Lista de obras - Drakoulis Yannoukakos - Dominio Público Uruguay

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

artículo científico publicado en 2012

A Mendelian randomization analysis of circulating lipid traits and breast cancer risk

artículo científico publicado en 2019

A Paternally Inherited BRCA1 Mutation Associated with an Unusual Aggressive Clinical Phenotype

artículo científico publicado en 2014

A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the FANCM Mutation.

artículo científico publicado en 2019

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

article

A change in the last base of BRCA1 exon 23, 5586G-->A, results in abnormal RNA splicing

artículo científico publicado en 2002

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

artículo científico publicado en 2011

A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype

artículo científico publicado en 2010

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

artículo científico publicado en 2013

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

artículo científico publicado en 2010

A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A.

artículo científico publicado en 2007

A point mutation in the extracellular domain activates LET-23, the Caenorhabditis elegans epidermal growth factor receptor homolog.

artículo científico publicado en 1996

A rareRETgene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: implications for screening

AE anion exchanger mRNA and protein expression in vascular smooth muscle cells, aorta, and renal microvessels ⬇️

artículo científico publicado el 1 de diciembre de 1997

Absence of association with cancer risk and low frequency of alterations at a p53 responsive PIG3 gene polymorphism in breast and lung carcinomas

artículo científico publicado en 2004

Absence of mutations in the functional domains of the human MDM2 oncogene in non-small cell lung carcinomas

artículo científico publicado en 2000

Abstract 3266: Expression quantitative trait locus analysis of triple negative breast cancer

artículo científico publicado en 2014

An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2008

An in-frame exon-skipping MUTYH mutation is associated with early-onset colorectal cancer

artículo científico publicado en 2010

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

artículo científico publicado en 2015

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

artículo científico publicado en 2019

Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer

scientific article published on 10 September 2020

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

artículo científico publicado en 2015

Atypical Medullary Breast Carcinoma in a Family Carrying the 5382insC BRCA-1 Mutation

artículo científico publicado en 2003

BRCA1 and BRCA2 genes mutation analysis in patients with a family history of breast and ovarian cancer

article

BRCA1 and BRCA2 germline testing in Cretan isolates reveals novel and strong founder effects

artículo científico publicado en 2020

BRCA1 mutation analysis in breast and ovarian cancer families from Greece.

artículo científico publicado en 2000

BRCA1 mutation analysis in breast/ovarian cancer families from Greece

artículo científico publicado en 2000

BRCA1 wild-type allele modifies risk of ovarian cancer in carriers of BRCA1 germ-line mutations

artículo científico publicado en 2003

BRCA2 gene mutations in Greek patients with familial breast cancer

artículo científico publicado en 2002

Breast cancer risk inBRCA1 andBRCA2 mutation carriers and polyglutamine repeat length in theAIB1 gene

article

Breast-Cancer Risk in Families With Mutations in PALB2

Breast-cancer risk in families with mutations in PALB2

artículo científico publicado en 2014

CHEK2 c.1100delC allele is rarely identified in Greek breast cancer cases

artículo científico publicado en 2015

CanVaS: Documenting the genetic variation spectrum of Greek cancer patients

artículo científico publicado en 2021

Cancer Risks Associated With and Pathogenic Variants

artículo científico publicado en 2022

Characterization and prevalence of two novel CHEK2 large deletions in Greek breast cancer patients.

artículo científico publicado en 2018

Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

artículo científico publicado en 2004

Collaborative genomics for human health and cooperation in the Mediterranean region

article

Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriers

scientific article published on 01 January 2005

Common breast cancer susceptibility loci are associated with triple-negative breast cancer

artículo científico publicado en 2011

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2014

Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases

scientific article published on 02 June 2009

Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece

artículo científico publicado en 2018

Correction: Prevalence of BRCA1 Mutations in Familial andSporadic Greek Ovarian Cancer Cases

artículo científico publicado en 2013

Cross-cancer genome-wide association study of endometrial cancer and epithelial ovarian cancer identifies genetic risk regions associated with risk of both cancers

artículo científico publicado en 2020

Culture of primary epithelial adenoma cells from familial adenomatous polyposis patients

artículo científico publicado en 2008

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

Efficacy and safety of pulsatile gonadotropin-releasing hormone therapy among patients with idiopathic and functional hypothalamic amenorrhea: a systematic review of the literature and a meta-analysis.

artículo científico publicado en 2018

Epidemiological and clinicopathological characteristics of BRCA-positive and BRCA-negative breast cancer patients in Greece

artículo científico publicado en 2015

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).

artículo científico publicado en 2009

Evaluation of dHPLC in mutation screening of the APC gene in a Greek FAP cohort.

artículo científico publicado en 2003

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

artículo científico publicado en 2014

Extending the clinical phenotype associated with biallelic NTHL1 germline mutations

scientific article published on 24 September 2018

FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium

artículo científico publicado en 2014

Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus

artículo científico publicado en 2016

Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

artículo científico publicado en 2015

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

article

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

artículo científico publicado en 2020

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

artículo científico publicado en 2014

Fully integrated monolithic optoelectronic transducer for real-time protein and DNA detection: the NEMOSLAB approach

artículo científico publicado en 2010

Functional characterization of CHEK2 variants in a Saccharomyces cerevisiae system

artículo científico publicado en 2019

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

artículo científico publicado en 2016

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

artículo científico publicado en 2013

G1738R is a BRCA1 founder mutation in Greek breast/ovarian cancer patients: evaluation of its pathogenicity and inferences on its genealogical history

article published in 2007

Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes

artículo científico publicado en 2016

Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk

artículo científico publicado en 2018

Genetic alterations of the APC gene in familial adenomatous polyposis patients of the hellenic group for the study of colorectal cancer.

artículo científico publicado en 2003

Genetic analysis and clinical description of Greek patients with Peutz-Jeghers syndrome: Creation of a National Registry.

artículo científico publicado en 2017

Genetic counseling of medullary breast cancer patients

scientific article published on 01 April 2004

Genetic evaluation based on family history and Her2 status correctly identifies TP53 mutations in very early onset breast cancer cases.

artículo científico publicado en 2014

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

artículo científico publicado en 2014

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

artículo científico publicado en 2014

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

article

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

artículo científico publicado en 2013

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

scientific article published on 18 May 2020

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

artículo científico publicado en 2013

Germ line BRCA1 & BRCA2 mutations in Greek breast/ovarian cancer families: 5382insC is the most frequent mutation observed

artículo científico publicado en 2002

Germline deleterious mutations in genes other than BRCA2 are infrequent in male breast cancer

artículo científico publicado en 2018

Glutathione-mediated metabolism of technetium-99m SNS/S mixed ligand complexes: a proposed mechanism of brain retention

artículo científico publicado en 1999

Greek BRCA1 and BRCA2 mutation spectrum: two BRCA1 mutations account for half the carriers found among high-risk breast/ovarian cancer patients

Growth index is independent of microvessel density in non–small-cell lung carcinomas

artículo científico publicado en 2002

Haplotype analysis of two recurrent genomic rearrangements in the BRCA1 gene suggests they are founder mutations for the Greek population

article

Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation

artículo científico publicado en 2016

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

artículo científico publicado en 2019

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

artículo científico publicado en 2015

Hereditary cancer syndromes

artículo científico publicado en 2007

High prevalence of BRCA1 founder mutations in Greek breast/ovarian families

artículo científico publicado en 2013

Human erythrocyte band 3 polymorphism (band 3 Memphis): characterization of the structural modification (Lys 56----Glu) by protein chemistry methods

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

artículo científico publicado en 2016

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Identifying and testing for hereditary susceptibility to breast/ovarian cancer in Serbia: Where are we now?

Improved DNA microarray detection sensitivity through immobilization of preformed in solution streptavidin/biotinylated oligonucleotide conjugates.

artículo científico publicado en 2015

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

artículo científico publicado en 2014

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

artículo científico publicado en 2015

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation

artículo científico publicado en 2010

Lack of association between RNASEL Arg462Gln variant and the risk of breast cancer

article

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

scientific article published on 19 June 2019

MicroRNA related polymorphisms and breast cancer risk

artículo científico publicado en 2014

Molecular cloning, expression, and chromosomal localization of two isoforms of the AE3 anion exchanger from human heart

artículo científico publicado en 1994

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

artículo científico publicado en 2013

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

artículo científico publicado en 2018

Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece.

artículo científico publicado en 2017

Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients

artículo científico publicado en 2010

Novel genomic rearrangements in the BRCA1 gene detected in Greek breast/ovarian cancer patients.

artículo científico publicado en 2006

Novel mutations of the APC gene in familial adenomatous polyposis in Greek patients

article

On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations

artículo científico publicado en 2010

One in three highly selected Greek patients with breast cancer carries a loss-of-function variant in a cancer susceptibility gene

artículo científico publicado en 2019

PALB2 c.2257C>T truncating variant is a Greek founder and is associated with high breast cancer risk

scientific article published on 14 May 2019

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

artículo científico publicado en 2016

Pathology of BRCA1- and BRCA2-associated Breast Cancers: Known and Less Known Connections

scientific article published on 22 August 2019

Phosphorylation sites in human erythrocyte band 3 protein

artículo científico publicado en 1991

Pitfalls in variant annotation for hereditary cancer diagnostics: The example of Illumina® VariantStudio®

artículo científico publicado en 2020

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

artículo científico publicado en 2019

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

artículo científico publicado en 2020

Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.

artículo científico publicado en 2002

Prevalence and founder effect of the BRCA1 p.(Val1833Met) variant in the Greek population, with further evidence for pathogenicity and risk modification

scientific article published on 12 June 2019

Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a Hellenic Cooperative Oncology Group Study.

artículo científico publicado en 2012

Prevalence of BRCA1 mutations in familial and sporadic greek ovarian cancer cases

artículo científico publicado en 2013

Prevalence of GJB2 mutations in prelingual deafness in the Greek population

artículo científico publicado en 2002

Primary structure of the cytoplasmic domain of human erythrocyte protein band 3. Comparison with its sequence in the mouse

artículo científico publicado en 1989

Proteolytic Cleavage Sites of Native AE2 Anion Exchanger in Gastric Mucosal Membranes†

scientific article published on 01 August 1996

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

artículo científico publicado en 2018

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

scientific article published on 23 September 2019

RAD51B in Familial Breast Cancer

artículo científico publicado en 2016

Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected families

artículo científico publicado en 2010

Shared heritability and functional enrichment across six solid cancers

artículo científico publicado en 2019

Shared heritability and functional enrichment across six solid cancers

The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

artículo científico publicado en 2018

The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases

scientific article published on 26 January 2020

The fate of BRCA1-related germline mutations in triple-negative breast tumors

scientific article published on January 2017

The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries

scientific article published on 26 July 2019

Thermal denaturation of the BRCT tandem repeat region of human tumour suppressor gene product BRCA1

article

Thermal unfolding of human BRCA1 BRCT-domain variants

artículo científico publicado en 2007

Thermodynamic study of the BRCT domain of BARD1 and its interaction with the -pSER-X-X-Phe- motif-containing BRIP1 peptide

artículo científico publicado en 2010

Three regions of erythrocyte band 3 protein are phosphorylated on tyrosines: characterization of the phosphorylation sites by solid phase sequencing combined with capillary electrophoresis

artículo científico publicado en 1991

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

artículo científico publicado en 2020

Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing

article

rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

artículo científico publicado en 2016

Lista de obras de Drakoulis Yannoukakos

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

A Mendelian randomization analysis of circulating lipid traits and breast cancer risk

A Paternally Inherited BRCA1 Mutation Associated with an Unusual Aggressive Clinical Phenotype

A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the FANCM Mutation.

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

A change in the last base of BRCA1 exon 23, 5586G-->A, results in abnormal RNA splicing

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A.

A point mutation in the extracellular domain activates LET-23, the Caenorhabditis elegans epidermal growth factor receptor homolog.

A rareRETgene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: implications for screening

AE anion exchanger mRNA and protein expression in vascular smooth muscle cells, aorta, and renal microvessels ⬇️

Absence of association with cancer risk and low frequency of alterations at a p53 responsive PIG3 gene polymorphism in breast and lung carcinomas

Absence of mutations in the functional domains of the human MDM2 oncogene in non-small cell lung carcinomas

Abstract 3266: Expression quantitative trait locus analysis of triple negative breast cancer

An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriers

An in-frame exon-skipping MUTYH mutation is associated with early-onset colorectal cancer

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

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

Atypical Medullary Breast Carcinoma in a Family Carrying the 5382insC BRCA-1 Mutation

BRCA1 and BRCA2 genes mutation analysis in patients with a family history of breast and ovarian cancer

BRCA1 and BRCA2 germline testing in Cretan isolates reveals novel and strong founder effects

BRCA1 mutation analysis in breast and ovarian cancer families from Greece.

BRCA1 mutation analysis in breast/ovarian cancer families from Greece

BRCA1 wild-type allele modifies risk of ovarian cancer in carriers of BRCA1 germ-line mutations

BRCA2 gene mutations in Greek patients with familial breast cancer

Breast cancer risk inBRCA1 andBRCA2 mutation carriers and polyglutamine repeat length in theAIB1 gene

Breast-Cancer Risk in Families With Mutations in PALB2

Breast-cancer risk in families with mutations in PALB2

CHEK2 c.1100delC allele is rarely identified in Greek breast cancer cases

CanVaS: Documenting the genetic variation spectrum of Greek cancer patients

Cancer Risks Associated With and Pathogenic Variants

Characterization and prevalence of two novel CHEK2 large deletions in Greek breast cancer patients.

Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

Collaborative genomics for human health and cooperation in the Mediterranean region

Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriers

Common breast cancer susceptibility loci are associated with triple-negative breast cancer

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases

Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece

Correction: Prevalence of BRCA1 Mutations in Familial andSporadic Greek Ovarian Cancer Cases

Cross-cancer genome-wide association study of endometrial cancer and epithelial ovarian cancer identifies genetic risk regions associated with risk of both cancers

Culture of primary epithelial adenoma cells from familial adenomatous polyposis patients

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

Efficacy and safety of pulsatile gonadotropin-releasing hormone therapy among patients with idiopathic and functional hypothalamic amenorrhea: a systematic review of the literature and a meta-analysis.

Epidemiological and clinicopathological characteristics of BRCA-positive and BRCA-negative breast cancer patients in Greece

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).

Evaluation of dHPLC in mutation screening of the APC gene in a Greek FAP cohort.

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

Extending the clinical phenotype associated with biallelic NTHL1 germline mutations

FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium

Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus

Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

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

Fully integrated monolithic optoelectronic transducer for real-time protein and DNA detection: the NEMOSLAB approach

Functional characterization of CHEK2 variants in a Saccharomyces cerevisiae system

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

G1738R is a BRCA1 founder mutation in Greek breast/ovarian cancer patients: evaluation of its pathogenicity and inferences on its genealogical history

Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes

Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk

Genetic alterations of the APC gene in familial adenomatous polyposis patients of the hellenic group for the study of colorectal cancer.

Genetic analysis and clinical description of Greek patients with Peutz-Jeghers syndrome: Creation of a National Registry.

Genetic counseling of medullary breast cancer patients

Genetic evaluation based on family history and Her2 status correctly identifies TP53 mutations in very early onset breast cancer cases.

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

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

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk