(Q26799562)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26210231%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

review article

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title

Genomic risk prediction of complex human disease and its clinical application (English)

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20 February 2020

1

1 reference

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20 February 2020

Michael Inouye

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26210231%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

2

Michael Inouye

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Gad Abraham

series ordinal

1

object named as

Gad Abraham

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language of work or name

English

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publication date

24 July 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26210231%20AND%20SRC:MED&resulttype=core&format=json

Current Opinion in Genetics & Development

20 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26210231%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

volume

33

1 reference

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20 February 2020

page(s)

10-16

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Association between a literature-based genetic risk score and cardiovascular events in women

20 February 2020

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Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

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Newly identified genetic risk variants for celiac disease related to the immune response

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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

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Large-scale association analysis identifies new risk loci for coronary artery disease

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7 January 2021

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

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Multiple common variants for celiac disease influencing immune gene expression

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7 January 2021

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

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Rare and common variants: twenty arguments

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Computational neuroanatomy of speech production.

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7 January 2021

Pitfalls of predicting complex traits from SNPs

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7 January 2021

What are the sensitivity and specificity of serologic tests for celiac disease? Do sensitivity and specificity vary in different populations?

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7 January 2021

The prevalence of celiac disease in average-risk and at-risk Western European populations: a systematic review

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7 January 2021

TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program

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7 January 2021

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk

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7 January 2021

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7 January 2021

MultiBLUP: improved SNP-based prediction for complex traits

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7 January 2021

Joint BSPGHAN and Coeliac UK guidelines for the diagnosis and management of coeliac disease in children

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7 January 2021

Diagnostic tests 2: Predictive values

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7 January 2021

Recent advances in coeliac disease

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7 January 2021

Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants

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7 January 2021

The behavioral response to personalized genetic information: will genetic risk profiles motivate individuals and families to choose more healthful behaviors?

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7 January 2021

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7 January 2021

Prediction of Coronary Heart Disease Using Risk Factor Categories

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7 January 2021

Genetic risk prediction and a 2-stage risk screening strategy for coronary heart disease

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7 January 2021

Multilocus genetic risk scores for coronary heart disease prediction

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7 January 2021

A genetic risk score is associated with incident cardiovascular disease and coronary artery calcium: the Framingham Heart Study

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7 January 2021

Systematic Examination of the Updated Framingham Heart Study General Cardiovascular Risk Profile

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7 January 2021

A blood pressure genetic risk score is a significant predictor of incident cardiovascular events in 32,669 individuals

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7 January 2021

Predicting stroke through genetic risk functions: the CHARGE Risk Score Project

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7 January 2021

Twelve-single nucleotide polymorphism genetic risk score identifies individuals at increased risk for future atrial fibrillation and stroke

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7 January 2021

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7 January 2021

A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways.

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7 January 2021

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7 January 2021

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7 January 2021

Data and theory point to mainly additive genetic variance for complex traits

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Accurate and robust genomic prediction of celiac disease using statistical learning

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7 January 2021

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7 January 2021

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7 January 2021

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Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26210231%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26210231%20AND%20SRC:MED&resulttype=core&format=json