A citation-based method for searching scientific literature

Chiara Tocco, Michele Bertacchi, Michèle Studer. Front Mol Neurosci 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


COUP-TFI regulates the balance of cortical patterning between frontal/motor and sensory areas.
Maria Armentano, Shen-Ju Chou, Giulio Srubek Tomassy, Axel Leingärtner, Dennis D M O'Leary, Michèle Studer. Nat Neurosci 2007
160
100

The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations.
Chun-An Chen, Daniëlle G M Bosch, Megan T Cho, Jill A Rosenfeld, Marwan Shinawi, Richard Alan Lewis, John Mann, Parul Jayakar, Katelyn Payne, Laurence Walsh,[...]. Genet Med 2016
44
50

Nonsense-mediated decay approaches the clinic.
Jill A Holbrook, Gabriele Neu-Yilik, Matthias W Hentze, Andreas E Kulozik. Nat Genet 2004
477
50



Neurobiological bases of autism-epilepsy comorbidity: a focus on excitation/inhibition imbalance.
Yuri Bozzi, Giovanni Provenzano, Simona Casarosa. Eur J Neurosci 2018
106
50

A neurodegenerative perspective on mitochondrial optic neuropathies.
Patrick Yu-Wai-Man, Marcela Votruba, Florence Burté, Chiara La Morgia, Piero Barboni, Valerio Carelli. Acta Neuropathol 2016
86
50

Human iPSC-Derived Cerebral Organoids Model Cellular Features of Lissencephaly and Reveal Prolonged Mitosis of Outer Radial Glia.
Marina Bershteyn, Tomasz J Nowakowski, Alex A Pollen, Elizabeth Di Lullo, Aishwarya Nene, Anthony Wynshaw-Boris, Arnold R Kriegstein. Cell Stem Cell 2017
279
50

The human hippocampus: cognitive maps or relational memory?
Dharshan Kumaran, Eleanor A Maguire. J Neurosci 2005
131
50

NR2F1 mediated down-regulation of osteoblast differentiation was rescued by bone morphogenetic protein-2 (BMP-2) in human MSC.
Muthurangan Manikandan, Sarah Abuelreich, Mona Elsafadi, Hussain Alsalman, Hassan Almalak, Abdulaziz Siyal, Jamil Amjad Hashmi, Abdullah Aldahmash, Moustapha Kassem, Musaad Alfayez,[...]. Differentiation 2018
10
50

The Optic Nerve Hypoplasia Spectrum: Review of the Literature and Clinical Guidelines.
Anna Ryabets-Lienhard, Carly Stewart, Mark Borchert, Mitchell E Geffner. Adv Pediatr 2016
27
50

Neurodevelopmental Disorders: From Genetics to Functional Pathways.
Ilaria Parenti, Luis G Rabaneda, Hanna Schoen, Gaia Novarino. Trends Neurosci 2020
79
50

Molecular logic of neocortical projection neuron specification, development and diversity.
L C Greig, M B Woodworth, M J Galazo, H Padmanabhan, J D Macklis. Nat Rev Neurosci 2013
457
50

Characteristics of Brains in Autism Spectrum Disorder: Structure, Function and Connectivity across the Lifespan.
Sungji Ha, In-Jung Sohn, Namwook Kim, Hyeon Jeong Sim, Keun-Ah Cheon. Exp Neurobiol 2015
112
50

Optic nerve hypoplasia syndrome: a review of the epidemiology and clinical associations.
Pamela Garcia-Filion, Mark Borchert. Curr Treat Options Neurol 2013
53
50

Medial temporal lobe contributions to cued retrieval of items and contexts.
Deborah E Hannula, Laura A Libby, Andrew P Yonelinas, Charan Ranganath. Neuropsychologia 2013
39
50

Netrin-1 and DCC mediate axon guidance locally at the optic disc: loss of function leads to optic nerve hypoplasia.
M S Deiner, T E Kennedy, A Fazeli, T Serafini, M Tessier-Lavigne, D W Sretavan. Neuron 1997
343
50

Epileptic seizures.
Haleema Anwar, Qudsia Umaira Khan, Natasha Nadeem, Iqra Pervaiz, Muhammad Ali, Fatima Fayyaz Cheema. Discoveries (Craiova) 2020
7
50

Catastrophic epilepsy in childhood.
W D Shields. Epilepsia 2000
64
50


Autism spectrum and obsessive-compulsive disorders: OC behaviors, phenotypes and genetics.
Suma Jacob, Angeli Landeros-Weisenberger, James F Leckman. Autism Res 2009
43
50

Whole genome sequencing unveils genetic heterogeneity in optic nerve hypoplasia.
Sara Dahl, Maria Pettersson, Jesper Eisfeldt, Anna Katharina Schröder, Ronny Wickström, Kristina Teär Fahnehjelm, Britt-Marie Anderlid, Anna Lindstrand. PLoS One 2020
4
50

Sustained Pax6 Expression Generates Primate-like Basal Radial Glia in Developing Mouse Neocortex.
Fong Kuan Wong, Ji-Feng Fei, Felipe Mora-Bermúdez, Elena Taverna, Christiane Haffner, Jun Fu, Konstantinos Anastassiadis, A Francis Stewart, Wieland B Huttner. PLoS Biol 2015
61
50

Astrocytes as Guardians of Neuronal Excitability: Mechanisms Underlying Epileptogenesis.
Quirijn P Verhoog, Linda Holtman, Eleonora Aronica, Erwin A van Vliet. Front Neurol 2020
29
50


Effect of Seizures on the Developing Brain and Cognition.
Gregory L Holmes. Semin Pediatr Neurol 2016
44
50

Recent advances in cortical visual impairment.
W V Good, J E Jan, S K Burden, A Skoczenski, R Candy. Dev Med Child Neurol 2001
97
50

Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction.
Elizabeth M Powell, Daniel B Campbell, Gregg D Stanwood, Caleb Davis, Jeffrey L Noebels, Pat Levitt. J Neurosci 2003
245
50

Missense NR2F1 variant in monozygotic twins affected with the Bosch-Boonstra-Schaaf optic atrophy syndrome.
Catia Mio, Federico Fogolari, Laura Pezzoli, Angela V D'Elia, Maria Iascone, Giuseppe Damante. Mol Genet Genomic Med 2020
4
50

Manneristic behaviors of visually impaired children.
Alysha Molloy, Fiona J Rowe. Strabismus 2011
13
50

Dynamic expression of NR2F1 and SOX2 in developing and adult human cortex: comparison with cortical malformations.
Benedetta Foglio, Laura Rossini, Rita Garbelli, Maria Cristina Regondi, Sara Mercurio, Michele Bertacchi, Laura Avagliano, Gaetano Bulfamante, Roland Coras, Antonino Maiorana,[...]. Brain Struct Funct 2021
4
50


Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.
Manuel A Rivas, Matti Pirinen, Donald F Conrad, Monkol Lek, Emily K Tsang, Konrad J Karczewski, Julian B Maller, Kimberly R Kukurba, David S DeLuca, Menachem Fromer,[...]. Science 2015
147
50

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
50

Drug-based modulation of endogenous stem cells promotes functional remyelination in vivo.
Fadi J Najm, Mayur Madhavan, Anita Zaremba, Elizabeth Shick, Robert T Karl, Daniel C Factor, Tyler E Miller, Zachary S Nevin, Christopher Kantor, Alex Sargent,[...]. Nature 2015
255
50

Nonsense-mediated decay in genetic disease: friend or foe?
Jake N Miller, David A Pearce. Mutat Res Rev Mutat Res 2014
123
50

Motor development and delay: advances in assessment of motor skills in autism spectrum disorders.
Rujuta B Wilson, Peter G Enticott, Nicole J Rinehart. Curr Opin Neurol 2018
28
50


FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders.
Jessica Mariani, Gianfilippo Coppola, Ping Zhang, Alexej Abyzov, Lauren Provini, Livia Tomasini, Mariangela Amenduni, Anna Szekely, Dean Palejev, Michael Wilson,[...]. Cell 2015
597
50

Renal-coloboma syndrome: report of a novel PAX2 gene mutation.
G W Chung, A O Edwards, L A Schimmenti, G S Manligas, Y H Zhang, R Ritter. Am J Ophthalmol 2001
19
50

COUP-TFI mitotically regulates production and migration of dentate granule cells and modulates hippocampal Cxcr4 expression.
Joséphine Parisot, Gemma Flore, Michele Bertacchi, Michèle Studer. Development 2017
14
50

The topography of corticopontine projections is controlled by postmitotic expression of the area-mapping gene Nr2f1.
Chiara Tocco, Martin Øvsthus, Jan G Bjaalie, Trygve B Leergaard, Michèle Studer. Development 2022
1
100


A staged screening of registered drugs highlights remyelinating drug candidates for clinical trials.
C Eleuteri, S Olla, C Veroni, R Umeton, R Mechelli, S Romano, M C Buscarinu, F Ferrari, G Calò, G Ristori,[...]. Sci Rep 2017
21
50

The intolerance to functional genetic variation of protein domains predicts the localization of pathogenic mutations within genes.
Ayal B Gussow, Slavé Petrovski, Quanli Wang, Andrew S Allen, David B Goldstein. Genome Biol 2016
77
50

Clinical whole-exome sequencing results impact medical management.
Nancy Niguidula, Christina Alamillo, Layla Shahmirzadi Mowlavi, Zöe Powis, Julie S Cohen, Kelly D Farwell Hagman. Mol Genet Genomic Med 2018
18
50

Early-Life Exposure to Environmental Air Pollution and Autism Spectrum Disorder: A Review of Available Evidence.
Giovanni Imbriani, Alessandra Panico, Tiziana Grassi, Adele Idolo, Francesca Serio, Francesco Bagordo, Giovanni De Filippis, Donato De Giorgi, Gianfranco Antonucci, Prisco Piscitelli,[...]. Int J Environ Res Public Health 2021
8
50

Clinical and neurocognitive issues associated with Bosch-Boonstra-Schaaf optic atrophy syndrome: A case study.
Erin K Bojanek, Matthew W Mosconi, Stephen Guter, Catalina Betancur, Carol Macmillan, Edwin H Cook. Am J Med Genet A 2020
7
50

OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling.
Simone A Fietz, Iva Kelava, Johannes Vogt, Michaela Wilsch-Bräuninger, Denise Stenzel, Jennifer L Fish, Denis Corbeil, Axel Riehn, Wolfgang Distler, Robert Nitsch,[...]. Nat Neurosci 2010
508
50



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.