A citation-based method for searching scientific literature

Frederick Furniss, Asit B Biswas, Rohit Gumber, Niraj Singh. Res Dev Disabil 2011
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


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
43

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
203
43

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
43

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
43

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
37

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
37

Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?
Kate Baker, Jacob A S Vorstman. Curr Opin Neurol 2012
46
31

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
31

Cognitive development in children with 22q11.2 deletion syndrome.
Sasja N Duijff, Petra W J Klaassen, Henriette F N Swanenburg de Veye, Frits A Beemer, Gerben Sinnema, Jacob A S Vorstman. Br J Psychiatry 2012
67
31

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
31

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
31

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
25


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
104
25

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
25

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
25

Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study.
Wendy R Kates, Kevin M Antshel, Stephen V Faraone, Wanda P Fremont, Anne Marie Higgins, Robert J Shprintzen, Jo-Anna Botti, Lauren Kelchner, Christopher McCarthy. Biol Psychiatry 2011
68
25

Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹⁰⁸/¹⁵⁸Met polymorphism, gender and symptomatology.
Erik Boot, Jan Booij, Nico Abeling, Julia Meijer, Fabiana da Silva Alves, Janneke Zinkstok, Frank Baas, Don Linszen, Thérèse van Amelsvoort. J Psychopharmacol 2011
25
25


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
59
25

The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.
Rachel K Jonas, Caroline A Montojo, Carrie E Bearden. Biol Psychiatry 2014
118
25

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
25

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
25


Risk factors and the evolution of psychosis in 22q11.2 deletion syndrome: a longitudinal 2-site study.
Doron Gothelf, Maude Schneider, Tamar Green, Martin Debbané, Amos Frisch, Bronwyn Glaser, Hadas Zilkha, Marie Schaer, Abraham Weizman, Stephan Eliez. J Am Acad Child Adolesc Psychiatry 2013
77
25

Comparing phenotypes in patients with idiopathic autism to patients with velocardiofacial syndrome (22q11 DS) with and without autism.
Wendy R Kates, Kevin M Antshel, Wanda P Fremont, Robert J Shprintzen, Leslie A Strunge, Courtney P Burnette, Anne Marie Higgins. Am J Med Genet A 2007
64
25

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
25

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
25

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.
R E Gur, J J Yi, D M McDonald-McGinn, S X Tang, M E Calkins, D Whinna, M C Souders, A Savitt, E H Zackai, P J Moberg,[...]. Mol Psychiatry 2014
64
25

Neuropsychiatric disorders in the 22q11 deletion syndrome.
L Niklasson, P Rasmussen, S Oskarsdóttir, C Gillberg. Genet Med 2001
105
18

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
352
18

Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome.
H M Lachman, B Morrow, R Shprintzen, S Veit, S S Parsia, G Faedda, R Goldberg, R Kucherlapati, D F Papolos. Am J Med Genet 1996
228
18

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
18

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
18

Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.
Wendy R Kates, Ravi Bansal, Wanda Fremont, Kevin M Antshel, Xuejun Hao, Anne Marie Higgins, Jun Liu, Robert J Shprintzen, Bradley S Peterson. J Am Acad Child Adolesc Psychiatry 2011
23
18

22q11 deletion syndrome in childhood onset schizophrenia: an update.
A Sporn, A Addington, A L Reiss, M Dean, N Gogtay, U Potocnik, D Greenstein, J Hallmayer, P Gochman, M Lenane,[...]. Mol Psychiatry 2004
63
18

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
18

Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome.
Doron Gothelf, Gadi Presburger, Ada H Zohar, Merav Burg, Ariela Nahmani, Moshe Frydman, Mordechai Shohat, Dov Inbar, Ayala Aviram-Goldring, Josepha Yeshaya,[...]. Am J Med Genet B Neuropsychiatr Genet 2004
112
18

A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome.
Heather M Shapiro, Yukari Takarae, Danielle J Harvey, Margarita H Cabaral, Tony J Simon. J Neurodev Disord 2012
16
18

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
18

Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
Doron Gothelf, Amanda J Law, Amos Frisch, Jingshan Chen, Omer Zarchi, Elena Michaelovsky, Renee Ren-Patterson, Barbara K Lipska, Miri Carmel, Bhaskar Kolachana,[...]. Biol Psychiatry 2014
42
18

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus.
P J Scambler, D Kelly, E Lindsay, R Williamson, R Goldberg, R Shprintzen, D I Wilson, J A Goodship, I E Cross, J Burn. Lancet 1992
363
18

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
318
18

The longitudinal course of attention deficit/hyperactivity disorder in velo-cardio-facial syndrome.
Kevin M Antshel, Kaitlin Hendricks, Robert Shprintzen, Wanda Fremont, Anne Marie Higgins, Stephen V Faraone, Wendy R Kates. J Pediatr 2013
22
18

Velo-cardio-facial syndrome: a distinctive behavioral phenotype.
R J Shprintzen. Ment Retard Dev Disabil Res Rev 2000
153
18

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
137
18

Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus.
Eva W C Chow, Andrew Ho, Corie Wei, Eduard H J Voormolen, Adrian P Crawley, Anne S Bassett. Am J Psychiatry 2011
40
18

Elevated prevalence of generalized anxiety disorder in adults with 22q11.2 deletion syndrome.
Wai Lun Alan Fung, Rebecca McEvilly, Jessica Fong, Candice Silversides, Eva Chow, Anne Bassett. Am J Psychiatry 2010
70
18


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
18


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.