A citation-based method for searching scientific literature

Dianne F Newbury, Nuala H Simpson, Paul A Thompson, Dorothy V M Bishop. Wellcome Open Res 2018
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Autism, language and communication in children with sex chromosome trisomies.
Dorothy V M Bishop, Patricia A Jacobs, Katherine Lachlan, Diana Wellesley, Angela Barnicoat, Patricia A Boyd, Alan Fryer, Prisca Middlemiss, Sarah Smithson, Kay Metcalfe,[...]. Arch Dis Child 2011
100
80

Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review.
Victoria Leggett, Patricia Jacobs, Kate Nation, Gaia Scerif, Dorothy V M Bishop. Dev Med Child Neurol 2010
116
80

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
60

Understanding Language from a Genomic Perspective.
Sarah A Graham, Simon E Fisher. Annu Rev Genet 2015
45
60

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
60

Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.
Judith L Ross, David P Roeltgen, Harvey Kushner, Andrew R Zinn, Allan Reiss, Martha Zeger Bardsley, Elizabeth McCauley, Nicole Tartaglia. Pediatrics 2012
90
60


A functional genetic link between distinct developmental language disorders.
Sonja C Vernes, Dianne F Newbury, Brett S Abrahams, Laura Winchester, Jérôme Nicod, Matthias Groszer, Maricela Alarcón, Peter L Oliver, Kay E Davies, Daniel H Geschwind,[...]. N Engl J Med 2008
390
60

Pathway-based association study of multiple candidate genes and multiple traits using structural equation models.
Hela Romdhani, Heungsun Hwang, Gilles Paradis, Marie-Helene Roy-Gagnon, Aurelie Labbe. Genet Epidemiol 2015
6
60

CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Dianne F Newbury, Laura Winchester, Laura Addis, Silvia Paracchini, Lyn-Louise Buckingham, Ann Clark, Wendy Cohen, Hilary Cowie, Katharina Dworzynski, Andrea Everitt,[...]. Am J Hum Genet 2009
101
60

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
D F Newbury, S Paracchini, T S Scerri, L Winchester, L Addis, Alex J Richardson, J Walter, J F Stein, J B Talcott, A P Monaco. Behav Genet 2011
132
60


Sex chromosome trisomies are not associated with atypical lateralization for language.
Alexander C Wilson, Dorothy V M Bishop. Dev Med Child Neurol 2018
5
60

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
Daniel J Weiner, Emilie M Wigdor, Stephan Ripke, Raymond K Walters, Jack A Kosmicki, Jakob Grove, Kaitlin E Samocha, Jacqueline I Goldstein, Aysu Okbay, Jonas Bybjerg-Grauholm,[...]. Nat Genet 2017
182
40


A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat Genet 2010
411
40


Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.
Maricela Alarcón, Brett S Abrahams, Jennifer L Stone, Jacqueline A Duvall, Julia V Perederiy, Jamee M Bomar, Jonathan Sebat, Michael Wigler, Christa L Martin, David H Ledbetter,[...]. Am J Hum Genet 2008
535
40


Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.
Chelsea Lowther, Marsha Speevak, Christine M Armour, Elaine S Goh, Gail E Graham, Chumei Li, Susan Zeesman, Malgorzata J M Nowaczyk, Lee-Anne Schultz, Antonella Morra,[...]. Genet Med 2017
37
40

A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population.
Andreas Pampanos, Konstantina Volaki, Emmanuel Kanavakis, Ourania Papandreou, Sotiris Youroukos, Loretta Thomaidis, Savvas Karkelis, Maria Tzetis, Sophia Kitsiou-Tzeli. Genet Test Mol Biomarkers 2009
35
40

What Causes Specific Language Impairment in Children?
Dorothy V M Bishop. Curr Dir Psychol Sci 2006
128
40

Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection.
Francesca Blasi, Elena Bacchelli, Giulia Pesaresi, Simona Carone, Anthony J Bailey, Elena Maestrini. Am J Med Genet B Neuropsychiatr Genet 2006
68
40

Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers.
Sylwia Chocholska, Eva Rossier, Gotthold Barbi, Hildegard Kehrer-Sawatzki. Am J Med Genet A 2006
46
40

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.
Frédéric Laumonnier, Frédérique Bonnet-Brilhault, Marie Gomot, Romuald Blanc, Albert David, Marie-Pierre Moizard, Martine Raynaud, Nathalie Ronce, Eric Lemonnier, Patrick Calvas,[...]. Am J Hum Genet 2004
507
40

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
Nuala H Simpson, Laura Addis, William M Brandler, Vicky Slonims, Ann Clark, Jocelynne Watson, Thomas S Scerri, Elizabeth R Hennessy, Patrick F Bolton, Gina Conti-Ramsden,[...]. Dev Med Child Neurol 2014
23
40

Data quality control in genetic case-control association studies.
Carl A Anderson, Fredrik H Pettersson, Geraldine M Clarke, Lon R Cardon, Andrew P Morris, Krina T Zondervan. Nat Protoc 2010
582
40

Connecting genes to brain in the autism spectrum disorders.
Brett S Abrahams, Daniel H Geschwind. Arch Neurol 2010
114
40

Genes that escape from X inactivation.
Joel B Berletch, Fan Yang, Jun Xu, Laura Carrel, Christine M Disteche. Hum Genet 2011
184
40

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
Dan E Arking, David J Cutler, Camille W Brune, Tanya M Teslovich, Kristen West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin, Edwin H Cook,[...]. Am J Hum Genet 2008
401
40

Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features.
J L Ross, N Tartaglia, D E Merry, M Dalva, A R Zinn. Genes Brain Behav 2015
35
40

Analysis of the neuroligin 4Y gene in patients with autism.
Jin Yan, Jinong Feng, Richard Schroer, Wenyan Li, Cindy Skinner, Charles E Schwartz, Edwin H Cook, Steve S Sommer. Psychiatr Genet 2008
53
40

Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.
M Macarov, M Zeigler, J P Newman, D Strich, V Sury, A Tennenbaum, V Meiner. J Intellect Disabil Res 2007
47
40

Logical and Methodological Issues Affecting Genetic Studies of Humans Reported in Top Neuroscience Journals.
Clara R Grabitz, Katherine S Button, Marcus R Munafò, Dianne F Newbury, Cyril R Pernet, Paul A Thompson, Dorothy V M Bishop. J Cogn Neurosci 2018
7
40

Genetic background effects in Neuroligin-3 mutant mice: Minimal behavioral abnormalities on C57 background.
Thomas C Jaramillo, Christine Ochoa Escamilla, Shunan Liu, Lauren Peca, Shari G Birnbaum, Craig M Powell. Autism Res 2018
13
40


Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder.
Kumiko Yanagi, Tadashi Kaname, Keiko Wakui, Ohiko Hashimoto, Yoshimitsu Fukushima, Kenji Naritomi. Autism Res Treat 2012
17
40

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism.
Z Talebizadeh, D Y Lam, M F Theodoro, D C Bittel, G H Lushington, M G Butler. J Med Genet 2006
117
40

The impact of nonverbal ability on prevalence and clinical presentation of language disorder: evidence from a population study.
Courtenay Frazier Norbury, Debbie Gooch, Charlotte Wray, Gillian Baird, Tony Charman, Emily Simonoff, George Vamvakas, Andrew Pickles. J Child Psychol Psychiatry 2016
155
40

Familial deletion within NLGN4 associated with autism and Tourette syndrome.
Amy Lawson-Yuen, Juan-Sebastian Saldivar, Steve Sommer, Jonathan Picker. Eur J Hum Genet 2008
182
40

Cognitive, behavioral, and neural consequences of sex chromosome aneuploidy.
Frida Printzlau, Jeanne Wolstencroft, David H Skuse. J Neurosci Res 2017
25
40

Neuroscience. Making synapses: a balancing act.
Natasha K Hussain, Morgan Sheng. Science 2005
19
40

CNTNAP2 variants affect early language development in the general population.
A J O Whitehouse, D V M Bishop, Q W Ang, C E Pennell, S E Fisher. Genes Brain Behav 2011
104
40

When the Lyon(ized chromosome) roars: ongoing expression from an inactive X chromosome.
Laura Carrel, Carolyn J Brown. Philos Trans R Soc Lond B Biol Sci 2017
31
40

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
40


Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2).
Zhuoyang Lu, M V V V Sekhar Reddy, Jianfang Liu, Ana Kalichava, Jiankang Liu, Lei Zhang, Fang Chen, Yun Wang, Luis Marcelo F Holthauzen, Mark A White,[...]. J Biol Chem 2016
29
40

Principal components analysis corrects for stratification in genome-wide association studies.
Alkes L Price, Nick J Patterson, Robert M Plenge, Michael E Weinblatt, Nancy A Shadick, David Reich. Nat Genet 2006
40

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.
John B Vincent, Debbie Kolozsvari, Wendy S Roberts, Patrick F Bolton, Hugh M D Gurling, Stephen W Scherer. Am J Med Genet B Neuropsychiatr Genet 2004
86
40

Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
Yanyan Liu, Yasong Du, Wenwen Liu, Caohua Yang, Yan Liu, Hongyan Wang, Xiaohong Gong. PLoS One 2013
18
40


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.