A citation-based method for searching scientific literature

Mohammad A Al-Muhaizea, Faten AlMutairi, Rawan Almass, Safinaz AlHarthi, Mazhor S Aldosary, Maysoon Alsagob, Ali AlOdaib, Dilek Colak, Namik Kaya. Cerebellum 2018
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


De novo point mutations in patients diagnosed with ataxic cerebral palsy.
Ricardo Parolin Schnekenberg, Emma M Perkins, Jack W Miller, Wayne I L Davies, Maria Cristina D'Adamo, Mauro Pessia, Katherine A Fawcett, David Sims, Elodie Gillard, Karl Hudspith,[...]. Brain 2015
91
63

Case of infantile onset spinocerebellar ataxia type 5.
Francois-Dominique Jacob, Eugenia S Ho, Mayra Martinez-Ojeda, Basil T Darras, Omar S Khwaja. J Child Neurol 2013
27
63

Spectrin mutations cause spinocerebellar ataxia type 5.
Yoshio Ikeda, Katherine A Dick, Marcy R Weatherspoon, Dan Gincel, Karen R Armbrust, Joline C Dalton, Giovanni Stevanin, Alexandra Dürr, Christine Zühlke, Katrin Bürk,[...]. Nat Genet 2006
244
63

A Japanese SCA5 family with a novel three-nucleotide in-frame deletion mutation in the SPTBN2 gene: a clinical and genetic study.
Ying Wang, Kishin Koh, Michiaki Miwa, Nobuo Yamashiro, Kazumasa Shindo, Yoshihisa Takiyama. J Hum Genet 2014
17
45


Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development.
Stefano Lise, Yvonne Clarkson, Emma Perkins, Alexandra Kwasniewska, Elham Sadighi Akha, Ricardo Parolin Schnekenberg, Daumante Suminaite, Jilly Hope, Ian Baker, Lorna Gregory,[...]. PLoS Genet 2012
64
45

Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain.
Esra Yıldız Bölükbaşı, Muhammad Afzal, Sara Mumtaz, Nafees Ahmad, Sajid Malik, Aslıhan Tolun. Am J Med Genet A 2017
12
36

Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.
Solaf M Elsayed, Raoul Heller, Michaela Thoenes, Maha S Zaki, Daniel Swan, Ezzat Elsobky, Christine Zühlke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg,[...]. Eur J Hum Genet 2014
27
36

Between SCA5 and SCAR14: delineation of the SPTBN2 p.R480W-associated phenotype.
Sara Nuovo, Alessia Micalizzi, Stefano D'Arrigo, Monia Ginevrino, Tommaso Biagini, Tommaso Mazza, Enza Maria Valente. Eur J Hum Genet 2018
12
36

Infantile-onset spinocerebellar ataxia type 5 associated with a novel SPTBN2 mutation: A case report.
Tomoko Mizuno, Ayako Kashimada, Toshihiro Nomura, Kengo Moriyama, Haruna Yokoyama, Setsuko Hasegawa, Masatoshi Takagi, Shuki Mizutani. Brain Dev 2019
8
50

Cerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathways.
Emma Perkins, Daumante Suminaite, Mandy Jackson. J Physiol 2016
18
27

Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.
K Bürk, C Zühlke, I R König, A Ziegler, E Schwinger, C Globas, J Dichgans, Y Hellenbroich. Neurology 2004
44
27

Autosomal-dominant cerebellar ataxias.
Andrew Mundwiler, Vikram G Shakkottai. Handb Clin Neurol 2018
14
18

Spinocerebellar ataxia type 5.
Katherine A Dick, Yoshio Ikeda, John W Day, Laura P W Ranum. Handb Clin Neurol 2012
21
18

Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi.
Yvonne L Clarkson, Trudi Gillespie, Emma M Perkins, Alastair R Lyndon, Mandy Jackson. Hum Mol Genet 2010
37
18

Spectrins: a structural platform for stabilization and activation of membrane channels, receptors and transporters.
Beata Machnicka, Aleksander Czogalla, Anita Hryniewicz-Jankowska, Dżamila M Bogusławska, Renata Grochowalska, Elżbieta Heger, Aleksander F Sikorski. Biochim Biophys Acta 2014
105
18

β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations.
Yvonne L Clarkson, Emma M Perkins, Callum J Cairncross, Alastair R Lyndon, Paul A Skehel, Mandy Jackson. Hum Mol Genet 2014
18
18

Loss of beta-III spectrin leads to Purkinje cell dysfunction recapitulating the behavior and neuropathology of spinocerebellar ataxia type 5 in humans.
Emma M Perkins, Yvonne L Clarkson, Nancy Sabatier, David M Longhurst, Christopher P Millward, Jennifer Jack, Junko Toraiwa, Mitsunori Watanabe, Jeffrey D Rothstein, Alastair R Lyndon,[...]. J Neurosci 2010
86
18

Spectrin mutations that cause spinocerebellar ataxia type 5 impair axonal transport and induce neurodegeneration in Drosophila.
Damaris N Lorenzo, Min-gang Li, Sarah E Mische, Karen R Armbrust, Laura P W Ranum, Thomas S Hays. J Cell Biol 2010
61
18

Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay.
Moeenaldeen D Al-Sayed, Hamad Al-Zaidan, Albandary Albakheet, Hana Hakami, Rosan Kenana, Yusra Al-Yafee, Mazhor Al-Dosary, Alya Qari, Tarfa Al-Sheddi, Muhammed Al-Muheiza,[...]. Am J Hum Genet 2013
52
18

Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy.
Mohammed AlMuhaizea, Rawan AlMass, Aljouhra AlHargan, Anoud AlBader, Eva Medico Salsench, Jude Howaidi, Jacie Ihinger, Peter Karachunski, Amber Begtrup, Monica Segura Castell,[...]. Acta Neuropathol 2020
11
18

ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder.
Zuhair N Al-Hassnan, Mazhor Al-Dosary, Majid Alfadhel, Eissa A Faqeih, Maysoon Alsagob, Rosan Kenana, Rawan Almass, Olfat S Al-Harazi, Hindi Al-Hindi, Omhani I Malibari,[...]. J Med Genet 2015
63
18

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability.
Namik Kaya, Maysoon Alsagob, Maria Cristina D'Adamo, Albandary Al-Bakheet, Sonia Hasan, Maria Muccioli, Faten B Almutairi, Rawan Almass, Mazhor Aldosary, Dorota Monies,[...]. J Med Genet 2016
11
18

Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia.
Andrea Accogli, Judith St-Onge, Nassima Addour-Boudrahem, Joël Lafond-Lapalme, Alexandre Dionne Laporte, Guy A Rouleau, Jean-Baptiste Rivière, Myriam Srour. J Child Neurol 2020
5
40

Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia.
Francesco Nicita, Marta Nardella, Emanuele Bellacchio, Paolo Alfieri, Gaetano Terrone, Giorgia Piccini, Federica Graziola, Claudio Pignata, Alessandro Capuano, Enrico Bertini,[...]. Clin Genet 2019
14
18

The FoldX web server: an online force field.
Joost Schymkowitz, Jesper Borg, Francois Stricher, Robby Nys, Frederic Rousseau, Luis Serrano. Nucleic Acids Res 2005
9

Degrees of alcohol intoxication in 117 hospitalized cases.
J Adachi, Y Mizoi, T Fukunaga, Y Ogawa, Y Ueno, H Imamichi. J Stud Alcohol 1991
86
9

Sulforaphane restores acetyl-histone H3 binding to Bcl-2 promoter and prevents apoptosis in ethanol-exposed neural crest cells and mouse embryos.
Fuqiang Yuan, Xiaopan Chen, Jie Liu, Wenke Feng, Lu Cai, Xiaoyang Wu, Shao-Yu Chen. Exp Neurol 2018
16
9



Sequential histone modifications at Hoxd4 regulatory regions distinguish anterior from posterior embryonic compartments.
Mojgan Rastegar, Laila Kobrossy, Erzsebet Nagy Kovacs, Isabel Rambaldi, Mark Featherstone. Mol Cell Biol 2004
55
9


Ethanol alters the balance of Sox2, Oct4, and Nanog expression in distinct subpopulations during differentiation of embryonic stem cells.
Joshua W Ogony, Evangelia Malahias, Rajanikanth Vadigepalli, Helen Anni. Stem Cells Dev 2013
22
9

Gene-ethanol interactions underlying fetal alcohol spectrum disorders.
Neil McCarthy, Johann K Eberhart. Cell Mol Life Sci 2014
18
9


Stage-Specific Transcription Factors Drive Astrogliogenesis by Remodeling Gene Regulatory Landscapes.
Neha Tiwari, Abhijeet Pataskar, Sophie Péron, Sudhir Thakurela, Sanjeeb Kumar Sahu, María Figueres-Oñate, Nicolás Marichal, Laura López-Mascaraque, Vijay K Tiwari, Benedikt Berninger. Cell Stem Cell 2018
25
9

Incidence and prevalence of fetal alcohol spectrum disorder by sex and age group in Alberta, Canada.
Nguyen Xuan Thanh, Egon Jonsson, Amy Salmon, Meghan Sebastianski. J Popul Ther Clin Pharmacol 2014
32
9

Brain region-specific expression of MeCP2 isoforms correlates with DNA methylation within Mecp2 regulatory elements.
Carl O Olson, Robby M Zachariah, Chinelo D Ezeonwuka, Vichithra R B Liyanage, Mojgan Rastegar. PLoS One 2014
52
9

MECP2 isoform-specific vectors with regulated expression for Rett syndrome gene therapy.
Mojgan Rastegar, Akitsu Hotta, Peter Pasceri, Maisam Makarem, Aaron Y L Cheung, Shauna Elliott, Katya J Park, Megumi Adachi, Frederick S Jones, Ian D Clarke,[...]. PLoS One 2009
51
9

Overview of the Genetic Basis and Epigenetic Mechanisms that Contribute to FASD Pathobiology.
Vichithra R B Liyanage, Kyle Curtis, Robby M Zachariah, Albert E Chudley, Mojgan Rastegar. Curr Top Med Chem 2017
19
9

Exposure of Rat Neural Stem Cells to Ethanol Affects Cell Numbers and Alters Expression of 28 Proteins.
Mohammed A Kashem, Nilufa Sultana, Vladimir J Balcar. Neurochem Res 2018
6
16


DNA modifications: function and applications in normal and disease States.
Vichithra R B Liyanage, Jessica S Jarmasz, Nanditha Murugeshan, Marc R Del Bigio, Mojgan Rastegar, James R Davie. Biology (Basel) 2014
66
9

Dynamic expression of MEIS1 homeoprotein in E14.5 forebrain and differentiated forebrain-derived neural stem cells.
Benjamin A Barber, Vichithra R B Liyanage, Robby M Zachariah, Carl O Olson, Melissa A G Bailey, Mojgan Rastegar. Ann Anat 2013
28
9

Ethanol-induced methylation of cell cycle genes in neural stem cells.
Steven D Hicks, Frank A Middleton, Michael W Miller. J Neurochem 2010
57
9


Copy number variation in fetal alcohol spectrum disorder.
Mehdi Zarrei, Geoffrey G Hicks, James N Reynolds, Bhooma Thiruvahindrapuram, Worrawat Engchuan, Molly Pind, Sylvia Lamoureux, John Wei, Zhouzhi Wang, Christian R Marshall,[...]. Biochem Cell Biol 2018
7
14

The axonal glycoprotein TAG-1 is an immunoglobulin superfamily member with neurite outgrowth-promoting activity.
A J Furley, S B Morton, D Manalo, D Karagogeos, J Dodd, T M Jessell. Cell 1990
534
9

GABA signaling promotes synapse elimination and axon pruning in developing cortical inhibitory interneurons.
Xiaoyun Wu, Yu Fu, Graham Knott, Jiangteng Lu, Graziella Di Cristo, Z Josh Huang. J Neurosci 2012
71
9



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.