about
TP53-binding protein variants and breast cancer risk: a case-control studyAbove and beyond state-of-the-art approaches to investigate sequence data: summary of methods and results from the population-based association group at the Genetic Analysis Workshop 19Using next-generation DNA sequence data for genetic association tests based on allele counts with and without consideration of zero inflation.The 'common disease-common variant' hypothesis and familial risks.Socio-economic status and overall and cause-specific mortality in SwedenRepresentation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis.The updated Swedish family-cancer database used to assess familial risks of prostate cancer during rapidly increasing incidence.Subtypes of Native American ancestry and leading causes of death: Mapuche ancestry-specific associations with gallbladder cancer risk in Chile.Contribution of the Defective BRCA1, BRCA2 and CHEK2 Genes to the Familial Aggregation of Breast Cancer: a Simulation Study Based on the Swedish Family-Cancer DatabaseTumor location and patient characteristics of colon and rectal adenocarcinomas in relation to survival and TNM classes.Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk.Association of inherited variation in Toll-like receptor genes with malignant melanoma susceptibility and survivalNuclear expression of the deubiquitinase CYLD is associated with improved survival in human hepatocellular carcinoma.Accuracy of estimation of graft size for living-related liver transplantation: first results of a semi-automated interactive software for CT-volumetry.Assessing responsiveness of health care services within a health insurance scheme in Nigeria: users' perspectives.Influence of genetic variants in type I interferon genes on melanoma survival and therapy.Variants at the 9p21 locus and melanoma riskBeyond cell death - antiapoptotic Bcl-2 proteins regulate migration and invasion of colorectal cancer cells in vitroLocal and global ancestry inference and applications to genetic association analysis for admixed populations.Performance evaluation of a health insurance in Nigeria using optimal resource use: health care providers perspectives.Neonatal variables, altitude of residence and Aymara ancestry in northern Chile.User experience with a health insurance coverage and benefit-package access: implications for policy implementation towards expansion in Nigeria.Genetic epidemiology of cancer: from families to heritable genes.Chemotherapy with BCNU in recurrent glioma: Analysis of clinical outcome and side effects in chemotherapy-naïve patients.High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients.Relationships between familial risks of cancer and the effects of heritable genes and their SNP variants.Familial risks and temporal incidence trends of multiple myeloma.The balance between heritable and environmental aetiology of human disease.Etiologic impact of known cancer susceptibility genes.Single-dose radiosurgical treatment for hepatic metastases--therapeutic outcome of 138 treated lesions from a single institution.Circulating fibronectin controls tumor growthWhole brain helical Tomotherapy with integrated boost for brain metastases in patients with malignant melanoma-a randomized trial.Long-term oncological outcomes after laparoscopic radical prostatectomy.Prostate cancer screening, changing age-specific incidence trends and implications on familial risk.Application of the lymphocyte Cytokinesis-Block Micronucleus Assay to populations exposed to petroleum and its derivatives: Results from a systematic review and meta-analysis.Methylome analysis and integrative profiling of human HCCs identify novel protumorigenic factors.Robust logistic regression to narrow down the winner's curse for rare and recessive susceptibility variants.Environmental exposure to benzene, micronucleus formation and polymorphisms in DNA-repair genes: a pilot study.Prognostic factors and long-term survival in surgically treated brain metastases from non-small cell lung cancer.Inherited variability in a master regulator polymorphism (rs4846126) associates with survival in 5-FU treated colorectal cancer patients.
P50
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P50
description
hulumtues
@sq
researcher
@en
ricercatore
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wetenschapper
@nl
հետազոտող
@hy
name
Justo Lorenzo Bermejo
@ast
Justo Lorenzo Bermejo
@en
Justo Lorenzo Bermejo
@es
Justo Lorenzo Bermejo
@nl
Justo Lorenzo Bermejo
@sl
type
label
Justo Lorenzo Bermejo
@ast
Justo Lorenzo Bermejo
@en
Justo Lorenzo Bermejo
@es
Justo Lorenzo Bermejo
@nl
Justo Lorenzo Bermejo
@sl
prefLabel
Justo Lorenzo Bermejo
@ast
Justo Lorenzo Bermejo
@en
Justo Lorenzo Bermejo
@es
Justo Lorenzo Bermejo
@nl
Justo Lorenzo Bermejo
@sl
P214
P227
P106
P21
P214
P227
P31
P496
0000-0002-6568-5333
P569
1972-01-01T00:00:00Z
P7859
viaf-45243501