(Q37585393)

English

Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects.

scholarly article

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15492219%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15492219%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

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4 January 2020

author name string

Anish Kejariwal

2

1 reference

Europe PubMed Central

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4 January 2020

language of work or name

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publication date

18 October 2004

1 reference

Europe PubMed Central

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4 January 2020

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

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4 January 2020

101

1 reference

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4 January 2020

43

1 reference

Europe PubMed Central

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4 January 2020

15398-15403

1 reference

Europe PubMed Central

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4 January 2020

Database resources of the National Center for Biotechnology Information: update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

PANTHER: a library of protein families and subfamilies indexed by function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Methylenetetrahydrofolate reductase (MTHFR) allele frequencies in Amerindians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Finding genes that underlie complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Beyond Mendel: an evolving view of human genetic disease transmission

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

A comprehensive review of genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Haplotype variation and linkage disequilibrium in 313 human genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Quantitative trait loci in Drosophila

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

dbSNP: the NCBI database of genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

RefSeq and LocusLink: NCBI gene-centered resources

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Amino acid difference formula to help explain protein evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

Evolution at two levels in humans and chimpanzees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

23 August 2017

JSNP: a database of common gene variations in the Japanese population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

6 September 2017

The human gene mutation database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

14 September 2017

Accounting for human polymorphisms predicted to affect protein function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

14 September 2017

Understanding human disease mutations through the use of interspecific genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=523449

1 September 2018

The last CTD repeat of the mammalian RNA polymerase II large subunit is important for its stability.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0404380101

21 January 2018

Inferences from protein and nucleic acid sequences: early molecular evolution, divergence of kingdoms and rates of change

1 reference

https://pubmed.ncbi.nlm.nih.gov/15492219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mannose-binding protein genetic polymorphisms in black patients with systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/15492219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

From QTL to gene: the harvest begins

1 reference

https://pubmed.ncbi.nlm.nih.gov/15492219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.0404380101

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15492219%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

2004PNAS..10115398T

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15492219%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15492219%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

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