A citation-based method for searching scientific literature

Shalini Mani, Geeta Swargiary, Radhika Chadha. Mitochondrion 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Mutant huntingtin impairs Ku70-mediated DNA repair.
Yasushi Enokido, Takuya Tamura, Hikaru Ito, Anup Arumughan, Akihiko Komuro, Hiroki Shiwaku, Masaki Sone, Raphaele Foulle, Hirohide Sawada, Hiroshi Ishiguro,[...]. J Cell Biol 2010
73
66

ATM functions at the peroxisome to induce pexophagy in response to ROS.
Jiangwei Zhang, Durga Nand Tripathi, Ji Jing, Angela Alexander, Jinhee Kim, Reid T Powell, Ruhee Dere, Jacqueline Tait-Mulder, Ji-Hoon Lee, Tanya T Paull,[...]. Nat Cell Biol 2015
233
66

Huntington's disease: from molecular pathogenesis to clinical treatment.
Christopher A Ross, Sarah J Tabrizi. Lancet Neurol 2011
895
66

PGC-1α rescues Huntington's disease proteotoxicity by preventing oxidative stress and promoting TFEB function.
Taiji Tsunemi, Travis D Ashe, Bradley E Morrison, Kathryn R Soriano, Jonathan Au, Ruben A Vázquez Roque, Eduardo R Lazarowski, Vincent A Damian, Eliezer Masliah, Albert R La Spada. Sci Transl Med 2012
294
66

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
66



Leucine-rich repeat kinase 2 disturbs mitochondrial dynamics via Dynamin-like protein.
Jingwen Niu, Mei Yu, Chunyan Wang, Zhiheng Xu. J Neurochem 2012
105
66

Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin.
Atsushi Tanaka, Megan M Cleland, Shan Xu, Derek P Narendra, Der-Fen Suen, Mariusz Karbowski, Richard J Youle. J Cell Biol 2010
882
66

OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells.
Irina V Kovtun, Yuan Liu, Magnar Bjoras, Arne Klungland, Samuel H Wilson, Cynthia T McMurray. Nature 2007
324
66

Huntington disease.
Gillian P Bates, Ray Dorsey, James F Gusella, Michael R Hayden, Chris Kay, Blair R Leavitt, Martha Nance, Christopher A Ross, Rachael I Scahill, Ronald Wetzel,[...]. Nat Rev Dis Primers 2015
558
66

ATF4 protects against neuronal death in cellular Parkinson's disease models by maintaining levels of parkin.
Xiaotian Sun, Jin Liu, John F Crary, Cristina Malagelada, David Sulzer, Lloyd A Greene, Oren A Levy. J Neurosci 2013
83
66

Mitochondrial DNA damage is associated with reduced mitochondrial bioenergetics in Huntington's disease.
Almas Siddiqui, Sulay Rivera-Sánchez, María del R Castro, Karina Acevedo-Torres, Anand Rane, Carlos A Torres-Ramos, David G Nicholls, Julie K Andersen, Sylvette Ayala-Torres. Free Radic Biol Med 2012
82
66

S-nitrosylation of dynamin-related protein 1 mediates mutant huntingtin-induced mitochondrial fragmentation and neuronal injury in Huntington's disease.
Florian Haun, Tomohiro Nakamura, Alicia D Shiu, Dong-Hyung Cho, Taiji Tsunemi, Emily A Holland, Albert R La Spada, Stuart A Lipton. Antioxid Redox Signal 2013
71
66

Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration.
Libin Cui, Hyunkyung Jeong, Fran Borovecki, Christopher N Parkhurst, Naoko Tanese, Dimitri Krainc. Cell 2006
744
66


Aging and neurodegeneration are associated with increased mutations in single human neurons.
Michael A Lodato, Rachel E Rodin, Craig L Bohrson, Michael E Coulter, Alison R Barton, Minseok Kwon, Maxwell A Sherman, Carl M Vitzthum, Lovelace J Luquette, Chandri N Yandava,[...]. Science 2018
212
33

Oxidative stress in Fanconi anaemia: from cells and molecules towards prospects in clinical management.
Giovanni Pagano, Annarita Aiello Talamanca, Giuseppe Castello, Federico V Pallardó, Adriana Zatterale, Paolo Degan. Biol Chem 2012
43
33

Brain insulin resistance in type 2 diabetes and Alzheimer disease: concepts and conundrums.
Steven E Arnold, Zoe Arvanitakis, Shannon L Macauley-Rambach, Aaron M Koenig, Hoau-Yan Wang, Rexford S Ahima, Suzanne Craft, Sam Gandy, Christoph Buettner, Luke E Stoeckel,[...]. Nat Rev Neurol 2018
396
33

Dysregulated Ca2+ homeostasis in Fanconi anemia cells.
Cesare Usai, Silvia Ravera, Paola Cuccarolo, Isabella Panfoli, Carlo Dufour, Enrico Cappelli, Paolo Degan. Sci Rep 2015
11
33

Nuclear localization sequence of FUS and induction of stress granules by ALS mutants.
Jozsef Gal, Jiayu Zhang, David M Kwinter, Jianjun Zhai, Hongge Jia, Jianhang Jia, Haining Zhu. Neurobiol Aging 2011
143
33

Genomic integrity and the ageing brain.
Hei-man Chow, Karl Herrup. Nat Rev Neurosci 2015
96
33

Mitochondrial Dysfunction, Neurogenesis, and Epigenetics: Putative Implications for Amyotrophic Lateral Sclerosis Neurodegeneration and Treatment.
Michele Longoni Calió, Elisandra Henriques, Amanda Siena, Clélia Rejane Antonio Bertoncini, Joana Gil-Mohapel, Tatiana Rosado Rosenstock. Front Neurosci 2020
13
33

Altered DNA base excision repair profile in brain tissue and blood in Alzheimer's disease.
Meryl S Lillenes, Alberto Rabano, Mari Støen, Tahira Riaz, Dorna Misaghian, Linda Møllersen, Ying Esbensen, Clara-Cecilie Günther, Per Selnes, Vidar T V Stenset,[...]. Mol Brain 2016
25
33


SIRT1 protects against α-synuclein aggregation by activating molecular chaperones.
Gizem Donmez, Anirudh Arun, Chee-Yeun Chung, Pamela J McLean, Susan Lindquist, Leonard Guarente. J Neurosci 2012
141
33

Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect.
Hiva Fassihi, Mieran Sethi, Heather Fawcett, Jonathan Wing, Natalie Chandler, Shehla Mohammed, Emma Craythorne, Ana M S Morley, Rongxuan Lim, Sally Turner,[...]. Proc Natl Acad Sci U S A 2016
86
33

ATP-dependent chromatin remodeling and DNA double-strand break repair.
Haico van Attikum, Susan M Gasser. Cell Cycle 2005
78
33

Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy.
Hiroshi Takashima, Cornelius F Boerkoel, Joy John, Gulam Mustafa Saifi, Mustafa A M Salih, Dawna Armstrong, Yuxin Mao, Florante A Quiocho, Benjamin B Roa, Masanori Nakagawa,[...]. Nat Genet 2002
364
33

Genome instability in Alzheimer disease.
Yujun Hou, Hyundong Song, Deborah L Croteau, Mansour Akbari, Vilhelm A Bohr. Mech Ageing Dev 2017
48
33

Oxidative DNA damage: mechanisms, mutation, and disease.
Marcus S Cooke, Mark D Evans, Miral Dizdaroglu, Joseph Lunec. FASEB J 2003
33

Reversal of mitochondrial defects with CSB-dependent serine protease inhibitors in patient cells of the progeroid Cockayne syndrome.
Laurent Chatre, Denis S F Biard, Alain Sarasin, Miria Ricchetti. Proc Natl Acad Sci U S A 2015
36
33

Oxidative lipid modification of nicastrin enhances amyloidogenic γ-secretase activity in Alzheimer's disease.
A-Ryeong Gwon, Jong-Sung Park, Thiruma V Arumugam, Yong-Kook Kwon, Sic L Chan, Seol-Hee Kim, Sang-Ha Baik, Sunghee Yang, Young-Kwang Yun, Yuri Choi,[...]. Aging Cell 2012
60
33

The Role of Cholesterol in α-Synuclein and Lewy Body Pathology in GBA1 Parkinson's Disease.
Patricia García-Sanz, Johannes M F G Aerts, Rosario Moratalla. Mov Disord 2021
5
33

The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin.
M C Moreira, C Barbot, N Tachi, N Kozuka, E Uchida, T Gibson, P Mendonça, M Costa, J Barros, T Yanagisawa,[...]. Nat Genet 2001
314
33

Human Cockayne syndrome B protein reciprocally communicates with mitochondrial proteins and promotes transcriptional elongation.
Brian R Berquist, Chandrika Canugovi, Peter Sykora, David M Wilson, Vilhelm A Bohr. Nucleic Acids Res 2012
46
33

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.
H Date, O Onodera, H Tanaka, K Iwabuchi, K Uekawa, S Igarashi, R Koike, T Hiroi, T Yuasa, Y Awaya,[...]. Nat Genet 2001
274
33

FUS is phosphorylated by DNA-PK and accumulates in the cytoplasm after DNA damage.
Qiudong Deng, Christopher J Holler, Georgia Taylor, Kathryn F Hudson, William Watkins, Marla Gearing, Daisuke Ito, Melissa E Murray, Dennis W Dickson, Nicholas T Seyfried,[...]. J Neurosci 2014
82
33

DNA repair deficiency in neurodegeneration.
Dennis Kjølhede Jeppesen, Vilhelm A Bohr, Tinna Stevnsner. Prog Neurobiol 2011
201
33


Poly(GR) in C9ORF72-Related ALS/FTD Compromises Mitochondrial Function and Increases Oxidative Stress and DNA Damage in iPSC-Derived Motor Neurons.
Rodrigo Lopez-Gonzalez, Yubing Lu, Tania F Gendron, Anna Karydas, Helene Tran, Dejun Yang, Leonard Petrucelli, Bruce L Miller, Sandra Almeida, Fen-Biao Gao. Neuron 2016
178
33

Lack of XPC leads to a shift between respiratory complexes I and II but sensitizes cells to mitochondrial stress.
Mateus P Mori, Rute A P Costa, Daniela T Soltys, Thiago de S Freire, Franco A Rossato, Ignácio Amigo, Alicia J Kowaltowski, Aníbal E Vercesi, Nadja C de Souza-Pinto. Sci Rep 2017
15
33

SCAN1-TDP1 trapping on mitochondrial DNA promotes mitochondrial dysfunction and mitophagy.
Arijit Ghosh, Sangheeta Bhattacharjee, Srijita Paul Chowdhuri, Abhik Mallick, Ishita Rehman, Sudipta Basu, Benu Brata Das. Sci Adv 2019
16
33

ATM directs DNA damage responses and proteostasis via genetically separable pathways.
Ji-Hoon Lee, Michael R Mand, Chung-Hsuan Kao, Yi Zhou, Seung W Ryu, Alicia L Richards, Joshua J Coon, Tanya T Paull. Sci Signal 2018
44
33

Mutant SOD1G93A triggers mitochondrial fragmentation in spinal cord motor neurons: neuroprotection by SIRT3 and PGC-1α.
Wenjun Song, Yuting Song, Brad Kincaid, Blaise Bossy, Ella Bossy-Wetzel. Neurobiol Dis 2013
140
33

Mitochondrial respiratory complex I defects in Fanconi anemia.
Enrico Cappelli, Silvia Ravera, Daniele Vaccaro, Paola Cuccarolo, Martina Bartolucci, Isabella Panfoli, Carlo Dufour, Paolo Degan. Trends Mol Med 2013
28
33

Activation of the DNA damage response in vivo in synucleinopathy models of Parkinson's disease.
Chiara Milanese, Silvia Cerri, Ayse Ulusoy, Simona V Gornati, Audrey Plat, Sylvia Gabriels, Fabio Blandini, Donato A Di Monte, Jan H Hoeijmakers, Pier G Mastroberardino. Cell Death Dis 2018
43
33

Neurological symptoms and natural course of xeroderma pigmentosum.
Anu Anttinen, Leena Koulu, Eeva Nikoskelainen, Raija Portin, Timo Kurki, Matti Erkinjuntti, Nicolaas G J Jaspers, Anja Raams, Michael H L Green, Alan R Lehmann,[...]. Brain 2008
76
33

The Response to Oxidative DNA Damage in Neurons: Mechanisms and Disease.
Laura Narciso, Eleonora Parlanti, Mauro Racaniello, Valeria Simonelli, Alessio Cardinale, Daniela Merlo, Eugenia Dogliotti. Neural Plast 2016
40
33

Cockayne syndrome group B protein prevents the accumulation of damaged mitochondria by promoting mitochondrial autophagy.
Morten Scheibye-Knudsen, Mahesh Ramamoorthy, Peter Sykora, Scott Maynard, Ping-Chang Lin, Robin K Minor, David M Wilson, Marcus Cooper, Richard Spencer, Rafael de Cabo,[...]. J Exp Med 2012
136
33


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.