A citation-based method for searching scientific literature

Elena A Repnikova, Dmitry A Lyalin, Kimberly McDonald, Caroline Astbury, Emily Hansen-Kiss, Linda D Cooley, Ruthann Pfau, Gail E Herman, Robert E Pyatt, Scott E Hickey. Eur J Med Genet 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
100

The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
482
100

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
922
100

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
100

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
100

Valproic acid silencing of ascl1b/Ascl1 results in the failure of serotonergic differentiation in a zebrafish model of fetal valproate syndrome.
John Jacob, Vanessa Ribes, Steven Moore, Sean C Constable, Noriaki Sasai, Sebastian S Gerety, Darren J Martin, Chris P Sergeant, David G Wilkinson, James Briscoe. Dis Model Mech 2014
20
50

Rate of de novo mutations and the importance of father's age to disease risk.
Augustine Kong, Michael L Frigge, Gisli Masson, Soren Besenbacher, Patrick Sulem, Gisli Magnusson, Sigurjon A Gudjonsson, Asgeir Sigurdsson, Aslaug Jonasdottir, Adalbjorg Jonasdottir,[...]. Nature 2012
50

Unexplained autism is frequently associated with low-level mosaic aneuploidy.
Y B Yurov, S G Vorsanova, I Y Iourov, I A Demidova, A K Beresheva, V S Kravetz, V V Monakhov, A D Kolotii, V Y Voinova-Ulas, N L Gorbachevskaya. J Med Genet 2007
80
50

Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders.
Aisling Mulligan, Richard J L Anney, Myra O'Regan, Wai Chen, Louise Butler, Michael Fitzgerald, Jan Buitelaar, Hans-Christoph Steinhausen, Aribert Rothenberger, Ruud Minderaa,[...]. J Autism Dev Disord 2009
128
50

Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males.
J Clayton-Smith, P Watson, S Ramsden, G C Black. Lancet 2000
117
50

Mapping a shared genetic basis for neurodevelopmental disorders.
Matthew Jensen, Santhosh Girirajan. Genome Med 2017
13
50

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
Yujun Shao, M L Cuccaro, E R Hauser, K L Raiford, M M Menold, C M Wolpert, S A Ravan, L Elston, K Decena, S L Donnelly,[...]. Am J Hum Genet 2003
242
50

Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.
F Gurrieri, A Battaglia, L Torrisi, R Tancredi, C Cavallaro, E Sangiorgi, G Neri. Neurology 1999
50
50

Examining and interpreting the female protective effect against autistic behavior.
Elise B Robinson, Paul Lichtenstein, Henrik Anckarsäter, Francesca Happé, Angelica Ronald. Proc Natl Acad Sci U S A 2013
193
50

Sex-specific serum biomarker patterns in adults with Asperger's syndrome.
E Schwarz, P C Guest, H Rahmoune, L Wang, Y Levin, E Ingudomnukul, L Ruta, L Kent, M Spain, S Baron-Cohen,[...]. Mol Psychiatry 2011
96
50

Increased female autosomal burden of rare copy number variants in human populations and in autism families.
G Desachy, L A Croen, A R Torres, M Kharrazi, G N Delorenze, G C Windham, C K Yoshida, L A Weiss. Mol Psychiatry 2015
24
50

Partial tetrasomy of chromosome 3q and mosaicism in a child with autism.
Guiomar Oliveira, Eunice Matoso, Astrid Vicente, Patricia Ribeiro, Carla Marques, Assunção Ataíde, Teresa Miguel, Jorge Saraiva, Isabel Carreira. J Autism Dev Disord 2003
8
50

Autism and maternally derived aberrations of chromosome 15q.
R J Schroer, M C Phelan, R C Michaelis, E C Crawford, S A Skinner, M Cuccaro, R J Simensen, J Bishop, C Skinner, D Fender,[...]. Am J Med Genet 1998
273
50

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.
A M Persico, L D'Agruma, N Maiorano, A Totaro, R Militerni, C Bravaccio, T H Wassink, C Schneider, R Melmed, S Trillo,[...]. Mol Psychiatry 2001
248
50

Kctd13 deletion reduces synaptic transmission via increased RhoA.
Christine Ochoa Escamilla, Irina Filonova, Angela K Walker, Zhong X Xuan, Roopashri Holehonnur, Felipe Espinosa, Shunan Liu, Summer B Thyme, Isabel A López-García, Dorian B Mendoza,[...]. Nature 2017
49
50

Autism: in search of susceptibility genes.
Janine A Lamb, Jeremy R Parr, Anthony J Bailey, Anthony P Monaco. Neuromolecular Med 2002
29
50


Autism.
Meng-Chuan Lai, Michael V Lombardo, Simon Baron-Cohen. Lancet 2014
892
50

Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.
Emily L Casanova, Julia L Sharp, Hrishikesh Chakraborty, Nahid Sultana Sumi, Manuel F Casanova. Mol Autism 2016
19
50

Role of UBE3A and ATP10A genes in autism susceptibility region 15q11-q13 in an Italian population: a positive replication for UBE3A.
Guia Guffanti, Luisa Strik Lievers, Maria Teresa Bonati, Margherita Marchi, Lupo Geronazzo, Nardo Nardocci, Margherita Estienne, Lidia Larizza, Fabio Macciardi, Silvia Russo. Psychiatry Res 2011
16
50

Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders.
Sofia Stamouli, Britt-Marie Anderlid, Charlotte Willfors, Bhooma Thiruvahindrapuram, John Wei, Steve Berggren, Ann Nordgren, Stephen W Scherer, Paul Lichtenstein, Kristiina Tammimies,[...]. Twin Res Hum Genet 2018
14
50

An Autism-Linked Mutation Disables Phosphorylation Control of UBE3A.
Jason J Yi, Janet Berrios, Jason M Newbern, William D Snider, Benjamin D Philpot, Klaus M Hahn, Mark J Zylka. Cell 2015
88
50



Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
50

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.
Sébastien Jacquemont, Bradley P Coe, Micha Hersch, Michael H Duyzend, Niklas Krumm, Sven Bergmann, Jacques S Beckmann, Jill A Rosenfeld, Evan E Eichler. Am J Hum Genet 2014
250
50

Sex Differences in Autism Spectrum Disorder: a Review.
Sarah L Ferri, Ted Abel, Edward S Brodkin. Curr Psychiatry Rep 2018
67
50

Investigation of modifier genes within copy number variations in Rett syndrome.
Rosangela Artuso, Filomena T Papa, Elisa Grillo, Mafalda Mucciolo, Dag H Yasui, Keith W Dunaway, Vittoria Disciglio, Maria A Mencarelli, Marzia Pollazzon, Michele Zappella,[...]. J Hum Genet 2011
18
50

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
Santhosh Girirajan, Megan Y Dennis, Carl Baker, Maika Malig, Bradley P Coe, Catarina D Campbell, Kenneth Mark, Tiffany H Vu, Can Alkan, Ze Cheng,[...]. Am J Hum Genet 2013
184
50

Autism risk factors: genes, environment, and gene-environment interactions.
Pauline Chaste, Marion Leboyer. Dialogues Clin Neurosci 2012
191
50

GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability.
F Bonnet-Brilhault, S Alirol, R Blanc, S Bazaud, S Marouillat, R-A Thépault, C R Andres, É Lemonnier, C Barthélémy, M Raynaud,[...]. Mol Psychiatry 2016
18
50

Sibling recurrence and the genetic epidemiology of autism.
John N Constantino, Yi Zhang, Thomas Frazier, Anna M Abbacchi, Paul Law. Am J Psychiatry 2010
256
50

Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb.
Andrew S McCallion, Erine Stames, Ronald A Conlon, Aravinda Chakravarti. Proc Natl Acad Sci U S A 2003
111
50

Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits.
Guomei Tang, Kathryn Gudsnuk, Sheng-Han Kuo, Marisa L Cotrina, Gorazd Rosoklija, Alexander Sosunov, Mark S Sonders, Ellen Kanter, Candace Castagna, Ai Yamamoto,[...]. Neuron 2014
501
50

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
50

Convergence of Sex Differences and the Neuroimmune System in Autism Spectrum Disorder.
Margaret M McCarthy, Christopher L Wright. Biol Psychiatry 2017
64
50

Variation in GABA-A subunit gene copy number in an autistic patient with mosaic 4 p duplication (p12p16).
Hiroaki Kakinuma, Mamoru Ozaki, Hitoshi Sato, Hiroaki Takahashi. Am J Med Genet B Neuropsychiatr Genet 2008
23
50

A Rare Variant Identified Within the GluN2B C-Terminus in a Patient with Autism Affects NMDA Receptor Surface Expression and Spine Density.
Shuxi Liu, Liang Zhou, Hongjie Yuan, Marta Vieira, Antonio Sanz-Clemente, John D Badger, Wei Lu, Stephen F Traynelis, Katherine W Roche. J Neurosci 2017
29
50

Maternal viral infection during pregnancy impairs development of fetal serotonergic neurons.
Takeshi Ohkawara, Takashi Katsuyama, Michiru Ida-Eto, Naoko Narita, Masaaki Narita. Brain Dev 2015
25
50

Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder.
Deidre R Krupp, Rebecca A Barnard, Yannis Duffourd, Sara A Evans, Ryan M Mulqueen, Raphael Bernier, Jean-Baptiste Rivière, Eric Fombonne, Brian J O'Roak. Am J Hum Genet 2017
75
50

Channelopathy pathogenesis in autism spectrum disorders.
Galina Schmunk, J Jay Gargus. Front Genet 2013
51
50

The Contribution of Mosaic Variants to Autism Spectrum Disorder.
Donald Freed, Jonathan Pevsner. PLoS Genet 2016
51
50

Increased signaling by the autism-related Engrailed-2 protein enhances dendritic branching and spine density, alters synaptic structural matching, and exaggerates protein synthesis.
Asma Soltani, Solène Lebrun, Gilles Carpentier, Giulia Zunino, Sandrine Chantepie, Auriane Maïza, Yuri Bozzi, Claire Desnos, François Darchen, Olivier Stettler. PLoS One 2017
10
50

Prenatal exposure to valproic acid leads to reduced expression of synaptic adhesion molecule neuroligin 3 in mice.
E Kolozsi, R N Mackenzie, F I Roullet, D deCatanzaro, J A Foster. Neuroscience 2009
71
50

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment.
Andrew J Schork, Hyejung Won, Vivek Appadurai, Ron Nudel, Mike Gandal, Olivier Delaneau, Malene Revsbech Christiansen, David M Hougaard, Marie Bækved-Hansen, Jonas Bybjerg-Grauholm,[...]. Nat Neurosci 2019
60
50


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.