A citation-based method for searching scientific literature

Thomas Arbogast, Abdel-Mouttalib Ouagazzal, Claire Chevalier, Maksym Kopanitsa, Nurudeen Afinowi, Eugenia Migliavacca, Belinda S Cowling, Marie-Christine Birling, Marie-France Champy, Alexandre Reymond, Yann Herault. PLoS Genet 2016
Times Cited: 55







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



Times Cited
  Times     Co-cited
Similarity


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
156
7

Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia.
Torfi Sigurdsson, Kimberly L Stark, Maria Karayiorgou, Joseph A Gogos, Joshua A Gordon. Nature 2010
423
7

The pattern of cortical dysfunction in a mouse model of a schizophrenia-related microdeletion.
Karine Fénelon, Bin Xu, Cora S Lai, Jun Mukai, Sander Markx, Kimberly L Stark, Pei-Ken Hsu, Wen-Biao Gan, Gerald D Fischbach, Amy B MacDermott,[...]. J Neurosci 2013
70
7

Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits.
Melanie Lacaria, Corinne Spencer, Wenli Gu, Richard Paylor, James R Lupski. Hum Mol Genet 2012
35
11


Absence of strong strain effects in behavioral analyses of Shank3-deficient mice.
Elodie Drapeau, Nate P Dorr, Gregory A Elder, Joseph D Buxbaum. Dis Model Mech 2014
30
13

Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice.
Michael Didriksen, Kim Fejgin, Simon R O Nilsson, Michelle R Birknow, Hannah M Grayton, Peter H Larsen, Jes B Lauridsen, Vibeke Nielsen, Pau Celada, Noemi Santana,[...]. J Psychiatry Neurosci 2017
29
13

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
7

The 16p11.2 homologs fam57ba and doc2a generate certain brain and body phenotypes.
Jasmine M McCammon, Alicia Blaker-Lee, Xiao Chen, Hazel Sive. Hum Mol Genet 2017
12
33

Pharmacological Inhibition of ERK Signaling Rescues Pathophysiology and Behavioral Phenotype Associated with 16p11.2 Chromosomal Deletion in Mice.
Joanna Pucilowska, Joseph Vithayathil, Marco Pagani, Caitlin Kelly, J Colleen Karlo, Camilla Robol, Ilaria Morella, Alessandro Gozzi, Riccardo Brambilla, Gary E Landreth. J Neurosci 2018
33
12

The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs.
Maria Nicla Loviglio, Thomas Arbogast, Aia Elise Jønch, Stephan C Collins, Konstantin Popadin, Camille S Bonnet, Giuliana Giannuzzi, Anne M Maillard, Sébastien Jacquemont, Binnaz Yalcin,[...]. Am J Hum Genet 2017
15
26

Chemogenetic Activation of Prefrontal Cortex Rescues Synaptic and Behavioral Deficits in a Mouse Model of 16p11.2 Deletion Syndrome.
Wei Wang, Benjamin Rein, Freddy Zhang, Tao Tan, Ping Zhong, Luye Qin, Zhen Yan. J Neurosci 2018
24
16

Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions.
Thomas Arbogast, Parisa Razaz, Jacob Ellegood, Spencer U McKinstry, Serkan Erdin, Benjamin Currall, Tanya Aneichyk, Jason P Lerch, Lily R Qiu, Ramona M Rodriguiz,[...]. Hum Mol Genet 2019
11
36

Increased Excitation-Inhibition Ratio Stabilizes Synapse and Circuit Excitability in Four Autism Mouse Models.
Michelle W Antoine, Tomer Langberg, Philipp Schnepel, Daniel E Feldman. Neuron 2019
116
7


16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.
Eva M Reinthaler, Dennis Lal, Sebastien Lebon, Michael S Hildebrand, Hans-Henrik M Dahl, Brigid M Regan, Martha Feucht, Hannelore Steinböck, Birgit Neophytou, Gabriel M Ronen,[...]. Hum Mol Genet 2014
41
7

A general framework for weighted gene co-expression network analysis.
Bin Zhang, Steve Horvath. Stat Appl Genet Mol Biol 2005
5

Cytoscape: a software environment for integrated models of biomolecular interaction networks.
Paul Shannon, Andrew Markiel, Owen Ozier, Nitin S Baliga, Jonathan T Wang, Daniel Ramage, Nada Amin, Benno Schwikowski, Trey Ideker. Genome Res 2003
5

Copy number variation in schizophrenia in Sweden.
J P Szatkiewicz, C O'Dushlaine, G Chen, K Chambert, J L Moran, B M Neale, M Fromer, D Ruderfer, S Akterin, S E Bergen,[...]. Mol Psychiatry 2014
161
5

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
50
6

Copy number variations in neurodevelopmental disorders.
Hannah M Grayton, Cathy Fernandes, Dan Rujescu, David A Collier. Prog Neurobiol 2012
106
5

The relationship between sleep and behavior in autism spectrum disorder (ASD): a review.
Simonne Cohen, Russell Conduit, Steven W Lockley, Shantha Mw Rajaratnam, Kim M Cornish. J Neurodev Disord 2014
128
5

Nocturnal excretion of 6-sulphatoxymelatonin in children and adolescents with autistic disorder.
Sylvie Tordjman, George M Anderson, Nadège Pichard, Henriette Charbuy, Yvan Touitou. Biol Psychiatry 2005
162
5

Circadian rhythms and sleep in children with autism.
Gena Glickman. Neurosci Biobehav Rev 2010
91
5

Sex differences in autism spectrum disorders.
Donna M Werling, Daniel H Geschwind. Curr Opin Neurol 2013
422
5

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
5

7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages.
Antonio Adamo, Sina Atashpaz, Pierre-Luc Germain, Matteo Zanella, Giuseppe D'Agostino, Veronica Albertin, Josh Chenoweth, Lucia Micale, Carmela Fusco, Christian Unger,[...]. Nat Genet 2015
76
5

A human neurodevelopmental model for Williams syndrome.
Thanathom Chailangkarn, Cleber A Trujillo, Beatriz C Freitas, Branka Hrvoj-Mihic, Roberto H Herai, Diana X Yu, Timothy T Brown, Maria C Marchetto, Cedric Bardy, Lauren McHenry,[...]. Nature 2016
96
5

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
5

Patches of disorganization in the neocortex of children with autism.
Rich Stoner, Maggie L Chow, Maureen P Boyle, Susan M Sunkin, Peter R Mouton, Subhojit Roy, Anthony Wynshaw-Boris, Sophia A Colamarino, Ed S Lein, Eric Courchesne. N Engl J Med 2014
383
5

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
Anthony R Isles, Andrés Ingason, Chelsea Lowther, James Walters, Micha Gawlick, Gerald Stöber, Elliott Rees, Joanna Martin, Rosie B Little, Harry Potter,[...]. PLoS Genet 2016
32
9

Population analysis of large copy number variants and hotspots of human genetic disease.
Andy Itsara, Gregory M Cooper, Carl Baker, Santhosh Girirajan, Jun Li, Devin Absher, Ronald M Krauss, Richard M Myers, Paul M Ridker, Daniel I Chasman,[...]. Am J Hum Genet 2009
419
5

Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
5


Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
5

Doc2alpha is an activity-dependent modulator of excitatory synaptic transmission.
G Sakaguchi, T Manabe, K Kobayashi, S Orita, T Sasaki, A Naito, M Maeda, H Igarashi, G Katsuura, H Nishioka,[...]. Eur J Neurosci 1999
49
6

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
681
5

Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
Megan R Glassford, Jill A Rosenfeld, Alexa A Freedman, Michael E Zwick, Jennifer G Mulle. Am J Med Genet A 2016
39
7

The complex behavioral phenotype of 15q13.3 microdeletion syndrome.
Mark N Ziats, Robin P Goin-Kochel, Leandra N Berry, May Ali, Jun Ge, Danielle Guffey, Jill A Rosenfeld, Patricia Bader, Michael J Gambello, Varina Wolf,[...]. Genet Med 2016
27
11

Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.
Derek J C Tai, Ashok Ragavendran, Poornima Manavalan, Alexei Stortchevoi, Catarina M Seabra, Serkan Erdin, Ryan L Collins, Ian Blumenthal, Xiaoli Chen, Yiping Shen,[...]. Nat Neurosci 2016
30
10

Evidence that duplications of 22q11.2 protect against schizophrenia.
E Rees, G Kirov, A Sanders, J T R Walters, K D Chambert, J Shi, J Szatkiewicz, C O'Dushlaine, A L Richards, E K Green,[...]. Mol Psychiatry 2014
85
5

A mouse model for Down syndrome exhibits learning and behaviour deficits.
R H Reeves, N G Irving, T H Moran, A Wohn, C Kitt, S S Sisodia, C Schmidt, R T Bronson, M T Davisson. Nat Genet 1995
674
5

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
5

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.
Hong Hua Li, Madhuri Roy, Unsal Kuscuoglu, Corinne M Spencer, Birgit Halm, Katharine C Harrison, Joseph H Bayle, Alessandra Splendore, Feng Ding, Leslie A Meltzer,[...]. EMBO Mol Med 2009
68
5

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
393
5

Behavioral alterations in rats prenatally exposed to valproic acid: animal model of autism.
Tomasz Schneider, Ryszard Przewłocki. Neuropsychopharmacology 2005
495
5

Structure and function of neonatal social communication in a genetic mouse model of autism.
T Takahashi, S Okabe, P Ó Broin, A Nishi, K Ye, M V Beckert, T Izumi, A Machida, G Kang, S Abe,[...]. Mol Psychiatry 2016
46
6

Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.
Mark R Etherton, Cory A Blaiss, Craig M Powell, Thomas C Südhof. Proc Natl Acad Sci U S A 2009
284
5

Applying the ARRIVE Guidelines to an In Vivo Database.
Natasha A Karp, Terry F Meehan, Hugh Morgan, Jeremy C Mason, Andrew Blake, Natalja Kurbatova, Damian Smedley, Julius Jacobsen, Richard F Mott, Vivek Iyer,[...]. PLoS Biol 2015
49
6

Down syndrome and the complexity of genome dosage imbalance.
Stylianos E Antonarakis. Nat Rev Genet 2017
116
5


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.