A citation-based method for searching scientific literature

Xuemin Jian, Jianhua Chen, Zhiqiang Li, Aamir Fahira, Weihuan Shao, Juan Zhou, Ke Wang, Yanqin Wen, Jinmai Zhang, Qiangzhen Yang, Dun Pan, Zhuo Wang, Yongyong Shi. Prog Neuropsychopharmacol Biol Psychiatry 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Structural basis for novel interactions between human translesion synthesis polymerases and proliferating cell nuclear antigen.
Asami Hishiki, Hiroshi Hashimoto, Tomo Hanafusa, Keijiro Kamei, Eiji Ohashi, Toshiyuki Shimizu, Haruo Ohmori, Mamoru Sato. J Biol Chem 2009
100
100

Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1.
R G Lafrenière, D L Rochefort, N Chrétien, J M Rommens, J I Cochius, R Kälviäinen, U Nousiainen, G Patry, K Farrell, B Söderfeldt,[...]. Nat Genet 1997
139
100

DNA Repair in Huntington's Disease and Spinocerebellar Ataxias: Somatic Instability and Alternative Hypotheses.
Tamara Maiuri, Claudia L K Hung, Celeste Suart, Nola Begeja, Carlos Barba-Bazan, Yi Peng, Natasha Savic, Timothy Wong, Ray Truant. J Huntingtons Dis 2021
5
100

The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair.
Puck Knipscheer, Markus Räschle, Agata Smogorzewska, Milica Enoiu, The Vinh Ho, Orlando D Schärer, Stephen J Elledge, Johannes C Walter. Science 2009
358
100

Double-strand break repair-independent role for BRCA2 in blocking stalled replication fork degradation by MRE11.
Katharina Schlacher, Nicole Christ, Nicolas Siaud, Akinori Egashira, Hong Wu, Maria Jasin. Cell 2011
682
100


The Werner syndrome protein promotes CAG/CTG repeat stability by resolving large (CAG)(n)/(CTG)(n) hairpins.
Nelson L S Chan, Caixia Hou, Tianyi Zhang, Fenghua Yuan, Amrita Machwe, Jian Huang, David K Orren, Liya Gu, Guo-Min Li. J Biol Chem 2012
14
100

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
107
100

Physical and functional interactions of human DNA polymerase eta with PCNA.
L Haracska, R E Johnson, I Unk, B Phillips, J Hurwitz, L Prakash, S Prakash. Mol Cell Biol 2001
201
100

The role of copy number variation in schizophrenia.
George Kirov. Expert Rev Neurother 2010
41
100


XPF-ERCC1 acts in Unhooking DNA interstrand crosslinks in cooperation with FANCD2 and FANCP/SLX4.
Daisy Klein Douwel, Rick A C M Boonen, David T Long, Anna A Szypowska, Markus Räschle, Johannes C Walter, Puck Knipscheer. Mol Cell 2014
187
100

Functional and physical interaction between the mismatch repair and FA-BRCA pathways.
Stacy A Williams, James B Wilson, Allison P Clark, Alyssa Mitson-Salazar, Andrei Tomashevski, Sahana Ananth, Peter M Glazer, O John Semmes, Allen E Bale, Nigel J Jones,[...]. Hum Mol Genet 2011
34
100

Cardiac circRNAs arise mainly from constitutive exons rather than alternatively spliced exons.
Simona Aufiero, Maarten M G van den Hoogenhof, Yolan J Reckman, Abdelaziz Beqqali, Ingeborg van der Made, Jolanda Kluin, Mohsin A F Khan, Yigal M Pinto, Esther E Creemers. RNA 2018
30
100

Age of onset in Huntington's disease is influenced by CAG repeat variations in other polyglutamine disease-associated genes.
Geerte Stuitje, Martine J van Belzen, Sarah L Gardiner, Willeke M C van Roon-Mom, Merel W Boogaard, Sarah J Tabrizi, Raymund A C Roos, N A Aziz. Brain 2017
6
100

On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability.
Alexandra N Khristich, Sergei M Mirkin. J Biol Chem 2020
30
100

Alternative DNA Structures In Vivo: Molecular Evidence and Remaining Questions.
Lucie Poggi, Guy-Franck Richard. Microbiol Mol Biol Rev 2020
5
100

Genes with triplet repeats: candidate mediators of neuropsychiatric disorders.
C A Ross, M G McInnis, R L Margolis, S H Li. Trends Neurosci 1993
166
100

Ubiquitinated Fancd2 recruits Fan1 to stalled replication forks to prevent genome instability.
Christophe Lachaud, Alberto Moreno, Francesco Marchesi, Rachel Toth, J Julian Blow, John Rouse. Science 2016
78
100


Human KIAA1018/FAN1 localizes to stalled replication forks via its ubiquitin-binding domain.
Robert D Shereda, Yuka Machida, Yuichi J Machida. Cell Cycle 2010
19
100

Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy.
M D Lalioti, H S Scott, C Buresi, C Rossier, A Bottani, M A Morris, A Malafosse, S E Antonarakis. Nature 1997
236
100

Spartan/C1orf124, a reader of PCNA ubiquitylation and a regulator of UV-induced DNA damage response.
Richard C Centore, Stephanie A Yazinski, Alice Tse, Lee Zou. Mol Cell 2012
91
100

Trinucleotide repeat expansion and neuropsychiatric disease.
R L Margolis, M G McInnis, A Rosenblatt, C A Ross. Arch Gen Psychiatry 1999
61
100

Double-strand break repair plays a role in repeat instability in a fragile X mouse model.
Inbal Gazy, Bruce Hayward, Svetlana Potapova, Xiaonan Zhao, Karen Usdin. DNA Repair (Amst) 2019
7
100

FAN1 protects against repeat expansions in a Fragile X mouse model.
Xiao-Nan Zhao, Karen Usdin. DNA Repair (Amst) 2018
28
100

Patterns of de novo tandem repeat mutations and their role in autism.
Ileena Mitra, Bonnie Huang, Nima Mousavi, Nichole Ma, Michael Lamkin, Richard Yanicky, Sharona Shleizer-Burko, Kirk E Lohmueller, Melissa Gymrek. Nature 2021
9
100


Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathology.
Adebola Enikanolaiye, Julie Ruston, Rong Zeng, Christine Taylor, Marijke Schrock, Christie M Buchovecky, Jay Shendure, Elif Acar, Monica J Justice. Genome Res 2020
4
100

Karyomegalic interstitial nephritis: further support for a distinct entity and evidence for a genetic defect.
M Spoendlin, H Moch, F Brunner, W Brunner, H R Burger, D Kiss, W Wegmann, P Dalquen, M Oberholzer, G Thiel. Am J Kidney Dis 1995
36
100

Protein tyrosine phosphatases in the human genome.
Andres Alonso, Joanna Sasin, Nunzio Bottini, Ilan Friedberg, Iddo Friedberg, Andrei Osterman, Adam Godzik, Tony Hunter, Jack Dixon, Tomas Mustelin. Cell 2004
100


Anticipation in bipolar affective disorder.
M G McInnis, F J McMahon, G A Chase, S G Simpson, C A Ross, J R DePaulo. Am J Hum Genet 1993
226
100

Pulmonary manifestations of systemic karyomegaly.
Levent M Akyürek, Aziz Hussein, Andrew G Nicholson, Nils-Johan Mauritz, Johan Mölne. Respir Med Case Rep 2020
1
100

Artemis, a novel guardian of the genome.
Z Dudásová, M Chovanec. Neoplasma 2003
11
100

Fen1 does not control somatic hypermutability of the (CTG)(n)*(CAG)(n) repeat in a knock-in mouse model for DM1.
Walther J A A van den Broek, Marcel R Nelen, Godfried W van der Heijden, Derick G Wansink, Bé Wieringa. FEBS Lett 2006
29
100

DNA mismatch repair complex MutSβ promotes GAA·TTC repeat expansion in human cells.
Anasheh Halabi, Scott Ditch, Jeffrey Wang, Ed Grabczyk. J Biol Chem 2012
47
100

Ubiquitin-binding domains in Y-family polymerases regulate translesion synthesis.
Marzena Bienko, Catherine M Green, Nicola Crosetto, Fabian Rudolf, Grzegorz Zapart, Barry Coull, Patricia Kannouche, Gerhard Wider, Matthias Peter, Alan R Lehmann,[...]. Science 2005
524
100

The mechanism and regulation of chromosomal V(D)J recombination.
Craig H Bassing, Wojciech Swat, Frederick W Alt. Cell 2002
605
100



The Bloom's syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repair.
G Langland, J Kordich, J Creaney, K H Goss, K Lillard-Wetherell, K Bebenek, T A Kunkel, J Groden. J Biol Chem 2001
84
100

Copy number variation in bipolar disorder.
E K Green, E Rees, J T R Walters, K-G Smith, L Forty, D Grozeva, J L Moran, P Sklar, S Ripke, K D Chambert,[...]. Mol Psychiatry 2016
92
100

POLE proofreading defects: Contributions to mutagenesis and cancer.
Vivian S Park, Zachary F Pursell. DNA Repair (Amst) 2019
15
100

Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review.
Sami Belhadj, Mariona Terradas, Pau M Munoz-Torres, Gemma Aiza, Matilde Navarro, Gabriel Capellá, Laura Valle. Hum Mutat 2020
6
100

Purified human BRCA2 stimulates RAD51-mediated recombination.
Ryan B Jensen, Aura Carreira, Stephen C Kowalczykowski. Nature 2010
406
100

What is the Pathogenic CAG Expansion Length in Huntington's Disease?
Jasmine Donaldson, Sophie Powell, Nadia Rickards, Peter Holmans, Lesley Jones. J Huntingtons Dis 2021
5
100

Functional FEN1 polymorphisms are associated with DNA damage levels and lung cancer risk.
Ming Yang, Huan Guo, Chen Wu, Yuefeng He, Dianke Yu, Li Zhou, Fang Wang, Jian Xu, Wen Tan, Guanghai Wang,[...]. Hum Mutat 2009
66
100

Crystal structures of the structure-selective nuclease Mus81-Eme1 bound to flap DNA substrates.
Gwang Hyeon Gwon, Aera Jo, Kyuwon Baek, Kyeong Sik Jin, Yaoyao Fu, Jong-Bong Lee, Youngchang Kim, Yunje Cho. EMBO J 2014
20
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.