(Q54243556)

4

object named as

Peter Donnelly

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Gilean McVean

5

object named as

Gil McVean

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Adam Auton

3

object named as

Adam Auton

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author name string

Colin Freeman

https://scigraph.springernature.com/pub.10.1038/ng.213

2

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language of work or name

English

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publication date

24 August 2008

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published in

Nature Genetics

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volume

40

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page(s)

1124-1129

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issue

9

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exact match

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cites work

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Factors influencing recombination frequency and distribution in a human meiotic crossover hotspot.

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A second generation human haplotype map of over 3.1 million SNPs

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Cis- and trans-acting elements regulate the mouse Psmb9 meiotic recombination hotspot

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Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation.

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Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

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Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

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A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

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Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

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Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion.

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A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination

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Two modes of germline instability at human minisatellite MS1 (locus D1S7): complex rearrangements and paradoxical hyperdeletion.

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Influences of array size and homogeneity on minisatellite mutation.

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Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90).

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Repeat instability at human minisatellites arising from meiotic recombination

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Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7.

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Complex minisatellite rearrangements generated in the total or partial absence of Rad27/hFEN1 activity occur in a single generation and are Rad51 and Rad52 dependent.

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Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans

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High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans.

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Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro

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Minisatellites: mutability and genome architecture.

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Mutational mechanisms of Williams-Beuren syndrome deletions

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Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion

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High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot

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