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Mourad Sahbatou

Showing results (21-30 of 37) with videos related to

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Human Molecular Genetics|July 6, 2004
Significant linkage to spondyloarthropathy on 9q31-34Corinne Miceli-Richard, Habib Zouali, Roula Said-Nahal, et al.
Pharmaceutics|June 27, 2024
Constitutional DNA Polymorphisms Associated with the Plasma Imatinib Concentration in Chronic Myeloid Leukemia PatientsHeriberto Bruzzoni-Giovanelli, Habib Zouali, Mourad Sahbatou, et al.
Aging Cell|June 19, 2025
Integrative Multiparametric Analysis of Circulating Cell-Free Nucleic Acids of Plasma in Healthy Individuals During AgingNicolas P Tessier, Lise M Hardy, Florence Mauger, et al.
Geroscience|January 25, 2024
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 studiesAlexandre How-Kit, Mourad Sahbatou, Lise M Hardy, et al.
Geroscience|December 23, 2023
The CEPH aging cohort and biobank: a valuable collection of biological samples from exceptionally long-lived French individuals and their offspring for longevity studiesAlexandre How-Kit, Mourad Sahbatou, Lise M Hardy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
A new F-box protein 7 gene mutation causing typical Parkinson's diseaseEbba Lohmann, Anne-Sophie Coquel, Aurélie Honoré, et al.
Nature Genetics|August 21, 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotypeHilde Brems, Magdalena Chmara, Mourad Sahbatou, et al.
European Journal of Human Genetics : EJHG|August 10, 2018
Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosisPhilip Farrell, Claude Férec, Milan Macek, et al.
Clinical Epigenetics|March 25, 2026
The 12 o'clock assay: an optimized dodecaplex droplet digital PCR assay for robust DNA methylation quantification and epigenetic clock-based age-predictionsIlef Hchaichi, Imène Garali, Alina-Madalina Popa, et al.
Science (New York, N.Y.)|April 9, 2011
Association of TALS developmental disorder with defect in minor splicing component U4atac snRNAPatrick Edery, Charles Marcaillou, Mourad Sahbatou, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|July 6, 2004
Significant linkage to spondyloarthropathy on 9q31-34Corinne Miceli-Richard, Habib Zouali, Roula Said-Nahal, et al.
Pharmaceutics|June 27, 2024
Constitutional DNA Polymorphisms Associated with the Plasma Imatinib Concentration in Chronic Myeloid Leukemia PatientsHeriberto Bruzzoni-Giovanelli, Habib Zouali, Mourad Sahbatou, et al.
Aging Cell|June 19, 2025
Integrative Multiparametric Analysis of Circulating Cell-Free Nucleic Acids of Plasma in Healthy Individuals During AgingNicolas P Tessier, Lise M Hardy, Florence Mauger, et al.
Geroscience|January 25, 2024
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 studiesAlexandre How-Kit, Mourad Sahbatou, Lise M Hardy, et al.
Geroscience|December 23, 2023
The CEPH aging cohort and biobank: a valuable collection of biological samples from exceptionally long-lived French individuals and their offspring for longevity studiesAlexandre How-Kit, Mourad Sahbatou, Lise M Hardy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
A new F-box protein 7 gene mutation causing typical Parkinson's diseaseEbba Lohmann, Anne-Sophie Coquel, Aurélie Honoré, et al.
Nature Genetics|August 21, 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotypeHilde Brems, Magdalena Chmara, Mourad Sahbatou, et al.
European Journal of Human Genetics : EJHG|August 10, 2018
Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosisPhilip Farrell, Claude Férec, Milan Macek, et al.
Clinical Epigenetics|March 25, 2026
The 12 o'clock assay: an optimized dodecaplex droplet digital PCR assay for robust DNA methylation quantification and epigenetic clock-based age-predictionsIlef Hchaichi, Imène Garali, Alina-Madalina Popa, et al.
Science (New York, N.Y.)|April 9, 2011
Association of TALS developmental disorder with defect in minor splicing component U4atac snRNAPatrick Edery, Charles Marcaillou, Mourad Sahbatou, et al.
Pageof 4