(Q29095288)

5

0 references

Piotr Dworzynski

object named as

P. Dworzynski

2

0 references

Tune H Pers

1 reference

ORCID Public Data File 2021

author name string

T. H. Pers

1

0 references

K. Lage

Creative Commons Attribution 3.0 Unported

4

0 references

language of work or name

English

0 references

publication date

22 May 2013

0 references

published in

Nucleic Acids Research

0 references

volume

41

0 references

issue

W1

0 references

page(s)

W104-W108

0 references

copyright license

start time

4 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Exome sequencing and complex disease: practical aspects of rare variant association studies

1 reference

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Hundreds of variants clustered in genomic loci and biological pathways affect human height

6 April 2017

1 reference

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Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

6 April 2017

1 reference

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Network medicine: a network-based approach to human disease

6 April 2017

1 reference

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A human phenome-interactome network of protein complexes implicated in genetic disorders

7 April 2017

1 reference

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ROCR: visualizing classifier performance in R

7 April 2017

1 reference

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Genome-wide association studies for common diseases and complex traits

7 April 2017

1 reference

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Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

7 April 2017

1 reference

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Synthesizing genome-wide association studies and expression microarray reveals novel genes that act in the human growth plate to modulate height

3 June 2018

1 reference

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Computational tools for prioritizing candidate genes: boosting disease gene discovery

3 June 2018

1 reference

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Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants

3 June 2018

1 reference

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The Mouse Genome Database (MGD): comprehensive resource for genetics and genomics of the laboratory mouse

3 June 2018

1 reference

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Protein interaction-based genome-wide analysis of incident coronary heart disease

3 June 2018

1 reference

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Rare-variant association testing for sequencing data with the sequence kernel association test

3 June 2018

1 reference

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Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes

3 June 2018

1 reference

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Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology

3 June 2018

1 reference

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Rare variant association analysis methods for complex traits

3 June 2018

1 reference

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Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk

3 June 2018

1 reference

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Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3692047

CANDID: a flexible method for prioritizing candidate genes for complex human traits.

3 June 2018

1 reference

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Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes

3 June 2018

1 reference

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Gene prioritization through genomic data fusion

3 June 2018

1 reference

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GeneCards 2002: towards a complete, object-oriented, human gene compendium

3 June 2018

1 reference

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A new measure of the effective number of tests, a practical tool for comparing families of non-independent significance tests

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3692047

Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

26 November 2018

1 reference

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Factors affecting the effective number of tests in genetic association studies: a comparative study of three PCA-based methods

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23703204

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKT387

1 reference

DBLP publication ID

journals/nar/PersDTLB13

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

1 reference

PubMed publication ID

23703204

1 reference