A citation-based method for searching scientific literature

Erik Boot, Jan Booij, Janneke Zinkstok, Nico Abeling, Lieuwe de Haan, Frank Baas, Don Linszen, Thérèse van Amelsvoort. Neuropsychopharmacology 2008
Times Cited: 44







List of co-cited articles
399 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
738
45

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
253
40

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
395
36

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele.
Jacob A S Vorstman, Bruce I Turetsky, Monique E J Sijmens-Morcus, Monique G de Sain, Bert Dorland, Mirjam Sprong, Eric F Rappaport, Frits A Beemer, Beverly S Emanuel, René S Kahn,[...]. Neuropsychopharmacology 2009
68
29

Striatal D₂ receptor binding in 22q11 deletion syndrome: an [¹²³I]IBZM SPECT study.
E Boot, J Booij, J R Zinkstok, L de Haan, D H Linszen, F Baas, T A van Amelsvoort. J Psychopharmacol 2010
18
72

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
285
27

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
Doron Gothelf, Marie Schaer, Stephan Eliez. Dev Disabil Res Rev 2008
97
27

COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome.
Erik Boot, Jan Booij, Janneke R Zinkstok, Frank Baas, Ann Swillen, Michael J Owen, Declan G Murphy, Kieran C Murphy, Don H Linszen, Thérèse A Van Amelsvoort. Synapse 2011
16
75

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
24
50

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
41
26

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.
Elizabeth M Tunbridge, Paul J Harrison, Daniel R Weinberger. Biol Psychiatry 2006
519
22

Functional gene-expression analysis shows involvement of schizophrenia-relevant pathways in patients with 22q11 deletion syndrome.
Nico J M van Beveren, Lianne C Krab, Sigrid Swagemakers, Gabriëlle H S Buitendijk, Erik Boot, Peter van der Spek, Ype Elgersma, Therese A M J van Amelsvoort. PLoS One 2012
24
41

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
193
22

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
20

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
108
20

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
20

The positive and negative syndrome scale (PANSS) for schizophrenia.
S R Kay, A Fiszbein, L A Opler. Schizophr Bull 1987
20


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
104
20



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
182
18

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
218
18

Proton magnetic resonance spectroscopy in 22q11 deletion syndrome.
Fabiana da Silva Alves, Erik Boot, Nicole Schmitz, Aart Nederveen, Jacob Vorstman, Christina Lavini, Petra J Pouwels, Lieuwe de Haan, Don Linszen, Therese van Amelsvoort. PLoS One 2011
30
26

Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome.
Erik Boot, Nancy J Butcher, Thérèse A M J van Amelsvoort, Anthony E Lang, Connie Marras, Margarita Pondal, Danielle M Andrade, Wai Lun Alan Fung, Anne S Bassett. Am J Med Genet A 2015
39
20

Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease.
Nancy J Butcher, Connie Marras, Margarita Pondal, Pablo Rusjan, Erik Boot, Leigh Christopher, Gabriela M Repetto, Rosemarie Fritsch, Eva W C Chow, Mario Masellis,[...]. Brain 2017
26
30

Catechol-o-methyltransferase enzyme activity and protein expression in human prefrontal cortex across the postnatal lifespan.
E M Tunbridge, C S Weickert, J E Kleinman, M M Herman, J Chen, B S Kolachana, P J Harrison, D R Weinberger. Cereb Cortex 2007
105
15

A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).
Wendy R Kates, Kevin M Antshel, Nuria Abdulsabur, Deirdre Colgan, Birgit Funke, Wanda Fremont, Anne Marie Higgins, Raju Kucherlapati, Robert J Shprintzen. Am J Med Genet B Neuropsychiatr Genet 2006
64
15

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
111
15

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
265
15

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
77
15

Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
Marie Schaer, Martin Debbané, Meritxell Bach Cuadra, Marie-Christine Ottet, Bronwyn Glaser, Jean-Philippe Thiran, Stephan Eliez. Schizophr Res 2009
86
15

Elevated striatal dopamine function linked to prodromal signs of schizophrenia.
Oliver D Howes, Andrew J Montgomery, Marie-Claude Asselin, Robin M Murray, Isabel Valli, Paul Tabraham, Elvira Bramon-Bosch, Lucia Valmaggia, Louise Johns, Matthew Broome,[...]. Arch Gen Psychiatry 2009
481
15

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
129
15

Practical guidelines for managing adults with 22q11.2 deletion syndrome.
Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, Danielle M Andrade, Erik Boot, Eva W C Chow, Brian Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman,[...]. Genet Med 2015
114
15

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
397
15

Lower prepulse inhibition in children with the 22q11 deletion syndrome.
Christina Sobin, Karen Kiley-Brabeck, Maria Karayiorgou. Am J Psychiatry 2005
80
13

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome.
Doron Gothelf, Elena Michaelovsky, Amos Frisch, Ada H Zohar, Gadi Presburger, Merav Burg, Ayala Aviram-Goldring, Moshe Frydman, Josepha Yeshaya, Mordechai Shohat,[...]. Int J Neuropsychopharmacol 2007
53
13


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
227
13

A common molecular basis for rearrangement disorders on chromosome 22q11.
L Edelmann, R K Pandita, E Spiteri, B Funke, R Goldberg, N Palanisamy, R S Chaganti, E Magenis, R J Shprintzen, B E Morrow. Hum Mol Genet 1999
337
13

Site-specific role of catechol-O-methyltransferase in dopamine overflow within prefrontal cortex and dorsal striatum.
Leonid Yavich, Markus M Forsberg, Maria Karayiorgou, Joseph A Gogos, Pekka T Männistö. J Neurosci 2007
188
13

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
169
13


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
163
13

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
13

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
13

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
76
13

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
T van Amelsvoort, J Zinkstok, M Figee, E Daly, R Morris, M J Owen, K C Murphy, L De Haan, D H Linszen, B Glaser,[...]. Psychol Med 2008
38
15



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.