Florence Le Calvez-Kelm

发表

Needlestack: an ultra-sensitive variant caller for multi-sample next generation sequencing data

Paul Brennan, Elisabeth Brambilla, Matthieu Foll, 2019, bioRxiv.

Methylome analysis reveals Jak-STAT pathway deregulation in putative breast cancer stem cells

Florence Le Calvez-Kelm, Sean V Tavtigian, Zdenko Herceg, 2011, Epigenetics.

Genome-wide association study identifies multiple risk loci for renal cell carcinoma

Bin Tean Teh, Tony Fletcher, Peter Kraft, 2017, Nature Communications.

Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer.

Alun Thomas, Sue Healey, John L Hopper, 2009, American journal of human genetics.

Integrative Genome-Wide Gene Expression Profiling of Clear Cell Renal Cell Carcinoma in Czech Republic and in the United States

Ivana Holcatova, Vladimir Janout, Ghislaine Scelo, 2013, PloS one.

Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation

Elisabeth Cardis, Florence Le Calvez-Kelm, Irina Malakhova, 2017, BMC Cancer.

Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer

William Wheeler, Paolo Vineis, Andres Metspalu, 2014, Nature Genetics.

Exposure to aflatoxin B1 in utero is associated with DNA methylation in white blood cells of infants in The Gambia.

Paula Dominguez-Salas, Florence Le Calvez-Kelm, Zdenko Herceg, 2015, International journal of epidemiology.

Hepatocellular Carcinoma Displays Distinct DNA Methylation Signatures with Potential as Clinical Predictors

Sean V. Tavtigian, Florence Le Calvez-Kelm, Zdenko Herceg, 2010, PloS one.

Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus

Catherine Voegele, Tú Nguyen-Dumont, Federica Gemignani, 2009, BMC Genetics.

Tobacco smoking-associated genome-wide DNA methylation changes in the EPIC study.

Paolo Vineis, Salvatore Panico, Vittorio Krogh, 2016, Epigenomics.