Lista de obras -

A Finnish founder mutation in RAD51D: analysis in breast, ovarian, prostate, and colorectal cancer

artículo científico publicado en 2012

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

article

A combined array-based comparative genomic hybridization and functional library screening approach identifies mir-30d as an oncomir in cancer

artículo científico publicado en 2011

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.

artículo científico publicado en 2010

Adult body mass index and risk of ovarian cancer by subtype: a Mendelian randomization study

artículo científico

Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study

artículo científico publicado en 2018

Allelic imbalance of HER2 variant in sporadic breast and ovarian cancer

artículo científico publicado en 2006

Assessing the genetic architecture of epithelial ovarian cancer histological subtypes

artículo científico publicado en 2016

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

artículo científico publicado en 2016

Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study

artículo científico publicado en 2016

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

artículo científico publicado en 2015

Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer

artículo científico publicado en 2015

Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk

artículo científico publicado en 2015

Common Genetic Variation in Circadian Rhythm Genes and Risk of Epithelial Ovarian Cancer (EOC).

artículo científico publicado en 2015

Common variants at 19p13 are associated with susceptibility to ovarian cancer

artículo científico publicado en 2010

Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer

artículo científico publicado en 2015

Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk

artículo científico publicado en 2014

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

Distinct expression levels and patterns of stem cell marker, aldehyde dehydrogenase isoform 1 (ALDH1), in human epithelial cancers

artículo científico publicado en 2010

Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci

artículo científico publicado en 2017

Epidermal growth factor receptor domain II, IV, and kinase domain mutations in human solid tumors

artículo científico publicado en 2005

Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer

artículo científico publicado en 2013

Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk

artículo científico publicado en 2015

Erratum: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer

scholarly article published in Nature Genetics

Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

artículo científico publicado en 2014

FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population

artículo científico publicado en 2017

Frequent genetic abnormalities of the PI3K/AKT pathway in primary ovarian cancer predict patient outcome

artículo científico publicado en 2011

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

artículo científico publicado en 2016

GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

artículo científico publicado en 2013

Gene amplification, mutation, and protein expression of EGFR and mutations of ERBB2 in serous ovarian carcinoma

artículo científico publicado en 2006

Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

artículo científico

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

artículo científico publicado en 2018

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 study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.

artículo científico publicado en 2013

Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.

artículo científico publicado en 2013

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

artículo científico publicado en 2017

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

artículo científico publicado en 2015

Incidence of and risk factors for surgical site infections in women undergoing hysterectomy for endometrial carcinoma

artículo científico publicado en 2015

Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration

artículo científico publicado en 2016

MiR-34a expression has an effect for lower risk of metastasis and associates with expression patterns predicting clinical outcome in breast cancer

artículo científico publicado en 2011

Molecular subtypes of breast cancers detected in mammography screening and outside of screening

artículo científico publicado en 2008

Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland

article

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

artículo científico publicado en 2013

Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Parity associates with chromosomal damage in uterine leiomyomas

artículo científico publicado en 2021

Pathology of ovarian cancers in BRCA1 and BRCA2 carriers

artículo científico publicado en 2004

Polymorphisms in stromal genes and susceptibility to serous epithelial ovarian cancer: a report from the Ovarian Cancer Association Consortium

artículo científico publicado en 2011

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

scientific article published on 23 September 2019

RAD51C is a susceptibility gene for ovarian cancer

article

Recurrent moderate-risk mutations in Finnish breast and ovarian cancer patients

artículo científico publicado en 2019

Risk of ovarian cancer and the NF-κB pathway: genetic association with IL1A and TNFSF10

artículo científico publicado en 2013

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

artículo científico publicado en 2015

Shared heritability and functional enrichment across six solid cancers

artículo científico publicado en 2019

Shared heritability and functional enrichment across six solid cancers

The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing

artículo científico publicado en 2011

Transcriptional regulation of PIK3CA oncogene by NF-kappaB in ovarian cancer microenvironment

artículo científico publicado en 2008

Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility

artículo científico publicado en 2018

rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology

artículo científico publicado en 2018

Lista de obras de

A Finnish founder mutation in RAD51D: analysis in breast, ovarian, prostate, and colorectal cancer

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

A combined array-based comparative genomic hybridization and functional library screening approach identifies mir-30d as an oncomir in cancer

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.

Adult body mass index and risk of ovarian cancer by subtype: a Mendelian randomization study

Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study

Allelic imbalance of HER2 variant in sporadic breast and ovarian cancer

Assessing the genetic architecture of epithelial ovarian cancer histological subtypes

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer

Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk

Common Genetic Variation in Circadian Rhythm Genes and Risk of Epithelial Ovarian Cancer (EOC).

Common variants at 19p13 are associated with susceptibility to ovarian cancer

Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer

Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk

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

Distinct expression levels and patterns of stem cell marker, aldehyde dehydrogenase isoform 1 (ALDH1), in human epithelial cancers

Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci

Epidermal growth factor receptor domain II, IV, and kinase domain mutations in human solid tumors

Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer

Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk

Erratum: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer

Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population

Frequent genetic abnormalities of the PI3K/AKT pathway in primary ovarian cancer predict patient outcome

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

GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

Gene amplification, mutation, and protein expression of EGFR and mutations of ERBB2 in serous ovarian carcinoma

Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

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

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 study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.

Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Incidence of and risk factors for surgical site infections in women undergoing hysterectomy for endometrial carcinoma

Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration

MiR-34a expression has an effect for lower risk of metastasis and associates with expression patterns predicting clinical outcome in breast cancer

Molecular subtypes of breast cancers detected in mammography screening and outside of screening

Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland

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

Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk

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

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

Parity associates with chromosomal damage in uterine leiomyomas

Pathology of ovarian cancers in BRCA1 and BRCA2 carriers

Polymorphisms in stromal genes and susceptibility to serous epithelial ovarian cancer: a report from the Ovarian Cancer Association Consortium

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

RAD51C is a susceptibility gene for ovarian cancer

Recurrent moderate-risk mutations in Finnish breast and ovarian cancer patients

Risk of ovarian cancer and the NF-κB pathway: genetic association with IL1A and TNFSF10

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

Shared heritability and functional enrichment across six solid cancers

Shared heritability and functional enrichment across six solid cancers

The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing

Transcriptional regulation of PIK3CA oncogene by NF-kappaB in ovarian cancer microenvironment

Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility

rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology