List of works - Helen Tsimiklis

Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies

scientific article

Body mass index and breast cancer survival: a Mendelian randomization analysis

scientific article published in December 2017

Breast Cancer Risk Prediction Using Clinical Models and 77 Independent Risk-Associated SNPs for Women Aged Under 50 Years: Australian Breast Cancer Family Registry

scientific article published on 16 December 2015

Common germline polymorphisms associated with breast cancer-specific survival

scientific article published on 22 April 2015

Epigenome-wide methylation in DNA from peripheral blood as a marker of risk for breast cancer

article

Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

scientific article

FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine

scientific article published on 19 January 2018

Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.

scientific article

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

scientific article

Genome-wide association analysis identifies three new breast cancer susceptibility loci

scientific article published on 22 January 2012

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

scientific article

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

scientific article published in April 2013

Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

scientific article

Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2

scientific article

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

scientific article

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

scientific article published on 27 April 2016

Identification of novel genetic markers of breast cancer survival

scientific article published on 18 April 2015

Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

scientific article

Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?

scientific article published on 8 February 2018

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

scientific article

MicroRNA related polymorphisms and breast cancer risk

scientific article

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

scientific article published on April 2013

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

scientific article published in May 2015

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

scientific article published in December 2016

Prediction of breast cancer risk based on profiling with common genetic variants

scientific article published on 8 April 2015

Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

scientific article published on 10 April 2018

Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers

scientific article

Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine

scientific article

The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array

scientific article

Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model

scientific article

List of works by Helen Tsimiklis

Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies

Body mass index and breast cancer survival: a Mendelian randomization analysis

Breast Cancer Risk Prediction Using Clinical Models and 77 Independent Risk-Associated SNPs for Women Aged Under 50 Years: Australian Breast Cancer Family Registry

Common germline polymorphisms associated with breast cancer-specific survival

Epigenome-wide methylation in DNA from peripheral blood as a marker of risk for breast cancer

Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine

Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

Genome-wide association analysis identifies three new breast cancer susceptibility loci

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

Identification of novel genetic markers of breast cancer survival

Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

MicroRNA related polymorphisms and breast cancer risk

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Prediction of breast cancer risk based on profiling with common genetic variants

Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers

Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine

The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array

Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model