A citation-based method for searching scientific literature

Amrutha Pattamatta, Lien Nguyen, Hailey R Olafson, Marina M Scotti, Lauren A Laboissonniere, Jared Richardson, J Andrew Berglund, Tao Zu, Eric T Wang, Laura P W Ranum. Hum Mol Genet 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Incomplete penetrance of the C9ORF72 hexanucleotide repeat expansions: frequency in a cohort of geriatric non-demented subjects.
Daniela Galimberti, Beatrice Arosio, Chiara Fenoglio, Maria Serpente, Sara M G Cioffi, Rossana Bonsi, Paolo Rossi, Carlo Abbate, Daniela Mari, Elio Scarpini. J Alzheimers Dis 2014
26
50

Antibody Therapy Targeting RAN Proteins Rescues C9 ALS/FTD Phenotypes in C9orf72 Mouse Model.
Lien Nguyen, Fabio Montrasio, Amrutha Pattamatta, Solaleh Khoramian Tusi, Olgert Bardhi, Kevin D Meyer, Lindsey Hayes, Katsuya Nakamura, Monica Banez-Coronel, Alyssa Coyne,[...]. Neuron 2020
28
50

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
Elisa Majounie, Alan E Renton, Kin Mok, Elise G P Dopper, Adrian Waite, Sara Rollinson, Adriano Chiò, Gabriella Restagno, Nayia Nicolaou, Javier Simon-Sanchez,[...]. Lancet Neurol 2012
752
50

Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansions.
Elaine M Cleary, Suvankar Pal, Tara Azam, David J Moore, Robert Swingler, George Gorrie, Laura Stephenson, Shuna Colville, Siddharthan Chandran, Mary Porteous,[...]. Mol Cell Probes 2016
25
50

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
50

Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice.
Owen M Peters, Gabriela Toro Cabrera, Helene Tran, Tania F Gendron, Jeanne E McKeon, Jake Metterville, Alexandra Weiss, Nicholas Wightman, Johnny Salameh, Juyhun Kim,[...]. Neuron 2015
165
50

C9orf72 deficiency promotes motor deficits of a C9ALS/FTD mouse model in a dose-dependent manner.
Qiang Shao, Chen Liang, Qing Chang, Wei Zhang, Mei Yang, Jian-Fu Chen. Acta Neuropathol Commun 2019
25
50

Pumilio1 haploinsufficiency leads to SCA1-like neurodegeneration by increasing wild-type Ataxin1 levels.
Vincenzo A Gennarino, Ravi K Singh, Joshua J White, Antonia De Maio, Kihoon Han, Ji-Yoen Kim, Paymaan Jafar-Nejad, Alberto di Ronza, Hyojin Kang, Layal S Sayegh,[...]. Cell 2015
87
50


Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
50

C9orf72 BAC Transgenic Mice Display Typical Pathologic Features of ALS/FTD.
Jacqueline G O'Rourke, Laurent Bogdanik, A K M G Muhammad, Tania F Gendron, Kevin J Kim, Andrew Austin, Janet Cady, Elaine Y Liu, Jonah Zarrow, Sharday Grant,[...]. Neuron 2015
180
50

Sudden onset of mortality within a colony of FVB/n mice.
Matthew D Rosenbaum, Sue VandeWoude, Helle Bielefeldt-Ohmann. Lab Anim (NY) 2007
5
50

G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences.
Franz Faul, Edgar Erdfelder, Albert-Georg Lang, Axel Buchner. Behav Res Methods 2007
50

Genetic control of sensitivity to hippocampal cell death induced by kainic acid: a quantitative trait loci analysis.
Paula Elyse Schauwecker, Robert W Williams, Julia Belen Santos. J Comp Neurol 2004
39
50

Absence of Survival and Motor Deficits in 500 Repeat C9ORF72 BAC Mice.
Daniel A Mordes, Brett M Morrison, Xanthe H Ament, Christopher Cantrell, Joanie Mok, Pierce Eggan, Carolyn Xue, Jin-Yuan Wang, Kevin Eggan, Jeffrey D Rothstein. Neuron 2020
11
50

C9orf72 BAC Mouse Model with Motor Deficits and Neurodegenerative Features of ALS/FTD.
Yuanjing Liu, Amrutha Pattamatta, Tao Zu, Tammy Reid, Olgert Bardhi, David R Borchelt, Anthony T Yachnis, Laura P W Ranum. Neuron 2016
191
50

Spontaneous lesions in aging FVB/N mice.
J F Mahler, W Stokes, P C Mann, M Takaoka, R R Maronpot. Toxicol Pathol 1996
139
50

Gain of Toxicity from ALS/FTD-Linked Repeat Expansions in C9ORF72 Is Alleviated by Antisense Oligonucleotides Targeting GGGGCC-Containing RNAs.
Jie Jiang, Qiang Zhu, Tania F Gendron, Shahram Saberi, Melissa McAlonis-Downes, Amanda Seelman, Jennifer E Stauffer, Paymaan Jafar-Nejad, Kevin Drenner, Derek Schulte,[...]. Neuron 2016
280
50

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
C Gunter, W Paradee, D C Crawford, K A Meadows, J Newman, C B Kunst, D L Nelson, C Schwartz, A Murray, J N Macpherson,[...]. Hum Mol Genet 1998
54
50

RAN translation at C9orf72-associated repeat expansions is selectively enhanced by the integrated stress response.
Katelyn M Green, M Rebecca Glineburg, Michael G Kearse, Brittany N Flores, Alexander E Linsalata, Stephen J Fedak, Aaron C Goldstrohm, Sami J Barmada, Peter K Todd. Nat Commun 2017
87
50


Repeat-Associated Non-ATG Translation: Molecular Mechanisms and Contribution to Neurological Disease.
Lien Nguyen, John Douglas Cleary, Laura P W Ranum. Annu Rev Neurosci 2019
33
50

Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.
Claudia Braida, Rhoda K A Stefanatos, Berit Adam, Navdeep Mahajan, Hubert J M Smeets, Florence Niel, Cyril Goizet, Benoit Arveiler, Michel Koenig, Clotilde Lagier-Tourenne,[...]. Hum Mol Genet 2010
97
50

C9orf72 Poly(PR) Dipeptide Repeats Disturb Biomolecular Phase Separation and Disrupt Nucleolar Function.
Michael R White, Diana M Mitrea, Peipei Zhang, Christopher B Stanley, Devon E Cassidy, Amanda Nourse, Aaron H Phillips, Michele Tolbert, J Paul Taylor, Richard W Kriwacki. Mol Cell 2019
62
50

Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.
Yoshio Ikeda, Joline C Dalton, Melinda L Moseley, Kathy L Gardner, Thomas D Bird, Tetsuo Ashizawa, William K Seltzer, Massimo Pandolfo, Aubrey Milunsky, Nicholas T Potter,[...]. Am J Hum Genet 2004
62
50

Non-ATG-initiated translation directed by microsatellite expansions.
Tao Zu, Brian Gibbens, Noelle S Doty, Mário Gomes-Pereira, Aline Huguet, Matthew D Stone, Jamie Margolis, Mark Peterson, Todd W Markowski, Melissa A C Ingram,[...]. Proc Natl Acad Sci U S A 2011
539
50

Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.
R A M Buijsen, J A Visser, P Kramer, E A W F M Severijnen, M Gearing, N Charlet-Berguerand, S L Sherman, R F Berman, R Willemsen, R K Hukema. Hum Reprod 2016
46
50

Repeat-associated non-AUG (RAN) translation: insights from pathology.
Monica Banez-Coronel, Laura P W Ranum. Lab Invest 2019
16
50

Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports.
A Zeman, J Stone, M Porteous, E Burns, L Barron, J Warner. J Neurol Neurosurg Psychiatry 2004
30
50

Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36.
Zachary T McEachin, Tania F Gendron, Nisha Raj, María García-Murias, Anwesha Banerjee, Ryan H Purcell, Patricia J Ward, Tiffany W Todd, Megan E Merritt-Garza, Karen Jansen-West,[...]. Neuron 2020
16
50


Repeat-associated non-ATG (RAN) translation.
John Douglas Cleary, Amrutha Pattamatta, Laura P W Ranum. J Biol Chem 2018
39
50

Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease.
Galen E B Wright, Jennifer A Collins, Chris Kay, Cassandra McDonald, Egor Dolzhenko, Qingwen Xia, Kristina Bečanović, Britt I Drögemöller, Alicia Semaka, Charlotte M Nguyen,[...]. Am J Hum Genet 2019
43
50

Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule Dynamics.
Steven Boeynaems, Elke Bogaert, Denes Kovacs, Albert Konijnenberg, Evy Timmerman, Alex Volkov, Mainak Guharoy, Mathias De Decker, Tom Jaspers, Veronica H Ryan,[...]. Mol Cell 2017
249
50

Translation of dipeptide repeat proteins from the C9ORF72 expanded repeat is associated with cellular stress.
Yoshifumi Sonobe, Ghanashyam Ghadge, Katsuhisa Masaki, Ataman Sendoel, Elaine Fuchs, Raymond P Roos. Neurobiol Dis 2018
36
50

Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia.
P F Worth, H Houlden, P Giunti, M B Davis, N W Wood. Nat Genet 2000
81
50

Facile FMR1 mRNA structure regulation by interruptions in CGG repeats.
Marek Napierala, Daniel Michalowski, Mateusz de Mezer, Wlodzimierz J Krzyzosiak. Nucleic Acids Res 2005
70
50

Are (CTG)n expansions at the SCA8 locus rare polymorphisms?
G Stevanin, A Herman, A Dürr, C Jodice, M Frontali, Y Agid, A Brice. Nat Genet 2000
65
50

Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects.
Yajun Hu, Yuji Hashimoto, Takashi Ishii, Mamut Rayle, Kazumasa Soga, Nozomu Sato, Michi Okita, Miwa Higashi, Kokoro Ozaki, Hidehiro Mizusawa,[...]. J Neurol Sci 2017
7
50

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
Melinda L Moseley, Tao Zu, Yoshio Ikeda, Wangcai Gao, Anne K Mosemiller, Randy S Daughters, Gang Chen, Marcy R Weatherspoon, H Brent Clark, Timothy J Ebner,[...]. Nat Genet 2006
305
50

C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins.
Sarah Mizielinska, Sebastian Grönke, Teresa Niccoli, Charlotte E Ridler, Emma L Clayton, Anny Devoy, Thomas Moens, Frances E Norona, Ione O C Woollacott, Julian Pietrzyk,[...]. Science 2014
402
50

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
M D Koob, M L Moseley, L J Schut, K A Benzow, T D Bird, J W Day, L P Ranum. Nat Genet 1999
447
50

Reply-
Moseley, Schut, Bird, Day, Ranum. Nat Genet 2000
7
50


Incoordinated thought and emotion in spinocerebellar ataxia type 8.
J Stone, L Smith, K Watt, L Barron, A Zeman. J Neurol 2001
17
50

C9orf72 Dipeptide Repeats Impair the Assembly, Dynamics, and Function of Membrane-Less Organelles.
Kyung-Ha Lee, Peipei Zhang, Hong Joo Kim, Diana M Mitrea, Mohona Sarkar, Brian D Freibaum, Jaclyn Cika, Maura Coughlin, James Messing, Amandine Molliex,[...]. Cell 2016
348
50

Metformin inhibits RAN translation through PKR pathway and mitigates disease in C9orf72 ALS/FTD mice.
Tao Zu, Shu Guo, Olgert Bardhi, Daniel A Ryskamp, Jian Li, Solaleh Khoramian Tusi, Avery Engelbrecht, Kelena Klippel, Paramita Chakrabarty, Lien Nguyen,[...]. Proc Natl Acad Sci U S A 2020
20
50

Poly-dipeptides encoded by the C9orf72 repeats bind nucleoli, impede RNA biogenesis, and kill cells.
Ilmin Kwon, Siheng Xiang, Masato Kato, Leeju Wu, Pano Theodoropoulos, Tao Wang, Jiwoong Kim, Jonghyun Yun, Yang Xie, Steven L McKnight. Science 2014
375
50

Advances in understanding the role of disease-associated proteins in spinal muscular atrophy.
Seyyedmohsen Hosseinibarkooie, Svenja Schneider, Brunhilde Wirth. Expert Rev Proteomics 2017
22
50

Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31.
Taro Ishiguro, Nozomu Sato, Morio Ueyama, Nobuhiro Fujikake, Chantal Sellier, Akemi Kanegami, Eiichi Tokuda, Bita Zamiri, Terence Gall-Duncan, Mila Mirceta,[...]. Neuron 2017
62
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.