A Swillen, K Devriendt, E Legius, P Prinzie, A Vogels, P Ghesquière, J P Fryns. Genet Couns 1999
Times Cited: 154
Times Cited: 154
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
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
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
A Swillen, K Devriendt, E Legius, B Eyskens, M Dumoulin, M Gewillig, J P Fryns. J Med Genet 1997
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
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
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
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
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
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
28
Velo-cardio-facial syndrome: language and psychological profiles.
K J Golding-Kushner, G Weller, R J Shprintzen. J Craniofac Genet Dev Biol 1985
K J Golding-Kushner, G Weller, R J Shprintzen. J Craniofac Genet Dev Biol 1985
27
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
D F Papolos, G L Faedda, S Veit, R Goldberg, B Morrow, R Kucherlapati, R J Shprintzen. Am J Psychiatry 1996
D F Papolos, G L Faedda, S Veit, R Goldberg, B Morrow, R Kucherlapati, R J Shprintzen. Am J Psychiatry 1996
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
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
26
Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk.
Carl Feinstein, Stephan Eliez, Christine Blasey, Allan L Reiss. Biol Psychiatry 2002
Carl Feinstein, Stephan Eliez, Christine Blasey, Allan L Reiss. Biol Psychiatry 2002
24
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
M Woodin, P P Wang, D Aleman, D McDonald-McGinn, E Zackai, E Moss. Genet Med 2001
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
R J Shprintzen, R Goldberg, K J Golding-Kushner, R W Marion. Am J Med Genet 1992
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
Tamar Green, Doron Gothelf, Bronwyn Glaser, Martin Debbane, Amos Frisch, Moshe Kotler, Abraham Weizman, Stephan Eliez. J Am Acad Child Adolesc Psychiatry 2009
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
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
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
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
22
Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group.
Kate D Baker, David H Skuse. Br J Psychiatry 2005
Kate D Baker, David H Skuse. Br J Psychiatry 2005
21
Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden.
S Oskarsdóttir, M Vujic, A Fasth. Arch Dis Child 2004
S Oskarsdóttir, M Vujic, A Fasth. Arch Dis Child 2004
21
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
Doron Gothelf, Stephan Eliez, Tracy Thompson, Christine Hinard, Lauren Penniman, Carl Feinstein, Hower Kwon, Shuting Jin, Booil Jo, Stylianos E Antonarakis,[...]. Nat Neurosci 2005
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
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
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
Tony J Simon, Lijun Ding, Joel P Bish, Donna M McDonald-McGinn, Elaine H Zackai, James Gee. Neuroimage 2005
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
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
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
P D Arnold, J Siegel-Bartelt, C Cytrynbaum, I Teshima, R Schachar. Am J Med Genet 2001
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
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
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
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
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
Doron Gothelf, Carl Feinstein, Tracy Thompson, Eugene Gu, Lauren Penniman, Ellen Van Stone, Hower Kwon, Stephan Eliez, Allan L Reiss. Am J Psychiatry 2007
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
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
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
R J Shprintzen, R B Goldberg, M L Lewin, E J Sidoti, M D Berkman, R V Argamaso, D Young. Cleft Palate J 1978
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
Tony J Simon, Carrie E Bearden, Donna McDonald Mc-Ginn, Elaine Zackai. Cortex 2005
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
B De Smedt, K Devriendt, J-P Fryns, A Vogels, M Gewillig, A Swillen. J Intellect Disabil Res 2007
16
16
22q11 deletion syndrome: a genetic subtype of schizophrenia.
A S Bassett, E W Chow. Biol Psychiatry 1999
A S Bassett, E W Chow. Biol Psychiatry 1999
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
A S Bassett, K Hodgkinson, E W Chow, S Correia, L E Scutt, R Weksberg. Am J Med Genet 1998
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
P P Wang, M F Woodin, R Kreps-Falk, E M Moss. Dev Med Child Neurol 2000
17
Neuropsychiatric disorders in the 22q11 deletion syndrome.
L Niklasson, P Rasmussen, S Oskarsdóttir, C Gillberg. Genet Med 2001
L Niklasson, P Rasmussen, S Oskarsdóttir, C Gillberg. Genet Med 2001
15
Velo-cardio-facial syndrome: a distinctive behavioral phenotype.
R J Shprintzen. Ment Retard Dev Disabil Res Rev 2000
R J Shprintzen. Ment Retard Dev Disabil Res Rev 2000
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
Anne S Bassett, Eva W C Chow, Philip AbdelMalik, Mirona Gheorghiu, Janice Husted, Rosanna Weksberg. Am J Psychiatry 2003
15
Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?
A Swillen, L Vandeputte, J Cracco, B Maes, P Ghesquière, K Devriendt, J P Fryns. Child Neuropsychol 1999
A Swillen, L Vandeputte, J Cracco, B Maes, P Ghesquière, K Devriendt, J P Fryns. Child Neuropsychol 1999
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
S Eliez, J E Schmitt, C D White, A L Reiss. Am J Psychiatry 2000
14
Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.
Lena Niklasson, Peder Rasmussen, Sólveig Oskarsdóttir, Christopher Gillberg. Dev Med Child Neurol 2002
Lena Niklasson, Peder Rasmussen, Sólveig Oskarsdóttir, Christopher Gillberg. Dev Med Child Neurol 2002
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
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
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
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
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
R Goldberg, B Motzkin, R Marion, P J Scambler, R J Shprintzen. Am J Med Genet 1993
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
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
13
Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications.
A Swillen, A Vogels, K Devriendt, J P Fryns. Am J Med Genet 2000
A Swillen, A Vogels, K Devriendt, J P Fryns. Am J Med Genet 2000
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
Therese van Amelsvoort, Eileen Daly, Jayne Henry, Dene Robertson, Virginia Ng, Michael Owen, Kieran C Murphy, Declan G M Murphy. Arch Gen Psychiatry 2004
13
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.
L A Jerome, V E Papaioannou. Nat Genet 2001
L A Jerome, V E Papaioannou. Nat Genet 2001
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
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
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
Linda E Campbell, Eileen Daly, Fiona Toal, Angela Stevens, Rayna Azuma, Marco Catani, Virginia Ng, Therese van Amelsvoort, Xavier Chitnis, William Cutter,[...]. Brain 2006
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
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
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.