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
Times Cited: 127
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
Gregory Costain, Eva W C Chow, Candice K Silversides, Anne S Bassett. J Med Genet 2011
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
G Costain, E W C Chow, P N Ray, A S Bassett. J Intellect Disabil Res 2012
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
Jacob A S Vorstman, Elemi J Breetvelt, Kirstin I Thode, Eva W C Chow, Anne S Bassett. Schizophr Res 2013
8
Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.
L Edelmann, R K Pandita, B E Morrow. Am J Hum Genet 1999
L Edelmann, R K Pandita, B E Morrow. Am J Hum Genet 1999
4
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
Christina Zaleski, Anne S Bassett, Karen Tam, Andrea L Shugar, Eva W C Chow, Elizabeth McPherson. Am J Med Genet A 2009
11
Atypical Antipsychotics and Relapsing Psychoses in 22q11.2 Deletion Syndrome: A Long-term Evaluation of 28 Patients.
W M A Verhoeven, J I M Egger. Pharmacopsychiatry 2015
W M A Verhoeven, J I M Egger. Pharmacopsychiatry 2015
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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
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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
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
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
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
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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
D A Driscoll, J Salvin, B Sellinger, M L Budarf, D M McDonald-McGinn, E H Zackai, B S Emanuel. J Med Genet 1993
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
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
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DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.
L A Jerome, V E Papaioannou. Nat Genet 2001
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A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.
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In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
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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
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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
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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
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
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
A Swillen, K Devriendt, E Legius, B Eyskens, M Dumoulin, M Gewillig, J P Fryns. J Med Genet 1997
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
Elfi Vergaelen, Stephan Claes, Stefan Kempke, Ann Swillen. Am J Med Genet A 2017
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Non-pharmacological treatment of psychiatric disorders in individuals with 22q11.2 deletion syndrome; a systematic review.
Petra C M Buijs, Anne S Bassett, Erik Boot. Am J Med Genet A 2018
Petra C M Buijs, Anne S Bassett, Erik Boot. Am J Med Genet A 2018
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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
Kathleen Angkustsiri, Ingrid Leckliter, Nicole Tartaglia, Elliott A Beaton, Janice Enriquez, Tony J Simon. J Dev Behav Pediatr 2012
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
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
4
Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia.
Lily Van, Erik Boot, Anne S Bassett. Curr Opin Psychiatry 2017
Lily Van, Erik Boot, Anne S Bassett. Curr Opin Psychiatry 2017
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
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
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
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
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
R J Shprintzen, R Goldberg, K J Golding-Kushner, R W Marion. Am J Med Genet 1992
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
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
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
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
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
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
7
Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.
Ann Swillen, Edward Moss, Sasja Duijff. Am J Med Genet A 2018
Ann Swillen, Edward Moss, Sasja Duijff. Am J Med Genet A 2018
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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
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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
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The annual incidence of DiGeorge/velocardiofacial syndrome.
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
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11
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
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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
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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
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
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
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
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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
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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
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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
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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
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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
Bert De Smedt, Ann Swillen, Lieven Verschaffel, Pol Ghesquière. Dev Disabil Res Rev 2009
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Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
Doron Gothelf, Marie Schaer, Stephan Eliez. Dev Disabil Res Rev 2008
Doron Gothelf, Marie Schaer, Stephan Eliez. Dev Disabil Res Rev 2008
3
miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome.
Linda M Brzustowicz, Anne S Bassett. Front Genet 2012
Linda M Brzustowicz, Anne S Bassett. Front Genet 2012
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
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
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
Naim M Maalouf, Khashayar Sakhaee, Clarita V Odvina. J Clin Endocrinol Metab 2004
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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
T R Kiehl, E W C Chow, D J Mikulis, S R George, A S Bassett. Cereb Cortex 2009
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.