A citation-based method for searching scientific literature

Kate Baker, Torsten Baldeweg, Sinthuja Sivagnanasundaram, Peter Scambler, David Skuse. Biol Psychiatry 2005
Times Cited: 103







List of co-cited articles
1388 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
254
44

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
39

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.
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,[...]. Am J Psychiatry 2004
103
31

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
29

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
28

Mismatch negativity in schizophrenia: a meta-analysis.
Daniel Umbricht, Sanya Krljes. Schizophr Res 2005
492
26

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
182
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
58

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
22

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
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
31

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
27

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
56
35

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
29

Duration mismatch negativity in biological relatives of patients with schizophrenia spectrum disorders.
Patricia T Michie, Hamish Innes-Brown, Juanita Todd, Assen V Jablensky. Biol Psychiatry 2002
132
19

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
177
19


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
266
18

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.
Elizabeth M Tunbridge, Paul J Harrison, Daniel R Weinberger. Biol Psychiatry 2006
521
18

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
18


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
17

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
194
17

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

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
60
26

Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications.
Martin Debbané, Bronwyn Glaser, Melissa K David, Carl Feinstein, Stephan Eliez. Schizophr Res 2006
104
16

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
Doron Gothelf, Marie Schaer, Stephan Eliez. Dev Disabil Res Rev 2008
97
16

Mismatch negativity potentials and cognitive impairment in schizophrenia.
Torsten Baldeweg, Anthony Klugman, John Gruzelier, Steven R Hirsch. Schizophr Res 2004
199
15


Amplitude reduction of the mismatch negativity in first-degree relatives of patients with schizophrenia.
F Jessen, T Fries, C Kucharski, T Nishimura, K Hoenig, W Maier, P Falkai, R Heun. Neurosci Lett 2001
79
18

Lower prepulse inhibition in children with the 22q11 deletion syndrome.
Christina Sobin, Karen Kiley-Brabeck, Maria Karayiorgou. Am J Psychiatry 2005
80
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
170
15

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
15

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
15

22q11 deletion syndrome in adults with schizophrenia.
A S Bassett, K Hodgkinson, E W Chow, S Correia, L E Scutt, R Weksberg. Am J Med Genet 1998
170
14

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
513
14

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
14

Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome.
Doron Gothelf, Gadi Presburger, Ada H Zohar, Merav Burg, Ariela Nahmani, Moshe Frydman, Mordechai Shohat, Dov Inbar, Ayala Aviram-Goldring, Josepha Yeshaya,[...]. Am J Med Genet B Neuropsychiatr Genet 2004
111
14

Brain potential evidence for an auditory sensory memory deficit in schizophrenia.
S V Catts, A M Shelley, P B Ward, B Liebert, N McConaghy, S Andrews, P T Michie. Am J Psychiatry 1995
259
14

Mismatch negativity: an index of a preattentive processing deficit in schizophrenia.
A M Shelley, P B Ward, S V Catts, P T Michie, S Andrews, N McConaghy. Biol Psychiatry 1991
323
14

Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome.
Joel P Bish, Samantha M Ferrante, Donna McDonald-McGinn, Elaine Zackai, Tony J Simon. Dev Sci 2005
63
22

Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study.
Doron Gothelf, Lauren Penniman, Eugene Gu, Stephan Eliez, Allan L Reiss. Schizophr Res 2007
78
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
220
14


The endophenotype concept in psychiatry: etymology and strategic intentions.
Irving I Gottesman, Todd D Gould. Am J Psychiatry 2003
13


A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
414
13

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study.
Therese van Amelsvoort, Eileen Daly, Jayne Henry, Dene Robertson, Virginia Ng, Michael Owen, Kieran C Murphy, Declan G M Murphy. Arch Gen Psychiatry 2004
100
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.