A citation-based method for searching scientific literature

Doron Gothelf, Fumiko Hoeft, Christine Hinard, Joachim F Hallmayer, John Van Dover Stoecker, Stylianos E Antonarakis, Michael A Morris, Allan L Reiss. Hum Brain Mapp 2007
Times Cited: 45







List of co-cited articles
511 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
754
42

The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome).
Wendy R Kates, Beth R Krauss, Nuria Abdulsabur, Deirdre Colgan, Kevin M Antshel, Anne Marie Higgins, Robert J Shprintzen. Neuropsychologia 2007
50
33

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
31

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
28

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.
Linda E Campbell, Eileen Daly, Fiona Toal, Angela Stevens, Rayna Azuma, Marco Catani, Virginia Ng, Therese van Amelsvoort, Xavier Chitnis, William Cutter,[...]. Brain 2006
136
26

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
24

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
24

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
24

Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study.
Tony J Simon, Lijun Ding, Joel P Bish, Donna M McDonald-McGinn, Elaine H Zackai, James Gee. Neuroimage 2005
150
24

Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
Marie Schaer, Martin Debbané, Meritxell Bach Cuadra, Marie-Christine Ottet, Bronwyn Glaser, Jean-Philippe Thiran, Stephan Eliez. Schizophr Res 2009
92
24

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
22

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
22

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
22

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
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
22

Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2).
S Eliez, C M Blasey, V Menon, C D White, J E Schmitt, A L Reiss. Genet Med 2001
56
20

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
20

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
23

Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2).
Stephan Eliez, Naama Barnea-Goraly, J Eric Schmitt, Yung Liu, Allan L Reiss. Biol Psychiatry 2002
56
20

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
106
20

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
20

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
166
20

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.
Elizabeth M Tunbridge, Paul J Harrison, Daniel R Weinberger. Biol Psychiatry 2006
531
20

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
20

Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome.
Frédéric Andersson, Bronwyn Glaser, Mona Spiridon, Martin Debbané, Patrik Vuilleumier, Stephan Eliez. Biol Psychiatry 2008
52
20

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
20

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
20

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
20

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
17


Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2).
Wendy R Kates, Courtney P Burnette, Brandy A Bessette, Bradley S Folley, Leslie Strunge, Ethylin W Jabs, Godfrey D Pearlson. J Child Neurol 2004
82
17

Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).
Kevin M Antshel, Alka Aneja, Leslie Strunge, Jena Peebles, Wanda P Fremont, Kimberly Stallone, Nuria Abdulsabur, Anne Marie Higgins, Robert J Shprintzen, Wendy R Kates. J Autism Dev Disord 2007
124
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

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
17

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
T van Amelsvoort, J Zinkstok, M Figee, E Daly, R Morris, M J Owen, K C Murphy, L De Haan, D H Linszen, B Glaser,[...]. Psychol Med 2008
38
21

Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.
Kathryn Eve Lewandowski, Vandana Shashi, Peggy M Berry, Thomas R Kwapil. Am J Med Genet B Neuropsychiatr Genet 2007
87
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
323
17

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
Doron Gothelf, Marie Schaer, Stephan Eliez. Dev Disabil Res Rev 2008
98
17

Resting-state networks in adolescents with 22q11.2 deletion syndrome: associations with prodromal symptoms and executive functions.
Martin Debbané, Marine Lazouret, Annalaura Lagioia, Maude Schneider, Dimitri Van De Ville, Stephan Eliez. Schizophr Res 2012
44
18

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
15

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
105
15

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
431
15

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
15


Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.
C Carlson, H Sirotkin, R Pandita, R Goldberg, J McKie, R Wadey, S R Patanjali, S M Weissman, K Anyane-Yeboa, D Warburton,[...]. Am J Hum Genet 1997
293
15

Investigation of white matter structure in velocardiofacial syndrome: a diffusion tensor imaging study.
Naama Barnea-Goraly, Vinod Menon, Ben Krasnow, Alex Ko, Allan Reiss, Stephan Eliez. Am J Psychiatry 2003
99
15

Lower prepulse inhibition in children with the 22q11 deletion syndrome.
Christina Sobin, Karen Kiley-Brabeck, Maria Karayiorgou. Am J Psychiatry 2005
81
15

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
15

Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging.
Therese van Amelsvoort, Nicole Schmitz, Eileen Daly, Quinton Deeley, Hugo Critchley, Jayne Henry, Dene Robertson, Michael Owen, Kieran C Murphy, Declan G Murphy. Br J Psychiatry 2006
32
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.