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1. Cluster effect for SNP–SNP interaction pairs for predicting complex traits

2. BUB1B monoallelic germline variants contribute to prostate cancer predisposition by triggering chromosomal instability

4. Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

5. Exome sequencing of affected duos and trios uncovers PRUNE2 as a novel prostate cancer predisposition gene

6. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

7. Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score

10. PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants

11. Aerobic exercise improves central blood pressure and blood pressure variability among patients with resistant hypertension: results of the EnRicH trial

16. The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.

17. Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis

18. Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility

19. Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer.

21. Polygenic hazard score is associated with prostate cancer in multi-ethnic populations.

22. Cellular Aging Secretes: a Comparison of Bone-Marrow-Derived and Induced Mesenchymal Stem Cells and Their Secretome Over Long-Term Culture

23. Haplotype analysis of the internationally distributed BRCA1 c.3331_3334delCAAG founder mutation reveals a common ancestral origin in Iberia

24. The effect of sample size on polygenic hazard models for prostate cancer

25. A Genetic Risk Score to Personalize Prostate Cancer Screening, Applied to Population Data

27. Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes

28. Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry.

30. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

31. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

32. Understanding the complex geomorphology of a deep sea area affected by continental tectonic indentation: The case of the Gulf of Vera (Western Mediterranean)

33. Genetic Cancer Susceptibility in Adolescents and Adults 25 Years or Younger With Colorectal Cancer

35. Polygenic hazard score to guide screening for aggressive prostate cancer: development and validation in large scale cohorts.

37. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

39. Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study

41. Deep Sea Sedimentation

43. Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer

44. Identification of novel candidate predisposing genes in familial nonmedullary thyroid carcinoma implicating DNA damage repair pathways.

46. Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2

47. Observational and genetic associations between cardiorespiratory fitness and cancer : a UK Biobank and international consortia study

48. Observational and genetic associations between cardiorespiratory fitness and cancer:a UK Biobank and international consortia study

49. Initial clinical evidence on biperiden as antiepileptogenic after traumatic brain injury--a randomized clinical trial.

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