About: Angela Risch

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) chercheuse (fr) investigadora (es) ഗവേഷക (ml) araştırmacı (tr) wetenschapper (nl) дослідниця (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast)
rdfs:label	Angela Risch (en) Angela Risch (es) Angela Risch (it) Angela Risch (nl) Angela Risch (ast)
skos:prefLabel	Angela Risch (en) Angela Risch (es) Angela Risch (it) Angela Risch (nl) Angela Risch (ast)
name	Angela Risch (en) Angela Risch (es) Angela Risch (it) Angela Risch (nl) Angela Risch (ast)
given name	wds:Q40580057-E1E077FC-3859-4F2D-A6CB-4B5D3D944DD4
given name	Angela
instance of	wds:Q40580057-93FAD782-5CB9-4D4F-AF21-85EB86C4D396
instance of	Homo sapiens
occupation	wds:Q40580057-7E32D08B-8652-4197-8C62-A51B086657E8
sex or gender	wds:Q40580057-36CD9B4C-C601-488F-9E52-65A557EA6E6E
VIAF ID	wds:Q40580057-5835C0FF-75EE-4E27-B4D9-2AE393A28CE4
GND ID	wds:Q40580057-511064d5-a922-41d4-80df-9bcec4caede9
WorldCat Identities ID (superseded)	wds:Q40580057-5698BFE3-B211-4C32-84BA-99535A2797E8
VIAF ID	http://viaf.org/viaf/317082479
GND ID	https://d-nb.info/gnd/1076185630
occupation	researcher
sex or gender	female organism
VIAF ID	317082479
GND ID	1076185630
WorldCat Identities ID (superseded)	viaf-317082479
ORCID iD	wds:Q40580057-D33B509B-BC8F-4810-812B-CB403A27C0D9
ORCID iD	https://orcid.org/0000-0002-8026-5505
ORCID iD	0000-0002-8026-5505
ResearcherID	wds:Q40580057-7AD946DA-B449-4D9B-8678-949C7D942882
Publons author ID	wds:Q40580057-0bcf1337-e205-456c-95c0-e9ca35a17d44
ResearcherID	H-2669-2013
Publons author ID	1590965
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q40580057
is author of	Short telomeres in patients with vascular dementia: an indicator of low antioxidative capacity and a possible risk factor? Specific combinations of DNA repair gene variants and increased risk for non-small cell lung cancer. Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study Informed conditioning on clinical covariates increases power in case-control association studies Slow N-acetylation genotype is a susceptibility factor in occupational and smoking related bladder cancer. Metabolic gene polymorphisms and lung cancer risk in non-smokers. An update of the GSEC study Metabolic gene polymorphism frequencies in control populations Rapid screening assay for mutagen sensitivity and DNA repair capacity in human peripheral blood lymphocytes Meta- and pooled analysis of GSTP1 polymorphism and lung cancer: a HuGE-GSEC review Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium Polymorphisms in transporter and phase II metabolism genes as potential modifiers of the predisposition to and treatment outcome of de novo acute myeloid leukemia in Israeli ethnic groups Polymorphisms in ABCG2, ABCC3 and CNT1 genes and their possible impact on chemotherapy outcome of lung cancer patients. A comprehensive study of polymorphisms inABCB1, ABCC2andABCG2and lung cancer chemotherapy response and prognosis Polymorphisms in the Apoptotic Pathway Gene BCL-2 and Survival in Small Cell Lung Cancer Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer International Lung Cancer Consortium: pooled analysis of sequence variants in DNA repair and cell cycle pathways Principles for the post-GWAS functional characterization of cancer risk loci Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations The CYP3A4*1B allele increases risk for small cell lung cancer: effect of gender and smoking dose Effect of NAT1 and NAT2 genetic polymorphisms on colorectal cancer risk associated with exposure to tobacco smoke and meat consumption SULT1A1 genotype and susceptibility to colorectal cancer. Occupation, exposure to polycyclic aromatic hydrocarbons and laryngeal cancer risk Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls Genotyping human polymorphic arylamine N-acetyltransferase: identification of new slow allotypic variants. Genome-wide prediction of splice-modifying SNPs in human genes using a new analysis pipeline called AASsites A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma Lung cancer epigenetics and genetics Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls Comparison of pathway analysis approaches using lung cancer GWAS data sets A common coding variant in CASP8 is associated with breast cancer risk Comparison of multiple DNA adduct types in tumor adjacent human lung tissue: effect of cigarette smoking Long noncoding RNA TARID directs demethylation and activation of the tumor suppressor TCF21 via GADD45A. Matrix metalloproteinase 1 (MMP1) is associated with early-onset lung cancer Mapping AAC1 AAC2 and AACP, the genes for arylamine N-acetyltransferases, carcinogen metabolising enzymes on human chromosome 8p22, a region frequently deleted in tumours Myeloperoxidase (MPO) genotype and lung cancer histologic types: the MPO -463 A allele is associated with reduced risk for small cell lung cancer in smokers

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