A citation-based method for searching scientific literature

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
Times Cited: 32







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



Times Cited
  Times     Co-cited
Similarity


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
78

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
316
50

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
971
43

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome.
Alexander Hoischen, Bregje W M van Bon, Christian Gilissen, Peer Arts, Bart van Lier, Marloes Steehouwer, Petra de Vries, Rick de Reuver, Nienke Wieskamp, Geert Mortier,[...]. Nat Genet 2010
318
40

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
653
28

A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay.
Sonia Bouquillon, Joris Andrieux, Emilie Landais, Bénédicte Duban-Bedu, Françoise Boidein, Bruno Lenne, Louis Vallée, Teresinha Leal, Martine Doco-Fenzy, Bruno Delobel. Eur J Med Genet 2011
17
41

FOXP2 as a molecular window into speech and language.
Simon E Fisher, Constance Scharff. Trends Genet 2009
267
21

Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map.
Ilse Feenstra, Lisenka E L M Vissers, Mirjam Orsel, Ad Geurts van Kessel, Han G Brunner, Joris A Veltman, Conny M A van Ravenswaaij-Arts. Am J Med Genet A 2007
91
18

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
389
18

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
18

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
754
18

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
190
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

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
247
18

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.
Rocco Piazza, Simona Valletta, Nils Winkelmann, Sara Redaelli, Roberta Spinelli, Alessandra Pirola, Laura Antolini, Luca Mologni, Carla Donadoni, Elli Papaemmanuil,[...]. Nat Genet 2013
239
18

Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.
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
17
35

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
30

Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndrome.
Karen Buysse, Björn Menten, Ann Oostra, Sylvie Tavernier, Geert R Mortier, Frank Speleman. Am J Med Genet A 2008
25
20

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

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction.
Ikuko Teramitsu, Lili C Kudo, Sarah E London, Daniel H Geschwind, Stephanie A White. J Neurosci 2004
220
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

MRI analysis of an inherited speech and language disorder: structural brain abnormalities.
K E Watkins, F Vargha-Khadem, J Ashburner, R E Passingham, A Connelly, K J Friston, R S J Frackowiak, M Mishkin, D G Gadian. Brain 2002
207
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

SRPX2 mutations in disorders of language cortex and cognition.
Patrice Roll, Gabrielle Rudolf, Sandrine Pereira, Barbara Royer, Ingrid E Scheffer, Annick Massacrier, Maria-Paola Valenti, Nathalie Roeckel-Trevisiol, Sarah Jamali, Christophe Beclin,[...]. Hum Mol Genet 2006
179
15


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
15

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
244
15

Progressive brain atrophy in Schinzel-Giedion syndrome with a SETBP1 mutation.
Akihito Takeuchi, Nobuhiko Okamoto, Shoko Fujinaga, Hirosuke Morita, Junya Shimizu, Tomoyuki Akiyama, Shinsuke Ninomiya, Jun-ichi Takanashi, Toshihide Kubo. Eur J Med Genet 2015
15
33

Schinzel-Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features.
Ellaine Carvalho, Rachel Honjo, Monize Magalhães, Guilherme Yamamoto, Katia Rocha, Michel Naslavsky, Mayana Zatz, Maria Rita Passos-Bueno, Chong Kim, Debora Bertola. Am J Med Genet A 2015
14
35

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
43
15

Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delay.
Jannine D Cody, Courtney Sebold, Amtul Malik, Patricia Heard, Erika Carter, Analisa Crandall, Bridgette Soileau, Margaret Semrud-Clikeman, Catherine M Cody, L Jean Hardies,[...]. Am J Med Genet A 2007
26
15

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
168
12

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
69
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
185
12

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
171
12

Decoding the genetics of speech and language.
Sarah A Graham, Simon E Fisher. Curr Opin Neurobiol 2013
79
12

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
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
116
12

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
148
12

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
103
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

Evo-devo, deep homology and FoxP2: implications for the evolution of speech and language.
Constance Scharff, Jana Petri. Philos Trans R Soc Lond B Biol Sci 2011
56
12

Somatic SETBP1 mutations in myeloid malignancies.
Hideki Makishima, Kenichi Yoshida, Nhu Nguyen, Bartlomiej Przychodzen, Masashi Sanada, Yusuke Okuno, Kwok Peng Ng, Kristbjorn O Gudmundsson, Bandana A Vishwakarma, Andres Jerez,[...]. Nat Genet 2013
170
12

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
12

De novo mutations in moderate or severe intellectual disability.
Fadi F Hamdan, Myriam Srour, Jose-Mario Capo-Chichi, Hussein Daoud, Christina Nassif, Lysanne Patry, Christine Massicotte, Amirthagowri Ambalavanan, Dan Spiegelman, Ousmane Diallo,[...]. PLoS Genet 2014
223
12

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
12

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

SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome.
K Suphapeetiporn, C Srichomthong, V Shotelersuk. Clin Genet 2011
20
20

West syndrome in a patient with Schinzel-Giedion syndrome.
Fuyu Miyake, Yukiko Kuroda, Takuya Naruto, Ikuko Ohashi, Kyoko Takano, Kenji Kurosawa. J Child Neurol 2015
12
33

Del(18)(q12.2q21.1) caused by a paternal sister chromatid rearrangement in a developmentally delayed girl.
Dieter Kotzot, Edda Haberlandt, Christine Fauth, Sara Baumgartner, Sabine Scholl-Bürgi, Gerd Utermann. Am J Med Genet A 2005
11
27


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.