(Q34587101)

3 August 2017

A Markov chain Monte Carlo technique for identification of combinations of allelic variants underlying complex diseases in humans (English)

1 reference

3 August 2017

Markov chain Monte Carlo

1 reference

0 references

Olga O Favorova

4

0 references

author name string

Alexander V Favorov

1

1 reference

3 August 2017

Timophey V Andreewski

2

1 reference

3 August 2017

Marina A Sudomoina

3

1 reference

3 August 2017

Giovanni Parmigiani

5

1 reference

3 August 2017

Michael F Ochs

6

1 reference

3 August 2017

language of work or name

English

0 references

publication date

22 August 2005

1 reference

3 August 2017

1 reference

3 August 2017

171

1 reference

3 August 2017

4

1 reference

3 August 2017

2113-2121

1 reference

Genetics, statistics and human disease: analytical retooling for complexity

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

The Bayesian revolution in genetics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

The International HapMap Project

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

Finding genes influencing susceptibility to complex diseases in the post-genome era.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

A physical map of the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

The Sequence of the Human Genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

dbSNP: the NCBI database of genetic variation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

Empirical bayes methods and false discovery rates for microarrays

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

Candidate-gene approaches for studying complex genetic traits: practical considerations

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

Sequence analysis using logic regression.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1456130

Association and linkage of juvenile MS with HLA-DR2(15) in Russians

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16118183

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifying interacting SNPs using Monte Carlo logic regression

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16118183

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The chemokine receptor CCR5 deletion mutation is associated with MS in HLA-DR4-positive Russians

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16118183

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1534/GENETICS.105.048090

1 reference

3 August 2017

1 reference

3 August 2017

1 reference