A citation-based method for searching scientific literature

R J Shprintzen, R Goldberg, K J Golding-Kushner, R W Marion. Am J Med Genet 1992
Times Cited: 317







List of co-cited articles
1021 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
743
61

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
339
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
195
24

Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
22


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
408
22

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
220
21

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
230
21

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
177
20

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
131
20

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
266
19


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
414
19

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
274
19

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
402
19

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
164
19


Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
George Kirov, Detelina Grozeva, Nadine Norton, Dobril Ivanov, Kiran K Mantripragada, Peter Holmans, Nick Craddock, Michael J Owen, Michael C O'Donovan. Hum Mol Genet 2009
307
18

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Tom Walsh, Jon M McClellan, Shane E McCarthy, Anjené M Addington, Sarah B Pierce, Greg M Cooper, Alex S Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari,[...]. Science 2008
16

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
288
16

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
E M Moss, M L Batshaw, C B Solot, M Gerdes, D M McDonald-McGinn, D A Driscoll, B S Emanuel, E H Zackai, P P Wang. J Pediatr 1999
220
16

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
120
16

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
254
16

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
513
16

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
16

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
821
15

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
84
17

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
139
15

Common variants conferring risk of schizophrenia.
Hreinn Stefansson, Roel A Ophoff, Stacy Steinberg, Ole A Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli P H Pietiläinen, Ole Mors, Preben B Mortensen,[...]. Nature 2009
15

22q11 deletion syndrome in adults with schizophrenia.
A S Bassett, K Hodgkinson, E W Chow, S Correia, L E Scutt, R Weksberg. Am J Med Genet 1998
170
15

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
104
15

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
301
15

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update.
B De Smedt, K Devriendt, J-P Fryns, A Vogels, M Gewillig, A Swillen. J Intellect Disabil Res 2007
105
15

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
14

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
197
14

Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan,[...]. J Pediatr 2011
299
14

Velo-cardio-facial syndrome: language and psychological profiles.
K J Golding-Kushner, G Weller, R J Shprintzen. J Craniofac Genet Dev Biol 1985
202
13

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
18

Common variants on chromosome 6p22.1 are associated with schizophrenia.
Jianxin Shi, Douglas F Levinson, Jubao Duan, Alan R Sanders, Yonglan Zheng, Itsik Pe'er, Frank Dudbridge, Peter A Holmans, Alice S Whittemore, Bryan J Mowry,[...]. Nature 2009
817
13

Identification of loci associated with schizophrenia by genome-wide association and follow-up.
Michael C O'Donovan, Nicholas Craddock, Nadine Norton, Hywel Williams, Timothy Peirce, Valentina Moskvina, Ivan Nikolov, Marian Hamshere, Liam Carroll, Lyudmila Georgieva,[...]. Nat Genet 2008
804
13

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
13

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
362
13

22q11 deletion syndrome: a genetic subtype of schizophrenia.
A S Bassett, E W Chow. Biol Psychiatry 1999
222
13

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
93
13

Strong association of de novo copy number mutations with sporadic schizophrenia.
Bin Xu, J Louw Roos, Shawn Levy, E J van Rensburg, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2008
589
12

Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
487
12


The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.
A Swillen, K Devriendt, E Legius, P Prinzie, A Vogels, P Ghesquière, J P Fryns. Genet Couns 1999
154
12

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
109
12


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.