A citation-based method for searching scientific literature

Maria Yamasaki, Takashi Makino, Seik-Soon Khor, Hiromi Toyoda, Taku Miyagawa, Xiaoxi Liu, Hitoshi Kuwabara, Yukiko Kano, Takafumi Shimada, Toshiro Sugiyama, Hisami Nishida, Nagisa Sugaya, Mamoru Tochigi, Takeshi Otowa, Yuji Okazaki, Hisanobu Kaiya, Yoshiya Kawamura, Akinori Miyashita, Ryozo Kuwano, Kiyoto Kasai, Hisashi Tanii, Tsukasa Sasaki, Makoto Honda, Katsushi Tokunaga. BMC Med Genomics 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Structures, alternative splicing, and neurexin binding of multiple neuroligins.
K Ichtchenko, T Nguyen, T C Südhof. J Biol Chem 1996
335
25

Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, David Hardekopf, Sona Pekova, Samarth Bhatt, Nadezda Kosyakova, Thomas Liehr. J Histochem Cytochem 2012
78
25

Concurrent Loss of Heterozygosity and Mosaic Deletion of 12p13.32pter.
Rosana S Faria, Claudiner P de Oliveira, Marcella M da Costa, Maria T A da S Rosa, Mara S Córdoba, Aline Pic-Taylor, Iris Ferrari, Silviene F de Oliveira, Juliana F Mazzeu. Cytogenet Genome Res 2016
2
50

The FTLD risk factor TMEM106B and MAP6 control dendritic trafficking of lysosomes.
Benjamin M Schwenk, Christina M Lang, Sebastian Hogl, Sabina Tahirovic, Denise Orozco, Kristin Rentzsch, Stefan F Lichtenthaler, Casper C Hoogenraad, Anja Capell, Christian Haass,[...]. EMBO J 2014
83
25

Differences in cyclin D2 and D1 protein expression distinguish forebrain progenitor subsets.
Sara B Glickstein, Suzy Alexander, M Elizabeth Ross. Cereb Cortex 2007
61
25

Gene expression in cortical interneuron precursors is prescient of their mature function.
Renata Batista-Brito, Robert Machold, Corinna Klein, Gord Fishell. Cereb Cortex 2008
86
25

Changing interpretation of chromosomal microarray over time in a community cohort with intellectual disability.
Emma Palmer, Helen Speirs, Peter J Taylor, Glenda Mullan, Gill Turner, Stewart Einfeld, Bruce Tonge, David Mowat. Am J Med Genet A 2014
30
25

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, Alice Chen-Plotkin, Li-San Wang, Neill R Graff-Radford, Dennis W Dickson, Rosa Rademakers, Bradley F Boeve, Murray Grossman,[...]. Nat Genet 2010
316
25

Dystroglycan binding to α-neurexin competes with neurexophilin-1 and neuroligin in the brain.
Carsten Reissner, Johanna Stahn, Dorothee Breuer, Martin Klose, Gottfried Pohlentz, Michael Mormann, Markus Missler. J Biol Chem 2014
37
25

Pathogenic or not? Assessing the clinical relevance of copy number variants.
J Y Hehir-Kwa, R Pfundt, J A Veltman, N de Leeuw. Clin Genet 2013
36
25


Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis.
Shashirekha Shetty, Kym M Boycott, Tanya L Gillan, Kathy Bowser, Jillian S Parboosingh, Brenda McInnes, Judy E Chernos, Francois P Bernier. Clin Dysmorphol 2007
3
33

PRMT8, a new membrane-bound tissue-specific member of the protein arginine methyltransferase family.
Jaeho Lee, Joyce Sayegh, Jeremy Daniel, Steven Clarke, Mark T Bedford. J Biol Chem 2005
173
25

A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins.
Antony A Boucard, Alexander A Chubykin, Davide Comoletti, Palmer Taylor, Thomas C Südhof. Neuron 2005
330
25


Structure and evolution of neurexophilin.
A G Petrenko, B Ullrich, M Missler, V Krasnoperov, T W Rosahl, T C Südhof. J Neurosci 1996
68
25




PRMT8 as a phospholipase regulates Purkinje cell dendritic arborization and motor coordination.
Jun-Dal Kim, Kyung-Eui Park, Junji Ishida, Koichiro Kako, Juri Hamada, Shuichi Kani, Miki Takeuchi, Kana Namiki, Hajime Fukui, Shigetomo Fukuhara,[...]. Sci Adv 2015
25
25

12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.
Julien Thevenon, Patrick Callier, Joris Andrieux, Bruno Delobel, Albert David, Sylvie Sukno, Delphine Minot, Laure Mosca Anne, Nathalie Marle, Damien Sanlaville,[...]. Eur J Hum Genet 2013
43
25

The frontotemporal lobar degeneration risk factor, TMEM106B, regulates lysosomal morphology and function.
Owen A Brady, Yanqiu Zheng, Kira Murphy, Marshall Huang, Fenghua Hu. Hum Mol Genet 2013
98
25

PRMT1 and PRMT8 regulate retinoic acid-dependent neuronal differentiation with implications to neuropathology.
Zoltan Simandi, Erik Czipa, Attila Horvath, Aron Koszeghy, Csilla Bordas, Szilárd Póliska, István Juhász, László Imre, Gábor Szabó, Balazs Dezso,[...]. Stem Cells 2015
32
25

Cerebellar histogenesis is disturbed in mice lacking cyclin D2.
J M Huard, C C Forster, M L Carter, P Sicinski, M E Ross. Development 1999
146
25

Loss of Protein Arginine Methyltransferase 8 Alters Synapse Composition and Function, Resulting in Behavioral Defects.
Jay Penney, Jinsoo Seo, Oleg Kritskiy, Sara Elmsaouri, Fan Gao, Ping-Chieh Pao, Susan C Su, Li-Huei Tsai. J Neurosci 2017
17
25

Ion channels in glial cells.
A Verkhratsky, C Steinhäuser. Brain Res Brain Res Rev 2000
360
25

A 4.5 Mb terminal deletion of chromosome 12p helps further define a psychosis-associated locus.
Hilda Vargas, Gail Beldia, William Korosh, Vicki Sudhalter, Anwar Iqbal, Jose Arturo Sanchez-Lacay, Milen Velinov. Eur J Med Genet 2012
8
25

Psychotic manifestations in a patient with mental retardation and a 6.2 megabase deletion at the distal short arm of chromosome 12.
Milen Velinov, Gail Beldia, Hong Gu, John A Tsiouris, Edmund C Jenkins, W T Brown. CNS Spectr 2008
11
25

Selective cortical interneuron and GABA deficits in cyclin D2-null mice.
Sara B Glickstein, Holly Moore, Bozena Slowinska, Joelle Racchumi, Minah Suh, Nao Chuhma, M Elizabeth Ross. Development 2007
61
25

Identification of two inherited copy number variants in a male with autism supports two-hit and compound heterozygosity models of autism.
Susan Shur-Fen Gau, Hsiao-Mei Liao, Chao-Chun Hong, Wei-Hsien Chien, Chia-Hsiang Chen. Am J Med Genet B Neuropsychiatr Genet 2012
24
25

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories.
Karen D Tsuchiya, Lisa G Shaffer, Swaroop Aradhya, Julie M Gastier-Foster, Ankita Patel, M Katharine Rudd, Julie Sanford Biggerstaff, Warren G Sanger, Stuart Schwartz, James H Tepperberg,[...]. Genet Med 2009
41
25

Spatio-temporal transcriptome of the human brain.
Hyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, Ying Zhu, Xuming Xu, Mingfeng Li, André M M Sousa, Mihovil Pletikos, Kyle A Meyer, Goran Sedmak,[...]. Nature 2011
25

International Union of Pharmacology. XLI. Compendium of voltage-gated ion channels: potassium channels.
George A Gutman, K George Chandy, John P Adelman, Jayashree Aiyar, Douglas A Bayliss, David E Clapham, Manuel Covarriubias, Gary V Desir, Kiyoshi Furuichi, Barry Ganetzky,[...]. Pharmacol Rev 2003
218
25

Modulation of synaptic function through the α-neurexin-specific ligand neurexophilin-1.
Gesche Born, Dorothee Breuer, Shaopeng Wang, Astrid Rohlmann, Philippe Coulon, Puja Vakili, Carsten Reissner, Friedemann Kiefer, Martin Heine, Hans-Christian Pape,[...]. Proc Natl Acad Sci U S A 2014
24
25

De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.
Ghayda Mirzaa, David A Parry, Andrew E Fry, Kristin A Giamanco, Jeremy Schwartzentruber, Megan Vanstone, Clare V Logan, Nicola Roberts, Colin A Johnson, Shawn Singh,[...]. Nat Genet 2014
86
25


12p13 rearrangements: 6 Mb deletion responsible for ID/MCA and reciprocal duplication without clinical responsibility.
Irene Madrigal, Margarita Martinez, Laia Rodriguez-Revenga, Ana Carrió, Montserrat Milà. Am J Med Genet A 2012
8
25

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.
J B Ravnan, J H Tepperberg, P Papenhausen, A N Lamb, J Hedrick, D Eash, D H Ledbetter, C L Martin. J Med Genet 2006
263
25

Partial monosomy 12p13.1----13.3.
D R Romain, J Goldsmith, L M Columbano-Green, C J Chapman, R H Smythe, R G Parfitt. J Med Genet 1987
15
25

Arginine methylation an emerging regulator of protein function.
Mark T Bedford, Stéphane Richard. Mol Cell 2005
793
25

Genotype-phenotype relationship in a child with 2.3 Mb de novo interstitial 12p13.33-p13.32 deletion.
Isabella Fanizza, Sara Bertuzzo, Silvana Beri, Elisabetta Scalera, Angelo Massagli, Maria Enrica Sali, Roberto Giorda, Maria Clara Bonaglia. Eur J Med Genet 2014
4
25

Localization and targeting of voltage-dependent ion channels in mammalian central neurons.
Helene Vacher, Durga P Mohapatra, James S Trimmer. Physiol Rev 2008
311
25

Mouse Genome Database (MGD) 2019.
Carol J Bult, Judith A Blake, Cynthia L Smith, James A Kadin, Joel E Richardson. Nucleic Acids Res 2019
202
25

Development of mice expressing a single D-type cyclin.
Maria A Ciemerych, Anna M Kenney, Ewa Sicinska, Ilona Kalaszczynska, Roderick T Bronson, David H Rowitch, Humphrey Gardner, Piotr Sicinski. Genes Dev 2002
210
25

Neuroligin 1: a splice site-specific ligand for beta-neurexins.
K Ichtchenko, Y Hata, T Nguyen, B Ullrich, M Missler, C Moomaw, T C Südhof. Cell 1995
520
25

G1-phase regulators, cyclin D1, cyclin D2, and cyclin D3: up-regulation at gastrulation and dynamic expression during neurulation.
F Wianny, F X Real, C L Mummery, M Van Rooijen, J Lahti, J Samarut, P Savatier. Dev Dyn 1998
55
25

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.
D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
574
25

A case of a female infant with simultaneous occurrence of de novo terminal deletions on chromosome 14q and 20p.
S Uehara, Y Akai, Y Takeyama, K Okamura, T Takabayashi, A Yajima, M Natsui, H Nakai. Clin Genet 1993
16
25

Constitutional chromosomal events at 22q11 and 15q26 in a child with a pilocytic astrocytoma of the spinal cord.
Samantha Mascelli, Mariasavina Severino, Alessandro Raso, Paolo Nozza, Elisa Tassano, Giovanni Morana, Patrizia De Marco, Elisa Merello, Claudia Milanaccio, Marco Pavanello,[...]. Mol Cytogenet 2014
2
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.