Replicating genotype-phenotype associations (Q29614919)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17554299

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Abecasis G

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Boehnke M

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Bailey-Wilson JE

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Boerwinkle E

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Daly M

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Chanock SJ

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Altshuler D

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Donnelly P

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Wacholder S

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Hunter DJ

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Manolio T

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Ellen M. Wijsman

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object named as

Wijsman EM

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Vogan KJ

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Collins FS

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Freimer NB

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Palmer LJ

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Rotimi C

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author name string

Thomas G

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Hirschhorn JN

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Brooks LD

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Cardon LR

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Fraumeni JF Jr

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Gerhard DS

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Gunter C

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Guttmacher AE

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Guyer MS

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Harris EL

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Hoh J

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Hoover R

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Kong CA

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Merikangas KR

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Morton CC

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Phimister EG

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Rice JP

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Roberts J

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17554299

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Tucker MA

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Winn DM

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17554299

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language of work or name

1 reference

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publication date

7 June 2007

1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17554299

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volume

447

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issue

7145

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30 April 2017

page(s)

655-60

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17554299

Finishing the euchromatic sequence of the human genome

30 April 2017

cites work

1 reference

7 January 2021

A haplotype map of the human genome

1 reference

7 January 2021

Whole-genome patterns of common DNA variation in three human populations

1 reference

7 January 2021

A comprehensive review of genetic association studies

1 reference

7 January 2021

Replication validity of genetic association studies

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

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7 January 2021

Common genetic variants for breast cancer: 32 largely refuted candidates and larger prospects

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Statistical false positive or true disease pathway?

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

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7 January 2021

Determinants of the success of whole-genome association testing

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7 January 2021

Variants in common diseases

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7 January 2021

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

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7 January 2021

Analysis of the type 2 diabetes gene, TCF7L2, in 13,795 type 1 diabetes cases and control subjects

1 reference

7 January 2021

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

1 reference

7 January 2021

Association Analysis of 6,736 U.K. Subjects Provides Replication and ConfirmsTCF7L2as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk

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7 January 2021

Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals

1 reference

7 January 2021

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

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7 January 2021

A genome-wide association study identifies novel risk loci for type 2 diabetes

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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Differential effects of NOD2 variants on Crohn's disease risk and phenotype in diverse populations: a metaanalysis.

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Complement factor H polymorphism and age-related macular degeneration

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7 January 2021

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

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7 January 2021

Complement factor H polymorphism in age-related macular degeneration

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7 January 2021

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

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7 January 2021

Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men.

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7 January 2021

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

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7 January 2021

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

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7 January 2021

Multiple regions within 8q24 independently affect risk for prostate cancer

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7 January 2021

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

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7 January 2021

Problems of reporting genetic associations with complex outcomes

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7 January 2021

Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases.

1 reference

7 January 2021

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

1 reference

7 January 2021

The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease

1 reference

7 January 2021

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.

1 reference

7 January 2021

Association of the DTNBP1 locus with schizophrenia in a U.S. population

1 reference

7 January 2021

Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

1 reference

7 January 2021

Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia

1 reference

7 January 2021

A common genetic variant is associated with adult and childhood obesity

1 reference

7 January 2021

INSIG-2 promoter polymorphism and obesity related phenotypes: association study in 1428 members of 248 families

1 reference

7 January 2021

Comment on "A common genetic variant is associated with adult and childhood obesity"

1 reference

7 January 2021

Comment on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity"

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7 January 2021

Comment on "A common genetic variant is associated with adult and childhood obesity"

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7 January 2021

Comment on the phosphodiesterase 4D replication study by Bevan et al

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7 January 2021

Many hypotheses but no replication for the association between PDE4D and stroke

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7 January 2021

Genes, environment and the value of prospective cohort studies

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7 January 2021

Using linkage genome scans to improve power of association in genome scans

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7 January 2021

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

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7 January 2021

The future of genetic studies of complex human diseases

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7 January 2021

Searching for genetic determinants in the new millennium

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7 January 2021

The interpretation of epidemiologic studies

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7 January 2021

Overcoming the winner's curse: estimating penetrance parameters from case-control data

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7 January 2021

Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium.

1 reference

7 January 2021

Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus

1 reference

7 January 2021

The human phenome project

1 reference

7 January 2021

The endophenotype concept in psychiatric genetics

1 reference

7 January 2021

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

1 reference

7 January 2021

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

7 January 2021

Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population.

1 reference

7 January 2021

A genetic variation of the transcription factor 7-like 2 gene is associated with risk of type 2 diabetes in the Japanese population

1 reference

7 January 2021

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

1 reference

7 January 2021

High-resolution whole-genome association study of Parkinson disease.

1 reference

7 January 2021

Considerations for genomewide association studies in Parkinson disease

1 reference

7 January 2021

Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease

1 reference

7 January 2021

Genomewide association, Parkinson disease, and PARK10

1 reference

7 January 2021

No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

1 reference

7 January 2021

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan

1 reference

7 January 2021

Replication publication

1 reference

7 January 2021

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

1 reference

7 January 2021

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

1 reference

7 January 2021

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

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7 January 2021

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

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7 January 2021

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17554299

Identifiers

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1027012183

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17554299

PubMed publication ID

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017