New common variants affecting susceptibility to basal cell carcinoma - Test2 - elhamkhani - TriplyDB

New common variants affecting susceptibility to basal cell carcinoma

New common variants affecting susceptibility to basal cell carcinoma

http://www.wikidata.org/entity/Q24615109

about

Krüppel-like factors: three fingers in control Functional characterization of CLPTM1L as a lung cancer risk candidate gene in the 5p15.33 locus Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"Imputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33 A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis Mammalian Krüppel-like factors in health and diseases Genetic variations in TERT-CLPTM1L genes and risk of squamous cell carcinoma of the head and neck Pancreatic Cancer Genetics Long Non-Coding RNAs as Master Regulators in Cardiovascular Diseases Long Non-coding RNA ANRIL and Polycomb in Human Cancers and Cardiovascular Disease Epidemiology and Inherited Predisposition for Sporadic Pancreatic Adenocarcinoma Defining keratin protein function in skin epithelia: epidermolysis bullosa simplex and its aftermath Long non-coding RNAs and complex human diseases The Triple-Code Model for Pancreatic Cancer: Cross Talk Among Genetics, Epigenetics, and Nuclear Structure Telomerase reverse transcriptase locus polymorphisms and cancer risk: a field synopsis and meta-analysis Variation at the TERT locus and predisposition for cancer A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese Genetics of type 2 diabetes: pathophysiologic and clinical relevance Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk TERT gene harbors multiple variants associated with pancreatic cancer susceptibility Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications The long non-coding RNA ANRIL promotes proliferation and cell cycle progression and inhibits apoptosis and senescence in epithelial ovarian cancer ANRIL: molecular mechanisms and implications in human health The identification of two regulatory ESCC susceptibility genetic variants in the TERT-CLPTM1L loci Functional evaluation of TERT-CLPTM1L genetic variants associated with susceptibility of papillary thyroid carcinoma Characterization of population-based variation and putative functional elements for the multiple-cancer susceptibility loci at 5p15.33 CLPTM1L is overexpressed in lung cancer and associated with apoptosis The emergence of human-evolutionary medical genomics Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21 Genetic variants at 9p21.3 are associated with risk of esophageal squamous cell carcinoma in a Chinese population

P2860

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P2860

New common variants affecting susceptibility to basal cell carcinoma

http://www.wikidata.org/entity/Q24615109

description

2009 nî lūn-bûn

@nan

2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

New common variants affecting susceptibility to basal cell carcinoma

@ast

New common variants affecting susceptibility to basal cell carcinoma

@en

New common variants affecting susceptibility to basal cell carcinoma

@nl

type

label

New common variants affecting susceptibility to basal cell carcinoma

@ast

New common variants affecting susceptibility to basal cell carcinoma

@en

New common variants affecting susceptibility to basal cell carcinoma

@nl

prefLabel

New common variants affecting susceptibility to basal cell carcinoma

@ast

New common variants affecting susceptibility to basal cell carcinoma

@en

New common variants affecting susceptibility to basal cell carcinoma

@nl

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Nature Genetics

P1476

New common variants affecting susceptibility to basal cell carcinoma

@en

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Asgeir Sigurdsson

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Bardur Sigurgeirsson

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Berta Saez

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Cristina Corredera

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Dominique Scherer

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Droplaug N Magnusdottir

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Eugene Gurzau

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Gisli Masson

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Hilma Holm

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Hjördis Bjarnason

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P2860

Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution

The genetic basis of Weber-Cockayne epidermolysis bullosa simplex

MicroRNA-29 family reverts aberrant methylation in lung cancer by targeting DNA methyltransferases 3A and 3B

Quantifying heterogeneity in a meta-analysis

Genetic determinants of hair, eye and skin pigmentation in Europeans

Many sequence variants affecting diversity of adult human height

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

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909-14

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1601052

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10.1038/NG.412

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8

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41

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Gudmar Thorleifsson

Unnur Þorsteinsdóttir

Valgerdur Steinthorsdottir

Daniel F Gudbjartsson

Solveig Gretarsdottir

Jona Saemundsdottir

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2009-08-01T00:00:00Z

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26648277

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1033015538

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19578363

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2973331

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