A citation-based method for searching scientific literature

Peter A Perrino, Lidiya Talbot, Rose Kirkland, Amanda Hill, Amanda R Rendall, Hayley S Mountford, Jenny Taylor, Alexzandrea N Buscarello, Nayana Lahiri, Anand Saggar, R Holly Fitch, Dianne F Newbury. Commun Biol 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
J D Eudy, M D Weston, S Yao, D M Hoover, H L Rehm, M Ma-Edmonds, D Yan, I Ahmad, J J Cheng, C Ayuso,[...]. Science 1998
272
50

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells.
Xiaoqing Liu, Oleg V Bulgakov, Keith N Darrow, Basil Pawlyk, Michael Adamian, M Charles Liberman, Tiansen Li. Proc Natl Acad Sci U S A 2007
149
50

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Michael D Weston, Mirjam W J Luijendijk, Kurt D Humphrey, Claes Möller, William J Kimberling. Am J Hum Genet 2004
210
50

Lifelong plasticity in the rat auditory cortex: basic mechanisms and role of sensory experience.
Etienne de Villers-Sidani, Michael M Merzenich. Prog Brain Res 2011
71
50

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
Inga Ebermann, Hendrik P N Scholl, Peter Charbel Issa, Elvir Becirovic, Jürgen Lamprecht, Bernhard Jurklies, José M Millán, Elena Aller, Diana Mitter, Hanno Bolz. Hum Genet 2007
154
50

Sensory Neuron Diversity in the Inner Ear Is Shaped by Activity.
Brikha R Shrestha, Chester Chia, Lorna Wu, Sharon G Kujawa, M Charles Liberman, Lisa V Goodrich. Cell 2018
101
50

Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction.
Baptiste Libé-Philippot, Vincent Michel, Jacques Boutet de Monvel, Sébastien Le Gal, Typhaine Dupont, Paul Avan, Christine Métin, Nicolas Michalski, Christine Petit. Proc Natl Acad Sci U S A 2017
19
50

Hair-Bundle Links: Genetics as the Gateway to Function.
Guy P Richardson, Christine Petit. Cold Spring Harb Perspect Med 2019
19
50

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.
Angeles Mencía, Silvia Modamio-Høybjør, Nick Redshaw, Matías Morín, Fernando Mayo-Merino, Leticia Olavarrieta, Luis A Aguirre, Ignacio del Castillo, Karen P Steel, Tamas Dalmay,[...]. Nat Genet 2009
360
50

Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
Mark I McCarthy, Gonçalo R Abecasis, Lon R Cardon, David B Goldstein, Julian Little, John P A Ioannidis, Joel N Hirschhorn. Nat Rev Genet 2008
25

A case of 17q21.31 microduplication and 7q31.33 microdeletion, associated with developmental delay, microcephaly, and mild dysmorphic features.
Adrian Mc Cormack, Juliet Taylor, Leah Te Weehi, Donald R Love, Alice M George. Case Rep Genet 2014
6
25

LocusZoom: regional visualization of genome-wide association scan results.
Randall J Pruim, Ryan P Welch, Serena Sanna, Tanya M Teslovich, Peter S Chines, Terry P Gliedt, Michael Boehnke, Gonçalo R Abecasis, Cristen J Willer. Bioinformatics 2010
25

PCSK6 is associated with handedness in individuals with dyslexia.
Thomas S Scerri, William M Brandler, Silvia Paracchini, Andrew P Morris, Susan M Ring, Alex J Richardson, Joel B Talcott, John Stein, Anthony P Monaco. Hum Mol Genet 2011
89
25

Imprinted genes and mental dysfunction.
W Davies, A R Isles, L S Wilkinson. Ann Med 2001
40
25

Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins.
Angela M Reiersen, John N Constantino, Marisa Grimmer, Nicholas G Martin, Richard D Todd. Twin Res Hum Genet 2008
95
25

Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree.
Sahar V Mozaffari, Jeanne M DeCara, Sanjiv J Shah, Carlo Sidore, Edoardo Fiorillo, Francesco Cucca, Roberto M Lang, Dan L Nicolae, Carole Ober. Commun Biol 2019
5
25



PhenoScanner V2: an expanded tool for searching human genotype-phenotype associations.
Mihir A Kamat, James A Blackshaw, Robin Young, Praveen Surendran, Stephen Burgess, John Danesh, Adam S Butterworth, James R Staley. Bioinformatics 2019
134
25


What Causes Specific Language Impairment in Children?
Dorothy V M Bishop. Curr Dir Psychol Sci 2006
128
25

Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk.
Ron Nudel, Camilla A J Christiani, Jessica Ohland, Md Jamal Uddin, Nicoline Hemager, Ditte V Ellersgaard, Katrine S Spang, Birgitte K Burton, Aja N Greve, Ditte L Gantriis,[...]. Autism Res 2020
2
50

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
25

Clinical features of microdeletion 9q22.3 (pat).
K Shimojima, M Adachi, M Tanaka, Y Tanaka, K Kurosawa, T Yamamoto. Clin Genet 2009
19
25

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
25

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
25

The SNAP-25 gene is associated with cognitive ability: evidence from a family-based study in two independent Dutch cohorts.
M F Gosso, E J C de Geus, M J van Belzen, T J C Polderman, P Heutink, D I Boomsma, D Posthuma. Mol Psychiatry 2006
54
25

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype.
Marcella Zollino, Daniela Orteschi, Marina Murdolo, Serena Lattante, Domenica Battaglia, Chiara Stefanini, Eugenio Mercuri, Pietro Chiurazzi, Giovanni Neri, Giuseppe Marangi. Nat Genet 2012
91
25

Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements.
Trilochan Sahoo, Jia-Chi Wang, Mohamed M Elnaggar, Pedro Sanchez-Lara, Leslie P Ross, Loretta W Mahon, Katayoun Hafezi, Abigail Deming, Lynne Hinman, Yovana Bruno,[...]. Eur J Hum Genet 2015
18
25

A general test of association for quantitative traits in nuclear families.
G R Abecasis, L R Cardon, W O Cookson. Am J Hum Genet 2000
915
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

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.
Gonçalo R Abecasis, Stacey S Cherny, William O Cookson, Lon R Cardon. Nat Genet 2002
25

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
25

Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data.
J Kaufman, B Birmaher, D Brent, U Rao, C Flynn, P Moreci, D Williamson, N Ryan. J Am Acad Child Adolesc Psychiatry 1997
25

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
25

Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil.
Gustavo R Nascimento, Irene P Pinto, Aldaires V de Melo, Damiana M da Cruz, Cristiano L Ribeiro, Claudio C da Silva, Aparecido D da Cruz, Lysa B Minasi. Mol Syndromol 2017
3
33


Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.
Tanja Zeller, Philipp Wild, Silke Szymczak, Maxime Rotival, Arne Schillert, Raphaele Castagne, Seraya Maouche, Marine Germain, Karl Lackner, Heidi Rossmann,[...]. PLoS One 2010
473
25

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
S Hong Lee, Stephan Ripke, Benjamin M Neale, Stephen V Faraone, Shaun M Purcell, Roy H Perlis, Bryan J Mowry, Anita Thapar, Michael E Goddard, John S Witte,[...]. Nat Genet 2013
25


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
25

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
25

A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13.
P D Evans, K L Mueller, E R Gamazon, N J Cox, J B Tomblin. Genes Brain Behav 2015
3
33

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index.
Clive J Hoggart, Giulia Venturini, Massimo Mangino, Felicia Gomez, Giulia Ascari, Jing Hua Zhao, Alexander Teumer, Thomas W Winkler, Natalia Tšernikova, Jian'an Luan,[...]. PLoS Genet 2014
40
25


Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders.
Kari M Ersland, Andrea Christoforou, Christine Stansberg, Thomas Espeseth, Manuel Mattheisen, Morten Mattingsdal, Gudmundur A Hardarson, Thomas Hansen, Carla P D Fernandes, Sudheer Giddaluru,[...]. PLoS One 2012
31
25

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.
Kerry A Pettigrew, Emily Frinton, Ron Nudel, May T M Chan, Paul Thompson, Marianna E Hayiou-Thomas, Joel B Talcott, John Stein, Anthony P Monaco, Charles Hulme,[...]. J Neurodev Disord 2016
16
25

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
25

A genome-wide scan for common alleles affecting risk for autism.
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams, Nuala Sykes, Alistair T Pagnamenta,[...]. Hum Mol Genet 2010
396
25

FOXP2.
Ron Nudel, Dianne F Newbury. Wiley Interdiscip Rev Cogn Sci 2013
13
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.