John C. Schimenti
Reproducibility track record
1
assessed papers
66/100
mean reproducibility
0
reproduced (C1–C2)
0
flagged
98
total citations
flag rate:
0%
(0/1)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
Funders
—
Frequent co-authors
David R. Liu 1Mi‐Hyun Choi 1Wei Zhang 1Shengdar Q. Tsai 1Christian M. Abratte 1Joseph M. Miano 1Rob J. Munroe 1Orazio J. Slivano 1Qing Lyu 1Xiaochun Long 1
Institutions
Augusta University 1St. Jude Children's Research Hospital 1Broad Institute 1Howard Hughes Medical Institute 1Harvard University 1Albany Medical Center Hospital 1
Geography (author institutions)
US 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
Complete publication record (278)
Request a reproduction →1 assessed by us (0 reproduced) · 277 not yet assessed — every PubMed paper on record, linked below.
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Multiplex organoid mutagenesis reveals gene combinations driving transformation, pathology, and chemosensitivity in ovarian carcinoma ↗Genetics · 2026 · PMID 41986871not yet assessed
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Genome integrity checkpoints in mammalian oogenesis ↗Biology of Reproduction · 2026 · PMID 42275079not yet assessed
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Aggressive Serous Carcinomas of the Female Reproductive Tract: Cancer-Prone Cell States and Genetic Drivers ↗Cancers · 2025 · PMID 40002199not yet assessed
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A primordial germ cell-like-cell platform enables CRISPRi screen for epigenetic fertility modifiers ↗EMBO Reports · 2025 · PMID 41233591not yet assessed
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Combinatorial organoid mutagenesis screen reveals gene constellations driving malignant transformation, pathology and chemosensitivity in high-grade serous ovarian carcinoma ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025 · PMID 40654781not yet assessed
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Spermatocytes ↗Elsevier eBooks · 2025not yet assessed
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Embryonic Stem Cell-Specific Responses to DNA Replication Stress ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025 · PMID 40463205not yet assessed
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not yet assessed
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Pre-ciliated tubal epithelial cells are prone to initiation of high-grade serous ovarian carcinoma ↗Nature Communications · 2024 · PMID 39366996not yet assessed
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Gene regulation during meiosis ↗Trends in Genetics · 2024 · PMID 38177041not yet assessed
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Relevance, strategies, and added value of mouse models in androgenetics ↗Andrology · 2024 · PMID 39300831not yet assessed
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Scalable primordial germ cell-like-cell platform for functional genomics identifies epigenetic fertility modifiers ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024 · PMID 38405756not yet assessed
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WITHDRAWN: High throughput CRISPR perturbation screens identify epigenetic regulators impacting primordial germ cell development ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024 · PMID 38463983not yet assessed
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Author Correction: Pre-ciliated tubal epithelial cells are prone to initiation of high-grade serous ovarian carcinoma ↗Nature Communications · 2024 · PMID 39567528not yet assessed
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In vivo versus in silico assessment of potentially pathogenic missense variants in human reproductive genes ↗Proceedings of the National Academy of Sciences · 2023 · PMID 37459509not yet assessed
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New allele of mouse DNA/RNA helicase senataxin causes meiotic arrest and infertility ↗Reproduction · 2023 · PMID 37801077not yet assessed
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Female infertility from oocyte maturation arrest: assembling the genetic puzzle ↗EMBO Molecular Medicine · 2023 · PMID 37073822not yet assessed
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Practical strategies for robust and inexpensive imaging of aqueous‐cleared tissues ↗Journal of Microscopy · 2023 · PMID 37413663not yet assessed
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Integrative genome-scale analyses reveal post-transcriptional signatures of early human small intestinal development in a directed differentiation organoid model ↗BMC Genomics · 2023 · PMID 37884859not yet assessed
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Pre-ciliated tubal epithelial cells are prone to initiation of high-grade serous ovarian carcinoma ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Abstract 175: Determining the genetic alterations in initiation and progression of high-grade serous ovarian carcinoma ↗Cancer Research · 2023not yet assessed
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A novel mouse allele of the DNA/RNA helicase senataxin ( Setx spcar3 ) causing meiotic arrest of spermatocytes and male infertility ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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not yet assessed
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Rescue of deficits by Brwd1 copy number restoration in the Ts65Dn mouse model of Down syndrome ↗Nature Communications · 2022 · PMID 36289231not yet assessed
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Bone mass and adaptation to mechanical loading are sexually dimorphic in adult osteoblast-specific ERα knockout mice ↗Bone · 2022 · PMID 35123146not yet assessed
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Genome Maintenance in Mammalian Stem Cells ↗Annual Review of Genetics · 2022 · PMID 35977408not yet assessed
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Integrative genome-scale analyses reveal post-transcriptional signatures of early human small intestinal development in a directed differentiation organoid model ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Imaging optically thick tissues simply and reproducibly: a practical guide to Lightsheet Macroscopy ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expressionGenome biology · 2021 · PMID 33722289L1 66/100
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Human MLH1/3 variants causing aneuploidy, pregnancy loss, and premature reproductive aging ↗Nature Communications · 2021 · PMID 34408140not yet assessed
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Strategies to Identify Genetic Variants Causing Infertility ↗Trends in Molecular Medicine · 2021 · PMID 33431240not yet assessed
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Genome maintenance during embryogenesis ↗DNA repair · 2021 · PMID 34358805not yet assessed
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Sequencing Micronuclei Reveals the Landscape of Chromosomal Instability ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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In vivo versus in silico assessment of potentially pathogenic missense variants in human reproductive genes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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MLH1/3 variants causing aneuploidy, pregnancy loss, and premature reproductive aging ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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Additional file 6 of Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression ↗Figshare · 2021not yet assessed
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Additional file 8 of Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression ↗Figshare · 2021not yet assessed
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Additional file 7 of Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression ↗Figshare · 2021not yet assessed
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Additional file 5 of Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression ↗Figshare · 2021not yet assessed
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Additional file 2 of Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression ↗Figshare · 2021not yet assessed
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Additional file 4 of Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression ↗Figshare · 2021not yet assessed
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Additional file 3 of Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression ↗Figshare · 2021not yet assessed
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SKP1 drives the prophase I to metaphase I transition during male meiosis ↗Science Advances · 2020 · PMID 32232159not yet assessed
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Testis formation in XX individuals resulting from novel pathogenic variants in Wilms’ tumor 1 ( WT1 ) gene ↗Proceedings of the National Academy of Sciences · 2020 · PMID 32493750not yet assessed
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Oocyte Elimination Through DNA Damage Signaling from CHK1/CHK2 to p53 and p63 ↗Genetics · 2020 · PMID 32273296not yet assessed
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Most Commonly Mutated Genes in High-Grade Serous Ovarian Carcinoma Are Nonessential for Ovarian Surface Epithelial Stem Cell Transformation ↗Cell Reports · 2020 · PMID 32877668not yet assessed
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A novel function for CDK2 activity at meiotic crossover sites ↗PLoS Biology · 2020 · PMID 33075054not yet assessed
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Gastric squamous-columnar junction contains a large pool of cancer-prone immature osteopontin responsive Lgr5−CD44+ cells ↗Nature Communications · 2020 · PMID 31901081not yet assessed
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Variants in RABL2A causing male infertility and ciliopathy ↗Human Molecular Genetics · 2020 · PMID 33075816not yet assessed
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Comparative Oncogenomics Implicates the Neurofibromin 1 Gene (NF1) as a Breast Cancer Driver ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2020not yet assessed
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Meiotic epigenetic factor PRDM9 impacts sperm quality of hybrid mice ↗Reproduction · 2020 · PMID 32272448not yet assessed
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A reporter mouse for in vivo detection of DNA damage in embryonic germ cells ↗genesis · 2020 · PMID 32343484not yet assessed
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Copy-number variation introduced by long transgenes compromises mouse male fertility independently of pachytene checkpoints ↗Chromosoma · 2020 · PMID 31940063not yet assessed
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Sexually dimorphic DNA damage responses and mutation avoidance in the mouse germline ↗Genes & Development · 2020 · PMID 33184219not yet assessed
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Prime Editing in Mice Reveals the Essentiality of a Single Base in Driving Tissue-Specific Gene Expression ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Most commonly mutated genes in High Grade Serous Ovarian Carcinoma are nonessential for ovarian surface epithelial stem cell transformation ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Single Cell Analysis Reveals Multi-faceted miR-375 Regulation of the Intestinal Crypt ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Sexually Dimorphic DNA Damage Responses and Mutation Avoidance in the Mouse Germline ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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A Reporter Mouse for In Vivo Detection of DNA Damage in Embryonic Germ Cells ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Variants in RABL2A causing male infertility and ciliopathy ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Conditional surrender in one generation: determining the reproductive roles of mouse embryo lethal genes by embryo complementation ↗Biology of Reproduction · 2020 · PMID 33057575not yet assessed
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Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations ↗Nature Communications · 2019 · PMID 31515488not yet assessed
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Female-biased embryonic death from inflammation induced by genomic instability ↗Nature · 2019 · PMID 30787433not yet assessed
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Germline genome protection: implications for gamete quality and germ cell tumorigenesis ↗Andrology · 2019 · PMID 31119900not yet assessed
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CDK2 kinase activity is a regulator of male germ cell fate ↗Development · 2019 · PMID 31582414not yet assessed
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A segregating human allele of SPO11 modeled in mice disrupts timing and amounts of meiotic recombination, causing oligospermia and a decreased ovarian reserve† ↗Biology of Reproduction · 2019 · PMID 31074776not yet assessed
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ENU‐induced mutant allele of Dnah1, ferf1, causes abnormal sperm behavior and fertilization failure in mice ↗Molecular Reproduction and Development · 2019 · PMID 30734403not yet assessed
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A predicted deleterious allele of the essential meiosis gene MND1, present in ~ 3% of East Asians, does not disrupt reproduction in mice ↗Molecular Human Reproduction · 2019 · PMID 31393579not yet assessed
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CDK2 kinase activity is a regulator of male germ cell fate ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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Signaling to TRP53 and TAp63 from CHK1/CHK2 is responsible for elimination of most oocytes defective for either chromosome synapsis or recombination ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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A segregating human allele of SPO11 modeled in mice disrupts timing and amounts of meiotic recombination, causing oligospermia and a decreased ovarian reserve ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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A predicted deleterious allele of the essential meiosis gene MND1 , present in ~3% of East Asians, does not disrupt reproduction in mice ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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Abstract 4611: Identifying drivers of mammary tumorigenesis & elucidating the mechanisms of cancer initiation in DNA replication defective Chaos3 mice ↗Cancer Research · 2019not yet assessed
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Abstract 4611: Identifying drivers of mammary tumorigenesis & elucidating the mechanisms of cancer initiation in DNA replication defective Chaos3 mice ↗Tumor Biology · 2019not yet assessed
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Unpackaging the genetics of mammalian fertility: strategies to identify the “reproductive genome”† ↗Biology of Reproduction · 2018 · PMID 29878059not yet assessed
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A putative human infertility allele of the meiotic recombinase DMC1 does not affect fertility in mice ↗Human Molecular Genetics · 2018 · PMID 30085085not yet assessed
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Whole Mount Immunofluorescence and Follicle Quantification of Cultured Mouse Ovaries ↗Journal of Visualized Experiments · 2018 · PMID 29782020not yet assessed
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Whole Mount Immunofluorescence and Follicle Quantification of Cultured Mouse Ovaries ↗Journal of Visualized Experiments · 2018not yet assessed
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A putative human infertility allele of the meiotic recombinase DMC1 does not affect fertility in mice ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
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Spermatocytes ↗Elsevier eBooks · 2018not yet assessed
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Female-biased embryonic death from genomic instability-induced inflammation ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
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Validation of Arid1a as a Mammary Tumor Driver in Mice ↗The FASEB Journal · 2018not yet assessed
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The DNA Damage Checkpoint Eliminates Mouse Oocytes with Chromosome Synapsis Failure ↗Molecular Cell · 2017 · PMID 28844861not yet assessed
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Pharmacological Inhibition of the DNA Damage Checkpoint Prevents Radiation-Induced Oocyte Death ↗Genetics · 2017 · PMID 28576861not yet assessed
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Pharmacological inhibition of the DNA damage checkpoint prevents radiation-induced oocyte death ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
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A single checkpoint pathway eliminates mouse oocytes with dna damage or chromosome synapsis failure ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
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Transcriptional profiling of cortical versus cancellous bone from mechanically-loaded murine tibiae reveals differential gene expression ↗Bone · 2016 · PMID 26876048not yet assessed
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Chronic DNA Replication Stress Reduces Replicative Lifespan of Cells by TRP53-Dependent, microRNA-Assisted MCM2-7 Downregulation ↗PLoS Genetics · 2016 · PMID 26765334not yet assessed
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Repair of Meiotic DNA Breaks and Homolog Pairing in Mouse Meiosis Requires a Minichromosome Maintenance (MCM) Paralog ↗Genetics · 2016 · PMID 27986806not yet assessed
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The Chromatin Remodeling ComponentArid1aIs a Suppressor of Spontaneous Mammary Tumors in Mice ↗Genetics · 2016 · PMID 27280691not yet assessed
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L. C. Dunn and Donald Charles on Quantitative Traits in the Mouse ↗Genetics · 2016 · PMID 26953264not yet assessed
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Mcmdc2 , a minichromosome maintenance (MCM) paralog, is required for repair of meiotic DNA breaks and homolog pairing in mouse meiosis ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
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How DNA‐Damage Machinery Protects the Genomes of Mouse Oocytes ↗The FASEB Journal · 2016not yet assessed
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Mechanism and Regulation of Rapid Telomere Prophase Movements in Mouse Meiotic Chromosomes ↗Cell Reports · 2015 · PMID 25892231not yet assessed
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MEI4: a central player in the regulation of meiotic DNA double strand break formation in the mouse ↗Journal of Cell Science · 2015 · PMID 25795304not yet assessed
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MCM 9 deficiency delays primordial germ cell proliferation independent of the ATM pathway ↗genesis · 2015 · PMID 26388201not yet assessed
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The genetics of human infertility by functional interrogation of SNPs in mice ↗Proceedings of the National Academy of Sciences · 2015 · PMID 26240362not yet assessed
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Effects of Deletion of ERα in Osteoblast-Lineage Cells on Bone Mass and Adaptation to Mechanical Loading Differ in Female and Male Mice ↗Journal of Bone and Mineral Research · 2015 · PMID 25707500not yet assessed
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miR-34 Cooperates with p53 in Suppression of Prostate Cancer by Joint Regulation of Stem Cell Compartment ↗Cell Reports · 2015not yet assessed
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A Mouse Geneticist’s Practical Guide to CRISPR Applications ↗Genetics · 2014 · PMID 25271304not yet assessed
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Reversal of Female Infertility by Chk2 Ablation Reveals the Oocyte DNA Damage Checkpoint Pathway ↗Science · 2014 · PMID 24482479not yet assessed
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Antagonistic roles of ubiquitin ligase HEI10 and SUMO ligase RNF212 regulate meiotic recombination ↗Nature Genetics · 2014 · PMID 24390283not yet assessed
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miR-34 Cooperates with p53 in Suppression of Prostate Cancer by Joint Regulation of Stem Cell Compartment ↗Cell Reports · 2014 · PMID 24630988not yet assessed
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Applying “Gold Standards” to In-Vitro-Derived Germ Cells ↗Cell · 2014 · PMID 24906145not yet assessed
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STAG3 is a strong candidate gene for male infertility ↗Human Molecular Genetics · 2014 · PMID 24608227not yet assessed
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Hypersensitivity of Primordial Germ Cells to Compromised Replication-Associated DNA Repair Involves ATM-p53-p21 Signaling ↗PLoS Genetics · 2014 · PMID 25010009not yet assessed
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A method for isolating high quality RNA from mouse cortical and cancellous bone ↗Bone · 2014 · PMID 25073031not yet assessed
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Mouse BRWD1 is critical for spermatid postmeiotic transcription and female meiotic chromosome stability ↗The Journal of Cell Biology · 2014 · PMID 25547156not yet assessed
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Induced Pluripotent Stem Cells have Similar Immunogenic and More Potent Immunomodulatory Properties Compared with Bone Marrow-Derived Stromal Cells in Vitro ↗Regenerative Medicine · 2014 · PMID 24773530not yet assessed
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not yet assessed
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Meiosis-specific cohesin mediates homolog recognition in mouse spermatocytes ↗Genes & Development · 2014 · PMID 24589552not yet assessed
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Cohesin mediates DSB-independent homolog pairing during meiosis ↗F1000Research · 2014not yet assessed
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An Ancient Transcription Factor Initiates the Burst of piRNA Production during Early Meiosis in Mouse Testes ↗Molecular Cell · 2013 · PMID 23523368not yet assessed
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The MCM8-MCM9 Complex Promotes RAD51 Recruitment at DNA Damage Sites To Facilitate Homologous Recombination ↗Molecular and Cellular Biology · 2013 · PMID 23401855not yet assessed
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Female Mice Lacking Estrogen Receptor-Alpha in Osteoblasts Have Compromised Bone Mass and Strength ↗Journal of Bone and Mineral Research · 2013 · PMID 24038209not yet assessed
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IQ Motif-Containing G (Iqcg) Is Required for Mouse Spermiogenesis ↗G3 Genes Genomes Genetics · 2013 · PMID 24362311not yet assessed
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AKAP9 Is Essential for Spermatogenesis and Sertoli Cell Maturation in Mice ↗Genetics · 2013 · PMID 23608191not yet assessed
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Role of DNA damage response pathways in preventing carcinogenesis caused by intrinsic replication stress ↗Oncogene · 2013 · PMID 23975433not yet assessed
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The 2013 Genetics Society of America Medal ↗Genetics · 2013 · PMID 23633134not yet assessed
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MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans ↗Journal of Clinical Investigation · 2012 · PMID 22354170not yet assessed
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Tissue-Specific Functional Networks for Prioritizing Phenotype and Disease Genes ↗PLoS Computational Biology · 2012 · PMID 23028291not yet assessed
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Meiotic cohesin complexes are essential for the formation of the axial element in mice ↗The Journal of Cell Biology · 2012 · PMID 22711701not yet assessed
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MARF1 Regulates Essential Oogenic Processes in Mice ↗Science · 2012 · PMID 22442484not yet assessed
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Genetics of Meiosis and Recombination in Mice ↗International review of cytology · 2012 · PMID 22878107not yet assessed
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Phosphorylation of Chromosome Core Components May Serve as Axis Marks for the Status of Chromosomal Events during Mammalian Meiosis ↗PLoS Genetics · 2012 · PMID 22346761not yet assessed
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Interallelic and Intergenic Incompatibilities of the Prdm9 (Hst1) Gene in Mouse Hybrid Sterility ↗PLoS Genetics · 2012 · PMID 23133405not yet assessed
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Comparative Oncogenomics Implicates the Neurofibromin 1 Gene (NF1) as a Breast Cancer Driver ↗Genetics · 2012 · PMID 22851646not yet assessed
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Meiosis arrest female 1 (MARF1) has nuage-like function in mammalian oocytes ↗Proceedings of the National Academy of Sciences · 2012 · PMID 23090997not yet assessed
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Using Genetic Networks and Homology to Understand the Evolution of Phenotypic Traits ↗Current Genomics · 2012 · PMID 22942677not yet assessed
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Post-transcriptional homeostasis and regulation of MCM2–7 in mammalian cells ↗Nucleic Acids Research · 2012 · PMID 22362746not yet assessed
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Genetic background affects induced pluripotent stem cell generation ↗Stem Cell Research & Therapy · 2012 · PMID 22862934not yet assessed
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Mutations Affecting Male Meiosis. ↗Biology of Reproduction · 2012not yet assessed
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A-MYB (MYBL1) transcription factor is a master regulator of male meiosis ↗Development · 2011 · PMID 21750041not yet assessed
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Minichromosome maintenance helicase paralog MCM9 is dispensible for DNA replication but functions in germ-line stem cells and tumor suppression ↗Proceedings of the National Academy of Sciences · 2011 · PMID 21987787not yet assessed
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Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells1 ↗Biology of Reproduction · 2011 · PMID 22011390not yet assessed
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Genetic Evidence That Synaptonemal Complex Axial Elements Govern Recombination Pathway Choice in Mice ↗Genetics · 2011 · PMID 21750255not yet assessed
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A reduction of licensed origins reveals strain-specific replication dynamics in mice ↗Mammalian Genome · 2011 · PMID 21611832not yet assessed
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Haploid Embryonic Stem Cells and the Dominance of Recessive Traits ↗Cell stem cell · 2011 · PMID 22136917not yet assessed
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A-MYB (MYBL1) transcription factor is a master regulator of male meiosis ↗Journal of Cell Science · 2011not yet assessed
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Regulating RNA polymerase pausing and transcription elongation in embryonic stem cells ↗Genes & Development · 2011 · PMID 21460038not yet assessed
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MCM4 mutation causes a novel DNA replication disorder associated with short stature and adrenal failure39th Meeting of the British Society for Paediatric Endocrinology and Diabetes · 2011not yet assessed
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Genetics of mammalian meiosis: regulation, dynamics and impact on fertility ↗Nature Reviews Genetics · 2010 · PMID 20051984not yet assessed
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Deficiency of Suppressor Enhancer Lin12 1 Like (SEL1L) in Mice Leads to Systemic Endoplasmic Reticulum Stress and Embryonic Lethality ↗Journal of Biological Chemistry · 2010 · PMID 20197277not yet assessed
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Incremental Genetic Perturbations to MCM2-7 Expression and Subcellular Distribution Reveal Exquisite Sensitivity of Mice to DNA Replication Stress ↗PLoS Genetics · 2010 · PMID 20838603not yet assessed
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Evidence Implicating CCNB1IP1, a RING Domain-Containing Protein Required for Meiotic Crossing Over in Mice, as an E3 SUMO Ligase ↗Genes · 2010 · PMID 21779533not yet assessed
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PDCD2 is essential for inner cell mass development and embryonic stem cell maintenance ↗Developmental Biology · 2010 · PMID 20813103not yet assessed
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The full‐length isoform of the mouse pleckstrin homology domain‐interacting protein (PHIP) is required for postnatal growth ↗FEBS Letters · 2010 · PMID 20816727not yet assessed
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Defective imprint resetting in carriers of Robertsonian translocation Rb (8.12) ↗Mammalian Genome · 2010 · PMID 20577743not yet assessed
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High resolution mapping and positional cloning of ENU-induced mutations in the Rw region of mouse chromosome 5 ↗BMC Genetics · 2010 · PMID 21118569not yet assessed
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SEL1L deficiency impairs growth and differentiation of pancreatic epithelial cells ↗BMC Developmental Biology · 2010 · PMID 20170518not yet assessed
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An allele separating skeletal patterning and spermatogonial renewal functions of PLZF ↗BMC Developmental Biology · 2010 · PMID 20338044not yet assessed
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Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass ↗BMC Developmental Biology · 2009 · PMID 19379485not yet assessed
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Aneuploidy and Improved Growth Are Coincident but Not Causal in a Yeast Cancer Model ↗PLoS Biology · 2009 · PMID 19636358not yet assessed
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Development and use of DNA archives at veterinary teaching hospitals to investigate the genetic basis of disease in dogs ↗Journal of the American Veterinary Medical Association · 2009 · PMID 19119968not yet assessed
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Mutagenesis of Mouse Embryonic Stem Cells with Ethylmethanesulfonate ↗Methods in molecular biology · 2009 · PMID 19266326not yet assessed
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Oocyte-Maturation Defective 1 (omd1): An ENU-Induced Mutation in Mouse Affecting the Oocyte-to-Embryo Transition. ↗Biology of Reproduction · 2009not yet assessed
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A Mouse Speciation Gene Encodes a Meiotic Histone H3 Methyltransferase ↗Science · 2008 · PMID 19074312not yet assessed
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The dual bromodomain and WD repeat-containing mouse protein BRWD1 is required for normal spermiogenesis and the oocyte–embryo transition ↗Developmental Biology · 2008 · PMID 18353305not yet assessed
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An Allelic Series Uncovers Novel Roles of the BRCT Domain-Containing Protein PTIP in Mouse Embryonic Vascular Development ↗Molecular and Cellular Biology · 2008 · PMID 18710940not yet assessed
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Mouse Pachytene Checkpoint 2 (Trip13) Is Required for Completing Meiotic Recombination but Not Synapsis ↗PLoS Genetics · 2007 · PMID 17696610not yet assessed
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Mutation in Mouse Hei10, an E3 Ubiquitin Ligase, Disrupts Meiotic Crossing Over ↗PLoS Genetics · 2007 · PMID 17784788not yet assessed
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Sperm Motility Defects and Infertility in Male Mice with a Mutation in Nsun7, a Member of the Sun Domain-Containing Family of Putative RNA Methyltransferases1 ↗Biology of Reproduction · 2007 · PMID 17442852not yet assessed
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A Dominant, Recombination-Defective Allele of Dmc1 Causing Male-Specific Sterility ↗PLoS Biology · 2007 · PMID 17425408not yet assessed
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Genetic Screen for Chromosome Instability in Mice: Mcm4 and Breast Cancer ↗Cell Cycle · 2007 · PMID 17495541not yet assessed
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Different regulatory systems operate in the midpiece and principal piece of the mammalian sperm flagellum. ↗PubMed · 2007 · PMID 17644973not yet assessed
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Correction: Mouse Pachytene Checkpoint 2 (Trip13) Is Required for Completing Meiotic Recombination but Not Synapsis ↗PLoS Genetics · 2007not yet assessed
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MUTAGENESIS AND PHENOTYPE-DRIVEN APPROACHES FOR IDENTIFICATION OF MALE FERTILITY GENES ↗Biology of Reproduction · 2007not yet assessed
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A viable allele of Mcm4 causes chromosome instability and mammary adenocarcinomas in mice ↗Nature Genetics · 2006 · PMID 17143284not yet assessed
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Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages ↗Experimental Cell Research · 2006 · PMID 17010969not yet assessed
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Mutagenesis as an unbiased approach to identify novel contraceptive targets ↗Molecular and Cellular Endocrinology · 2006 · PMID 16412559not yet assessed
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Mutation of a Ubiquitously Expressed Mouse Transmembrane Protein (Tapt1) Causes Specific Skeletal Homeotic Transformations ↗Genetics · 2006 · PMID 17151244not yet assessed
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Fast forward to new genes in mammalian reproduction ↗The Journal of Physiology · 2006 · PMID 16973708not yet assessed
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Mutagenesis-generated mouse models of human infertility with abnormal sperm ↗Human Reproduction · 2006 · PMID 16920728not yet assessed
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The mouse gcd2 mutation causes primordial germ cell depletion ↗Mechanisms of Development · 2006 · PMID 16822657not yet assessed
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Mutations in Col4a1 Cause Perinatal Cerebral Hemorrhage and Porencephaly ↗Science · 2005 · PMID 15905400not yet assessed
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Mei1 is epistatic to Dmc1 during mouse meiosis ↗Chromosoma · 2005 · PMID 15928951not yet assessed
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Mutations in Serac1 or Synj2 cause proximal t haplotype-mediated male mouse sterility but not transmission ratio distortion ↗Proceedings of the National Academy of Sciences · 2005 · PMID 15722415not yet assessed
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The translesion DNA polymerase θ plays a dominant role in immunoglobulin gene somatic hypermutation ↗The EMBO Journal · 2005 · PMID 16222339not yet assessed
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Transgenic rescue of the mouse t complex haplolethal locus Thl1 ↗Mammalian Genome · 2005 · PMID 16284799not yet assessed
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Mouse Pachytene Checkpoint 2 (Trip13) is Required for Completing Meiotic Recombination but not Synapsis ↗PLoS Genetics · 2005not yet assessed
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Mutation in Mouse Hei10, an E3 Ubiquitin Ligase, Disrupts Meiotic Crossing-over ↗PLoS Genetics · 2005not yet assessed
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Random mutagenesis of proximal mouse chromosome 5 uncovers predominantly embryonic lethal mutations ↗Genome Research · 2005 · PMID 16024820not yet assessed
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Positional cloning and characterization of mouse mei8 , a disrupted allele of the meiotic cohesin Rec8 ↗genesis · 2004 · PMID 15515002not yet assessed
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Synapsis or silence ↗Nature Genetics · 2004 · PMID 15624015not yet assessed
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The Mouse Genomic Instability Mutation chaos1 Is an Allele of Polq That Exhibits Genetic Interaction with Atm ↗Molecular and Cellular Biology · 2004 · PMID 15542845not yet assessed
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Homologous recombinational repair proteins in mouse meiosis ↗Cytogenetic and Genome Research · 2004 · PMID 15467364not yet assessed
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Forward Genetic Screens for Meiotic and Mitotic Recombination-Defective Mutants in Mice ↗Humana Press eBooks · 2004 · PMID 14769957not yet assessed
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New mouse genetic models for human contraceptive development ↗Cytogenetic and Genome Research · 2004 · PMID 15237210not yet assessed
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Functional annotation of mouse mutations in embryonic stem cells by use of expression profiling ↗Mammalian Genome · 2004 · PMID 14727137not yet assessed
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Genomewide two-generation screens for recessive mutations by ES cell mutagenesis ↗Mammalian Genome · 2004 · PMID 15599554not yet assessed
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Identification of a cryptic lethal mutation in the mouse tw73 haplotype ↗Genetics Research · 2004 · PMID 15822604not yet assessed
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Vestibular defects in head-tilt mice result from mutations in Nox3 , encoding an NADPH oxidase ↗Genes & Development · 2004 · PMID 15014044not yet assessed
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Contents Vol. 107, 2004 ↗Cytogenetic and Genome Research · 2004not yet assessed
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Contents Vol. 105, 2004 ↗Cytogenetic and Genome Research · 2004not yet assessed
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Subject Index Vol. 107, 3–4, 2004 ↗Cytogenetic and Genome Research · 2004not yet assessed
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Author Index Vol. 105, No. 2–4, 2004 ↗Cytogenetic and Genome Research · 2004not yet assessed
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Title Page / Table of Contents ↗Cytogenetic and Genome Research · 2004not yet assessed
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Author Index Vol. 105, 2004 ↗Cytogenetic and Genome Research · 2004not yet assessed
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Author Index Vol. 107, 3–4, 2004 ↗Cytogenetic and Genome Research · 2004not yet assessed
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Positional cloning and characterization of Mei1 , a vertebrate-specific gene required for normal meiotic chromosome synapsis in mice ↗Proceedings of the National Academy of Sciences · 2003 · PMID 14668445not yet assessed
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Phenotype-Based Identification of Mouse Chromosome Instability Mutants ↗Genetics · 2003 · PMID 12663541not yet assessed
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Toward the Genetics of Mammalian Reproduction: Induction and Mapping of Gametogenesis Mutants in Mice1 ↗Biology of Reproduction · 2003 · PMID 12855593not yet assessed
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Overlapping deletions spanning the proximal two-thirds of the mouse t complex ↗Mammalian Genome · 2003 · PMID 14724736not yet assessed
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Overlapping deletions define novel embryonic lethal loci in the mouse t complex ↗genesis · 2003 · PMID 12533796not yet assessed
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The Mouse Meiotic Mutation mei1 Disrupts Chromosome Synapsis with Sexually Dimorphic Consequences for Meiotic Progression ↗Developmental Biology · 2002 · PMID 11820814not yet assessed
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A Haplolethal Locus Uncovered by Deletions in the Mouse t Complex ↗Genetics · 2002 · PMID 11861570not yet assessed
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New Mutagenesis Technologies for Generating Mouse Models of Human DiseaseJapanese Circulation Journal-english Edition · 2002not yet assessed
-
Advances in basic research : from mouse to men.Japanese Circulation Journal-english Edition · 2002not yet assessed
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Functional Annotation of Mouse Genome Sequences ↗Science · 2001 · PMID 11233449not yet assessed
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Reciprocal Mouse and Human Limb Phenotypes Caused by Gain- and Loss-of-Function Mutations Affecting Lmbr1 ↗Genetics · 2001 · PMID 11606546not yet assessed
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Mutations of the Mouse Twist and sy (Fibrillin 2) Genes Induced by Chemical Mutagenesis of ES Cells ↗Genomics · 2001 · PMID 11350121not yet assessed
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DelBank: a mouse ES-cell resource for generating deletions ↗Nature Genetics · 2001 · PMID 11479588not yet assessed
-
Monoallelic Gene Expression in Mice: Who? When? How? Why? ↗Genome Research · 2001 · PMID 11691841not yet assessed
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Experimental and computational approaches yield a high-resolution, 1-Mb physical map of the region harboring the mouse t haplotype sterility factor, tcs1 ↗Mammalian Genome · 2001 · PMID 11471064not yet assessed
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Preface ↗Current Genomics · 2001not yet assessed
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Midgestation lethality in mice deficient for the RecA-related gene,Rad51d/Rad51l3 ↗genesis · 2000 · PMID 10705376not yet assessed
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Mouse mutants from chemically mutagenized embryonic stem cells ↗Nature Genetics · 2000 · PMID 10700192not yet assessed
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Segregation distortion of mouse t haplotypes ↗Trends in Genetics · 2000 · PMID 10827448not yet assessed
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Physical Mapping of Male Fertility and Meiotic Drive Quantitative Trait Loci in the Mouse t Complex Using Chromosome Deficiencies ↗Genetics · 2000 · PMID 10835401not yet assessed
-
Narrowing the Critical Regions for Mouse t Complex Transmission Ratio Distortion Factors by Use of Deletions ↗Genetics · 2000 · PMID 10835400not yet assessed
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Interdigitated Deletion Complexes on Mouse Chromosome 5 Induced by Irradiation of Embryonic Stem Cells ↗Genome Research · 2000 · PMID 10899153not yet assessed
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Toward the yeastification of mouse genetics: chemical mutagenesis of embryonic stem cells ↗Mammalian Genome · 2000 · PMID 10886030not yet assessed
-
Physical mapping of male fertility and meiotic drive quantitative trait loci in the mouse t complex using chromosome deficiencies [In Process Citation]The Mouseion at the JAXlibrary (Jackson Laboratory) · 2000not yet assessed
-
Narrowing the critical regions for mouse t complex transmission ratio distortion factors by use of deletions [In Process Citation]The Mouseion at the JAXlibrary (Jackson Laboratory) · 2000not yet assessed
-
Segregation distortion of mouse t haplotypes the molecular basis emerges [In Process Citation]The Mouseion at the JAXlibrary (Jackson Laboratory) · 2000not yet assessed
-
Mutagenesis in Mice Modern Times ↗Current Genomics · 2000not yet assessed
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Vestibular responses to linear acceleration are absent in otoconia-deficient C57BL/6JEi-het mice ↗Hearing Research · 1999 · PMID 10491954not yet assessed
-
Mice and the Role of Unequal Recombination in Gene-Family Evolution ↗The American Journal of Human Genetics · 1999 · PMID 9915941not yet assessed
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ORFless, intronless, and mutant transcription units in the mouse t complex responder ( Tcr ) locus ↗Mammalian Genome · 1999 · PMID 10501965not yet assessed
-
Transgenic and Mutational Analyses of Meiotic Recombination in Micea ↗Annals of the New York Academy of Sciences · 1999 · PMID 10415485not yet assessed
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Note to the Community ↗Mammalian Genome · 1999 · PMID 10341107not yet assessed
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Meiotic Prophase Arrest with Failure of Chromosome Synapsis in Mice Deficient for Dmc1 , a Germline-Specific RecA Homolog ↗Molecular Cell · 1998 · PMID 9660953not yet assessed
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Identification, Characterization, and Genetic Mapping ofRad51d,a New Mouse and HumanRAD51/RecA-Related Gene ↗Genomics · 1998 · PMID 9570954not yet assessed
-
Deletion Mapping of the Head Tilt (het) Gene in Mice: A Vestibular Mutation Causing Specific Absence of Otoliths ↗Genetics · 1998 · PMID 9755211not yet assessed
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Factors affecting ectopic gene conversion in mice ↗Mammalian Genome · 1998 · PMID 9545491not yet assessed
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Utility of C57BL/6J × 129/SvJae embryonic stem cells for generating chromosomal deletions: tolerance to γ radiation and microsatellite polymorphism ↗Mammalian Genome · 1998 · PMID 9501308not yet assessed
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Global analysis of gene function in mammals: Integration of physical, mutational and expression strategies ↗LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · 1998not yet assessed
-
Functional Genomics in the Mouse: Phenotype-Based Mutagenesis Screens ↗Genome Research · 1998 · PMID 9685317not yet assessed
-
Global analysis of gene function in mammals: Integration of physical, mutational and expression strategies ↗Electronic Journal of Biotechnology · 1998not yet assessed
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Chromosomal deletion complexes in mice by radiation of embryonic stem cells ↗Nature Genetics · 1997 · PMID 9054943not yet assessed
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1 Recombination in the Mammalian Germ Line ↗Current topics in developmental biology/Current Topics in Developmental Biology · 1997 · PMID 9352182not yet assessed
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Evidence for Cyclophosphamide-Induced Gene Conversion and Mutation in Mouse Germ Cells ↗Toxicology and Applied Pharmacology · 1997 · PMID 9439729not yet assessed
-
Generation of Radiation-Induced Deletion Complexes in the Mouse Genome Using Embryonic Stem Cells ↗Methods · 1997 · PMID 9480785not yet assessed
-
Cisplatin increases meiotic crossing-over in mice ↗Proceedings of the National Academy of Sciences · 1997 · PMID 9238037not yet assessed
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Molecular analysis of gene conversion in spermatids from transgenic mice ↗Gene · 1997 · PMID 9373154not yet assessed
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Decennial tails ↗Trends in Genetics · 1997 · PMID 9009842not yet assessed
-
Function of Untranslated Regions in the Mouse Spermatogenesis-Specific Gene Tcp10 Evaluated in Transgenic Mice ↗DNA and Cell Biology · 1997 · PMID 9174169not yet assessed
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A new spontaneous deletion on Chromosome 17 including brachyury ↗Mammalian Genome · 1997 · PMID 9383288not yet assessed
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Targeted Mutagenesis of a Candidate t Complex Responder Gene in Mouse t Haplotypes Does Not Eliminate Transmission Ratio Distortion ↗Genetics · 1996 · PMID 8889539not yet assessed
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Promoter mapping of the mouseTcp-10bt gene in transgenic mice identifies essential male germ cell regulatory sequences ↗Molecular Reproduction and Development · 1996 · PMID 8868241not yet assessed
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Promoter mapping of the mouse Tcp10bt gene in transgenic mice identifies essential male germ cell regulatory sequences ↗Molecular Reproduction and Development · 1996not yet assessed
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Gene conversion between unlinked sequences in the germline of mice. ↗Genetics · 1994 · PMID 8088528not yet assessed
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A recombination-based transgenic mouse system for genotoxicity testing ↗Mutation research. Fundamental and molecular mechanisms of mutagenesis · 1994 · PMID 7514731not yet assessed
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Functional and molecular characterization of the transcriptional regulatory region of Tcp-10bt, a testes-expressed gene from the t complex responder locus ↗Development · 1993 · PMID 8223262not yet assessed
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High-Frequency Germ Line Gene Conversion in Transgenic Mice ↗Molecular and Cellular Biology · 1992 · PMID 1588956not yet assessed
-
High-frequency germ line gene conversion in transgenic mice. ↗Molecular and Cellular Biology · 1992not yet assessed
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Functional analysis of a t complex responder locus transgene in mice ↗Mammalian Genome · 1992 · PMID 1421767not yet assessed
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H chain C domains influence the strength of binding of IgG for streptococcal group A carbohydrate ↗The Journal of Immunology · 1991 · PMID 1901882not yet assessed
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Microwave-accelerated fixation and lacZ activity staining of testicular cells in transgenic mice ↗Analytical Biochemistry · 1991 · PMID 1724120not yet assessed
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Molecular structure of Tcp-10 genes from the t complex responder locus ↗Mammalian Genome · 1991 · PMID 1794051not yet assessed
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Sodium butyrate causes reexpression of three membrane proteins on glycolipid-anchoring mutants ↗Somatic Cell and Molecular Genetics · 1991 · PMID 1679568not yet assessed
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Rapid identification of mouse t haplotypes by PCR polymorphism (PCRP).1990not yet assessed
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Molecular cloning of the t complex responder genetic locus ↗Genomics · 1990 · PMID 1981992not yet assessed
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Molecular cloning and genetic mapping of the t complex responder candidate gene family. ↗Genetics · 1990 · PMID 2323558not yet assessed
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Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes. ↗Proceedings of the National Academy of Sciences · 1989 · PMID 2717616not yet assessed
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Human homologs of two testes-expressed loci on mouse chromosome 17 map to opposite arms of chromosome 6 ↗Genomics · 1989 · PMID 2767684not yet assessed
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A candidate gene family for the mouse t complex responder (Tcr) locus responsible for haploid effects on sperm function ↗Cell · 1988 · PMID 3167978not yet assessed
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An unstable family of large DNA elements in the center of the mouse t complex ↗Journal of Molecular Biology · 1987 · PMID 2821263not yet assessed
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Dual evolutionary modes in the bovine globin locus ↗Biochemistry · 1986 · PMID 3768329not yet assessed
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Amplification and Rearrangement of DNA Sequences During the Evolutionary Divergence of t Haplotypes and Wild-Type Forms of Mouse Chromosome 17 ↗Current topics in microbiology and immunology · 1986 · PMID 3731843not yet assessed
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Structure and organization of the bovine beta-globin genes. ↗Molecular Biology and Evolution · 1985 · PMID 3870874not yet assessed
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Concerted evolution of the cow epsilon 2 and epsilon 4 beta-globin genes. ↗Molecular Biology and Evolution · 1985 · PMID 3870873not yet assessed
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Ruminant globin gene structures suggest an evolutionary role for Alu-type repeats ↗Nucleic Acids Research · 1984 · PMID 6322113not yet assessed
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DNA methylation and expression of baboon globin genes. ↗PubMed · 1984 · PMID 6209730not yet assessed
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Fetal hemoglobin production in adult baboons by 5-azacytidine or by phenylhydrazine-induced hemolysis is associated with hypomethylation of globin gene DNA. ↗PubMed · 1983 · PMID 6198662not yet assessed
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Selection of Hypercellulolytic Mutants of Trichoderma reesei Based on Resistance to Nystatin ↗Mycologia · 1983not yet assessed
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Is increase of fetal hemoglobin due to erythropoietic stress the result of DNA hypomethylation? ↗PubMed · 1983 · PMID 6208664not yet assessed
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Selection of Hypercellulolytic Mutants of Trichoderma Reesei Based on Resistance to Nystatin ↗Mycologia · 1983not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Schimenti J” paper on PubMed ↗