Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families. - Wikidata - wikimedia - TriplyDB

Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families.

Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families.

http://www.wikidata.org/entity/Q37131918

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Genetic-epigenetic interactions in cis: a major focus in the post-GWAS era Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study Novel Implications in Molecular Diagnosis of Lynch Syndrome.

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Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families.

http://www.wikidata.org/entity/Q37131918

description

article científic

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article scientifique

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artigo científico

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bilimsel makale

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scientific article published on 20 July 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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Polygenic risk score is associ ...... innish breast cancer families.

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Polygenic risk score is associ ...... innish breast cancer families.

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Polygenic risk score is associ ...... innish breast cancer families.

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Polygenic risk score is associ ...... innish breast cancer families.

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Polygenic risk score is associ ...... innish breast cancer families.

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Polygenic risk score is associ ...... innish breast cancer families.

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S10549-016-3897-6

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Breast Cancer Research and Treatment

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Polygenic risk score is associ ...... innish breast cancer families.

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Andrew Lee

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Kristiina Aittomäki

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Rainer Fagerholm

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P2860

DNA sequencing with chain-terminating inhibitors

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

Large-scale genotyping identifies 41 new loci associated with breast cancer risk.

Missing heritability and strategies for finding the underlying causes of complex disease

Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease.

An approximate model of polygenic inheritance.

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes.

Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

The contributions of breast density and common genetic variation to breast cancer risk

CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer.

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Kristiina Aittomäki

Heli Nevanlinna

Douglas F. Easton

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