A citation-based method for searching scientific literature

Robert J Shprintzen. Dev Disabil Res Rev 2008
Times Cited: 271







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



Times Cited
  Times     Co-cited
Similarity


Why IQ is not a covariate in cognitive studies of neurodevelopmental disorders.
Maureen Dennis, David J Francis, Paul T Cirino, Russell Schachar, Marcia A Barnes, Jack M Fletcher. J Int Neuropsychol Soc 2009
545
4

Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow.
P S Eicher, D M McDonald-Mcginn, C A Fox, D A Driscoll, B S Emanuel, E H Zackai. J Pediatr 2000
68
5

Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome.
D Gothelf, A Frisch, H Munitz, R Rockah, N Laufer, T Mozes, H Hermesh, A Weizman, M Frydman. Schizophr Res 1999
70
4

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
Doron Gothelf, Marie Schaer, Stephan Eliez. Dev Disabil Res Rev 2008
97
3

Structural changes to the fusiform gyrus: a cerebral marker for social impairments in 22q11.2 deletion syndrome?
Bronwyn Glaser, Marie Schaer, Sandra Berney, Martin Debbane, Patrik Vuilleumier, Stephan Eliez. Schizophr Res 2007
22
13

Individuals with 22q11.2 deletion syndrome are impaired at explicit, but not implicit, discrimination of local forms embedded in global structures.
Anne Giersch, Bronwyn Glaser, Catherine Pasca, Mélanie Chabloz, Martin Debbané, Stephan Eliez. Am J Intellect Dev Disabil 2014
5
60

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
71
4

Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study.
Marie Schaer, J Eric Schmitt, Bronwyn Glaser, François Lazeyras, Jacqueline Delavelle, Stephan Eliez. Psychiatry Res 2006
61
4

Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions.
Carrie E Bearden, Theo G M van Erp, Rebecca A Dutton, Agatha D Lee, Tony J Simon, Tyrone D Cannon, Beverly S Emanuel, Donna McDonald-McGinn, Elaine H Zackai, Paul M Thompson. Cereb Cortex 2009
66
4

Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2).
Wendy R Kates, Courtney P Burnette, Brandy A Bessette, Bradley S Folley, Leslie Strunge, Ethylin W Jabs, Godfrey D Pearlson. J Child Neurol 2004
81
3

Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?
S Eliez, C M Blasey, E J Schmitt, C D White, D Hu, A L Reiss. Am J Psychiatry 2001
87
3

Behavioral problems in relation to intelligence in children with 22q11.2 deletion syndrome: a matched control study.
P W Jansen, S N Duijff, F A Beemer, J A S Vorstman, P W J Klaassen, M E J Morcus, J A Heineman-de Boer. Am J Med Genet A 2007
31
9

The diverse clinical features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome).
Solrun Melkorka Maggadottir, Kathleen E Sullivan. J Allergy Clin Immunol Pract 2013
26
11

Lower prepulse inhibition in children with the 22q11 deletion syndrome.
Christina Sobin, Karen Kiley-Brabeck, Maria Karayiorgou. Am J Psychiatry 2005
80
3

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
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
681
3


Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm.
Amélie Calmont, Sarah Ivins, Kelly Lammerts Van Bueren, Irinna Papangeli, Vanessa Kyriakopoulou, William D Andrews, James F Martin, Anne M Moon, Elizabeth A Illingworth, M Albert Basson,[...]. Development 2009
87
3

Neural crest cells contribute to normal aorticopulmonary septation.
M L Kirby, T F Gale, D E Stewart. Science 1983
853
3


Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.
Fabíola P Monteiro, Társis P Vieira, Ilária C Sgardioli, Miriam C Molck, Ana Paula Damiano, Josiane Souza, Isabella L Monlleó, Marshall I B Fontes, Agnes C Fett-Conte, Têmis M Félix,[...]. Eur J Pediatr 2013
35
8

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
175
3

Psychopathology in adults with 22q11 deletion syndrome and moderate and severe intellectual disability.
L J M Evers, T A M J van Amelsvoort, M J J M Candel, H Boer, J J M Engelen, L M G Curfs. J Intellect Disabil Res 2014
19
15


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
311
3

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
77
3

Negative and paranoid symptoms are associated with negative performance beliefs and social cognition in 22q11.2 deletion syndrome.
Maude Schneider, Martial Van der Linden, Sarah Menghetti, Martin Debbané, Stephan Eliez. Early Interv Psychiatry 2017
10
30

Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?
Kate Baker, Jacob A S Vorstman. Curr Opin Neurol 2012
44
6

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
62
4

Sex differences in the behavior of children with the 22q11 deletion syndrome.
Christina Sobin, Karen Kiley-Brabeck, Samantha Hadley Monk, Jananne Khuri, Maria Karayiorgou. Psychiatry Res 2009
14
21

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
7

Altered white matter microstructure is associated with social cognition and psychotic symptoms in 22q11.2 microdeletion syndrome.
Maria Jalbrzikowski, Julio E Villalon-Reina, Katherine H Karlsgodt, Damla Senturk, Carolyn Chow, Paul M Thompson, Carrie E Bearden. Front Behav Neurosci 2014
45
6

Neuropsychological profile of Italian children and adolescents with 22q11.2 deletion syndrome with and without intellectual disability.
Stefano Vicari, Manuela Mantovan, Francesca Addona, Floriana Costanzo, Lorena Verucci, Deny Menghini. Behav Genet 2012
12
25

Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.
Ling M Wong, Tracy Riggins, Danielle Harvey, Margarita Cabaral, Tony J Simon. Am J Intellect Dev Disabil 2014
14
21

Cortical gyrification in velo-cardio-facial (22q11.2 deletion) syndrome: a longitudinal study.
Arun Kunwar, Seethalakshmi Ramanathan, Joshua Nelson, Kevin M Antshel, Wanda Fremont, Anne Marie Higgins, Robert J Shprintzen, Wendy R Kates. Schizophr Res 2012
26
11

Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS).
Kathryn Louise McCabe, Rebbekah Josephine Atkinson, Gavin Cooper, Jessica Lauren Melville, Jill Harris, Ulrich Schall, Carmel Maree Loughland, Renate Thienel, Linda Elisabet Campbell. J Neurodev Disord 2014
11
27

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
3

Schizophrenia.
Jim van Os, Shitij Kapur. Lancet 2009
3

Genetic counseling for the 22q11.2 deletion.
Donna M McDonald-McGinn, Elaine H Zackai. Dev Disabil Res Rev 2008
42
7

Altered auditory processing in frontal and left temporal cortex in 22q11.2 deletion syndrome: a group at high genetic risk for schizophrenia.
Tonia A Rihs, Miralena I Tomescu, Juliane Britz, Vincent Rochas, Anna Custo, Maude Schneider, Martin Debbané, Stephan Eliez, Christoph M Michel. Psychiatry Res 2013
34
8

Language skills in children with velocardiofacial syndrome (deletion 22q11.2).
Bronwyn Glaser, Donna L Mumme, Christine Blasey, Michael A Morris, Sophie P Dahoun, Stylianos E Antonarakis, Allan L Reiss, Stephan Eliez. J Pediatr 2002
50
6

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
3



Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms.
Maria Jalbrzikowski, Rachel Jonas, Damla Senturk, Arati Patel, Carolyn Chow, Michael F Green, Carrie E Bearden. Neuroimage Clin 2013
67
4

Structural and functional connectivity in the default mode network in 22q11.2 deletion syndrome.
Maria Carmela Padula, Marie Schaer, Elisa Scariati, Maude Schneider, Dimitri Van De Ville, Martin Debbané, Stephan Eliez. J Neurodev Disord 2015
31
9

Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
223
3

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
Andrew J Sharp, Heather C Mefford, Kelly Li, Carl Baker, Cindy Skinner, Roger E Stevenson, Richard J Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone,[...]. Nat Genet 2008
405
3

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
357
3

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
Regina E Ensenauer, Adewale Adeyinka, Heather C Flynn, Virginia V Michels, Noralane M Lindor, D Brian Dawson, Erik C Thorland, Cindy Pham Lorentz, Jennifer L Goldstein, Marie T McDonald,[...]. Am J Hum Genet 2003
254
3


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.