Publications by authors named "Celine Besse"

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Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes.
Gaëlle Munsch, Florian Thibord, Ohanna C Bezerra, Jennifer A Brody, Astrid van Hylckama Vlieg, Céline Besse

Blood· November 2025

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Genomic Landscape of Thrombosis Recurrence Risk Across Venous Thromboembolism Subtypes.
Gaëlle Munsch, Florian Thibord, Ohanna C Bezerra, Jennifer A Brody, Astrid van Hylckama Vlieg, Céline Besse

medRxiv· December 2024

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Human genetic structure in Northwest France provides new insights into West European historical demography.
Isabel Alves, Joanna Giemza, Michael G B Blum, Carolina Bernhardsson, Stéphanie Chatel, Céline Besse

Nat Commun· August 2024

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A Case-Only Genome-Wide Interaction Study of Smoking and Bladder Cancer Risk: Results from the COBLAnCE Cohort.
Maryam Karimi, Sebastian Mendez-Pineda, Hélène Blanché, Anne Boland, Céline Besse

Cancers (Basel)· August 2023

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Accelerated genome sequencing with controlled costs for infants in intensive care units: a feasibility study in a French hospital network.
Anne-Sophie Denommé-Pichon, Antonio Vitobello, Robert Olaso, Alban Ziegler, Médéric Jeanne, Céline Besse

Eur J Hum Genet· May 2022

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New insights into the genetic etiology of Alzheimer's disease and related dementias.
Céline Bellenguez, Fahri Küçükali, Iris E Jansen, Luca Kleineidam, Sonia Moreno-Grau, Céline Besse

Nat Genet· April 2022

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Experimental evolution links post-transcriptional regulation to Leishmania fitness gain.
Laura Piel, K Shanmugha Rajan, Giovanni Bussotti, Hugo Varet, Rachel Legendre, Céline Besse

PLoS Pathog· March 2022

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Mutations and variants of ONECUT1 in diabetes.
Anne Philippi, Sandra Heller, Ivan G Costa, Valérie Senée, Markus Breunig, Céline Besse

Nat Med· November 2021

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Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.
Sophie Garnier, Magdalena Harakalova, Stefan Weiss, Michal Mokry, Vera Regitz-Zagrosek, Céline Besse

Eur Heart J· May 2021

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Fine-mapping of two differentiated thyroid carcinoma susceptibility loci at 2q35 and 8p12 in Europeans, Melanesians and Polynesians.
Julie Guibon, Pierre-Emmanuel Sugier, Om Kulkarni, Mojgan Karimi, Delphine Bacq-Daian, Céline Besse

Oncotarget· March 2021

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Papuan mitochondrial genomes and the settlement of Sahul.
Nicole Pedro, Nicolas Brucato, Veronica Fernandes, Mathilde André, Lauri Saag, Céline Besse

J Hum Genet· October 2020

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Prediction of Breast Cancer Treatment-Induced Fatigue by Machine Learning Using Genome-Wide Association Data.
Sangkyu Lee, Joseph O Deasy, Jung Hun Oh, Antonio Di Meglio, Agnes Dumas, Celine Besse

JNCI Cancer Spectr· October 2020

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A novel rare c.-39C>T mutation in the PROS1 5'UTR causing PS deficiency by creating a new upstream translation initiation codon.
Sylvie Labrouche-Colomer, Omar Soukarieh, Carole Proust, Christine Mouton, Yoann Huguenin, Céline Besse

Clin Sci (Lond)· May 2020

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Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia.
Nicolas Brucato, Veronica Fernandes, Pradiptajati Kusuma, Viktor Černý, Connie J Mulligan, Céline Besse

Genome Biol Evol· March 2019

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Corrigendum re "Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma" [Eur Urol 2017;72:747-54].
Mitchell J Machiela, Jonathan N Hofmann, Robert Carreras-Torres, Kevin M Brown, Mattias Johansson, Celine Besse

Eur Urol· September 2018

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Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma.
Mitchell J Machiela, Jonathan N Hofmann, Robert Carreras-Torres, Kevin M Brown, Mattias Johansson, Celine Besse

Eur Urol· November 2017

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Assessment of the prognostic role of a 94-single nucleotide polymorphisms risk score in early breast cancer in the SIGNAL/PHARE prospective cohort: no correlation with clinico-pathological characteristics and outcomes.
Elsa Curtit, Xavier Pivot, Julie Henriques, Sophie Paget-Bailly, Pierre Fumoleau, Céline Besse

Breast Cancer Res· August 2017

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Genome-wide association study identifies multiple risk loci for renal cell carcinoma.
Ghislaine Scelo, Mark P Purdue, Kevin M Brown, Mattias Johansson, Zhaoming Wang, Celine Besse

Nat Commun· June 2017

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dUTPase () Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure.
Reinaldo Sousa Dos Santos, Mathilde Daures, Anne Philippi, Sophie Romero, Lorella Marselli, Céline Besse

Diabetes· April 2017

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Genome-Wide Methylation Analysis Identifies Specific Epigenetic Marks In Severely Obese Children.
Delphine Fradin, Pierre-Yves Boëlle, Marie-Pierre Belot, Fanny Lachaux, Jorg Tost, Céline Besse

Sci Rep· April 2017

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A GWAS in uveal melanoma identifies risk polymorphisms in the locus.
Lenha Mobuchon, Aude Battistella, Claire Bardel, Ghislaine Scelo, Alexia Renoud, Céline Besse

NPJ Genom Med· March 2017

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Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort.
Xavier Pivot, Gilles Romieu, Pierre Fumoleau, Maria Rios, Hervé Bonnefoi, Céline Besse

NPJ Breast Cancer· February 2017

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GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients.
David G Cox, Elsa Curtit, Gilles Romieu, Pierre Fumoleau, Maria Rios, Céline Besse

Oncotarget· November 2016

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Analysis with the exome array identifies multiple new independent variants in lipid loci.
Stavroula Kanoni, Nicholas G D Masca, Kathleen E Stirrups, Tibor V Varga, Helen R Warren, Céline Besse

Hum Mol Genet· September 2016

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Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations.
Fabienne Jabot-Hanin, Aurélie Cobat, Jacqueline Feinberg, Ghislain Grange, Natascha Remus, Céline Besse

J Infect Dis· April 2016

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