On the public citation graph
Frequency of mosaicism points towards mutation-prone early cleavage cell divisions in cattle
0 signed · 89 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.cell.2012.11.019openalex-snapshot
Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation
inferredcites →https://doi.org/10.1016/j.tig.2015.03.013openalex-snapshot
Somatic mosaicism: implications for disease and transmission genetics
inferredcites →https://doi.org/10.1038/nature11396openalex-snapshot
Rate of de novo mutations and the importance of father’s age to disease risk
inferredcites →https://doi.org/10.1038/nature21703openalex-snapshot
Somatic mutations reveal asymmetric cellular dynamics in the early human embryo
inferredcites →https://doi.org/10.1038/ng.2418openalex-snapshot
Estimating the human mutation rate using autozygosity in a founder population
inferredcites →https://doi.org/10.1038/ng.3034openalex-snapshot
Whole-genome sequencing of 234 bulls facilitates mapping of monogenic and complex traits in cattle
inferredcites →https://doi.org/10.1038/ng.3469openalex-snapshot
Timing, rates and spectra of human germline mutation
inferredcites →https://doi.org/10.1038/ng.862openalex-snapshot
Variation in genome-wide mutation rates within and between human families
inferredcites →https://doi.org/10.1038/s41467-019-12023-wopenalex-snapshot
Similarities and differences in patterns of germline mutation between mice and humans
inferredcites →https://doi.org/10.1046/j.1420-9101.1992.5030457.xopenalex-snapshot
Have premeiotic clusters of mutation been overlooked in evolutionary theory?
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/genetics/163.1.453openalex-snapshot
Mosaicism of Solid Gold Supports the Causality of a Noncoding A-to-G Transition in the Determinism of the Callipyge Phenotype
inferredcites →https://doi.org/10.1098/rstb.2015.0137openalex-snapshot
Mutation rates and the evolution of germline structure
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1101/gr.204669.116openalex-snapshot
Direct estimate of the rate of germline mutation in a bird
inferredcites →https://doi.org/10.1126/science.1186802openalex-snapshot
Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing
inferredcites →https://doi.org/10.1126/science.344.6189.1272openalex-snapshot
Strong male bias drives germline mutation in chimpanzees
inferredcites →https://doi.org/10.1146/annurev-genom-031714-125740openalex-snapshot
Determinants of Mutation Rate Variation in the Human Germline
inferredcites →https://doi.org/10.1186/1471-2105-9-253openalex-snapshot
BatchPrimer3: A high throughput web application for PCR and sequencing primer design
inferredcites →https://doi.org/10.48550/arxiv.1207.3907openalex-snapshot
Haplotype-based variant detection from short-read sequencing
inferredcites →https://doi.org/10.7554/elife.23907openalex-snapshot
Moderate nucleotide diversity in the Atlantic herring is associated with a low mutation rate
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s11248-019-00141-6openalex-snapshot
Application of genome editing in farm animals: cattle
inferred← citeshttps://doi.org/10.1016/j.tig.2019.08.005openalex-snapshot
De Novo Mutations Reflect Development and Aging of the Human Germline
inferred← citeshttps://doi.org/10.1038/s41437-020-00383-9openalex-snapshot
An evaluation of inbreeding measures using a whole-genome sequenced cattle pedigree
inferred← citeshttps://doi.org/10.1038/s41437-021-00446-5openalex-snapshot
Pedigree-based and phylogenetic methods support surprising patterns of mutation rate and spectrum in the gray mouse lemur
inferred← citeshttps://doi.org/10.1038/s41467-017-00323-yopenalex-snapshot
Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes
inferred← citeshttps://doi.org/10.1038/s41467-019-12023-wopenalex-snapshot
Similarities and differences in patterns of germline mutation between mice and humans
inferred← citeshttps://doi.org/10.1038/s41467-024-46434-1openalex-snapshot
GWAS reveals determinants of mobilization rate and dynamics of an active endogenous retrovirus of cattle
inferred← citeshttps://doi.org/10.1038/s41467-026-70342-1openalex-snapshot
Long-read sequencing of families reveals increased germline and postzygotic mutation rates in repetitive DNA
inferred← citeshttps://doi.org/10.1038/s41538-019-0035-yopenalex-snapshot
Proposed U.S. regulation of gene-edited food animals is not fit for purpose
inferred← citeshttps://doi.org/10.1038/s41576-018-0082-2openalex-snapshot
Harnessing genomic information for livestock improvement
inferred← citeshttps://doi.org/10.1038/s41576-021-00376-2openalex-snapshot
The origin of human mutation in light of genomic data
inferred← citeshttps://doi.org/10.1038/s41586-023-05752-yopenalex-snapshot
Evolution of the germline mutation rate across vertebrates
inferred← citeshttps://doi.org/10.1038/s41587-019-0266-0openalex-snapshot
Genomic and phenotypic analyses of six offspring of a genome-edited hornless bull
inferred← citeshttps://doi.org/10.1038/s41588-018-0285-7openalex-snapshot
Error-prone bypass of DNA lesions during lagging-strand replication is a common source of germline and cancer mutations
inferred← citeshttps://doi.org/10.1038/s41588-020-00755-1openalex-snapshot
Differences between germline genomes of monozygotic twins
inferred← citeshttps://doi.org/10.1038/s42003-019-0476-5openalex-snapshot
Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspring
inferred← citeshttps://doi.org/10.1073/pnas.1900714116openalex-snapshot
Signatures of replication timing, recombination, and sex in the spectrum of rare variants on the human X chromosome and autosomes
inferred← citeshttps://doi.org/10.1073/pnas.1901259116openalex-snapshot
Overlooked roles of DNA damage and maternal age in generating human germline mutations
inferred← citeshttps://doi.org/10.1073/pnas.1915664117openalex-snapshot
Changes in life history and population size can explain the relative neutral diversity levels on X and autosomes in extant human populations
inferred← citeshttps://doi.org/10.1093/evlett/qrad027openalex-snapshot
Experimental estimates of germline mutation rate in eukaryotes: a phylogenetic meta-analysis
inferred← citeshttps://doi.org/10.1093/genetics/iyac087openalex-snapshot
The impact of genetic modifiers on variation in germline mutation rates within and among human populations
inferred← citeshttps://doi.org/10.1093/genetics/iyae166openalex-snapshot
A maternal germline mutator phenotype in a family affected by heritable colorectal cancer
inferred← citeshttps://doi.org/10.1093/genetics/iyaf177openalex-snapshot
Low mutation rate but high male-bias in the germline of a short-lived opossum
inferred← citeshttps://doi.org/10.1093/molbev/msac134openalex-snapshot
Warthog Genomes Resolve an Evolutionary Conundrum and Reveal Introgression of Disease Resistance Genes
inferred← citeshttps://doi.org/10.1093/molbev/msac147openalex-snapshot
De novo Mutations in Domestic Cat are Consistent with an Effect of Reproductive Longevity on Both the Rate and Spectrum of Mutations
inferred← citeshttps://doi.org/10.1098/rstb.2015.0137openalex-snapshot
Mutation rates and the evolution of germline structure
inferred← citeshttps://doi.org/10.1101/2022.10.29.514266openalex-snapshot
Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.1101/2023.03.22.533860openalex-snapshot
Extensive variation in germline de novo mutations in Poecilia reticulata
inferred← citeshttps://doi.org/10.1101/2024.09.05.611523openalex-snapshot
Mutation and recombination parameters in zebra finch are similar to those in mammals
inferred← citeshttps://doi.org/10.1101/2024.12.13.628352openalex-snapshot
Unprecedented female mutation bias in aye-ayes
inferred← citeshttps://doi.org/10.1101/348441openalex-snapshot
Base pair editing of goat embryos: nonsense codon introgression into FGF5 to improve cashmere yield
inferred← citeshttps://doi.org/10.1101/gr.277884.123openalex-snapshot
The rate of de novo structural variation is increased in in vitro–produced offspring and preferentially affects the paternal genome
inferred← citeshttps://doi.org/10.1101/gr.277936.123openalex-snapshot
Extensive variation in germline de novo mutations in Poecilia reticulata
inferred← citeshttps://doi.org/10.1101/gr.279542.124openalex-snapshot
Overcoming limitations to customize DeepVariant for domesticated animals with TrioTrain
inferred← citeshttps://doi.org/10.1111/mec.16007openalex-snapshot
The challenge and promise of estimating the de novo mutation rate from whole‐genome comparisons among closely related individuals
inferred← citeshttps://doi.org/10.1126/science.adf2160openalex-snapshot
Wild pedigrees inform mutation rates and historic abundance in baleen whales
inferred← citeshttps://doi.org/10.1146/annurev-animal-050622-055534openalex-snapshot
Identification of Genetic Risk Factors for Monogenic and Complex Canine Diseases
inferred← citeshttps://doi.org/10.1186/s12711-017-0321-6openalex-snapshot
A strategy to improve phasing of whole-genome sequenced individuals through integration of familial information from dense genotype panels
inferred← citeshttps://doi.org/10.1186/s12711-025-00967-1openalex-snapshot
Estimating mutation rate and characterising single nucleotide de novo mutations in pigs
inferred← citeshttps://doi.org/10.1186/s12711-026-01085-2openalex-snapshot
The rate and spectrum of germline mutations in chicken from a commercial pedigree line
inferred← citeshttps://doi.org/10.1186/s12864-018-4712-zopenalex-snapshot
Low incidence of SNVs and indels in trio genomes of Cas9-mediated multiplex edited sheep
inferred← citeshttps://doi.org/10.1186/s12864-021-07804-xopenalex-snapshot
The genomes of precision edited cloned calves show no evidence for off-target events or increased de novo mutagenesis
inferred← citeshttps://doi.org/10.1186/s12864-022-08354-6openalex-snapshot
Benchmarking phasing software with a whole-genome sequenced cattle pedigree
inferred← citeshttps://doi.org/10.1186/s12864-023-09296-3openalex-snapshot
Identification and characterisation of de novo germline structural variants in two commercial pig lines using trio-based whole genome sequencing
inferred← citeshttps://doi.org/10.1371/journal.pbio.3000838openalex-snapshot
A comparison of humans and baboons suggests germline mutation rates do not track cell divisions
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003799openalex-snapshot
What sets the mutation rate of a cell type in an animal species?
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006651openalex-snapshot
A de novo variant in the ASPRV1 gene in a dog with ichthyosis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008055openalex-snapshot
Loss of function mutations in essential genes cause embryonic lethality in pigs
inferred← citeshttps://doi.org/10.1534/genetics.117.1114openalex-snapshot
Contrasting Determinants of Mutation Rates in Germline and Soma
inferred← citeshttps://doi.org/10.18174/515207openalex-snapshot
From sequence to phenotype: the impact of deleterious variation in livestock
inferred← citeshttps://doi.org/10.22215/etd/2017-11975openalex-snapshot
Harnessing New Genomics Technologies to Assess Environmental Risk Factors That May Cause Heritable Genetic Disease
inferred← citeshttps://doi.org/10.3389/fgene.2018.00449openalex-snapshot
Trio-Based Deep Sequencing Reveals a Low Incidence of Off-Target Mutations in the Offspring of Genetically Edited Goats
inferred← citeshttps://doi.org/10.3389/fgene.2019.00215openalex-snapshot
Programmable Base Editing of the Sheep Genome Revealed No Genome-Wide Off-Target Mutations
inferred← citeshttps://doi.org/10.7554/elife.23907openalex-snapshot
Moderate nucleotide diversity in the Atlantic herring is associated with a low mutation rate
inferred← citeshttps://doi.org/10.7554/elife.46922openalex-snapshot
Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation
inferred← citeshttps://doi.org/10.7554/elife.73577openalex-snapshot
The Mutationathon highlights the importance of reaching standardization in estimates of pedigree-based germline mutation rates
inferred← citeshttps://doi.org/10.7554/elife.80008openalex-snapshot
A paternal bias in germline mutation is widespread in amniotes and can arise independently of cell division numbers
inferred← citeshttps://doi.org/10.7554/elife.84874openalex-snapshot
Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.7554/elife.84874.1openalex-snapshot
Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.7554/elife.84874.1.sa0openalex-snapshot
Author Response: Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.7554/elife.84874.1.sa1openalex-snapshot
Reviewer #3 (Public Review): Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.7554/elife.84874.1.sa2openalex-snapshot
Reviewer #2 (Public Review): Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.7554/elife.84874.1.sa3openalex-snapshot
Reviewer #1 (Public Review): Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.7554/elife.84874.1.sa4openalex-snapshot
eLife Assessment: Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.7554/elife.84874.2openalex-snapshot
Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
inferred← citeshttps://doi.org/10.7554/elife.84874.3openalex-snapshot
Expanding the stdpopsim species catalog, and lessons learned for realistic genome simulations
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.