Lista de obras - Katri Pylkäs - Dominio Público Uruguay

11q13 is a susceptibility locus for hormone receptor positive breast cancer

artículo científico publicado en 2012

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

artículo científico publicado en 2012

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

artículo científico publicado en 2014

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium

artículo científico publicado en 2012

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

artículo científico publicado en 2011

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 novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development

scientific article published on 28 January 2022

A recurrent mutation in PALB2 in Finnish cancer families.

artículo científico publicado en 2007

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

artículo científico publicado en 2018

Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families

artículo científico publicado en 2008

Assessment of targeted and non-targeted responses in cells deficient in ATM function following exposure to low and high dose X-rays

artículo científico publicado en 2014

Association analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.

scientific article published on 21 October 2016

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

artículo científico publicado en 2016

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

artículo científico publicado en 2010

Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2011

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

article by Xiang Shu et al published 1 October 2018 in International Journal of Epidemiology

BRCA1 mislocalization leads to aberrant DNA damage response in heterozygous ABRAXAS1 mutation carrier cells

scientific article published on 01 December 2019

BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

artículo científico publicado en 2020

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

artículo científico publicado en 2016

Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions

artículo científico publicado en 2012

Breast-Cancer Risk in Families With Mutations in PALB2

Breast-cancer risk in families with mutations in PALB2

artículo científico publicado en 2014

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

artículo científico publicado en 2019

Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility

artículo científico publicado en 2017

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

artículo científico publicado en 2011

Common germline polymorphisms associated with breast cancer-specific survival

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

artículo científico publicado en 2012

Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer

artículo científico publicado en 2011

Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

artículo científico publicado en 2012

Evaluating the role of MLH3 p.Ser1188Ter variant in inherited breast cancer predisposition

scientific article published on 05 November 2019

Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition

scientific article published on 19 September 2020

Evaluation of the need for routine clinical testing of PALB2 c.1592delT mutation in BRCA negative Northern Finnish breast cancer families

artículo científico publicado en 2013

Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer

artículo científico publicado en 2006

Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

artículo científico publicado en 2011

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

artículo científico publicado en 2014

Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

scientific article published on 03 September 2016

FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

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 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

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

artículo científico publicado en 2013

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer

Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

artículo científico publicado en 2021

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

Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility

article

Genetic predisposition to ductal carcinoma in situ of the breast

artículo científico publicado en 2016

Genetic predisposition to in situ and invasive lobular carcinoma of the breast

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

Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

artículo científico publicado en 2016

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

artículo científico publicado en 2012

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 studies identify four ER negative-specific breast cancer risk loci

artículo científico publicado en 2013

Genome-wide association study of germline variants and breast cancer-specific mortality

artículo científico publicado en 2019

Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families

artículo científico publicado en 2010

Germline alterations in the CLSPN gene in breast cancer families

artículo científico publicado en 2008

Haplotypes of the I157T CHEK2 germline mutation in ethnically diverse populations

artículo científico publicado en 2009

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

artículo científico publicado en 2015

Heterozygous mutations in PALB2 cause DNA replication and damage response defects

artículo científico publicado en 2013

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 novel genetic markers of breast cancer survival

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice

scientific journal article

Incorporating progesterone receptor expression into the PREDICT breast prognostic model

artículo científico publicado en 2022

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

KEAP1 Genetic Polymorphisms Associate with Breast Cancer Risk and Survival Outcomes

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

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 genotyping identifies 41 new loci associated with breast cancer risk

artículo científico publicado en 2013

MicroRNA related polymorphisms and breast cancer risk

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Mutation analysis of the AATF gene in breast cancer families

artículo científico publicado en 2009

Mutation analysis of the gene encoding the PALB2-binding protein MRG15 in BRCA1/2-negative breast cancer families

article

Mutation screening of the MERIT40 gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families

artículo científico publicado en 2009

Mutation screening of the RNF8, UBC13 and MMS2 genes in Northern Finnish breast cancer families

artículo científico publicado en 2011

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

artículo científico publicado en 2015

No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer families

artículo científico publicado en 2003

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

scientific article published on 26 February 2016

Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies

artículo científico publicado en 2006

Novel variants and phenotypes widen the phenotypic spectrum of GABRG2-related disorders

scientific article published on 19 March 2019

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

artículo científico publicado en 2016

PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.

artículo científico publicado en 2017

PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2.

artículo científico publicado en 2012

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association Consortium

artículo científico publicado en 2016

Penetrance analysis of the PALB2 c.1592delT founder mutation

artículo científico publicado en 2008

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

artículo científico publicado en 2019

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

artículo científico publicado en 2015

Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders

artículo científico publicado en 2018

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

artículo científico publicado en 2018

Rare copy number variants observed in hereditary breast cancer cases disrupt genes in estrogen signaling and TP53 tumor suppression network

artículo científico publicado en 2012

Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer

artículo científico publicado en 2014

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

artículo científico publicado en 2014

Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study.

artículo científico publicado en 2017

SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival

artículo científico publicado en 2015

Screening for large genomic rearrangements in the FANCA gene reveals extensive deletion in a Finnish breast cancer family

artículo científico publicado en 2011

Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families

artículo científico publicado en 2010

Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility

artículo científico publicado en 2016

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

artículo científico publicado en 2018

The UGT1A6_19_GG genotype is a breast cancer risk factor

artículo científico publicado en 2013

The role of genetic breast cancer susceptibility variants as prognostic factors

artículo científico publicado en 2012

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

artículo científico publicado en 2020

Tumor suppressor MCPH1 regulates gene expression profiles related to malignant conversion and chromosomal assembly

scientific article published on 21 March 2019

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 Katri Pylkäs

11q13 is a susceptibility locus for hormone receptor positive breast cancer

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

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium

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

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 novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development

A recurrent mutation in PALB2 in Finnish cancer families.

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families

Assessment of targeted and non-targeted responses in cells deficient in ATM function following exposure to low and high dose X-rays

Association analysis identifies 65 new breast cancer risk loci.

Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

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

Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

BRCA1 mislocalization leads to aberrant DNA damage response in heterozygous ABRAXAS1 mutation carrier cells

BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

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

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

Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions

Breast-Cancer Risk in Families With Mutations in PALB2

Breast-cancer risk in families with mutations in PALB2

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility

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

Common germline polymorphisms associated with breast cancer-specific survival

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

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer

Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

Evaluating the role of MLH3 p.Ser1188Ter variant in inherited breast cancer predisposition

Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition

Evaluation of the need for routine clinical testing of PALB2 c.1592delT mutation in BRCA negative Northern Finnish breast cancer families

Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer

Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

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

Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome

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

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

Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

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

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.

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

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer

Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

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

Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility

Genetic predisposition to ductal carcinoma in situ of the breast

Genetic predisposition to in situ and invasive lobular carcinoma of the breast

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

Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

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

Genome-wide association study of germline variants and breast cancer-specific mortality

Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families

Germline alterations in the CLSPN gene in breast cancer families

Haplotypes of the I157T CHEK2 germline mutation in ethnically diverse populations

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

Heterozygous mutations in PALB2 cause DNA replication and damage response defects

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

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

Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice

Incorporating progesterone receptor expression into the PREDICT breast prognostic model

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

KEAP1 Genetic Polymorphisms Associate with Breast Cancer Risk and Survival Outcomes

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

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