A citation-based method for searching scientific literature

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, Sixto García-Miñaúr, Susan George, Anthony E Lang, Gabriela Repetto, Andrea Shugar, Candice Silversides, Ann Swillen, Therese van Amelsvoort, Donna M McDonald-McGinn, Anne S Bassett. Genet Med 2015
Times Cited: 127







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



Times Cited
  Times     Co-cited
Similarity


Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions.
Gregory Costain, Eva W C Chow, Candice K Silversides, Anne S Bassett. J Med Genet 2011
36
11

Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome.
G Costain, E W C Chow, P N Ray, A S Bassett. J Intellect Disabil Res 2012
36
11

Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion.
Jacob A S Vorstman, Elemi J Breetvelt, Kirstin I Thode, Eva W C Chow, Anne S Bassett. Schizophr Res 2013
45
8


The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome.
Christina Zaleski, Anne S Bassett, Karen Tam, Andrea L Shugar, Eva W C Chow, Elizabeth McPherson. Am J Med Genet A 2009
35
11


Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Raphael Bernier, Kyle J Steinman, Beau Reilly, Arianne Stevens Wallace, Elliott H Sherr, Nicholas Pojman, Heather C Mefford, Jennifer Gerdts, Rachel Earl, Ellen Hanson,[...]. Genet Med 2016
85
4

Presenting symptoms in adults with the 22q11 deletion syndrome.
Annick Vogels, Sara Schevenels, Richard Cayenberghs, Eddy Weyts, Griet Van Buggenhout, Ann Swillen, Hilde Van Esch, Thomy de Ravel, Pieter Corveleyn, Koen Devriendt. Eur J Med Genet 2014
11
36

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.
Nancy J Butcher, Daniele Merico, Mehdi Zarrei, Lucas Ogura, Christian R Marshall, Eva W C Chow, Anthony E Lang, Stephen W Scherer, Anne S Bassett. PLoS One 2017
11
36

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
D A Driscoll, J Salvin, B Sellinger, M L Budarf, D M McDonald-McGinn, E H Zackai, B S Emanuel. J Med Genet 1993
406
4

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.
Elisabeth E Mlynarski, Molly B Sheridan, Michael Xie, Tingwei Guo, Silvia E Racedo, Donna M McDonald-McGinn, Xiaowu Gai, Eva W C Chow, Jacob Vorstman, Ann Swillen,[...]. Am J Hum Genet 2015
48
8


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
4

In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
84
4

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
348
4

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.
Louise K Hoeffding, Betina B Trabjerg, Line Olsen, Wiktor Mazin, Thomas Sparsø, Anders Vangkilde, Preben B Mortensen, Carsten B Pedersen, Thomas Werge. JAMA Psychiatry 2017
55
7

Cognitive development in children with 22q11.2 deletion syndrome.
Sasja N Duijff, Petra W J Klaassen, Henriette F N Swanenburg de Veye, Frits A Beemer, Gerben Sinnema, Jacob A S Vorstman. Br J Psychiatry 2012
65
6

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
4

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
267
4

High prevalence of fatigue in adults with a 22q11.2 deletion syndrome.
Elfi Vergaelen, Stephan Claes, Stefan Kempke, Ann Swillen. Am J Med Genet A 2017
8
50


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
41
9

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
234
4

Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia.
Lily Van, Erik Boot, Anne S Bassett. Curr Opin Psychiatry 2017
46
8

Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study.
Omri Weisman, Yael Guri, Raquel E Gur, Donna M McDonald-McGinn, Monica E Calkins, Sunny X Tang, Beverly Emanuel, Elaine H Zackai, Stephan Eliez, Maude Schneider,[...]. Schizophr Bull 2017
22
18

Psychopathology and cognition in children with 22q11.2 deletion syndrome.
Maria Niarchou, Stanley Zammit, Stephanie H M van Goozen, Anita Thapar, Hayley M Tierling, Michael J Owen, Marianne B M van den Bree. Br J Psychiatry 2014
52
7

Late-onset psychosis in the velo-cardio-facial syndrome.
R J Shprintzen, R Goldberg, K J Golding-Kushner, R W Marion. Am J Med Genet 1992
317
4

Autism genetics: opportunities and challenges for clinical translation.
Jacob A S Vorstman, Jeremy R Parr, Daniel Moreno-De-Luca, Richard J L Anney, John I Nurnberger, Joachim F Hallmayer. Nat Rev Genet 2017
198
4

Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.
Erica Schindewolf, Nahla Khalek, Mark P Johnson, Juliana Gebb, Beverly Coleman, Terrence Blaine Crowley, Elaine H Zackai, Donna M McDonald-McGinn, Julie S Moldenhauer. Am J Med Genet A 2018
17
23

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study.
Line Olsen, Thomas Sparsø, Shantel M Weinsheimer, Marcelo Bertalan Quintanilha Dos Santos, Wiktor Mazin, Anders Rosengren, Xabier Calle Sanchez, Louise K Hoeffding, Henriette Schmock, Marie Baekvad-Hansen,[...]. Lancet Psychiatry 2018
53
7

Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.
Ann Swillen, Edward Moss, Sasja Duijff. Am J Med Genet A 2018
12
33

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Anne S Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W C Chow, Therese van Amelsvoort, Donna McDonald-McGinn, Raquel E Gur, Ann Swillen, Marianne Van den Bree,[...]. Am J Psychiatry 2017
44
9

Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.
Ania M Fiksinski, Maude Schneider, Clodagh M Murphy, Marco Armando, Stefano Vicari, Jaume M Canyelles, Doron Gothelf, Stephan Eliez, Elemi J Breetvelt, Celso Arango,[...]. Am J Med Genet A 2018
31
12

The annual incidence of DiGeorge/velocardiofacial syndrome.
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
257
4



Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Mari E K Niemi, Hilary C Martin, Daniel L Rice, Giuseppe Gallone, Scott Gordon, Martin Kelemen, Kerrie McAloney, Jeremy McRae, Elizabeth J Radford, Sui Yu,[...]. Nature 2018
130
4

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
423
4

Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders.
Johan H Thygesen, Kate Wolfe, Andrew McQuillin, Marina Viñas-Jornet, Neus Baena, Nathalie Brison, Greet D'Haenens, Susanna Esteba-Castillo, Elisabeth Gabau, Núria Ribas-Vidal,[...]. Br J Psychiatry 2018
14
28

Education and employment trajectories from childhood to adulthood in individuals with 22q11.2 deletion syndrome.
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
10
40

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
402
4

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
10
40

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
35
11

Syndrome-specific growth charts for 22q11.2 deletion syndrome in Caucasian children.
Alex Habel, Michael-John McGinn, Elaine H Zackai, Nancy Unanue, Donna M McDonald-McGinn. Am J Med Genet A 2012
21
14

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
40
7

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

miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome.
Linda M Brzustowicz, Anne S Bassett. Front Genet 2012
27
11

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS.
Donna M McDonald-McGinn, Somayyeh Fahiminiya, Timothée Revil, Beata A Nowakowska, Joshua Suhl, Alice Bailey, Elisabeth Mlynarski, David R Lynch, Albert C Yan, Larissa T Bilaniuk,[...]. J Med Genet 2013
78
3

A case of chromosome 22q11 deletion syndrome diagnosed in a 32-year-old man with hypoparathyroidism.
Naim M Maalouf, Khashayar Sakhaee, Clarita V Odvina. J Clin Endocrinol Metab 2004
19
15

Neuropathologic features in adults with 22q11.2 deletion syndrome.
T R Kiehl, E W C Chow, D J Mikulis, S R George, A S Bassett. Cereb Cortex 2009
60
5


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.