A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


The genome-wide effects of ionizing radiation on mutation induction in the mammalian germline.
Adeolu B Adewoye, Sarah J Lindsay, Yuri E Dubrova, Matthew E Hurles. Nat Commun 2015
70
40

Hydroxyurea induces de novo copy number variants in human cells.
Martin F Arlt, Alev Cagla Ozdemir, Shanda R Birkeland, Thomas E Wilson, Thomas W Glover. Proc Natl Acad Sci U S A 2011
62
40

A copy number variation map of the human genome.
Mehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, Stephen W Scherer. Nat Rev Genet 2015
383
40

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
655
40

Copy number variants are produced in response to low-dose ionizing radiation in cultured cells.
Martin F Arlt, Sountharia Rajendran, Shanda R Birkeland, Thomas E Wilson, Thomas W Glover. Environ Mol Mutagen 2014
30
40

De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining.
Martin F Arlt, Sountharia Rajendran, Shanda R Birkeland, Thomas E Wilson, Thomas W Glover. PLoS Genet 2012
46
40

Replication stress and mechanisms of CNV formation.
Martin F Arlt, Thomas E Wilson, Thomas W Glover. Curr Opin Genet Dev 2012
64
40


Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
40

Gene copy-number variation in haploid and diploid strains of the yeast Saccharomyces cerevisiae.
Hengshan Zhang, Ane F B Zeidler, Wei Song, Christopher M Puccia, Ewa Malc, Patricia W Greenwell, Piotr A Mieczkowski, Thomas D Petes, Juan Lucas Argueso. Genetics 2013
48
40

Large-scale copy number polymorphism in the human genome.
Jonathan Sebat, B Lakshmi, Jennifer Troge, Joan Alexander, Janet Young, Pär Lundin, Susanne Månér, Hillary Massa, Megan Walker, Maoyen Chi,[...]. Science 2004
40


Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
Jacob J Michaelson, Yujian Shi, Madhusudan Gujral, Hancheng Zheng, Dheeraj Malhotra, Xin Jin, Minghan Jian, Guangming Liu, Douglas Greer, Abhishek Bhandari,[...]. Cell 2012
334
20

Increased paternal age and the influence on burden of genomic copy number variation in the general population.
Jacobine E Buizer-Voskamp, Hylke M Blauw, Marco P M Boks, Kristel R van Eijk, Jan H Veldink, Eric A M Hennekam, Jacob A S Vorstman, Flip Mulder, Henning Tiemeier, André G Uitterlinden,[...]. Hum Genet 2013
21
20



Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.
Xin-Yan Lu, Mai T Phung, Chad A Shaw, Kim Pham, Sarah E Neil, Ankita Patel, Trilochan Sahoo, Carlos A Bacino, Pawel Stankiewicz, Sung-Hae Lee Kang,[...]. Pediatrics 2008
106
20

Human copy number variation and complex genetic disease.
Santhosh Girirajan, Catarina D Campbell, Evan E Eichler. Annu Rev Genet 2011
209
20

Delayed fathering and risk of mental disorders in adult offspring.
Saroja Krishnaswamy, Kavitha Subramaniam, Padma Ramachandran, Tishya Indran, Jemain Abdul Aziz. Early Hum Dev 2011
5
20

Increased de novo copy number variants in the offspring of older males.
T Flatscher-Bader, C J Foldi, S Chong, E Whitelaw, R J Moser, T H J Burne, D W Eyles, J J McGrath. Transl Psychiatry 2011
32
20

Peripheral blood gene expression signature differentiates children with autism from unaffected siblings.
S W Kong, Y Shimizu-Motohashi, M G Campbell, I H Lee, C D Collins, S J Brewster, I A Holm, L Rappaport, I S Kohane, L M Kunkel. Neurogenetics 2013
27
20

The genetic risk in mice from radiation: an estimate of the mutation induction rate per genome.
Jun-ichi Asakawa, Mieko Kodaira, Harry M Cullings, Hiroaki Katayama, Nori Nakamura. Radiat Res 2013
10
20


A kinetic model of single-strand annealing for the repair of DNA double-strand breaks.
Reza Taleei, Michael Weinfeld, Hooshang Nikjoo. Radiat Prot Dosimetry 2011
16
20

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.
Jayne Y Hehir-Kwa, Benjamín Rodríguez-Santiago, Lisenka E Vissers, Nicole de Leeuw, Rolph Pfundt, Jan K Buitelaar, Luis A Pérez-Jurado, Joris A Veltman. J Med Genet 2011
75
20


Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
20

Copy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarray.
Guorui Hu, Yanjie Fan, Lili Wang, Ru-En Yao, Xiaodong Huang, Yiping Shen, Yongguo Yu, Xuefan Gu. Mol Cytogenet 2016
6
20

Radiation induced DNA DSBs: Contribution from stalled replication forks?
Jane V Harper, Jennifer A Anderson, Peter O'Neill. DNA Repair (Amst) 2010
49
20

A rare de novo interstitial duplication of 15q15.3q21.2 in a boy with severe short stature, hypogonadism, global developmental delay and intellectual disability.
Haiming Yuan, Zhe Meng, Lina Zhang, Xiangyang Luo, Liping Liu, Mengfan Chen, Xinwei Li, Weiwei Zhao, Liyang Liang. Mol Cytogenet 2016
4
25

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders.
Daniel J Turner, Marcos Miretti, Diana Rajan, Heike Fiegler, Nigel P Carter, Martyn L Blayney, Stephan Beck, Matthew E Hurles. Nat Genet 2008
215
20

Assessment of BCL2/J(H) translocation in healthy individuals exposed to low-level radiation of 137CsCl in Goiânia, Goiás, Brazil.
H F Nunes, A B A Laranjeira, J A Yunes, E O A Costa, C O de A Melo, D de M e Silva, A D da Cruz. Genet Mol Res 2013
2
50

Stillbirth and neonatal death in relation to radiation exposure before conception: a retrospective cohort study.
Lisa B Signorello, John J Mulvihill, Daniel M Green, Heather M Munro, Marilyn Stovall, Rita E Weathers, Ann C Mertens, John A Whitton, Leslie L Robison, John D Boice. Lancet 2010
96
20



Timing, rates and spectra of human germline mutation.
Raheleh Rahbari, Arthur Wuster, Sarah J Lindsay, Robert J Hardwick, Ludmil B Alexandrov, Saeed Al Turki, Anna Dominiczak, Andrew Morris, David Porteous, Blair Smith,[...]. Nat Genet 2016
244
20


Microsatellite mutations in the offspring of irradiated parents 19 years after the Cesium-137 accident.
Aparecido Divino da Cruz, Daniela de Melo e Silva, Cláudio Carlos da Silva, R John Nelson, Lígia Maria Ribeiro, Eduardo Rocha Pedrosa, Jivago Carneiro Jayme, Maria Paula Curado. Mutat Res 2008
18
20

Population analysis of large copy number variants and hotspots of human genetic disease.
Andy Itsara, Gregory M Cooper, Carl Baker, Santhosh Girirajan, Jun Li, Devin Absher, Ronald M Krauss, Richard M Myers, Paul M Ridker, Daniel I Chasman,[...]. Am J Hum Genet 2009
420
20

Novel biodosimetry methods applied to victims of the Goiânia accident.
T Straume, R G Langlois, J Lucas, R H Jensen, W L Bigbee, A T Ramalho, C E Brandão-Mello. Health Phys 1991
67
20

De novo rates and selection of large copy number variation.
Andy Itsara, Hao Wu, Joshua D Smith, Deborah A Nickerson, Isabelle Romieu, Stephanie J London, Evan E Eichler. Genome Res 2010
194
20

Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.
Andrew Dauber, Yongguo Yu, Michael C Turchin, Charleston W Chiang, Yan A Meng, Ellen W Demerath, Sanjay R Patel, Stephen S Rich, Jerome I Rotter, Pamela J Schreiner,[...]. Am J Hum Genet 2011
47
20

Ionizing radiation biomarkers for potential use in epidemiological studies.
Eileen Pernot, Janet Hall, Sarah Baatout, Mohammed Abderrafi Benotmane, Eric Blanchardon, Simon Bouffler, Houssein El Saghire, Maria Gomolka, Anne Guertler, Mats Harms-Ringdahl,[...]. Mutat Res 2012
130
20

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
20


Copy number variation in human health, disease, and evolution.
Feng Zhang, Wenli Gu, Matthew E Hurles, James R Lupski. Annu Rev Genomics Hum Genet 2009
701
20

Properties and rates of germline mutations in humans.
Catarina D Campbell, Evan E Eichler. Trends Genet 2013
132
20

Radiation-induced biomarkers for the detection and assessment of absorbed radiation doses.
Sudha Rana, Raj Kumar, Sarwat Sultana, Rakesh Kumar Sharma. J Pharm Bioallied Sci 2010
27
20




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.