A citation-based method for searching scientific literature

Mariela Mosheva, Virginie Pouillard, Yael Fishman, Lydia Dubourg, Dafna Sofrin-Frumer, Yaffa Serur, Abraham Weizman, Stephan Eliez, Doron Gothelf, Maude Schneider. Eur Child Adolesc Psychiatry 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
411
55

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
55


22q11.2 deletion syndrome: behaviour problems of children and adolescents and parental stress.
W Briegel, M Schneider, K Otfried Schwab. Child Care Health Dev 2008
26
33

Developmental trajectories in 22q11.2 deletion.
Ann Swillen, Donna McDonald-McGinn. Am J Med Genet C Semin Med Genet 2015
83
33

An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome.
Kathleen Angkustsiri, Ingrid Leckliter, Nicole Tartaglia, Elliott A Beaton, Janice Enriquez, Tony J Simon. J Dev Behav Pediatr 2012
39
33

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
117
33

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
33

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.
Ian M Campbell, Sarah E Sheppard, T Blaine Crowley, Daniel E McGinn, Alice Bailey, Michael J McGinn, Marta Unolt, Jelle F Homans, Erin Y Chen, Harold I Salmons,[...]. Am J Med Genet A 2018
30
33

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
33

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kimberley M Kendall, Elliott Rees, Valentina Escott-Price, Mark Einon, Rhys Thomas, Jonathan Hewitt, Michael C O'Donovan, Michael J Owen, James T R Walters, George Kirov. Biol Psychiatry 2017
76
33

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Jacob A S Vorstman, Elemi J Breetvelt, Sasja N Duijff, Stephan Eliez, Maude Schneider, Maria Jalbrzikowski, Marco Armando, Stefano Vicari, Vandana Shashi, Stephen R Hooper,[...]. JAMA Psychiatry 2015
120
33

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Robert W Davies, Ania M Fiksinski, Elemi J Breetvelt, Nigel M Williams, Stephen R Hooper, Thomas Monfeuga, Anne S Bassett, Michael J Owen, Raquel E Gur, Bernice E Morrow,[...]. Nat Med 2020
26
33

Childhood Executive Functioning Predicts Young Adult Outcomes in 22q11.2 Deletion Syndrome.
Avery B Albert, Tamara Abu-Ramadan, Wendy R Kates, Wanda Fremont, Kevin M Antshel. J Int Neuropsychol Soc 2018
6
50

A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.
Stephen R Hooper, Kathleen Curtiss, Kelly Schoch, Matcheri S Keshavan, Andrew Allen, Vandana Shashi. Res Dev Disabil 2013
38
33

Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.
Florence Bretelle, Laura Beyer, Marie Christine Pellissier, Chantal Missirian, Sabine Sigaudy, Marc Gamerre, Claude D'Ercole, Nicole Philip. Eur J Med Genet 2010
31
22

Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.
Bert De Smedt, Ann Swillen, Lieven Verschaffel, Pol Ghesquière. Dev Disabil Res Rev 2009
39
22


Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome.
Kelly Schoch, Waverly Harrell, Stephen R Hooper, Edward H Ip, Santiago Saldana, Thomas R Kwapil, Vandana Shashi. J Learn Disabil 2014
10
22

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
22

Reciprocal Copy Number Variations at 22q11.2 Produce Distinct and Convergent Neurobehavioral Impairments Relevant for Schizophrenia and Autism Spectrum Disorder.
Amy Lin, Ariana Vajdi, Leila Kushan-Wells, Gerhard Helleman, Laura Pacheco Hansen, Rachel K Jonas, Maria Jalbrzikowski, Lyle Kingsbury, Armin Raznahan, Carrie E Bearden. Biol Psychiatry 2020
9
22

Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?
Renée R Lajiness-O'Neill, Isabelle Beaulieu, Jeffrey B Titus, Alexander Asamoah, Erin D Bigler, Erawati V Bawle, Rebecca Pollack. Child Neuropsychol 2005
64
22

Mother-Child Interaction as a Window to a Unique Social Phenotype in 22q11.2 Deletion Syndrome and in Williams Syndrome.
Omri Weisman, Ruth Feldman, Merav Burg-Malki, Miri Keren, Ronny Geva, Gil Diesendruck, Doron Gothelf. J Autism Dev Disord 2015
12
22

Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.
Ann Swillen, Edward Moss, Sasja Duijff. Am J Med Genet A 2018
10
22

Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Guillaume Huguet, Catherine Schramm, Elise Douard, Lai Jiang, Aurélie Labbe, Frédérique Tihy, Géraldine Mathonnet, Sonia Nizard, Emmanuelle Lemyre, Alexandre Mathieu,[...]. JAMA Psychiatry 2018
37
22

Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
Christa Lese Martin, Karen E Wain, Matthew T Oetjens, Kasia Tolwinski, Emily Palen, Abby Hare-Harris, Lukas Habegger, Evan K Maxwell, Jeffrey G Reid, Lauren Kasparson Walsh,[...]. JAMA Psychiatry 2020
13
22

Predicting Cognition and Psychosis in Young Adults With 22q11.2 Deletion Syndrome.
Kevin M Antshel, Wanda Fremont, Seetha Ramanathan, Wendy R Kates. Schizophr Bull 2017
22
22

Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Samuel J R A Chawner, Michael J Owen, Peter Holmans, F Lucy Raymond, David Skuse, Jeremy Hall, Marianne B M van den Bree. Lancet Psychiatry 2019
34
22

The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome.
Samuel J R A Chawner, Maria Niarchou, Joanne L Doherty, Hayley Moss, Michael J Owen, Marianne B M van den Bree. J Psychiatr Res 2019
6
33

Effectiveness and side effects of psychopharmacotherapy in individuals with 22q11.2 deletion syndrome with comorbid psychiatric disorders: a systematic review.
Mariela Mosheva, Liran Korotkin, Raquel E Gur, Abraham Weizman, Doron Gothelf. Eur Child Adolesc Psychiatry 2020
8
25

The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
Andres Moreno-De-Luca, David W Evans, K B Boomer, Ellen Hanson, Raphael Bernier, Robin P Goin-Kochel, Scott M Myers, Thomas D Challman, Daniel Moreno-De-Luca, Mylissa M Slane,[...]. JAMA Psychiatry 2015
87
22

Response to clozapine in a clinically identifiable subtype of schizophrenia.
Nancy J Butcher, Wai Lun Alan Fung, Laura Fitzpatrick, Alina Guna, Danielle M Andrade, Anthony E Lang, Eva W C Chow, Anne S Bassett. Br J Psychiatry 2015
43
22


Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.
Karen Crawford, Matthew Bracher-Smith, David Owen, Kimberley M Kendall, Elliott Rees, Antonio F Pardiñas, Mark Einon, Valentina Escott-Price, James T R Walters, Michael C O'Donovan,[...]. J Med Genet 2019
42
22

Association of Rare Copy Number Variants With Risk of Depression.
Kimberley Marie Kendall, Elliott Rees, Matthew Bracher-Smith, Sophie Legge, Lucy Riglin, Stanley Zammit, Michael Conlon O'Donovan, Michael John Owen, Ian Jones, George Kirov,[...]. JAMA Psychiatry 2019
29
22


Ultra high risk status and transition to psychosis in 22q11.2 deletion syndrome.
Maude Schneider, Marco Armando, Maria Pontillo, Stefano Vicari, Martin Debbané, Frauke Schultze-Lutter, Stephan Eliez. World Psychiatry 2016
35
22

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
820
22

Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology.
Sinead Morrison, Samuel J R A Chawner, Therese A M J van Amelsvoort, Ann Swillen, Claudia Vingerhoets, Elfi Vergaelen, David E J Linden, Stefanie Linden, Michael J Owen, Marianne B M van den Bree. Transl Psychiatry 2020
9
22

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
421
22

Prodromal assessment with the structured interview for prodromal syndromes and the scale of prodromal symptoms: predictive validity, interrater reliability, and training to reliability.
Tandy J Miller, Thomas H McGlashan, Joanna L Rosen, Kristen Cadenhead, Tyrone Cannon, Joseph Ventura, William McFarlane, Diana O Perkins, Godfrey D Pearlson, Scott W Woods. Schizophr Bull 2003
22

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.
R E Gur, A S Bassett, D M McDonald-McGinn, C E Bearden, E Chow, B S Emanuel, M Owen, A Swillen, M Van den Bree, J Vermeesch,[...]. Mol Psychiatry 2017
40
22

Negative subthreshold psychotic symptoms distinguish 22q11.2 deletion syndrome from other neurodevelopmental disorders: A two-site study.
Ehud Mekori-Domachevsky, Yael Guri, James Yi, Omri Weisman, Monica E Calkins, Sunny X Tang, Raz Gross, Donna M McDonald-McGinn, Beverly S Emanuel, Elaine H Zackai,[...]. Schizophr Res 2017
11
22

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
22

Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data.
J Kaufman, B Birmaher, D Brent, U Rao, C Flynn, P Moreci, D Williamson, N Ryan. J Am Acad Child Adolesc Psychiatry 1997
22

The Psychosis Spectrum in 22q11.2 Deletion Syndrome Is Comparable to That of Nondeleted Youths.
Sunny X Tang, Tyler M Moore, Monica E Calkins, James J Yi, Adam Savitt, Christian G Kohler, Margaret C Souders, Elaine H Zackai, Donna M McDonald-McGinn, Beverly S Emanuel,[...]. Biol Psychiatry 2017
31
22

Detailed analysis of 22q11.2 with a high density MLPA probe set.
G R Jalali, J A S Vorstman, Ab Errami, R Vijzelaar, J Biegel, T Shaikh, B S Emanuel. Hum Mutat 2008
71
22

Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohorts.
James J Yi, Ronnie Weinberger, Tyler M Moore, Monica E Calkins, Yael Guri, Donna M McDonald-McGinn, Elaine H Zackai, Beverly S Emanuel, Raquel E Gur, Doron Gothelf,[...]. Brain Cogn 2016
11
22

Psychiatric disorders in 22q11.2 deletion syndrome are prevalent but undertreated.
S X Tang, J J Yi, M E Calkins, D A Whinna, C G Kohler, M C Souders, D M McDonald-McGinn, E H Zackai, B S Emanuel, R C Gur,[...]. Psychol Med 2014
74
22



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.