A citation-based method for searching scientific literature

Simon E Fisher, Constance Scharff. Trends Genet 2009
Times Cited: 269







List of co-cited articles
736 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
50

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
29

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
26

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
170
24

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
Wolfgang Enard, Sabine Gehre, Kurt Hammerschmidt, Sabine M Hölter, Torsten Blass, Mehmet Somel, Martina K Brückner, Christiane Schreiweis, Christine Winter, Reinhard Sohr,[...]. Cell 2009
277
23

Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.
Sebastian Haesler, Christelle Rochefort, Benjamin Georgi, Pawel Licznerski, Pavel Osten, Constance Scharff. PLoS Biol 2007
242
22

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
20

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.
Russell J Ferland, Timothy J Cherry, Patricia O Preware, Edward E Morrisey, Christopher A Walsh. J Comp Neurol 2003
331
20

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
19

Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability.
Malavika Murugan, Stephen Harward, Constance Scharff, Richard Mooney. Neuron 2013
80
23

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
19

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
Cecilia S L Lai, Dianne Gerrelli, Anthony P Monaco, Simon E Fisher, Andrew J Copp. Brain 2003
207
18

An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning.
C A French, X Jin, T G Campbell, E Gerfen, M Groszer, S E Fisher, R M Costa. Mol Psychiatry 2012
68
25

FoxP2 expression in avian vocal learners and non-learners.
Sebastian Haesler, Kazuhiro Wada, A Nshdejan, Edward E Morrisey, Thierry Lints, Eric D Jarvis, Constance Scharff. J Neurosci 2004
222
17

Human-specific transcriptional regulation of CNS development genes by FOXP2.
Genevieve Konopka, Jamee M Bomar, Kellen Winden, Giovanni Coppola, Zophonias O Jonsson, Fuying Gao, Sophia Peng, Todd M Preuss, James A Wohlschlegel, Daniel H Geschwind. Nature 2009
216
16

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
16

Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells.
Eriko Fujita, Yuko Tanabe, Akira Shiota, Masatsugu Ueda, Kiyotaka Suwa, Mariko Y Momoi, Takashi Momoi. Proc Natl Acad Sci U S A 2008
140
16

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
15



Molecular evolution of FOXP2, a gene involved in speech and language.
Wolfgang Enard, Molly Przeworski, Simon E Fisher, Cecilia S L Lai, Victor Wiebe, Takashi Kitano, Anthony P Monaco, Svante Pääbo. Nature 2002
628
15


Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene.
Weiguo Shu, Julie Y Cho, Yuhui Jiang, Minhua Zhang, Donald Weisz, Gregory A Elder, James Schmeidler, Rita De Gasperi, Miguel A Gama Sosa, Donald Rabidou,[...]. Proc Natl Acad Sci U S A 2005
253
14

Understanding Language from a Genomic Perspective.
Sarah A Graham, Simon E Fisher. Annu Rev Genet 2015
45
28

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
208
12

What can mice tell us about Foxp2 function?
Catherine A French, Simon E Fisher. Curr Opin Neurobiol 2014
42
28

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
560
11

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
70
15

FoxP2 regulates neurogenesis during embryonic cortical development.
David Tsui, John P Vessey, Hideaki Tomita, David R Kaplan, Freda D Miller. J Neurosci 2013
91
12

Decoding the genetics of speech and language.
Sarah A Graham, Simon E Fisher. Curr Opin Neurobiol 2013
79
13

FOXP2 and the neuroanatomy of speech and language.
Faraneh Vargha-Khadem, David G Gadian, Andrew Copp, Mortimer Mishkin. Nat Rev Neurosci 2005
214
11

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
Fadi F Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, Mathieu Langlois, Gila Foomani, Sylvia Dobrzeniecka, Marie-Odile Krebs, Ridha Joober,[...]. Am J Hum Genet 2010
141
10

Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.
Elliot Sollis, Sarah A Graham, Arianna Vino, Henning Froehlich, Maaike Vreeburg, Danai Dimitropoulou, Christian Gilissen, Rolph Pfundt, Gudrun A Rappold, Han G Brunner,[...]. Hum Mol Genet 2016
42
23

Expression of FOXP2 in the developing monkey forebrain: comparison with the expression of the genes FOXP1, PBX3, and MEIS2.
Kaoru Takahashi, Fu-Chin Liu, Takao Oishi, Takuma Mori, Noriyuki Higo, Motoharu Hayashi, Katsuiku Hirokawa, Hiroshi Takahashi. J Comp Neurol 2008
51
17

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
760
9

Conservation and diversity of Foxp2 expression in muroid rodents: functional implications.
Polly Campbell, Roger L Reep, Margaret L Stoll, Alexander G Ophir, Steven M Phelps. J Comp Neurol 2009
71
12

Birdsong and human speech: common themes and mechanisms.
A J Doupe, P K Kuhl. Annu Rev Neurosci 1999
838
9

Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum.
Kaoru Takahashi, Fu-Chin Liu, Katsuiku Hirokawa, Hiroshi Takahashi. J Neurosci Res 2003
119
9

Humanized Foxp2 specifically affects cortico-basal ganglia circuits.
S Reimers-Kipping, W Hevers, S Pääbo, W Enard. Neuroscience 2011
73
12


The structure of innate vocalizations in Foxp2-deficient mouse pups.
S Gaub, M Groszer, S E Fisher, G Ehret. Genes Brain Behav 2010
65
13

Knockdown of FoxP2 alters spine density in Area X of the zebra finch.
S B Schulz, S Haesler, C Scharff, C Rochefort. Genes Brain Behav 2010
65
13


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
9

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
26

A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice.
Jonathan Chabout, Abhra Sarkar, Sheel R Patel, Taylor Radden, David B Dunson, Simon E Fisher, Erich D Jarvis. Front Behav Neurosci 2016
48
18

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
8

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
19

De novo TBR1 mutations in sporadic autism disrupt protein functions.
Pelagia Deriziotis, Brian J O'Roak, Sarah A Graham, Sara B Estruch, Danai Dimitropoulou, Raphael A Bernier, Jennifer Gerdts, Jay Shendure, Evan E Eichler, Simon E Fisher. Nat Commun 2014
73
10

Assessing the effects of common variation in the FOXP2 gene on human brain structure.
Martine Hoogman, Tulio Guadalupe, Marcel P Zwiers, Patricia Klarenbeek, Clyde Francks, Simon E Fisher. Front Hum Neurosci 2014
23
34


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.