(Q30874389)

14 September 2017

High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools (English)

1 reference

high-throughput screening

14 September 2017

0 references

author

Francis Collins

9

0 references

Karen L Mohlke

1

object named as

Karen L Mohlke

1 reference

14 September 2017

8

Michael Boehnke

1 reference

14 September 2017

5

Anne U Jackson

1 reference

14 September 2017

6

Kaisa Silander

1 reference

14 September 2017

4

Tasha E Fingerlin

1 reference

14 September 2017

Michael R Erdos

2

1 reference

14 September 2017

Laura J Scott

3

1 reference

14 September 2017

Pablo Hollstein

7

1 reference

14 September 2017

language of work or name

English

0 references

publication date

13 December 2002

1 reference

14 September 2017

6

1 reference

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

inferred from page(s)

published in

1 reference

14 September 2017

99

1 reference

14 September 2017

16928-16933

1 reference

14 September 2017

26

1 reference

describes a project that uses

14 September 2017

1 reference

Large-scale determination of SNP allele frequencies in DNA pools using MALDI-TOF mass spectrometry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

How many SNPs does a genome-wide haplotype map require?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

Quantification of single nucleotide polymorphisms: a novel method that combines primer extension assay and capillary electrophoresis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

Precise estimation of allele frequencies of single-nucleotide polymorphisms by a quantitative SSCP analysis of pooled DNA.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

Quantitative approach to single-nucleotide polymorphism analysis using MALDI-TOF mass spectrometry

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

A new MALDI-TOF based mini-sequencing assay for genotyping of SNPS.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

Detection of RET proto-oncogene codon 634 mutations using mass spectrometry

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

The future of genetic studies of complex human diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: studies of the HLA class II loci

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139246

Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

21 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262661399

Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262661399

The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262661399

Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262661399

High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC)

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262661399

Determination of SNP allele frequencies in pooled DNAs by primer extension genotyping and denaturing high-performance liquid chromatography

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262661399

Fluorescence-based DHPLC for allelic quantification by single-nucleotide primer extension

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262661399

Estimation of single nucleotide polymorphism allele frequency in DNA pools by using Pyrosequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262661399

Rapid SNP allele frequency determination in genomic DNA pools by pyrosequencing

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12482934

12 December 2020

inferred from PubMed ID database lookup

Assessing allele frequencies of single nucleotide polymorphisms in DNA pools by pyrosequencing technology

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12482934

12 December 2020

inferred from PubMed ID database lookup

Determining SNP allele frequencies in DNA pools

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12482934

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.262661399

1 reference

14 September 2017

0 references

1 reference

14 September 2017

1 reference