A citation-based method for searching scientific literature

Christina Sobin, Karen Kiley-Brabeck, Maria Karayiorgou. Am J Psychiatry 2005
Times Cited: 80







List of co-cited articles
973 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
753
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
30

Prestimulus effects on human startle reflex in normals and schizophrenics.
D Braff, C Stone, E Callaway, M Geyer, I Glick, L Bali. Psychophysiology 1978
954
28


Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.
Richard Paylor, Beate Glaser, Annalisa Mupo, Paris Ataliotis, Corinne Spencer, Angela Sobotka, Chelsey Sparks, Chul-Hee Choi, John Oghalai, Sarah Curran,[...]. Proc Natl Acad Sci U S A 2006
201
23

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
188
22

Brain anatomy and sensorimotor gating in Asperger's syndrome.
Grainne M McAlonan, Eileen Daly, Veena Kumari, Hugo D Critchley, Therese van Amelsvoort, John Suckling, Andrew Simmons, Thordur Sigmundsson, Kathyrn Greenwood, Ailsa Russell,[...]. Brain 2002
311
21


Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.
R Paylor, K L McIlwain, R McAninch, A Nellis, L A Yuva-Paylor, A Baldini, E A Lindsay. Hum Mol Genet 2001
107
21

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
240
21

Impaired prepulse inhibition of acoustic and tactile startle response in patients with Huntington's disease.
N R Swerdlow, J Paulsen, D L Braff, N Butters, M A Geyer, M R Swenson. J Neurol Neurosurg Psychiatry 1995
363
20

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice.
J A Gogos, M Santha, Z Takacs, K D Beck, V Luine, L R Lucas, J V Nadler, M Karayiorgou. Nat Genet 1999
202
20

Realistic expectations of prepulse inhibition in translational models for schizophrenia research.
Neal R Swerdlow, Martin Weber, Ying Qu, Gregory A Light, David L Braff. Psychopharmacology (Berl) 2008
396
20

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
18

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
426
18

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
103
18

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model.
Kimberly L Stark, Bin Xu, Anindya Bagchi, Wen-Sung Lai, Hui Liu, Ruby Hsu, Xiang Wan, Paul Pavlidis, Alea A Mills, Maria Karayiorgou,[...]. Nat Genet 2008
424
18

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
839
17

Sensorimotor gating in boys with Tourette's syndrome and ADHD: preliminary results.
F X Castellanos, E J Fine, D Kaysen, W L Marsh, J L Rapoport, M Hallett. Biol Psychiatry 1996
314
17

Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome.
Joel P Bish, Samantha M Ferrante, Donna McDonald-McGinn, Elaine Zackai, Tony J Simon. Dev Sci 2005
63
22

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
143
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
173
17

Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.
Kathryn Eve Lewandowski, Vandana Shashi, Peggy M Berry, Thomas R Kwapil. Am J Med Genet B Neuropsychiatr Genet 2007
86
17

Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice.
P W Frankland, Y Wang, B Rosner, T Shimizu, B W Balleine, E M Dykens, E M Ornitz, A J Silva. Mol Psychiatry 2004
207
16

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
17

Networks of attention in children with the 22q11 deletion syndrome.
Christina Sobin, Karen Kiley-Brabeck, Sarah Daniels, Maude Blundell, Kwame Anyane-Yeboa, Maria Karayiorgou. Dev Neuropsychol 2004
76
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
223
16

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia.
Hui Liu, Simon C Heath, Christina Sobin, J Louw Roos, Brandi L Galke, Maude L Blundell, Marge Lenane, Brian Robertson, Ellen M Wijsman, Judith L Rapoport,[...]. Proc Natl Acad Sci U S A 2002
237
16



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
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

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
15

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
104
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
268
15

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
406
15

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
137
15


Men are more inhibited than women by weak prepulses.
N R Swerdlow, P Auerbach, S M Monroe, H Hartston, M A Geyer, D L Braff. Biol Psychiatry 1993
181
15

Impaired prepulse inhibition of acoustic startle in obsessive-compulsive disorder.
Klaus Hoenig, Andrea Hochrein, Boris B Quednow, Wolfgang Maier, Michael Wagner. Biol Psychiatry 2005
131
15

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
113
15

Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome.
Jeffrey M Long, Patricia LaPorte, Sandra Merscher, Birgit Funke, Bruno Saint-Jore, Anne Puech, Raju Kucherlapati, Bernice E Morrow, Arthur I Skoultchi, Anthony Wynshaw-Boris. Neurogenetics 2006
54
22

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
235
15

A preliminary assessment of sensorimotor gating in patients with obsessive compulsive disorder.
N R Swerdlow, C H Benbow, S Zisook, M A Geyer, D L Braff. Biol Psychiatry 1993
281
13

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
700
13

A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.
Tony J Simon, Joel P Bish, Carrie E Bearden, Lijun Ding, Samantha Ferrante, Vy Nguyen, James C Gee, Donna M McDonald-McGinn, Elaine H Zackai, Beverly S Emanuel. Dev Psychopathol 2005
61
18

Tactile prepuff inhibition of startle in children with Tourette's syndrome: in search of an "fMRI-friendly" startle paradigm.
N R Swerdlow, B Karban, Y Ploum, R Sharp, M A Geyer, A Eastvold. Biol Psychiatry 2001
129
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
135
13


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.