43 results on '"Sahbatou, Mourad"'
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2. The CEPH aging cohort and biobank: a valuable collection of biological samples from exceptionally long-lived French individuals and their offspring for longevity studies
3. A high-throughput real-time PCR tissue-of-origin test to distinguish blood from lymphoblastoid cell line DNA for (epi)genomic studies
4. Constitutional DNA Polymorphisms Associated with the Plasma Imatinib Concentration in Chronic Myeloid Leukemia Patients.
5. The CEPH aging cohort and biobank: a valuable collection of biological samples from exceptionally long-lived French individuals and their offspring for longevity studies
6. Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosis
7. Improvements and inter-laboratory implementation and optimization of blood-based single-locus age prediction models using DNA methylation of the ELOVL2 promoter
8. Centenarians consistently present a younger epigenetic age than their chronological age with four epigenetic clocks based on a small number of CpG sites
9. Major improvement in the detection of microsatellite instability in colorectal cancer using HSP110 T17 E‐ice‐COLD‐PCR
10. Inbreeding Coefficient Estimation with Dense SNP Data : Comparison of Strategies and Application to HapMap III
11. Could Inbred Cases Identified in GWAS Data Succeed in Detecting Rare Recessive Variants Where Affected Sib-Pairs Have Failed?
12. Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA
13. Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort
14. A new F-box protein 7 gene mutation causing typical Parkinsonʼs disease
15. FSuite: exploiting inbreeding in dense SNP chip and exome data
16. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
17. Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis
18. Tumor DNA hypomethylation of LINE‑1 is associated with low tumor grade of breast cancer in Tunisian patients
19. Significant linkage to spondyloarthropathy on 9q31–34
20. SREBF-1 Gene Polymorphisms Are Associated With Obesity and Type 2 Diabetes in French Obese and Diabetic Cohorts
21. Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum
22. Additional file 2: of 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
23. Major improvement in the detection of microsatellite instability in colorectal cancer using HSP110 T17 E-ice -COLD-PCR
24. 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
25. A new F-box protein 7 gene mutation causing typical Parkinson's disease
26. GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients
27. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
28. High level of inbreeding in final phase of 1000 Genomes Project
29. Major improvement in the detection of microsatellite instability in colorectal cancer using HSP110 T17 E‐<italic>ice</italic>‐COLD‐PCR.
30. Erratum: Genome-wide inbreeding estimation within Lebanese communities using SNP arrays
31. Genome-wide inbreeding estimation within Lebanese communities using SNP arrays
32. Comparative Power of Family-Based Association Strategies to Detect Disease-Causing Variants Under Two-Locus Models
33. Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?
34. Human longevity and 11p15.5: a study in 1321 centenarians
35. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype
36. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
37. Estimating the odds ratios of Crohn disease for the main CARD15/NOD2 mutations using a conditional maximum likelihood method in pedigrees collected via affected family members
38. Genome-wide inbreeding estimation within Lebanese communities using SNP arrays.
39. Foetal haemoglobin in normal healthy adults: relationship with polymorphic sequences cis to the β globin gene
40. A study of French centenarians: are ACE and APOE associated with longevity?
41. The efficiency of genetic analysis of DNA from aged siblings to detect chromosomal regions implicated in longevity
42. Could Inbred Cases Identified in GWAS Data Succeed in Detecting Rare Recessive Variants Where Affected Sib-Pairs Have Failed?
43. Foetal haemoglobin in normal healthy adults: relationship with polymorphic sequences cis to the beta globin gene.
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