Evidence map›Paper›PMID 15998910›Full record

ArticleGenome research2005

Mutation scanning by meltMADGE: validations using BRCA1 and LDLR, and demonstration of the potential to identify severe, moderate, silent, rare, and paucimorphic mutations in the general population.

Khalid K Alharbi, Mohammed A Aldahmesh, Emmanuel Spanakis, Lema Haddad, Roslyn A Whittall, Xiao-he Chen, Hamid Rassoulian, Matt J Smith, Julie Sillibourne, Nicola J Ball and 12 more

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in Genome research, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 7 institutions in 2 countries.

Khalid K AlharbiHuman Genetics Division, School of Medicine, University of Southampton, Southampton University Hospitals NHS Trust, Southampton SO16 6YD, United Kingdom.
Mohammed A Aldahmesh
Emmanuel Spanakis
Lema Haddad
Roslyn A Whittall
Xiao-he Chen
Hamid Rassoulian
Matt J Smith
Julie Sillibourne
Nicola J Ball
Nikki J Graham
Patricia J Briggs
Iain A Simpson
David I W Phillips
Deborah A Lawlor
Shu Ye
Stephen E Humphries
Cyrus Cooper
George Davey Smith
Shah Ebrahim
Diana M Eccles
Ian N M Day
University of Southampton · GBUniversity of Bristol · GBThe Royal Free Hospital · GBEssex Cardiothoracic Centre · GBGenomics Medicine (Ireland) · IEGreat Ormond Street Hospital · GBUniversity Hospital Southampton NHS Foundation Trust · GB

Funding

Breast Cancer Now 2001:191
6 · The paper itself

Abstract

We have developed a mutation-scanning approach suitable for whole population screening for unknown mutations. The method, meltMADGE, combines thermal ramp electrophoresis with MADGE to achieve suitable cost efficiency and throughput. The sensitivity was tested in blind trials using 54 amplicons representing the BRCA1 coding region and a panel of 94 unrelated family breast cancer risk consultands previously screened in a clinical diagnostic laboratory. All 10 common polymorphisms, 15/15 previously identified disease-causing mutations, and three previously untested single base changes were identified. Assays of LDLR exons 3 and 8 were validated in 460 familial hypercholesteremics and detected 8/9 known variants. We then applied the exon 3 assay in several DNA banks representing approximately 8000 subjects with known cholesterol values and applied both assays in one DNA bank (n = 3600). In exon 3 we identified one previously reported moderate mutation, P84S (n = 1), also associated with moderate hypercholesteremia in this subject; an unreported silent variant, N76N (n = 1); and known severe hypercholesteremia splice mutation 313+1G-->A (n = 2). Around exon 8 we identified a paucimorphism (n = 35) at the splice site 1061-8T-->C (known to be in complete linkage disequilibrium with T705I) and unreported sequence variants 1186+11G-->A (n = 1) and D335N G-->A (n = 1). The cholesterol value for D335N was on the 96.2 percentile and for T705I, 2/35 carriers were above the 99th percentile. Thus, variants with predicted severe, moderate, and no effect were identified at the population level. In contrast with case collections, CpG mutations predominated. MeltMADGE will enable definition of the full population spectrum of rare, paucimorphic, severe, moderate (forme fruste), and silent mutations and effects.

Indexed as

MutationBreast NeoplasmsDNA Mutational AnalysisElectrophoresis, Polyacrylamide GelFemaleGenes, BRCA1HumansHyperlipoproteinemia Type IIMalePolymorphism, GeneticPopulation SurveillanceReceptors, LDLSensitivity and SpecificityReceptors, LDL

Identifiers

PMID15998910
PMCPMC1172041
OpenAlexW2099481104

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.