A citation-based method for searching scientific literature

Dianne F Newbury, Laura Winchester, Laura Addis, Silvia Paracchini, Lyn-Louise Buckingham, Ann Clark, Wendy Cohen, Hilary Cowie, Katharina Dworzynski, Andrea Everitt, Ian M Goodyer, Elizabeth Hennessy, A David Kindley, Laura L Miller, Jamal Nasir, Anne O'Hare, Duncan Shaw, Zoe Simkin, Emily Simonoff, Vicky Slonims, Jocelynne Watson, Jiannis Ragoussis, Simon E Fisher, Jonathon R Seckl, Peter J Helms, Patrick F Bolton, Andrew Pickles, Gina Conti-Ramsden, Gillian Baird, Dorothy V M Bishop, Anthony P Monaco. Am J Hum Genet 2009
Times Cited: 101







List of co-cited articles
1029 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
65

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
44


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
36


DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
Tom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, Dianne F Newbury, Laura L Miller, Anthony P Monaco, Dorothy V M Bishop, Silvia Paracchini. Biol Psychiatry 2011
102
34

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
29

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
29

A major susceptibility locus for specific language impairment is located on 13q21.
Christopher W Bartlett, Judy F Flax, Mark W Logue, Veronica J Vieland, Anne S Bassett, Paula Tallal, Linda M Brzustowicz. Am J Hum Genet 2002
140
27

Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.
M Falcaro, A Pickles, D F Newbury, L Addis, E Banfield, S E Fisher, A P Monaco, Z Simkin, G Conti-Ramsden. Genes Brain Behav 2008
61
42

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

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
22

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
22


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
22

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

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
21

FOXP2 as a molecular window into speech and language.
Simon E Fisher, Constance Scharff. Trends Genet 2009
269
20

FOXP2 is not a major susceptibility gene for autism or specific language impairment.
D F Newbury, E Bonora, J A Lamb, S E Fisher, C S L Lai, G Baird, L Jannoun, V Slonims, C M Stott, M J Merricks,[...]. Am J Hum Genet 2002
149
20

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
48

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
19

Relations among speech, language, and reading disorders.
Bruce F Pennington, Dorothy V M Bishop. Annu Rev Psychol 2009
249
18

Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.
Christopher W Bartlett, Judy F Flax, Mark W Logue, Brett J Smith, Veronica J Vieland, Paula Tallal, Linda M Brzustowicz. Hum Hered 2004
65
27

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.
Natalie Cope, Denise Harold, Gary Hill, Valentina Moskvina, Jim Stevenson, Peter Holmans, Michael J Owen, Michael C O'Donovan, Julie Williams. Am J Hum Genet 2005
198
18


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
36

The Children's Test of Nonword Repetition: a test of phonological working memory.
S E Gathercole, C S Willis, A D Baddeley, H Emslie. Memory 1994
363
17


Localisation of a gene implicated in a severe speech and language disorder.
S E Fisher, F Vargha-Khadem, K E Watkins, A P Monaco, M E Pembrey. Nat Genet 1998
260
17

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
Silvia Paracchini, Colin D Steer, Lyn-Louise Buckingham, Andrew P Morris, Susan Ring, Thomas Scerri, John Stein, Marcus E Pembrey, Jiannis Ragoussis, Jean Golding,[...]. Am J Psychiatry 2008
92
18

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
32

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
16

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
Megan Y Dennis, Silvia Paracchini, Thomas S Scerri, Ludmila Prokunina-Olsson, Julian C Knight, Richard Wade-Martins, Penny Coggill, Stephan Beck, Eric D Green, Anthony P Monaco. PLoS Genet 2009
73
21

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.
Beate Peter, Wendy H Raskind, Mark Matsushita, Mark Lisowski, Tiffany Vu, Virginia W Berninger, Ellen M Wijsman, Zoran Brkanac. J Neurodev Disord 2011
74
21

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
27


Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.
Pia Villanueva, Dianne F Newbury, Lilian Jara, Zulema De Barbieri, Ghazala Mirza, Hernán M Palomino, María Angélica Fernández, Jean-Baptiste Cazier, Anthony P Monaco, Hernán Palomino. Eur J Hum Genet 2011
27
55

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
14

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
14

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Silvia Paracchini, Ankur Thomas, Sandra Castro, Cecilia Lai, Murugan Paramasivam, Yu Wang, Brendan J Keating, Jennifer M Taylor, Douglas F Hacking, Thomas Scerri,[...]. Hum Mol Genet 2006
173
14

Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation.
T C Bates, P A Lind, M Luciano, G W Montgomery, N G Martin, M J Wright. Mol Psychiatry 2010
56
25

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Heidi Anthoni, Marco Zucchelli, Hans Matsson, Bertram Müller-Myhsok, Ingegerd Fransson, Johannes Schumacher, Satu Massinen, Päivi Onkamo, Andreas Warnke, Heide Griesemann,[...]. Hum Mol Genet 2007
75
18

Decoding the genetics of speech and language.
Sarah A Graham, Simon E Fisher. Curr Opin Neurobiol 2013
79
17

Mutations in the lysosomal enzyme-targeting pathway and persistent stuttering.
Changsoo Kang, Sheikh Riazuddin, Jennifer Mundorff, Donna Krasnewich, Penelope Friedman, James C Mullikin, Dennis Drayna. N Engl J Med 2010
98
13

Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.
Lawrence D Shriberg, Kirrie J Ballard, J Bruce Tomblin, Joseph R Duffy, Katharine H Odell, Charles A Williams. J Speech Lang Hear Res 2006
94
13

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
13

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
Betul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, Abha R Gupta, Jesse F Abelson, Thomas M Morgan, Katarzyna Chawarska, Ami Klin, A Gulhan Ercan-Sencicek, Althea A Stillman,[...]. Am J Hum Genet 2008
375
13

Genetic basis of specific language impairment: evidence from a twin study.
D V Bishop, T North, C Donlan. Dev Med Child Neurol 1995
203
13

Heritable risk factors associated with language impairments.
J G Barry, I Yasin, D V M Bishop. Genes Brain Behav 2007
66
19

Recent advances in the genetics of language impairment.
Dianne F Newbury, Simon E Fisher, Anthony P Monaco. Genome Med 2010
55
23


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.