(Q35616540)

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Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies

scientific article published on 6 December 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

9 August 2017

Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies (English)

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Europe PubMed Central

PubMed publication ID

9 August 2017

single-nucleotide polymorphism

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based on heuristic

inferred from title

20

object named as

Eric M Reiman

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Europe PubMed Central

PubMed publication ID

9 August 2017

12

object named as

Thomas Beach

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9 August 2017

16

object named as

Frank Jessen

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9 August 2017

13

object named as

Sigrid B Sando

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PubMed publication ID

9 August 2017

author name string

John V Pearson

1

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9 August 2017

Matthew J Huentelman

2

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9 August 2017

Rebecca F Halperin

3

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Europe PubMed Central

PubMed publication ID

9 August 2017

Waibhav D Tembe

4

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9 August 2017

Stacey Melquist

5

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9 August 2017

Nils Homer

6

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9 August 2017

Marcel Brun

7

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9 August 2017

Szabolcs Szelinger

8

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9 August 2017

Keith D Coon

9

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9 August 2017

Victoria L Zismann

10

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9 August 2017

Jennifer A Webster

11

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9 August 2017

Jan O Aasly

14

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9 August 2017

Reinhard Heun

15

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9 August 2017

Heike Kolsch

17

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9 August 2017

Magdalini Tsolaki

18

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9 August 2017

Makrina Daniilidou

19

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9 August 2017

Andreas Papassotiropoulos

21

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9 August 2017

Michael L Hutton

22

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9 August 2017

Dietrich A Stephan

23

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9 August 2017

David W Craig

24

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9 August 2017

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publication date

6 December 2006

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9 August 2017

American Journal of Human Genetics

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9 August 2017

80

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9 August 2017

1

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9 August 2017

126-139

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PubMed publication ID

9 August 2017

A genome-wide study of preferential amplification/hybridization in microarray-based pooled DNA experiments

1 reference

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12 July 2018

Pooled association genome scanning for alcohol dependence using 104,268 SNPs: validation and use to identify alcoholism vulnerability loci in unrelated individuals from the collaborative study on the genetics of alcoholism

1 reference

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12 July 2018

PDA: Pooled DNA analyzer

1 reference

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Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates

1 reference

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Two-stage designs in case-control association analysis

1 reference

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How to decide? Different methods of calculating gene expression from short oligonucleotide array data will give different results

1 reference

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Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans

1 reference

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12 July 2018

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

1 reference

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SNiPer: improved SNP genotype calling for Affymetrix 10K GeneChip microarray data

1 reference

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A haplotype map of the human genome

1 reference

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12 July 2018

PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays

1 reference

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12 July 2018

Identification of disease causing loci using an array-based genotyping approach on pooled DNA.

1 reference

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12 July 2018

Pooled association genome scanning: validation and use to identify addiction vulnerability loci in two samples

1 reference

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12 July 2018

Applications of whole-genome high-density SNP genotyping

1 reference

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12 July 2018

Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs

1 reference

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Complement factor H polymorphism in age-related macular degeneration

1 reference

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12 July 2018

Silhouette scores for assessment of SNP genotype clusters

1 reference

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12 July 2018

A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays

1 reference

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12 July 2018

Streamlined analysis of pooled genotype data in SNP-based association studies

1 reference

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A common inversion under selection in Europeans

1 reference

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Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels

1 reference

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12 July 2018

Large-scale validation of single nucleotide polymorphisms in gene regions

1 reference

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Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

1 reference

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Risk and protective effects of the APOE gene towards Alzheimer's disease in the Kungsholmen project: variation by age and sex.

1 reference

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DNA pooling as a tool for large-scale association studies in complex traits

1 reference

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Mining disease susceptibility genes through SNP analyses and expression profiling using MALDI-TOF mass spectrometry

1 reference

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12 July 2018

Amino acid variant in the kinase binding domain of dual-specific A kinase-anchoring protein 2: a disease susceptibility polymorphism

1 reference

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12 July 2018

Apolipoprotein E epsilon4 allele, AD pathology, and the clinical expression of Alzheimer's disease

1 reference

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Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design

1 reference

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12 July 2018

Association testing by DNA pooling: an effective initial screen

1 reference

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12 July 2018

DNA Pooling: a tool for large-scale association studies

1 reference

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The use of MassARRAY technology for high throughput genotyping

1 reference

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SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis.

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Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

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LRRK2 mutations are not common in Alzheimer's disease.

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SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children.

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Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms.

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

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Automated genotyping using the DNA MassArray technology

1 reference

https://pubmed.ncbi.nlm.nih.gov/17160900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein E and intellectual achievement

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

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Europe PubMed Central

PubMed publication ID

9 August 2017

PMC publication ID

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Europe PubMed Central

PubMed publication ID

9 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

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