A citation-based method for searching scientific literature

Ashley P L Marsh, Delphine Heron, Timothy J Edwards, Angélique Quartier, Charles Galea, Caroline Nava, Agnès Rastetter, Marie-Laure Moutard, Vicki Anderson, Pierre Bitoun, Jens Bunt, Anne Faudet, Catherine Garel, Greta Gillies, Ilan Gobius, Justine Guegan, Solveig Heide, Boris Keren, Fabien Lesne, Vesna Lukic, Simone A Mandelstam, George McGillivray, Alissandra McIlroy, Aurélie Méneret, Cyril Mignot, Laura R Morcom, Sylvie Odent, Annalisa Paolino, Kate Pope, Florence Riant, Gail A Robinson, Megan Spencer-Smith, Myriam Srour, Sarah E M Stephenson, Rick Tankard, Oriane Trouillard, Quentin Welniarz, Amanda Wood, Alexis Brice, Guy Rouleau, Tania Attié-Bitach, Martin B Delatycki, Jean-Louis Mandel, David J Amor, Emmanuel Roze, Amélie Piton, Melanie Bahlo, Thierry Billette de Villemeur, Elliott H Sherr, Richard J Leventer, Linda J Richards, Paul J Lockhart, Christel Depienne. Nat Genet 2017
Times Cited: 48







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



Times Cited
  Times     Co-cited
Similarity


Mutations in DCC cause congenital mirror movements.
Myriam Srour, Jean-Baptiste Rivière, Jessica M T Pham, Marie-Pierre Dubé, Simon Girard, Steves Morin, Patrick A Dion, Géraldine Asselin, Daniel Rochefort, Pascale Hince,[...]. Science 2010
104
39

Biallelic mutations in human DCC cause developmental split-brain syndrome.
Saumya S Jamuar, Klaus Schmitz-Abe, Alissa M D'Gama, Marie Drottar, Wai-Man Chan, Maya Peeva, Sarah Servattalab, Anh-Thu N Lam, Mauricio R Delgado, Nancy J Clegg,[...]. Nat Genet 2017
30
63

Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene.
A Fazeli, S L Dickinson, M L Hermiston, R V Tighe, R G Steen, C G Small, E T Stoeckli, K Keino-Masu, M Masu, H Rayburn,[...]. Nature 1997
625
29

DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.
Ashley P L Marsh, Timothy J Edwards, Charles Galea, Helen M Cooper, Elizabeth C Engle, Saumya S Jamuar, Aurélie Méneret, Marie-Laure Moutard, Caroline Nava, Agnès Rastetter,[...]. Hum Mutat 2018
23
52

Deleted in Colorectal Cancer (DCC) encodes a netrin receptor.
K Keino-Masu, M Masu, L Hinck, E D Leonardo, S S Chan, J G Culotti, M Tessier-Lavigne. Cell 1996
807
22

Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity.
Lynn K Paul, Warren S Brown, Ralph Adolphs, J Michael Tyszka, Linda J Richards, Pratik Mukherjee, Elliott H Sherr. Nat Rev Neurosci 2007
463
22

Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline.
Quentin Welniarz, Marie-Pierre Morel, Oriane Pourchet, Cécile Gallea, Jean-Charles Lamy, Massimo Cincotta, Mohamed Doulazmi, Morgane Belle, Aurélie Méneret, Oriane Trouillard,[...]. Sci Rep 2017
19
52

Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.
Timothy J Edwards, Elliott H Sherr, A James Barkovich, Linda J Richards. Brain 2014
155
18

The netrin 1 receptors Unc5h3 and Dcc are necessary at multiple choice points for the guidance of corticospinal tract axons.
Jacqueline H Finger, Rod T Bronson, Belinda Harris, Kenneth Johnson, Stefan A Przyborski, Susan L Ackerman. J Neurosci 2002
127
14

A novel DCC mutation and genetic heterogeneity in congenital mirror movements.
C Depienne, M Cincotta, S Billot, D Bouteiller, S Groppa, V Brochard, C Flamand, C Hubsch, S Meunier, F Giovannelli,[...]. Neurology 2011
52
14

Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system.
T Serafini, S A Colamarino, E D Leonardo, H Wang, R Beddington, W C Skarnes, M Tessier-Lavigne. Cell 1996
989
14

Netrin-DCC signaling regulates corpus callosum formation through attraction of pioneering axons and by modulating Slit2-mediated repulsion.
Thomas Fothergill, Amber-Lee S Donahoo, Amelia Douglass, Oressia Zalucki, Jiajia Yuan, Tianzhi Shu, Geoffrey J Goodhill, Linda J Richards. Cereb Cortex 2014
55
14

Netrins are diffusible chemotropic factors for commissural axons in the embryonic spinal cord.
T E Kennedy, T Serafini, J R de la Torre, M Tessier-Lavigne. Cell 1994
14

Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations.
Elizabeth A Franz, Rachel Chiaroni-Clarke, Stephanie Woodrow, Kelly A Glendining, Christine L Jasoni, Stephen P Robertson, R J McKinlay Gardner, David Markie. J Neurol Sci 2015
18
38

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.
Aurélie Méneret, Christel Depienne, Florence Riant, Oriane Trouillard, Delphine Bouteiller, Massimo Cincotta, Pierre Bitoun, Julia Wickert, Isabelle Lagroua, Ana Westenberger,[...]. Neurology 2014
34
20

Netrin1 Produced by Neural Progenitors, Not Floor Plate Cells, Is Required for Axon Guidance in the Spinal Cord.
Supraja G Varadarajan, Jennifer H Kong, Keith D Phan, Tzu-Jen Kao, S Carmen Panaitof, Julie Cardin, Holger Eltzschig, Artur Kania, Bennett G Novitch, Samantha J Butler. Neuron 2017
94
14

RAD51 haploinsufficiency causes congenital mirror movements in humans.
Christel Depienne, Delphine Bouteiller, Aurélie Méneret, Ségolène Billot, Sergiu Groppa, Stephan Klebe, Fanny Charbonnier-Beaupel, Jean-Christophe Corvol, Jean-Paul Saraiva, Norbert Brueggemann,[...]. Am J Hum Genet 2012
49
14

Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.
Francesco D'Antonio, Giorgio Pagani, Alessandra Familiari, Asma Khalil, Tally-Lerman Sagies, Gustavo Malinger, Zvi Leibovitz, Catherine Garel, Marie Laure Moutard, Gianluigi Pilu,[...]. Pediatrics 2016
59
14

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
14

Floor-plate-derived netrin-1 is dispensable for commissural axon guidance.
Chloé Dominici, Juan Antonio Moreno-Bravo, Sergi Roig Puiggros, Quentin Rappeneau, Nicolas Rama, Pauline Vieugue, Agnes Bernet, Patrick Mehlen, Alain Chédotal. Nature 2017
101
12

Neural migration. Structures of netrin-1 bound to two receptors provide insight into its axon guidance mechanism.
Kai Xu, Zhuhao Wu, Nicolas Renier, Alexander Antipenko, Dorothea Tzvetkova-Robev, Yan Xu, Maria Minchenko, Vincenzo Nardi-Dei, Kanagalaghatta R Rajashankar, Juha Himanen,[...]. Science 2014
107
12

Mutations in the netrin-1 gene cause congenital mirror movements.
Aurélie Méneret, Elizabeth A Franz, Oriane Trouillard, Thomas C Oliver, Yvrick Zagar, Stephen P Robertson, Quentin Welniarz, R J MacKinlay Gardner, Cécile Gallea, Myriam Srour,[...]. J Clin Invest 2017
21
28

DCC mediated axon guidance of spinal interneurons is essential for normal locomotor central pattern generator function.
Nadine Rabe Bernhardt, Fatima Memic, Henrik Gezelius, Anja-Lena Thiebes, Anna Vallstedt, Klas Kullander. Dev Biol 2012
32
15

Deleted in colorectal carcinoma suppresses metastasis in p53-deficient mammary tumours.
Paul Krimpenfort, Ji-Ying Song, Natalie Proost, John Zevenhoven, Jos Jonkers, Anton Berns. Nature 2012
64
10

Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder.
Iltaf Ahmed, Kirti Mittal, Taimoor I Sheikh, Nasim Vasli, Muhammad Arshad Rafiq, Anna Mikhailov, Mehrnaz Ohadi, Huda Mahmood, Guy A Rouleau, Attya Bhatti,[...]. Hum Genet 2014
13
38

Mirror movements after childhood hemiparesis.
B T Woods, H L Teuber. Neurology 1978
165
10

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
10

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
10

Agenesis of the corpus callosum in California 1983-2003: a population-based study.
Hannah C Glass, Gary M Shaw, Chen Ma, Elliott H Sherr. Am J Med Genet A 2008
122
10

Unc5C and DCC act downstream of Ctip2 and Satb2 and contribute to corpus callosum formation.
Swathi Srivatsa, Srinivas Parthasarathy, Olga Britanova, Ingo Bormuth, Amber-Lee Donahoo, Susan L Ackerman, Linda J Richards, Victor Tarabykin. Nat Commun 2014
37
10

The crystal structure of netrin-1 in complex with DCC reveals the bifunctionality of netrin-1 as a guidance cue.
Lorenzo I Finci, Nina Krüger, Xiaqin Sun, Jie Zhang, Magda Chegkazi, Yu Wu, Gundolf Schenk, Haydyn D T Mertens, Dmitri I Svergun, Yan Zhang,[...]. Neuron 2014
66
8


RAD51 deficiency disrupts the corticospinal lateralization of motor control.
Cécile Gallea, Traian Popa, Cécile Hubsch, Romain Valabregue, Vanessa Brochard, Prantik Kundu, Benoît Schmitt, Eric Bardinet, Eric Bertasi, Constance Flamand-Roze,[...]. Brain 2013
37
10

dcc orchestrates the development of the prefrontal cortex during adolescence and is altered in psychiatric patients.
C Manitt, C Eng, M Pokinko, R T Ryan, A Torres-Berrío, J P Lopez, S V Yogendran, M J J Daubaras, A Grant, E R E Schmidt,[...]. Transl Psychiatry 2013
58
8

DCC Confers Susceptibility to Depression-like Behaviors in Humans and Mice and Is Regulated by miR-218.
Angélica Torres-Berrío, Juan Pablo Lopez, Rosemary C Bagot, Dominique Nouel, Gregory Dal Bo, Santiago Cuesta, Lei Zhu, Colleen Manitt, Conrad Eng, Helen M Cooper,[...]. Biol Psychiatry 2017
56
8


Neurophysiology of unimanual motor control and mirror movements.
M Cincotta, U Ziemann. Clin Neurophysiol 2008
140
8

Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum.
Loubna Jouan, Bouchra Ouled Amar Bencheikh, Hussein Daoud, Alexandre Dionne-Laporte, Sylvia Dobrzeniecka, Dan Spiegelman, Daniel Rochefort, Pascale Hince, Anna Szuto, Maryse Lassonde,[...]. Eur J Hum Genet 2016
16
25

Outcome of isolated agenesis of the corpus callosum: A population-based prospective study.
Vincent des Portes, Anne Rolland, Juan Velazquez-Dominguez, Emeline Peyric, Marie-Pierre Cordier, Pascal Gaucherand, Jérôme Massardier, Mona Massoud, Aurore Curie, Anne-Sophie Pellot,[...]. Eur J Paediatr Neurol 2018
18
22

Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum.
Ilan Gobius, Laura Morcom, Rodrigo Suárez, Jens Bunt, Polina Bukshpun, William Reardon, William B Dobyns, John L R Rubenstein, A James Barkovich, Elliott H Sherr,[...]. Cell Rep 2016
40
10



Signaling switch of the axon guidance receptor Robo3 during vertebrate evolution.
Pavol Zelina, Heike Blockus, Yvrick Zagar, Amélie Péres, François Friocourt, Zhuhao Wu, Nicolas Rama, Coralie Fouquet, Erhard Hohenester, Marc Tessier-Lavigne,[...]. Neuron 2014
93
8

Familial congenital mirror movements: report of a large 4-generation family.
M Srour, M Philibert, M-H Dion, A Duquette, F Richer, G A Rouleau, S Chouinard. Neurology 2009
15
26

frazzled encodes a Drosophila member of the DCC immunoglobulin subfamily and is required for CNS and motor axon guidance.
P A Kolodziej, L C Timpe, K J Mitchell, S R Fried, C S Goodman, L Y Jan, Y N Jan. Cell 1996
366
8


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
8

The divergent Robo family protein rig-1/Robo3 is a negative regulator of slit responsiveness required for midline crossing by commissural axons.
Christelle Sabatier, Andrew S Plump, Le Ma, Katja Brose, Atsushi Tamada, Fujio Murakami, Eva Y-H P Lee, Marc Tessier-Lavigne. Cell 2004
303
6

Hoxb8-Cre mice: A tool for brain-sparing conditional gene deletion.
Robert Witschi, Torbjörn Johansson, Giannina Morscher, Louis Scheurer, Jacqueline Deschamps, Hanns Ulrich Zeilhofer. Genesis 2010
28
10

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.
Joanna C Jen, Wai-Man Chan, Thomas M Bosley, Jijun Wan, Janai R Carr, Udo Rüb, David Shattuck, Georges Salamon, Lili C Kudo, Jing Ou,[...]. Science 2004
244
6


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.