Xenética
Servizo
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Pitié-Salpêtrière Hospital
París, FranciaPublicacións en colaboración con investigadores/as de Pitié-Salpêtrière Hospital (14)
2021
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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Nature Communications, Vol. 12, Núm. 1
2020
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Nature Genetics, Vol. 52, Núm. 1, pp. 56-73
2019
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Erratum to: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (Nature Communications, (2018), 9, 1, (1340), 10.1038/s41467-018-03178-z)
Nature Communications
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Erratum to: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (Nature Communications, (2017), 8, 1, (1892), 10.1038/s41467-017-00320-1)
Nature Communications
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Erratum to: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (Nature Communications, (2018), 9, 1, (3707), 10.1038/s41467-018-04989-w)
Nature Communications
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Erratum to: Large-scale transcriptome-wide association study identifies new prostate cancer risk regions (Nature Communications, (2018), 9, 1, (4079), 10.1038/s41467-018-06302-1)
Nature Communications
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The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
npj Breast Cancer, Vol. 5, Núm. 1
2018
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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia
Nature Communications, Vol. 9, Núm. 1
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Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
Nature Communications, Vol. 9, Núm. 1
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Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
Nature Communications, Vol. 9, Núm. 1
2017
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Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
Nature Communications, Vol. 8, Núm. 1
2016
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Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of european ancestry
Human Molecular Genetics, Vol. 25, Núm. 6, pp. 1203-1214
2014
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Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33
Human Molecular Genetics, Vol. 23, Núm. 24, pp. 6616-6633
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The 19q12 bladder cancer GWAS signal: Association with cyclin E function and aggressive disease
Cancer Research, Vol. 74, Núm. 20, pp. 5808-5818