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List of works by Charles Mein

A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature

article

A molecular genetic and statistical approach for the diagnosis of dual-site cancers.

scientific article published in October 2004

A new variation in the promoter region, the -604 C>T, and the Leu72Met polymorphism of the ghrelin gene are associated with protection to insulin resistance.

scientific article published on 11 December 2007

A search for type 1 diabetes susceptibility genes in families from the United Kingdom

article

A simple and novel method for RNA-seq library preparation of single cell cDNA analysis by hyperactive Tn5 transposase

scientific article

A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children

scientific article published in August 2002

ABCA12 is the major harlequin ichthyosis gene

scientific article

Adaptive from Innate: Human IFN-γ+CD4+ T Cells Can Arise Directly from CXCL8-Producing Recent Thymic Emigrants in Babies and Adults.

scientific article published on 28 July 2017

Association between gene expression biomarkers of immunosuppression and blood transfusion in severely injured polytrauma patients.

scientific article published in April 2015

Association between gene expression biomarkers of immunosuppression and blood transfusion in severely injured polytrauma patients.

scientific article published on 7 July 2014

Association of Melanin-Concentrating Hormone Receptor 1 5' Polymorphism With Early-Onset Extreme Obesity

scientific article published on 26 September 2005

Association studies on ghrelin and ghrelin receptor gene polymorphisms with obesity

scientific article published on 22 January 2009

BayMeth: improved DNA methylation quantification for affinity capture sequencing data using a flexible Bayesian approach

scientific article (publication date: 11 February 2014)

Comparison of transcriptome responses to glyphosate, isoxaflutole, quizalofop-p-ethyl and mesotrione in the HepaRG cell line

article

Control of spasticity in a multiple sclerosis model using central nervous system-excluded CB1 cannabinoid receptor agonists

scientific article published on 11 October 2013

CpG dinucleotide-specific hypermethylation of the TNS3 gene promoter in human renal cell carcinoma

scientific article

Cytokine responses to exercise and activity in patients with chronic fatigue syndrome: case-control study.

scientific article published on 5 August 2017

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

scientific article

Differences between disease-associated endoplasmic reticulum aminopeptidase 1 (ERAP1) isoforms in cellular expression, interactions with tumour necrosis factor receptor 1 (TNF-R1) and regulation by cytokines

scientific article

Distinctive patterns of microRNA expression associated with karyotype in acute myeloid leukaemia

scientific article

Double-blind randomised placebo-controlled trial of bolus-dose vitamin D3 supplementation in adults with asthma (ViDiAs).

scientific article

Ethnic variation in inflammatory profile in tuberculosis

scientific article

Evaluation of DNA extraction methods from mouse stomachs for the quantification of H. pylori by real-time PCR.

scientific article

Evidence of a role for GTP cyclohydrolase-1 in visceral pain

scientific article published on 17 March 2015

Examining the Candidacy of Ghrelin as a Gene Responsible for Variation in Adult Stature in a United Kingdom Population with Type 2 Diabetes

article

Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi population.

scientific article published on 9 March 2009

Functional analysis of tenocytes gene expression in tendon fascicles subjected to cyclic tensile strain

scientific article published on 24 May 2010

Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndrome

scientific article

Genetics of essential hypertension

scientific article published on 5 February 2004

Genome-wide Linkage Analysis for Severe Obesity in French Caucasians Finds Significant Susceptibility Locus on Chromosome 19q

article

Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing

scientific article published on January 2010

Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study

scientific article

Haplotype structure, LD blocks, and uneven recombination within the LRP5 gene.

scientific article published on May 2003

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study

article

Harlequin ichthyosis: a review of clinical and molecular findings in 45 cases

scientific article

Heterogeneous topographic profiles of kinetic and cell cycle regulator microsatellites in atypical (dysplastic) melanocytic nevi.

scientific article

High quality genomic DNA extraction from postmortem fetal tissue.

scientific article

High-dose vitamin D(3) during intensive-phase antimicrobial treatment of pulmonary tuberculosis: a double-blind randomised controlled trial

scientific article

Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in children

scientific article

Identification of type 1 diabetes-associated DNA methylation variable positions that precede disease diagnosis.

scientific article

Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study

article

Increased invasive behaviour in cutaneous squamous cell carcinoma with loss of basement-membrane type VII collagen.

scientific article published on 12 May 2009

Inflammatory transcriptome profiling of human monocytes exposed acutely to cigarette smoke.

scientific article

Integrated functional, gene expression and genomic analysis for the identification of cancer targets

scientific article

Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma

scientific article published on 22 December 2013

Integrative mRNA profiling comparing cultured primary cells with clinical samples reveals PLK1 and C20orf20 as therapeutic targets in cutaneous squamous cell carcinoma

scientific article published on 23 May 2011

Intestinal injury and endotoxemia in children undergoing surgery for congenital heart disease

scientific article published on 25 August 2011

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension

scientific article

Methylation of the FGFR2 gene is associated with high birth weight centile in humans

scientific article published on January 2014

Multiple common variants for celiac disease influencing immune gene expression

scientific article

Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis. ⬇️

scientific article

Mutations in EDA and EDAR Genes in a Large Mexican Hispanic Cohort with Hypohidrotic Ectodermal Dysplasia

scientific article

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

scientific article

Newly identified genetic risk variants for celiac disease related to the immune response

scientific article

No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases

article

PPAR-gamma2 Pro12Ala variant is associated with greater insulin sensitivity in childhood obesity

scientific article published on 5 November 2004

Quantification of X-chromosome inactivation patterns in haematological samples using the DNA PCR-based HUMARA assay

scientific article published on 01 February 1996

Quantitative genome-wide methylation analysis of high-grade non-muscle invasive bladder cancer.

scientific article published on March 2016

Quantitative, high-resolution epigenetic profiling of CpG loci identifies associations with cord blood plasma homocysteine and birth weight in humans

scientific article

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

scientific article

Selection of candidate genes in hypertension.

scientific article

Single-Cell Expression Profiling Reveals a Dynamic State of Cardiac Precursor Cells in the Early Mouse Embryo

scientific article published on 15 October 2015

Somatic mitochondrial DNA mutations in primary and metastatic ovarian cancer

scientific article published on 30 August 2006

Successful amplification of degraded DNA for use with high-throughput SNP genotyping platforms

scientific article published in December 2008

The EIF2AK3 gene region and type I diabetes in subjects from South India

scientific article

The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1.

scientific article

The common PPAR-gamma2 Pro12Ala variant is associated with greater insulin sensitivity

scientific article

Transcriptional consequences of schizophrenia candidate miR-137 manipulation in human neural progenitor cells

scientific article published on 18 February 2014

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension

article

Vitamin D accelerates resolution of inflammatory responses during tuberculosis treatment

scientific article

WWOX tumour suppressor gene polymorphisms and ovarian cancer pathology and prognosis.

scientific article published on 13 January 2010

Yes-associated protein (YAP) functions as a tumor suppressor in breast.

scientific article

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