A citation-based method for searching scientific literature

Doron Gothelf, Marie Schaer, Stephan Eliez. Dev Disabil Res Rev 2008
Times Cited: 97







List of co-cited articles
1176 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
749
41

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
36

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
23

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


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
165
21

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

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
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
267
19

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
310
19

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
87
21

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
425
19

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
197
18

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
276
17

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
233
17

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
21


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
16

Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.
T van Amelsvoort, E Daly, D Robertson, J Suckling, V Ng, H Critchley, M J Owen, J Henry, K C Murphy, D G Murphy. Br J Psychiatry 2001
122
16

Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome).
Giles M Tan, Danilo Arnone, Andrew M McIntosh, Klaus P Ebmeier. Schizophr Res 2009
50
32

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.
Elizabeth M Tunbridge, Paul J Harrison, Daniel R Weinberger. Biol Psychiatry 2006
524
15

Mapping cortical thickness in children with 22q11.2 deletions.
Carrie E Bearden, Theo G M van Erp, Rebecca A Dutton, Helen Tran, Lara Zimmermann, Daqiang Sun, Jennifer A Geaga, Tony J Simon, David C Glahn, Tyrone D Cannon,[...]. Cereb Cortex 2007
78
19

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
221
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
171
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
186
15

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
18

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
134
15

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
222
15

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
14

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome).
Wendy R Kates, Adam M Miller, Nuria Abdulsabur, Kevin M Antshel, Jena Conchelos, Wanda Fremont, Nancy Roizen. J Am Acad Child Adolesc Psychiatry 2006
62
22

Late-onset psychosis in the velo-cardio-facial syndrome.
R J Shprintzen, R Goldberg, K J Golding-Kushner, R W Marion. Am J Med Genet 1992
317
13

The neurocognitive phenotype in velo-cardio-facial syndrome: a developmental perspective.
Kevin M Antshel, Wanda Fremont, Wendy R Kates. Dev Disabil Res Rev 2008
57
22

22q11 deletion syndrome: a genetic subtype of schizophrenia.
A S Bassett, E W Chow. Biol Psychiatry 1999
223
13

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
13

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
34

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
13


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
294
13

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
90
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
121
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
142
12

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
12

Disrupted dopaminergic neurotransmission in 22q11 deletion syndrome.
Erik Boot, Jan Booij, Janneke Zinkstok, Nico Abeling, Lieuwe de Haan, Frank Baas, Don Linszen, Thérèse van Amelsvoort. Neuropsychopharmacology 2008
45
26

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
84
14

Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndrome.
Doron Gothelf, Fumiko Hoeft, Takefumi Ueno, Lisa Sugiura, Agatha D Lee, Paul Thompson, Allan L Reiss. J Psychiatr Res 2011
58
20

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
11

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
423
11

Arithmetic ability and parietal alterations: a diffusion tensor imaging study in velocardiofacial syndrome.
Naama Barnea-Goraly, Stephan Eliez, Vinod Menon, Roland Bammer, Allan L Reiss. Brain Res Cogn Brain Res 2005
82
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.