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



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Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Latha Soorya, Alexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, Lily Schwartz, Yitzchak Frank, A Ting Wang, Guiqing Cai, Elena Parkhomenko,[...]. Mol Autism 2013
143
65

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
784
43

Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.
Sara M Sarasua, Luigi Boccuto, Julia L Sharp, Alka Dwivedi, Chin-Fu Chen, Jonathan D Rollins, R Curtis Rogers, Katy Phelan, Barbara R DuPont. Hum Genet 2014
74
43

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.
Maria Clara Bonaglia, Roberto Giorda, Silvana Beri, Cristina De Agostini, Francesca Novara, Marco Fichera, Lucia Grillo, Ornella Galesi, Annalisa Vetro, Roberto Ciccone,[...]. PLoS Genet 2011
108
43

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Christelle M Durand, Catalina Betancur, Tobias M Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Rastam, I Carina Gillberg, Henrik Anckarsäter,[...]. Nat Genet 2007
933
39

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).
K Phelan, H E McDermid. Mol Syndromol 2012
217
39

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Claire S Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kevin Mouzat,[...]. PLoS Genet 2014
280
34

Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring.
Alexander Kolevzon, Benjamin Angarita, Lauren Bush, A Ting Wang, Yitzchak Frank, Amy Yang, Robert Rapaport, Jeffrey Saland, Shubhika Srivastava, Cristina Farrell,[...]. J Neurodev Disord 2014
63
34

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms.
H L Wilson, A C C Wong, S R Shaw, W-Y Tse, G A Stapleton, M C Phelan, S Hu, J Marshall, H E McDermid. J Med Genet 2003
238
34

SHANK proteins: roles at the synapse and in autism spectrum disorder.
Patricia Monteiro, Guoping Feng. Nat Rev Neurosci 2017
221
30

Characterizing regression in Phelan McDermid Syndrome (22q13 deletion syndrome).
Gillian Reierson, Jon Bernstein, Wendy Froehlich-Santino, Alexander Urban, Carolin Purmann, Sean Berquist, Josh Jordan, Ruth O'Hara, Joachim Hallmayer. J Psychiatr Res 2017
22
31

Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations.
Silvia De Rubeis, Paige M Siper, Allison Durkin, Jordana Weissman, François Muratet, Danielle Halpern, Maria Del Pilar Trelles, Yitzchak Frank, Reymundo Lozano, A Ting Wang,[...]. Mol Autism 2018
50
30

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3.
Xiaoming Wang, Portia A McCoy, Ramona M Rodriguiz, Yanzhen Pan, H Shawn Je, Adam C Roberts, Caroline J Kim, Janet Berrios, Jennifer S Colvin, Danielle Bousquet-Moore,[...]. Hum Mol Genet 2011
325
26

SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties.
Kihoon Han, J Lloyd Holder, Christian P Schaaf, Hui Lu, Hongmei Chen, Hyojin Kang, Jianrong Tang, Zhenyu Wu, Shuang Hao, Sau Wai Cheung,[...]. Nature 2013
212
26

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.
Julie Gauthier, Nathalie Champagne, Ronald G Lafrenière, Lan Xiong, Dan Spiegelman, Edna Brustein, Mathieu Lapointe, Huashan Peng, Mélanie Côté, Anne Noreau,[...]. Proc Natl Acad Sci U S A 2010
258
26

Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID.
Daniela M Cochoy, Alexander Kolevzon, Yuji Kajiwara, Michael Schoen, Maria Pascual-Lucas, Stacey Lurie, Joseph D Buxbaum, Tobias M Boeckers, Michael J Schmeisser. Mol Autism 2015
41
21

Shank3-mutant mice lacking exon 9 show altered excitation/inhibition balance, enhanced rearing, and spatial memory deficit.
Jiseok Lee, Changuk Chung, Seungmin Ha, Dongmin Lee, Do-Young Kim, Hyun Kim, Eunjoon Kim. Front Cell Neurosci 2015
83
21

Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism.
Thomas C Jaramillo, Haley E Speed, Zhong Xuan, Jeremy M Reimers, Shunan Liu, Craig M Powell. Autism Res 2016
73
21

Autism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlations.
Lindsay M Oberman, Luigi Boccuto, Lauren Cascio, Sara Sarasua, Walter E Kaufmann. Orphanet J Rare Dis 2015
24
21

Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism.
Xiaoming Wang, Alexandra L Bey, Brittany M Katz, Alexandra Badea, Namsoo Kim, Lisa K David, Lara J Duffney, Sunil Kumar, Stephen D Mague, Samuel W Hulbert,[...]. Nat Commun 2016
131
21

22q13.3 deletion syndrome: clinical and molecular analysis using array CGH.
S U Dhar, D del Gaudio, J R German, S U Peters, Z Ou, P I Bader, J S Berg, M Blazo, C W Brown, B H Graham,[...]. Am J Med Genet A 2010
88
21

Neuropsychological phenotype and psychopathology in seven adult patients with Phelan-McDermid syndrome: implications for treatment strategy.
J I M Egger, R J Zwanenburg, C M A van Ravenswaaij-Arts, T Kleefstra, W M A Verhoeven. Genes Brain Behav 2016
16
31

Phelan-McDermid syndrome in two adult brothers: atypical bipolar disorder as its psychopathological phenotype?
Willem Ma Verhoeven, Jos Im Egger, Marjolein H Willemsen, Gert Jm de Leijer, Tjitske Kleefstra. Neuropsychiatr Dis Treat 2012
36
21

Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome).
Sara M Sarasua, Alka Dwivedi, Luigi Boccuto, Jonathan D Rollins, Chin-Fu Chen, R Curtis Rogers, Katy Phelan, Barbara R DuPont, Julianne S Collins. J Med Genet 2011
71
21

Neurobehavioral profile and brain imaging study of the 22q13.3 deletion syndrome in childhood.
Anne Philippe, Nathalie Boddaert, Laurence Vaivre-Douret, Laurence Robel, Laurent Danon-Boileau, Valérie Malan, Marie-Christine de Blois, Delphine Heron, Laurence Colleaux, Bernard Golse,[...]. Pediatrics 2008
63
21

Seizures and EEG pattern in the 22q13.3 deletion syndrome: clinical report of six Italian cases.
Maria Grazia Figura, Antonietta Coppola, Maria Bottitta, Giuseppe Calabrese, Lucia Grillo, Daniela Luciano, Luigi Del Gaudio, Claudia Torniero, Salvatore Striano, Maurizio Elia. Seizure 2014
21
23

Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills.
A Denayer, H Van Esch, T de Ravel, J-P Frijns, G Van Buggenhout, A Vogels, K Devriendt, J Geutjens, P Thiry, A Swillen. Mol Syndromol 2012
49
21

Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletion.
Ksenija Vucurovic, Emilie Landais, Cécile Delahaigue, Julien Eutrope, Anouck Schneider, Camille Leroy, Hamza Kabbaj, Jacques Motte, Dominique Gaillard, Anne-Catherine Rolland,[...]. Eur J Med Genet 2012
29
21

Contribution of SHANK3 mutations to autism spectrum disorder.
Rainald Moessner, Christian R Marshall, James S Sutcliffe, Jennifer Skaug, Dalila Pinto, John Vincent, Lonnie Zwaigenbaum, Bridget Fernandez, Wendy Roberts, Peter Szatmari,[...]. Am J Hum Genet 2007
422
21

Deletion 22q13.3 syndrome.
Mary C Phelan. Orphanet J Rare Dis 2008
127
21

Lithium as a rescue therapy for regression and catatonia features in two SHANK3 patients with autism spectrum disorder: case reports.
Sylvie Serret, Susanne Thümmler, Emmanuelle Dor, Stephanie Vesperini, Andreia Santos, Florence Askenazy. BMC Psychiatry 2015
44
21

Model of autism: increased ratio of excitation/inhibition in key neural systems.
J L R Rubenstein, M M Merzenich. Genes Brain Behav 2003
17

Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.
Luigi Boccuto, Maria Lauri, Sara M Sarasua, Cindy D Skinner, Daniela Buccella, Alka Dwivedi, Daniela Orteschi, Julianne S Collins, Marcella Zollino, Paola Visconti,[...]. Eur J Hum Genet 2013
124
17

Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice.
Mu Yang, Ozlem Bozdagi, Maria Luisa Scattoni, Markus Wöhr, Florence I Roullet, Adam M Katz, Danielle N Abrams, David Kalikhman, Harrison Simon, Leuk Woldeyohannes,[...]. J Neurosci 2012
221
17

Modeling autism by SHANK gene mutations in mice.
Yong-Hui Jiang, Michael D Ehlers. Neuron 2013
271
17

Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators.
Lara J Duffney, Ping Zhong, Jing Wei, Emmanuel Matas, Jia Cheng, Luye Qin, Kaijie Ma, David M Dietz, Yuji Kajiwara, Joseph D Buxbaum,[...]. Cell Rep 2015
137
17


Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication.
Ozlem Bozdagi, Takeshi Sakurai, Danae Papapetrou, Xiaobin Wang, Dara L Dickstein, Nagahide Takahashi, Yuji Kajiwara, Mu Yang, Adam M Katz, Maria Luisa Scattoni,[...]. Mol Autism 2010
341
17

Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits.
Haley E Speed, Mehreen Kouser, Zhong Xuan, Jeremy M Reimers, Christine F Ochoa, Natasha Gupta, Shunan Liu, Craig M Powell. J Neurosci 2015
70
17

The emerging role of SHANK genes in neuropsychiatric disorders.
Audrey Guilmatre, Guillaume Huguet, Richard Delorme, Thomas Bourgeron. Dev Neurobiol 2014
146
17

22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndrome.
Sara M Sarasua, Alka Dwivedi, Luigi Boccuto, Chin-Fu Chen, Julia L Sharp, Jonathan D Rollins, Julianne S Collins, R Curtis Rogers, Katy Phelan, Barbara R DuPont. Genet Med 2014
38
17

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients.
Aleksandr Shcheglovitov, Olesya Shcheglovitova, Masayuki Yazawa, Thomas Portmann, Rui Shu, Vittorio Sebastiano, Anna Krawisz, Wendy Froehlich, Jonathan A Bernstein, Joachim F Hallmayer,[...]. Nature 2013
288
17

Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion.
Kimberly A Aldinger, Jillene Kogan, Virginia Kimonis, Bridget Fernandez, Denise Horn, Eva Klopocki, Brian Chung, Annick Toutain, Rosanna Weksberg, Kathleen J Millen,[...]. Am J Med Genet A 2013
39
17

Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons.
Fei Yi, Tamas Danko, Salome Calado Botelho, Christopher Patzke, ChangHui Pak, Marius Wernig, Thomas C Südhof. Science 2016
150
17


Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations.
J J Luciani, P de Mas, D Depetris, C Mignon-Ravix, A Bottani, M Prieur, P Jonveaux, A Philippe, G Bourrouillou, B de Martinville,[...]. J Med Genet 2003
79
17

Molecular and phenotypic characterization of ring chromosome 22.
Aaron R Jeffries, Sarah Curran, Frances Elmslie, Ajay Sharma, Sharon Wenger, Marybeth Hummel, John Powell. Am J Med Genet A 2005
67
17


Mice with Shank3 Mutations Associated with ASD and Schizophrenia Display Both Shared and Distinct Defects.
Yang Zhou, Tobias Kaiser, Patrícia Monteiro, Xiangyu Zhang, Marie S Van der Goes, Dongqing Wang, Boaz Barak, Menglong Zeng, Chenchen Li, Congyi Lu,[...]. Neuron 2016
153
17

Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children.
Renée J Zwanenburg, Selma A J Ruiter, Edwin R van den Heuvel, Boudien C T Flapper, Conny M A Van Ravenswaaij-Arts. J Neurodev Disord 2016
32
17


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.