Author

Martin Houlard

Centre for Human GeneticsORCID 0000-0001-6780-6939Unclaimed ORCID profile · follow to get notified of new preprints

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Approach:Bayesian inference· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Organism:mouse· 1 Assay:multiome· 1 Assay:scATAC-seq· 1

Frequent Co-Authors

Anjali Gupta HinchiD· 1 shared Brynelle Myers· 1 shared Emmanuelle BitouniD· 1 shared Ipsita AgarwaliD· 1 shared Simon Robert MyersiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

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5 top collaborators · 10 mutual co-author links

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1 shared paperGenetics

Anjali Gupta HinchORCID

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintSep 11, 2026

✦ In-depth digest

Mammalian spermatogenesis at single-cell resolution downstream of genetic perturbations in meiotic double-strand break repair

Ipsita Agarwal, Brynelle Myers, Martin Houlard…·Simon Robert Myers

Single-nucleus RNA+ATAC profiling of 32 mice shows asymmetric PRDM9 binding drives asynapsis, pachytene cell loss, aneuploidy and multi-megabase crossover redistribution, tuned by a chromosome 15 locus.

DOI 10.64898/2026.05.14.724910

mousemultiome

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