A citation-based method for searching scientific literature

Pierre Mattar, Christine Jolicoeur, Thanh Dang, Sujay Shah, Brian S Clark, Michel Cayouette. Sci Rep 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


A conserved regulatory logic controls temporal identity in mouse neural progenitors.
Pierre Mattar, Johan Ericson, Seth Blackshaw, Michel Cayouette. Neuron 2015
65
100

Ikaros confers early temporal competence to mouse retinal progenitor cells.
Jimmy Elliott, Christine Jolicoeur, Vasanth Ramamurthy, Michel Cayouette. Neuron 2008
119
100


Ikaros promotes early-born neuronal fates in the cerebral cortex.
Jessica M Alsiö, Basile Tarchini, Michel Cayouette, Frederick J Livesey. Proc Natl Acad Sci U S A 2013
53
66

Temporal patterning of apical progenitors and their daughter neurons in the developing neocortex.
L Telley, G Agirman, J Prados, N Amberg, S Fièvre, P Oberst, G Bartolini, I Vitali, C Cadilhac, S Hippenmeyer,[...]. Science 2019
86
66


Conserved microRNA pathway regulates developmental timing of retinal neurogenesis.
Anna La Torre, Sean Georgi, Thomas A Reh. Proc Natl Acad Sci U S A 2013
135
66


How variable clones build an invariant retina.
Jie He, Gen Zhang, Alexandra D Almeida, Michel Cayouette, Benjamin D Simons, William A Harris. Neuron 2012
133
66


Neuronal specification in space and time.
Isabel Holguera, Claude Desplan. Science 2018
50
66


Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets.
Evan Z Macosko, Anindita Basu, Rahul Satija, James Nemesh, Karthik Shekhar, Melissa Goldman, Itay Tirosh, Allison R Bialas, Nolan Kamitaki, Emily M Martersteck,[...]. Cell 2015
66

Math5 is required for retinal ganglion cell and optic nerve formation.
N L Brown, S Patel, J Brzezinski, T Glaser. Development 2001
363
66

Foxn4 is a temporal identity factor conferring mid/late-early retinal competence and involved in retinal synaptogenesis.
Shuting Liu, Xiaoning Liu, Shengguo Li, Xiuting Huang, Haohua Qian, Kangxin Jin, Mengqing Xiang. Proc Natl Acad Sci U S A 2020
8
66


Neuronal diversity and convergence in a visual system developmental atlas.
Mehmet Neset Özel, Félix Simon, Shadi Jafari, Isabel Holguera, Yen-Chung Chen, Najate Benhra, Rana Naja El-Danaf, Katarina Kapuralin, Jennifer Amy Malin, Nikolaos Konstantinides,[...]. Nature 2021
15
66

Pou2f1 and Pou2f2 cooperate to control the timing of cone photoreceptor production in the developing mouse retina.
Awais Javed, Pierre Mattar, Suying Lu, Kamil Kruczek, Magdalena Kloc, Anai Gonzalez-Cordero, Rod Bremner, Robin R Ali, Michel Cayouette. Development 2020
4
66

Reconstruction of rat retinal progenitor cell lineages in vitro reveals a surprising degree of stochasticity in cell fate decisions.
Francisco L A F Gomes, Gen Zhang, Felix Carbonell, José A Correa, William A Harris, Benjamin D Simons, Michel Cayouette. Development 2011
106
66

Temporal patterning of Drosophila medulla neuroblasts controls neural fates.
Xin Li, Ted Erclik, Claire Bertet, Zhenqing Chen, Roumen Voutev, Srinidhi Venkatesh, Javier Morante, Arzu Celik, Claude Desplan. Nature 2013
152
66

SATB1 targets chromatin remodelling to regulate genes over long distances.
Dag Yasui, Masaru Miyano, Shutao Cai, Patrick Varga-Weisz, Terumi Kohwi-Shigematsu. Nature 2002
361
33

The methyl binding domain 3/nucleosome remodelling and deacetylase complex regulates neural cell fate determination and terminal differentiation in the cerebral cortex.
Erin Knock, João Pereira, Patrick D Lombard, Andrew Dimond, Donna Leaford, Frederick J Livesey, Brian Hendrich. Neural Dev 2015
26
33

LHX2 Interacts with the NuRD Complex and Regulates Cortical Neuron Subtype Determinants Fezf2 and Sox11.
Bhavana Muralidharan, Zeba Khatri, Upasana Maheshwari, Ritika Gupta, Basabdatta Roy, Saurabh J Pradhan, Krishanpal Karmodiya, Hari Padmanabhan, Ashwin S Shetty, Chinthapalli Balaji,[...]. J Neurosci 2017
26
33


Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability.
Martin Chevarin, Yannis Duffourd, Rebecca A Barnard, Sébastien Moutton, François Lecoquierre, Fatma Daoud, Paul Kuentz, Caroline Cabret, Julien Thevenon, Elodie Gautier,[...]. J Med Genet 2020
1
100

Molecular mechanism for age-related memory loss: the histone-binding protein RbAp48.
Elias Pavlopoulos, Sidonie Jones, Stylianos Kosmidis, Maggie Close, Carla Kim, Olga Kovalerchik, Scott A Small, Eric R Kandel. Sci Transl Med 2013
70
33

Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.
Amy B Wilfert, Arvis Sulovari, Tychele N Turner, Bradley P Coe, Evan E Eichler. Genome Med 2017
52
33

Polycomb limits the neurogenic competence of neural precursor cells to promote astrogenic fate transition.
Yusuke Hirabayashi, Nao Suzki, Masafumi Tsuboi, Takaho A Endo, Tetsuro Toyoda, Jun Shinga, Haruhiko Koseki, Miguel Vidal, Yukiko Gotoh. Neuron 2009
283
33

The Mendelian disorders of the epigenetic machinery.
Hans Tomas Bjornsson. Genome Res 2015
72
33


Prevalence of intellectual disability: a meta-analysis of population-based studies.
Pallab K Maulik, Maya N Mascarenhas, Colin D Mathers, Tarun Dua, Shekhar Saxena. Res Dev Disabil 2011
560
33

Abnormal early brain development in autism.
E Courchesne. Mol Psychiatry 2002
72
33

Targeting Peripheral Somatosensory Neurons to Improve Tactile-Related Phenotypes in ASD Models.
Lauren L Orefice, Jacqueline R Mosko, Danielle T Morency, Michael F Wells, Aniqa Tasnim, Shawn M Mozeika, Mengchen Ye, Anda M Chirila, Alan J Emanuel, Genelle Rankin,[...]. Cell 2019
38
33


The human brain in numbers: a linearly scaled-up primate brain.
Suzana Herculano-Houzel. Front Hum Neurosci 2009
475
33

Casz1 controls higher-order nuclear organization in rod photoreceptors.
Pierre Mattar, Milanka Stevanovic, Ivana Nad, Michel Cayouette. Proc Natl Acad Sci U S A 2018
12
33

Neuronal activity-regulated gene transcription in synapse development and cognitive function.
Anne E West, Michael E Greenberg. Cold Spring Harb Perspect Biol 2011
309
33

Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.
Emily L Casanova, Julia L Sharp, Hrishikesh Chakraborty, Nahid Sultana Sumi, Manuel F Casanova. Mol Autism 2016
19
33

State of the Field: Differentiating Intellectual Disability From Autism Spectrum Disorder.
Audrey Thurm, Cristan Farmer, Emma Salzman, Catherine Lord, Somer Bishop. Front Psychiatry 2019
32
33


CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Lot Snijders Blok, Justine Rousseau, Joanna Twist, Sophie Ehresmann, Motoki Takaku, Hanka Venselaar, Lance H Rodan, Catherine B Nowak, Jessica Douglas, Kathryn J Swoboda,[...]. Nat Commun 2018
32
33


Ubiquitination-Independent Repression of PRC1 Targets during Neuronal Fate Restriction in the Developing Mouse Neocortex.
Masafumi Tsuboi, Yusuke Kishi, Wakana Yokozeki, Haruhiko Koseki, Yusuke Hirabayashi, Yukiko Gotoh. Dev Cell 2018
25
33

Epigenetic cues modulating the generation of cell-type diversity in the cerebral cortex.
Nicole Amberg, Susanne Laukoter, Simon Hippenmeyer. J Neurochem 2019
8
33

Proteomic analysis of Sox2-associated proteins during early stages of mouse embryonic stem cell differentiation identifies Sox21 as a novel regulator of stem cell fate.
Sunil K Mallanna, Briana D Ormsbee, Michelina Iacovino, Joshua M Gilmore, Jesse L Cox, Michael Kyba, Michael P Washburn, Angie Rizzino. Stem Cells 2010
77
33

DNA methylation directs genomic localization of Mbd2 and Mbd3 in embryonic stem cells.
Sarah J Hainer, Kurtis N McCannell, Jun Yu, Ly-Sha Ee, Lihua J Zhu, Oliver J Rando, Thomas G Fazzio. Elife 2016
13
33

Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum.
Christopher L Frank, Fang Liu, Ranjula Wijayatunge, Lingyun Song, Matthew T Biegler, Marty G Yang, Christopher M Vockley, Alexias Safi, Charles A Gersbach, Gregory E Crawford,[...]. Nat Neurosci 2015
86
33

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Hsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, Mingshan Xue, Maria Chahrour, Jong Yoo, Jeffrey L Neul, Shiaoching Gong, Hui-Chen Lu, Nathaniel Heintz,[...]. Nature 2010
733
33

dMi-2, a hunchback-interacting protein that functions in polycomb repression.
J Kehle, D Beuchle, S Treuheit, B Christen, J A Kennison, M Bienz, J Müller. Science 1998
290
33

Binding of the CHD4 PHD2 finger to histone H3 is modulated by covalent modifications.
Catherine A Musselman, Robyn E Mansfield, Adam L Garske, Foteini Davrazou, Ann H Kwan, Samuel S Oliver, Heather O'Leary, John M Denu, Joel P Mackay, Tatiana G Kutateladze. Biochem J 2009
81
33


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.