Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction-Reference-Cited by-同舟云学术

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Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction

Published:2012-05-30 Issue:9 Volume:131 Page:1519-1524
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Borel Christelle,Cheung Fanny,Stewart Helen,Koolen David A.,Phillips Christopher,Thomas N. Simon,Jacobs Patricia A.,Eliez Stephan,Sharp Andrew J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-012-1180-4.pdf

Reference20 articles.

1. Baudat F, Buard J, Grey C, Fledel-Alon A, Ober C, Przeworski M, Coop G, de Massy B (2010) PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice. Science 327(5967):836–840. doi: science.118343910.1126/science.1183439

2. Berg IL, Neumann R, Lam KW, Sarbajna S, Odenthal-Hesse L, May CA, Jeffreys AJ (2010) PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans. Nat Genet 42(10):859–863. doi: ng.65810.1038/ng.658

3. Berg IL, Neumann R, Sarbajna S, Odenthal-Hesse L, Butler NJ, Jeffreys AJ (2011) Variants of the protein PRDM9 differentially regulate a set of human meiotic recombination hotspots highly active in African populations. Proc Natl Acad Sci USA 108(30):12378–12383. doi: 110953110810.1073/pnas.1109531108

4. Bugge M, Collins A, Petersen MB, Fisher J, Brandt C, Hertz JM, Tranebjaerg L, de Lozier-Blanchet C, Nicolaides P, Brondum-Nielsen K, Morton N, Mikkelsen M (1998) Non-disjunction of chromosome 18. Hum Mol Genet 7(4):661–669. doi: ddb080

5. Bugge M, Collins A, Hertz JM, Eiberg H, Lundsteen C, Brandt CA, Bak M, Hansen C, Delozier CD, Lespinasse J, Tranebjaerg L, Hahnemann JM, Rasmussen K, Bruun-Petersen G, Duprez L, Tommerup N, Petersen MB (2007) Non-disjunction of chromosome 13. Hum Mol Genet 16(16):2004–2010. doi: ddm14810.1093/hmg/ddm148

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1. Variant Identification in BARD1, PRDM9, RCC1, and RECQL in Patients with Ovarian Cancer by Targeted Next-generation Sequencing of DNA Pools;Cancer Prevention Research;2021-12-14

2. Further evidence for lack of association of PRDM9 polymorphisms and 22q11.2 deletion syndrome;Meta Gene;2021-09

3. A new experimental system to study meiotic recurrent non-allelic homologous recombination in budding yeast;2020-06-25

4. The impact of recombination on human mutation load and disease;Philosophical Transactions of the Royal Society B: Biological Sciences;2017-11-06

5. An exploratory study of predisposing genetic factors for DiGeorge/velocardiofacial syndrome;Scientific Reports;2017-01-06

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