A citation-based method for searching scientific literature

Sau W Cheung, Weimin Bi. Expert Rev Mol Diagn 2018
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity



Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.
Desheng Liang, David S Cram, Hu Tan, Siyuan Linpeng, Yingdi Liu, Huaiyu Sun, Yu Zhang, Feng Tian, Hongmin Zhu, Mengnan Xu,[...]. Genet Med 2019
52
15

Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.
Kitty K Lo, Evangelia Karampetsou, Christopher Boustred, Fiona McKay, Sarah Mason, Melissa Hill, Vincent Plagnol, Lyn S Chitty. Am J Hum Genet 2016
67
15

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
320
15

Chromosome Imbalances in Cancer: Molecular Cytogenetics Meets Genomics.
Elisa Palumbo, Antonella Russo. Cytogenet Genome Res 2016
8
12

The development of chromosome-specific composite DNA probes for the mouse and their application to chromosome painting.
J W Breneman, M J Ramsey, D A Lee, G G Eveleth, J L Minkler, J D Tucker. Chromosoma 1993
58
7


Looping and interaction between hypersensitive sites in the active beta-globin locus.
Bas Tolhuis, Robert Jan Palstra, Erik Splinter, Frank Grosveld, Wouter de Laat. Mol Cell 2002
952
7

mBAND and mFISH analysis of chromosomal aberrations and breakpoint distribution in chromosome 1 of AG01522 human fibroblasts that were exposed to radiation of different qualities.
F Berardinelli, M De Vitis, D Nieri, R Cherubini, V De Nadal, S Gerardi, C Tanzarella, A Sgura, A Antoccia. Mutat Res Genet Toxicol Environ Mutagen 2015
5
20


Combining fluorescence imaging with Hi-C to study 3D genome architecture of the same single cell.
David Lando, Srinjan Basu, Tim J Stevens, Andy Riddell, Kai J Wohlfahrt, Yang Cao, Wayne Boucher, Martin Leeb, Liam P Atkinson, Steven F Lee,[...]. Nat Protoc 2018
4
25

Investigating chromosome damage using fluorescent in situ hybridization to identify biomarkers of radiosensitivity in prostate cancer patients.
Lindsay A Beaton, Leonora Marro, Sara Samiee, Shawn Malone, Scott Grimes, Kyle Malone, Ruth C Wilkins. Int J Radiat Biol 2013
16
7

High-resolution mapping of satellite DNA using biotin-labeled DNA probes.
L Manuelidis, P R Langer-Safer, D C Ward. J Cell Biol 1982
135
7

Current cytogenetic methods for detecting exposure and effects of mutagens and carcinogens.
A T Natarajan, J J Boei, F Darroudi, P C Van Diemen, F Dulout, M P Hande, A T Ramalho. Environ Health Perspect 1996
54
7

In situ hybridization with fluoresceinated DNA.
J Wiegant, T Ried, P M Nederlof, M van der Ploeg, H J Tanke, A K Raap. Nucleic Acids Res 1991
152
7

Multicolor FISH probe sets and their applications.
T Liehr, H Starke, A Weise, H Lehrer, U Claussen. Histol Histopathol 2004
41
7

Tumor cytogenetics revisited: comparative genomic hybridization and spectral karyotyping.
T Ried, M Liyanage, S du Manoir, K Heselmeyer, G Auer, M Macville, E Schröck. J Mol Med (Berl) 1997
70
7

Translocation analysis by the FISH-painting method for retrospective dose reconstruction in individuals exposed to ionizing radiation 10 years after exposure.
Marjori L Camparoto, Adriana T Ramalho, Adayapalam T Natarajan, Maria P Curado, Elza T Sakamoto-Hojo. Mutat Res 2003
34
7


High susceptibility of chromosome 16 to radiation-induced chromosome rearrangements in human lymphocytes under in vivo and in vitro exposure.
M L Camparoto, S A Takahashi-Hyodo, J G Dauwerse, A T Natarajan, E T Sakamoto-Hojo. Cytogenet Genome Res 2005
7
14

Chromosomal instability--mechanisms and consequences.
Shriram Venkatesan, Adayapalam T Natarajan, M Prakash Hande. Mutat Res Genet Toxicol Environ Mutagen 2015
31
7

The chromosomes of man.
C E FORD, J L HAMERTON. Nature 1956
280
7


Cytogenetic biodosimetry and dose-rate effect after radioiodine therapy for thyroid cancer.
Igor K Khvostunov, Vladimir A Saenko, Valeri Krylov, Andrei Rodichev, Shunichi Yamashita. Radiat Environ Biophys 2017
3
33


Localization of heterochromatin in human chromosomes.
F E Arrighi, T C Hsu. Cytogenetics 1971
867
7

The array CGH and its clinical applications.
Marwan Shinawi, Sau Wai Cheung. Drug Discov Today 2008
111
7



Chromosome banding.
D E Comings. J Histochem Cytochem 1975
12
8

Recent developments in the assessment of chromosomal damage.
A T Natarajan, A S Balajee, J J Boei, S Chatterjee, F Darroudi, M Grigorova, M Noditi, H J Oh, P Slijepcevic, S Vermeulen. Int J Radiat Biol 1994
62
7

mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations.
I Chudoba, G Hickmann, T Friedrich, A Jauch, P Kozlowski, G Senger. Cytogenet Genome Res 2004
36
7

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors.
A Kallioniemi, O P Kallioniemi, D Sudar, D Rutovitz, J W Gray, F Waldman, D Pinkel. Science 1992
7

Simultaneous G- and C- banding for human chromosomes.
R S Verma, H Dosik. J Med Genet 1980
4
25

Silver staining of nucleolus organizer regions during human spermatogenesis.
M Schmid, H Müller, S Stasch, W Engel. Hum Genet 1983
29
7


Long-range intrachromosomal interactions in the T helper type 2 cytokine locus.
Charalampos G Spilianakis, Richard A Flavell. Nat Immunol 2004
332
7

Multicolor spectral karyotyping of human chromosomes.
E Schröck, S du Manoir, T Veldman, B Schoell, J Wienberg, M A Ferguson-Smith, Y Ning, D H Ledbetter, I Bar-Am, D Soenksen,[...]. Science 1996
7


Fluorescence in situ hybridization: past, present and future.
Jeffrey M Levsky, Robert H Singer. J Cell Sci 2003
277
7

Cytogenetic damage of radiotherapy in long-term head and neck cancer survivors.
Dilek Unal, Aslihan Kiraz, Deniz Avci, Arzu Tasdemir, Tuba Dilay Unal, Sedat Cagli, Celalettin Eroglu, Imdat Yuce, Ibrahim Ozcan, Bunyamin Kaplan. Int J Radiat Biol 2016
3
33

Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotype.
J G Dauwerse, J Wiegant, A K Raap, M H Breuning, G J van Ommen. Hum Mol Genet 1992
109
7

Karyotyping human chromosomes by combinatorial multi-fluor FISH.
M R Speicher, S Gwyn Ballard, D C Ward. Nat Genet 1996
855
7


Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.
D Pinkel, T Straume, J W Gray. Proc Natl Acad Sci U S A 1986
7


Chromatin organization in the mammalian nucleus.
Nick Gilbert, Susan Gilchrist, Wendy A Bickmore. Int Rev Cytol 2005
111
7



Application of new staining techniques to the study of human chromosomes.
O J Miller, D A Miller, D Warburton. Prog Med Genet 1973
35
7


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.