A citation-based method for searching scientific literature

Nancy J Butcher, Tim-Rasmus Kiehl, Lili-Naz Hazrati, Eva W C Chow, Ekaterina Rogaeva, Anthony E Lang, Anne S Bassett. JAMA Neurol 2013
Times Cited: 83







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



Times Cited
  Times     Co-cited
Similarity


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
49
61


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
31

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
28

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
28

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
33
69

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
27

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
39
46


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
18

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
235
14

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
27

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
13

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
67
16

22q11.2 deletion syndrome presenting with early-onset Parkinson's disease.
Aliya F Rehman, Radhika Dhamija, Eli S Williams, Matthew J Barrett. Mov Disord 2015
13
84

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
26
42

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.
Eva W C Chow, Mark Watson, Donald A Young, Anne S Bassett. Schizophr Res 2006
131
12

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
40
25

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.
Erik Boot, Nancy J Butcher, Sean Udow, Connie Marras, Kin Y Mok, Satoshi Kaneko, Matthew J Barrett, Paolo Prontera, Brian D Berman, Mario Masellis,[...]. Neurology 2018
20
50

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
M H Polymeropoulos, C Lavedan, E Leroy, S E Ide, A Dehejia, A Dutra, B Pike, H Root, J Rubenstein, R Boyer,[...]. Science 1997
10

Schizophrenia and 22q11.2 deletion syndrome.
Anne S Bassett, Eva W C Chow. Curr Psychiatry Rep 2008
137
10

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
48
18

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
59
15

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
10

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
52
17

Psychopathology in adults with 22q11 deletion syndrome and moderate and severe intellectual disability.
L J M Evers, T A M J van Amelsvoort, M J J M Candel, H Boer, J J M Engelen, L M G Curfs. J Intellect Disabil Res 2014
20
40

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
9

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
408
9

22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.
Robert G Wither, Felippe Borlot, Alex MacDonald, Nancy J Butcher, Eva W C Chow, Anne S Bassett, Danielle M Andrade. Epilepsia 2017
19
42

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
128
8

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
Mike A Nalls, Nathan Pankratz, Christina M Lill, Chuong B Do, Dena G Hernandez, Mohamad Saad, Anita L DeStefano, Eleanna Kara, Jose Bras, Manu Sharma,[...]. Nat Genet 2014
8

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
8


Developmental trajectories in 22q11.2 deletion.
Ann Swillen, Donna McDonald-McGinn. Am J Med Genet C Semin Med Genet 2015
83
8

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
27
25

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
44
13

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
E Sidransky, M A Nalls, J O Aasly, J Aharon-Peretz, G Annesi, E R Barbosa, A Bar-Shira, D Berg, J Bras, A Brice,[...]. N Engl J Med 2009
7

Increased prevalence of unprovoked seizures in patients with a 22q11.2 deletion.
Amy Kao, Juliana Mariani, Donna M McDonald-McGinn, Melissa K Maisenbacher, Amy R Brooks-Kayal, Elaine H Zackai, David R Lynch. Am J Med Genet A 2004
41
14

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
46
13


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
7


DNAJC13 mutations in Parkinson disease.
Carles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, Brinda Shah, Chelsea Szu-Tu, Joanne Trinh, Irene Yu, Mary Encarnacion, Lise N Munsie, Lucia Tapia,[...]. Hum Mol Genet 2014
177
7

Staging of brain pathology related to sporadic Parkinson's disease.
Heiko Braak, Kelly Del Tredici, Udo Rüb, Rob A I de Vos, Ernst N H Jansen Steur, Eva Braak. Neurobiol Aging 2003
7

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study.
Manabu Funayama, Kenji Ohe, Taku Amo, Norihiko Furuya, Junji Yamaguchi, Shinji Saiki, Yuanzhe Li, Kotaro Ogaki, Maya Ando, Hiroyo Yoshino,[...]. Lancet Neurol 2015
174
7

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
7

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
7

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
377
7

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
32
18

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
32
18


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.