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: 113
Times Cited: 113
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
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
49
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
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
48
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
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
34
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
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
29
Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.
Nancy J Butcher, Tim-Rasmus Kiehl, Lili-Naz Hazrati, Eva W C Chow, Ekaterina Rogaeva, Anthony E Lang, Anne S Bassett. JAMA Neurol 2013
Nancy J Butcher, Tim-Rasmus Kiehl, Lili-Naz Hazrati, Eva W C Chow, Ekaterina Rogaeva, Anthony E Lang, Anne S Bassett. JAMA Neurol 2013
25
Premature death in adults with 22q11.2 deletion syndrome.
A S Bassett, E W C Chow, J Husted, K A Hodgkinson, E Oechslin, L Harris, C Silversides. J Med Genet 2009
A S Bassett, E W C Chow, J Husted, K A Hodgkinson, E Oechslin, L Harris, C Silversides. J Med Genet 2009
27
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
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
15
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega,[...]. Prenat Diagn 2015
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega,[...]. Prenat Diagn 2015
15
Functional outcomes of adults with 22q11.2 deletion syndrome.
Nancy J Butcher, Eva W C Chow, Gregory Costain, Dominique Karas, Andrew Ho, Anne S Bassett. Genet Med 2012
Nancy J Butcher, Eva W C Chow, Gregory Costain, Dominique Karas, Andrew Ho, Anne S Bassett. Genet Med 2012
29
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.
Kin Y Mok, Una Sheerin, Javier Simón-Sánchez, Afnan Salaka, Lucy Chester, Valentina Escott-Price, Kiran Mantripragada, Karen M Doherty, Alastair J Noyce, Niccolo E Mencacci,[...]. Lancet Neurol 2016
Kin Y Mok, Una Sheerin, Javier Simón-Sánchez, Afnan Salaka, Lucy Chester, Valentina Escott-Price, Kiran Mantripragada, Karen M Doherty, Alastair J Noyce, Niccolo E Mencacci,[...]. Lancet Neurol 2016
28
Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
14
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
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
14
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
12
High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
12
Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
12
Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome.
Erik Boot, Nancy J Butcher, Thérèse A M J van Amelsvoort, Anthony E Lang, Connie Marras, Margarita Pondal, Danielle M Andrade, Wai Lun Alan Fung, Anne S Bassett. Am J Med Genet A 2015
Erik Boot, Nancy J Butcher, Thérèse A M J van Amelsvoort, Anthony E Lang, Connie Marras, Margarita Pondal, Danielle M Andrade, Wai Lun Alan Fung, Anne S Bassett. Am J Med Genet A 2015
31
Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome.
Evelyn Ning Man Cheung, Susan R George, Gary A Costain, Danielle M Andrade, Eva W C Chow, Candice K Silversides, Anne S Bassett. Clin Endocrinol (Oxf) 2014
Evelyn Ning Man Cheung, Susan R George, Gary A Costain, Danielle M Andrade, Eva W C Chow, Candice K Silversides, Anne S Bassett. Clin Endocrinol (Oxf) 2014
31
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
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
25
Elevated prevalence of generalized anxiety disorder in adults with 22q11.2 deletion syndrome.
Wai Lun Alan Fung, Rebecca McEvilly, Jessica Fong, Candice Silversides, Eva Chow, Anne Bassett. Am J Psychiatry 2010
Wai Lun Alan Fung, Rebecca McEvilly, Jessica Fong, Candice Silversides, Eva Chow, Anne Bassett. Am J Psychiatry 2010
16
Developmental trajectories in 22q11.2 deletion.
Ann Swillen, Donna McDonald-McGinn. Am J Med Genet C Semin Med Genet 2015
Ann Swillen, Donna McDonald-McGinn. Am J Med Genet C Semin Med Genet 2015
13
Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.
Alina Guna, Nancy J Butcher, Anne S Bassett. J Neurodev Disord 2015
Alina Guna, Nancy J Butcher, Anne S Bassett. J Neurodev Disord 2015
22
Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden.
S Oskarsdóttir, M Vujic, A Fasth. Arch Dis Child 2004
S Oskarsdóttir, M Vujic, A Fasth. Arch Dis Child 2004
10
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
Tamar Green, Doron Gothelf, Bronwyn Glaser, Martin Debbane, Amos Frisch, Moshe Kotler, Abraham Weizman, Stephan Eliez. J Am Acad Child Adolesc Psychiatry 2009
10
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
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
10
Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!
D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, B Finucane, D A Driscoll, B S Emanuel, E H Zackai. Genet Med 2001
D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, B Finucane, D A Driscoll, B S Emanuel, E H Zackai. Genet Med 2001
10
Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome.
Evelyn Ning Man Cheung, Susan R George, Danielle M Andrade, Eva W C Chow, Candice K Silversides, Anne S Bassett. Genet Med 2014
Evelyn Ning Man Cheung, Susan R George, Danielle M Andrade, Eva W C Chow, Candice K Silversides, Anne S Bassett. Genet Med 2014
20
Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.
Nicole Philip, Anne Bassett. Behav Genet 2011
Nicole Philip, Anne Bassett. Behav Genet 2011
11
Co-occurrence of early-onset Parkinson disease and 22q11.2 deletion syndrome: Potential role for dopamine transporter imaging.
Jan Booij, Thérèse van Amelsvoort, Erik Boot. Am J Med Genet A 2010
Jan Booij, Thérèse van Amelsvoort, Erik Boot. Am J Med Genet A 2010
25
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.
Daniele Merico, Mehdi Zarrei, Gregory Costain, Lucas Ogura, Babak Alipanahi, Matthew J Gazzellone, Nancy J Butcher, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Eva W C Chow,[...]. G3 (Bethesda) 2015
Daniele Merico, Mehdi Zarrei, Gregory Costain, Lucas Ogura, Babak Alipanahi, Matthew J Gazzellone, Nancy J Butcher, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Eva W C Chow,[...]. G3 (Bethesda) 2015
29
Obesity in adults with 22q11.2 deletion syndrome.
Sarah L Voll, Erik Boot, Nancy J Butcher, Samantha Cooper, Tracy Heung, Eva W C Chow, Candice K Silversides, Anne S Bassett. Genet Med 2017
Sarah L Voll, Erik Boot, Nancy J Butcher, Samantha Cooper, Tracy Heung, Eva W C Chow, Candice K Silversides, Anne S Bassett. Genet Med 2017
34
Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.
Anne S Bassett, Christian R Marshall, Anath C Lionel, Eva W C Chow, Stephen W Scherer. Hum Mol Genet 2008
Anne S Bassett, Christian R Marshall, Anath C Lionel, Eva W C Chow, Stephen W Scherer. Hum Mol Genet 2008
8
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
B De Smedt, K Devriendt, J-P Fryns, A Vogels, M Gewillig, A Swillen. J Intellect Disabil Res 2007
8
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.
T H Shaikh, H Kurahashi, S C Saitta, A M O'Hare, P Hu, B A Roe, D A Driscoll, D M McDonald-McGinn, E H Zackai, M L Budarf,[...]. Hum Mol Genet 2000
T H Shaikh, H Kurahashi, S C Saitta, A M O'Hare, P Hu, B A Roe, D A Driscoll, D M McDonald-McGinn, E H Zackai, M L Budarf,[...]. Hum Mol Genet 2000
8
Clinical features and follow-up in patients with 22q11.2 deletion syndrome.
Caterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, Annarosa Soresina, Silvana Martino, Roberto Rondelli, Rita Consolini, Ezia Maria Ruga, Fabio Cardinale, Andrea Finocchi,[...]. J Pediatr 2014
Caterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, Annarosa Soresina, Silvana Martino, Roberto Rondelli, Rita Consolini, Ezia Maria Ruga, Fabio Cardinale, Andrea Finocchi,[...]. J Pediatr 2014
10
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
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
8
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
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
36
Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome.
Chrystal Chan, Gregory Costain, Lucas Ogura, Candice K Silversides, Eva W C Chow, Anne S Bassett. J Genet Couns 2015
Chrystal Chan, Gregory Costain, Lucas Ogura, Candice K Silversides, Eva W C Chow, Anne S Bassett. J Genet Couns 2015
53
MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome.
Daniele Merico, Gregory Costain, Nancy J Butcher, William Warnica, Lucas Ogura, Simon E Alfred, Linda M Brzustowicz, Anne S Bassett. Front Neurol 2014
Daniele Merico, Gregory Costain, Nancy J Butcher, William Warnica, Lucas Ogura, Simon E Alfred, Linda M Brzustowicz, Anne S Bassett. Front Neurol 2014
23
A population study of chromosome 22q11 deletions in infancy.
J Goodship, I Cross, J LiLing, C Wren. Arch Dis Child 1998
J Goodship, I Cross, J LiLing, C Wren. Arch Dis Child 1998
7
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
20
Case fatality rate and associated factors in patients with 22q11 microdeletion syndrome: a retrospective cohort study.
Gabriela M Repetto, M Luisa Guzmán, Iris Delgado, Hugo Loyola, Mirta Palomares, Guillermo Lay-Son, Cecilia Vial, Felipe Benavides, Karena Espinoza, Patricia Alvarez. BMJ Open 2014
Gabriela M Repetto, M Luisa Guzmán, Iris Delgado, Hugo Loyola, Mirta Palomares, Guillermo Lay-Son, Cecilia Vial, Felipe Benavides, Karena Espinoza, Patricia Alvarez. BMJ Open 2014
35
Genetic counseling for the 22q11.2 deletion.
Donna M McDonald-McGinn, Elaine H Zackai. Dev Disabil Res Rev 2008
Donna M McDonald-McGinn, Elaine H Zackai. Dev Disabil Res Rev 2008
17
Disrupted dopaminergic neurotransmission in 22q11 deletion syndrome.
Erik Boot, Jan Booij, Janneke Zinkstok, Nico Abeling, Lieuwe de Haan, Frank Baas, Don Linszen, Thérèse van Amelsvoort. Neuropsychopharmacology 2008
Erik Boot, Jan Booij, Janneke Zinkstok, Nico Abeling, Lieuwe de Haan, Frank Baas, Don Linszen, Thérèse van Amelsvoort. Neuropsychopharmacology 2008
15
Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome.
Lily Van, Nancy J Butcher, Gregory Costain, Lucas Ogura, Eva W C Chow, Anne S Bassett. Genet Med 2016
Lily Van, Nancy J Butcher, Gregory Costain, Lucas Ogura, Eva W C Chow, Anne S Bassett. Genet Med 2016
36
Fetal phenotype associated with the 22q11 deletion.
Anne-Claire Noël, Fanny Pelluard, Anne-Lise Delezoide, Louise Devisme, Laurence Loeuillet, Brigitte Leroy, Alain Martin, Raymonde Bouvier, Annie Laquerriere, Corinne Jeanne-Pasquier,[...]. Am J Med Genet A 2014
Anne-Claire Noël, Fanny Pelluard, Anne-Lise Delezoide, Louise Devisme, Laurence Loeuillet, Brigitte Leroy, Alain Martin, Raymonde Bouvier, Annie Laquerriere, Corinne Jeanne-Pasquier,[...]. Am J Med Genet A 2014
29
Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.
S J Gross, M Stosic, D M McDonald-McGinn, A S Bassett, A Norvez, R Dhamankar, K Kobara, E Kirkizlar, B Zimmermann, N Wayham,[...]. Ultrasound Obstet Gynecol 2016
S J Gross, M Stosic, D M McDonald-McGinn, A S Bassett, A Norvez, R Dhamankar, K Kobara, E Kirkizlar, B Zimmermann, N Wayham,[...]. Ultrasound Obstet Gynecol 2016
10
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
Anne S Bassett, Eva W C Chow, Philip AbdelMalik, Mirona Gheorghiu, Janice Husted, Rosanna Weksberg. Am J Psychiatry 2003
7
Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.
Lisa J Kobrynski, Kathleen E Sullivan. Lancet 2007
Lisa J Kobrynski, Kathleen E Sullivan. Lancet 2007
7
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
7
Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease.
Nancy J Butcher, Connie Marras, Margarita Pondal, Pablo Rusjan, Erik Boot, Leigh Christopher, Gabriela M Repetto, Rosemarie Fritsch, Eva W C Chow, Mario Masellis,[...]. Brain 2017
Nancy J Butcher, Connie Marras, Margarita Pondal, Pablo Rusjan, Erik Boot, Leigh Christopher, Gabriela M Repetto, Rosemarie Fritsch, Eva W C Chow, Mario Masellis,[...]. Brain 2017
26
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.