A citation-based method for searching scientific literature

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
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
44


Functional magnetic resonance imaging of chronic dysarthric speech after childhood brain injury: reliance on a left-hemisphere compensatory network.
Angela T Morgan, Richard Masterton, Lauren Pigdon, Alan Connelly, Frédérique J Liégeois. Brain 2013
23
33

Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia.
Angela T Morgan, Leenke van Haaften, Karen van Hulst, Carol Edley, Cristina Mei, Tiong Yang Tan, David Amor, Simon E Fisher, David A Koolen. Eur J Hum Genet 2018
11
45

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
27

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
27

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
22

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
22

Who to Refer for Speech Therapy at 4 Years of Age Versus Who to "Watch and Wait"?
Angela Morgan, Kyriaki Ttofari Eecen, Angela Pezic, Katherine Brommeyer, Cristina Mei, Patricia Eadie, Sheena Reilly, Barbara Dodd. J Pediatr 2017
22
22

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
22

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
22

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
16

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
16


Identifying and managing common childhood language and speech impairments.
Sheena Reilly, Cristina McKean, Angela Morgan, Melissa Wake. BMJ 2015
29
16

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
16

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
16

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
16

Cognitive and behavioral characterization of 16p11.2 deletion syndrome.
Ellen Hanson, Ramzi H Nasir, Alexa Fong, Alyss Lian, Rachel Hundley, Yiping Shen, Bai-Lin Wu, Ingrid A Holm, David T Miller. J Dev Behav Pediatr 2010
75
16

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
16

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
16

Understanding Language from a Genomic Perspective.
Sarah A Graham, Simon E Fisher. Annu Rev Genet 2015
45
16

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
16

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
16

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
16

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
16

Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays.
Beate Peter, Hope Lancaster, Caitlin Vose, Amna Fares, Isabelle Schrauwen, Matthew Huentelman. Am J Med Genet A 2017
13
15

Early neuroimaging markers of FOXP2 intragenic deletion.
Frédérique J Liégeois, Michael S Hildebrand, Alexandra Bonthrone, Samantha J Turner, Ingrid E Scheffer, Melanie Bahlo, Alan Connelly, Angela T Morgan. Sci Rep 2016
12
16

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
11

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
11

BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
Cristina Dias, Sara B Estruch, Sarah A Graham, Jeremy McRae, Stephen J Sawiak, Jane A Hurst, Shelagh K Joss, Susan E Holder, Jenny E V Morton, Claire Turner,[...]. Am J Hum Genet 2016
67
11

Motor and speech disorders in classic galactosemia.
Nancy L Potter, Yves Nievergelt, Lawrence D Shriberg. JIMD Rep 2013
35
11

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
11

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
11


Autism spectrum disorder and co-occurring developmental, psychiatric, and medical conditions among children in multiple populations of the United States.
Susan E Levy, Ellen Giarelli, Li-Ching Lee, Laura A Schieve, Russell S Kirby, Christopher Cunniff, Joyce Nicholas, Judy Reaven, Catherine E Rice. J Dev Behav Pediatr 2010
205
11

Phase 2 of CATALISE: a multinational and multidisciplinary Delphi consensus study of problems with language development: Terminology.
Dorothy V M Bishop, Margaret J Snowling, Paul A Thompson, Trisha Greenhalgh. J Child Psychol Psychiatry 2017
293
11

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
11

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
11

A motor speech assessment for children with severe speech disorders: reliability and validity evidence.
Edythe A Strand, Rebecca J McCauley, Stephen D Weigand, Ruth E Stoeckel, Becky S Baas. J Speech Lang Hear Res 2013
38
11

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
11

Developmental apraxia of speech: I. Descriptive and theoretical perspectives.
L D Shriberg, D M Aram, J Kwiatkowski. J Speech Lang Hear Res 1997
95
11

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
11

Data-driven subclassification of speech sound disorders in preschool children.
Jennell C Vick, Thomas F Campbell, Lawrence D Shriberg, Jordan R Green, Klaus Truemper, Heather Leavy Rusiewicz, Christopher A Moore. J Speech Lang Hear Res 2014
17
11

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
11

Interventions for childhood apraxia of speech.
Angela T Morgan, Elizabeth Murray, Frederique J Liégeois. Cochrane Database Syst Rev 2018
7
28

Clinical and molecular consequences of disease-associated de novo mutations in SATB2.
Hemant Bengani, Mark Handley, Mohsan Alvi, Rita Ibitoye, Melissa Lees, Sally Ann Lynch, Wayne Lam, Madeleine Fannemel, Ann Nordgren, H Malmgren,[...]. Genet Med 2017
24
11

Aetiology of childhood apraxia of speech: A clinical practice update for paediatricians.
Angela T Morgan, Richard Webster. J Paediatr Child Health 2018
7
28

FOXP2 as a molecular window into speech and language.
Simon E Fisher, Constance Scharff. Trends Genet 2009
269
11

Inhibition of Upf2-Dependent Nonsense-Mediated Decay Leads to Behavioral and Neurophysiological Abnormalities by Activating the Immune Response.
Jennifer L Johnson, Loredana Stoica, Yuwei Liu, Ping Jun Zhu, Abhisek Bhattacharya, Shelly A Buffington, Redwan Huq, N Tony Eissa, Ola Larsson, Bo T Porse,[...]. Neuron 2019
13
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.