A citation-based method for searching scientific literature

Takema Kato, Hidehito Inagaki, Maoqing Tong, Hiroshi Kogo, Tamae Ohye, Kouji Yamada, Makiko Tsutsumi, Beverly S Emanuel, Hiroki Kurahashi. Mol Cytogenet 2011
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity



Chromosomal translocations and palindromic AT-rich repeats.
Takema Kato, Hiroki Kurahashi, Beverly S Emanuel. Curr Opin Genet Dev 2012
49
57

The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions.
H Kehrer-Sawatzki, J Häussler, W Krone, H Bode, D E Jenne, K U Mehnert, U Tümmers, G Assum. Hum Genet 1997
72
42

The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.
Hiroki Kurahashi, Tamim Shaikh, Masayuki Takata, Tatsushi Toda, Beverly S Emanuel. Am J Hum Genet 2003
92
42


Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.
Maoqing Tong, Takema Kato, Kouji Yamada, Hidehito Inagaki, Hiroshi Kogo, Tamae Ohye, Makiko Tsutsumi, Jieru Wang, Beverly S Emanuel, Hiroki Kurahashi. Hum Mol Genet 2010
15
42

A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
Molly B Sheridan, Takema Kato, Chad Haldeman-Englert, G Reza Jalali, Jeff M Milunsky, Ying Zou, Ruediger Klaes, Georgio Gimelli, Stefania Gimelli, Robert M Gemmill,[...]. Am J Hum Genet 2010
32
42

A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies.
Anthony L Gotter, Manjunath A Nimmakayalu, G Reza Jalali, April M Hacker, Jacob Vorstman, Danielle Conforto Duffy, Livija Medne, Beverly S Emanuel. Genome Res 2007
47
42


Molecular cloning of a translocation breakpoint hotspot in 22q11.
Hiroki Kurahashi, Hidehito Inagaki, Eriko Hosoba, Takema Kato, Tamae Ohye, Hiroshi Kogo, Beverly S Emanuel. Genome Res 2007
37
42

Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).
H Kurahashi, T H Shaikh, E H Zackai, L Celle, D A Driscoll, M L Budarf, B S Emanuel. Am J Hum Genet 2000
67
42

A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
Manjunath A Nimmakayalu, Anthony L Gotter, Tamim H Shaikh, Beverly S Emanuel. Hum Mol Genet 2003
47
42

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.
Hiroki Kurahashi, Hidehito Inagaki, Kouji Yamada, Tamae Ohye, Mariko Taniguchi, Beverly S Emanuel, Tatsushi Toda. J Biol Chem 2004
83
42

A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.
Anthony L Gotter, Tamim H Shaikh, Marcia L Budarf, C Harker Rhodes, Beverly S Emanuel. Hum Mol Genet 2004
77
42

Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations.
Hidehito Inagaki, Tamae Ohye, Hiroshi Kogo, Makiko Tsutsumi, Takema Kato, Maoqing Tong, Beverly S Emanuel, Hiroki Kurahashi. Nat Commun 2013
35
42

Cruciform structures are a common DNA feature important for regulating biological processes.
Václav Brázda, Rob C Laister, Eva B Jagelská, Cheryl Arrowsmith. BMC Mol Biol 2011
149
42



Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.
Tamim H Shaikh, Ronald J O'Connor, Mary Ella Pierpont, James McGrath, April M Hacker, Manjunath Nimmakayalu, Elizabeth Geiger, Beverly S Emanuel, Sulagna C Saitta. Genome Res 2007
94
28

A constitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma.
Kathryn S Poland, Mohammed Azim, Matthew Folsom, Richard Goldfarb, Rizwan Naeem, Christopher Korch, Harry A Drabkin, Robert M Gemmill, Sharon E Plon. Genes Chromosomes Cancer 2007
30
28

The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers.
I Tapia-Páez, M Kost-Alimova, P Hu, B A Roe, E Blennow, L Fedorova, S Imreh, J P Dumanski. Hum Genet 2001
47
28

Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm.
Takema Kato, Kouji Yamada, Hidehito Inagaki, Hiroshi Kogo, Tamae Ohye, Beverly S Emanuel, Hiroki Kurahashi. Fertil Steril 2007
16
28

Paternal origin of the de novo constitutional t(11;22)(q23;q11).
Tamae Ohye, Hidehito Inagaki, Hiroshi Kogo, Makiko Tsutsumi, Takema Kato, Maoqing Tong, Merryn V E Macville, Livija Medne, Elaine H Zackai, Beverly S Emanuel,[...]. Eur J Hum Genet 2010
25
28

Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22).
Terry Ashley, Ann P Gaeth, Hidehito Inagaki, Allen Seftel, Maimon M Cohen, Lorinda K Anderson, Hiroki Kurahashi, Beverly S Emanuel. Am J Hum Genet 2006
30
28


Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).
H Kurahashi, T H Shaikh, P Hu, B A Roe, B S Emanuel, M L Budarf. Hum Mol Genet 2000
130
28

Hereditary renal-cell carcinoma associated with a chromosomal translocation.
A J Cohen, F P Li, S Berg, D J Marchetto, S Tsai, S C Jacobs, R S Brown. N Engl J Med 1979
612
28

Two different forms of palindrome resolution in the human genome: deletion or translocation.
Takema Kato, Hidehito Inagaki, Hiroshi Kogo, Tamae Ohye, Kouji Yamada, Beverly S Emanuel, Hiroki Kurahashi. Hum Mol Genet 2008
17
28

Genetic variation affects de novo translocation frequency.
Takema Kato, Hidehito Inagaki, Kouji Yamada, Hiroshi Kogo, Tamae Ohye, Hiroe Kowa, Kayuri Nagaoka, Mariko Taniguchi, Beverly S Emanuel, Hiroki Kurahashi. Science 2006
58
28

Inverted DNA repeats: a source of eukaryotic genomic instability.
D A Gordenin, K S Lobachev, N P Degtyareva, A L Malkova, E Perkins, M A Resnick. Mol Cell Biol 1993
150
28

Palindrome resolution and recombination in the mammalian germ line.
E Akgün, J Zahn, S Baumes, G Brown, F Liang, P J Romanienko, S Lewis, M Jasin. Mol Cell Biol 1997
151
28

Palindrome-mediated chromosomal translocations in humans.
Hiroki Kurahashi, Hidehito Inagaki, Tamae Ohye, Hiroshi Kogo, Takema Kato, Beverly S Emanuel. DNA Repair (Amst) 2006
79
28

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.
T H Shaikh, H Kurahashi, S C Saitta, A M O'Hare, P Hu, B A Roe, D A Driscoll, D M McDonald-McGinn, E H Zackai, M L Budarf,[...]. Hum Mol Genet 2000
383
28

The human genome-wide distribution of DNA palindromes.
Le Lu, Hui Jia, Peter Dröge, Jinming Li. Funct Integr Genomics 2007
29
28

AT-rich palindromes mediate the constitutional t(11;22) translocation.
L Edelmann, E Spiteri, K Koren, V Pulijaal, M G Bialer, A Shanske, R Goldberg, B E Morrow. Am J Hum Genet 2001
142
28

Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.
Hiroki Kurahashi, Hidehito Inagaki, Takema Kato, Eriko Hosoba, Hiroshi Kogo, Tamae Ohye, Makiko Tsutsumi, Hasbaira Bolor, Maoqing Tong, Beverly S Emanuel. Hum Mol Genet 2009
14
28

Instability of long inverted repeats within mouse transgenes.
A Collick, J Drew, J Penberth, P Bois, J Luckett, F Scaerou, A Jeffreys, W Reik. EMBO J 1996
84
28

Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.
Hiroshi Kogo, Hidehito Inagaki, Tamae Ohye, Takema Kato, Beverly S Emanuel, Hiroki Kurahashi. Nucleic Acids Res 2007
30
28

Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates.
Hidehito Inagaki, Tamae Ohye, Hiroshi Kogo, Kouji Yamada, Hiroe Kowa, Tamim H Shaikh, Beverly S Emanuel, Hiroki Kurahashi. Hum Mutat 2005
31
28

Chimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiency.
Xiaohui Tan, Sarah L Anzick, Sikandar G Khan, Takahiro Ueda, Gary Stone, John J Digiovanna, Deborah Tamura, Daniel Wattendorf, David Busch, Carmen C Brewer,[...]. Hum Mutat 2013
11
28

Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals.
Melissa T Carter, Stephanie A St Pierre, Elaine H Zackai, Beverly S Emanuel, Kym M Boycott. Am J Med Genet A 2009
49
28


Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.
Takema Kato, Colleen P Franconi, Molly B Sheridan, April M Hacker, Hidehito Inagakai, Thomas W Glover, Martin F Arlt, Harry A Drabkin, Robert M Gemmill, Hiroki Kurahashi,[...]. Cancer Genet 2014
15
28

A perfect palindrome in the Escherichia coli chromosome forms DNA hairpins on both leading- and lagging-strands.
Benura Azeroglu, Frédéric Lincker, Martin A White, Devanshi Jain, David R F Leach. Nucleic Acids Res 2014
9
28

Inverted Alu repeats unstable in yeast are excluded from the human genome.
K S Lobachev, J E Stenger, O G Kozyreva, J Jurka, D A Gordenin, M A Resnick. EMBO J 2000
111
28

T4 endonuclease VII cleaves holliday structures.
K Mizuuchi, B Kemper, J Hays, R A Weisberg. Cell 1982
258
28

Mre11-Sae2 and RPA Collaborate to Prevent Palindromic Gene Amplification.
Sarah K Deng, Yi Yin, Thomas D Petes, Lorraine S Symington. Mol Cell 2015
43
28

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
123
28

Long inverted repeat transiently stalls DNA replication by forming hairpin structures on both leading and lagging strands.
Pey Jiun Lai, Chew Theng Lim, Hang Phuong Le, Tsutomu Katayama, David R F Leach, Asako Furukohri, Hisaji Maki. Genes Cells 2016
11
28



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.