A citation-based method for searching scientific literature

Carrie E Bearden, Abbas F Jawad, David R Lynch, Set Sokol, Steven J Kanes, Donna M McDonald-McGinn, Sulagna C Saitta, Stacy E Harris, Edward Moss, Paul P Wang, Elaine Zackai, Beverly S Emanuel, Tony J Simon. Am J Psychiatry 2004
Times Cited: 106







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



Times Cited
  Times     Co-cited
Similarity


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
55

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia.
M F Egan, T E Goldberg, B S Kolachana, J H Callicott, C M Mazzanti, R E Straub, D Goldman, D R Weinberger. Proc Natl Acad Sci U S A 2001
52

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
44

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
38

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
104
34

A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition.
Anil K Malhotra, Lisa J Kestler, Chiara Mazzanti, John A Bates, Terry Goldberg, David Goldman. Am J Psychiatry 2002
453
31


Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
V Shashi, M S Keshavan, T D Howard, M N Berry, M J Basehore, E Lewandowski, T R Kwapil. Clin Genet 2006
57
47

Genetic and neurochemical modulation of prefrontal cognitive functions in children.
Adele Diamond, Lisa Briand, John Fossella, Lorrie Gehlbach. Am J Psychiatry 2004
261
26

Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia.
Terry E Goldberg, Michael F Egan, Tonya Gscheidle, Richard Coppola, Thomas Weickert, Bhaskar S Kolachana, David Goldman, Daniel R Weinberger. Arch Gen Psychiatry 2003
485
26

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.
A Swillen, K Devriendt, E Legius, B Eyskens, M Dumoulin, M Gewillig, J P Fryns. J Med Genet 1997
269
26

Neurocognitive correlates of the COMT Val(158)Met polymorphism in chronic schizophrenia.
Robert M Bilder, Jan Volavka, Pál Czobor, Anil K Malhotra, James L Kennedy, Xingqun Ni, Robert S Goldman, Matthew J Hoptman, Brian Sheitman, Jean-Pierre Lindenmayer,[...]. Biol Psychiatry 2002
269
25

No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.
Bronwyn Glaser, Martin Debbane, Christine Hinard, Michael A Morris, Sophie P Dahoun, Stylianos E Antonarakis, Stephan Eliez. Am J Psychiatry 2006
39
64


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
22

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
669
21

A highly significant association between a COMT haplotype and schizophrenia.
Sagiv Shifman, Michal Bronstein, Meira Sternfeld, Anne Pisanté-Shalom, Efrat Lev-Lehman, Avraham Weizman, Ilya Reznik, Baruch Spivak, Nimrod Grisaru, Leon Karp,[...]. Am J Hum Genet 2002
541
21

A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).
Wendy R Kates, Kevin M Antshel, Nuria Abdulsabur, Deirdre Colgan, Birgit Funke, Wanda Fremont, Anne Marie Higgins, Raju Kucherlapati, Robert J Shprintzen. Am J Med Genet B Neuropsychiatr Genet 2006
64
32



Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome.
Anne S Bassett, Oana Caluseriu, Rosanna Weksberg, Donald A Young, Eva W C Chow. Biol Psychiatry 2007
74
25

Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine.
Venkata S Mattay, Terry E Goldberg, Francesco Fera, Ahmad R Hariri, Alessandro Tessitore, Michael F Egan, Bhaskar Kolachana, Joseph H Callicott, Daniel R Weinberger. Proc Natl Acad Sci U S A 2003
709
18

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
17

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
E M Moss, M L Batshaw, C B Solot, M Gerdes, D M McDonald-McGinn, D A Driscoll, B S Emanuel, E H Zackai, P P Wang. J Pediatr 1999
223
17

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
17

Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis.
W R Kates, C P Burnette, E W Jabs, J Rutberg, A M Murphy, M Grados, M Geraghty, W E Kaufmann, G D Pearlson. Biol Psychiatry 2001
134
16

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.
M Woodin, P P Wang, D Aleman, D McDonald-McGinn, E Zackai, E Moss. Genet Med 2001
179
16

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
407
16

New evidence of association between COMT gene and prefrontal neurocognitive function in healthy individuals from sibling pairs discordant for psychosis.
Araceli Rosa, Víctor Peralta, Manuel J Cuesta, Amalia Zarzuela, Fermín Serrano, Alfredo Martínez-Larrea, Lourdes Fañanás. Am J Psychiatry 2004
152
16

A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.
Tony J Simon, Joel P Bish, Carrie E Bearden, Lijun Ding, Samantha Ferrante, Vy Nguyen, James C Gee, Donna M McDonald-McGinn, Elaine H Zackai, Beverly S Emanuel. Dev Psychopathol 2005
61
26

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
144
16

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.
Elizabeth M Tunbridge, Paul J Harrison, Daniel R Weinberger. Biol Psychiatry 2006
531
16

Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome.
Tony J Simon, Carrie E Bearden, Donna McDonald Mc-Ginn, Elaine Zackai. Cortex 2005
105
15

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.
R J Shprintzen, R B Goldberg, M L Lewin, E J Sidoti, M D Berkman, R V Argamaso, D Young. Cleft Palate J 1978
510
15

A comprehensive analysis of 22q11 gene expression in the developing and adult brain.
T M Maynard, G T Haskell, A Z Peters, L Sikich, J A Lieberman, A-S LaMantia. Proc Natl Acad Sci U S A 2003
107
15

Prefrontal neurons and the genetics of schizophrenia.
D R Weinberger, M F Egan, A Bertolino, J H Callicott, V S Mattay, B K Lipska, K F Berman, T E Goldberg. Biol Psychiatry 2001
532
14

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
340
14

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome.
Kevin M Antshel, Wanda Fremont, Nancy J Roizen, Robert Shprintzen, Anne Marie Higgins, Amit Dhamoon, Wendy R Kates. J Am Acad Child Adolesc Psychiatry 2006
122
14

Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.
Carrie E Bearden, Abbas F Jawad, David R Lynch, John R Monterossso, Set Sokol, Donna M McDonald-McGinn, Sulagna C Saitta, Stacy E Harris, Edward Moss, Paul P Wang,[...]. Child Neuropsychol 2005
35
40

An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS).
J C Henry, T van Amelsvoort, R G Morris, M J Owen, D G M Murphy, K C Murphy. Neuropsychologia 2002
90
15

Neuropsychiatric disorders in the 22q11 deletion syndrome.
L Niklasson, P Rasmussen, S Oskarsdóttir, C Gillberg. Genet Med 2001
105
14

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.
A Swillen, K Devriendt, E Legius, P Prinzie, A Vogels, P Ghesquière, J P Fryns. Genet Couns 1999
154
14

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
236
14


Children and adolescents with velocardiofacial syndrome: a volumetric MRI study.
S Eliez, J E Schmitt, C D White, A L Reiss. Am J Psychiatry 2000
195
13

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.
M Gerdes, C Solot, P P Wang, E Moss, D LaRossa, P Randall, E Goldmuntz, B J Clark, D A Driscoll, A Jawad,[...]. Am J Med Genet 1999
198
13

Variation in catechol-o-methyltransferase val158 met genotype associated with schizotypy but not cognition: a population study in 543 young men.
Nicholas C Stefanis, Jim Van Os, Dimitrios Avramopoulos, Nikolaos Smyrnis, Ioannis Evdokimidis, Ioanna Hantoumi, Costas N Stefanis. Biol Psychiatry 2004
117
13

The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes.
Robert M Bilder, Jan Volavka, Herbert M Lachman, Anthony A Grace. Neuropsychopharmacology 2004
569
13

Interaction of COMT (Val(108/158)Met) genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia.
Alessandro Bertolino, Grazia Caforio, Giuseppe Blasi, Mariapia De Candia, Valeria Latorre, Vittoria Petruzzella, Mario Altamura, Gaetano Nappi, Sergio Papa, Joseph H Callicott,[...]. Am J Psychiatry 2004
228
13



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.