On the public citation graph

De novo deletions and duplications at recombination hotspots in mouse germlines

https://doi.org/10.1101/2020.06.23.168138

0 signed · 72 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/bies.201400161openalex-snapshot

Replication protein A prevents promiscuous annealing between short sequence homologies: Implications for genome integrity

inferredcites →https://doi.org/10.1002/cyto.a.22463openalex-snapshot

Optimized flow cytometry isolation of murine spermatocytes

inferredcites →https://doi.org/10.1007/978-1-61779-129-1_15openalex-snapshot

Isolation of Meiotic Recombinants from Mouse Sperm

inferredcites →https://doi.org/10.1016/j.cell.2011.02.009openalex-snapshot

A Hierarchical Combination of Factors Shapes the Genome-wide Topography of Yeast Meiotic Recombination Initiation

inferredcites →https://doi.org/10.1016/j.cell.2013.10.043openalex-snapshot

ATR Prohibits Replication Catastrophe by Preventing Global Exhaustion of RPA

inferredcites →https://doi.org/10.1016/j.cell.2014.09.052openalex-snapshot

Sequencing the Mouse Y Chromosome Reveals Convergent Gene Acquisition and Amplification on Both Sex Chromosomes

inferredcites →https://doi.org/10.1016/j.cell.2016.09.035openalex-snapshot

The Landscape of Mouse Meiotic Double-Strand Break Formation, Processing, and Repair

inferredcites →https://doi.org/10.1016/j.molcel.2010.08.017openalex-snapshot

Comprehensive, Fine-Scale Dissection of Homologous Recombination Outcomes at a Hot Spot in Mouse Meiosis

inferredcites →https://doi.org/10.1016/j.molcel.2014.12.027openalex-snapshot

Gradual Implementation of the Meiotic Recombination Program via Checkpoint Pathways Controlled by Global DSB Levels

inferredcites →https://doi.org/10.1016/j.molcel.2018.02.032openalex-snapshot

Mechanistic View and Genetic Control of DNA Recombination during Meiosis

inferredcites →https://doi.org/10.1016/j.molcel.2020.04.009openalex-snapshot

Mechanistic Insight into Crossing over during Mouse Meiosis

inferredcites →https://doi.org/10.1016/j.mrfmmm.2010.02.004openalex-snapshot

Genetic probing of homologous recombination and non-homologous end joining during meiotic prophase in irradiated mouse spermatocytes

inferredcites →https://doi.org/10.1016/j.semcdb.2016.02.019openalex-snapshot

Mechanisms of germ line genome instability

inferredcites →https://doi.org/10.1016/j.tibs.2006.05.004openalex-snapshot

The ATM-mediated DNA-damage response: taking shape

inferredcites →https://doi.org/10.1016/j.tibs.2015.08.006openalex-snapshot

Microhomology-Mediated End Joining: A Back-up Survival Mechanism or Dedicated Pathway?

inferredcites →https://doi.org/10.1016/s0070-2153(01)52008-6openalex-snapshot

Mechanism and control of meiotic recombination initiation

inferredcites →https://doi.org/10.1016/s0092-8674(00)80086-0openalex-snapshot

Atm-Deficient Mice: A Paradigm of Ataxia Telangiectasia

inferredcites →https://doi.org/10.1016/s0092-8674(00)81876-0openalex-snapshot

Meiosis-Specific DNA Double-Strand Breaks Are Catalyzed by Spo11, a Member of a Widely Conserved Protein Family

inferredcites →https://doi.org/10.1038/35072078openalex-snapshot

Meiotic recombination hot spots and cold spots

inferredcites →https://doi.org/10.1038/nature03872openalex-snapshot

Endonucleolytic processing of covalent protein-linked DNA double-strand breaks

inferredcites →https://doi.org/10.1038/nature10508openalex-snapshot

ATM controls meiotic double-strand-break formation

inferredcites →https://doi.org/10.1038/nature11089openalex-snapshot

Genetic recombination is directed away from functional genomic elements in mice

inferredcites →https://doi.org/10.1038/nature13120openalex-snapshot

Homologue engagement controls meiotic DNA break number and distribution

inferredcites →https://doi.org/10.1038/nature13993openalex-snapshot

Tel1ATM-mediated interference suppresses clustered meiotic double-strand-break formation

inferredcites →https://doi.org/10.1038/nature16931openalex-snapshot

Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice

inferredcites →https://doi.org/10.1038/nbt.3583openalex-snapshot

Analyzing CRISPR genome-editing experiments with CRISPResso

inferredcites →https://doi.org/10.1038/ncb2451openalex-snapshot

Homeostatic control of recombination is implemented progressively in mouse meiosis

inferredcites →https://doi.org/10.1038/ncomms4347openalex-snapshot

ATM specifically mediates repair of double-strand breaks with blocked DNA ends

inferredcites →https://doi.org/10.1038/ng.3068openalex-snapshot

Mouse tetrad analysis provides insights into recombination mechanisms and hotspot evolutionary dynamics

inferredcites →https://doi.org/10.1038/nrg3573openalex-snapshot

Meiotic recombination in mammals: localization and regulation

inferredcites →https://doi.org/10.1038/nrm.2017.48openalex-snapshot

Non-homologous DNA end joining and alternative pathways to double-strand break repair

inferredcites →https://doi.org/10.1038/s41467-018-06417-5openalex-snapshot

Regulatory control of DNA end resection by Sae2 phosphorylation

inferredcites →https://doi.org/10.1038/s41467-019-11675-yopenalex-snapshot

A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination

inferredcites →https://doi.org/10.1038/s41467-020-14654-wopenalex-snapshot

ATM and PRDM9 regulate SPO11-bound recombination intermediates during meiosis

inferredcites →https://doi.org/10.1038/s41586-020-2287-8openalex-snapshot

A structural variation reference for medical and population genetics

inferredcites →https://doi.org/10.1038/s41586-021-03389-3openalex-snapshot

Concerted cutting by Spo11 illuminates meiotic DNA break mechanics

inferredcites →https://doi.org/10.1038/s41587-019-0032-3openalex-snapshot

CRISPResso2 provides accurate and rapid genome editing sequence analysis

inferredcites →https://doi.org/10.1073/pnas.1117937108openalex-snapshot

Meiotic double-strand breaks occur once per pair of (sister) chromatids and, via Mec1/ATR and Tel1/ATM, once per quartet of chromatids

inferredcites →https://doi.org/10.1073/pnas.1719029115openalex-snapshot

Interdependent and separable functions of Caenorhabditis elegans MRN-C complex members couple formation and repair of meiotic DSBs

inferredcites →https://doi.org/10.1073/pnas.1801920115openalex-snapshot

Physical basis for long-distance communication along meiotic chromosomes

inferredcites →https://doi.org/10.1080/15384101.2015.1093709openalex-snapshot

Meiotic DSB patterning: A multifaceted process

inferredcites →https://doi.org/10.1080/15384101.2017.1361065openalex-snapshot

Genomic and chromatin features shaping meiotic double-strand break formation and repair in mice

inferredcites →https://doi.org/10.1080/15384101.2018.1464847openalex-snapshot

Control of meiotic double-strand-break formation by ATM: local and global views

inferredcites →https://doi.org/10.1093/nar/gkaa1205openalex-snapshot

A pathway for error-free non-homologous end joining of resected meiotic double-strand breaks

inferredcites →https://doi.org/10.1093/nar/gku1341openalex-snapshot

Insight into biases and sequencing errors for amplicon sequencing with the Illumina MiSeq platform

inferredcites →https://doi.org/10.1093/nar/gky968openalex-snapshot

A chromatin-associated protein required for inducing and limiting meiotic DNA double-strand break formation

inferredcites →https://doi.org/10.1093/plcell/koab045openalex-snapshot

ATM controls meiotic DNA double-strand break formation and recombination and affects synaptonemal complex organization in plants

inferredcites →https://doi.org/10.1097/hp.0000000000000852openalex-snapshot

NHEJ Contributes to the Fast Repair of Radiation-induced DNA Double-strand Breaks at Late Prophase I Telomeres

inferredcites →https://doi.org/10.1101/2020.02.21.960245openalex-snapshot

DNA-dependent macromolecular condensation drives self-assembly of the meiotic DNA break machinery

inferredcites →https://doi.org/10.1101/527333openalex-snapshot

Removal of Spo11 from meiotic DNA breaks in vitro but not in vivo by Tyrosyl DNA Phosphodiesterase 2

inferredcites →https://doi.org/10.1101/cshperspect.a016618openalex-snapshot

Meiotic Recombination: The Essence of Heredity

inferredcites →https://doi.org/10.1101/gad.10.19.2411openalex-snapshot

Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma.

inferredcites →https://doi.org/10.1101/gad.270009.115openalex-snapshot

The evolutionary turnover of recombination hot spots contributes to speciation in mice

inferredcites →https://doi.org/10.1101/gad.336032.119openalex-snapshot

Molecular structures and mechanisms of DNA break processing in mouse meiosis

inferredcites →https://doi.org/10.1101/gr.213587.116openalex-snapshot

Numerical and spatial patterning of yeast meiotic DNA breaks by Tel1

inferredcites →https://doi.org/10.1126/science.aak9704openalex-snapshot

A global view of meiotic double-strand break end resection

inferredcites →https://doi.org/10.1128/mcb.00055-13openalex-snapshot

Impaired Resection of Meiotic Double-Strand Breaks Channels Repair to Nonhomologous End Joining in Caenorhabditis elegans

inferredcites →https://doi.org/10.1128/mcb.25.16.7203-7215.2005openalex-snapshot

Surveillance of Different Recombination Defects in Mouse Spermatocytes Yields Distinct Responses despite Elimination at an Identical Developmental Stage

inferredcites →https://doi.org/10.1128/mcb.25.8.3127-3139.2005openalex-snapshot

RAD-51-Dependent and -Independent Roles of a Caenorhabditis elegans BRCA2-Related Protein during DNA Double-Strand Break Repair

inferredcites →https://doi.org/10.1146/annurev-genet-110711-155423openalex-snapshot

Initiation of Meiotic Recombination: How and Where? Conservation and Specificities Among Eukaryotes

inferredcites →https://doi.org/10.1242/dev.125.20.4007openalex-snapshot

Atm deficiency results in severe meiotic disruption as early as leptonema of prophase I

inferredcites →https://doi.org/10.1371/journal.pgen.1003276openalex-snapshot

COM-1 Promotes Homologous Recombination during Caenorhabditis elegans Meiosis by Antagonizing Ku-Mediated Non-Homologous End Joining

inferredcites →https://doi.org/10.1371/journal.pgen.1004916openalex-snapshot

PRDM9 Drives Evolutionary Erosion of Hotspots in Mus musculus through Haplotype-Specific Initiation of Meiotic Recombination

inferredcites →https://doi.org/10.1371/journal.pgen.1005478openalex-snapshot

Reduced Crossover Interference and Increased ZMM-Independent Recombination in the Absence of Tel1/ATM

inferredcites →https://doi.org/10.1371/journal.pgen.1007439openalex-snapshot

Transition from a meiotic to a somatic-like DNA damage response during the pachytene stage in mouse meiosis

inferredcites →https://doi.org/10.1534/genetics.114.164152openalex-snapshot

Pseudosynapsis and Decreased Stringency of Meiotic Repair Pathway Choice on the Hemizygous Sex Chromosome of Caenorhabditis elegans Males

inferredcites →https://doi.org/10.1534/genetics.118.301402openalex-snapshot

Meiotic Double-Strand Break Proteins Influence Repair Pathway Utilization

inferredcites →https://doi.org/10.3389/fgene.2018.00521openalex-snapshot

Hotspots for Initiation of Meiotic Recombination

What points at this work

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

inferred← citeshttps://doi.org/10.1038/s41586-021-03389-3openalex-snapshot

Concerted cutting by Spo11 illuminates meiotic DNA break mechanics

inferred← citeshttps://doi.org/10.1038/s41586-021-03632-xopenalex-snapshot

Spo11 generates gaps through concerted cuts at sites of topological stress

inferred← citeshttps://doi.org/10.70675/26286691zf12dz4718z8320zc833ed23c04copenalex-snapshot

Régulation spatiale des cassures d’ADN double-brin méiotiques chez Saccharomyces cerevisiae : rôle de la protéine kinase Tel1

inferred← citeshttps://doi.org/10.7554/elife.77956openalex-snapshot

Phosphoregulation of DSB-1 mediates control of meiotic double-strand break activity

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.