Transcriptome and genome sequencing uncovers functional variation in humans
2013 · Nature · 2,118 citations
https://doi.org/10.1038/nature12531
J
Jean Monlong
Inserm(FR)
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Jean Monlong is an academic researcher from Inserm. The author has contributed to research in topics: Cancer Genomics and Diagnostics & Pancreatic and Hepatic Oncology Research & Genomics and Phylogenetic Studies. The author has an h-index of 34, co-authored 95 publications.
ORCID: 0000-0002-9737-5516Papers by this author
worksExploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
2018 · Nature Communications · 1,175 citations
https://doi.org/10.1038/s41467-018-03621-1
A draft human pangenome reference
2023 · Nature · 1,070 citations
https://doi.org/10.1038/s41586-023-05896-x
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
2020 · Nature Genetics · 463 citations
https://doi.org/10.1038/s41588-019-0562-0
Pangenomics enables genotyping of known structural variants in 5202 diverse genomes
2021 · Science · 392 citations
https://doi.org/10.1126/science.abg8871
Recombination between heterologous human acrocentric chromosomes
2023 · Nature · 133 citations
https://doi.org/10.1038/s41586-023-05976-y
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