PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans

Berg, Ingrid L, Neumann, Rita, Lam, Kwan-Wood G, Sarbajna, Shriparna, Odenthal-Hesse, Linda, May, Celia A, Jeffreys, Alec J·2010·Nature Genetics

Cited by (318)

Items 301–318 of 318

  1. Incorporating recombination into the study of recent human evolutionary history
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  2. Additional file 2 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits
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  3. Additional file 3 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits
    Yuan, Bo, Katharina Schulze, Assia Batzir, Nurit, Jefferson C. Sinson, Hongzheng Dai, Zhu, Wenmiao, Francia Bocanegra, ChinTo Fong, Holder, Jimmy, Nguyen, Joanne et al. · 2022 · Figshare
  4. Additional file 1 of Personalized genome structure via single gamete sequencing
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  5. Additional file 1 of Analysis of archaic human haplotypes suggests that 5hmC acts as an epigenetic guide for NCO recombination
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  6. Additional file 1 of Genome-wide recombination map construction from single sperm sequencing in cattle
    Yang, Liu, Gao, Yahui, Li, Mingxun, Park, Ki-Eun, Liu, Shuli, Kang, Xiaolong, Liu, Mei, Adam Oswalt, Fang, Lingzhao, Bhanu Prakash V. L. Telugu et al. · 2022 · Figshare
  7. Aberrant meiotic recombination mediated by maternal RNF212, PRDM9, and SPO11 variants increases risk of chromosome 21 nondisjunction and Down syndrome birth
    Upamanyu Pal, Pinku Halder, Agnish Ganguly, Sumantra Sarkar, Papiya Ghosh, Sujay Ghosh · 2025 · Egyptian Journal of Medical Human Genetics
  8. The evolution of recombination and genomic structures : a modelling approach
    Alexandra Popa · 2011
  9. NGS-based approaches for the diagnosis of intellectual disability and other genetically heterogeneous developmental disorders
    Claire E. Redin · 2014 · theses.fr (ABES)
  10. Rôle de l'activité méthyltransférase de la protéine PRDM9 dans la recombinaison méiotique chez la souris
    Boubou Diagouraga · 2015
  11. Meiotic recombination evolution : Prdm9 gene variation and evolution in mice
    Denis Dunoyer de Segonzac · 2016
  12. Biochemical properties and regulation of the TopoVI-like complex responsible for the initiation of meiotic recombination
    Alexandre Nore · 2018
  13. Gene editing approaches of microsatellite disorders : shortening expanded repeats
    Lucie Poggi · 2020 · theses.fr (ABES)
  14. Étude de la recombinaison méiotique chez la levure Lachancea kluyveri
    Sylvain Legrand · 2020
  15. Régulation spatiale des cassures d’ADN double-brin méiotiques chez Saccharomyces cerevisiae : rôle de la protéine kinase Tel1
    Marie Dorme · 2022
  16. Why recombination hotspots?
    Julien Joseph, Thomas Brazier, Marie Raynaud, Sylvain Glémin, Frédéric Baudat, Bernard de Massy, Nicolas Lartillot, Laurent Duret · 2026 · PLoS Genetics
  17. Modelling DMC1 mediated homologous recombination repair in mouse embryonic stem cells
    Aditya Mhaskar, Esther Sleddens–Linkels, Ivy Liang, Fiona Horne, Achmed Al-Kourdi, Johan A. Slotman, Wiggert A. van Cappellen, Maarten W. Paul, Mehrnaz Ghazvini, Adriaan B. Houtsmuller et al. · 2026 · Frontiers in Cell and Developmental Biology
  18. BindingDB Entry 8010: Trimethylation of histone H3 lysine 36 by human methyltransferase PRDM9 protein.
    BindingDB · 2017 · UC San Diego