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List of works by John A.L. Armour

33.6 (D1S111) and pMLAJ1 (D1S61) identify the same VNTR on chromosome 1

scientific article

A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation

scientific article

A highly polymorphic minisatellite (pMS626) on chromosome 13 (D13S103).

scientific article

Abnormal segregation of alleles in CEPH pedigree DNAs arising from allele loss in lymphoblastoid DNA

scientific article published on 01 January 1993

Accurate measurement of gene copy number for human alpha-defensin DEFA1A3.

scientific article

Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats.

scientific article published on 14 December 2006

Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability

scientific article published on 01 August 1993

Allelic imbalance on chromosome 1 in human breast cancer. I. Minisatellite and RFLP analysis

scientific article published on 01 January 1995

Allelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins.

scholarly article

Analysis of Multiallelic CNVs by Emulsion Haplotype Fusion PCR

scientific article published on 01 January 2017

Analysis of somatic mutations at human minisatellite loci in tumors and cell lines

scientific article published on 01 April 1989

Association of β-defensin copy number and psoriasis in three cohorts of European origin.

scientific article

Beta-defensin-2 protein is a serum biomarker for disease activity in psoriasis and reaches biologically relevant concentrations in lesional skin

scientific article

Biology and applications of human minisatellite loci

scientific article published on December 1, 1992

CCL3L1 copy number, CCR5 genotype and susceptibility to tuberculosis.

scientific article published on 9 January 2014

Cis-regulation of inter-allelic exchanges in mutation at human minisatellite MS205 in yeast

scientific article published on 01 May 1999

Complex gene conversion events in germline mutation at human minisatellites

article

Compound haplotypes at Xp11.23 and human population growth in Eurasia.

scientific article published in September 2004

Constitutional trisomy 8 and Behçet syndrome.

scientific article published in May 2009

Copy number polymorphism and expression level variation of the human alpha-defensin genes DEFA1 and DEFA3

scientific article

Copy number variation and antigenic repertoire

scientific article published on 01 December 2009

Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity.

scientific article published on 20 February 2017

Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis.

scientific article published on 8 April 2010

Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis

scientific article

Direct analysis by small-pool PCR of MS205 minisatellite mutation rates in sperm after mutagenic therapies

scientific article published on 01 September 1999

Directional and balancing selection in human beta-defensins

scientific article (publication date: 16 April 2008)

Distribution of tandem repeat polymorphism within minisatellite MS621 (D5S110).

scientific article published in January 1996

Evaluation of tetranucleotide repeat locus D7S809 (wg1g9) in the Japanese population

scientific article published on 01 August 1996

Evaluation of two new STR loci 9q2h2 and wg3f12 in a Japanese population

scientific article published on 01 September 1999

Evolution and population genetics of the H-ras minisatellite and cancer predisposition.

scientific article published in April 2003

Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy

scientific article (publication date: August 2007)

Functional effects of CCL3L1 copy number.

scientific article published on 5 April 2012

Genome-wide association study of handedness excludes simple genetic models

scientific article

Golli-MBP copy number analysis by FISH, QMPSF and MAPH in 195 patients with hypomyelinating leukodystrophies.

scientific article

Heritability of attractiveness to mosquitoes

scientific article published on 22 April 2015

Human genetics: measuring the raw material of evolution

scientific article published on 01 September 2009

Human minisatellite alleles detectable only after PCR amplification ⬇️

scientific article published on January 1, 1992

Human minisatellite loci composed of interspersed GGA-GGT triplet repeats

scientific article published on 01 September 1995

Isolation of human simple repeat loci by hybridization selection.

scientific article published on April 1994

Loss of heterozygosity on the X chromosome in human breast cancer

scientific article published on 01 August 1995

Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction.

scientific article published on June 2016

MS205 minisatellite diversity in Basques: evidence for a pre-Neolithic component.

scientific article published on December 1998

Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.

scientific article

Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6.

scientific article

Minisatellite diversity supports a recent African origin for modern humans

article

Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies.

scientific article

Multiplex Paralogue Ratio Tests for accurate measurement of multiallelic CNVs

scientific article published on 22 October 2008

Mutation processes at human minisatellites.

scientific article published on September 1995

Mutation rate heterogeneity and the generation of allele diversity at the human minisatellite MS205 (D16S309)

scientific article published on 01 November 1996

No Evidence for Association of BMI with Salivary Amylase Gene Copy Number in the UK 1958 Birth Cohort

scientific article published on 01 September 2019

No evidence for DNA copy number change associated with the DUP25 cytogenetic phenotype.

scientific article published in December 2003

Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes

scientific article

PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: Identification of one partial triplication and two partial deletions of PLP1.

scientific article published on 17 January 2006

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

scientific article

Quadruplex MAPH: improvement of throughput in high-resolution copy number screening.

scientific article

Recurrent Rearrangements of Human Amylase Genes Create Multiple Independent CNV Series.

scientific article published on 19 January 2017

Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993

scientific article published on 01 January 1993

Screening for common copy-number variants in cancer genes.

scientific article published in December 2010

Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH

article

Sequence analysis of alleles at a microsatellite locus D14S299 (wg1c5) and population genetic comparisons

scientific article published on 01 January 1999

Sharp focus on the variable genome

journal article; published in Nature on 2009-10-07

Simple repeat polymorphism at the D9S151 locus.

scientific article published on January 1994

Systematic cloning of human minisatellites from ordered array charomid libraries.

scientific article

Tandemly repeated DNA: why should anyone care?

scientific article

Tetrameric short tandem repeat (STR) system D15S233 (wg1d1): sequencing and frequency data in the japanese and Chinese populations.

scientific article

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

scientific article published in June 1992

The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells

scientific article published on 01 July 1995

Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome

scientific article

Uniparental paternal disomy in Angelman's syndrome ⬇️

scientific article published on March 23, 1991

α-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

scientific article

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