HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination (Q43149406)

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scientific article published on 21 January 2009

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English	HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination	scientific article published on 21 January 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination (English)

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

DNA methylation

0 references

Martin Sigurdsson

1

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Albert V. Smith

2

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

3

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

author name string

Jon J Jonsson

4

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Europe PubMed Central

PMC publication ID

14 November 2017

language of work or name

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based on heuristic

inferred from title

publication date

21 January 2009

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Europe PubMed Central

PMC publication ID

14 November 2017

Genome Research

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Europe PubMed Central

PMC publication ID

14 November 2017

19

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

4

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

581-589

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665777

25 May 2018

Sperm cross-over activity in regions of the human genome showing extreme breakdown of marker association

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25 May 2018

Intra-individual change over time in DNA methylation with familial clustering

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665777

25 May 2018

A second generation human haplotype map of over 3.1 million SNPs

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665777

25 May 2018

Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665777

25 May 2018

Gene body-specific methylation on the active X chromosome

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25 May 2018

Variation resources at UC Santa Cruz

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25 May 2018

DNA methylation profiling of human chromosomes 6, 20 and 22

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25 May 2018

The distribution and causes of meiotic recombination in the human genome

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25 May 2018

Human imprinted chromosomal regions are historical hot-spots of recombination.

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A map of recent positive selection in the human genome

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Transposon-derived repeats in the human genome and 5-methylcytosine-associated mutations in adjacent genes.

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Analysis of repetitive element DNA methylation by MethyLight

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25 May 2018

A haplotype map of the human genome

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665777

25 May 2018

Sequence features in regions of weak and strong linkage disequilibrium

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25 May 2018

A fine-scale map of recombination rates and hotspots across the human genome

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25 May 2018

Repbase Update, a database of eukaryotic repetitive elements

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25 May 2018

Association of tissue-specific differentially methylated regions (TDMs) with differential gene expression

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DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

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25 May 2018

The ENCODE (ENCyclopedia Of DNA Elements) Project

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25 May 2018

Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L

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25 May 2018

Comparative recombination rates in the rat, mouse, and human genomes

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25 May 2018

The DNA sequence and biology of human chromosome 19

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25 May 2018

Imprinted chromosomal regions of the human genome have unusually high recombination rates

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665777

25 May 2018

The UCSC Table Browser data retrieval tool

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25 May 2018

CpG methylation of human papillomavirus type 16 DNA in cervical cancer cell lines and in clinical specimens: genomic hypomethylation correlates with carcinogenic progression

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665777

25 May 2018

A high-resolution recombination map of the human genome

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25 May 2018

The human genome browser at UCSC

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25 May 2018

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665777

25 May 2018

DNA methylation in health and disease

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Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

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25 May 2018

CpG islands as genomic footprints of promoters that are associated with replication origins.

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Comprehensive human genetic maps: individual and sex-specific variation in recombination

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Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes

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Cytosine methylation and the ecology of intragenomic parasites

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25 May 2018

DNA methylation and the frequency of CpG in animal DNA.

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25 May 2018

Hypomethylation distinguishes genes of some human cancers from their normal counterparts

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25 May 2018

Transformation with DNA from 5-azacytidine-reactivated X chromosomes

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CpG islands in vertebrate genomes

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The CpG dinucleotide and human genetic disease

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CpG-rich islands and the function of DNA methylation

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Molecular basis of base substitution hotspots in Escherichia coli

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

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Developmental acquisition of genome-wide DNA methylation occurs prior to meiosis in male germ cells.

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CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1.

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

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Sequence context analysis of 8.2 million single nucleotide polymorphisms in the human genome

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Comparison of fine-scale recombination rates in humans and chimpanzees.

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Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.

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Reactivation of an inactive human X chromosome: evidence for X inactivation by DNA methylation

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Identifiers

10.1101/GR.086181.108

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

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