A citation-based method for searching scientific literature

Jannine DeMars Cody. Trends Genet 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Germline PALB2 Mutations in Cancers and Its Distinction From Somatic PALB2 Mutations in Breast Cancers.
Zhe-Yu Hu, Liping Liu, Ning Xie, Jun Lu, Zhentian Liu, Yu Tang, Yikai Wang, Jianbo Yang, Quchang Ouyang. Front Genet 2020
1
100

Pathology of Hereditary Breast and Ovarian Cancer.
Anjelica Hodgson, Gulisa Turashvili. Front Oncol 2020
7
100

Interplay between BRCA1 and GADD45A and Its Potential for Nucleotide Excision Repair in Breast Cancer Pathogenesis.
Sylwia Pietrasik, Gabriela Zajac, Jan Morawiec, Miroslaw Soszynski, Michal Fila, Janusz Blasiak. Int J Mol Sci 2020
7
100

The pattern of gene amplification is determined by the chromosomal location of hairpin-capped breaks.
Vidhya Narayanan, Piotr A Mieczkowski, Hyun-Min Kim, Thomas D Petes, Kirill S Lobachev. Cell 2006
120
100

BRCA1, PARP1 and γH2AX in acute myeloid leukemia: Role as biomarkers of response to the PARP inhibitor olaparib.
Isabella Faraoni, Mirco Compagnone, Serena Lavorgna, Daniela Francesca Angelini, Maria Teresa Cencioni, Eleonora Piras, Paola Panetta, Tiziana Ottone, Susanna Dolci, Adriano Venditti,[...]. Biochim Biophys Acta 2015
40
100

Double-strand break end resection and repair pathway choice.
Lorraine S Symington, Jean Gautier. Annu Rev Genet 2011
866
100



DNA end resection and its role in DNA replication and DSB repair choice in mammalian cells.
Fei Zhao, Wootae Kim, Jake A Kloeber, Zhenkun Lou. Exp Mol Med 2020
7
100

Impeding the single-strand annealing pathway of DNA double-strand break repair by withaferin A-mediated FANCA degradation.
Wenjun Liu, Guanying Wang, Anna Palovcak, Yan Li, Sophie Hao, Zhao-Jun Liu, Ralf Landgraf, Fenghua Yuan, Yanbin Zhang. DNA Repair (Amst) 2019
6
100

Mechanisms and Consequences of Double-Strand DNA Break Formation in Chromatin.
Wendy J Cannan, David S Pederson. J Cell Physiol 2016
107
100

Will CRISPR-Cas9 Have Cards to Play Against Cancer? An Update on its Applications.
Precilla S Daisy, Kuduvalli S Shreyas, T S Anitha. Mol Biotechnol 2021
1
100

DNA-PKcs, ATM, and ATR Interplay Maintains Genome Integrity during Neurogenesis.
Vanessa Enriquez-Rios, Lavinia C Dumitrache, Susanna M Downing, Yang Li, Eric J Brown, Helen R Russell, Peter J McKinnon. J Neurosci 2017
27
100

The Evolution, Functions and Applications of the Breast Cancer Genes BRCA1 and BRCA2.
Claire M Pfeffer, Benjamin N Ho, Amareshwar T K Singh. Cancer Genomics Proteomics 2017
14
100

Genetic Characterization of Three Distinct Mechanisms Supporting RNA-Driven DNA Repair and Modification Reveals Major Role of DNA Polymerase ζ.
Chance Meers, Havva Keskin, Gabor Banyai, Olga Mazina, Taehwan Yang, Alli L Gombolay, Kuntal Mukherjee, Efiyenia I Kaparos, Gary Newnam, Alexander Mazin,[...]. Mol Cell 2020
10
100


Chronic Myeloid Leukemia, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.
Michael W Deininger, Neil P Shah, Jessica K Altman, Ellin Berman, Ravi Bhatia, Bhavana Bhatnagar, Daniel J DeAngelo, Jason Gotlib, Gabriela Hobbs, Lori Maness,[...]. J Natl Compr Canc Netw 2020
12
100

The power of DNA double-strand break (DSB) repair testing to predict breast cancer susceptibility.
Marlen Keimling, Miriam Deniz, Dominic Varga, Andreea Stahl, Hubert Schrezenmeier, Rolf Kreienberg, Isabell Hoffmann, Jochem König, Lisa Wiesmüller. FASEB J 2012
28
100

53BP1 fosters fidelity of homology-directed DNA repair.
Fena Ochs, Kumar Somyajit, Matthias Altmeyer, Maj-Britt Rask, Jiri Lukas, Claudia Lukas. Nat Struct Mol Biol 2016
124
100

RPA antagonizes microhomology-mediated repair of DNA double-strand breaks.
Sarah K Deng, Bryan Gibb, Mariana Justino de Almeida, Eric C Greene, Lorraine S Symington. Nat Struct Mol Biol 2014
102
100

The use of CRISPR/Cas9-based gene editing strategies to explore cancer gene function in mice.
Louise van der Weyden, Jos Jonkers, David J Adams. Curr Opin Genet Dev 2021
2
100

Genome-wide analyses of LINE-LINE-mediated nonallelic homologous recombination.
Michał Startek, Przemyslaw Szafranski, Tomasz Gambin, Ian M Campbell, Patricia Hixson, Chad A Shaw, Paweł Stankiewicz, Anna Gambin. Nucleic Acids Res 2015
45
100

Chromosomal stability and the DNA double-stranded break connection.
D C van Gent, J H Hoeijmakers, R Kanaar. Nat Rev Genet 2001
850
100

Rad52 competes with Ku70/Ku86 for binding to S-region DSB ends to modulate antibody class-switch DNA recombination.
Hong Zan, Connie Tat, Zhifang Qiu, Julia R Taylor, Justin A Guerrero, Tian Shen, Paolo Casali. Nat Commun 2017
17
100

Dual-reporter surrogate systems for efficient enrichment of genetically modified cells.
Chonghua Ren, Kun Xu, Zhongtian Liu, Juncen Shen, Furong Han, Zhilong Chen, Zhiying Zhang. Cell Mol Life Sci 2015
24
100

Non-specific chemical inhibition of the Fanconi anemia pathway sensitizes cancer cells to cisplatin.
Céline Jacquemont, Julian A Simon, Alan D D'Andrea, Toshiyasu Taniguchi. Mol Cancer 2012
45
100


Is non-homologous end-joining really an inherently error-prone process?
Mireille Bétermier, Pascale Bertrand, Bernard S Lopez. PLoS Genet 2014
206
100


A multiplexed gRNA piggyBac transposon system facilitates efficient induction of CRISPRi and CRISPRa in human pluripotent stem cells.
Dane Z Hazelbaker, Amanda Beccard, Gabriella Angelini, Patrizia Mazzucato, Angelica Messana, Daisy Lam, Kevin Eggan, Lindy E Barrett. Sci Rep 2020
3
100

Increased single-strand annealing rather than non-homologous end-joining predicts hereditary ovarian carcinoma.
Miriam Deniz, Tatiana Romashova, Sarah Kostezka, Anke Faul, Theresa Gundelach, Maria Moreno-Villanueva, Wolfgang Janni, Thomas W P Friedl, Lisa Wiesmüller. Oncotarget 2017
4
100

Inverted DNA repeats channel repair of distant double-strand breaks into chromatid fusions and chromosomal rearrangements.
Kelly VanHulle, Francene J Lemoine, Vidhya Narayanan, Brandon Downing, Krista Hull, Christy McCullough, Melissa Bellinger, Kirill Lobachev, Thomas D Petes, Anna Malkova. Mol Cell Biol 2007
80
100

Chromothripsis drives the evolution of gene amplification in cancer.
Ofer Shoshani, Simon F Brunner, Rona Yaeger, Peter Ly, Yael Nechemia-Arbely, Dong Hyun Kim, Rongxin Fang, Guillaume A Castillon, Miao Yu, Julia S Z Li,[...]. Nature 2021
13
100


The RAD52 S346X variant reduces risk of developing breast cancer in carriers of pathogenic germline BRCA2 mutations.
Aaron W Adamson, Yuan Chun Ding, Carlos Mendez-Dorantes, Adam M Bailis, Jeremy M Stark, Susan L Neuhausen. Mol Oncol 2020
4
100

Genomic rearrangements induced by unscheduled DNA double strand breaks in somatic mammalian cells.
Ayeong So, Tangui Le Guen, Bernard S Lopez, Josée Guirouilh-Barbat. FEBS J 2017
16
100


Role of Mre11 in chromosomal nonhomologous end joining in mammalian cells.
Emilie Rass, Anastazja Grabarz, Isabelle Plo, Jean Gautier, Pascale Bertrand, Bernard S Lopez. Nat Struct Mol Biol 2009
223
100

BRCA1 accelerates CtIP-mediated DNA-end resection.
Andrés Cruz-García, Ana López-Saavedra, Pablo Huertas. Cell Rep 2014
138
100

Heterozygous PALB2 c.1592delT mutation channels DNA double-strand break repair into error-prone pathways in breast cancer patients.
K Obermeier, J Sachsenweger, T W P Friedl, H Pospiech, R Winqvist, L Wiesmüller. Oncogene 2016
26
100

TypeTE: a tool to genotype mobile element insertions from whole genome resequencing data.
Clément Goubert, Jainy Thomas, Lindsay M Payer, Jeffrey M Kidd, Julie Feusier, W Scott Watkins, Kathleen H Burns, Lynn B Jorde, Cédric Feschotte. Nucleic Acids Res 2020
6
100


Mutational signatures reveal the role of RAD52 in p53-independent p21-driven genomic instability.
Panagiotis Galanos, George Pappas, Alexander Polyzos, Athanassios Kotsinas, Ioanna Svolaki, Nickolaos N Giakoumakis, Christina Glytsou, Ioannis S Pateras, Umakanta Swain, Vassilis L Souliotis,[...]. Genome Biol 2018
32
100


Chromosomal translocation mechanisms at intronic alu elements in mammalian cells.
Beth Elliott, Christine Richardson, Maria Jasin. Mol Cell 2005
121
100

Repair of G1 induced DNA double-strand breaks in S-G2/M by alternative NHEJ.
Wei Yu, Chloé Lescale, Loelia Babin, Marie Bedora-Faure, Hélène Lenden-Hasse, Ludivine Baron, Caroline Demangel, José Yelamos, Erika Brunet, Ludovic Deriano. Nat Commun 2020
5
100

Microhomology-mediated end joining: Good, bad and ugly.
Ja-Hwan Seol, Eun Yong Shim, Sang Eun Lee. Mutat Res 2018
78
100


Improving gene targeting efficiency on pig IGF2 mediated by ZFNs and CRISPR/Cas9 by using SSA reporter system.
Wu Jinqing, Mei Gui, Liu Zhiguo, Chen Yaosheng, Cong Peiqing, He Zuyong. Yi Chuan 2015
2
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.