List of works - Shirley Hodgson

Utilisation of prophylactic mastectomy in 10 European centres

scientific article published on October 1999

Identification of nine new susceptibility loci for endometrial cancer

scientific article published in Nature Communications

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

scientific article

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

scientific article

Mechanisms of inherited cancer susceptibility

scientific article

Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist:Hip Ratio, Is Causal for Endometrial Cancer

scientific article published on 22 August 2016

Lymphocyte telomere length is long in BRCA1 and BRCA2 mutation carriers regardless of cancer-affected status

scientific article

APC mutation associated with late onset of familial adenomatous polyposis

scientific article published on November 1994

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

scientific article

Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer

scientific article published in October 2015

UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor gene

scientific article

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

scientific article published on 25 April 2015

Exploring the link between MORF4L1 and risk of breast cancer

scientific article

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA).

scientific article

Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family history

scientific article published in October 2000

GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer

scientific article published on 23 March 2016

Association between polymorphisms of the GPX1 gene and second primary tumours after index squamous cell cancer of the head and neck

scientific article published on 19 April 2005

Cancer genetics services in Europe

scientific article published on October 1999

Identification of a C/G polymorphism in the promoter region of the BRCA1 gene and its use as a marker for rapid detection of promoter deletions

scientific article published on February 1999

Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe

scientific article published on October 1999

Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome

scientific article

Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

scientific article

No evidence that GATA3 rs570613 SNP modifies breast cancer risk

scientific article published on 11 December 2008

Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases

scientific article published in April 2003

Diagnosis and Management of Hereditary Thyroid Cancer

scientific article published on January 1, 2016

Does the occurrence of certain rare cancers indicate an inherited cancer susceptibility?

No evidence of RET germline mutations in familial pituitary adenoma

scientific article

Breast cancer susceptibility polymorphisms and endometrial cancer risk: a Collaborative Endometrial Cancer Study

scientific article published on 30 September 2011

Risk estimation as a decision-making tool for genetic analysis of the breast cancer susceptibility genes. EC Demonstration Project on Familial Breast Cancer

scientific article published on October 1999

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

scientific article

A complex endocrine conundrum

scientific article published on September 1, 2013

Current Policies for Surveillance and Management in Women at Risk for Breast and Ovarian Cancer: A Survey among 16 European Family Cancer Clinics

Mutation-Specific Survival of Inherited Breast Cancer

scientific article published in January 1999

Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer

scientific article published on 13 July 2020

List of works by Shirley Hodgson

Utilisation of prophylactic mastectomy in 10 European centres

Identification of nine new susceptibility loci for endometrial cancer

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

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

Mechanisms of inherited cancer susceptibility

Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist:Hip Ratio, Is Causal for Endometrial Cancer

Lymphocyte telomere length is long in BRCA1 and BRCA2 mutation carriers regardless of cancer-affected status

APC mutation associated with late onset of familial adenomatous polyposis

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer

UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor gene

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

Exploring the link between MORF4L1 and risk of breast cancer

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA).

Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family history

GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer

Association between polymorphisms of the GPX1 gene and second primary tumours after index squamous cell cancer of the head and neck

Cancer genetics services in Europe

Identification of a C/G polymorphism in the promoter region of the BRCA1 gene and its use as a marker for rapid detection of promoter deletions

Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe

Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome

Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

No evidence that GATA3 rs570613 SNP modifies breast cancer risk

Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases

Diagnosis and Management of Hereditary Thyroid Cancer

Does the occurrence of certain rare cancers indicate an inherited cancer susceptibility?

No evidence of RET germline mutations in familial pituitary adenoma

Breast cancer susceptibility polymorphisms and endometrial cancer risk: a Collaborative Endometrial Cancer Study

Risk estimation as a decision-making tool for genetic analysis of the breast cancer susceptibility genes. EC Demonstration Project on Familial Breast Cancer

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

A complex endocrine conundrum

Current Policies for Surveillance and Management in Women at Risk for Breast and Ovarian Cancer: A Survey among 16 European Family Cancer Clinics

Mutation-Specific Survival of Inherited Breast Cancer

Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer