A citation-based method for searching scientific literature

Christina Sobin, Karen Kiley-Brabeck, Maria Karayiorgou. Am J Psychiatry 2005
Times Cited: 81



Kate Baker, Torsten Baldeweg, Sinthuja Sivagnanasundaram, Peter Scambler, David Skuse. Biol Psychiatry 2005
Times Cited: 104




List of shared articles



Times cited

Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.
Omer Zarchi, Miri Carmel, Chen Avni, Josef Attias, Amos Frisch, Elena Michaelovsky, Miriam Patya, Tamar Green, Ronnie Weinberger, Abraham Weizman,[...]. J Psychiatr Res 2013
29

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
323

Mouse Models of 22q11.2-Associated Autism Spectrum Disorder.
Noboru Hiroi, Takeshi Hiramoto, Kathryn M Harper, Go Suzuki, Shuken Boku. Autism Open Access 2012
12

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.
N Hiroi, T Takahashi, A Hishimoto, T Izumi, S Boku, T Hiramoto. Mol Psychiatry 2013
87

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
71

The development of cognitive control in children with chromosome 22q11.2 deletion syndrome.
Heather M Shapiro, Flora Tassone, Nimrah S Choudhary, Tony J Simon. Front Psychol 2014
37

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

Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome.
Doron Gothelf, Fumiko Hoeft, Christine Hinard, Joachim F Hallmayer, John Van Dover Stoecker, Stylianos E Antonarakis, Michael A Morris, Allan L Reiss. Hum Brain Mapp 2007
45

Cognitive phenotype of velocardiofacial syndrome: a review.
Frederick Furniss, Asit B Biswas, Rohit Gumber, Niraj Singh. Res Dev Disabil 2011
16

PRODH rs450046 and proline x COMT Val¹⁵⁸ Met interaction effects on intelligence and startle in adults with 22q11 deletion syndrome.
Mariken B de Koning, Esther D A van Duin, Erik Boot, Oswald J N Bloemen, Jaap A Bakker, Kathryn M Abel, Thérèse A M J van Amelsvoort. Psychopharmacology (Berl) 2015
8

The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.
Liam J Drew, Gregg W Crabtree, Sander Markx, Kimberly L Stark, Florence Chaverneff, Bin Xu, Jun Mukai, Karine Fenelon, Pei-Ken Hsu, Joseph A Gogos,[...]. Int J Dev Neurosci 2011
91

Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.
Sinthuja Sivagnanasundaram, Danielle Fletcher, Mike Hubank, Elizabeth Illingworth, David Skuse, Peter Scambler. Brain Res 2007
31


Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome.
Yukari Takarae, Linda Schmidt, Flora Tassone, Tony J Simon. Cogn Affect Behav Neurosci 2009
17

Neurophysiological endophenotypes of schizophrenia: the viability of selected candidate measures.
Bruce I Turetsky, Monica E Calkins, Gregory A Light, Ann Olincy, Allen D Radant, Neal R Swerdlow. Schizophr Bull 2007
410