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List of works by Fay Hosking

A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer

scientific article published on 20 May 2015

Allergy and glioma risk: test of association by genotype.

scientific article published on 25 May 2010

Chromosome 7p11.2 (EGFR) variation influences glioma risk

scientific journal article

Common variation at 10p12.31 near MLLT10 influences meningioma risk

scientific article

Deciphering the 8q24.21 association for glioma

scientific article published on 11 February 2013

Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer

scientific article published on 30 July 2013

Do health checks for adults with intellectual disability reduce emergency hospital admissions? Evaluation of a natural experiment.

scientific article published on 16 June 2016

Erratum: A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer

scientific article published on 3 August 2015

Genetic advances in glioma: susceptibility genes and networks

scientific article

Genetic risk profiles identify different molecular etiologies for glioma

scientific article

Genome-Wide High-Density SNP Linkage Search for Glioma Susceptibility Loci: Results from the Gliogene Consortium ⬇️

scientific article published on October 28, 2011

Genome-wide association studies for detecting cancer susceptibility

scientific article published on 18 January 2011

Genome-wide homozygosity signatures and childhood acute lymphoblastic leukemia risk

Health characteristics and consultation patterns of people with intellectual disability: a cross-sectional database study in English general practice.

scientific article published on 23 February 2016

Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis

scientific article

Inference from genome-wide association studies using a novel Markov model

scientific article published in September 2008

Inherited genetic susceptibility to monoclonal gammopathy of unknown significance

scientific article published on 21 January 2014

Inherited variation in immune genes and pathways and glioblastoma risk

scientific article

Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma

scientific article published on 12 June 2012

Interaction between 5 genetic variants and allergy in glioma risk

scientific article published on 12 May 2010

Learning disability registers in primary care

scientific article published on July 2016

Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia

scientific article

MHC variation and risk of childhood B-cell precursor acute lymphoblastic leukemia

Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

scientific article

Mortality Among Adults With Intellectual Disability in England: Comparisons With the General Population.

scientific article published on 16 June 2016

New insights into susceptibility to glioma

scientific article published on March 2010

Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study

scientific article published on 24 January 2011

Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival

scientific article

Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia

scientific article

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer ⬇️

scientific article

Risk of breast and prostate cancer is not associated with increased homozygosity in outbred populations

scientific article

Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population

scientific article

The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

scientific article

Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk

scientific article

Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood

scientific article

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