A citation-based method for searching scientific literature

Evelina Fedorenko, Angela Morgan, Elizabeth Murray, Annie Cardinaux, Cristina Mei, Helen Tager-Flusberg, Simon E Fisher, Nancy Kanwisher. Eur J Hum Genet 2016
Times Cited: 33







List of co-cited articles
230 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
42

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
128
30

Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
Gordana Raca, Becky S Baas, Salman Kirmani, Jennifer J Laffin, Craig A Jackson, Edythe A Strand, Kathy J Jakielski, Lawrence D Shriberg. Eur J Hum Genet 2013
35
27

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
Dianne F Newbury, Francesca Mari, Elham Sadighi Akha, Kay D Macdermot, Roberto Canitano, Anthony P Monaco, Jenny C Taylor, Alessandra Renieri, Simon E Fisher, Samantha J L Knight. Eur J Hum Genet 2013
27
29

Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria.
Samantha J Turner, Michael S Hildebrand, Susan Block, John Damiano, Michael Fahey, Sheena Reilly, Melanie Bahlo, Ingrid E Scheffer, Angela T Morgan. Am J Med Genet A 2013
42
24

De novo microdeletion of BCL11A is associated with severe speech sound disorder.
Beate Peter, Mark Matsushita, Kaori Oda, Wendy Raskind. Am J Med Genet A 2014
42
24

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
24

Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion.
Cristina Mei, Evelina Fedorenko, David J Amor, Amber Boys, Caitlyn Hoeflin, Peter Carew, Trent Burgess, Simon E Fisher, Angela T Morgan. Eur J Hum Genet 2018
18
44

Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization.
Jennifer J S Laffin, Gordana Raca, Craig A Jackson, Edythe A Strand, Kathy J Jakielski, Lawrence D Shriberg. Genet Med 2012
39
21

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

The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
Loyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, Aurélie Pain, Sandra Martin-Brevet, Carina Ferrari, Philippe Conus, Aurélien Macé, Nouchine Hadjikhani, Andres Metspalu,[...]. Biol Psychiatry 2016
49
21

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
Marwan Shinawi, Pengfei Liu, Sung-Hae L Kang, Joseph Shen, John W Belmont, Daryl A Scott, Frank J Probst, William J Craigen, Brett H Graham, Amber Pursley,[...]. J Med Genet 2010
317
21

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Kyle J Steinman, Sarah J Spence, Melissa B Ramocki, Monica B Proud, Sudha K Kessler, Elysa J Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K Chung,[...]. Am J Med Genet A 2016
70
21

GRIN2A: an aptly named gene for speech dysfunction.
Samantha J Turner, Angela K Mayes, Andrea Verhoeven, Simone A Mandelstam, Angela T Morgan, Ingrid E Scheffer. Neurology 2015
39
18

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
18

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

Speech sound disorder at 4 years: prevalence, comorbidities, and predictors in a community cohort of children.
Patricia Eadie, Angela Morgan, Obioha C Ukoumunne, Kyriaki Ttofari Eecen, Melissa Wake, Sheena Reilly. Dev Med Child Neurol 2015
56
18

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
15

Language fMRI abnormalities associated with FOXP2 gene mutation.
Frédérique Liégeois, Torsten Baldeweg, Alan Connelly, David G Gadian, Mortimer Mishkin, Faraneh Vargha-Khadem. Nat Neurosci 2003
191
15

Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech.
Beate Peter, Le Button, Carol Stoel-Gammon, Kathy Chapman, Wendy H Raskind. Clin Linguist Phon 2013
21
23

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
15

Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.
Lawrence D Shriberg, Nancy L Potter, Edythe A Strand. J Speech Lang Hear Res 2011
79
15



A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, Ellen Hanson, Anne M Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari, Zoltán Kutalik, Joris Andrieux,[...]. J Med Genet 2012
154
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

Speech and language in a genotyped cohort of individuals with Kabuki syndrome.
Angela T Morgan, Cristina Mei, Annette Da Costa, Joanne Fifer, Damien Lederer, Valérie Benoit, Margaret J McMillin, Kati J Buckingham, Michael J Bamshad, Kate Pope,[...]. Am J Med Genet A 2015
20
25


Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
15

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.
E K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, A van Haeringen, D E Fransen van de Putte, B-M Anderlid, J Lundin, P Lapunzina, L A Pérez Jurado, B Delle Chiaie,[...]. Eur J Med Genet 2009
168
15

Differential diagnosis of children with suspected childhood apraxia of speech.
Elizabeth Murray, Patricia McCabe, Robert Heard, Kirrie J Ballard. J Speech Lang Hear Res 2015
70
15

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.
Else Eising, Amaia Carrion-Castillo, Arianna Vino, Edythe A Strand, Kathy J Jakielski, Thomas S Scerri, Michael S Hildebrand, Richard Webster, Alan Ma, Bernard Mazoyer,[...]. Mol Psychiatry 2019
44
15

Insights into the genetic foundations of human communication.
Sarah A Graham, Pelagia Deriziotis, Simon E Fisher. Neuropsychol Rev 2015
13
30

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
12

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
12



FOXP2 as a molecular window into speech and language.
Simon E Fisher, Constance Scharff. Trends Genet 2009
269
12

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
12

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
12

Deciphering the genetic basis of speech and language disorders.
Simon E Fisher, Cecilia S L Lai, Anthony P Monaco. Annu Rev Neurosci 2003
88
12

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
Matthias Groszer, David A Keays, Robert M J Deacon, Joseph P de Bono, Shweta Prasad-Mulcare, Simone Gaub, Muriel G Baum, Catherine A French, Jérôme Nicod, Julie A Coventry,[...]. Curr Biol 2008
187
12

Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia.
Emma Belton, Claire H Salmond, Kate E Watkins, Faraneh Vargha-Khadem, David G Gadian. Hum Brain Mapp 2003
117
12

Genome-Wide Studies of Specific Language Impairment.
Rose H Reader, Laura E Covill, Ron Nudel, Dianne F Newbury. Curr Behav Neurosci Rep 2014
10
40

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
12

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
12

Extensions to the Speech Disorders Classification System (SDCS).
Lawrence D Shriberg, Marios Fourakis, Sheryl D Hall, Heather B Karlsson, Heather L Lohmeier, Jane L McSweeny, Nancy L Potter, Alison R Scheer-Cohen, Edythe A Strand, Christie M Tilkens,[...]. Clin Linguist Phon 2010
94
12

School-age follow-up of children with childhood apraxia of speech.
Barbara A Lewis, Lisa A Freebairn, Amy J Hansen, Sudha K Iyengar, H Gerry Taylor. Lang Speech Hear Serv Sch 2004
86
12


Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
461
12


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.