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Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.2011.743openalex-snapshot
Cancer Risks Associated With Germline Mutations in MLH1 , MSH2 , and MSH6 Genes in Lynch Syndrome
inferredcites →https://doi.org/10.1002/embj.201387330openalex-snapshot
Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesion
inferredcites →https://doi.org/10.1007/s00412-005-0346-4openalex-snapshot
Mei1 is epistatic to Dmc1 during mouse meiosis
inferredcites →https://doi.org/10.1007/s00412-008-0194-0openalex-snapshot
Protein SYCP2 provides a link between transverse filaments and lateral elements of mammalian synaptonemal complexes
inferredcites →https://doi.org/10.1007/s00412-015-0552-7openalex-snapshot
RPA homologs and ssDNA processing during meiotic recombination
inferredcites →https://doi.org/10.1007/s00412-017-0631-zopenalex-snapshot
The PRDM9 KRAB domain is required for meiosis and involved in protein interactions
inferredcites →https://doi.org/10.1007/s00412-020-00733-wopenalex-snapshot
Condensin I is required for faithful meiosis in Drosophila males
inferredcites →https://doi.org/10.1007/s00438-019-01594-4openalex-snapshot
Novel STAG3 mutations in a Caucasian family with primary ovarian insufficiency
inferredcites →https://doi.org/10.1007/s00439-020-02236-1openalex-snapshot
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia
inferredcites →https://doi.org/10.1016/j.ajhg.2008.12.002openalex-snapshot
Mutations of the SYCP3 Gene in Women with Recurrent Pregnancy Loss
inferredcites →https://doi.org/10.1016/j.ajhg.2014.11.002openalex-snapshot
MCM9 Mutations Are Associated with Ovarian Failure, Short Stature, and Chromosomal Instability
inferredcites →https://doi.org/10.1016/j.ajhg.2018.10.007openalex-snapshot
Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles
inferredcites →https://doi.org/10.1016/j.ajhg.2019.11.013openalex-snapshot
SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility
inferredcites →https://doi.org/10.1016/j.ajhg.2021.01.010openalex-snapshot
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans
inferredcites →https://doi.org/10.1016/j.ceb.2018.01.005openalex-snapshot
LINC complexes as regulators of meiosis
inferredcites →https://doi.org/10.1016/j.cell.2006.05.044openalex-snapshot
Crossover Homeostasis in Yeast Meiosis
inferredcites →https://doi.org/10.1016/j.cell.2007.05.035openalex-snapshot
BLM Ortholog, Sgs1, Prevents Aberrant Crossing-over by Suppressing Formation of Multichromatid Joint Molecules
inferredcites →https://doi.org/10.1016/j.cell.2008.04.047openalex-snapshot
Rapid Telomere Movement in Meiotic Prophase Is Promoted By NDJ1, MPS3, and CSM4 and Is Modulated by Recombination
inferredcites →https://doi.org/10.1016/j.cell.2009.07.035openalex-snapshot
Condensins Regulate Meiotic DNA Break Distribution, thus Crossover Frequency, by Controlling Chromosome Structure
inferredcites →https://doi.org/10.1016/j.cell.2013.11.040openalex-snapshot
Genome Analyses of Single Human Oocytes
inferredcites →https://doi.org/10.1016/j.cell.2015.10.030openalex-snapshot
MAJIN Links Telomeric DNA to the Nuclear Membrane by Exchanging Telomere Cap
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.cell.2017.02.002openalex-snapshot
Inefficient Crossover Maturation Underlies Elevated Aneuploidy in Human Female Meiosis
inferredcites →https://doi.org/10.1016/j.cell.2017.06.052openalex-snapshot
Multi-invasions Are Recombination Byproducts that Induce Chromosomal Rearrangements
inferredcites →https://doi.org/10.1016/j.cell.2019.02.021openalex-snapshot
Per-Nucleus Crossover Covariation and Implications for Evolution
inferredcites →https://doi.org/10.1016/j.cell.2021.02.036openalex-snapshot
Heritable human genome editing: Research progress, ethical considerations, and hurdles to clinical practice
inferredcites →https://doi.org/10.1016/j.celrep.2016.09.059openalex-snapshot
Cohesin Removal along the Chromosome Arms during the First Meiotic Division Depends on a NEK1-PP1γ-WAPL Axis in the Mouse
inferredcites →https://doi.org/10.1016/j.celrep.2019.05.096openalex-snapshot
HSF2BP Interacts with a Conserved Domain of BRCA2 and Is Required for Mouse Spermatogenesis
inferredcites →https://doi.org/10.1016/j.celrep.2020.107686openalex-snapshot
Meiosis-Specific C19orf57/4930432K21Rik/BRME1 Modulates Localization of RAD51 and DMC1 to DSBs in Mouse Meiotic Recombination
inferredcites →https://doi.org/10.1016/j.celrep.2020.108575openalex-snapshot
The Essential Function of SETDB1 in Homologous Chromosome Pairing and Synapsis during Meiosis
inferredcites →https://doi.org/10.1016/j.cub.2010.11.010openalex-snapshot
Evidence that Meiotic Sex Chromosome Inactivation Is Essential for Male Fertility
inferredcites →https://doi.org/10.1016/j.cub.2017.12.020openalex-snapshot
SMC1α Substitutes for Many Meiotic Functions of SMC1β but Cannot Protect Telomeres from Damage
inferredcites →https://doi.org/10.1016/j.cub.2019.02.007openalex-snapshot
Prdm9 and Meiotic Cohesin Proteins Cooperatively Promote DNA Double-Strand Break Formation in Mammalian Spermatocytes
inferredcites →https://doi.org/10.1016/j.cub.2019.11.064openalex-snapshot
The Initiation of Meiotic Sex Chromosome Inactivation Sequesters DNA Damage Signaling from Autosomes in Mouse Spermatogenesis
inferredcites →https://doi.org/10.1016/j.devcel.2005.03.018openalex-snapshot
Absence of Mouse REC8 Cohesin Promotes Synapsis of Sister Chromatids in Meiosis
inferredcites →https://doi.org/10.1016/j.devcel.2007.03.018openalex-snapshot
SUN1 Is Required for Telomere Attachment to Nuclear Envelope and Gametogenesis in Mice
inferredcites →https://doi.org/10.1016/j.devcel.2015.01.014openalex-snapshot
SCML2 Establishes the Male Germline Epigenome through Regulation of Histone H2A Ubiquitination
inferredcites →https://doi.org/10.1016/j.devcel.2018.10.004openalex-snapshot
SETDB1 Links the Meiotic DNA Damage Response to Sex Chromosome Silencing in Mice
inferredcites →https://doi.org/10.1016/j.devcel.2020.01.010openalex-snapshot
MEIOSIN Directs the Switch from Mitosis to Meiosis in Mammalian Germ Cells
inferredcites →https://doi.org/10.1016/j.ebiom.2019.03.075openalex-snapshot
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks
inferredcites →https://doi.org/10.1016/j.fertnstert.2013.07.1995openalex-snapshot
rs189037, a functional variant in ATM gene promoter, is associated with idiopathic nonobstructive azoospermia
inferredcites →https://doi.org/10.1016/j.gde.2012.12.002openalex-snapshot
Programmed induction of DNA double strand breaks during meiosis: setting up communication between DNA and the chromosome structure
inferredcites →https://doi.org/10.1016/j.jbc.2021.101231openalex-snapshot
Loss of TDP-43 in male germ cells causes meiotic failure and impairs fertility in mice
inferredcites →https://doi.org/10.1016/j.molcel.2005.09.021openalex-snapshot
Crossover and Noncrossover Pathways in Mouse Meiosis
inferredcites →https://doi.org/10.1016/j.molcel.2012.05.048openalex-snapshot
MCM8- and MCM9-Deficient Mice Reveal Gametogenesis Defects and Genome Instability Due to Impaired Homologous Recombination
inferredcites →https://doi.org/10.1016/j.molcel.2017.07.027openalex-snapshot
The DNA Damage Checkpoint Eliminates Mouse Oocytes with Chromosome Synapsis Failure
inferredcites →https://doi.org/10.1016/j.molcel.2018.06.035openalex-snapshot
Pericentromere-Specific Cohesin Complex Prevents Meiotic Pericentric DNA Double-Strand Breaks and Lethal Crossovers
inferredcites →https://doi.org/10.1016/j.molcel.2019.03.022openalex-snapshot
Mouse ANKRD31 Regulates Spatiotemporal Patterning of Meiotic Recombination Initiation and Ensures Recombination between X and Y Sex Chromosomes
inferredcites →https://doi.org/10.1016/j.molcel.2019.03.023openalex-snapshot
REC114 Partner ANKRD31 Controls Number, Timing, and Location of Meiotic DNA Breaks
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.molcel.2020.06.015openalex-snapshot
The Configuration of RPA, RAD51, and DMC1 Binding in Meiosis Reveals the Nature of Critical Recombination Intermediates
inferredcites →https://doi.org/10.1016/j.molmed.2020.11.003openalex-snapshot
Fertility Preservation: The Challenge of Freezing and Transplanting Ovarian Tissue
inferredcites →https://doi.org/10.1016/j.scib.2020.08.026openalex-snapshot
A TOP6BL mutation abolishes meiotic DNA double-strand break formation and causes human infertility
inferredcites →https://doi.org/10.1016/j.tcb.2011.03.004openalex-snapshot
Checkpoint mechanisms: the puppet masters of meiotic prophase
inferredcites →https://doi.org/10.1016/j.tcb.2016.09.002openalex-snapshot
Mechanisms of Aneuploidy in Human Eggs
inferredcites →https://doi.org/10.1016/j.tcb.2020.12.004openalex-snapshot
Phase Separation during Germline Development
inferredcites →https://doi.org/10.1016/j.tig.2017.12.017openalex-snapshot
PRDM9 and Its Role in Genetic Recombination
inferredcites →https://doi.org/10.1016/j.tig.2020.02.002openalex-snapshot
New Solutions to Old Problems: Molecular Mechanisms of Meiotic Crossover Control
inferredcites →https://doi.org/10.1016/j.tig.2020.06.008openalex-snapshot
Meiotic Executioner Genes Protect the Y from Extinction
inferredcites →https://doi.org/10.1016/j.urology.2010.10.001openalex-snapshot
Role of Genetics in Azoospermia
inferredcites →https://doi.org/10.1016/j.ydbio.2011.01.028openalex-snapshot
Cul4A is essential for spermatogenesis and male fertility
inferredcites →https://doi.org/10.1016/s0140-6736(03)14845-3openalex-snapshot
Azoospermia in patients heterozygous for a mutation in SYCP3
inferredcites →https://doi.org/10.1016/s1097-2765(00)00097-6openalex-snapshot
The Mouse Spo11 Gene Is Required for Meiotic Chromosome Synapsis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80069-6openalex-snapshot
Meiotic Prophase Arrest with Failure of Chromosome Synapsis in Mice Deficient for Dmc1 , a Germline-Specific RecA Homolog
inferredcites →https://doi.org/10.1016/s1097-2765(00)80070-2openalex-snapshot
The Mouse RecA-like Gene Dmc1 Is Required for Homologous Chromosome Synapsis during Meiosis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80404-9openalex-snapshot
The Murine SCP3 Gene Is Required for Synaptonemal Complex Assembly, Chromosome Synapsis, and Male Fertility
inferredcites →https://doi.org/10.1016/s2213-8587(16)30040-7openalex-snapshot
Novel concepts in the aetiology of male reproductive impairment
inferredcites →https://doi.org/10.1038/43932openalex-snapshot
Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination
inferredcites →https://doi.org/10.1038/celldisc.2015.25openalex-snapshot
Senataxin controls meiotic silencing through ATR activation and chromatin remodeling
inferredcites →https://doi.org/10.1038/d41586-021-01710-8openalex-snapshot
Genomic analysis identifies variants that can predict the timing of menopause
inferredcites →https://doi.org/10.1038/ejhg.2015.107openalex-snapshot
STAG3 truncating variant as the cause of primary ovarian insufficiency
inferredcites →https://doi.org/10.1038/emboj.2011.222openalex-snapshot
The cohesin subunit RAD21L functions in meiotic synapsis and exhibits sexual dimorphism in fertility
inferredcites →https://doi.org/10.1038/gim.2016.225openalex-snapshot
A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes
inferredcites →https://doi.org/10.1038/gim.2018.10openalex-snapshot
Point-of-care whole-exome sequencing of idiopathic male infertility
inferredcites →https://doi.org/10.1038/nature10331openalex-snapshot
Protection of repetitive DNA borders from self-induced meiotic instability
inferredcites →https://doi.org/10.1038/nature10508openalex-snapshot
ATM controls meiotic double-strand-break formation
inferredcites →https://doi.org/10.1038/ncb1135openalex-snapshot
Cohesin SMC1β is required for meiotic chromosome dynamics, sister chromatid cohesion and DNA recombination
inferredcites →https://doi.org/10.1038/ncb2896openalex-snapshot
The TRF1-binding protein TERB1 promotes chromosome movement and telomere rigidity in meiosis
inferredcites →https://doi.org/10.1038/ncb3417openalex-snapshot
Meiotic DNA break formation requires the unsynapsed chromosome axis-binding protein IHO1 (CCDC36) in mice
inferredcites →https://doi.org/10.1038/ncomms13298openalex-snapshot
C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
inferredcites →https://doi.org/10.1038/ncomms3788openalex-snapshot
MEIOB exhibits single-stranded DNA-binding and exonuclease activities and is essential for meiotic recombination
inferredcites →https://doi.org/10.1038/ng.2541openalex-snapshot
RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosis
inferredcites →https://doi.org/10.1038/ng.2858openalex-snapshot
Antagonistic roles of ubiquitin ligase HEI10 and SUMO ligase RNF212 regulate meiotic recombination
inferredcites →https://doi.org/10.1038/ng0796-336openalex-snapshot
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
inferredcites →https://doi.org/10.1038/ng1484openalex-snapshot
Silencing of unsynapsed meiotic chromosomes in the mouse
inferredcites →https://doi.org/10.1038/ng931openalex-snapshot
Meiotic arrest and aneuploidy in MLH3-deficient mice
inferredcites →https://doi.org/10.1038/nrg2505openalex-snapshot
The consequences of asynapsis for mammalian meiosis
inferredcites →https://doi.org/10.1038/nrm.2016.177openalex-snapshot
Control of structure-specific endonucleases to maintain genome stability
inferredcites →https://doi.org/10.1038/nrm2849openalex-snapshot
Genome destabilization by homologous recombination in the germ line
inferredcites →https://doi.org/10.1038/s41388-020-01542-2openalex-snapshot
Germline variants of DNA repair genes in early onset mantle cell lymphoma
inferredcites →https://doi.org/10.1038/s41392-021-00710-4openalex-snapshot
Mutations of MSH5 in nonobstructive azoospermia (NOA) and rescued via in vivo gene editing
inferredcites →https://doi.org/10.1038/s41418-020-0493-4openalex-snapshot
NBS1 is required for SPO11-linked DNA double-strand break repair in male meiosis
inferredcites →https://doi.org/10.1038/s41419-019-1720-0openalex-snapshot
BRCA2 deficiency is a potential driver for human primary ovarian insufficiency
inferredcites →https://doi.org/10.1038/s41436-020-0907-1openalex-snapshot
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men
inferredcites →https://doi.org/10.1038/s41436-020-0916-0openalex-snapshot
A genomics approach to male infertility
inferredcites →https://doi.org/10.1038/s41467-018-06384-xopenalex-snapshot
Shu complex SWS1-SWSAP1 promotes early steps in mouse meiotic recombination
inferredcites →https://doi.org/10.1038/s41467-019-08437-1openalex-snapshot
The meiotic TERB1-TERB2-MAJIN complex tethers telomeres to the nuclear envelope
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/s41467-020-15954-xopenalex-snapshot
The BRCA2-MEILB2-BRME1 complex governs meiotic recombination and impairs the mitotic BRCA2-RAD51 function in cancer cells
inferredcites →https://doi.org/10.1038/s41467-020-16885-3openalex-snapshot
Proline-rich protein PRR19 functions with cyclin-like CNTD1 to promote meiotic crossing over in mouse
inferredcites →https://doi.org/10.1038/s41467-021-23550-wopenalex-snapshot
The SUN1-SPDYA interaction plays an essential role in meiosis prophase I
inferredcites →https://doi.org/10.1038/s41467-022-28208-9openalex-snapshot
The toposiomerase IIIalpha-RMI1-RMI2 complex orients human Bloom’s syndrome helicase for efficient disruption of D-loops
inferredcites →https://doi.org/10.1038/s41585-018-0003-3openalex-snapshot
Genetics of male infertility
inferredcites →https://doi.org/10.1038/s41586-018-0492-5openalex-snapshot
Extensive sex differences at the initiation of genetic recombination
inferredcites →https://doi.org/10.1038/s41586-020-2327-4openalex-snapshot
Ensuring meiotic DNA break formation in the mouse pseudoautosomal region
inferredcites →https://doi.org/10.1038/s41586-020-2592-2openalex-snapshot
Regulation of the MLH1–MLH3 endonuclease in meiosis
inferredcites →https://doi.org/10.1038/s41586-020-2645-6openalex-snapshot
PCNA activates the MutLγ endonuclease to promote meiotic crossing over
inferredcites →https://doi.org/10.1038/s41586-021-03779-7openalex-snapshot
Genetic insights into biological mechanisms governing human ovarian ageing
inferredcites →https://doi.org/10.1038/s41594-018-0078-9openalex-snapshot
Structural basis of meiotic chromosome synapsis through SYCP1 self-assembly
inferredcites →https://doi.org/10.1038/s41594-021-00636-zopenalex-snapshot
Structural basis of meiotic chromosome synaptic elongation through hierarchical fibrous assembly of SYCE2-TEX12
inferredcites →https://doi.org/10.1056/nejmc1310150openalex-snapshot
Mutations in HFM1 in Recessive Primary Ovarian Insufficiency
inferredcites →https://doi.org/10.1056/nejmoa1309635openalex-snapshot
Mutant Cohesin in Premature Ovarian Failure
inferredcites →https://doi.org/10.1056/nejmoa1406192openalex-snapshot
X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men
inferredcites →https://doi.org/10.1056/nejmoa1800024openalex-snapshot
Essential Role of BRCA2 in Ovarian Development and Function
inferredcites →https://doi.org/10.1073/pnas.1601691113openalex-snapshot
BRCA2 regulates DMC1-mediated recombination through the BRC repeats
inferredcites →https://doi.org/10.1073/pnas.1712530114openalex-snapshot
DNA damage response protein TOPBP1 regulates X chromosome silencing in the mammalian germ line
inferredcites →https://doi.org/10.1073/pnas.1902440116openalex-snapshot
Molecular organization of mammalian meiotic chromosome axis revealed by expansion STORM microscopy
inferredcites →https://doi.org/10.1073/pnas.1914963117openalex-snapshot
Autologous transplantation of spermatogonial stem cells restores fertility in congenitally infertile mice
inferredcites →https://doi.org/10.1073/pnas.2004832117openalex-snapshot
Frequent loss of heterozygosity in CRISPR-Cas9–edited early human embryos
inferredcites →https://doi.org/10.1073/pnas.2025421118openalex-snapshot
The male germline-specific protein MAPS is indispensable for pachynema progression and fertility
inferredcites →https://doi.org/10.1073/pnas.2432067100openalex-snapshot
Positional cloning and characterization of Mei1 , a vertebrate-specific gene required for normal meiotic chromosome synapsis in mice
inferredcites →https://doi.org/10.1083/jcb.200603063openalex-snapshot
Mouse SYCP2 is required for synaptonemal complex assembly and chromosomal synapsis during male meiosis
inferredcites →https://doi.org/10.1083/jcb.200610027openalex-snapshot
SYCE2 is required for synaptonemal complex assembly, double strand break repair, and homologous recombination
inferredcites →https://doi.org/10.1083/jcb.200709057openalex-snapshot
Mouse TEX15 is essential for DNA double-strand break repair and chromosomal synapsis during male meiosis
inferredcites →https://doi.org/10.1083/jcb.200909048openalex-snapshot
Mammalian BLM helicase is critical for integrating multiple pathways of meiotic recombination
inferredcites →https://doi.org/10.1083/jcb.201008005openalex-snapshot
RAD21L, a novel cohesin subunit implicated in linking homologous chromosomes in mammalian meiosis
inferredcites →https://doi.org/10.1083/jcb.201304004openalex-snapshot
A mammalian KASH domain protein coupling meiotic chromosomes to the cytoskeleton
inferredcites →https://doi.org/10.1083/jcb.201311050openalex-snapshot
BRCA1 establishes DNA damage signaling and pericentric heterochromatin of the X chromosome in male meiosis
inferredcites →https://doi.org/10.1083/jcb.201401122openalex-snapshot
Mammalian CNTD1 is critical for meiotic crossover maturation and deselection of excess precrossover sites
inferredcites →https://doi.org/10.1089/dna.2015.3022openalex-snapshot
Gen1 and Eme1 Play Redundant Roles in DNA Repair and Meiotic Recombination in Mice
inferredcites →https://doi.org/10.1091/mbc.e16-09-0686openalex-snapshot
PRDM9 interactions with other proteins provide a link between recombination hotspots and the chromosomal axis in meiosis
inferredcites →https://doi.org/10.1091/mbc.e20-09-0604openalex-snapshot
EWSR1 affects PRDM9-dependent histone 3 methylation and provides a link between recombination hotspots and the chromosome axis protein REC8
inferredcites →https://doi.org/10.1093/emboj/19.24.6675openalex-snapshot
Xrcc2 is required for genetic stability, embryonic neurogenesis and viability in mice
inferredcites →https://doi.org/10.1093/hmg/ddu051openalex-snapshot
STAG3 is a strong candidate gene for male infertility
inferredcites →https://doi.org/10.1093/hmg/ddv290openalex-snapshot
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family
inferredcites →https://doi.org/10.1093/hmg/ddx044openalex-snapshot
Mutations in MSH5 in primary ovarian insufficiency
inferredcites →https://doi.org/10.1093/hmg/ddx199openalex-snapshot
A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency
inferredcites →https://doi.org/10.1093/humrep/deaa212openalex-snapshot
Should germline genome editing be allowed? The effect of treatment characteristics on public acceptability
inferredcites →https://doi.org/10.1093/humrep/deaa362openalex-snapshot
Rare missense variant inMSH4associated with primary gonadal failure in both 46, XX and 46, XY individuals
inferredcites →https://doi.org/10.1093/humrep/deab046openalex-snapshot
A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination
inferredcites →https://doi.org/10.1093/humrep/deab118openalex-snapshot
Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure
inferredcites →https://doi.org/10.1093/humrep/deab185openalex-snapshot
Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB
inferredcites →https://doi.org/10.1093/humrep/deab230openalex-snapshot
Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes
inferredcites →https://doi.org/10.1093/humrep/dey073openalex-snapshot
A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family
inferredcites →https://doi.org/10.1093/humrep/dez016openalex-snapshot
A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest
inferredcites →https://doi.org/10.1093/humrep/dez042openalex-snapshot
Sequencing of a ‘mouse azoospermia’ gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest
inferredcites →https://doi.org/10.1093/humrep/dez204openalex-snapshot
Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest
inferredcites →https://doi.org/10.1093/humupd/dmaa034openalex-snapshot
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice
inferredcites →https://doi.org/10.1093/humupd/dmab030openalex-snapshot
A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene–disease relationships
inferredcites →https://doi.org/10.1093/humupd/dmz028openalex-snapshot
Sperm recovery and ICSI outcomes in men with non-obstructive azoospermia: a systematic review and meta-analysis
inferredcites →https://doi.org/10.1093/humupd/dmz043openalex-snapshot
BRCA-related ATM-mediated DNA double-strand break repair and ovarian aging
inferredcites →https://doi.org/10.1093/molehr/gaaa032openalex-snapshot
Familial primary ovarian insufficiency associated with an SYCE1 point mutation: defective meiosis elucidated in humanized mice
inferredcites →https://doi.org/10.1093/molehr/gaaa050openalex-snapshot
STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermia
inferredcites →https://doi.org/10.1093/nar/gkaa1016openalex-snapshot
The ssDNA-binding protein MEIOB acts as a dosage-sensitive regulator of meiotic recombination
inferredcites →https://doi.org/10.1093/nar/gkab082openalex-snapshot
Four-pronged negative feedback of DSB machinery in meiotic DNA-break control in mice
inferredcites →https://doi.org/10.1093/nar/gkab722openalex-snapshot
ESA1 regulates meiotic chromosome axis and crossover frequency via acetylating histone H4
inferredcites →https://doi.org/10.1093/nar/gkz226openalex-snapshot
SCRE serves as a unique synaptonemal complex fastener and is essential for progression of meiosis prophase I in mice
inferredcites →https://doi.org/10.1093/nar/gkz992openalex-snapshot
FBXO47 regulates telomere-inner nuclear envelope integration by stabilizing TRF2 during meiosis
inferredcites →https://doi.org/10.1095/biolreprod.111.095752openalex-snapshot
Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells1
inferredcites →https://doi.org/10.1096/fj.202100756ropenalex-snapshot
A kaleidoscopic view of ovarian genes associated with premature ovarian insufficiency and senescence
inferredcites →https://doi.org/10.1097/00006254-198742030-00020openalex-snapshot
Incidence of Premature Ovarian Failure
inferredcites →https://doi.org/10.1101/cshperspect.a016410openalex-snapshot
An Overview of the Molecular Mechanisms of Recombinational DNA Repair
inferredcites →https://doi.org/10.1101/cshperspect.a016444openalex-snapshot
DNA-Pairing and Annealing Processes in Homologous Recombination and Homology-Directed Repair
inferredcites →https://doi.org/10.1101/cshperspect.a016451openalex-snapshot
Mediators of Homologous DNA Pairing
inferredcites →https://doi.org/10.1101/cshperspect.a016618openalex-snapshot
Meiotic Recombination: The Essence of Heredity
inferredcites →https://doi.org/10.1101/cshperspect.a016659openalex-snapshot
DNA Strand Exchange and RecA Homologs in Meiosis
inferredcites →https://doi.org/10.1101/cshperspect.a016675openalex-snapshot
The Meiotic Checkpoint Network: Step-by-Step through Meiotic Prophase
inferredcites →https://doi.org/10.1101/gad.13.5.523openalex-snapshot
Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis
inferredcites →https://doi.org/10.1101/gad.14.9.1085openalex-snapshot
MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice
inferredcites →https://doi.org/10.1101/gad.1613608openalex-snapshot
Meiotic failure in male mice lacking an X-linked factor
inferredcites →https://doi.org/10.1101/gad.187559.112openalex-snapshot
Meiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanisms
inferredcites →https://doi.org/10.1101/gad.2030811openalex-snapshot
MDC1 directs chromosome-wide silencing of the sex chromosomes in male germ cells
inferredcites →https://doi.org/10.1101/gad.219477.113openalex-snapshot
ATR acts stage specifically to regulate multiple aspects of mammalian meiotic silencing
inferredcites →https://doi.org/10.1101/gad.333542.119openalex-snapshot
HELLS and PRDM9 form a pioneer complex to open chromatin at meiotic recombination hot spots
inferredcites →https://doi.org/10.1101/gad.475308openalex-snapshot
Shugoshin-2 is essential for the completion of meiosis but not for mitotic cell division in mice
inferredcites →https://doi.org/10.1101/gad.571710openalex-snapshot
Functional conservation of Mei4 for meiotic DNA double-strand break formation from yeasts to mice
inferredcites →https://doi.org/10.1111/cge.13034openalex-snapshot
Whole‐exome sequencing identifies a homozygous donor splice‐site mutation in STAG3 that causes primary ovarian insufficiency
inferredcites →https://doi.org/10.1111/cge.13475openalex-snapshot
XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans
inferredcites →https://doi.org/10.1111/gtc.12652openalex-snapshot
The cohesin complex in mammalian meiosis
inferredcites →https://doi.org/10.1111/jcmm.17180openalex-snapshot
Novel exon mutation in SYCE1 gene is associated with non‐obstructive azoospermia
inferredcites →https://doi.org/10.1126/sciadv.aau9780openalex-snapshot
SPO16 binds SHOC1 to promote homologous recombination and crossing-over in meiotic prophase I
inferredcites →https://doi.org/10.1126/sciadv.aax1101openalex-snapshot
The histone modification reader ZCWPW1 is required for meiosis prophase I in male but not in female mice
inferredcites →https://doi.org/10.1126/sciadv.aaz2129openalex-snapshot
SKP1 drives the prophase I to metaphase I transition during male meiosis
inferredcites →https://doi.org/10.1126/sciadv.abb1660openalex-snapshot
Meiotic chromosome synapsis depends on multivalent SYCE1-SIX6OS1 interactions that are disrupted in cases of human infertility
inferredcites →https://doi.org/10.1126/sciadv.abi8683openalex-snapshot
Imaging and tracing the pattern of adult ovarian angiogenesis implies a strategy against female reproductive aging
inferredcites →https://doi.org/10.1126/sciadv.abk1789openalex-snapshot
RAD51AP2 is required for efficient meiotic recombination between X and Y chromosomes
inferredcites →https://doi.org/10.1126/science.1070594openalex-snapshot
Female Germ Cell Aneuploidy and Embryo Death in Mice Lacking the Meiosis-Specific Protein SCP3
inferredcites →https://doi.org/10.1126/science.1083022openalex-snapshot
Essential Role of Fkbp6 in Male Fertility and Homologous Chromosome Pairing in Meiosis
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.1195774openalex-snapshot
Distinct Properties of the XY Pseudoautosomal Region Crucial for Male Meiosis
inferredcites →https://doi.org/10.1126/science.aad5309openalex-snapshot
The TopoVIB-Like protein family is required for meiotic DNA double-strand break formation
inferredcites →https://doi.org/10.1126/science.aaf6407openalex-snapshot
A SUMO-ubiquitin relay recruits proteasomes to chromosome axes to regulate meiotic recombination
inferredcites →https://doi.org/10.1136/jmedgenet-2017-104992openalex-snapshot
DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing
inferredcites →https://doi.org/10.1136/jmedgenet-2017-105145openalex-snapshot
XRCC2 mutation causes meiotic arrest, azoospermia and infertility
inferredcites →https://doi.org/10.1136/jmedgenet-2020-107042openalex-snapshot
Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia
inferredcites →https://doi.org/10.1146/annurev-biochem-011520-104722openalex-snapshot
Checkpoint Responses to DNA Double-Strand Breaks
inferredcites →https://doi.org/10.1146/annurev-biochem-062917-012415openalex-snapshot
The MRE11–RAD50–NBS1 Complex Conducts the Orchestration of Damage Signaling and Outcomes to Stress in DNA Replication and Repair
showing the first 200 of 268 · page through all 268
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4741234openalex-extracted
A New Heterozygous Deletion Mutation of the Sycp2 Gene Caused Male Infertility Due to Non-Obstructive Azoospermia
inferred← citeshttps://doi.org/10.1002/2211-5463.13810openalex-snapshot
HELQ deficiency impairs the induction of primordial germ cell‐like cells
inferred← citeshttps://doi.org/10.1002/advs.202402412openalex-snapshot
HSF5 Deficiency Causes Male Infertility Involving Spermatogenic Arrest at Meiotic Prophase I in Humans and Mice
inferred← citeshttps://doi.org/10.1002/advs.202406332openalex-snapshot
METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis
inferred← citeshttps://doi.org/10.1002/advs.202412196openalex-snapshot
hnRNPC Functions with HuR to Regulate Alternative Splicing in an m6A‐Dependent Manner and is Essential for Meiosis
inferred← citeshttps://doi.org/10.1002/advs.202506600openalex-snapshot
m 6 A Reader hnRNPA2B1 Modulates Late Pachytene Progression in Male Meiosis Through Post‐Transcriptional Control
inferred← citeshttps://doi.org/10.1002/jat.70434openalex-snapshot
Microplastics and Nanoplastics and Their Effects on Reproductive Health: Potential Risks and Mechanisms
inferred← citeshttps://doi.org/10.1002/mgg3.2402openalex-snapshot
A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage
inferred← citeshttps://doi.org/10.1002/mrd.70061openalex-snapshot
Effects of Aging on Mammalian Spermatogenesis From a Cellular Perspective
inferred← citeshttps://doi.org/10.1007/s00018-024-05479-7openalex-snapshot
BCAS2 and hnRNPH1 orchestrate alternative splicing for DNA double-strand break repair and synapsis in meiotic prophase I
inferred← citeshttps://doi.org/10.1007/s00438-024-02113-wopenalex-snapshot
Novel MEI1 mutations cause chromosomal and DNA methylation abnormalities leading to embryonic arrest and implantation failure
inferred← citeshttps://doi.org/10.1007/s00439-022-02515-zopenalex-snapshot
Loss of SUN1 function in spermatocytes disrupts the attachment of telomeres to the nuclear envelope and contributes to non-obstructive azoospermia in humans
inferred← citeshttps://doi.org/10.1007/s10495-026-02354-7openalex-snapshot
The IAP family member BRUCE/BIRC6: an emerging new player in balancing life and death
inferred← citeshttps://doi.org/10.1007/s10815-023-02825-9openalex-snapshot
Identification of novel candidate genes associated with meiotic aneuploidy in human embryos by whole-exome sequencing
inferred← citeshttps://doi.org/10.1007/s10815-025-03443-3openalex-snapshot
A novel homozygous frameshift mutation in MCM8 causes primary gonadal dysgenesis in both genders
inferred← citeshttps://doi.org/10.1007/s10815-025-03559-6openalex-snapshot
Autophagy-related biomarkers in non-obstructive azoospermia: insights from transcriptomics and single-cell sequencing
inferred← citeshttps://doi.org/10.1007/s10815-025-03711-2openalex-snapshot
The role of resveratrol in male spermatogenesis: mechanisms and latest advances in clinical applications
inferred← citeshttps://doi.org/10.1007/s10815-026-03807-3openalex-snapshot
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics
inferred← citeshttps://doi.org/10.1007/s11154-022-09783-0openalex-snapshot
An update on the role and potential mechanisms of clock genes regulating spermatogenesis: A systematic review of human and animal experimental studies
inferred← citeshttps://doi.org/10.1016/j.ebiom.2025.105718openalex-snapshot
CKAP5 deficiency induces premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115503openalex-snapshot
Low dose PFDA induces DNA damage and DNA repair inhibition by promoting nuclear cGAS accumulation in ovarian epithelial cells
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.117478openalex-snapshot
Gestational exposure to arsenic reduces female offspring fertility by impairing the repair of DNA double-strand breaks and synapsis formation in oocytes
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.117980openalex-snapshot
Gestational exposure to PNMC reduces offspring gamete numbers by disrupting oocyte meiosis and spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.126200openalex-snapshot
Effects of polystyrene microparticles exposures on spermatogenic cell differentiation and reproductive endpoints in male mice
inferred← citeshttps://doi.org/10.1016/j.fct.2026.116168openalex-snapshot
Maternal PFBS exposure disrupts oocyte meiotic prophase I and reduces primordial follicle pool
inferred← citeshttps://doi.org/10.1016/j.gendis.2025.101868openalex-snapshot
HSF5: A novel switch for meiotic pachynema progression in male germ cells
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.150796openalex-snapshot
The Poly(rC) binding protein 2 is required for spermatogenesis by regulating alternative splicing and mRNA stability
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112878openalex-snapshot
UBE2J2 is essential for the progression of meiosis prophase I during spermatogenesis in mice
inferred← citeshttps://doi.org/10.1016/j.jare.2024.08.011openalex-snapshot
An essential role of the E3 ubiquitin ligase RNF126 in ensuring meiosis I completion during spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.jare.2026.02.047openalex-snapshot
Heterogeneous nuclear ribonucleoprotein L orchestrates alternative splicing critical for primordial follicle formation
inferred← citeshttps://doi.org/10.1016/j.jgg.2023.05.008openalex-snapshot
Homozygous nonsense variants of KCTD19 cause male infertility in humans and mice
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.12.005openalex-snapshot
MEI4 variations drive female reproductive disorders via impaired oocyte abundance and developmental potential
inferred← citeshttps://doi.org/10.1016/j.maturitas.2026.109034openalex-snapshot
MSH4 and MSH5 variants in premature ovarian insufficiency: A literature review and case study
inferred← citeshttps://doi.org/10.1016/j.purol.2023.09.027openalex-snapshot
Évaluation de l’homme du couple infertile
inferred← citeshttps://doi.org/10.1016/j.scib.2023.04.030openalex-snapshot
SRSF1 is crucial for male meiosis through alternative splicing during homologous pairing and synapsis in mice
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.08.016openalex-snapshot
DNA methylome of primary spermatocyte reveals epigenetic dysregulation associated with male sterility of cattleyak
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2025.117426openalex-snapshot
Germline-specific deletion of testis-highly expressed Lrwd1 reveals nonessential roles in male fertility
inferred← citeshttps://doi.org/10.1016/j.xhgg.2023.100256openalex-snapshot
Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192
inferred← citeshttps://doi.org/10.1038/s10038-025-01350-0openalex-snapshot
Bi-allelic KCTD19 variants associated with meiotic arrest and non-obstructive azoospermia in humans
inferred← citeshttps://doi.org/10.1038/s10038-025-01397-zopenalex-snapshot
A novel MCMDC2 variant causes meiotic arrest and non-obstructive azoospermia in a consanguineous Chinese family
inferred← citeshttps://doi.org/10.1038/s10038-026-01492-9openalex-snapshot
Novel variants in LINC and TTM complexes of meiotic chromosome dynamics are associated with meiotic arrest and non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1038/s41418-026-01768-9openalex-snapshot
LSM7 coordinates scaRNA-mediated snRNA modification to ensure spliceosome fidelity and spermatogonial stem cell differentiation
inferred← citeshttps://doi.org/10.1038/s41418-026-01872-wopenalex-snapshot
SMC1A is required for fate determinations of human spermatogonial stem cells and male fertility by interacting with YBX1 and stabilizing HMGA2 mRNA via an m5C modification
inferred← citeshttps://doi.org/10.1038/s41420-023-01433-xopenalex-snapshot
Age-related elevation of O-GlcNAc causes meiotic arrest in male mice
inferred← citeshttps://doi.org/10.1038/s41421-023-00580-wopenalex-snapshot
Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression
inferred← citeshttps://doi.org/10.1038/s41421-023-00638-9openalex-snapshot
Mapping crossover events of mouse meiotic recombination by restriction fragment ligation-based Refresh-seq
inferred← citeshttps://doi.org/10.1038/s41467-024-50930-9openalex-snapshot
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility
inferred← citeshttps://doi.org/10.1038/s42003-025-08426-9openalex-snapshot
Biallelic BRCA2 variants induce premature ovarian insufficiency by impaired meiotic homologous recombination
inferred← citeshttps://doi.org/10.1038/s44321-025-00244-0openalex-snapshot
Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes
inferred← citeshttps://doi.org/10.1080/15384101.2023.2171544openalex-snapshot
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1080/19491034.2024.2328719openalex-snapshot
Heterochromatin in plant meiosis
inferred← citeshttps://doi.org/10.1093/biolre/ioad008openalex-snapshot
Sohlh1loss of function male and female infertility model impacts overall health beyond gonadal dysfunction in mice
inferred← citeshttps://doi.org/10.1093/biolre/ioaf258openalex-snapshot
Mutations of SOX30 are identified in azoospermic human patients and reduce sperm in mice
inferred← citeshttps://doi.org/10.1093/hropen/hoag039openalex-snapshot
Meiotic gene variants contribute to recurrent blastulation failure
inferred← citeshttps://doi.org/10.1093/humrep/dead095openalex-snapshot
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia
inferred← citeshttps://doi.org/10.1093/humrep/deag086openalex-snapshot
Novel variants in YTHDC2 cause non-obstructive azoospermia by disrupting the mitotic-to-meiotic transition in humans and mice
inferred← citeshttps://doi.org/10.1093/humupd/dmaf002openalex-snapshot
Harnessing omics data for drug discovery and development in ovarian aging
inferred← citeshttps://doi.org/10.1093/humupd/dmag012openalex-snapshot
Maternal genetic variants associated with aneuploid conception: a narrative review
inferred← citeshttps://doi.org/10.1093/molehr/gaae002openalex-snapshot
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia
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/10.1093/procel/pwag033openalex-snapshot
Epigenetic dynamics of human spermatogenesis and their dysregulation in non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1093/qjmed/hcae034openalex-snapshot
Function and mechanism of lysine crotonylation in health and disease
inferred← citeshttps://doi.org/10.1096/fj.202403260ropenalex-snapshot
HELQ Maintains Genome Stability of Primordial Germ Cells by Inhibiting LINE ‐1 Expression
inferred← citeshttps://doi.org/10.1096/fj.202600580rropenalex-snapshot
Smek1 ‐Dependent Transcriptional Repression of Usp10 Is Essential for the Progression of Murine Spermatogenesis
inferred← citeshttps://doi.org/10.1097/cu9.0000000000000372openalex-snapshot
Chinese expert consensus on the classification for diagnosis and management of spermatogenic dysfunction
inferred← citeshttps://doi.org/10.1101/2023.07.22.23292907openalex-snapshot
Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192
inferred← citeshttps://doi.org/10.1101/2024.03.20.24304490openalex-snapshot
Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes
inferred← citeshttps://doi.org/10.1111/andr.13474openalex-snapshot
A novel SNP in HUWE1 promoter confers increased risk of NOA by affecting the RA/RARα pathway in Chinese individuals
inferred← citeshttps://doi.org/10.1111/andr.70270openalex-snapshot
Biallelic Variants of CHTF18 Are Associated With Male Infertility With Cryptozoospermia in Humans
inferred← citeshttps://doi.org/10.1111/cge.14392openalex-snapshot
A homozygous frameshift variant in SYCP2 caused meiotic arrest and non‐obstructive azoospermia
inferred← citeshttps://doi.org/10.1111/cge.70106openalex-snapshot
Identification of a Homozygous Nonsense Variant in KCTD19 Causing Meiotic Arrest and Non‐Obstructive Azoospermia in Humans
inferred← citeshttps://doi.org/10.1111/cpr.70079openalex-snapshot
YKT6 Is Essential for Male Fertility by Promoting Meiosis Progression During Spermatogenesis of Mice
inferred← citeshttps://doi.org/10.1134/s1022795425701704openalex-snapshot
Genetic Mechanisms of Premature Ovarian Insufficiency
inferred← citeshttps://doi.org/10.1177/15579883261468072openalex-snapshot
Integrated Ultrasound Localization Microscopy and Multi-Omics for Mechanism-Driven Stratification of Azoospermia
inferred← citeshttps://doi.org/10.1186/s12864-025-11431-1openalex-snapshot
Comparatively profiling the transcriptome of human, Porcine and mouse oocytes undergoing meiotic maturation
inferred← citeshttps://doi.org/10.1186/s12864-026-12649-3openalex-snapshot
The transcription factor E4F1 is crucial for spermatogonial differentiation and meiosis progression in mice
inferred← citeshttps://doi.org/10.1186/s12943-024-02187-5openalex-snapshot
Unveiling the mysteries of extrachromosomal circular DNA: from generation to clinical relevance in human cancers and health
inferred← citeshttps://doi.org/10.1186/s12958-025-01493-xopenalex-snapshot
The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study
inferred← citeshttps://doi.org/10.1186/s12958-026-01524-1openalex-snapshot
Mechanism and potential therapeutic strategies of genetic abnormalities involved in deoxyribonucleic acid double-strand breaks leading to the development of human non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1186/s12964-026-02817-zopenalex-snapshot
Orchestrating homolog segregation in meiosis I: molecular logic and regulatory networks with emphasis on male metaphase I
inferred← citeshttps://doi.org/10.1186/s13048-023-01221-2openalex-snapshot
DNA double-strand break genetic variants in patients with premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1360/tb-2023-0549openalex-snapshot
Regulatory functions of alternative splicing in homologous chromosome pairing and synapsis in male germ cells
inferred← citeshttps://doi.org/10.1360/tb-2024-1401openalex-snapshot
Physiological and pathological mechanisms of human oocyte development
inferred← citeshttps://doi.org/10.1371/journal.pone.0324948openalex-snapshot
Analysis of the inflammatory gene expression characteristics and immune microenvironment regulatory mechanisms in the testicular tissue of patients with non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1515/medgen-2024-2040openalex-snapshot
Genetics of female and male infertility
inferred← citeshttps://doi.org/10.21037/tau-23-485openalex-snapshot
Clinical management, differential diagnosis, follow-up and biomarkers of infertile men with nonobstructive azoospermia
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10361087/v1openalex-snapshot
A mechanistic framework for interspecific variation in vertebrate developmental radiosensitivity under chronic ionizing radiation
inferred← citeshttps://doi.org/10.3389/fendo.2026.1916743openalex-snapshot
A homozygous SPDYA variant associated with meiotic arrest and failed microdissection testicular sperm extraction in non-obstructive azoospermia
inferred← citeshttps://doi.org/10.3390/medicina61101864openalex-snapshot
Chromosomal Roadblocks in Male Fertility: Mechanisms, Risk Factors and Syndromes
inferred← citeshttps://doi.org/10.3390/medicina62010139openalex-snapshot
Follicular Klotho in the Ovarian Microenvironment: Exploring Its Role in IVF Outcome Prediction
inferred← citeshttps://doi.org/10.4103/aja202495openalex-snapshot
Novel biallelic MCMDC2 variants were associated with meiotic arrest and nonobstructive azoospermia
inferred← citeshttps://doi.org/10.5534/wjmh.240149openalex-snapshot
Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility
inferred← citeshttps://doi.org/10.5772/intechopen.1007775openalex-snapshot
Detection and Clinical Application of Sperm DNA Fragmentation
inferred← citeshttps://doi.org/10.7150/ijbs.82191openalex-snapshot
Application of single-cell RNA sequencing on human testicular samples: a comprehensive review
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