A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
Christina N Vallianatos, Shigeki Iwase. Epigenomics 2015
78
50

Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%).
Elise B Robinson, Karestan C Koenen, Marie C McCormick, Kerim Munir, Victoria Hallett, Francesca Happé, Robert Plomin, Angelica Ronald. Arch Gen Psychiatry 2011
175
25

BoxPlotR: a web tool for generation of box plots.
Michaela Spitzer, Jan Wildenhain, Juri Rappsilber, Mike Tyers. Nat Methods 2014
323
25

AutDB: a gene reference resource for autism research.
Saumyendra N Basu, Ravi Kollu, Sharmila Banerjee-Basu. Nucleic Acids Res 2009
240
25

Social Cognition in Autism and Other Neurodevelopmental Disorders: A Co-twin Control Study.
J Isaksson, A Van't Westeinde, É Cauvet, R Kuja-Halkola, K Lundin, J Neufeld, C Willfors, S Bölte. J Autism Dev Disord 2019
9
25

Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism.
Valerie W Hu, Tewarit Sarachana, Kyung Soon Kim, AnhThu Nguyen, Shreya Kulkarni, Mara E Steinberg, Truong Luu, Yinglei Lai, Norman H Lee. Autism Res 2009
130
25


Phenotypic and genetic overlap between autistic traits at the extremes of the general population.
Angelica Ronald, Francesca Happé, Thomas S Price, Simon Baron-Cohen, Robert Plomin. J Am Acad Child Adolesc Psychiatry 2006
130
25

A multivariate twin study of autistic traits in 12-year-olds: testing the fractionable autism triad hypothesis.
Elise B Robinson, Karestan C Koenen, Marie C McCormick, Kerim Munir, Victoria Hallett, Francesca Happé, Robert Plomin, Angelica Ronald. Behav Genet 2012
47
25



Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk.
Brooke McKenna, Tanner Koomar, Kevin Vervier, Jamie Kremsreiter, Jacob J Michaelson. Cold Spring Harb Mol Case Stud 2018
5
25

SNPper: retrieval and analysis of human SNPs.
A Riva, I S Kohane. Bioinformatics 2002
109
25

A twin study of heritable and shared environmental contributions to autism.
Thomas W Frazier, Lee Thompson, Eric A Youngstrom, Paul Law, Antonio Y Hardan, Charis Eng, Nathan Morris. J Autism Dev Disord 2014
57
25

Autism as a strongly genetic disorder: evidence from a British twin study.
A Bailey, A Le Couteur, I Gottesman, P Bolton, E Simonoff, E Yuzda, M Rutter. Psychol Med 1995
25

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
25

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
25

Heritability of autism spectrum disorders: a meta-analysis of twin studies.
Beata Tick, Patrick Bolton, Francesca Happé, Michael Rutter, Frühling Rijsdijk. J Child Psychol Psychiatry 2016
262
25

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
25

Whole-exome sequencing in a family with a monozygotic twin pair concordant for autism spectrum disorder and a follow-up study.
Jun Egawa, Yuichiro Watanabe, Atsunori Sugimoto, Ayako Nunokawa, Masako Shibuya, Hirofumi Igeta, Emiko Inoue, Satoshi Hoya, Naoki Orime, Taketsugu Hayashi,[...]. Psychiatry Res 2015
4
25


Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
662
25


Shorter sleep duration is associated with social impairment and comorbidities in ASD.
Olivia J Veatch, James S Sutcliffe, Zachary E Warren, Brendan T Keenan, Melissa H Potter, Beth A Malow. Autism Res 2017
31
25

An Overview of Autism Spectrum Disorder, Heterogeneity and Treatment Options.
Anne Masi, Marilena M DeMayo, Nicholas Glozier, Adam J Guastella. Neurosci Bull 2017
169
25

SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine.
Abu Z Dayem Ullah, Jorge Oscanoa, Jun Wang, Ai Nagano, Nicholas R Lemoine, Claude Chelala. Nucleic Acids Res 2018
59
25

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
537
25

Examining the Association Between Autistic Traits and Atypical Sensory Reactivity: A Twin Study.
Mark J Taylor, Peik Gustafsson, Henrik Larsson, Christopher Gillberg, Sebastian Lundström, Paul Lichstenstein. J Am Acad Child Adolesc Psychiatry 2018
14
25

The Roots of Autism and ADHD Twin Study in Sweden (RATSS).
Sven Bölte, Charlotte Willfors, Steve Berggren, Joakim Norberg, Lina Poltrago, Katell Mevel, Christina Coco, Peter Fransson, Jacqueline Borg, Rouslan Sitnikov,[...]. Twin Res Hum Genet 2014
38
25

Genetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay.
Olivia J Veatch, Julie S Pendergast, Melissa J Allen, Roberta M Leu, Carl Hirschie Johnson, Sarah H Elsea, Beth A Malow. J Autism Dev Disord 2015
34
25

Genetic heritability and shared environmental factors among twin pairs with autism.
Joachim Hallmayer, Sue Cleveland, Andrea Torres, Jennifer Phillips, Brianne Cohen, Tiffany Torigoe, Janet Miller, Angie Fedele, Jack Collins, Karen Smith,[...]. Arch Gen Psychiatry 2011
971
25



Autism risk across generations: a population-based study of advancing grandpaternal and paternal age.
Emma M Frans, Sven Sandin, Abraham Reichenberg, Niklas Långström, Paul Lichtenstein, John J McGrath, Christina M Hultman. JAMA Psychiatry 2013
71
25

Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample.
Emma Colvert, Beata Tick, Fiona McEwen, Catherine Stewart, Sarah R Curran, Emma Woodhouse, Nicola Gillan, Victoria Hallett, Stephanie Lietz, Tracy Garnett,[...]. JAMA Psychiatry 2015
195
25

Autism spectrum disorders and autistic traits: a decade of new twin studies.
Angelica Ronald, Rosa A Hoekstra. Am J Med Genet B Neuropsychiatr Genet 2011
297
25

Diverse transcription factor binding features revealed by genome-wide ChIP-seq in C. elegans.
Wei Niu, Zhi John Lu, Mei Zhong, Mihail Sarov, John I Murray, Cathleen M Brdlik, Judith Janette, Chao Chen, Pedro Alves, Elicia Preston,[...]. Genome Res 2011
156
25

A functional link between the histone demethylase PHF8 and the transcription factor ZNF711 in X-linked mental retardation.
Daniela Kleine-Kohlbrecher, Jesper Christensen, Julien Vandamme, Iratxe Abarrategui, Mads Bak, Niels Tommerup, Xiaobing Shi, Or Gozani, Juri Rappsilber, Anna Elisabetta Salcini,[...]. Mol Cell 2010
138
25

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
Patrick S Tarpey, Raffaella Smith, Erin Pleasance, Annabel Whibley, Sarah Edkins, Claire Hardy, Sarah O'Meara, Calli Latimer, Ed Dicks, Andrew Menzies,[...]. Nat Genet 2009
398
25

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability.
Tjitske Kleefstra, Jamie M Kramer, Kornelia Neveling, Marjolein H Willemsen, Tom S Koemans, Lisenka E L M Vissers, Willemijn Wissink-Lindhout, Michaela Fenckova, Willem M R van den Akker, Nael Nadif Kasri,[...]. Am J Hum Genet 2012
139
25


Caenorhabditis elegans aristaless/Arx gene alr-1 restricts variable gene expression.
Irini Topalidou, Alexander van Oudenaarden, Martin Chalfie. Proc Natl Acad Sci U S A 2011
31
25

Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesis.
Gaëlle Friocourt, Shigeaki Kanatani, Hidenori Tabata, Masato Yozu, Takao Takahashi, Mary Antypa, Odile Raguénès, Jamel Chelly, Claude Férec, Kazunori Nakajima,[...]. J Neurosci 2008
83
25

Dynamic transcriptomes during neural differentiation of human embryonic stem cells revealed by short, long, and paired-end sequencing.
Jia Qian Wu, Lukas Habegger, Parinya Noisa, Anna Szekely, Caihong Qiu, Stephen Hutchison, Debasish Raha, Michael Egholm, Haifan Lin, Sherman Weissman,[...]. Proc Natl Acad Sci U S A 2010
131
25

Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia.
F E Abidi, L Holloway, C A Moore, D D Weaver, R J Simensen, R E Stevenson, R C Rogers, C E Schwartz. J Med Genet 2008
58
25

Neuron-specific knock-down of SMN1 causes neuron degeneration and death through an apoptotic mechanism.
Ivan Gallotta, Nadia Mazzarella, Alessandra Donato, Alessandro Esposito, Justin C Chaplin, Silvana Castro, Giuseppina Zampi, Giorgio S Battaglia, Massimo A Hilliard, Paolo Bazzicalupo,[...]. Hum Mol Genet 2016
15
25

The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases.
Shigeki Iwase, Fei Lan, Peter Bayliss, Luis de la Torre-Ubieta, Maite Huarte, Hank H Qi, Johnathan R Whetstine, Azad Bonni, Thomas M Roberts, Yang Shi. Cell 2007
455
25

Affinity purification of protein complexes in C. elegans.
Esther Zanin, Julien Dumont, Reto Gassmann, Iain Cheeseman, Paul Maddox, Shirin Bahmanyar, Ana Carvalho, Sherry Niessen, John R Yates, Karen Oegema,[...]. Methods Cell Biol 2011
20
25

JMJD-1.2/PHF8 controls axon guidance by regulating Hedgehog-like signaling.
Alba Redo Riveiro, Luca Mariani, Emily Malmberg, Pier Giorgio Amendola, Juhani Peltonen, Garry Wong, Anna Elisabetta Salcini. Development 2017
9
25

A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARX.
Loredana Poeta, Francesca Fusco, Denise Drongitis, Cheryl Shoubridge, Genesia Manganelli, Stefania Filosa, Mariateresa Paciolla, Monica Courtney, Patrick Collombat, Maria Brigida Lioi,[...]. Am J Hum Genet 2013
26
25


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.