A citation-based method for searching scientific literature

Beate St Pourcain, Rolieke A M Cents, Andrew J O Whitehouse, Claire M A Haworth, Oliver S P Davis, Paul F O'Reilly, Susan Roulstone, Yvonne Wren, Qi W Ang, Fleur P Velders, David M Evans, John P Kemp, Nicole M Warrington, Laura Miller, Nicholas J Timpson, Susan M Ring, Frank C Verhulst, Albert Hofman, Fernando Rivadeneira, Emma L Meaburn, Thomas S Price, Philip S Dale, Demetris Pillas, Anneli Yliherva, Alina Rodriguez, Jean Golding, Vincent W V Jaddoe, Marjo-Riitta Jarvelin, Robert Plomin, Craig E Pennell, Henning Tiemeier, George Davey Smith. Nat Commun 2014
Times Cited: 42







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



Times Cited
  Times     Co-cited
Similarity


A forkhead-domain gene is mutated in a severe speech and language disorder.
C S Lai, S E Fisher, J A Hurst, F Vargha-Khadem, A P Monaco. Nature 2001
975
38

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
35

A genome-wide association study for reading and language abilities in two population cohorts.
M Luciano, D M Evans, N K Hansell, S E Medland, G W Montgomery, N G Martin, M J Wright, T C Bates. Genes Brain Behav 2013
49
35

Genome-wide screening for DNA variants associated with reading and language traits.
A Gialluisi, D F Newbury, E G Wilcutt, R K Olson, J C DeFries, W M Brandler, B F Pennington, S D Smith, T S Scerri, N H Simpson,[...]. Genes Brain Behav 2014
58
35

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
R Nudel, N H Simpson, G Baird, A O'Hare, G Conti-Ramsden, P F Bolton, E R Hennessy, S M Ring, G Davey Smith, C Francks,[...]. Genes Brain Behav 2014
41
31

Genome-wide association study of shared components of reading disability and language impairment.
J D Eicher, N R Powers, L L Miller, N Akshoomoff, D G Amaral, C S Bloss, O Libiger, N J Schork, B F Darst, B J Casey,[...]. Genes Brain Behav 2013
53
30

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
26

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.
Sonja C Vernes, Elizabeth Spiteri, Jérôme Nicod, Matthias Groszer, Jennifer M Taylor, Kay E Davies, Daniel H Geschwind, Simon E Fisher. Am J Hum Genet 2007
160
23

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia.
Katariina Hannula-Jouppi, Nina Kaminen-Ahola, Mikko Taipale, Ranja Eklund, Jaana Nopola-Hemmi, Helena Kääriäinen, Juha Kere. PLoS Genet 2005
206
23

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
23

A recent evolutionary change affects a regulatory element in the human FOXP2 gene.
Tomislav Maricic, Viola Günther, Oleg Georgiev, Sabine Gehre, Marija Curlin, Christiane Schreiweis, Ronald Naumann, Hernán A Burbano, Matthias Meyer, Carles Lalueza-Fox,[...]. Mol Biol Evol 2013
84
21

Decreased expression of axon-guidance receptors in the anterior cingulate cortex in autism.
Shiro Suda, Keiko Iwata, Chie Shimmura, Yosuke Kameno, Ayyappan Anitha, Ismail Thanseem, Kazuhiko Nakamura, Hideo Matsuzaki, Kenji J Tsuchiya, Genichi Sugihara,[...]. Mol Autism 2011
57
21

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
21

Decoding the genetics of speech and language.
Sarah A Graham, Simon E Fisher. Curr Opin Neurobiol 2013
79
19

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
Kay D MacDermot, Elena Bonora, Nuala Sykes, Anne-Marie Coupe, Cecilia S L Lai, Sonja C Vernes, Faraneh Vargha-Khadem, Fiona McKenzie, Robert L Smith, Anthony P Monaco,[...]. Am J Hum Genet 2005
249
19

The complete genome sequence of a Neanderthal from the Altai Mountains.
Kay Prüfer, Fernando Racimo, Nick Patterson, Flora Jay, Sriram Sankararaman, Susanna Sawyer, Anja Heinze, Gabriel Renaud, Peter H Sudmant, Cesare de Filippo,[...]. Nature 2014
845
19

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
Clyde Francks, Silvia Paracchini, Shelley D Smith, Alex J Richardson, Tom S Scerri, Lon R Cardon, Angela J Marlow, I Laurence MacPhie, Janet Walter, Bruce F Pennington,[...]. Am J Hum Genet 2004
166
19

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
19

Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.
Catherine M Stein, James H Schick, H Gerry Taylor, Lawrence D Shriberg, Christopher Millard, Amy Kundtz-Kluge, Karlie Russo, Nori Minich, Amy Hansen, Lisa A Freebairn,[...]. Am J Hum Genet 2004
93
16

A high-coverage genome sequence from an archaic Denisovan individual.
Matthias Meyer, Martin Kircher, Marie-Theres Gansauge, Heng Li, Fernando Racimo, Swapan Mallick, Joshua G Schraiber, Flora Jay, Kay Prüfer, Cesare de Filippo,[...]. Science 2012
821
16


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
16

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
Sonja C Vernes, Peter L Oliver, Elizabeth Spiteri, Helen E Lockstone, Rathi Puliyadi, Jennifer M Taylor, Joses Ho, Cedric Mombereau, Ariel Brewer, Ernesto Lowy,[...]. PLoS Genet 2011
170
16

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.
Patrice Roll, Sonja C Vernes, Nadine Bruneau, Jennifer Cillario, Magali Ponsole-Lenfant, Annick Massacrier, Gabrielle Rudolf, Manal Khalife, Edouard Hirsch, Simon E Fisher,[...]. Hum Mol Genet 2010
70
16

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.
Elizabeth Spiteri, Genevieve Konopka, Giovanni Coppola, Jamee Bomar, Michael Oldham, Jing Ou, Sonja C Vernes, Simon E Fisher, Bing Ren, Daniel H Geschwind. Am J Hum Genet 2007
172
16


Genome-wide association study of receptive language ability of 12-year-olds.
Nicole Harlaar, Emma L Meaburn, Marianna E Hayiou-Thomas, Oliver S P Davis, Sophia Docherty, Ken B Hanscombe, Claire M A Haworth, Thomas S Price, Maciej Trzaskowski, Philip S Dale,[...]. J Speech Lang Hear Res 2014
12
58

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
204
16

Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Nuala H Simpson, Fabiola Ceroni, Rose H Reader, Laura E Covill, Julian C Knight, Elizabeth R Hennessy, Patrick F Bolton, Gina Conti-Ramsden, Anne O'Hare, Gillian Baird,[...]. Eur J Hum Genet 2015
28
25


Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
Pía Villanueva, Ron Nudel, Alexander Hoischen, María Angélica Fernández, Nuala H Simpson, Christian Gilissen, Rose H Reader, Lillian Jara, María Magdalena Echeverry, Clyde Francks,[...]. PLoS Genet 2015
26
26

Human-specific transcriptional regulation of CNS development genes by FOXP2.
Genevieve Konopka, Jamee M Bomar, Kellen Winden, Giovanni Coppola, Zophonias O Jonsson, Fuying Gao, Sophia Peng, Todd M Preuss, James A Wohlschlegel, Daniel H Geschwind. Nature 2009
216
14

FOXP2 as a molecular window into speech and language.
Simon E Fisher, Constance Scharff. Trends Genet 2009
269
14

Molecular evolution of FOXP2, a gene involved in speech and language.
Wolfgang Enard, Molly Przeworski, Simon E Fisher, Cecilia S L Lai, Victor Wiebe, Takashi Kitano, Anthony P Monaco, Svante Pääbo. Nature 2002
628
14


Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.
L L Field, K Shumansky, J Ryan, D Truong, E Swiergala, B J Kaplan. Genes Brain Behav 2013
24
25

Prevalence of specific language impairment in kindergarten children.
J B Tomblin, N L Records, P Buckwalter, X Zhang, E Smith, M O'Brien. J Speech Lang Hear Res 1997
886
14

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
Mikko Taipale, Nina Kaminen, Jaana Nopola-Hemmi, Tuomas Haltia, Birgitta Myllyluoma, Heikki Lyytinen, Kurt Muller, Minna Kaaranen, Perttu J Lindsberg, Katariina Hannula-Jouppi,[...]. Proc Natl Acad Sci U S A 2003
223
14

Reading and language disorders: the importance of both quantity and quality.
Dianne F Newbury, Anthony P Monaco, Silvia Paracchini. Genes (Basel) 2014
21
28

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
760
14

Shining a light on CNTNAP2: complex functions to complex disorders.
Pedro Rodenas-Cuadrado, Joses Ho, Sonja C Vernes. Eur J Hum Genet 2014
136
14

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
Elizabeth A Worthey, Gordana Raca, Jennifer J Laffin, Brandon M Wilk, Jeremy M Harris, Kathy J Jakielski, David P Dimmock, Edythe A Strand, Lawrence D Shriberg. J Neurodev Disord 2013
43
14

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
323
14

Cohort Profile: the 'children of the 90s'--the index offspring of the Avon Longitudinal Study of Parents and Children.
Andy Boyd, Jean Golding, John Macleod, Debbie A Lawlor, Abigail Fraser, John Henderson, Lynn Molloy, Andy Ness, Susan Ring, George Davey Smith. Int J Epidemiol 2013
14

Association of the ROBO1 gene with reading disabilities in a family-based analysis.
C Tran, K G Wigg, K Zhang, T D Cate-Carter, E Kerr, L L Field, B J Kaplan, M W Lovett, C L Barr. Genes Brain Behav 2014
20
25

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Simon E Fisher, Clyde Francks, Angela J Marlow, I Laurence MacPhie, Dianne F Newbury, Lon R Cardon, Yumiko Ishikawa-Brush, Alex J Richardson, Joel B Talcott, Javier Gayán,[...]. Nat Genet 2002
175
11


Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.
Ashley A Scott-Van Zeeland, Brett S Abrahams, Ana I Alvarez-Retuerto, Lisa I Sonnenblick, Jeffrey D Rudie, Dara Ghahremani, Jeanette A Mumford, Russell A Poldrack, Mirella Dapretto, Daniel H Geschwind,[...]. Sci Transl Med 2010
167
11

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
Fadi F Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, Mathieu Langlois, Gila Foomani, Sylvia Dobrzeniecka, Marie-Odile Krebs, Ridha Joober,[...]. Am J Hum Genet 2010
141
11

Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain.
Guillermina López-Bendito, Nuria Flames, Le Ma, Coralie Fouquet, Thomas Di Meglio, Alain Chedotal, Marc Tessier-Lavigne, Oscar Marín. J Neurosci 2007
143
11


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.