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
DOI 10.1038/ng.658
Cited by (318)
Items 301–318 of 318
- Incorporating recombination into the study of recent human evolutionary historyMarta Melé · 2011 · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
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- Additional file 3 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traitsYuan, 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
- Additional file 1 of Personalized genome structure via single gamete sequencingRuqian Lyu, Vanessa Tsui, McCarthy, Davis J., Wayne Crismani · 2021 · Figshare
- Additional file 1 of Analysis of archaic human haplotypes suggests that 5hmC acts as an epigenetic guide for NCO recombinationLee, Bernett, Samantha L. Cyrill, Lee, Wendy, Rossella Melchiotti, Andiappan, Anand Kumar, Michael Poidinger, Rötzschke, Olaf · 2022 · Figshare
- Additional file 1 of Genome-wide recombination map construction from single sperm sequencing in cattleYang, 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
- Aberrant meiotic recombination mediated by maternal RNF212, PRDM9, and SPO11 variants increases risk of chromosome 21 nondisjunction and Down syndrome birthUpamanyu Pal, Pinku Halder, Agnish Ganguly, Sumantra Sarkar, Papiya Ghosh, Sujay Ghosh · 2025 · Egyptian Journal of Medical Human Genetics
- The evolution of recombination and genomic structures : a modelling approachAlexandra Popa · 2011
- NGS-based approaches for the diagnosis of intellectual disability and other genetically heterogeneous developmental disordersClaire E. Redin · 2014 · theses.fr (ABES)
- Rôle de l'activité méthyltransférase de la protéine PRDM9 dans la recombinaison méiotique chez la sourisBoubou Diagouraga · 2015
- Meiotic recombination evolution : Prdm9 gene variation and evolution in miceDenis Dunoyer de Segonzac · 2016
- Biochemical properties and regulation of the TopoVI-like complex responsible for the initiation of meiotic recombinationAlexandre Nore · 2018
- Gene editing approaches of microsatellite disorders : shortening expanded repeatsLucie Poggi · 2020 · theses.fr (ABES)
- Étude de la recombinaison méiotique chez la levure Lachancea kluyveriSylvain Legrand · 2020
- Régulation spatiale des cassures d’ADN double-brin méiotiques chez Saccharomyces cerevisiae : rôle de la protéine kinase Tel1Marie Dorme · 2022
- Why recombination hotspots?Julien Joseph, Thomas Brazier, Marie Raynaud, Sylvain Glémin, Frédéric Baudat, Bernard de Massy, Nicolas Lartillot, Laurent Duret · 2026 · PLoS Genetics
- Modelling DMC1 mediated homologous recombination repair in mouse embryonic stem cellsAditya 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
- BindingDB Entry 8010: Trimethylation of histone H3 lysine 36 by human methyltransferase PRDM9 protein.BindingDB · 2017 · UC San Diego