A citation-based method for searching scientific literature

Christina Sobin, Samantha H Monk, Karen Kiley-Brabeck, Jananne Khuri, Maria Karayiorgou. Mov Disord 2006
Times Cited: 28







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



Times Cited
  Times     Co-cited
Similarity


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

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
39

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
39

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
35

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
35

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
40
35

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
843
32

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
28

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
298
25

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
25

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
25

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
25

22q11.2DS deletion syndrome: developmental milestones in infants and toddlers.
Nancy J Roizen, Kevin M Antshel, Wanda Fremont, Nuria AbdulSabur, Anne Marie Higgins, Robert J Shprintzen, Wendy R Kates. J Dev Behav Pediatr 2007
26
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
179
21

Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis.
Christina Sobin, Karen Kiley-Brabeck, Sarah Daniels, Jananne Khuri, Lisa Taylor, Maude Blundell, Kwame Anyane-Yeboa, Maria Karayiorgou. Child Neuropsychol 2005
74
21

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
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
258
21

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
113
21

Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defect.
Ann Swillen, Hilde Feys, Tamara Adriaens, Loes Nelissen, Luc Mertens, Marc Gewillig, Koen Devriendt, Jean-Pierre Fryns. Dev Med Child Neurol 2005
24
25

22q11.2 deletion syndrome: are motor deficits more than expected for IQ level?
Nancy J Roizen, Anne M Higgins, Kevin M Antshel, Wanda Fremont, Robert Shprintzen, Wendy R Kates. J Pediatr 2010
16
37

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
52
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
452
21

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
497
21

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

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
17

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
137
17

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
675
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

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
17


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
223
17

Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls.
Katrijn Van Aken, Ann Swillen, Marc Beirinckx, Luc Janssens, Karen Caeyenberghs, Bouwien Smits-Engelsman. Res Dev Disabil 2010
10
50

The motor profile of primary school-age children with a 22q11.2 deletion syndrome (22q11.2DS) and an age- and IQ-matched control group.
Katrijn Van Aken, Karen Caeyenberghs, Bouwien Smits-Engelsman, Ann Swillen. Child Neuropsychol 2009
20
25

Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study.
Kevin M Antshel, Robert Shprintzen, Wanda Fremont, Anne Marie Higgins, Stephen V Faraone, Wendy R Kates. J Am Acad Child Adolesc Psychiatry 2010
94
17


Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.
Lena Niklasson, Peder Rasmussen, Sólveig Oskarsdóttir, Christopher Gillberg. Res Dev Disabil 2009
145
17

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
329
17

Otolaryngologic manifestations of the 22q11.2 deletion syndrome.
Orville Dyce, Donna McDonald-McGinn, Richard E Kirschner, Elaine Zackai, Kathleen Young, Ian N Jacobs. Arch Otolaryngol Head Neck Surg 2002
73
17

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives.
A E Pulver, G Nestadt, R Goldberg, R J Shprintzen, M Lamacz, P S Wolyniec, B Morrow, M Karayiorgou, S E Antonarakis, D Housman. J Nerv Ment Dis 1994
340
14

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
546
14

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
14

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
14

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
318
14

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
510
14

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia.
Jun Mukai, Hui Liu, Rachel A Burt, Dionne E Swor, Wen-Sung Lai, Maria Karayiorgou, Joseph A Gogos. Nat Genet 2004
241
14

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Grégory Raux, Emilie Bumsel, Bernadette Hecketsweiler, Therese van Amelsvoort, Janneke Zinkstok, Sylvie Manouvrier-Hanu, Carole Fantini, Georges-Marie M Brévière, Gabriella Di Rosa, Giuseppina Pustorino,[...]. Hum Mol Genet 2007
115
14

Genetic variation in the 22q11 locus and susceptibility to schizophrenia.
Hui Liu, Goncalo R Abecasis, Simon C Heath, Alyson Knowles, Sandra Demars, Ying-Jiun Chen, J Louw Roos, Judith L Rapoport, Joseph A Gogos, Maria Karayiorgou. Proc Natl Acad Sci U S A 2002
149
14

Velo-cardio-facial syndrome: a distinctive behavioral phenotype.
R J Shprintzen. Ment Retard Dev Disabil Res Rev 2000
153
14

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.
M Karayiorgou, M A Morris, B Morrow, R J Shprintzen, R Goldberg, J Borrow, A Gos, G Nestadt, P S Wolyniec, V K Lasseter. Proc Natl Acad Sci U S A 1995
407
14


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.