A citation-based method for searching scientific literature

Kelvin K Hui, Yi-Kai Chen, Ryo Endo, Motomasa Tanaka. Biomolecules 2019
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
Paige B Martin, Yu Kigoshi-Tansho, Roger B Sher, Gianina Ravenscroft, Jennifer E Stauffer, Rajesh Kumar, Ryo Yonashiro, Tina Müller, Christopher Griffith, William Allen,[...]. Nat Commun 2020
13
100

Protein synthesis. Rqc2p and 60S ribosomal subunits mediate mRNA-independent elongation of nascent chains.
Peter S Shen, Joseph Park, Yidan Qin, Xueming Li, Krishna Parsawar, Matthew H Larson, James Cox, Yifan Cheng, Alan M Lambowitz, Jonathan S Weissman,[...]. Science 2015
152
50

Polyneuropathies.
Claudia Sommer, Christian Geber, Peter Young, Raimund Forst, Frank Birklein, Benedikt Schoser. Dtsch Arztebl Int 2018
21
50

A novel complex neurological phenotype due to a homozygous mutation in FDX2.
Juliana Gurgel-Giannetti, David S Lynch, Anderson Rodrigues Brandão de Paiva, Leandro Tavares Lucato, Guilherme Yamamoto, Christer Thomsen, Somsuvro Basu, Fernando Freua, Alexandre Varella Giannetti, Bruno Della Ripa de Assis,[...]. Brain 2018
13
50


Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation.
Ales Maver, Luca Lovrecic, Marija Volk, Gorazd Rudolf, Karin Writzl, Ana Blatnik, Alenka Hodzic, Peterlin Borut. Genet Med 2016
23
50

Structure and assembly pathway of the ribosome quality control complex.
Sichen Shao, Alan Brown, Balaji Santhanam, Ramanujan S Hegde. Mol Cell 2015
110
50

The p75 neurotrophin receptor negatively modulates dendrite complexity and spine density in hippocampal neurons.
Marta Zagrebelsky, Andreas Holz, Georg Dechant, Yves-Alain Barde, Tobias Bonhoeffer, Martin Korte. J Neurosci 2005
201
50

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
50

Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population.
Peter Bauer, Krishna Kumar Kandaswamy, Maximilian E R Weiss, Omid Paknia, Martin Werber, Aida M Bertoli-Avella, Zafer Yüksel, Malgorzata Bochinska, Gabriela E Oprea, Shivendra Kishore,[...]. Genet Med 2019
14
50

Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms.
Daniela Zahorakova, Robert Rosipal, Jan Hadac, Alena Zumrova, Vladimir Bzduch, Nadezda Misovicova, Alice Baxova, Jiri Zeman, Pavel Martasek. J Hum Genet 2007
19
50

Spatiotemporal gene expression trajectories reveal developmental hierarchies of the human cortex.
Tomasz J Nowakowski, Aparna Bhaduri, Alex A Pollen, Beatriz Alvarado, Mohammed A Mostajo-Radji, Elizabeth Di Lullo, Maximilian Haeussler, Carmen Sandoval-Espinosa, Siyuan John Liu, Dmitry Velmeshev,[...]. Science 2017
274
50


MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism.
Akane Shibayama, Edwin H Cook, Jinong Feng, Cecile Glanzmann, Jin Yan, Nick Craddock, Ian R Jones, David Goldman, Leonard L Heston, Steve S Sommer. Am J Med Genet B Neuropsychiatr Genet 2004
102
50


CAT tails drive degradation of stalled polypeptides on and off the ribosome.
Cole S Sitron, Onn Brandman. Nat Struct Mol Biol 2019
33
50

A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing.
Steven W Long, Jenny Y Y Ooi, Peter M Yau, Peter L Jones. Biosci Rep 2011
42
50

Revealing 3D magnetization of thin films with soft X-ray tomography: magnetic singularities and topological charges.
A Hierro-Rodriguez, C Quirós, A Sorrentino, L M Alvarez-Prado, J I Martín, J M Alameda, S McVitie, E Pereiro, M Vélez, S Ferrer. Nat Commun 2020
1
100

Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.
S Anazi, S Maddirevula, E Faqeih, H Alsedairy, F Alzahrani, H E Shamseldin, N Patel, M Hashem, N Ibrahim, F Abdulwahab,[...]. Mol Psychiatry 2017
106
50

Hereditary Neuropathies.
Katja Eggermann, Burkhard Gess, Martin Häusler, Joachim Weis, Andreas Hahn, Ingo Kurth. Dtsch Arztebl Int 2018
20
50

Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases.
Gaber Bergant, Ales Maver, Luca Lovrecic, Goran Čuturilo, Alenka Hodzic, Borut Peterlin. Genet Med 2018
26
50

Autism and abnormal development of brain connectivity.
Matthew K Belmonte, Greg Allen, Andrea Beckel-Mitchener, Lisa M Boulanger, Ruth A Carper, Sara J Webb. J Neurosci 2004
691
50

Dendritic spine pathology: cause or consequence of neurological disorders?
John C Fiala, Josef Spacek, Kristen M Harris. Brain Res Brain Res Rev 2002
574
50

A mouse forward genetics screen identifies LISTERIN as an E3 ubiquitin ligase involved in neurodegeneration.
Jessie Chu, Nancy A Hong, Claudio A Masuda, Brian V Jenkins, Keats A Nelms, Christopher C Goodnow, Richard J Glynne, Hua Wu, Eliezer Masliah, Claudio A P Joazeiro,[...]. Proc Natl Acad Sci U S A 2009
132
50


HomozygosityMapper--an interactive approach to homozygosity mapping.
Dominik Seelow, Markus Schuelke, Friedhelm Hildebrandt, Peter Nürnberg. Nucleic Acids Res 2009
276
50

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
50

Charcot-Marie-Tooth Disease and Other Genetic Polyneuropathies.
Sindhu Ramchandren. Continuum (Minneap Minn) 2017
14
50

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
50

Global prevalence of autism and other pervasive developmental disorders.
Mayada Elsabbagh, Gauri Divan, Yun-Joo Koh, Young Shin Kim, Shuaib Kauchali, Carlos Marcín, Cecilia Montiel-Nava, Vikram Patel, Cristiane S Paula, Chongying Wang,[...]. Autism Res 2012
934
50

Variation in Gene Expression in Autism Spectrum Disorders: An Extensive Review of Transcriptomic Studies.
Ashley Ansel, Joshua P Rosenzweig, Philip D Zisman, Michal Melamed, Benjamin Gesundheit. Front Neurosci 2017
42
50


Increased burden of deleterious variants in essential genes in autism spectrum disorder.
Xiao Ji, Rachel L Kember, Christopher D Brown, Maja Bućan. Proc Natl Acad Sci U S A 2016
24
50

Gender and age differences in the core triad of impairments in autism spectrum disorders: a systematic review and meta-analysis.
Patricia J M Van Wijngaarden-Cremers, Evelien van Eeten, Wouter B Groen, Patricia A Van Deurzen, Iris J Oosterling, Rutger Jan Van der Gaag. J Autism Dev Disord 2014
188
50

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.
Dianne F Newbury, Pamela C Warburton, Natalie Wilson, Elena Bacchelli, Simona Carone, Janine A Lamb, Elena Maestrini, Emanuela V Volpi, Shehla Mohammed, Gillian Baird,[...]. Am J Med Genet A 2009
16
50

A ribosome-bound quality control complex triggers degradation of nascent peptides and signals translation stress.
Onn Brandman, Jacob Stewart-Ornstein, Daisy Wong, Adam Larson, Christopher C Williams, Gene-Wei Li, Sharleen Zhou, David King, Peter S Shen, Jimena Weibezahn,[...]. Cell 2012
330
50

A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.
Danielle Posthuma, Michelle Luciano, Eco J C de Geus, Margie J Wright, P Eline Slagboom, Grant W Montgomery, Dorret I Boomsma, Nicholas G Martin. Am J Hum Genet 2005
84
50

Expression Analysis of VDR-Related LncRNAs in Autism Spectrum Disorder.
Soudeh Ghafouri-Fard, Reyhane Eghtedarian, Bashdar Mahmud Hussen, Elahe Motevaseli, Shahram Arsang-Jang, Mohammad Taheri. J Mol Neurosci 2021
1
100

Ermin, a myelinating oligodendrocyte-specific protein that regulates cell morphology.
Damian Brockschnieder, Helena Sabanay, Dieter Riethmacher, Elior Peles. J Neurosci 2006
71
50


Comparative Multimodal Meta-analysis of Structural and Functional Brain Abnormalities in Autism Spectrum Disorder and Obsessive-Compulsive Disorder.
Christina O Carlisi, Luke J Norman, Steve S Lukito, Joaquim Radua, David Mataix-Cols, Katya Rubia. Biol Psychiatry 2017
71
50

Genetic Advances in Autism.
Anita Thapar, Michael Rutter. J Autism Dev Disord 2020
6
50

Brain region-specific altered expression and association of mitochondria-related genes in autism.
Ayyappan Anitha, Kazuhiko Nakamura, Ismail Thanseem, Kazuo Yamada, Yoshimi Iwayama, Tomoko Toyota, Hideo Matsuzaki, Taishi Miyachi, Satoru Yamada, Masatsugu Tsujii,[...]. Mol Autism 2012
74
50

Autism spectrum disorder: insights into convergent mechanisms from transcriptomics.
Mathieu Quesnel-Vallières, Robert J Weatheritt, Sabine P Cordes, Benjamin J Blencowe. Nat Rev Genet 2019
50
50

Changes in prefrontal axons may disrupt the network in autism.
Basilis Zikopoulos, Helen Barbas. J Neurosci 2010
209
50

Sex differences in autism spectrum disorders.
Donna M Werling, Daniel H Geschwind. Curr Opin Neurol 2013
414
50

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
E Maestrini, A T Pagnamenta, J A Lamb, E Bacchelli, N H Sykes, I Sousa, C Toma, G Barnby, H Butler, L Winchester,[...]. Mol Psychiatry 2010
91
50

Cdc48-associated complex bound to 60S particles is required for the clearance of aberrant translation products.
Quentin Defenouillère, Yanhua Yao, John Mouaikel, Abdelkader Namane, Aurélie Galopier, Laurence Decourty, Antonia Doyen, Christophe Malabat, Cosmin Saveanu, Alain Jacquier,[...]. Proc Natl Acad Sci U S A 2013
147
50

Genetic and epigenetic methylation defects and implication of the ERMN gene in autism spectrum disorders.
A Homs, M Codina-Solà, B Rodríguez-Santiago, C M Villanueva, D Monk, I Cuscó, L A Pérez-Jurado. Transl Psychiatry 2016
13
50

Ermin is a p116RIP -interacting protein promoting oligodendroglial differentiation and myelin maintenance.
Shan Wang, Tao Wang, Tao Liu, Rou-Gang Xie, Xiang-Hui Zhao, Lei Wang, Qian Yang, Lin-Tao Jia, Jing Han. Glia 2020
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.