(Q56565671)

Jean Golding

19

0 references

Jeremy Grimshaw

Jeremy Grimshaw

10

0 references

John Ioannidis

3

John P. A. Ioannidis

0 references

Isabel Fortier

24

Isabel Fortier

0 references

David Moher

4

David Moher

0 references

Marta Gwinn

12

Marta Gwinn

0 references

Muin J. Khoury

7

Muin J. Khoury

0 references

Julian Little

1

Julian Little

0 references

Cornelia M. van Duijn

20

Cornelia van Duijn

0 references

Julian Higgins

2

Julian P. T. Higgins

0 references

George Davey Smith

9

George Davey-Smith

0 references

Claire Infante-Rivard

28

Claire Infante-Rivard

0 references

George Wells

23

George Wells

0 references

Candice Y. Johnson

16

Candice Y. Johnson

0 references

Guang Yong Zou

14

Guang Yong Zou

0 references

Kim Hutchings

15

Kim Hutchings

0 references

Valerie Tait

17

Valerie Tait

0 references

Matthew L Freedman

25

Matthew Freedman

0 references

Maja Zecevic

26

Maja Zecevic

0 references

Nick Birkett

30

Nick Birkett

0 references

author name string

France Gagnon

5

0 references

Barbara Cohen

8

0 references

Paul Scheet

11

0 references

Robin E. Williamson

13

0 references

Miriam Wiens

18

0 references

John McLaughlin

21

0 references

Richard King

27

0 references

Alex Stewart

29

0 references

Andrew Paterson

https://scigraph.springernature.com/pub.10.1007/s00439-008-0592-7

22

0 references

publication date

1 February 2009

0 references

published in

Human Genetics

0 references

volume

125

0 references

issue

2

0 references

page(s)

131-151

0 references

exact match

0 references

cites work

The revised CONSORT statement for reporting randomized trials: explanation and elaboration

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0592-7

Minimum information about a microarray experiment (MIAME)-toward standards for microarray data

21 January 2018

1 reference

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Publication guidelines for improvement studies in health care: evolution of the SQUIRE Project

21 January 2018

1 reference

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When is a "positive" association truly a "positive" in psychiatric genetics? A commentary based on issues debated at the World Congress of Psychiatric Genetics, Boston, October 12-18, 2005.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0592-7

Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0592-7

Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): explanation and elaboration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0592-7

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0592-7

Association studies in asthma genetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0592-7

Does haplotype diversity predict power for association mapping of disease susceptibility?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0592-7

Elaboración de directrices para la publicación de investigación biomédica: proceso y fundamento científico

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0592-7

Reliability of statistical associations between genes and disease

21 January 2018

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12 December 2020

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

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12 December 2020

GERBIL: Genotype resolution and block identification using likelihood

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12 December 2020

Guidelines for human gene nomenclature

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12 December 2020

Use of methodological standards in diagnostic test research. Getting better but still not good.

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12 December 2020

Assessing the quality of case-control association studies on the genetic basis of sepsis

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12 December 2020

A method to address differential bias in genotyping in large-scale association studies

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12 December 2020

Are we ready for genome-wide association studies?

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12 December 2020

Identifying outcome reporting bias in randomised trials on PubMed: review of publications and survey of authors

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12 December 2020

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

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12 December 2020

A common genetic risk factor for colorectal and prostate cancer

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12 December 2020

Evaluating bias due to population stratification in case-control association studies of admixed populations.

1 reference

12 December 2020

Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test

1 reference

12 December 2020

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

1 reference

12 December 2020

Mendelian proportions in a mixed population

1 reference

12 December 2020

Clinical epidemiological quality in molecular genetic research: the need for methodological standards

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12 December 2020

Genome-wide association study identifies novel breast cancer susceptibility loci

1 reference

12 December 2020

Detection of genotyping errors by Hardy-Weinberg equilibrium testing.

1 reference

12 December 2020

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

1 reference

12 December 2020

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

1 reference

12 December 2020

Problems of reporting genetic associations with complex outcomes

1 reference

12 December 2020

The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomized trials

1 reference

12 December 2020

Joint effect of genes and environment distorted by selection biases: implications for hospital-based case-control studies.

1 reference

12 December 2020

Estimation of magnitude in gene-environment interactions in the presence of measurement error.

1 reference

12 December 2020

Jesting Pilate, genetic case-control association studies, and Heart

1 reference

12 December 2020

A second generation human haplotype map of over 3.1 million SNPs

1 reference

12 December 2020

Empirical evidence for selective reporting of outcomes in randomized trials: comparison of protocols to published articles

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12 December 2020

Prospects and pitfalls in whole genome association studies

1 reference

12 December 2020

The human genome project is complete. How do we develop a handle for the pump?

1 reference

12 December 2020

Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays

1 reference

12 December 2020

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

1 reference

12 December 2020

Confounding from cryptic relatedness in case-control association studies

1 reference

12 December 2020

Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms

1 reference

12 December 2020

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

1 reference

12 December 2020

Model-based inference of haplotype block variation.

1 reference

12 December 2020

Missing data imputation and haplotype phase inference for genome-wide association studies

1 reference

12 December 2020

dbSNP: the NCBI database of genetic variation

1 reference

12 December 2020

Comparison of strategies for selecting single nucleotide polymorphisms for case/control association studies

1 reference

12 December 2020

Race and ethnicity in medical research: requirements meet reality.

1 reference

12 December 2020

A common variant on chromosome 9p21 affects the risk of myocardial infarction

1 reference

12 December 2020

On the synthesis and interpretation of consistent but weak gene-disease associations in the era of genome-wide association studies

1 reference

12 December 2020

Using haplotype blocks to map human complex trait loci

1 reference

12 December 2020

Genetic association studies in epilepsy: "the truth is out there".

1 reference

12 December 2020

Candidate gene approach in association studies: would the factor V Leiden mutation have been found by this approach?

1 reference

12 December 2020

A systematic review of the quality of genetic association studies in human sepsis

1 reference

12 December 2020

Outcome reporting bias in randomized trials funded by the Canadian Institutes of Health Research

1 reference

12 December 2020

Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group.

1 reference

12 December 2020

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

1 reference

12 December 2020

Framework for a fully powered risk engine

1 reference

12 December 2020

'Racial' differences in genetic effects for complex diseases

1 reference

12 December 2020

Genetic association studies: time for a new paradigm?

1 reference

12 December 2020

How to interpret a genome-wide association study

1 reference

12 December 2020

Bias in clinical intervention research.

1 reference

12 December 2020

Case-control association studies in pharmacogenetics

1 reference

12 December 2020

Misclassification of genetic susceptibility biomarkers: implications for case-control studies and cross-population comparisons.

1 reference

12 December 2020

How should we use information about HWE in the meta-analyses of genetic association studies?

1 reference

12 December 2020

Genotyping errors: causes, consequences and solutions

1 reference

12 December 2020

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

12 December 2020

The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies

1 reference

12 December 2020

Protecting aggregate genomic data

1 reference

12 December 2020

Nonreplication in genetic studies of complex diseases--lessons learned from studies of osteoporosis and tentative remedies

1 reference

12 December 2020

Imputation-based analysis of association studies: candidate regions and quantitative traits

1 reference

12 December 2020

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

1 reference

12 December 2020

Case-control genetic association studies in gastrointestinal disease: review and recommendations.

1 reference

12 December 2020

The scandal of poor epidemiological research

1 reference

12 December 2020

What makes a good genetic association study?

1 reference

12 December 2020

A Bayesian characterization of Hardy-Weinberg disequilibrium

1 reference

12 December 2020

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

1 reference

12 December 2020

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

1 reference

12 December 2020

Hardy–Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations and power

1 reference

12 December 2020

1 reference

12 December 2020

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

1 reference

12 December 2020

Population stratification and spurious allelic association

1 reference

12 December 2020

The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures

1 reference

12 December 2020

Good prospects for genetic and molecular epidemiologic studies in the European Journal of Epidemiology

1 reference

12 December 2020

Evaluation of candidate genes in case-control studies: a statistical method to account for related subjects

1 reference

12 December 2020

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

1 reference

12 December 2020

Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure.

1 reference

12 December 2020

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

1 reference

12 December 2020

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

1 reference

12 December 2020

Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wi

1 reference

12 December 2020

A network of investigator networks in human genome epidemiology

1 reference

12 December 2020

Multiple regions within 8q24 independently affect risk for prostate cancer

1 reference

12 December 2020

A common allele on chromosome 9 associated with coronary heart disease

1 reference

12 December 2020

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

1 reference

12 December 2020

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

12 December 2020

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

12 December 2020

Methodologic quality and genotyping reproducibility in studies of tumor necrosis factor -308 G-->A single nucleotide polymorphism and bacterial sepsis: implications for studies of complex traits

1 reference

12 December 2020

Positive results in association studies are associated with departure from Hardy-Weinberg equilibrium: hint for genotyping error?

1 reference

12 December 2020

The Reliable Identification of Disease-Gene Associations

1 reference

12 December 2020

Publication environment and broad investigation of the genome

1 reference

12 December 2020

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

1 reference

12 December 2020

Quality control in molecular genetic testing

1 reference

12 December 2020

The impact of SNP density on fine-scale patterns of linkage disequilibrium

1 reference

12 December 2020

Assessing the impact of population stratification on genetic association studies

1 reference

12 December 2020

Non-replication and inconsistency in the genome-wide association setting

1 reference

12 December 2020

Bias in psychiatric case-control studies: literature survey

1 reference

12 December 2020

The merits of testing Hardy-Weinberg equilibrium in the analysis of unmatched case-control data: a cautionary note

1 reference

12 December 2020

Associations, populations, and the truth: recommendations for genetic association studies in Arthritis & Rheumatism

1 reference

12 December 2020

SNP judgments and freedom of association

1 reference

12 December 2020

Estimation of pairwise relatedness with molecular markers.

1 reference

12 December 2020

A road map for efficient and reliable human genome epidemiology

1 reference

12 December 2020

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

12 December 2020

Genetic variation and cancer: improving the environment for publication of association studies

1 reference

12 December 2020

Point: population stratification: a problem for case-control studies of candidate-gene associations?

1 reference

12 December 2020

A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies

1 reference

12 December 2020

Guidelines for conducting and reporting whole genome/large-scale association studies.

1 reference

12 December 2020

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

1 reference

12 December 2020

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

1 reference

12 December 2020

Association study designs for complex diseases

1 reference

12 December 2020

The design, execution, and interpretation of genetic association studies to decipher complex diseases.

1 reference

12 December 2020

Publication policy or publication bias?

1 reference

12 December 2020

Robustness of case-control studies of genetic factors to population stratification: magnitude of bias and type I error.

1 reference

12 December 2020

Population structure, differential bias and genomic control in a large-scale, case-control association study

1 reference

12 December 2020

Replicating genotype-phenotype associations

1 reference

12 December 2020

Gm3;5,13,14 and type 2 diabetes mellitus: an association in American Indians with genetic admixture

1 reference

12 December 2020

Genetic association studies in Thorax

1 reference

12 December 2020

Measuring departures from Hardy-Weinberg: a Markov chain Monte Carlo method for estimating the inbreeding coefficient.

1 reference

12 December 2020

The effects of human population structure on large genetic association studies

1 reference

12 December 2020

Impact of Violations and Deviations in Hardy-Weinberg Equilibrium on Postulated Gene-Disease Associations

1 reference

12 December 2020

Tracking the epidemiology of human genes in the literature: the HuGE Published Literature database

1 reference

12 December 2020

An empirical evaluation of multifarious outcomes in pharmacogenetics: beta-2 adrenoceptor gene polymorphisms in asthma treatment

1 reference

12 December 2020

CYP3A4-V and prostate cancer in African Americans: causal or confounding association because of population stratification?

1 reference

12 December 2020

Genew: the human gene nomenclature database

1 reference

12 December 2020

Issues in the reporting of epidemiological studies: a survey of recent practice

1 reference

12 December 2020

A tutorial on statistical methods for population association studies

1 reference

12 December 2020

Recommendations for Reporting of Clinical Research Studies

1 reference

12 December 2020

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

12 December 2020

Proposed guidelines for papers describing DNA polymorphism-disease associations.

1 reference

12 December 2020

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

1 reference

12 December 2020

Reporting of human genome epidemiology (HuGE) association studies: an empirical assessment

1 reference

12 December 2020

Guidelines for association studies in Human Molecular Genetics

1 reference

12 December 2020

Turning the Pump Handle: Evolving Methods for Integrating the Evidence on Gene-Disease Association

1 reference

12 December 2020

Genetic association studies in Alzheimer's disease research: challenges and opportunities

1 reference

12 December 2020

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

1 reference

12 December 2020

Reflections on publication criteria for genetic association studies

1 reference

12 December 2020