A citation-based method for searching scientific literature

Bhaskar Roy, Robert Griggs. Neurol Clin 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy.
Ewout J N Groen, Elena Perenthaler, Natalie L Courtney, Crispin Y Jordan, Hannah K Shorrock, Dinja van der Hoorn, Yu-Ting Huang, Lyndsay M Murray, Gabriella Viero, Thomas H Gillingwater. Hum Mol Genet 2018
31
50

A nomenclature and classification for the congenital myasthenic syndromes: preparing for FAIR data in the genomic era.
Rachel Thompson, Angela Abicht, David Beeson, Andrew G Engel, Bruno Eymard, Emmanuel Maxime, Hanns Lochmüller. Orphanet J Rare Dis 2018
9
50

Monitoring disease activity noninvasively in the mdx model of Duchenne muscular dystrophy.
Antonio Filareto, Katie Maguire-Nguyen, Qiang Gan, Garazi Aldanondo, Léo Machado, Jeffrey S Chamberlain, Thomas A Rando. Proc Natl Acad Sci U S A 2018
3
50

Innovative genomic collaboration using the GENESIS (GEM.app) platform.
Michael Gonzalez, Marni J Falk, Xiaowu Gai, Richard Postrel, Rebecca Schüle, Stephan Zuchner. Hum Mutat 2015
60
50

Assessing non-Mendelian inheritance in inherited axonopathies.
Dana M Bis-Brewer, Ziv Gan-Or, Patrick Sleiman, Hakon Hakonarson, Sarah Fazal, Steve Courel, Vivian Cintra, Feifei Tao, Mehrdad A Estiar, Mark Tarnopolsky,[...]. Genet Med 2020
6
50

An artificial niche preserves the quiescence of muscle stem cells and enhances their therapeutic efficacy.
Marco Quarta, Jamie O Brett, Rebecca DiMarco, Antoine De Morree, Stephane C Boutet, Robert Chacon, Michael C Gibbons, Victor A Garcia, James Su, Joseph B Shrager,[...]. Nat Biotechnol 2016
90
50

Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials.
Jordi Diaz-Manera, Roberto Fernandez-Torron, Jaume LLauger, Meredith K James, Anna Mayhew, Fiona E Smith, Ursula R Moore, Andrew M Blamire, Pierre G Carlier, Laura Rufibach,[...]. J Neurol Neurosurg Psychiatry 2018
39
50

Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular Transmission.
Amina Chaouch, Vito Porcelli, Daniel Cox, Shimon Edvardson, Pasquale Scarcia, Anna De Grassi, Ciro L Pierri, Judith Cossins, Steven H Laval, Helen Griffin,[...]. J Neuromuscul Dis 2014
40
50

MYO-MRI diagnostic protocols in genetic myopathies.
Jodi Warman Chardon, Jordi Díaz-Manera, Giorgio Tasca, Carsten G Bönnemann, David Gómez-Andrés, Arend Heerschap, Eugenio Mercuri, Francesco Muntoni, Anna Pichiecchio, Enzo Ricci,[...]. Neuromuscul Disord 2019
19
50

The CNDR: collaborating to translate new therapies for Canadians.
Lawrence Korngut, Craig Campbell, Megan Johnston, Timothy Benstead, Angela Genge, Alex Mackenzie, Anna McCormick, Douglas Biggar, Pierre Bourque, Hannah Briemberg,[...]. Can J Neurol Sci 2013
15
50

G3BP1 promotes stress-induced RNA granule interactions to preserve polyadenylated mRNA.
Anaïs Aulas, Guillaume Caron, Christos G Gkogkas, Nguyen-Vi Mohamed, Laurie Destroismaisons, Nahum Sonenberg, Nicole Leclerc, J Alex Parker, Christine Vande Velde. J Cell Biol 2015
62
50

CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis.
Eva Janzen, Natalia Mendoza-Ferreira, Seyyedmohsen Hosseinibarkooie, Svenja Schneider, Kristina Hupperich, Theresa Tschanz, Vanessa Grysko, Markus Riessland, Matthias Hammerschmidt, Frank Rigo,[...]. Brain 2018
30
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

The origins and non-canonical functions of macrophages in development and regeneration.
Marine Theret, Remi Mounier, Fabio Rossi. Development 2019
38
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

Diet-resistant obesity is characterized by a distinct plasma proteomic signature and impaired muscle fiber metabolism.
A B Thrush, G Antoun, M Nikpay, D A Patten, C DeVlugt, J-F Mauger, B L Beauchamp, P Lau, R Reshke, É Doucet,[...]. Int J Obes (Lond) 2018
9
50

Channelopathies of skeletal muscle excitability.
Stephen C Cannon. Compr Physiol 2015
111
50

Assessment of disease activity in muscular dystrophies by noninvasive imaging.
Katie K Maguire, Leland Lim, Sedona Speedy, Thomas A Rando. J Clin Invest 2013
11
50

Mutations in glycyl-tRNA synthetase impair mitochondrial metabolism in neurons.
Veronika Boczonadi, Kathrin Meyer, Humberto Gonczarowska-Jorge, Helen Griffin, Andreas Roos, Marina Bartsakoulia, Boglarka Bansagi, Giulia Ricci, Fanni Palinkas, René P Zahedi,[...]. Hum Mol Genet 2018
13
50

ALS biomarkers for therapy development: State of the field and future directions.
Michael Benatar, Kevin Boylan, Andreas Jeromin, Seward B Rutkove, James Berry, Nazem Atassi, Lucie Bruijn. Muscle Nerve 2016
58
50

Spinal Muscular Atrophy in the Treatment Era.
Megan A Waldrop, Bakri H Elsheikh. Neurol Clin 2020
6
50

Regenerative Rehabilitation: Applied Biophysics Meets Stem Cell Therapeutics.
Thomas A Rando, Fabrisia Ambrosio. Cell Stem Cell 2018
26
50

Neurocalcin Delta Suppression Protects against Spinal Muscular Atrophy in Humans and across Species by Restoring Impaired Endocytosis.
Markus Riessland, Anna Kaczmarek, Svenja Schneider, Kathryn J Swoboda, Heiko Löhr, Cathleen Bradler, Vanessa Grysko, Maria Dimitriadi, Seyyedmohsen Hosseinibarkooie, Laura Torres-Benito,[...]. Am J Hum Genet 2017
88
50

TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype.
S Donkervoort, M Papadaki, J M de Winter, M B Neu, J Kirschner, V Bolduc, M L Yang, M A Gibbons, Y Hu, J Dastgir,[...]. Ann Neurol 2015
23
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

Single-cell RNA sequencing in facioscapulohumeral muscular dystrophy disease etiology and development.
Anita van den Heuvel, Ahmed Mahfouz, Susan L Kloet, Judit Balog, Baziel G M van Engelen, Rabi Tawil, Stephen J Tapscott, Silvère M van der Maarel. Hum Mol Genet 2019
23
50

An analysis of disease severity based on SMN2 copy number in adults with spinal muscular atrophy.
Bakri Elsheikh, Thomas Prior, Xiaoli Zhang, Robert Miller, Stephen J Kolb, Dan Moore, Walter Bradley, Richard Barohn, Wilson Bryan, Deborah Gelinas,[...]. Muscle Nerve 2009
53
50

mTORC1 controls the adaptive transition of quiescent stem cells from G0 to G(Alert).
Joseph T Rodgers, Katherine Y King, Jamie O Brett, Melinda J Cromie, Gregory W Charville, Katie K Maguire, Christopher Brunson, Namrata Mastey, Ling Liu, Chang-Ru Tsai,[...]. Nature 2014
346
50

The Canadian Neuromuscular Disease Registry 2010-2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease Registry.
V Hodgkinson, J Lounsberry, S M'Dahoma, A Russell, G Jewett, T Benstead, B Brais, C Campbell, W Johnston, H Lochmüller,[...]. J Neuromuscul Dis 2021
5
50

Novel mutations in MYBPC1 are associated with myogenic tremor and mild myopathy.
Janis Stavusis, Baiba Lace, Jochen Schäfer, Janelle Geist, Inna Inashkina, Dita Kidere, Sander Pajusalu, Nathan T Wright, Annika Saak, Manja Weinhold,[...]. Ann Neurol 2019
9
50

Anti-HMGCR myopathy may resemble limb-girdle muscular dystrophy.
Payam Mohassel, Océane Landon-Cardinal, A Reghan Foley, Sandra Donkervoort, Katherine S Pak, Colleen Wahl, Robert T Shebert, Amy Harper, Pierre Fequiere, Matthew Meriggioli,[...]. Neurol Neuroimmunol Neuroinflamm 2018
29
50

Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture.
Zachary A Miller, Virginia E Sturm, Gamze Balci Camsari, Anna Karydas, Jennifer S Yokoyama, Lea T Grinberg, Adam L Boxer, Howard J Rosen, Katherine P Rankin, Maria Luisa Gorno-Tempini,[...]. Neurol Neuroimmunol Neuroinflamm 2016
46
50

Spinal muscular atrophy: going beyond the motor neuron.
Gillian Hamilton, Thomas H Gillingwater. Trends Mol Med 2013
213
50

Recovery from acidosis is a robust trigger for loss of force in murine hypokalemic periodic paralysis.
Wentao Mi, Fenfen Wu, Marbella Quinonez, Marino DiFranco, Stephen C Cannon. J Gen Physiol 2019
5
50

A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene.
Dwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, Dhekra Al-Basha, Kinga I Gawlik, Kyle Lindsay, Elzbieta Hyatt, Rebekah Kember, Kara M Place, Ryan M Marks,[...]. Nature 2019
42
50

C9orf72 is required for proper macrophage and microglial function in mice.
J G O'Rourke, L Bogdanik, A Yáñez, D Lall, A J Wolf, A K M G Muhammad, R Ho, S Carmona, J P Vit, J Zarrow,[...]. Science 2016
289
50

Defining pre-symptomatic amyotrophic lateral sclerosis.
Michael Benatar, Martin R Turner, Joanne Wuu. Amyotroph Lateral Scler Frontotemporal Degener 2019
21
50

Myopathy With SQSTM1 and TIA1 Variants: Clinical and Pathological Features.
Zhiyv Niu, Carly Sabine Pontifex, Sarah Berini, Leslie E Hamilton, Elie Naddaf, Eric Wieben, Ross A Aleff, Kristina Martens, Angela Gruber, Andrew G Engel,[...]. Front Neurol 2018
12
50

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy.
Matthew M Goddeeris, Biming Wu, David Venzke, Takako Yoshida-Moriguchi, Fumiaki Saito, Kiichiro Matsumura, Steven A Moore, Kevin P Campbell. Nature 2013
70
50

Provincial Differences in the Diagnosis and Care of Amyotrophic Lateral Sclerosis.
Victoria L Hodgkinson, Josh Lounsberry, Ario Mirian, Angela Genge, Timothy Benstead, Hannah Briemberg, Ian Grant, Walter Hader, Wendy S Johnston, Sanjay Kalra,[...]. Can J Neurol Sci 2018
9
50


Intermittent glucocorticoid steroid dosing enhances muscle repair without eliciting muscle atrophy.
Mattia Quattrocelli, David Y Barefield, James L Warner, Andy H Vo, Michele Hadhazy, Judy U Earley, Alexis R Demonbreun, Elizabeth M McNally. J Clin Invest 2017
53
50

New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy.
Jorge Alonso-Pérez, Lidia González-Quereda, Luca Bello, Michela Guglieri, Volker Straub, Pia Gallano, Claudio Semplicini, Elena Pegoraro, Vittoria Zangaro, Andrés Nascimento,[...]. Brain 2020
11
50

Comparison of independent screens on differentially vulnerable motor neurons reveals alpha-synuclein as a common modifier in motor neuron diseases.
Rachel A Kline, Kevin A Kaifer, Erkan Y Osman, Francesco Carella, Ariana Tiberi, Jolill Ross, Giuseppa Pennetta, Christian L Lorson, Lyndsay M Murray. PLoS Genet 2017
19
50

Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.
Takako Yoshida-Moriguchi, Kevin P Campbell. Glycobiology 2015
105
50

Therapeutic Applications of CRISPR/Cas for Duchenne Muscular Dystrophy.
Tatianna Wai Ying Wong, Ronald D Cohn. Curr Gene Ther 2017
15
50

Follow-up of late-onset Pompe disease patients with muscle magnetic resonance imaging reveals increase in fat replacement in skeletal muscles.
Claudia Nuñez-Peralta, Jorge Alonso-Pérez, Jaume Llauger, Sonia Segovia, Paula Montesinos, Izaskun Belmonte, Irene Pedrosa, Elena Montiel, Alicia Alonso-Jiménez, Javier Sánchez-González,[...]. J Cachexia Sarcopenia Muscle 2020
14
50

Control of phosphorothioate stereochemistry substantially increases the efficacy of antisense oligonucleotides.
Naoki Iwamoto, David C D Butler, Nenad Svrzikapa, Susovan Mohapatra, Ivan Zlatev, Dinah W Y Sah, Meena, Stephany M Standley, Genliang Lu, Luciano H Apponi,[...]. Nat Biotechnol 2017
120
50

Report on the 4th Ottawa International Conference on Neuromuscular Disease and Biology - September 5-7, 2017, Ottawa, Canada.
Jodi Warman Chardon, Bernard J Jasmin, Rashmi Kothary, Robin J Parks. J Neuromuscul Dis 2018
1
100


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.