A citation-based method for searching scientific literature

Fulya Akçimen, Sandra Martins, Calwing Liao, Cynthia V Bourassa, Hélène Catoire, Garth A Nicholson, Olaf Riess, Mafalda Raposo, Marcondes C França, João Vasconcelos, Manuela Lima, Iscia Lopes-Cendes, Maria Luiza Saraiva-Pereira, Laura B Jardim, Jorge Sequeiros, Patrick A Dion, Guy A Rouleau. Aging (Albany NY) 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Asian origin for the worldwide-spread mutational event in Machado-Joseph disease.
Sandra Martins, Francesc Calafell, Claudia Gaspar, Virginia C N Wong, Isabel Silveira, Garth A Nicholson, Ewout R Brunt, Lisbeth Tranebjaerg, Giovanni Stevanin, Mingli Hsieh,[...]. Arch Neurol 2007
47
75

ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions.
Egor Dolzhenko, Viraj Deshpande, Felix Schlesinger, Peter Krusche, Roman Petrovski, Sai Chen, Dorothea Emig-Agius, Andrew Gross, Giuseppe Narzisi, Brett Bowman,[...]. Bioinformatics 2019
42
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

Polyglutamine Repeats in Neurodegenerative Diseases.
Andrew P Lieberman, Vikram G Shakkottai, Roger L Albin. Annu Rev Pathol 2019
75
50

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Conceição Bettencourt, Davina Hensman-Moss, Michael Flower, Sarah Wiethoff, Alexis Brice, Cyril Goizet, Giovanni Stevanin, Georgios Koutsis, Georgia Karadima, Marios Panas,[...]. Ann Neurol 2016
114
50


CRISPR/Cas9 Editing of the Mutant Huntingtin Allele In Vitro and In Vivo.
Alex Mas Monteys, Shauna A Ebanks, Megan S Keiser, Beverly L Davidson. Mol Ther 2017
141
50

Variation in DNA Repair System Gene as an Additional Modifier of Age at Onset in Spinocerebellar Ataxia Type 3/Machado-Joseph Disease.
Rafaella Mergener, Gabriel Vasata Furtado, Eduardo Preusser de Mattos, Vanessa Bielefeldt Leotti, Laura Bannach Jardim, Maria Luiza Saraiva-Pereira. Neuromolecular Med 2020
5
50

Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1.
Ricardo Mouro Pinto, Larissa Arning, James V Giordano, Pedram Razghandi, Marissa A Andrew, Tammy Gillis, Kevin Correia, Jayalakshmi S Mysore, Debora-M Grote Urtubey, Constanze R Parwez,[...]. Hum Mol Genet 2020
21
50


CAG repeat expansion of Machado-Joseph disease in the Japanese: analysis of the repeat instability for parental transmission, and correlation with disease phenotype.
H Sasaki, A Wakisaka, T Fukazawa, K Iwabuchi, T Hamada, A Takada, E Mukai, T Matsuura, T Yoshiki, K Tashiro. J Neurol Sci 1995
18
50

The gene for Machado-Joseph disease maps to human chromosome 14q.
Y Takiyama, M Nishizawa, H Tanaka, S Kawashima, H Sakamoto, Y Karube, H Shimazaki, M Soutome, K Endo, S Ohta. Nat Genet 1993
297
50

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
A Dürr, G Stevanin, G Cancel, C Duyckaerts, N Abbas, O Didierjean, H Chneiweiss, A Benomar, O Lyon-Caen, J Julien,[...]. Ann Neurol 1996
337
50

Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations.
Dineke S Verbeek, Sytse J Piersma, Eric F A M Hennekam, Elly F Ippel, Peter L Pearson, Richard J Sinke. Eur J Hum Genet 2004
9
50

Is the High Frequency of Machado-Joseph Disease in China Due to New Mutational Origins?
Tianjiao Li, Sandra Martins, Yun Peng, Puzhi Wang, Xiaocan Hou, Zhao Chen, Chunrong Wang, Zhaoli Tang, Rong Qiu, Chao Chen,[...]. Front Genet 2019
6
50

Machado-Joseph disease in a Nigerian family: mutational origin and review of the literature.
Shamsideen Abayomi Ogun, Sandra Martins, Philip B Adebayo, Clara O Dawodu, Jorge Sequeiros, Michael F Finkel. Eur J Hum Genet 2015
7
50

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.
Y Kawaguchi, T Okamoto, M Taniwaki, M Aizawa, M Inoue, S Katayama, H Kawakami, S Nakamura, M Nishimura, I Akiguchi. Nat Genet 1994
50

Correlation between CAG repeat length and clinical features in Machado-Joseph disease.
P Maciel, C Gaspar, A L DeStefano, I Silveira, P Coutinho, J Radvany, D M Dawson, L Sudarsky, J Guimarães, J E Loureiro. Am J Hum Genet 1995
220
50

The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease.
Jae Whan Keum, Aram Shin, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Kawther Abu Elneel, Diane Lucente, Tiffany Hadzi, Peter Holmans, Lesley Jones, Michael Orth,[...]. Am J Hum Genet 2016
65
25

A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
D R Langbehn, R R Brinkman, D Falush, J S Paulsen, M R Hayden. Clin Genet 2004
518
25


FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair.
Weibin Zhou, Edgar A Otto, Andrew Cluckey, Rannar Airik, Toby W Hurd, Moumita Chaki, Katrina Diaz, Francis P Lach, Geoffrey R Bennett, Heon Yung Gee,[...]. Nat Genet 2012
144
25

Somatic expansion in mouse and human carriers of fragile X premutation alleles.
Rachel Adihe Lokanga, Ali Entezam, Daman Kumari, Dmitry Yudkin, Mei Qin, Carolyn Beebe Smith, Karen Usdin. Hum Mutat 2013
54
25

Precise Excision of the CAG Tract from the Huntingtin Gene by Cas9 Nickases.
Magdalena Dabrowska, Wojciech Juzwa, Wlodzimierz J Krzyzosiak, Marta Olejniczak. Front Neurosci 2018
47
25

Evaluating drug targets through human loss-of-function genetic variation.
Eric Vallabh Minikel, Konrad J Karczewski, Hilary C Martin, Beryl B Cummings, Nicola Whiffin, Daniel Rhodes, Jessica Alföldi, Richard C Trembath, David A van Heel, Mark J Daly,[...]. Nature 2020
41
25

Potent and sustained huntingtin lowering via AAV5 encoding miRNA preserves striatal volume and cognitive function in a humanized mouse model of Huntington disease.
Nicholas S Caron, Amber L Southwell, Cynthia C Brouwers, Louisa Dal Cengio, Yuanyun Xie, Hailey Findlay Black, Lisa M Anderson, Seunghyun Ko, Xiang Zhu, Sander J van Deventer,[...]. Nucleic Acids Res 2020
19
25


Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles.
Sarah L Nolin, Anne Glicksman, Nicole Tortora, Emily Allen, James Macpherson, Montserrat Mila, Angela M Vianna-Morgante, Stephanie L Sherman, Carl Dobkin, Gary J Latham,[...]. Am J Med Genet A 2019
19
25

MutLγ promotes repeat expansion in a Fragile X mouse model while EXO1 is protective.
Xiaonan Zhao, Yongwei Zhang, Kenneth Wilkins, Winfried Edelmann, Karen Usdin. PLoS Genet 2018
24
25

Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.
S S Chong, A E McCall, J Cota, S H Subramony, H T Orr, M R Hughes, H Y Zoghbi. Nat Genet 1995
153
25

PolyQ Tract Toxicity in SCA1 is Length Dependent in the Absence of CAG Repeat Interruption.
Suran Nethisinghe, Maria Lucia Pigazzini, Sally Pemble, Mary G Sweeney, Robyn Labrum, Katarina Manso, David Moore, Jon Warner, Mary B Davis, Paola Giunti. Front Cell Neurosci 2018
8
25


Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.
Davina J Hensman Moss, Antonio F Pardiñas, Douglas Langbehn, Kitty Lo, Blair R Leavitt, Raymund Roos, Alexandra Durr, Simon Mead, Peter Holmans, Lesley Jones,[...]. Lancet Neurol 2017
129
25

Deregulated Splicing Is a Major Mechanism of RNA-Induced Toxicity in Huntington's Disease.
Judith Schilling, Meike Broemer, Ilian Atanassov, Yvonne Duernberger, Ina Vorberg, Christoph Dieterich, Alina Dagane, Gunnar Dittmar, Erich Wanker, Willeke van Roon-Mom,[...]. J Mol Biol 2019
22
25

Results from a phase 1 study of nusinersen (ISIS-SMN(Rx)) in children with spinal muscular atrophy.
Claudia A Chiriboga, Kathryn J Swoboda, Basil T Darras, Susan T Iannaccone, Jacqueline Montes, Darryl C De Vivo, Daniel A Norris, C Frank Bennett, Kathie M Bishop. Neurology 2016
332
25

Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.
Meera Swami, Audrey E Hendricks, Tammy Gillis, Tiffany Massood, Jayalakshmi Mysore, Richard H Myers, Vanessa C Wheeler. Hum Mol Genet 2009
159
25

Ultrasensitive measurement of huntingtin protein in cerebrospinal fluid demonstrates increase with Huntington disease stage and decrease following brain huntingtin suppression.
Amber L Southwell, Stephen E P Smith, Tessa R Davis, Nicholas S Caron, Erika B Villanueva, Yuanyun Xie, Jennifer A Collins, Min Li Ye, Aaron Sturrock, Blair R Leavitt,[...]. Sci Rep 2015
48
25

The somatic mutation landscape of the human body.
Pablo E García-Nieto, Ashby J Morrison, Hunter B Fraser. Genome Biol 2019
27
25

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
25

Immune responses to AAV in a phase I study for Canavan disease.
S W J McPhee, C G Janson, C Li, R J Samulski, A S Camp, J Francis, D Shera, L Lioutermann, M Feely, A Freese,[...]. J Gene Med 2006
171
25

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein.
K Nakamura, S Y Jeong, T Uchihara, M Anno, K Nagashima, T Nagashima, S Ikeda, S Tsuji, I Kanazawa. Hum Mol Genet 2001
456
25

CRISPR-Cas9-Mediated Genome Editing Increases Lifespan and Improves Motor Deficits in a Huntington's Disease Mouse Model.
Freja K Ekman, David S Ojala, Maroof M Adil, Paola A Lopez, David V Schaffer, Thomas Gaj. Mol Ther Nucleic Acids 2019
32
25

Unbiased Profiling of Isogenic Huntington Disease hPSC-Derived CNS and Peripheral Cells Reveals Strong Cell-Type Specificity of CAG Length Effects.
Jolene Ooi, Sarah R Langley, Xiaohong Xu, Kagistia H Utami, Bernice Sim, Yihui Huang, Nathan P Harmston, Yi Lin Tay, Amin Ziaei, Ruizhu Zeng,[...]. Cell Rep 2019
28
25

Elimination of Toxic Microsatellite Repeat Expansion RNA by RNA-Targeting Cas9.
Ranjan Batra, David A Nelles, Elaine Pirie, Steven M Blue, Ryan J Marina, Harrison Wang, Isaac A Chaim, James D Thomas, Nigel Zhang, Vu Nguyen,[...]. Cell 2017
131
25

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.
H Telenius, B Kremer, Y P Goldberg, J Theilmann, S E Andrew, J Zeisler, S Adam, C Greenberg, E J Ives, L A Clarke. Nat Genet 1994
301
25


Interruptions in the triplet repeats of SCA1 and FRAXA reduce the propensity and complexity of slipped strand DNA (S-DNA) formation.
C E Pearson, E E Eichler, D Lorenzetti, S F Kramer, H Y Zoghbi, D L Nelson, R R Sinden. Biochemistry 1998
115
25

Cancer Risks for PMS2-Associated Lynch Syndrome.
Sanne W Ten Broeke, Heleen M van der Klift, Carli M J Tops, Stefan Aretz, Inge Bernstein, Daniel D Buchanan, Albert de la Chapelle, Gabriel Capella, Mark Clendenning, Christoph Engel,[...]. J Clin Oncol 2018
80
25

Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects.
Kyung-Hee Kim, Eun Pyo Hong, Jun Wan Shin, Michael J Chao, Jacob Loupe, Tammy Gillis, Jayalakshmi S Mysore, Peter Holmans, Lesley Jones, Michael Orth,[...]. Am J Hum Genet 2020
17
25

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
25


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.