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



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  Times     Co-cited
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Genetic correction of Huntington's disease phenotypes in induced pluripotent stem cells.
Mahru C An, Ningzhe Zhang, Gary Scott, Daniel Montoro, Tobias Wittkop, Sean Mooney, Simon Melov, Lisa M Ellerby. Cell Stem Cell 2012
236
50


Reversal of Phenotypic Abnormalities by CRISPR/Cas9-Mediated Gene Correction in Huntington Disease Patient-Derived Induced Pluripotent Stem Cells.
Xiaohong Xu, Yilin Tay, Bernice Sim, Su-In Yoon, Yihui Huang, Jolene Ooi, Kagistia Hana Utami, Amin Ziaei, Bryan Ng, Carola Radulescu,[...]. Stem Cell Reports 2017
111
43

The first reported generation of several induced pluripotent stem cell lines from homozygous and heterozygous Huntington's disease patients demonstrates mutation related enhanced lysosomal activity.
Stefano Camnasio, Alessia Delli Carri, Angelo Lombardo, Iwona Grad, Caterina Mariotti, Alessia Castucci, Björn Rozell, Pietro Lo Riso, Valentina Castiglioni, Chiara Zuccato,[...]. Neurobiol Dis 2012
125
37

Characterization of Human Huntington's Disease Cell Model from Induced Pluripotent Stem Cells.
Ningzhe Zhang, Mahru C An, Daniel Montoro, Lisa M Ellerby. PLoS Curr 2010
173
37

Quantitative proteomic analysis of induced pluripotent stem cells derived from a human Huntington's disease patient.
Jung-Il Chae, Dong-Wook Kim, Nayeon Lee, Young-Joo Jeon, Iksoo Jeon, Jihye Kwon, Jumi Kim, Yunjo Soh, Dong-Seok Lee, Kang Seok Seo,[...]. Biochem J 2012
70
37


Disease-specific induced pluripotent stem cells.
In-Hyun Park, Natasha Arora, Hongguang Huo, Nimet Maherali, Tim Ahfeldt, Akiko Shimamura, M William Lensch, Chad Cowan, Konrad Hochedlinger, George Q Daley. Cell 2008
31

Striatal neurons directly converted from Huntington's disease patient fibroblasts recapitulate age-associated disease phenotypes.
Matheus B Victor, Michelle Richner, Hannah E Olsen, Seong Won Lee, Alejandro M Monteys, Chunyu Ma, Christine J Huh, Bo Zhang, Beverly L Davidson, X William Yang,[...]. Nat Neurosci 2018
94
31

Human Huntington's Disease iPSC-Derived Cortical Neurons Display Altered Transcriptomics, Morphology, and Maturation.
Shagun R Mehta, Colton M Tom, Yizhou Wang, Catherine Bresee, David Rushton, Pranav P Mathkar, Jie Tang, Virginia B Mattis. Cell Rep 2018
42
31

Inhibition of mitochondrial fragmentation diminishes Huntington's disease-associated neurodegeneration.
Xing Guo, Marie-Helene Disatnik, Marie Monbureau, Mehrdad Shamloo, Daria Mochly-Rosen, Xin Qi. J Clin Invest 2013
218
31

Manifestation of Huntington's disease pathology in human induced pluripotent stem cell-derived neurons.
Evgeny D Nekrasov, Vladimir A Vigont, Sergey A Klyushnikov, Olga S Lebedeva, Ekaterina M Vassina, Alexandra N Bogomazova, Ilya V Chestkov, Tatiana A Semashko, Elena Kiseleva, Lyubov A Suldina,[...]. Mol Neurodegener 2016
80
31

Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity.
Wenjun Song, Jin Chen, Alejandra Petrilli, Geraldine Liot, Eva Klinglmayr, Yue Zhou, Patrick Poquiz, Jonathan Tjong, Mahmoud A Pouladi, Michael R Hayden,[...]. Nat Med 2011
357
25

Molecular mechanisms and potential therapeutical targets in Huntington's disease.
Chiara Zuccato, Marta Valenza, Elena Cattaneo. Physiol Rev 2010
550
25

Mitochondrial loss, dysfunction and altered dynamics in Huntington's disease.
Jinho Kim, Jennifer P Moody, Christina K Edgerly, Olivia L Bordiuk, Kerry Cormier, Karen Smith, M Flint Beal, Robert J Ferrante. Hum Mol Genet 2010
208
25

Human iPSC-based modeling of late-onset disease via progerin-induced aging.
Justine D Miller, Yosif M Ganat, Sarah Kishinevsky, Robert L Bowman, Becky Liu, Edmund Y Tu, Pankaj K Mandal, Elsa Vera, Jae-won Shim, Sonja Kriks,[...]. Cell Stem Cell 2013
419
25

Mutant huntingtin's interaction with mitochondrial protein Drp1 impairs mitochondrial biogenesis and causes defective axonal transport and synaptic degeneration in Huntington's disease.
Ulziibat P Shirendeb, Marcus J Calkins, Maria Manczak, Vishwanath Anekonda, Brett Dufour, Jodi L McBride, Peizhong Mao, P Hemachandra Reddy. Hum Mol Genet 2012
218
25

N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking.
Adam L Orr, Shihua Li, Chuan-En Wang, He Li, Jianjun Wang, Juan Rong, Xingshun Xu, Pier Giorgio Mastroberardino, J Timothy Greenamyre, Xiao-Jiang Li. J Neurosci 2008
281
25

Characterization of forebrain neurons derived from late-onset Huntington's disease human embryonic stem cell lines.
Jonathan C Niclis, Anita Pinar, John M Haynes, Walaa Alsanie, Robert Jenny, Mirella Dottori, David S Cram. Front Cell Neurosci 2013
29
25

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
25

Genomic Analysis Reveals Disruption of Striatal Neuronal Development and Therapeutic Targets in Human Huntington's Disease Neural Stem Cells.
Karen L Ring, Mahru C An, Ningzhe Zhang, Robert N O'Brien, Eliana Marisa Ramos, Fuying Gao, Robert Atwood, Barbara J Bailus, Simon Melov, Sean D Mooney,[...]. Stem Cell Reports 2015
56
25

Neuronal properties, in vivo effects, and pathology of a Huntington's disease patient-derived induced pluripotent stem cells.
Iksoo Jeon, Nayeon Lee, Jia-Yi Li, In-Hyun Park, Kyoung Sun Park, Jisook Moon, Sung Han Shim, Chunggab Choi, Da-Jeong Chang, Jihye Kwon,[...]. Stem Cells 2012
125
25

HD iPSC-derived neural progenitors accumulate in culture and are susceptible to BDNF withdrawal due to glutamate toxicity.
Virginia B Mattis, Colton Tom, Sergey Akimov, Jasmine Saeedian, Michael E Østergaard, Amber L Southwell, Crystal N Doty, Loren Ornelas, Anais Sahabian, Lindsay Lenaeus,[...]. Hum Mol Genet 2015
64
25

Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9.
Jun Wan Shin, Kyung-Hee Kim, Michael J Chao, Ranjit S Atwal, Tammy Gillis, Marcy E MacDonald, James F Gusella, Jong-Min Lee. Hum Mol Genet 2016
123
25

Proteomics of Huntington's disease-affected human embryonic stem cells reveals an evolving pathology involving mitochondrial dysfunction and metabolic disturbances.
Leon R McQuade, Anushree Balachandran, Heather A Scott, Simer Khaira, Mark S Baker, Uli Schmidt. J Proteome Res 2014
35
25

Generation of human striatal neurons by microRNA-dependent direct conversion of fibroblasts.
Matheus B Victor, Michelle Richner, Tracey O Hermanstyne, Joseph L Ransdell, Courtney Sobieski, Pan-Yue Deng, Vitaly A Klyachko, Jeanne M Nerbonne, Andrew S Yoo. Neuron 2014
173
25

Oxidative metabolism in YAC128 mouse model of Huntington's disease.
James Hamilton, Jessica J Pellman, Tatiana Brustovetsky, Robert A Harris, Nickolay Brustovetsky. Hum Mol Genet 2015
31
18

Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease.
Elizabeth J Slow, Jeremy van Raamsdonk, Daniel Rogers, Sarah H Coleman, Rona K Graham, Yu Deng, Rosemary Oh, Nagat Bissada, Sazzad M Hossain, Yu-Zhou Yang,[...]. Hum Mol Genet 2003
569
18

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice.
L Mangiarini, K Sathasivam, M Seller, B Cozens, A Harper, C Hetherington, M Lawton, Y Trottier, H Lehrach, S W Davies,[...]. Cell 1996
18

Huntington disease.
J P Vonsattel, M DiFiglia. J Neuropathol Exp Neurol 1998
18

Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage.
Ulziibat Shirendeb, Arubala P Reddy, Maria Manczak, Marcus J Calkins, Peizhong Mao, Danilo A Tagle, P Hemachandra Reddy. Hum Mol Genet 2011
248
18

Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond.
Hristelina Ilieva, Magdalini Polymenidou, Don W Cleveland. J Cell Biol 2009
725
18

Age-dependent neurovascular abnormalities and altered microglial morphology in the YAC128 mouse model of Huntington disease.
Sonia Franciosi, Jae K Ryu, Yaein Shim, Austin Hill, Colum Connolly, Michael R Hayden, James G McLarnon, Blair R Leavitt. Neurobiol Dis 2012
72
18

Role of brain-derived neurotrophic factor in Huntington's disease.
Chiara Zuccato, Elena Cattaneo. Prog Neurobiol 2007
372
18

Microglial activation correlates with severity in Huntington disease: a clinical and PET study.
N Pavese, A Gerhard, Y F Tai, A K Ho, F Turkheimer, R A Barker, D J Brooks, P Piccini. Neurology 2006
273
18

Brain-derived neurotrophic factor regulates the onset and severity of motor dysfunction associated with enkephalinergic neuronal degeneration in Huntington's disease.
Josep M Canals, José R Pineda, Jesús F Torres-Peraza, Miquel Bosch, Raquel Martín-Ibañez, M Teresa Muñoz, Guadalupe Mengod, Patrik Ernfors, Jordi Alberch. J Neurosci 2004
249
18

Astrocytes generated from patient induced pluripotent stem cells recapitulate features of Huntington's disease patient cells.
Tarja A Juopperi, Woon Ryoung Kim, Cheng-Hsuan Chiang, Huimei Yu, Russell L Margolis, Christopher A Ross, Guo-li Ming, Hongjun Song. Mol Brain 2012
154
18

Microglial activation in presymptomatic Huntington's disease gene carriers.
Yen F Tai, Nicola Pavese, Alexander Gerhard, Sarah J Tabrizi, Roger A Barker, David J Brooks, Paola Piccini. Brain 2007
274
18

Polyglutamine Disease Modeling: Epitope Based Screen for Homologous Recombination using CRISPR/Cas9 System.
Mahru C An, Robert N O'Brien, Ningzhe Zhang, Biranchi N Patra, Michael De La Cruz, Animesh Ray, Lisa M Ellerby. PLoS Curr 2014
49
18

PPARδ activation by bexarotene promotes neuroprotection by restoring bioenergetic and quality control homeostasis.
Audrey S Dickey, Dafne N Sanchez, Martin Arreola, Kunal R Sampat, Weiwei Fan, Nicolas Arbez, Sergey Akimov, Michael J Van Kanegan, Kohta Ohnishi, Stephen K Gilmore-Hall,[...]. Sci Transl Med 2017
33
18

Targeting Huntingtin Expression in Patients with Huntington's Disease.
Sarah J Tabrizi, Blair R Leavitt, G Bernhard Landwehrmeyer, Edward J Wild, Carsten Saft, Roger A Barker, Nick F Blair, David Craufurd, Josef Priller, Hugh Rickards,[...]. N Engl J Med 2019
249
18

Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects.
Jerome Mertens, Apuã C M Paquola, Manching Ku, Emily Hatch, Lena Böhnke, Shauheen Ladjevardi, Sean McGrath, Benjamin Campbell, Hyungjun Lee, Joseph R Herdy,[...]. Cell Stem Cell 2015
344
18

The ubiquitin ligase UBR5 suppresses proteostasis collapse in pluripotent stem cells from Huntington's disease patients.
Seda Koyuncu, Isabel Saez, Hyun Ju Lee, Ricardo Gutierrez-Garcia, Wojciech Pokrzywa, Azra Fatima, Thorsten Hoppe, David Vilchez. Nat Commun 2018
42
18

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
18

Huntington disease iPSCs show early molecular changes in intracellular signaling, the expression of oxidative stress proteins and the p53 pathway.
Wojciech J Szlachcic, Pawel M Switonski, Wlodzimierz J Krzyzosiak, Marek Figlerowicz, Maciej Figiel. Dis Model Mech 2015
32
18

Human pluripotent stem cell differentiation into authentic striatal projection neurons.
Alessia Delli Carri, Marco Onorati, Valentina Castiglioni, Andrea Faedo, Stefano Camnasio, Mauro Toselli, Gerardo Biella, Elena Cattaneo. Stem Cell Rev Rep 2013
44
18

Targeting ATM ameliorates mutant Huntingtin toxicity in cell and animal models of Huntington's disease.
Xiao-Hong Lu, Virginia B Mattis, Nan Wang, Ismael Al-Ramahi, Nick van den Berg, Silvina A Fratantoni, Henry Waldvogel, Erin Greiner, Alex Osmand, Karla Elzein,[...]. Sci Transl Med 2014
71
18

Energy Metabolism and Mitochondrial Superoxide Anion Production in Pre-symptomatic Striatal Neurons Derived from Human-Induced Pluripotent Stem Cells Expressing Mutant Huntingtin.
James Hamilton, Tatiana Brustovetsky, Akshayalakshmi Sridhar, Yanling Pan, Theodore R Cummins, Jason S Meyer, Nickolay Brustovetsky. Mol Neurobiol 2020
9
33

Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling.
Stuart M Chambers, Christopher A Fasano, Eirini P Papapetrou, Mark Tomishima, Michel Sadelain, Lorenz Studer. Nat Biotechnol 2009
18


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.