A citation-based method for searching scientific literature

Annemarie Hübers, Nicolai Marroquin, Birgit Schmoll, Stefan Vielhaber, Marlies Just, Benjamin Mayer, Josef Högel, Johannes Dorst, Thomas Mertens, Walter Just, Anna Aulitzky, Verena Wais, Albert C Ludolph, Christian Kubisch, Jochen H Weishaupt, Alexander E Volk. Neurobiol Aging 2014
Times Cited: 45







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



Times Cited
  Times     Co-cited
Similarity


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
77

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
68

Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.
Jon Beck, Mark Poulter, Davina Hensman, Jonathan D Rohrer, Colin J Mahoney, Gary Adamson, Tracy Campbell, James Uphill, Aaron Borg, Pietro Fratta,[...]. Am J Hum Genet 2013
232
48

Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study.
Marka van Blitterswijk, Mariely DeJesus-Hernandez, Ellis Niemantsverdriet, Melissa E Murray, Michael G Heckman, Nancy N Diehl, Patricia H Brown, Matthew C Baker, NiCole A Finch, Peter O Bauer,[...]. Lancet Neurol 2013
191
44

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.
Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee, Kristel Sleegers, Stéphanie Philtjens, Gernot Kleinberger, Jonathan Janssens, Karolien Bettens, Caroline Van Cauwenberghe, Sandra Pereson,[...]. Lancet Neurol 2012
480
40

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
794
40

Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion.
Adrian J Waite, Dirk Bäumer, Simon East, James Neal, Huw R Morris, Olaf Ansorge, Derek J Blake. Neurobiol Aging 2014
189
37

Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia.
Oriol Dols-Icardo, Alberto García-Redondo, Ricard Rojas-García, Raquel Sánchez-Valle, Aina Noguera, Estrella Gómez-Tortosa, Pau Pastor, Isabel Hernández, Jesús Esteban-Pérez, Marc Suárez-Calvet,[...]. Hum Mol Genet 2014
83
35

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.
Bradley N Smith, Stephen Newhouse, Aleksey Shatunov, Caroline Vance, Simon Topp, Lauren Johnson, Jack Miller, Younbok Lee, Claire Troakes, Kirsten M Scott,[...]. Eur J Hum Genet 2013
163
28

Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration.
Clotilde Lagier-Tourenne, Michael Baughn, Frank Rigo, Shuying Sun, Patrick Liu, Hai-Ri Li, Jie Jiang, Andrew T Watt, Seung Chun, Melanie Katz,[...]. Proc Natl Acad Sci U S A 2013
398
28

C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking.
Manal A Farg, Vinod Sundaramoorthy, Jessica M Sultana, Shu Yang, Rachel A K Atkinson, Vita Levina, Mark A Halloran, Paul A Gleeson, Ian P Blair, Kai Y Soo,[...]. Hum Mol Genet 2014
310
28

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.
Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben,[...]. Hum Mutat 2013
201
28

RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention.
Christopher J Donnelly, Ping-Wu Zhang, Jacqueline T Pham, Aaron R Haeusler, Nipun A Mistry, Svetlana Vidensky, Elizabeth L Daley, Erin M Poth, Benjamin Hoover, Daniel M Fines,[...]. Neuron 2013
619
28

Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion.
Dhruv Sareen, Jacqueline G O'Rourke, Pratap Meera, A K M G Muhammad, Sharday Grant, Megan Simpkinson, Shaughn Bell, Sharon Carmona, Loren Ornelas, Anais Sahabian,[...]. Sci Transl Med 2013
470
28

C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci.
Sarah Mizielinska, Tammaryn Lashley, Frances E Norona, Emma L Clayton, Charlotte E Ridler, Pietro Fratta, Adrian M Isaacs. Acta Neuropathol 2013
221
26

Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion.
Zhengrui Xi, Lorne Zinman, Danielle Moreno, Jennifer Schymick, Yan Liang, Christine Sato, Yonglan Zheng, Mahdi Ghani, Samar Dib, Julia Keith,[...]. Am J Hum Genet 2013
191
26

Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS.
Peter E A Ash, Kevin F Bieniek, Tania F Gendron, Thomas Caulfield, Wen-Lang Lin, Mariely Dejesus-Hernandez, Marka M van Blitterswijk, Karen Jansen-West, Joseph W Paul, Rosa Rademakers,[...]. Neuron 2013
747
26

The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.
Kohji Mori, Shih-Ming Weng, Thomas Arzberger, Stephanie May, Kristin Rentzsch, Elisabeth Kremmer, Bettina Schmid, Hans A Kretzschmar, Marc Cruts, Christine Van Broeckhoven,[...]. Science 2013
843
26

RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia.
Tao Zu, Yuanjing Liu, Monica Bañez-Coronel, Tammy Reid, Olga Pletnikova, Jada Lewis, Timothy M Miller, Matthew B Harms, Annet E Falchook, S H Subramony,[...]. Proc Natl Acad Sci U S A 2013
518
26

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72.
Bradley F Boeve, Kevin B Boylan, Neill R Graff-Radford, Mariely DeJesus-Hernandez, David S Knopman, Otto Pedraza, Prashanthi Vemuri, David Jones, Val Lowe, Melissa E Murray,[...]. Brain 2012
260
26

Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD.
Angelica Nordin, Chizuru Akimoto, Anna Wuolikainen, Helena Alstermark, Pär Jonsson, Anna Birve, Stefan L Marklund, Karin S Graffmo, Karin Forsberg, Thomas Brännström,[...]. Hum Mol Genet 2015
69
26

Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic.
Youn-Bok Lee, Han-Jou Chen, João N Peres, Jorge Gomez-Deza, Jan Attig, Maja Stalekar, Claire Troakes, Agnes L Nishimura, Emma L Scotter, Caroline Vance,[...]. Cell Rep 2013
318
24

C9orf72 nucleotide repeat structures initiate molecular cascades of disease.
Aaron R Haeusler, Christopher J Donnelly, Goran Periz, Eric A J Simko, Patrick G Shaw, Min-Sik Kim, Nicholas J Maragakis, Juan C Troncoso, Akhilesh Pandey, Rita Sattler,[...]. Nature 2014
592
24

Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation.
Vladimir L Buchman, Johnathan Cooper-Knock, Natalie Connor-Robson, Adrian Higginbottom, Janine Kirby, Olga D Razinskaya, Natalia Ninkina, Pamela J Shaw. Mol Neurodegener 2013
39
28

Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS.
Tania F Gendron, Kevin F Bieniek, Yong-Jie Zhang, Karen Jansen-West, Peter E A Ash, Thomas Caulfield, Lillian Daughrity, Judith H Dunmore, Monica Castanedes-Casey, Jeannie Chew,[...]. Acta Neuropathol 2013
381
24

C9orf72 hypermethylation protects against repeat expansion-associated pathology in ALS/FTD.
Elaine Y Liu, Jenny Russ, Kathryn Wu, Donald Neal, Eunran Suh, Anna G McNally, David J Irwin, Vivianna M Van Deerlin, Edward B Lee. Acta Neuropathol 2014
124
24

Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifier.
Jenny Russ, Elaine Y Liu, Kathryn Wu, Donald Neal, EunRan Suh, David J Irwin, Corey T McMillan, Matthew B Harms, Nigel J Cairns, Elisabeth M Wood,[...]. Acta Neuropathol 2015
92
24

Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.
Kohji Mori, Thomas Arzberger, Friedrich A Grässer, Ilse Gijselinck, Stephanie May, Kristin Rentzsch, Shih-Ming Weng, Martin H Schludi, Julie van der Zee, Marc Cruts,[...]. Acta Neuropathol 2013
329
22

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.
Pietro Fratta, Mark Poulter, Tammaryn Lashley, Jonathan D Rohrer, James M Polke, Jon Beck, Natalie Ryan, Davina Hensman, Sarah Mizielinska, Adrian J Waite,[...]. Acta Neuropathol 2013
108
22

C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan.
Hiroyuki Ishiura, Yuji Takahashi, Jun Mitsui, Sohei Yoshida, Tameko Kihira, Yasumasa Kokubo, Shigeki Kuzuhara, Laura P W Ranum, Tomoko Tamaoki, Yaeko Ichikawa,[...]. Arch Neurol 2012
75
22

C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients.
Carol Dobson-Stone, Marianne Hallupp, Clement T Loy, Elizabeth M Thompson, Eric Haan, Carolyn M Sue, Peter K Panegyres, Cristina Razquin, Manuel Seijo-Martínez, Ramon Rene,[...]. PLoS One 2013
49
22

Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study.
Susan Byrne, Marwa Elamin, Peter Bede, Aleksey Shatunov, Cathal Walsh, Bernie Corr, Mark Heverin, Norah Jordan, Kevin Kenna, Catherine Lynch,[...]. Lancet Neurol 2012
336
22

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations.
Julie S Snowden, Sara Rollinson, Jennifer C Thompson, Jennifer M Harris, Cheryl L Stopford, Anna M T Richardson, Matthew Jones, Alex Gerhard, Yvonne S Davidson, Andrew Robinson,[...]. Brain 2012
374
22

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.
Elizabeth T Cirulli, Brittany N Lasseigne, Slavé Petrovski, Peter C Sapp, Patrick A Dion, Claire S Leblond, Julien Couthouis, Yi-Fan Lu, Quanli Wang, Brian J Krueger,[...]. Science 2015
618
22

Semi-automated quantification of C9orf72 expansion size reveals inverse correlation between hexanucleotide repeat number and disease duration in frontotemporal degeneration.
EunRan Suh, Edward B Lee, Donald Neal, Elisabeth M Wood, Jon B Toledo, Lior Rennert, David J Irwin, Corey T McMillan, Bryan Krock, Lauren B Elman,[...]. Acta Neuropathol 2015
50
22

Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations.
Ian R Mackenzie, Thomas Arzberger, Elisabeth Kremmer, Dirk Troost, Stefan Lorenzl, Kohji Mori, Shih-Ming Weng, Christian Haass, Hans A Kretzschmar, Dieter Edbauer,[...]. Acta Neuropathol 2013
242
20

Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood.
Veronique V Belzil, Peter O Bauer, Mercedes Prudencio, Tania F Gendron, Caroline T Stetler, Irene K Yan, Luc Pregent, Lillian Daughrity, Matthew C Baker, Rosa Rademakers,[...]. Acta Neuropathol 2013
204
20

Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis.
Sorana Ciura, Serena Lattante, Isabelle Le Ber, Morwena Latouche, Hervé Tostivint, Alexis Brice, Edor Kabashi. Ann Neurol 2013
234
20

C9orf72 repeat expansions are a rare genetic cause of parkinsonism.
Suzanne Lesage, Isabelle Le Ber, Christel Condroyer, Emmanuel Broussolle, Audrey Gabelle, Stéphane Thobois, Florence Pasquier, Karl Mondon, Patrick A Dion, Daniel Rochefort,[...]. Brain 2013
121
20

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.
Johnathan Cooper-Knock, Christopher Hewitt, J Robin Highley, Alice Brockington, Antonio Milano, Somai Man, Joanne Martindale, Judith Hartley, Theresa Walsh, Catherine Gelsthorpe,[...]. Brain 2012
230
20

Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients.
Zhengrui Xi, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Amalia C Bruni, Raffaele G Maletta, Benedetta Nacmias, Sandro Sorbi, Daniela Galimberti, Ezequiel I Surace,[...]. Hum Mol Genet 2014
64
20

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.
Adriano Chiò, Giuseppe Borghero, Gabriella Restagno, Gabriele Mora, Carsten Drepper, Bryan J Traynor, Michael Sendtner, Maura Brunetti, Irene Ossola, Andrea Calvo,[...]. Brain 2012
155
20

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
437
20

C9orf72 FTLD/ALS-associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration.
Stephanie May, Daniel Hornburg, Martin H Schludi, Thomas Arzberger, Kristin Rentzsch, Benjamin M Schwenk, Friedrich A Grässer, Kohji Mori, Elisabeth Kremmer, Julia Banzhaf-Strathmann,[...]. Acta Neuropathol 2014
211
20

Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p.
Heather Stewart, Nicola J Rutherford, Hannah Briemberg, Charles Krieger, Neil Cashman, Marife Fabros, Matt Baker, Alice Fok, Mariely DeJesus-Hernandez, Andrew Eisen,[...]. Acta Neuropathol 2012
131
20

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis.
B R Brooks, R G Miller, M Swash, T L Munsat. Amyotroph Lateral Scler Other Motor Neuron Disord 2000
20

The C9orf72 repeat expansion disrupts nucleocytoplasmic transport.
Ke Zhang, Christopher J Donnelly, Aaron R Haeusler, Jonathan C Grima, James B Machamer, Peter Steinwald, Elizabeth L Daley, Sean J Miller, Kathleen M Cunningham, Svetlana Vidensky,[...]. Nature 2015
612
20

The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter.
I Gijselinck, S Van Mossevelde, J van der Zee, A Sieben, S Engelborghs, J De Bleecker, A Ivanoiu, O Deryck, D Edbauer, M Zhang,[...]. Mol Psychiatry 2016
145
20

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.
Axel Freischmidt, Thomas Wieland, Benjamin Richter, Wolfgang Ruf, Veronique Schaeffer, Kathrin Müller, Nicolai Marroquin, Frida Nordin, Annemarie Hübers, Patrick Weydt,[...]. Nat Neurosci 2015
514
20

C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease.
Karen Nuytemans, Güney Bademci, Martin M Kohli, Gary W Beecham, Liyong Wang, Juan I Young, Fatta Nahab, Eden R Martin, John R Gilbert, Michael Benatar,[...]. Ann Hum Genet 2013
54
17


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.