On the public citation graph

High Diversity at PRDM9 in Chimpanzees and Bonobos

https://doi.org/10.1371/journal.pone.0039064
0 signed · 99 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/anbe.1996.0077openalex-snapshot
Using randomization techniques to analyse behavioural data
inferredcites →https://doi.org/10.1007/bf00179796openalex-snapshot
Elimination of heteroduplex artifacts when sequencing HLA genes amplified by polymerase chain reaction (PCR)
inferredcites →https://doi.org/10.1016/0168-9525(96)10040-8openalex-snapshot
Hybrid sterility in the mouse
inferredcites →https://doi.org/10.1016/j.cub.2006.04.033openalex-snapshot
Demographic History and Genetic Differentiation in Apes
inferredcites →https://doi.org/10.1016/j.cub.2010.01.048openalex-snapshot
Meiosis: A PRDM9 Guide to the Hotspots of Recombination
inferredcites →https://doi.org/10.1016/j.tig.2011.02.001openalex-snapshot
What are the genomic drivers of the rapid evolution of PRDM9?
inferredcites →https://doi.org/10.1016/s0021-9258(19)39621-8openalex-snapshot
DNA damage promotes jumping between templates during enzymatic amplification.
inferredcites →https://doi.org/10.1017/s0016672300015214openalex-snapshot
Genetic studies on male sterility of hybrids between laboratory and wild mice ( Mus musculus L.)
inferredcites →https://doi.org/10.1038/35072078openalex-snapshot
Meiotic recombination hot spots and cold spots
inferredcites →https://doi.org/10.1038/hdy.2010.88openalex-snapshot
Is the control of recombination conserved among diverse eukaryotes?
inferredcites →https://doi.org/10.1038/nature04112openalex-snapshot
A histone H3 methyltransferase controls epigenetic events required for meiotic prophase
inferredcites →https://doi.org/10.1038/nature09525openalex-snapshot
Fine-scale recombination rate differences between sexes, populations and individuals
inferredcites →https://doi.org/10.1038/nature10336openalex-snapshot
The landscape of recombination in African Americans
inferredcites →https://doi.org/10.1038/ng.213openalex-snapshot
A common sequence motif associated with recombination hot spots and genome instability in humans
inferredcites →https://doi.org/10.1038/ng.346openalex-snapshot
The rise and fall of a human recombination hot spot
inferredcites →https://doi.org/10.1038/ng.658openalex-snapshot
PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans
inferredcites →https://doi.org/10.1038/ng1010-821openalex-snapshot
PRDM9 marks the spot
inferredcites →https://doi.org/10.1038/ng1529openalex-snapshot
Fine-scale recombination patterns differ between chimpanzees and humans
inferredcites →https://doi.org/10.1038/nrg1947openalex-snapshot
An evolutionary view of human recombination
inferredcites →https://doi.org/10.1046/j.1365-2370.2002.00356.xopenalex-snapshot
Recombinant DRB sequences produced by mismatch repair of heteroduplexes during cloning in Escherichia coli
inferredcites →https://doi.org/10.1046/j.1440-1711.1998.00772.xopenalex-snapshot
PCR amplification of murine immunoglobulin germline V genes: Strategies for minimization of recombination artefacts
inferredcites →https://doi.org/10.1073/pnas.1109531108openalex-snapshot
Variants of the protein PRDM9 differentially regulate a set of human meiotic recombination hotspots highly active in African populations
inferredcites →https://doi.org/10.1073/pnas.87.7.2833openalex-snapshot
Rapid cloning of HLA-A,B cDNA by using the polymerase chain reaction: frequency and nature of errors produced in amplification.
inferredcites →https://doi.org/10.1073/pnas.94.15.8058openalex-snapshot
The hotspot conversion paradox and the evolution of meiotic recombination
inferredcites →https://doi.org/10.1093/bioinformatics/btl498openalex-snapshot
Meisetz and the birth of the KRAB motif
inferredcites →https://doi.org/10.1093/genetics/148.3.929openalex-snapshot
Likelihood Models for Detecting Positively Selected Amino Acid Sites and Applications to the HIV-1 Envelope Gene
inferredcites →https://doi.org/10.1093/genetics/155.1.431openalex-snapshot
Codon-Substitution Models for Heterogeneous Selection Pressure at Amino Acid Sites
inferredcites →https://doi.org/10.1093/molbev/msi097openalex-snapshot
Bayes Empirical Bayes Inference of Amino Acid Sites Under Positive Selection
inferredcites →https://doi.org/10.1093/molbev/msm088openalex-snapshot
PAML 4: Phylogenetic Analysis by Maximum Likelihood
inferredcites →https://doi.org/10.1093/molbev/msp259openalex-snapshot
SeaView Version 4: A Multiplatform Graphical User Interface for Sequence Alignment and Phylogenetic Tree Building
inferredcites →https://doi.org/10.1093/nar/23.11.2049openalex-snapshot
Template-switching during DNA synthesis byThermus aquaticusDNA polymerase I
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003945openalex-snapshot
Accuracy and Power of the Likelihood Ratio Test in Detecting Adaptive Molecular Evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004007openalex-snapshot
A Novel Use of Equilibrium Frequencies in Models of Sequence Evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040152openalex-snapshot
A likelihood approach for comparing synonymous and nonsynonymous nucleotide substitution rates, with application to the chloroplast genome.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040153openalex-snapshot
A codon-based model of nucleotide substitution for protein-coding DNA sequences.
inferredcites →https://doi.org/10.1101/gr.124123.111openalex-snapshot
Death of PRDM9 coincides with stabilization of the recombination landscape in the dog genome
inferredcites →https://doi.org/10.1111/j.1471-8286.2007.01821.xopenalex-snapshot
FaBox: an online toolbox for fasta sequences
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00257.xopenalex-snapshot
ASYMMETRY AND POLYMORPHISM OF HYBRID MALE STERILITY DURING THE EARLY STAGES OF SPECIATION IN HOUSE MICE
inferredcites →https://doi.org/10.1126/science.1105322openalex-snapshot
Comparison of Fine-Scale Recombination Rates in Humans and Chimpanzees
inferredcites →https://doi.org/10.1126/science.1163601openalex-snapshot
A Mouse Speciation Gene Encodes a Meiotic Histone H3 Methyltransferase
inferredcites →https://doi.org/10.1126/science.1181495openalex-snapshot
Prdm9 Controls Activation of Mammalian Recombination Hotspots
inferredcites →https://doi.org/10.1126/science.1182363openalex-snapshot
Drive Against Hotspot Motifs in Primates Implicates the PRDM9 Gene in Meiotic Recombination
inferredcites →https://doi.org/10.1126/science.1183439openalex-snapshot
PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice
inferredcites →https://doi.org/10.1126/science.1187155openalex-snapshot
Genetic Control of Hotspots
inferredcites →https://doi.org/10.1126/science.1216872openalex-snapshot
A Fine-Scale Chimpanzee Genetic Map from Population Sequencing
inferredcites →https://doi.org/10.1146/annurev.biochem.70.1.313openalex-snapshot
Design and Selection of Novel Cys2His2 Zinc Finger Proteins
inferredcites →https://doi.org/10.1146/annurev.ge.29.120195.002231openalex-snapshot
MEIOTIC RECOMBINATION HOTSPOTS
inferredcites →https://doi.org/10.1146/annurev.genet.41.110306.130301openalex-snapshot
Mammalian Meiotic Recombination Hot Spots
inferredcites →https://doi.org/10.1186/1471-2148-7-187openalex-snapshot
Family expansion and gene rearrangements contributed to the functional specialization of PRDM genes in vertebrates
inferredcites →https://doi.org/10.1201/9781315273075openalex-snapshot
Randomization, Bootstrap and Monte Carlo Methods in Biology
inferredcites →https://doi.org/10.1371/journal.pbio.1001176openalex-snapshot
Mouse PRDM9 DNA-Binding Specificity Determines Sites of Histone H3 Lysine 4 Trimethylation for Initiation of Meiotic Recombination
inferredcites →https://doi.org/10.1371/journal.pbio.1001211openalex-snapshot
The Case of the Fickle Fingers: How the PRDM9 Zinc Finger Protein Specifies Meiotic Recombination Hotspots in Humans
inferredcites →https://doi.org/10.1371/journal.pgen.1000753openalex-snapshot
Accelerated Evolution of the Prdm9 Speciation Gene across Diverse Metazoan Taxa
inferredcites →https://doi.org/10.1371/journal.pone.0008505openalex-snapshot
Extraordinary Molecular Evolution in the PRDM9 Fertility Gene
inferredcites →https://doi.org/10.1371/journal.pone.0020321openalex-snapshot
Variation in Human Recombination Rates and Its Genetic Determinants
inferredcites →https://doi.org/10.1371/journal.pone.0021605openalex-snapshot
Bonobos Fall within the Genomic Variation of Chimpanzees
inferredcites →https://doi.org/10.1371/journal.pone.0025498openalex-snapshot
Prdm9, a Major Determinant of Meiotic Recombination Hotspots, Is Not Functional in Dogs and Their Wild Relatives, Wolves and Coyotes
inferredcites →https://doi.org/10.1534/genetics.104.032144openalex-snapshot
Detecting Amino Acid Sites Under Positive Selection and Purifying Selection
inferredcites →https://doi.org/10.2164/jandrol.108.006262openalex-snapshot
Single‐Nucleotide Polymorphisms of the PRDM9 (MEISETZ) Gene in Patients With Nonobstructive Azoospermia
inferredcites →https://doi.org/10.2307/2533527openalex-snapshot
Randomization, Bootstrap and Monte Carlo Methods in Biology.
inferredcites →https://doi.org/10.3410/b2-37openalex-snapshot
PRDM9 sticks its zinc fingers into recombination hotspots and between species

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.5281/zenodo.5096357openalex-extracted
inferred← citeshttps://doi.org/10.1002/bies.201400047openalex-snapshot
Unraveling recombination rate evolution using ancestral recombination maps
inferred← citeshttps://doi.org/10.1007/s00412-017-0631-zopenalex-snapshot
The PRDM9 KRAB domain is required for meiosis and involved in protein interactions
inferred← citeshttps://doi.org/10.1007/s00438-013-0784-2openalex-snapshot
High-resolution linkage map for two honeybee chromosomes: the hotspot quest
inferred← citeshttps://doi.org/10.1007/s00438-016-1260-6openalex-snapshot
Evolutionary dynamics of meiotic recombination hotspots regulator PRDM9 in bovids
inferred← citeshttps://doi.org/10.1016/j.tig.2017.12.017openalex-snapshot
PRDM9 and Its Role in Genetic Recombination
inferred← citeshttps://doi.org/10.1038/ncomms5370openalex-snapshot
Primate evolution of the recombination regulator PRDM9
inferred← citeshttps://doi.org/10.1038/nrg3573openalex-snapshot
Meiotic recombination in mammals: localization and regulation
inferred← citeshttps://doi.org/10.1038/srep34618openalex-snapshot
The pioneering role of PRDM9 indel mutations in tarsier evolution
inferred← citeshttps://doi.org/10.1074/jbc.m116.721472openalex-snapshot
PR Domain-containing Protein 7 (PRDM7) Is a Histone 3 Lysine 4 Trimethyltransferase
inferred← citeshttps://doi.org/10.1074/jbc.m117.805754openalex-snapshot
Structural basis of human PR/SET domain 9 (PRDM9) allele C–specific recognition of its cognate DNA sequence
inferred← citeshttps://doi.org/10.1093/biolinnean/bly063openalex-snapshot
What is Speciation Genomics? The roles of ecology, gene flow, and genomic architecture in the formation of species
inferred← citeshttps://doi.org/10.1093/dnares/dst059openalex-snapshot
Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks
inferred← citeshttps://doi.org/10.1093/gbe/evw022openalex-snapshot
No Distinction of Orthology/Paralogy between Human and Chimpanzee Rh Blood Group Genes
inferred← citeshttps://doi.org/10.1093/jhered/esy060openalex-snapshot
Hybrid Sterility with Meiotic Metaphase Arrest in Intersubspecific Mouse Crosses
inferred← citeshttps://doi.org/10.1093/molbev/msae063openalex-snapshot
Multiple Genomic Landscapes of Recombination and Genomic Divergence in Wild Populations of House Mice—The Role of Chromosomal Fusions and Prdm9
inferred← citeshttps://doi.org/10.1093/nar/gkag049openalex-snapshot
A novel dual histone mark reader ZCWPW2 regulates meiotic recombination through lactylation and transcriptional regulation in humans and mice
inferred← citeshttps://doi.org/10.1098/rsob.250171openalex-snapshot
The evolutionary entanglement of flipons with zinc fingers and retroelements has engendered a large family of Z-DNA and G-quadruplex binding proteins
inferred← citeshttps://doi.org/10.1101/498428openalex-snapshot
PRDM9 forms an active trimer mediated by its repetitive zinc finger array
inferred← citeshttps://doi.org/10.1101/gad.274928.115openalex-snapshot
Structural basis for human PRDM9 action at recombination hot spots
inferred← citeshttps://doi.org/10.1101/gr.151472.112openalex-snapshot
Global analysis of Drosophila Cys2-His2 zinc finger proteins reveals a multitude of novel recognition motifs and binding determinants
inferred← citeshttps://doi.org/10.1111/age.12487openalex-snapshot
Evidence of positive selection and concerted evolution in the rapidly evolving PRDM 9 zinc finger domain in goats and sheep
inferred← citeshttps://doi.org/10.1146/annurev-genet-110711-155423openalex-snapshot
Initiation of Meiotic Recombination: How and Where? Conservation and Specificities Among Eukaryotes
inferred← citeshttps://doi.org/10.1186/s12711-017-0330-5openalex-snapshot
The potential of shifting recombination hotspots to increase genetic gain in livestock breeding
inferred← citeshttps://doi.org/10.1186/s12864-022-08305-1openalex-snapshot
Evolution of the recombination regulator PRDM9 in minke whales
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004916openalex-snapshot
PRDM9 Drives Evolutionary Erosion of Hotspots in Mus musculus through Haplotype-Specific Initiation of Meiotic Recombination
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005011openalex-snapshot
Pervasive Variation of Transcription Factor Orthologs Contributes to Regulatory Network Evolution
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005512openalex-snapshot
Multimer Formation Explains Allelic Suppression of PRDM9 Recombination Hotspots
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007479openalex-snapshot
PRDM9, a driver of the genetic map
inferred← citeshttps://doi.org/10.1371/journal.pone.0085021openalex-snapshot
Diversity of Prdm9 Zinc Finger Array in Wild Mice Unravels New Facets of the Evolutionary Turnover of this Coding Minisatellite
inferred← citeshttps://doi.org/10.1371/journal.pone.0156159openalex-snapshot
Zinc Finger Domain of the PRDM9 Gene on Chromosome 1 Exhibits High Diversity in Ruminants but Its Paralog PRDM7 Contains Multiple Disruptive Mutations
inferred← citeshttps://doi.org/10.15173/nexus.v23i2.894openalex-snapshot
Dmanisi hominin fossils and the problem of the multiple species in the early Homo genus
inferred← citeshttps://doi.org/10.3389/fgene.2021.593725openalex-snapshot
Pinpointing the PRDM9-PRDM7 Gene Duplication Event During Primate Divergence
inferred← citeshttps://doi.org/10.3389/fgene.2021.662239openalex-snapshot
Positive Selection in Gene Regulatory Factors Suggests Adaptive Pleiotropic Changes During Human Evolution
inferred← citeshttps://doi.org/10.56093/ijans.v92i12.112968openalex-snapshot
Fertility of hybrids of dromedary and Bactrian camels: A possible role of conserved architecture of zinc finger domain of recombination regulator PRDM9
inferred← citeshttps://doi.org/10.64898/2026.05.22.727067openalex-snapshot
Dual histone methylation reader ZCWPW2 links histone methylation to initiation of meiotic recombination
inferred← citeshttps://doi.org/10.70675/4f23518fz0509z4fa5z96f0zb94275a9db50openalex-snapshot
Meiotic recombination evolution : Prdm9 gene variation and evolution in mice
inferred← citeshttps://doi.org/10.70675/6992b6c8z7c66z4afbz8a88z34168d0ab438openalex-snapshot
Rôle de l'activité méthyltransférase de la protéine PRDM9 dans la recombinaison méiotique chez la souris
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.