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  1. Article

    Open Access

    Correction to: The CEPH aging cohort and biobank: a valuable collection of biological samples from exceptionally long‑lived French individuals and their offspring for longevity studies

    Alexandre How‑Kit, Mourad Sahbatou, Lise M. Hardy, Nicolas P. Tessier in GeroScience (2024)

  2. Article

    Open Access

    The CEPH aging cohort and biobank: a valuable collection of biological samples from exceptionally long-lived French individuals and their offspring for longevity studies

    The increasing aging of the human population is currently and for the coming decades a major public health issue in many countries, requiring the implementation of global public health policies promoting healt...

    Alexandre How-Kit, Mourad Sahbatou, Lise M. Hardy, Nicolas P. Tessier in GeroScience (2024)

  3. Article

    Open Access

    SARS-CoV-2 infection prevalence and associated factors among primary healthcare workers in France after the third COVID-19 wave

    Data on the SARS-CoV-2 infection among primary health care workers (PHCWs) are scarce but essential to reflect on policy regarding prevention and control measures. We assessed the prevalence of PHCWs who have ...

    Marie Pouquet, Dorine Decarreaux, Laura Di Domenico in Scientific Reports (2024)

  4. Article

    Open Access

    Correction: Antibody response, associated symptoms and profile of patients presumably infected by SARS-CoV-2 with taste or smell disorders in the SAPRIS multicohort study

    Julien Ramillon, Xavier de Lamballerie, Olivier Robineau in BMC Infectious Diseases (2023)

  5. Article

    Open Access

    Antibody response, associated symptoms and profile of patients presumably infected by SARS-CoV-2 with taste or smell disorders in the SAPRIS multicohort study

    Taste or smell disorders have been reported as strongly associated with COVID-19 diagnosis. We aimed to identify subject characteristics, symptom associations, and antibody response intensity associated with t...

    Julien Ramillon, Xavier de Lamballerie, Olivier Robineau in BMC Infectious Diseases (2023)

  6. Article

    Open Access

    Publisher Correction: Heterogeneous SARS-CoV-2 humoral response after COVID-19 vaccination and/or infection in the general population

    Fabrice Carrat, Paola Mariela Saba Villarroel, Nathanael Lapidus in Scientific Reports (2022)

  7. Article

    Open Access

    Heterogeneous SARS-CoV-2 humoral response after COVID-19 vaccination and/or infection in the general population

    Assessment of the intensity, dynamics and determinants of the antibody response after SARS-CoV-2 infection or vaccination in the general population is critical to guide vaccination policies. This study charact...

    Fabrice Carrat, Paola Mariela Saba Villarroel, Nathanael Lapidus in Scientific Reports (2022)

  8. Article

    Open Access

    A high-throughput real-time PCR tissue-of-origin test to distinguish blood from lymphoblastoid cell line DNA for (epi)genomic studies

    Lymphoblastoid cell lines (LCLs) derive from blood infected in vitro by Epstein–Barr virus and were used in several genetic, transcriptomic and epigenomic studies. Although few changes were shown between LCL a...

    Lise M. Hardy, Yosra Bouyacoub, Antoine Daunay, Mourad Sahbatou in Scientific Reports (2022)

  9. Article

    Open Access

    Age, COVID-19-like symptoms and SARS-CoV-2 seropositivity profiles after the first wave of the pandemic in France

    The interplay between age and symptoms intensity on antibody response to SARS-CoV-2 infection has not been studied in a general population setting.

    Fabrice Carrat, Nathanael Lapidus, Laetitia Ninove, Hélène Blanché in Infection (2022)

  10. Article

    Open Access

    Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes

    A Correction to this paper has been published: https://doi.org/10.1038/s41467-021-22613-2

    Joris Deelen, Daniel S. Evans, Dan E. Arking, Niccolò Tesi in Nature Communications (2021)

  11. Article

    Open Access

    A meta-analysis of genome-wide association studies identifies multiple longevity genes

    Human longevity is heritable, but genome-wide association (GWA) studies have had limited success. Here, we perform two meta-analyses of GWA studies of a rigorous longevity phenotype definition including 11,262...

    Joris Deelen, Daniel S. Evans, Dan E. Arking, Niccolò Tesi in Nature Communications (2019)

  12. Article

    Open Access

    Publisher Correction: Identification and characterization of two functional variants in the human longevity gene FOXO3

    The original version of this Article contained an error in the spelling of the author Robert Häsler, which was incorrectly given as Robert Häesler. This has now been corrected in both the PDF and HTML versions...

    Friederike Flachsbart, Janina Dose, Liljana Gentschew in Nature Communications (2018)

  13. Article

    Open Access

    Identification and characterization of two functional variants in the human longevity gene FOXO3

    FOXO3 is consistently annotated as a human longevity gene. However, functional variants and underlying mechanisms for the association remain unknown. Here, we perform resequencing of the FOXO3 locus and single-nu...

    Friederike Flachsbart, Janina Dose, Liljana Gentschew in Nature Communications (2017)

  14. Article

    Open Access

    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

    Genome-wide association studies (GWAS) have to date identified 94 genetic variants (single nucleotide polymorphisms (SNPs)) associated with risk of develo** breast cancer. A score based on the combined effec...

    Elsa Curtit, Xavier Pivot, Julie Henriques, Sophie Paget-Bailly in Breast Cancer Research (2017)

  15. Article

    Open Access

    Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort

    Human epidermal growth factor receptor 2-positive breast cancer is a subtype of interest regarding its outcome and the impressive impact of human epidermal growth factor receptor 2 targeted therapy. Constituti...

    Xavier Pivot, Gilles Romieu, Pierre Fumoleau, Maria Rios in npj Breast Cancer (2017)

  16. Article

    Open Access

    A whole-genome sequence and transcriptome perspective on HER2-positive breast cancers

    HER2-positive breast cancer has long proven to be a clinically distinct class of breast cancers for which several targeted therapies are now available. However, resistance to the treatment associated with spec...

    Anthony Ferrari, Anne Vincent-Salomon, Xavier Pivot in Nature Communications (2016)

  17. Article

    Correction: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

    Nature 480, 94–98 (2011); doi:10.1038/nature10539 In this Letter, one image was mistakenly duplicated during preparation of the artwork. In the original Fig. 3d, the left image illustrating migration of RCC4 c...

    Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub in Nature (2016)

  18. No Access

    Article

    A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

    Iris Heid, Gonçalo Abecasis, Sudha Iyengar and colleagues report the results of a large genome-wide association meta-analysis of macular degeneration based on over 43,000 subjects. They identify 16 new risk lo...

    Lars G Fritsche, Wilmar Igl, Jessica N Cooke Bailey, Felix Grassmann in Nature Genetics (2016)

  19. No Access

    Article

    Variation in genomic landscape of clear cell renal cell carcinoma across Europe

    The incidence of renal cell carcinoma (RCC) is increasing worldwide, and its prevalence is particularly high in some parts of Central Europe. Here we undertake whole-genome and transcriptome sequencing of clea...

    Ghislaine Scelo, Yasser Riazalhosseini, Liliana Greger in Nature Communications (2014)

  20. No Access

    Article

    A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

    Two papers in this issue of Nature demonstrate that missense substitutions in the gene encoding for microphthalmia-associated transcription factor (MITF) are associated with susceptibility to melanoma and renal c...

    Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub in Nature (2011)

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