos. Nat Genet 2004
233
22

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.
M Karayiorgou, M A Morris, B Morrow, R J Shprintzen, R Goldberg, J Borrow, A Gos, G Nestadt, P S Wolyniec, V K Lasseter. Proc Natl Acad Sci U S A 1995
402
22

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives.
A E Pulver, G Nestadt, R Goldberg, R J Shprintzen, M Lamacz, P S Wolyniec, B Morrow, M Karayiorgou, S E Antonarakis, D Housman. J Nerv Ment Dis 1994
339
20

Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior.
J A Gogos, M Morgan, V Luine, M Santha, S Ogawa, D Pfaff, M Karayiorgou. Proc Natl Acad Sci U S A 1998
662
20

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.
Hélène Jacquet, Grégory Raux, Florence Thibaut, Bernadette Hecketsweiler, Emmanuelle Houy, Caroline Demilly, Sadeq Haouzir, Gabrielle Allio, Gael Fouldrin, Valérie Drouin,[...]. Hum Mol Genet 2002
135
20

Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and function.
Lucas Kempf, Kristin K Nicodemus, Bhaskar Kolachana, Radhakrishna Vakkalanka, Beth A Verchinski, Michael F Egan, Richard E Straub, Venkata A Mattay, Joseph H Callicott, Daniel R Weinberger,[...]. PLoS Genet 2008
77
25

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia.
Hui Liu, Simon C Heath, Christina Sobin, J Louw Roos, Brandi L Galke, Maude L Blundell, Marge Lenane, Brian Robertson, Ellen M Wijsman, Judith L Rapoport,[...]. Proc Natl Acad Sci U S A 2002
235
20

Genetic dissection of the role of catechol-O-methyltransferase in cognition and stress reactivity in mice.
Francesco Papaleo, Jacqueline N Crawley, Jian Song, Barbara K Lipska, Jim Pickel, Daniel R Weinberger, Jingshan Chen. J Neurosci 2008
230
18

Strong association of de novo copy number mutations with sporadic schizophrenia.
Bin Xu, J Louw Roos, Shawn Levy, E J van Rensburg, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2008
589
18

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
182
18

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
16

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
16

The molecular genetics of the 22q11-associated schizophrenia.
Maria Karayiorgou, Joseph A Gogos. Brain Res Mol Brain Res 2004
103
16


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
16

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.
Elizabeth M Tunbridge, Paul J Harrison, Daniel R Weinberger. Biol Psychiatry 2006
521
15

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.
Jingshan Chen, Barbara K Lipska, Nader Halim, Quang D Ma, Mitsuyuki Matsumoto, Samer Melhem, Bhaskar S Kolachana, Thomas M Hyde, Mary M Herman, Jose Apud,[...]. Am J Hum Genet 2004
15

Evidence for association of hyperprolinemia with schizophrenia and a measure of clinical outcome.
Catherine L Clelland, Laura L Read, Amanda N Baraldi, Corinne P Bart, Carrie A Pappas, Laura J Panek, Robert H Nadrich, James D Clelland. Schizophr Res 2011
46
32

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.
Jacob A S Vorstman, Monique E J Morcus, Sasja N Duijff, Petra W J Klaassen, Josien A Heineman-de Boer, Frits A Beemer, Hanna Swaab, René S Kahn, Herman van Engeland. J Am Acad Child Adolesc Psychiatry 2006
230
14

Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome.
Doron Gothelf, Carl Feinstein, Tracy Thompson, Eugene Gu, Lauren Penniman, Ellen Van Stone, Hower Kwon, Stephan Eliez, Allan L Reiss. Am J Psychiatry 2007
164
14

A mutation in mouse Disc1 that models a schizophrenia risk allele leads to specific alterations in neuronal architecture and cognition.
Mirna Kvajo, Heather McKellar, P Alexander Arguello, Liam J Drew, Holly Moore, Amy B MacDermott, Maria Karayiorgou, Joseph A Gogos. Proc Natl Acad Sci U S A 2008
219
14

COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome.
Kate Baker, Torsten Baldeweg, Sinthuja Sivagnanasundaram, Peter Scambler, David Skuse. Biol Psychiatry 2005
103
14

Genetic variation in the 22q11 locus and susceptibility to schizophrenia.
Hui Liu, Goncalo R Abecasis, Simon C Heath, Alyson Knowles, Sandra Demars, Ying-Jiun Chen, J Louw Roos, Judith L Rapoport, Joseph A Gogos, Maria Karayiorgou. Proc Natl Acad Sci U S A 2002
147
14

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
14

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
89
15

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
136
14

Disc1 is mutated in the 129S6/SvEv strain and modulates working memory in mice.
Hiroko Koike, P Alexander Arguello, Mirna Kvajo, Maria Karayiorgou, Joseph A Gogos. Proc Natl Acad Sci U S A 2006
214
13

Modeling madness in mice: one piece at a time.
P Alexander Arguello, Joseph A Gogos. Neuron 2006
229
13

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.
R Paylor, K L McIlwain, R McAninch, A Nellis, L A Yuva-Paylor, A Baldini, E A Lindsay. Hum Mol Genet 2001
105
13

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
13

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
377
13

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
131
13

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
Doron Gothelf, Marie Schaer, Stephan Eliez. Dev Disabil Res Rev 2008
97
13

Proline-induced potentiation of glutamate transmission.
S M Cohen, J V Nadler. Brain Res 1997
71
18

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
13

A common molecular basis for rearrangement disorders on chromosome 22q11.
L Edelmann, R K Pandita, E Spiteri, B Funke, R Goldberg, N Palanisamy, R S Chaganti, E Magenis, R J Shprintzen, B E Morrow. Hum Mol Genet 1999
338
12

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome.
Sarah E Fine, Alison Weissman, Marsha Gerdes, Jennifer Pinto-Martin, Elaine H Zackai, Donna M McDonald-McGinn, Beverly S Emanuel. J Autism Dev Disord 2005
141
12

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
170
12

Behavioral phenotypes of Disc1 missense mutations in mice.
Steven J Clapcote, Tatiana V Lipina, J Kirsty Millar, Shaun Mackie, Sheila Christie, Fumiaki Ogawa, Jason P Lerch, Keith Trimble, Masashi Uchiyama, Yoshiyuki Sakuraba,[...]. Neuron 2007
392
12

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
12



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.