A citation-based method for searching scientific literature

Xihan Guo, Juan Ni, Ziqing Liang, Jinglun Xue, Michael F Fenech, Xu Wang. Mutat Res Rev Mutat Res 2019
Times Cited: 38







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



Times Cited
  Times     Co-cited
Similarity




Nuclear morphologies: their diversity and functional relevance.
Benjamin M Skinner, Emma E P Johnson. Chromosoma 2017
50
5


Sequestration of mammalian Rad51-recombination protein into micronuclei.
T Haaf, E Raderschall, G Reddy, D C Ward, C M Radding, E I Golub. J Cell Biol 1999
104
5

Expression of neural markers by undifferentiated mesenchymal-like stem cells from different sources.
Dana Foudah, Marianna Monfrini, Elisabetta Donzelli, Stefania Niada, Anna T Brini, Monia Orciani, Giovanni Tredici, Mariarosaria Miloso. J Immunol Res 2014
49
5

Detection and Phenotypic Characterization of Adult Neurogenesis.
H Georg Kuhn, Amelia J Eisch, Kirsty Spalding, Daniel A Peterson. Cold Spring Harb Perspect Biol 2016
32
6

Subpopulations of proliferating cells of the adult hippocampus respond differently to physiologic neurogenic stimuli.
Golo Kronenberg, Katja Reuter, Barbara Steiner, Moritz D Brandt, Sebastian Jessberger, Masahiro Yamaguchi, Gerd Kempermann. J Comp Neurol 2003
474
5


Age-related changes in astrocytic and ependymal cells of the subventricular zone.
Vivian Capilla-Gonzalez, Arantxa Cebrian-Silla, Hugo Guerrero-Cazares, Jose Manuel Garcia-Verdugo, Alfredo Quiñones-Hinojosa. Glia 2014
58
5

Deciphering the Code of the Cancer Genome: Mechanisms of Chromosome Rearrangement.
Nicholas A Willis, Emilie Rass, Ralph Scully. Trends Cancer 2015
30
6

Catastrophic chromosomal restructuring during genome elimination in plants.
Ek Han Tan, Isabelle M Henry, Maruthachalam Ravi, Keith R Bradnam, Terezie Mandakova, Mohan Pa Marimuthu, Ian Korf, Martin A Lysak, Luca Comai, Simon Wl Chan. Elife 2015
55
5

Catastrophic Unbalanced Genome Rearrangements Cause Somatic Loss of Berry Color in Grapevine.
Pablo Carbonell-Bejerano, Carolina Royo, Rafael Torres-Pérez, Jérôme Grimplet, Lucie Fernandez, José Manuel Franco-Zorrilla, Diego Lijavetzky, Elisa Baroja, Juana Martínez, Enrique García-Escudero,[...]. Plant Physiol 2017
28
7

The Flow of the Gibbon LAVA Element Is Facilitated by the LINE-1 Retrotransposition Machinery.
Thomas J Meyer, Ulrike Held, Kimberly A Nevonen, Sabine Klawitter, Thomas Pirzer, Lucia Carbone, Gerald G Schumann. Genome Biol Evol 2016
10
20

Genome chaos: survival strategy during crisis.
Guo Liu, Joshua B Stevens, Steven D Horne, Batoul Y Abdallah, Karen J Ye, Steven W Bremer, Christine J Ye, David J Chen, Henry H Heng. Cell Cycle 2014
64
5

Reflections on a lifetime in cytogenetics.
Adayapalam T Natarajan. Mutat Res Rev Mutat Res 2012
7
28

Germline Chromothripsis Driven by L1-Mediated Retrotransposition and Alu/Alu Homologous Recombination.
Lusine Nazaryan-Petersen, Birgitte Bertelsen, Mads Bak, Lars Jønson, Niels Tommerup, Dustin C Hancks, Zeynep Tümer. Hum Mutat 2016
34
5

Breaking TADs: How Alterations of Chromatin Domains Result in Disease.
Darío G Lupiáñez, Malte Spielmann, Stefan Mundlos. Trends Genet 2016
189
5

Population genomics of picophytoplankton unveils novel chromosome hypervariability.
Romain Blanc-Mathieu, Marc Krasovec, Maxime Hebrard, Sheree Yau, Elodie Desgranges, Joel Martin, Wendy Schackwitz, Alan Kuo, Gerald Salin, Cecile Donnadieu,[...]. Sci Adv 2017
30
6

Catastrophic cellular events leading to complex chromosomal rearrangements in the germline.
M Fukami, H Shima, E Suzuki, T Ogata, K Matsubara, T Kamimaki. Clin Genet 2017
25
8

Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens.
Haoyang Cai, Nitin Kumar, Homayoun C Bagheri, Christian von Mering, Mark D Robinson, Michael Baudis. BMC Genomics 2014
71
5

Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.
Christopher M Grochowski, Shen Gu, Bo Yuan, Julia Tcw, Kristen J Brennand, Jonathan Sebat, Dheeraj Malhotra, Shane McCarthy, Uwe Rudolph, Anna Lindstrand,[...]. Hum Mutat 2018
13
15

Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis.
Brooke Weckselblatt, Karen E Hermetz, M Katharine Rudd. Genome Res 2015
39
5

Chromatin three-dimensional interactions mediate genetic effects on gene expression.
O Delaneau, M Zazhytska, C Borel, G Giannuzzi, G Rey, C Howald, S Kumar, H Ongen, K Popadin, D Marbach,[...]. Science 2019
60
5

Highly rearranged chromosomes reveal uncoupling between genome topology and gene expression.
Yad Ghavi-Helm, Aleksander Jankowski, Sascha Meiers, Rebecca R Viales, Jan O Korbel, Eileen E M Furlong. Nat Genet 2019
96
5

The genomic characteristics and cellular origin of chromothripsis.
Zuzana Storchová, Wigard P Kloosterman. Curr Opin Cell Biol 2016
35
5

Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring.
Mirjam S de Pagter, Markus J van Roosmalen, Annette F Baas, Ivo Renkens, Karen J Duran, Ellen van Binsbergen, Masoumeh Tavakoli-Yaraki, Ron Hochstenbach, Lars T van der Veken, Edwin Cuppen,[...]. Am J Hum Genet 2015
47
5

Chromothriptic cure of WHIM syndrome.
David H McDermott, Ji-Liang Gao, Qian Liu, Marie Siwicki, Craig Martens, Paejonette Jacobs, Daniel Velez, Erin Yim, Christine R Bryke, Nancy Hsu,[...]. Cell 2015
108
5

What Is Karyotype Coding and Why Is Genomic Topology Important for Cancer and Evolution?
Christine J Ye, Lukas Stilgenbauer, Amanda Moy, Guo Liu, Henry H Heng. Front Genet 2019
18
11

Intrachromosomal Rearrangements in Rodents from the Perspective of Comparative Region-Specific Painting.
Svetlana A Romanenko, Natalya A Serdyukova, Polina L Perelman, Svetlana V Pavlova, Nina S Bulatova, Feodor N Golenishchev, Roscoe Stanyon, Alexander S Graphodatsky. Genes (Basel) 2017
8
25

N-Ethyl-N-Nitrosourea (ENU) Mutagenesis Reveals an Intronic Residue Critical for Caenorhabditis elegans 3' Splice Site Function in Vivo.
Omar A Itani, Stephane Flibotte, Kathleen J Dumas, Chunfang Guo, Thomas Blumenthal, Patrick J Hu. G3 (Bethesda) 2016
2
100

Chromosome rearrangements via template switching between diverged repeated sequences.
Ranjith P Anand, Olga Tsaponina, Patricia W Greenwell, Cheng-Sheng Lee, Wei Du, Thomas D Petes, James E Haber. Genes Dev 2014
69
5

A germline chromothripsis event stably segregating in 11 individuals through three generations.
Birgitte Bertelsen, Lusine Nazaryan-Petersen, Wei Sun, Mana M Mehrjouy, Gangcai Xie, Wei Chen, Lena E Hjermind, Peter E M Taschner, Zeynep Tümer. Genet Med 2016
36
5

Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells.
Atsushi Hattori, Kohji Okamura, Yumiko Terada, Rika Tanaka, Yuko Katoh-Fukui, Yoichi Matsubara, Keiko Matsubara, Masayo Kagami, Reiko Horikawa, Maki Fukami. BMC Med Genomics 2019
5
40

Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant.
Peter J B Sabatini, Resham Ejaz, Dimitri J Stavropoulos, Roberto Mendoza-Londono, Ann M Joseph-George. Mol Cytogenet 2018
5
40

Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations.
Erina Suzuki, Hirohito Shima, Machiko Toki, Kunihiko Hanew, Keiko Matsubara, Hiroki Kurahashi, Satoshi Narumi, Tsutomu Ogata, Tsutomu Kamimaki, Maki Fukami. Cytogenet Genome Res 2016
13
15

The Iceberg under Water: Unexplored Complexity of Chromoanagenesis in Congenital Disorders.
Cinthya J Zepeda-Mendoza, Cynthia C Morton. Am J Hum Genet 2019
19
10


On the Complexity of Mechanisms and Consequences of Chromothripsis: An Update.
Alla S Koltsova, Anna A Pendina, Olga A Efimova, Olga G Chiryaeva, Tatyana V Kuznetzova, Vladislav S Baranov. Front Genet 2019
29
6

Sex reduces genetic variation: a multidisciplinary review.
Root Gorelick, Henry H Q Heng. Evolution 2011
38
5

A genomic view of mosaicism and human disease.
Leslie G Biesecker, Nancy B Spinner. Nat Rev Genet 2013
330
5

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.
Florian Zink, Simon N Stacey, Gudmundur L Norddahl, Michael L Frigge, Olafur T Magnusson, Ingileif Jonsdottir, Thorgeir E Thorgeirsson, Asgeir Sigurdsson, Sigurjon A Gudjonsson, Julius Gudmundsson,[...]. Blood 2017
291
5

Age-dependent inclusion of sex chromosomes in lymphocyte micronuclei of man.
J Catalán, K Autio, E Kuosma, H Norppa. Am J Hum Genet 1998
63
5

Change of human chromosome count distribution with age: evidence for a sex differences.
P A JACOBS, M BRUNTON, W M COURT BROWN, R DOLL, H GOLDSTEIN. Nature 1963
216
5

Loss of chromosome Y in blood, but not in brain, of suicide completers.
Atsushi Kimura, Akitoyo Hishimoto, Ikuo Otsuka, Satoshi Okazaki, Shuken Boku, Tadasu Horai, Takeshi Izumi, Motonori Takahashi, Yasuhiro Ueno, Osamu Shirakawa,[...]. PLoS One 2018
16
12

Somatic mosaicism of sex chromosomes in the blood and brain.
Emma J Graham, Michael Vermeulen, Badri Vardarajan, David Bennett, Phil De Jager, Richard V Pearse, Tracy L Young-Pearse, Sara Mostafavi. Brain Res 2019
7
28

Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility.
Daniel J Wright, Felix R Day, Nicola D Kerrison, Florian Zink, Alexia Cardona, Patrick Sulem, Deborah J Thompson, Svanhvit Sigurjonsdottir, Daniel F Gudbjartsson, Agnar Helgason,[...]. Nat Genet 2017
53
5

Outdoor air pollution and mosaic loss of chromosome Y in older men from the Cardiovascular Health Study.
Jason Y Y Wong, Helene G Margolis, Mitchell Machiela, Weiyin Zhou, Michelle C Odden, Bruce M Psaty, John Robbins, Rena R Jones, Jerome I Rotter, Stephen J Chanock,[...]. Environ Int 2018
15
13

Characterization of large structural genetic mosaicism in human autosomes.
Mitchell J Machiela, Weiyin Zhou, Joshua N Sampson, Michael C Dean, Kevin B Jacobs, Amanda Black, Louise A Brinton, I-Shou Chang, Chu Chen, Constance Chen,[...]. Am J Hum Genet 2015
65
5

Detectable clonal mosaicism from birth to old age and its relationship to cancer.
Cathy C Laurie, Cecelia A Laurie, Kenneth Rice, Kimberly F Doheny, Leila R Zelnick, Caitlin P McHugh, Hua Ling, Kurt N Hetrick, Elizabeth W Pugh, Chris Amos,[...]. Nat Genet 2012
359
5


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.