(Q36670492)

15 August 2017

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title

The balance between heritable and environmental aetiology of human disease (English)

1 reference

15 August 2017

3

Asta Försti

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15 August 2017

1

Kari Hemminki

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PubMed ID

17139327

15 August 2017

Justo Lorenzo Bermejo

object named as

Justo Lorenzo Bermejo

series ordinal

2

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language of work or name

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1 December 2006

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15 August 2017

Nature Reviews Genetics

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15 August 2017

7

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15 August 2017

958-965

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15 August 2017

12

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https://scigraph.springernature.com/pub.10.1038/nrg2009

15 August 2017

0 references

cites work

Do we need genomic research for the prevention of common diseases with environmental causes?

1 reference

The Causes of Cancer: Quantitative Estimates of Avoidable Risks of Cancer in the United States Today

21 January 2018

1 reference

Balancing life-style and genomics research for disease prevention

21 January 2018

1 reference

Genomic Priorities and Public Health

21 January 2018

1 reference

Dissecting complex disease: the quest for the Philosopher's Stone?

21 January 2018

1 reference

Common susceptibility genes for cancer: search for the end of the rainbow

21 January 2018

1 reference

Genetic epidemiology and public health: hope, hype, and future prospects

21 January 2018

1 reference

Genome-wide association studies: theoretical and practical concerns

21 January 2018

1 reference

Searching for genetic determinants in the new millennium

21 January 2018

1 reference

Genomics and medicine. Dissecting human disease in the postgenomic era.

21 January 2018

1 reference

A self-fulfilling prophecy: are we underestimating the role of the environment in gene-environment interaction research?

21 January 2018

1 reference

Gene-environment interactions in psychiatry: joining forces with neuroscience

21 January 2018

1 reference

Key concepts in genetic epidemiology

21 January 2018

1 reference

Confounding, ascertainment bias, and the blind quest for a genetic 'fountain of youth'.

21 January 2018

1 reference

Population-based family studies in genetic epidemiology

21 January 2018

1 reference

Genetics and the common cancers

21 January 2018

1 reference

Single nucleotide polymorphisms (SNPs) are inherited from parents and they measure heritable events

21 January 2018

1 reference

Relationships between familial risks of cancer and the effects of heritable genes and their SNP variants

21 January 2018

1 reference

Familial risks of cancer as a guide to gene identification and mode of inheritance.

21 January 2018

1 reference

Characterization of BRCA1 and BRCA2 mutations in a large United States sample

21 January 2018

1 reference

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

First experimental demonstration of the multipotential carcinogenic effects of aspartame administered in the feed to Sprague-Dawley rats

21 January 2018

1 reference

Mortality in relation to smoking: 50 years' observations on male British doctors

21 January 2018

1 reference

Studies of cancer in migrants: rationale and methodology

21 January 2018

1 reference

Trends in cancer incidence in Connecticut, 1935-1991.

21 January 2018

1 reference

A census of human cancer genes

21 January 2018

1 reference

Dual origins of Finns revealed by Y chromosome haplotype variation

21 January 2018

1 reference

Finnish and Swedish genotypes and risk of cancer in Sweden

21 January 2018

1 reference

The scandal of poor epidemiological research

21 January 2018

1 reference

How many diseases does it take to map a gene with SNPs?

21 January 2018

1 reference

The allelic architecture of human disease genes: common disease-common variant... or not?

21 January 2018

1 reference

An utter refutation of the "fundamental theorem of the HapMap".

21 January 2018

1 reference

Highly penetrant hereditary cancer syndromes.

21 January 2018

1 reference

Population-Based Study of BRCA1 and BRCA2 Mutations in 1035 Unselected Finnish Breast Cancer Patients

21 January 2018

1 reference

Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer

21 January 2018

1 reference

NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses

21 January 2018

1 reference

Replication validity of genetic association studies

21 January 2018

1 reference

How many genes underlie the occurrence of common complex diseases in the population?

21 January 2018

1 reference

Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.

21 January 2018

1 reference

A systematic review and meta-analysis of familial colorectal cancer risk

21 January 2018

1 reference

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

21 January 2018

1 reference

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

21 January 2018

1 reference

Familial risk of cancer: data for clinical counseling and cancer genetics

21 January 2018

1 reference

Implications of the Human Genome Project for medical science.

21 January 2018

1 reference

Welcome to the genomic era.

21 January 2018

1 reference

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

21 January 2018

1 reference

A common variant associated with prostate cancer in European and African populations.

21 January 2018

1 reference

Variants in the GH-IGF axis confer susceptibility to lung cancer

21 January 2018

1 reference

Epidemiology — identifying the causes and preventability of cancer?

21 January 2018

1 reference

Cancer risks in first-generation immigrants to Sweden

21 January 2018

1 reference

Genetics as a tool to improve cancer outcomes: ethics and policy

21 January 2018

1 reference

The family history--more important than ever

21 January 2018

1 reference

A haplotype map of the human genome

31 March 2020

1 reference

Association mapping of complex diseases in linked regions: estimation of genetic effects and feasibility of testing rare variants

31 March 2020

1 reference

A cohort study of cancer risk in relation to family histories of cancer in the Utah population database

31 March 2020

1 reference

Cancer risks in second-generation immigrants to Sweden

31 March 2020

1 reference

Increasing colorectal cancer incidence rates in Japan

31 March 2020

1 reference

Language replacement in Scandinavia

31 March 2020

1 reference

On the resolution and feasibility of genome scanning approaches

31 March 2020

1 reference

Hereditary colorectal cancer

31 March 2020

1 reference

Cancer epidemiology in migrant populations

31 March 2020

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NRG2009

1 reference

PubMed ID

17139327

Dimensions Publication ID

15 August 2017

0 references

1 reference

PubMed ID

17139327