A citation-based method for searching scientific literature

A Swillen, K Devriendt, E Legius, P Prinzie, A Vogels, P Ghesquière, J P Fryns. Genet Couns 1999
Times Cited: 154







List of co-cited articles
819 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
46

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
40

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
35

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
32

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
829
28

Velo-cardio-facial syndrome: language and psychological profiles.
K J Golding-Kushner, G Weller, R J Shprintzen. J Craniofac Genet Dev Biol 1985
202
27


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
26


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
24

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
23

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
23

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
22

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
22



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
19

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
18

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
17

Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
533
17

Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders.
P D Arnold, J Siegel-Bartelt, C Cytrynbaum, I Teshima, R Schachar. Am J Med Genet 2001
73
23

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
D M McDonald-McGinn, R Kirschner, E Goldmuntz, K Sullivan, P Eicher, M Gerdes, E Moss, C Solot, P Wang, I Jacobs,[...]. Genet Couns 1999
313
17

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
17

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
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

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
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
16

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update.
B De Smedt, K Devriendt, J-P Fryns, A Vogels, M Gewillig, A Swillen. J Intellect Disabil Res 2007
108
16

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
276
16

22q11 deletion syndrome: a genetic subtype of schizophrenia.
A S Bassett, E W Chow. Biol Psychiatry 1999
223
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
171
15

Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).
P P Wang, M F Woodin, R Kreps-Falk, E M Moss. Dev Med Child Neurol 2000
84
17

Neuropsychiatric disorders in the 22q11 deletion syndrome.
L Niklasson, P Rasmussen, S Oskarsdóttir, C Gillberg. Genet Med 2001
101
15

Velo-cardio-facial syndrome: a distinctive behavioral phenotype.
R J Shprintzen. Ment Retard Dev Disabil Res Rev 2000
154
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


The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
346
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
14

Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.
Lena Niklasson, Peder Rasmussen, Sólveig Oskarsdóttir, Christopher Gillberg. Dev Med Child Neurol 2002
66
21

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
382
14

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
14

Velo-cardio-facial syndrome: a review of 120 patients.
R Goldberg, B Motzkin, R Marion, P J Scambler, R J Shprintzen. Am J Med Genet 1993
343
13

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
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


The annual incidence of DiGeorge/velocardiofacial syndrome.
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
257
13

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
13

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
S Merscher, B Funke, J A Epstein, J Heyer, A Puech, M M Lu, R J Xavier, M B Demay, R G Russell, S Factor,[...]. Cell 2001
665
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.