Germline copy number variation analysis in Finnish families with hereditary prostate cancer.

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Germline copy number variations are associated with breast cancer risk and prognosis.Candidate predisposing germline copy number variants in early onset colorectal cancer patients.Expressional profiling of prostate cancer risk SNPs at 11q13.5 identifies DGAT2 as a new target gene.

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P2860

Germline copy number variation analysis in Finnish families with hereditary prostate cancer.

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name

Germline copy number variation ...... th hereditary prostate cancer.

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Germline copy number variation ...... th hereditary prostate cancer.

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Germline copy number variation ...... th hereditary prostate cancer.

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Germline copy number variation ...... th hereditary prostate cancer.

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Teuvo L J Tammela

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Tiina Wahlfors

http://www.w3.org/2001/XMLSchema#string

Tommi Rantapero

http://www.w3.org/2001/XMLSchema#string

Virpi H Laitinen

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P2860

Copy number variation at 1q21.1 associated with neuroblastoma

PLINK: a tool set for whole-genome association and population-based linkage analyses

WebGestalt: an integrated system for exploring gene sets in various biological contexts.

Germline mutations in the ribonuclease L gene in families showing linkage with HPC1

BEDTools: a flexible suite of utilities for comparing genomic features.

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

PALB2 variants in hereditary and unselected Finnish prostate cancer cases.

Molecular genetics of the Finnish disease heritage.

Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients.

Human prostate cancer risk factors.

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316-324

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scholarly article

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10.1002/PROS.23123

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http://www.w3.org/2001/XMLSchema#string

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http://www.w3.org/2001/XMLSchema#string

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Johanna Schleutker

Oyediran Akinrinade

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2015-11-10T00:00:00Z

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283687921

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26552734

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P921

Finland

Germline copy number variation analysis in Finnish families with hereditary prostate cancer.

about

P2860

P2860

Germline copy number variation analysis in Finnish families with hereditary prostate cancer.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921