1
|
The B73 maize genome: complexity, diversity, and dynamics.
|
Science
|
2009
|
18.73
|
2
|
A standardized kinesin nomenclature.
|
J Cell Biol
|
2004
|
4.43
|
3
|
Centromeric retroelements and satellites interact with maize kinetochore protein CENH3.
|
Plant Cell
|
2002
|
2.55
|
4
|
A molecular view of plant centromeres.
|
Trends Plant Sci
|
2003
|
2.26
|
5
|
Chromatin immunoprecipitation reveals that the 180-bp satellite repeat is the key functional DNA element of Arabidopsis thaliana centromeres.
|
Genetics
|
2003
|
2.05
|
6
|
Maize centromeres: organization and functional adaptation in the genetic background of oat.
|
Plant Cell
|
2004
|
2.01
|
7
|
Centromere-encoded RNAs are integral components of the maize kinetochore.
|
Proc Natl Acad Sci U S A
|
2004
|
1.95
|
8
|
Molecular and cytological analyses of large tracks of centromeric DNA reveal the structure and evolutionary dynamics of maize centromeres.
|
Genetics
|
2003
|
1.92
|
9
|
Maize centromere structure and evolution: sequence analysis of centromeres 2 and 5 reveals dynamic Loci shaped primarily by retrotransposons.
|
PLoS Genet
|
2009
|
1.71
|
10
|
Partitioning of the maize epigenome by the number of methyl groups on histone H3 lysines 9 and 27.
|
Genetics
|
2006
|
1.47
|
11
|
Molecular and functional dissection of the maize B chromosome centromere.
|
Plant Cell
|
2005
|
1.43
|
12
|
DNA binding of centromere protein C (CENPC) is stabilized by single-stranded RNA.
|
PLoS Genet
|
2010
|
1.38
|
13
|
CHH islands: de novo DNA methylation in near-gene chromatin regulation in maize.
|
Genome Res
|
2012
|
1.36
|
14
|
Widespread gene conversion in centromere cores.
|
PLoS Biol
|
2010
|
1.29
|
15
|
Spreading of heterochromatin is limited to specific families of maize retrotransposons.
|
PLoS Genet
|
2012
|
1.25
|
16
|
Maximum likelihood methods reveal conservation of function among closely related kinesin families.
|
J Mol Evol
|
2002
|
1.24
|
17
|
Fused sister kinetochores initiate the reductional division in meiosis I.
|
Nat Cell Biol
|
2009
|
1.23
|
18
|
Independently regulated neocentromere activity of two classes of tandem repeat arrays.
|
Plant Cell
|
2002
|
1.13
|
19
|
Distribution of retroelements in centromeres and neocentromeres of maize.
|
Genetics
|
2003
|
1.07
|
20
|
Megabase-scale inversion polymorphism in the wild ancestor of maize.
|
Genetics
|
2012
|
1.05
|
21
|
Phosphoserines on maize CENTROMERIC HISTONE H3 and histone H3 demarcate the centromere and pericentromere during chromosome segregation.
|
Plant Cell
|
2005
|
1.03
|
22
|
Strong epigenetic similarity between maize centromeric and pericentromeric regions at the level of small RNAs, DNA methylation and H3 chromatin modifications.
|
Nucleic Acids Res
|
2011
|
1.02
|
23
|
Precise centromere mapping using a combination of repeat junction markers and chromatin immunoprecipitation-polymerase chain reaction.
|
Genetics
|
2006
|
1.01
|
24
|
RNA as a structural and regulatory component of the centromere.
|
Annu Rev Genet
|
2012
|
1.00
|
25
|
Maize centromeres expand and adopt a uniform size in the genetic background of oat.
|
Genome Res
|
2013
|
0.97
|
26
|
Four loci on abnormal chromosome 10 contribute to meiotic drive in maize.
|
Genetics
|
2003
|
0.95
|
27
|
Marcus rhoades, preferential segregation and meiotic drive.
|
Genetics
|
2003
|
0.95
|
28
|
Reinterpreting pericentromeric heterochromatin.
|
Curr Opin Plant Biol
|
2006
|
0.93
|
29
|
The meiotic drive system on maize abnormal chromosome 10 contains few essential genes.
|
Genetica
|
2003
|
0.93
|
30
|
Distinct influences of tandem repeats and retrotransposons on CENH3 nucleosome positioning.
|
Epigenetics Chromatin
|
2011
|
0.91
|
31
|
Intragenomic conflict between the two major knob repeats of maize.
|
Genetics
|
2013
|
0.90
|
32
|
Transformation of rice with long DNA-segments consisting of random genomic DNA or centromere-specific DNA.
|
Transgenic Res
|
2006
|
0.90
|
33
|
The maize Ab10 meiotic drive system maps to supernumerary sequences in a large complex haplotype.
|
Genetics
|
2006
|
0.89
|
34
|
Mechanisms of plant spindle formation.
|
Chromosome Res
|
2011
|
0.89
|
35
|
Total centromere size and genome size are strongly correlated in ten grass species.
|
Chromosome Res
|
2012
|
0.87
|
36
|
Diversity and evolution of centromere repeats in the maize genome.
|
Chromosoma
|
2014
|
0.86
|
37
|
Maize NDC80 is a constitutive feature of the central kinetochore.
|
Chromosome Res
|
2007
|
0.84
|
38
|
Maize chromosomal knobs are located in gene-dense areas and suppress local recombination.
|
Chromosoma
|
2012
|
0.83
|
39
|
Engineered plant minichromosomes: a bottom-up success?
|
Plant Cell
|
2008
|
0.81
|
40
|
Centromeres: long intergenic spaces with adaptive features.
|
Funct Integr Genomics
|
2009
|
0.80
|
41
|
Live imaging of chromosome dynamics.
|
Methods Mol Biol
|
2013
|
0.79
|
42
|
An Arabidopsis tissue-specific RNAi method for studying genes essential to mitosis.
|
PLoS One
|
2012
|
0.78
|
43
|
Stable integration of an engineered megabase repeat array into the maize genome.
|
Plant J
|
2012
|
0.77
|
44
|
RNA interference on chromosomes.
|
Nat Genet
|
2004
|
0.76
|
45
|
LumberJack: a heuristic tool for sequence alignment exploration and phylogenetic inference.
|
Bioinformatics
|
2004
|
0.75
|