A citation-based method for searching scientific literature

Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, Jonathan Lévy, Julien Buratti, Alexandre Mathieu, Damien Haye, Laurence Perrin, Céline Dupont, Sandrine Passemard, Yline Capri, Alain Verloes, Séverine Drunat, Boris Keren, Cyril Mignot, Isabelle Marey, Aurélia Jacquette, Sandra Whalen, Eva Pipiras, Brigitte Benzacken, Sandra Chantot-Bastaraud, Alexandra Afenjar, Delphine Héron, Cédric Le Caignec, Claire Beneteau, Olivier Pichon, Bertrand Isidor, Albert David, Laila El Khattabi, Stephan Kemeny, Laetitia Gouas, Philippe Vago, Anne-Laure Mosca-Boidron, Laurence Faivre, Chantal Missirian, Nicole Philip, Damien Sanlaville, Patrick Edery, Véronique Satre, Charles Coutton, Françoise Devillard, Klaus Dieterich, Marie-Laure Vuillaume, Caroline Rooryck, Didier Lacombe, Lucile Pinson, Vincent Gatinois, Jacques Puechberty, Jean Chiesa, James Lespinasse, Christèle Dubourg, Chloé Quelin, Mélanie Fradin, Hubert Journel, Annick Toutain, Dominique Martin, Abdelamdjid Benmansour, Claire S Leblond, Roberto Toro, Frédérique Amsellem, Richard Delorme, Thomas Bourgeron. NPJ Genom Med 2017
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).
K Phelan, H E McDermid. Mol Syndromol 2012
217
71

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
61

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
52

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
47

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
42

Identification of 22q13 genes most likely to contribute to Phelan McDermid syndrome.
Andrew R Mitz, Travis J Philyaw, Luigi Boccuto, Aleksandr Shcheglovitov, Sara M Sarasua, Walter E Kaufmann, Audrey Thurm. Eur J Hum Genet 2018
20
40

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
38

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
38

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
38

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
38

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
33


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
28

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
28

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
28

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
28

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
23

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
23

Modeling autism by SHANK gene mutations in mice.
Yong-Hui Jiang, Michael D Ehlers. Neuron 2013
271
23

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
23

Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome.
Vittoria Disciglio, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Mafalda Mucciolo, Annabella Marozza, Chiara Di Marco, Antonio Massarelli, Valentina Canocchi, Margherita Baldassarri, Enea Ndoni,[...]. Am J Med Genet A 2014
25
23

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome.
M C Bonaglia, R Giorda, R Borgatti, G Felisari, C Gagliardi, A Selicorni, O Zuffardi. Am J Hum Genet 2001
195
23

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
23

Human Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome.
Hélène Darville, Aurélie Poulet, Frédérique Rodet-Amsellem, Laure Chatrousse, Julie Pernelle, Claire Boissart, Delphine Héron, Caroline Nava, Anselme Perrier, Margot Jarrige,[...]. EBioMedicine 2016
48
19

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
19

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
19

Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development.
Heather L Wilson, John A Crolla, Dena Walker, Lina Artifoni, Bruno Dallapiccola, Takako Takano, Pradeep Vasudevan, Shuwen Huang, Vivienne Maloney, Twila Yobb,[...]. Eur J Hum Genet 2008
44
19

SHANK proteins: roles at the synapse and in autism spectrum disorder.
Patricia Monteiro, Guoping Feng. Nat Rev Neurosci 2017
221
19

22q13 deletion syndrome: communication disorder or autism? Evidence from a specific clinical and neurophysiological phenotype.
Laura Ponson, Marie Gomot, Romuald Blanc, Catherine Barthelemy, Sylvie Roux, Arnold Munnich, Serge Romana, Nadia Aguillon-Hernandez, Valérie Malan, Frédérique Bonnet-Brilhault. Transl Psychiatry 2018
12
33

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
25

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
19

A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case.
Claudia Ismania Samogy-Costa, Elisa Varella-Branco, Frederico Monfardini, Helen Ferraz, Rodrigo Ambrósio Fock, Ricardo Henrique Almeida Barbosa, André Luiz Santos Pessoa, Ana Beatriz Alvarez Perez, Naila Lourenço, Maria Vibranovski,[...]. J Neurodev Disord 2019
7
57

The emerging role of SHANK genes in neuropsychiatric disorders.
Audrey Guilmatre, Guillaume Huguet, Richard Delorme, Thomas Bourgeron. Dev Neurobiol 2014
146
14

Stem cell-derived neurons from autistic individuals with SHANK3 mutation show morphogenetic abnormalities during early development.
A Kathuria, P Nowosiad, R Jagasia, S Aigner, R D Taylor, L C Andreae, N J F Gatford, W Lucchesi, D P Srivastava, J Price. Mol Psychiatry 2018
45
14

Three-dimensional Quantification of Dendritic Spines from Pyramidal Neurons Derived from Human Induced Pluripotent Stem Cells.
Laura Gouder, Jean-Yves Tinevez, Hany Goubran-Botros, Alexandra Benchoua, Thomas Bourgeron, Isabelle Cloëz-Tayarani. J Vis Exp 2015
4
75

Differentiation from human pluripotent stem cells of cortical neurons of the superficial layers amenable to psychiatric disease modeling and high-throughput drug screening.
C Boissart, A Poulet, P Georges, H Darville, E Julita, R Delorme, T Bourgeron, M Peschanski, A Benchoua. Transl Psychiatry 2013
64
14

Deficits in the Proline-Rich Synapse-Associated Shank3 Protein in Multiple Neuropsychiatric Disorders.
Peter N Alexandrov, Yuhai Zhao, Vivian Jaber, Lin Cong, Walter J Lukiw. Front Neurol 2017
21
14

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
14

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
14

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
14

Deletion of the last exon of SHANK3 gene produces the full Phelan-McDermid phenotype: a case report.
Marta Macedoni-Lukšič, Danijela Krgović, Boris Zagradišnik, Nadja Kokalj-Vokač. Gene 2013
9
33

22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay.
Kristina Cusmano-Ozog, Melanie A Manning, H Eugene Hoyme. Am J Med Genet C Semin Med Genet 2007
65
14

Altered neurogenesis and disrupted expression of synaptic proteins in prefrontal cortex of SHANK3-deficient non-human primate.
Hui Zhao, Zhuchi Tu, Huijuan Xu, Sen Yan, Huanhuan Yan, Yinghui Zheng, Weili Yang, Jiezhao Zheng, Zhujun Li, Rui Tian,[...]. Cell Res 2017
35
14

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
14

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
14

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
14

Deletion 22q13.3 syndrome.
Mary C Phelan. Orphanet J Rare Dis 2008
127
14

Volumetric Analysis of the Basal Ganglia and Cerebellar Structures in Patients with Phelan-McDermid Syndrome.
Siddharth Srivastava, Benoit Scherrer, Anna K Prohl, Rajna Filip-Dhima, Kush Kapur, Alexander Kolevzon, Joseph D Buxbaum, Elizabeth Berry-Kravis, Latha Soorya, Audrey Thurm,[...]. Pediatr Neurol 2019
9
33

Deletion of Autism Risk Gene Shank3 Disrupts Prefrontal Connectivity.
Marco Pagani, Alice Bertero, Adam Liska, Alberto Galbusera, Mara Sabbioni, Noemi Barsotti, Nigel Colenbier, Daniele Marinazzo, Maria Luisa Scattoni, Massimo Pasqualetti,[...]. J Neurosci 2019
24
14



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.