A citation-based method for searching scientific literature

Sergey A Kornilov, Natalia Rakhlin, Roman Koposov, Maria Lee, Carolyn Yrigollen, Ahmet Okay Caglayan, James S Magnuson, Shrikant Mane, Joseph T Chang, Elena L Grigorenko. Pediatrics 2016
Times Cited: 19







List of co-cited articles
176 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
47

Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndrome.
Isabel Filges, Keiko Shimojima, Nobuhiko Okamoto, Benno Röthlisberger, Peter Weber, Andreas R Huber, Tsutomu Nishizawa, Alexandre N Datta, Peter Miny, Toshiyuki Yamamoto. J Med Genet 2011
46
42

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
36

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
31

372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.
Giuseppina Marseglia, Maria Rosaria Scordo, Chiara Pescucci, Genni Nannetti, Elisabetta Biagini, Valeria Scandurra, Francesca Gerundino, Alberto Magi, Matteo Benelli, Francesca Torricelli. Eur J Med Genet 2012
32
31

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
31

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
Xiaowei Sylvia Chen, Rose H Reader, Alexander Hoischen, Joris A Veltman, Nuala H Simpson, Clyde Francks, Dianne F Newbury, Simon E Fisher. Sci Rep 2017
42
31

12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.
Julien Thevenon, Patrick Callier, Joris Andrieux, Bruno Delobel, Albert David, Sylvie Sukno, Delphine Minot, Laure Mosca Anne, Nathalie Marle, Damien Sanlaville,[...]. Eur J Hum Genet 2013
43
26

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

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.
Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, Natalia Lozovaya, Audrey Labalme, Nadia Boutry-Kryza, Manal Salmi, Timur Tsintsadze, Laura Addis, Jacques Motte,[...]. Nat Genet 2013
246
21

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
21

Understanding Language from a Genomic Perspective.
Sarah A Graham, Simon E Fisher. Annu Rev Genet 2015
45
21

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
21


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
21

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
21

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
21

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
21

Common variation near ROBO2 is associated with expressive vocabulary in infancy.
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,[...]. Nat Commun 2014
42
21

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
21

Common variation within the SETBP1 gene is associated with reading-related skills and patterns of functional neural activation.
Meaghan V Perdue, Sara Mascheretti, Sergey A Kornilov, Kaja K Jasińska, Kayleigh Ryherd, W Einar Mencl, Stephen J Frost, Elena L Grigorenko, Kenneth R Pugh, Nicole Landi. Neuropsychologia 2019
7
57

Speech and Language: Translating the Genome.
Pelagia Deriziotis, Simon E Fisher. Trends Genet 2017
25
21

A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Mark A DePristo, Eric Banks, Ryan Poplin, Kiran V Garimella, Jared R Maguire, Christopher Hartl, Anthony A Philippakis, Guillermo del Angel, Manuel A Rivas, Matt Hanna,[...]. Nat Genet 2011
15

A map of human genome variation from population-scale sequencing.
Gonçalo R Abecasis, David Altshuler, Adam Auton, Lisa D Brooks, Richard M Durbin, Richard A Gibbs, Matt E Hurles, Gil A McVean. Nature 2010
15

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
15

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
15

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
15

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
15

DCDC2 is associated with reading disability and modulates neuronal development in the brain.
Haiying Meng, Shelley D Smith, Karl Hager, Matthew Held, Jonathan Liu, Richard K Olson, Bruce F Pennington, John C DeFries, Joel Gelernter, Thomas O'Reilly-Pol,[...]. Proc Natl Acad Sci U S A 2005
256
15

FOXP2 as a molecular window into speech and language.
Simon E Fisher, Constance Scharff. Trends Genet 2009
269
15

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
J Elia, X Gai, H M Xie, J C Perin, E Geiger, J T Glessner, M D'arcy, R deBerardinis, E Frackelton, C Kim,[...]. Mol Psychiatry 2010
352
15

GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
Gemma L Carvill, Brigid M Regan, Simone C Yendle, Brian J O'Roak, Natalia Lozovaya, Nadine Bruneau, Nail Burnashev, Adiba Khan, Joseph Cook, Eileen Geraghty,[...]. Nat Genet 2013
213
15

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
15

Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.
Elliot Sollis, Sarah A Graham, Arianna Vino, Henning Froehlich, Maaike Vreeburg, Danai Dimitropoulou, Christian Gilissen, Rolph Pfundt, Gudrun A Rappold, Han G Brunner,[...]. Hum Mol Genet 2016
42
15

Distribution and intensity of constraint in mammalian genomic sequence.
Gregory M Cooper, Eric A Stone, George Asimenos, Eric D Green, Serafim Batzoglou, Arend Sidow. Genome Res 2005
849
15

De novo TBR1 mutations in sporadic autism disrupt protein functions.
Pelagia Deriziotis, Brian J O'Roak, Sarah A Graham, Sara B Estruch, Danai Dimitropoulou, Raphael A Bernier, Jennifer Gerdts, Jay Shendure, Evan E Eichler, Simon E Fisher. Nat Commun 2014
73
15

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
15

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.
Sara B Estruch, Sarah A Graham, Swathi M Chinnappa, Pelagia Deriziotis, Simon E Fisher. J Neurodev Disord 2016
15
20

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.
Kevin A Strauss, Erik G Puffenberger, Matthew J Huentelman, Steven Gottlieb, Seth E Dobrin, Jennifer M Parod, Dietrich A Stephan, D Holmes Morton. N Engl J Med 2006
411
15

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.
P Devanna, X S Chen, J Ho, D Gajewski, S D Smith, A Gialluisi, C Francks, S E Fisher, D F Newbury, S C Vernes. Mol Psychiatry 2018
28
15

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.
Evelina Fedorenko, Angela Morgan, Elizabeth Murray, Annie Cardinaux, Cristina Mei, Helen Tager-Flusberg, Simon E Fisher, Nancy Kanwisher. Eur J Hum Genet 2016
33
15

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
15

FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
Miriam S Reuter, Angelika Riess, Ute Moog, Tracy A Briggs, Kate E Chandler, Anita Rauch, Miriam Stampfer, Katharina Steindl, Dieter Gläser, Pascal Joset,[...]. J Med Genet 2017
34
15

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
15

The COMT Val/Met polymorphism is associated with reading-related skills and consistent patterns of functional neural activation.
Nicole Landi, Stephen J Frost, W Einar Mencl, Jonathan L Preston, Leslie K Jacobsen, Maria Lee, Carolyn Yrigollen, Kenneth R Pugh, Elena L Grigorenko. Dev Sci 2013
18
16

Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutation.
Jung Min Ko, Byung Chan Lim, Ki Joong Kim, Yong Seung Hwang, Hye Won Ryu, Jung Ho Lee, Jon Su Kim, Jong-Hee Chae. Childs Nerv Syst 2013
20
15

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.
Heather C Whalley, Garret O'Connell, Jessika E Sussmann, Anna Peel, Andrew C Stanfield, Marianna E Hayiou-Thomas, Eve C Johnstone, Stephen M Lawrie, Andrew M McIntosh, Jeremy Hall. Am J Med Genet B Neuropsychiatr Genet 2011
65
15

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
15

Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Stephan Ripke, Colm O'Dushlaine, Kimberly Chambert, Jennifer L Moran, Anna K Kähler, Susanne Akterin, Sarah E Bergen, Ann L Collins, James J Crowley, Menachem Fromer,[...]. Nat Genet 2013
979
15

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
15


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.