A citation-based method for searching scientific literature

M Gerdes, C Solot, P P Wang, E Moss, D LaRossa, P Randall, E Goldmuntz, B J Clark, D A Driscoll, A Jawad, B S Emanuel, D M McDonald-McGinn, M L Batshaw, E H Zackai. Am J Med Genet 1999
Times Cited: 198







List of co-cited articles
787 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
38

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
38

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
30

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
821
29

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
28

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
24

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
24

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.
A Swillen, K Devriendt, E Legius, P Prinzie, A Vogels, P Ghesquière, J P Fryns. Genet Couns 1999
154
21

Velo-cardio-facial syndrome: language and psychological profiles.
K J Golding-Kushner, G Weller, R J Shprintzen. J Craniofac Genet Dev Biol 1985
202
20

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
274
20


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
17

Communication issues in 22q11.2 deletion syndrome: children at risk.
C B Solot, M Gerdes, R E Kirschner, D M McDonald-McGinn, E Moss, M Woodin, D Aleman, E H Zackai, P P Wang. Genet Med 2001
51
33

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
311
17


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
105
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

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
16

Language skills in children with velocardiofacial syndrome (deletion 22q11.2).
Bronwyn Glaser, Donna L Mumme, Christine Blasey, Michael A Morris, Sophie P Dahoun, Stylianos E Antonarakis, Allan L Reiss, Stephan Eliez. J Pediatr 2002
51
31

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
19

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
15

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
120
15

Early speech and language development in children with velocardiofacial syndrome.
N J Scherer, L L D'Antonio, J H Kalbfleisch. Am J Med Genet 1999
69
21

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
15


Velo-cardio-facial syndrome: a distinctive behavioral phenotype.
R J Shprintzen. Ment Retard Dev Disabil Res Rev 2000
154
14


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
141
13

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
104
13


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
13

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
343
12

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
12

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
12


Communication disorders in the 22Q11.2 microdeletion syndrome.
C B Solot, C Knightly, S D Handler, M Gerdes, D M McDonald-McGinn, E Moss, P Wang, M Cohen, P Randall, D Larossa,[...]. J Commun Disord 2000
40
30

Disabilities and cognition in children and adolescents with 22q11 deletion syndrome.
S Oskarsdóttir, M Belfrage, E Sandstedt, G Viggedal, P Uvebrant. Dev Med Child Neurol 2005
39
30

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
12

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
12

Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?
Renée R Lajiness-O'Neill, Isabelle Beaulieu, Jeffrey B Titus, Alexander Asamoah, Erin D Bigler, Erawati V Bawle, Rebecca Pollack. Child Neuropsychol 2005
64
18

Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome).
Katrijn Van Aken, Bert De Smedt, Annelies Van Roie, Marc Gewillig, Koen Devriendt, Jean-Pierre Fryns, Johan Simons, Ann Swillen. Dev Med Child Neurol 2007
27
44

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
12

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
12

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
235
12

Neuropsychiatric disorders in the 22q11 deletion syndrome.
L Niklasson, P Rasmussen, S Oskarsdóttir, C Gillberg. Genet Med 2001
101
11

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
11

Prevalence of 22q11 microdeletion.
S Tézenas Du Montcel, H Mendizabai, S Aymé, A Lévy, N Philip. J Med Genet 1996
194
11

Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan,[...]. J Pediatr 2011
299
11


Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
687
10


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.