(Q28678675)

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Properties and rates of germline mutations in humans

scientific article (publication date: October 2013)

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Properties and rates of germline mutations in humans (English)

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Evan E. Eichler

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Catarina D Campbell

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Catarina D Campbell

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publication date

October 2013

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Trends in Genetics

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29

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575-84

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

3 June 2018

Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

3 June 2018

Birth prevalence study of the Apert syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

3 June 2018

Revising the human mutation rate: implications for understanding human evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Genetics: The rate of human mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Variation in the ratio of nucleotide substitution and indel rates across genomes in mammals and bacteria.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Template switching during break-induced replication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Estimating the retrotransposition rate of human Alu elements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Transcription-associated mutational asymmetry in mammalian evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Sex biases in the mutation rate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3785239

27 November 2018

Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/23684843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of paternal age in achondroplasia, thanatophoric dysplasia, and osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/23684843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/23684843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mutation rate of the gene for haemophilia, and its segregation ratios in males and females

1 reference

https://pubmed.ncbi.nlm.nih.gov/23684843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of unequal crossover in alpha-satellite DNA evolution: a computational analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23684843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/23684843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent DNA copy number variation in the laboratory mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/23684843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.TIG.2013.04.005

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

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