A citation-based method for searching scientific literature

J V Cabral-Costa, D Z Andreotti, N P Mello, C Scavone, S Camandola, E M Kawamoto. Sci Rep 2018
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Intermittent fasting attenuates lipopolysaccharide-induced neuroinflammation and memory impairment.
Andrea R Vasconcelos, Lidia M Yshii, Tania A Viel, Hudson S Buck, Mark P Mattson, Cristoforo Scavone, Elisa M Kawamoto. J Neuroinflammation 2014
97
40

SIRT3 mediates hippocampal synaptic adaptations to intermittent fasting and ameliorates deficits in APP mutant mice.
Yong Liu, Aiwu Cheng, Yu-Jiao Li, Ying Yang, Yuki Kishimoto, Shi Zhang, Yue Wang, Ruiqian Wan, Sophia M Raefsky, Daoyuan Lu,[...]. Nat Commun 2019
51
30

Autistic-Like Traits and Cerebellar Dysfunction in Purkinje Cell PTEN Knock-Out Mice.
Dario Cupolillo, Eriola Hoxha, Alessio Faralli, Annarita De Luca, Ferdinando Rossi, Filippo Tempia, Daniela Carulli. Neuropsychopharmacology 2016
66
30

Intermittent Fasting Confers Protection in CNS Autoimmunity by Altering the Gut Microbiota.
Francesca Cignarella, Claudia Cantoni, Laura Ghezzi, Amber Salter, Yair Dorsett, Lei Chen, Daniel Phillips, George M Weinstock, Luigi Fontana, Anne H Cross,[...]. Cell Metab 2018
140
30

Intermittent fasting and caloric restriction ameliorate age-related behavioral deficits in the triple-transgenic mouse model of Alzheimer's disease.
Veerendra Kumar Madala Halagappa, Zhihong Guo, Michelle Pearson, Yasuji Matsuoka, Roy G Cutler, Frank M Laferla, Mark P Mattson. Neurobiol Dis 2007
325
30

Effects of eight weeks of time-restricted feeding (16/8) on basal metabolism, maximal strength, body composition, inflammation, and cardiovascular risk factors in resistance-trained males.
Tatiana Moro, Grant Tinsley, Antonino Bianco, Giuseppe Marcolin, Quirico Francesco Pacelli, Giuseppe Battaglia, Antonio Palma, Paulo Gentil, Marco Neri, Antonio Paoli. J Transl Med 2016
193
30

Fasting: molecular mechanisms and clinical applications.
Valter D Longo, Mark P Mattson. Cell Metab 2014
557
30

Age and energy intake interact to modify cell stress pathways and stroke outcome.
Thiruma V Arumugam, Terry M Phillips, Aiwu Cheng, Christopher H Morrell, Mark P Mattson, Ruiqian Wan. Ann Neurol 2010
173
30

Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndrome.
Joan C Han, Audrey Thurm, Christine Golden Williams, Lisa A Joseph, Wadih M Zein, Brian P Brooks, John A Butman, Sheila M Brady, Shannon R Fuhr, Melanie D Hicks,[...]. Cortex 2013
36
20

Intermittent metabolic switching, neuroplasticity and brain health.
Mark P Mattson, Keelin Moehl, Nathaniel Ghena, Maggie Schmaedick, Aiwu Cheng. Nat Rev Neurosci 2018
152
20

A ketone ester diet exhibits anxiolytic and cognition-sparing properties, and lessens amyloid and tau pathologies in a mouse model of Alzheimer's disease.
Yoshihiro Kashiwaya, Christian Bergman, Jong-Hwan Lee, Ruiqian Wan, M Todd King, Mohamed R Mughal, Eitan Okun, Kieran Clarke, Mark P Mattson, Richard L Veech. Neurobiol Aging 2013
183
20

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
148
20

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
358
20

Mutations causing syndromic autism define an axis of synaptic pathophysiology.
Benjamin D Auerbach, Emily K Osterweil, Mark F Bear. Nature 2011
413
20

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
568
20

A modified ketogenic gluten-free diet with MCT improves behavior in children with autism spectrum disorder.
Ryan W Y Lee, Michael J Corley, Alina Pang, Gaye Arakaki, Lisa Abbott, Michael Nishimoto, Rob Miyamoto, Erica Lee, Susan Yamamoto, Alika K Maunakea,[...]. Physiol Behav 2018
37
20

Cntnap2 Knockout Rats and Mice Exhibit Epileptiform Activity and Abnormal Sleep-Wake Physiology.
Alexia M Thomas, Michael D Schwartz, Michael D Saxe, Thomas S Kilduff. Sleep 2017
31
20

Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autism.
Olga Peñagarikano, María T Lázaro, Xiao-Hong Lu, Aaron Gordon, Hongmei Dong, Hoa A Lam, Elior Peles, Nigel T Maidment, Niall P Murphy, X William Yang,[...]. Sci Transl Med 2015
195
20

CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.
Aarathi Sugathan, Marta Biagioli, Christelle Golzio, Serkan Erdin, Ian Blumenthal, Poornima Manavalan, Ashok Ragavendran, Harrison Brand, Diane Lucente, Judith Miles,[...]. Proc Natl Acad Sci U S A 2014
174
20

The autism/neuroprotection-linked ADNP/NAP regulate the excitatory glutamatergic synapse.
Shlomo Sragovich, Anna Malishkevich, Yael Piontkewitz, Eliezer Giladi, Olga Touloumi, Roza Lagoudaki, Nikolaos Grigoriadis, Illana Gozes. Transl Psychiatry 2019
20
20

Chd2 Is Necessary for Neural Circuit Development and Long-Term Memory.
Young J Kim, Sattar Khoshkhoo, Jan C Frankowski, Bingyao Zhu, Saad Abbasi, Sunyoung Lee, Ye Emily Wu, Robert F Hunt. Neuron 2018
28
20

Altered Auditory Processing, Filtering, and Reactivity in the Cntnap2 Knock-Out Rat Model for Neurodevelopmental Disorders.
Kaela E Scott, Ashley L Schormans, Katharine Y Pacoli, Cleusa De Oliveira, Brian L Allman, Susanne Schmid. J Neurosci 2018
13
20

Oxytocin improves behavioral and electrophysiological deficits in a novel Shank3-deficient rat.
Hala Harony-Nicolas, Maya Kay, Johann du Hoffmann, Matthew E Klein, Ozlem Bozdagi-Gunal, Mohammed Riad, Nikolaos P Daskalakis, Sankalp Sonar, Pablo E Castillo, Patrick R Hof,[...]. Elife 2017
67
20


Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality.
Tzyy-Nan Huang, Hsiu-Chun Chuang, Wen-Hsi Chou, Chiung-Ya Chen, Hsiao-Fang Wang, Shen-Ju Chou, Yi-Ping Hsueh. Nat Neurosci 2014
106
20

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
Nicole A Hawkins, Melinda S Martin, Wayne N Frankel, Jennifer A Kearney, Andrew Escayg. Neurobiol Dis 2011
57
20

Role of chromodomain helicase DNA-binding protein 2 in DNA damage response signaling and tumorigenesis.
P Nagarajan, T M Onami, S Rajagopalan, S Kania, R Donnell, S Venkatachalam. Oncogene 2009
69
20

Germline Chd8 haploinsufficiency alters brain development in mouse.
Andrea L Gompers, Linda Su-Feher, Jacob Ellegood, Nycole A Copping, M Asrafuzzaman Riyadh, Tyler W Stradleigh, Michael C Pride, Melanie D Schaffler, A Ayanna Wade, Rinaldo Catta-Preta,[...]. Nat Neurosci 2017
109
20

Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment.
Cemre Celen, Jen-Chieh Chuang, Xin Luo, Nadine Nijem, Angela K Walker, Fei Chen, Shuyuan Zhang, Andrew S Chung, Liem H Nguyen, Ibrahim Nassour,[...]. Elife 2017
48
20

Involvement of synaptic genes in the pathogenesis of autism spectrum disorders: the case of synapsins.
Silvia Giovedí, Anna Corradi, Anna Fassio, Fabio Benfenati. Front Pediatr 2014
38
20

Neuronal death and perinatal lethality in voltage-gated sodium channel alpha(II)-deficient mice.
R Planells-Cases, M Caprini, J Zhang, E M Rockenstein, R R Rivera, C Murre, E Masliah, M Montal. Biophys J 2000
107
20

The Histone Methyltransferase Gene Absent, Small, or Homeotic Discs-1 Like Is Required for Normal Hox Gene Expression and Fertility in Mice.
Michelle L Brinkmeier, Krista A Geister, Morgan Jones, Meriam Waqas, Ivan Maillard, Sally A Camper. Biol Reprod 2015
19
20

Peripheral Mechanosensory Neuron Dysfunction Underlies Tactile and Behavioral Deficits in Mouse Models of ASDs.
Lauren L Orefice, Amanda L Zimmerman, Anda M Chirila, Steven J Sleboda, Joshua P Head, David D Ginty. Cell 2016
142
20

Trans-synaptic zinc mobilization improves social interaction in two mouse models of autism through NMDAR activation.
Eun-Jae Lee, Hyejin Lee, Tzyy-Nan Huang, Changuk Chung, Wangyong Shin, Kyungdeok Kim, Jae-Young Koh, Yi-Ping Hsueh, Eunjoon Kim. Nat Commun 2015
60
20

CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
Yuta Katayama, Masaaki Nishiyama, Hirotaka Shoji, Yasuyuki Ohkawa, Atsuki Kawamura, Tetsuya Sato, Mikita Suyama, Toru Takumi, Tsuyoshi Miyakawa, Keiichi I Nakayama. Nature 2016
154
20

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
65
20

Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice.
Philipp Suetterlin, Shaun Hurley, Conor Mohan, Kimberley L H Riegman, Marco Pagani, Angela Caruso, Jacob Ellegood, Alberto Galbusera, Ivan Crespo-Enriquez, Caterina Michetti,[...]. Cereb Cortex 2018
53
20

Rodent models in neuroscience research: is it a rat race?
Bart Ellenbroek, Jiun Youn. Dis Model Mech 2016
239
20

Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
Mihiro Shibutani, Takuro Horii, Hirotaka Shoji, Sumiyo Morita, Mika Kimura, Naomi Terawaki, Tsuyoshi Miyakawa, Izuho Hatada. Int J Mol Sci 2017
29
20

Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling.
Omer Durak, Fan Gao, Yea Jin Kaeser-Woo, Richard Rueda, Anthony J Martorell, Alexi Nott, Carol Y Liu, L Ashley Watson, Li-Huei Tsai. Nat Neurosci 2016
113
20

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
20

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
584
20

Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity.
Siavash Fazel Darbandi, Sarah E Robinson Schwartz, Qihao Qi, Rinaldo Catta-Preta, Emily Ling-Lin Pai, Jeffrey D Mandell, Amanda Everitt, Anna Rubin, Rebecca A Krasnoff, Sol Katzman,[...]. Neuron 2018
33
20

Histone methyltransferase Ash1L mediates activity-dependent repression of neurexin-1α.
Τao Zhu, Chen Liang, Dongdong Li, Miaomiao Tian, Sanxiong Liu, Guanjun Gao, Ji-Song Guan. Sci Rep 2016
18
20

CHD8 suppresses p53-mediated apoptosis through histone H1 recruitment during early embryogenesis.
Masaaki Nishiyama, Kiyotaka Oshikawa, Yu-ichi Tsukada, Tadashi Nakagawa, Shun-ichiro Iemura, Tohru Natsume, Yuhong Fan, Akira Kikuchi, Arthur I Skoultchi, Keiichi I Nakayama. Nat Cell Biol 2009
122
20

Sexually dimorphic behavior, neuronal activity, and gene expression in Chd8-mutant mice.
Hwajin Jung, Haram Park, Yeonsoo Choi, Hyojin Kang, Eunee Lee, Hanseul Kweon, Junyeop Daniel Roh, Jacob Ellegood, Woochul Choi, Jaeseung Kang,[...]. Nat Neurosci 2018
59
20

Sexual divergence in microtubule function: the novel intranasal microtubule targeting SKIP normalizes axonal transport and enhances memory.
N Amram, G Hacohen-Kleiman, S Sragovich, A Malishkevich, J Katz, O Touloumi, R Lagoudaki, N C Grigoriadis, E Giladi, A Yeheskel,[...]. Mol Psychiatry 2016
45
20

Histone methyltransferase Ash1l suppresses interleukin-6 production and inflammatory autoimmune diseases by inducing the ubiquitin-editing enzyme A20.
Meng Xia, Juan Liu, Xiaohui Wu, Shuxun Liu, Gang Li, Chaofeng Han, Lijun Song, Zhiqing Li, Qingqing Wang, Jianli Wang,[...]. Immunity 2013
97
20

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
506
20

Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits.
Randall J Platt, Yang Zhou, Ian M Slaymaker, Ashwin S Shetty, Niels R Weisbach, Jin-Ah Kim, Jitendra Sharma, Mitul Desai, Sabina Sood, Hannah R Kempton,[...]. Cell Rep 2017
96
20


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.