A citation-based method for searching scientific literature

Dario Cupolillo, Eriola Hoxha, Alessio Faralli, Annarita De Luca, Ferdinando Rossi, Filippo Tempia, Daniela Carulli. Neuropsychopharmacology 2016
Times Cited: 64







List of co-cited articles
1111 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.
Peter T Tsai, Court Hull, YunXiang Chu, Emily Greene-Colozzi, Abbey R Sadowski, Jarrett M Leech, Jason Steinberg, Jacqueline N Crawley, Wade G Regehr, Mustafa Sahin. Nature 2012
480
48

Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice.
Saša Peter, Michiel M Ten Brinke, Jeffrey Stedehouder, Claudia M Reinelt, Bin Wu, Haibo Zhou, Kuikui Zhou, Henk-Jan Boele, Steven A Kushner, Min Goo Lee,[...]. Nat Commun 2016
93
35

Pten regulates neuronal arborization and social interaction in mice.
Chang-Hyuk Kwon, Bryan W Luikart, Craig M Powell, Jing Zhou, Sharon A Matheny, Wei Zhang, Yanjiao Li, Suzanne J Baker, Luis F Parada. Neuron 2006
661
29

Loss of Tsc2 in Purkinje cells is associated with autistic-like behavior in a mouse model of tuberous sclerosis complex.
R Michelle Reith, James McKenna, Henry Wu, S Shahrukh Hashmi, Seo-Hee Cho, Pramod K Dash, Michael J Gambello. Neurobiol Dis 2013
102
28

The cerebellum, sensitive periods, and autism.
Samuel S-H Wang, Alexander D Kloth, Aleksandra Badura. Neuron 2014
318
26

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
806
21

Altered cerebellar connectivity in autism and cerebellar-mediated rescue of autism-related behaviors in mice.
Catherine J Stoodley, Anila M D'Mello, Jacob Ellegood, Vikram Jakkamsetti, Pei Liu, Mary Beth Nebel, Jennifer M Gibson, Elyza Kelly, Fantao Meng, Christopher A Cano,[...]. Nat Neurosci 2017
117
21


Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome.
S K E Koekkoek, K Yamaguchi, B A Milojkovic, B R Dortland, T J H Ruigrok, R Maex, W De Graaf, A E Smit, F VanderWerf, C E Bakker,[...]. Neuron 2005
296
18

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
M G Butler, M J Dasouki, X-P Zhou, Z Talebizadeh, M Brown, T N Takahashi, J H Miles, C H Wang, R Stratton, R Pilarski,[...]. J Med Genet 2005
504
18

Cerebellar gray matter and lobular volumes correlate with core autism symptoms.
Anila M D'Mello, Deana Crocetti, Stewart H Mostofsky, Catherine J Stoodley. Neuroimage Clin 2015
101
18

Consensus paper: pathological role of the cerebellum in autism.
S Hossein Fatemi, Kimberly A Aldinger, Paul Ashwood, Margaret L Bauman, Charles D Blaha, Gene J Blatt, Abha Chauhan, Ved Chauhan, Stephen R Dager, Price E Dickson,[...]. Cerebellum 2012
351
17

Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.
Kim L McBride, Elizabeth A Varga, Matthew T Pastore, Thomas W Prior, Kandamurugu Manickam, Joan F Atkin, Gail E Herman. Autism Res 2010
160
17

Autism spectrum disorders and neuropathology of the cerebellum.
David R Hampson, Gene J Blatt. Front Neurosci 2015
97
17

Cerebellar plasticity and motor learning deficits in a copy-number variation mouse model of autism.
Claire Piochon, Alexander D Kloth, Giorgio Grasselli, Heather K Titley, Hisako Nakayama, Kouichi Hashimoto, Vivian Wan, Dana H Simmons, Tahra Eissa, Jin Nakatani,[...]. Nat Commun 2014
90
17

Cerebellar associative sensory learning defects in five mouse autism models.
Alexander D Kloth, Aleksandra Badura, Amy Li, Adriana Cherskov, Sara G Connolly, Andrea Giovannucci, M Ali Bangash, Giorgio Grasselli, Olga Peñagarikano, Claire Piochon,[...]. Elife 2015
66
15

Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease.
S A Backman, V Stambolic, A Suzuki, J Haight, A Elia, J Pretorius, M S Tsao, P Shannon, B Bolon, G O Ivy,[...]. Nat Genet 2001
360
15

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.
Elizabeth A Varga, Matthew Pastore, Thomas Prior, Gail E Herman, Kim L McBride. Genet Med 2009
183
14

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
574
14

Deletion of PTEN produces autism-like behavioral deficits and alterations in synaptic proteins.
Joaquin N Lugo, Gregory D Smith, Erin P Arbuckle, Jessika White, Andrew J Holley, Crina M Floruta, Nowrin Ahmed, Maribel C Gomez, Obi Okonkwo. Front Mol Neurosci 2014
88
14


Pten regulates neuronal soma size: a mouse model of Lhermitte-Duclos disease.
C H Kwon, X Zhu, J Zhang, L L Knoop, R Tharp, R J Smeyne, C G Eberhart, P C Burger, S J Baker. Nat Genet 2001
337
14

The parvalbumin/somatostatin ratio is increased in Pten mutant mice and by human PTEN ASD alleles.
Daniel Vogt, Kathleen K A Cho, Anthony T Lee, Vikaas S Sohal, John L R Rubenstein. Cell Rep 2015
60
15

Cerebro-cerebellar circuits in autism spectrum disorder.
Anila M D'Mello, Catherine J Stoodley. Front Neurosci 2015
114
14

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
12

Purkinje cell size is reduced in cerebellum of patients with autism.
S Hossein Fatemi, Amy R Halt, George Realmuto, Julie Earle, David A Kist, Paul Thuras, Amelia Merz. Cell Mol Neurobiol 2002
188
12

Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephaly.
Judith A Hobert, Rebecca Embacher, Jessica L Mester, Thomas W Frazier, Charis Eng. Eur J Hum Genet 2014
50
16

Adult restoration of Shank3 expression rescues selective autistic-like phenotypes.
Yuan Mei, Patricia Monteiro, Yang Zhou, Jin-Ah Kim, Xian Gao, Zhanyan Fu, Guoping Feng. Nature 2016
183
12

Cerebellar Shank2 Regulates Excitatory Synapse Density, Motor Coordination, and Specific Repetitive and Anxiety-Like Behaviors.
Seungmin Ha, Dongwon Lee, Yi Sul Cho, Changuk Chung, Ye-Eun Yoo, Jihye Kim, Jiseok Lee, Woohyun Kim, Hyosang Kim, Yong Chul Bae,[...]. J Neurosci 2016
37
21

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
861
12

Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity.
J Ellegood, E Anagnostou, B A Babineau, J N Crawley, L Lin, M Genestine, E DiCicco-Bloom, J K Y Lai, J A Foster, O Peñagarikano,[...]. Mol Psychiatry 2015
151
12


Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function.
Hyejung Won, Hye-Ryeon Lee, Heon Yung Gee, Won Mah, Jae-Ick Kim, Jiseok Lee, Seungmin Ha, Changuk Chung, Eun Suk Jung, Yi Sul Cho,[...]. Nature 2012
412
12

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Brian J O'Roak, Laura Vives, Wenqing Fu, Jarrett D Egertson, Ian B Stanaway, Ian G Phelps, Gemma Carvill, Akash Kumar, Choli Lee, Katy Ankenman,[...]. Science 2012
787
10

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
10

Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2.
Michael J Schmeisser, Elodie Ey, Stephanie Wegener, Juergen Bockmann, A Vanessa Stempel, Angelika Kuebler, Anna-Lena Janssen, Patrick T Udvardi, Ehab Shiban, Christina Spilker,[...]. Nature 2012
380
10

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
287
10

Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.
Joseph D Buxbaum, Guiqing Cai, Pauline Chaste, Gudrun Nygren, Juliet Goldsmith, Jennifer Reichert, Henrik Anckarsäter, Maria Rastam, Christopher J Smith, Jeremy M Silverman,[...]. Am J Med Genet B Neuropsychiatr Genet 2007
174
10

Regional alterations in purkinje cell density in patients with autism.
Jerry Skefos, Christopher Cummings, Katelyn Enzer, Jarrod Holiday, Katrina Weed, Ezra Levy, Tarik Yuce, Thomas Kemper, Margaret Bauman. PLoS One 2014
74
10

Neuroanatomic observations of the brain in autism: a review and future directions.
Margaret L Bauman, Thomas L Kemper. Int J Dev Neurosci 2005
511
10

Cerebellar lesions in tuberous sclerosis complex: neurobehavioral and neuroimaging correlates.
Thomas J Eluvathingal, Michael E Behen, Harry T Chugani, James Janisse, Bruno Bernardi, Pulak Chakraborty, Csaba Juhasz, Otto Muzik, Diane C Chugani. J Child Neurol 2006
74
10

Most genetic risk for autism resides with common variation.
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
556
10

Does cerebellar injury in premature infants contribute to the high prevalence of long-term cognitive, learning, and behavioral disability in survivors?
Catherine Limperopoulos, Haim Bassan, Kimberlee Gauvreau, Richard L Robertson, Nancy R Sullivan, Carol B Benson, Lauren Avery, Jane Stewart, Janet S Soul, Steven A Ringer,[...]. Pediatrics 2007
321
10

Pharmacological inhibition of mTORC1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific Pten knock-out mice.
Jing Zhou, Jacqueline Blundell, Shiori Ogawa, Chang-Hyuk Kwon, Wei Zhang, Christopher Sinton, Craig M Powell, Luis F Parada. J Neurosci 2009
286
10

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
331
10

Shared synaptic pathophysiology in syndromic and nonsyndromic rodent models of autism.
Stéphane J Baudouin, Julien Gaudias, Stefan Gerharz, Laetitia Hatstatt, Kuikui Zhou, Pradeep Punnakkal, Kenji F Tanaka, Will Spooren, Rene Hen, Chris I De Zeeuw,[...]. Science 2012
195
10

Hyperactivity of newborn Pten knock-out neurons results from increased excitatory synaptic drive.
Michael R Williams, Tyrone DeSpenza, Meijie Li, Allan T Gulledge, Bryan W Luikart. J Neurosci 2015
63
11

Cerebellar granule cells encode the expectation of reward.
Mark J Wagner, Tony Hyun Kim, Joan Savall, Mark J Schnitzer, Liqun Luo. Nature 2017
188
10

Cerebellar modulation of the reward circuitry and social behavior.
Ilaria Carta, Christopher H Chen, Amanda L Schott, Schnaude Dorizan, Kamran Khodakhah. Science 2019
150
10

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
9


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.