(Q36542324)

14 August 2017

1 reference

title

Case-control studies in the genomic era: a clinician's guide (English)

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14 August 2017

Daniel G Healy

1

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14 August 2017

1 August 2006

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14 August 2017

1 reference

14 August 2017

5

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14 August 2017

701-707

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14 August 2017

8

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Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?

14 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Complement factor H variant increases the risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Complement factor H polymorphism and age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Variation is the spice of life

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Tackling common disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Localization and identification of human quantitative trait loci: king harvest has surely come

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

MULTIFACTORIAL GENETICSUNDERSTANDING QUANTITATIVE GENETIC VARIATION

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Functional analysis of human promoter polymorphisms.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

A Gene Map of the Human Genome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Initial sequencing and analysis of the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The Sequence of the Human Genome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Human genome. HapMap launched with pledges of $100 million

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Genetics of idiopathic epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

New strategies for the identification of drugs to prevent the development or progression of epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The future of association studies: gene-based analysis and replication

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Applications of whole-genome high-density SNP genotyping

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Toward genome-wide SNP genotyping

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Islands of linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The structure of haplotype blocks in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Haplotype tagging for the identification of common disease genes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Genome scans and candidate gene approaches in the study of common diseases and variable drug responses

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

A single-nucleotide polymorphism tagging set for human drug metabolism and transport

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Optimal selection of SNP markers for disease association studies.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Mapping complex disease loci in whole-genome association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

A comprehensive review of genetic association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Replication validity of genetic association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The human phenome project

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Research criteria for defining patients with CIDP.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Systematic review of methods and results of studies of the genetic epidemiology of ischemic stroke

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Subarachnoid haemorrhage in first and second degree relatives of patients with subarachnoid haemorrhage

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Is family history an independent risk factor for stroke?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Genetic association studies in stroke: methodological issues and proposed standard criteria

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Potential biological markers for cerebrovascular disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Silent stroke: pathogenesis, genetic factors and clinical implications as a risk factor

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Pharmacogenetics goes genomic

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

UCHL-1 gene in multiple system atrophy: a haplotype tagging approach

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Epidemiological evidence on multiple system atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Association of genetic loci: replication or not, that is the question

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Parameters for reliable results in genetic association studies in common disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Problems of reporting genetic associations with complex outcomes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Allelic association of human dopamine D2 receptor gene in alcoholism

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The A1 allele at the D2 dopamine receptor gene and alcoholism. A reappraisal

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Population stratification and spurious allelic association

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Testing for population subdivision and association in four case-control studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Population stratification in epidemiologic studies of common genetic variants and cancer: quantification of bias

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

An Icelandic example of the impact of population structure on association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Genotype-environment interaction in transmission disequilibrium tests

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Genomic control for association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Use of unlinked genetic markers to detect population stratification in association studies.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Control of confounding of genetic associations in stratified populations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Detecting association in a case-control study while correcting for population stratification

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The file drawer problem and tolerance for null results

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The old file-drawer problem.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Meta-analysis in clinical trials

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Pharmacogenetics in the laboratory and the clinic.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Finding Functional Features in Saccharomyces Genomes by Phylogenetic Footprinting

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Neurogenomics: at the intersection of neurobiology and genome sciences

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

The ENCODE (ENCyclopedia Of DNA Elements) Project

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Comparative genomics, genome cross-referencing and XREFdb

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Initial sequence of the chimpanzee genome and comparison with the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Mouse-human comparative map resources on the Web.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Single-cell transcriptional analysis of neuronal progenitors

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

BRCA1--lots of mutations, lots of dilemmas

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Diagnostic testing in neurogenetics. Principles, limitations, and ethical considerations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

Physicians' knowledge of genetics and genetic tests

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970524-5

7 January 2021

10.1016/S1474-4422(06)70524-5

Identifiers

DOI

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14 August 2017

1 reference

PubMed ID

16857576