A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer. - Wikidata - awgldk - TriplyDB

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.

http://www.wikidata.org/entity/Q36582798

about

Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology In search of low-frequency and rare variants affecting complex traits A comparison of genetic risk score with family history for estimating prostate cancer risk Insights into metabolic disease from studying genetics in isolated populations: stories from Greece to Greenland Rare-variant association analysis: study designs and statistical tests The MKK7 p.Glu116Lys Rare Variant Serves as a Predictor for Lung Cancer Risk and Prognosis in Chinese.Mapping asthma-associated variants in admixed populations Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort Progress in methods for rare variant association Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.Rare and low-frequency coding variants alter human adult height The perfect neuroimaging-genetics-computation storm: collision of petabytes of data, millions of hardware devices and thousands of software tools A Pilot Genome-Wide Association Study Identifies Potential Metabolic Pathways Involved in Tinnitus.Reducing INDEL calling errors in whole genome and exome sequencing data.Prediction of potential cancer-risk regions based on transcriptome data: towards a comprehensive view Prostate cancer risk regions at 8q24 and 17q24 are differentially associated with somatic TMPRSS2:ERG fusion status.Prediction of gene expression with cis-SNPs using mixed models and regularization methods Loss-of-function mutations in SLC30A8 protect against type 2 diabetes Genotyping the High Altitude Mestizo Ecuadorian Population Affected with Prostate Cancer Prostate cancer risk alleles are associated with prostate cancer volume and prostate size.Distribution and medical impact of loss-of-function variants in the Finnish founder population.Discussing race-related limitations of genomic testing for colon cancer risk: implications for education and counseling.Prostate cancer in young men: an important clinical entity.A comprehensive resequence-analysis of 250 kb region of 8q24.21 in men of African ancestry Inactivating Mutations in GT198 in Familial and Early-Onset Breast and Ovarian Cancers.Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants Using genetically isolated populations to understand the genomic basis of disease.Prostate cancer risk locus at 8q24 as a regulatory hub by physical interactions with multiple genomic loci across the genome.A rare 8q24 single nucleotide polymorphism (SNP) predisposes North American men to prostate cancer and possibly more aggressive disease Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets.Genetics of complex traits in psychiatry Prostate cancer in East Asia: evolving trend over the last decade.Personalized sequencing and the future of medicine: discovery, diagnosis and defeat of disease.Rare variant association studies: considerations, challenges and opportunities.Genetic dissection of Anopheles gambiae gut epithelial responses to Serratia marcescens Rare variants detection with kernel machine learning based on likelihood ratio test.Assessing the Power of Exome Chips.Germline HOXB13 p.Gly84Glu mutation and cancer susceptibility: a pooled analysis of 25 epidemiological studies with 145,257 participates.Association of three 8q24 polymorphisms with prostate cancer susceptibility: evidence from a meta-analysis with 50,854 subjects.KNOWLEDGE DRIVEN BINNING AND PHEWAS ANALYSIS IN MARSHFIELD PERSONALIZED MEDICINE RESEARCH PROJECT USING BIOBIN

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A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.

http://www.wikidata.org/entity/Q36582798

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A study based on whole-genome ...... sociated with prostate cancer.

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A study based on whole-genome ...... sociated with prostate cancer.

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Nature Genetics

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Asgeir Sigurdsson

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Bjarni A Agnarsson

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Brian T Helfand

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Droplaug N Magnusdottir

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Eirikur Jonsson

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Fernando Fuertes

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Freddy C Hamdy

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Gisli Masson

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Gudmundur V Einarsson

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Hafdis Th Helgadottir

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Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family

Genome-wide association study identifies novel breast cancer susceptibility loci

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

Mutations in BRIP1 confer high risk of ovarian cancer

Germline mutations in HOXB13 and prostate-cancer risk

Discovery of common variants associated with low TSH levels and thyroid cancer risk

A new multipoint method for genome-wide association studies by imputation of genotypes

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

Detection of sharing by descent, long-range phasing and haplotype imputation.

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

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1326-1329

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10.1038/NG.2437

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12

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44

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Gudmar Thorleifsson

Unnur Þorsteinsdóttir

Daniel F Gudbjartsson

Laufey Tryggvadottir

Hrefna Johannsdottir

Adalbjorg Jonasdottir

Lambertus Kiemeney

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2012-10-28T00:00:00Z

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232720491

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23104005

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3562711

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