Lista de obras - Silje H Nordgard - Dominio Público Uruguay

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

artículo científico publicado en 2014

A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients

artículo científico publicado en 2015

ABCB1 and GST polymorphisms associated with TP53 status in breast cancer

article published in 2007

ABI3 mediates expression of the peroxiredoxin antioxidant AtPER1 gene and induction by oxidative stress

artículo científico publicado en 2003

Allele-specific copy number analysis of tumors

artículo científico publicado en 2010

Analyzing cancer samples with SNP arrays

artículo científico publicado en 2012

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

artículo científico publicado en 2015

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

artículo científico publicado en 2016

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

Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors

artículo científico publicado en 2018

Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors

scholarly article published in Nature Communications

Basal-like Breast cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival

artículo científico publicado en 2011

Basal-like breast cancer engages tumor-supportive macrophages via secreted factors induced by extracellular S100A4

scholarly article by Lina Prasmickaite et al published September 2018 in Molecular Oncology

Breast cancer quantitative proteome and proteogenomic landscape

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

artículo científico publicado en 2016

Canine Mammary Tumours Are Affected by Frequent Copy Number Aberrations, including Amplification of MYC and Loss of PTEN

artículo científico publicado en 2015

Deregulation of cancer-related miRNAs is a common event in both benign and malignant human breast tumors

artículo científico publicado en 2013

Differential in vivo tumorigenicity of distinct subpopulations from a luminal-like breast cancer xenograft

artículo científico publicado en 2014

ESR1 gene amplification in breast cancer: a common phenomenon?

artículo científico publicado en 2008

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

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-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

artículo científico publicado en 2016

Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Genes harbouring susceptibility SNPs are differentially expressed in the breast cancer subtypes

artículo científico publicado en 2007

Genetic variation in putative regulatory loci controlling gene expression in breast cancer

artículo científico publicado en 2006

Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients.

artículo científico publicado en 2008

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

artículo científico publicado en 2015

Glycan-related gene expression signatures in breast cancer subtypes; relation to survival

artículo científico publicado en 2015

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 novel genetic markers of breast cancer survival

artículo científico publicado en 2015

Integrated molecular profiles of invasive breast tumors and ductal carcinoma in situ (DCIS) reveal differential vascular and interleukin signaling

artículo científico publicado en 2011

Integrated study of copy number states and genotype calls using high-density SNP arrays

artículo científico publicado en 2009

Integrative clustering reveals a novel split in the luminal A subtype of breast cancer with impact on outcome

artículo científico publicado en 2017

Intrinsic subtypes and benefit from postmastectomy radiotherapy in node-positive premenopausal breast cancer patients who received adjuvant chemotherapy - results from two independent randomized trials

artículo científico publicado en 2017

Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size

artículo científico publicado en 2013

Methylation profiling with a panel of cancer related genes: association with estrogen receptor, TP53 mutation status and expression subtypes in sporadic breast cancer

artículo científico publicado en 2010

Next-generation sequencing of disseminated tumor cells

artículo científico publicado en 2013

Overrepresentation of transcription factor families in the genesets underlying breast cancer subtypes

artículo científico publicado en 2012

Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors.

artículo científico publicado en 2017

Pathway based analysis of SNPs with relevance to 5-FU therapy: relation to intratumoral mRNA expression and survival.

artículo científico publicado en 2008

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

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

artículo científico publicado en 2018

Relationship between the prognostic and predictive value of the intrinsic subtypes and a validated gene profile predictive of loco-regional control and benefit from post-mastectomy radiotherapy in patients with high-risk breast cancer.

artículo científico publicado en 2014

Seed 1-cysteine peroxiredoxin antioxidants are not involved in dormancy, but contribute to inhibition of germination during stress

artículo científico publicado en 2003

Single nucleotide polymorphisms in the multidrug resistance gene 1 (ABCB1): effects on its expression and clinicopathological characteristics in breast cancer patients.

artículo científico publicado en 2008

The 5p12 breast cancer susceptibility locus affects MRPS30 expression in estrogen-receptor positive tumors

artículo científico publicado en 2013

The Genomic Landscape of Pancreatic and Periampullary Adenocarcinoma

artículo científico publicado en 2016

The Longitudinal Transcriptional Response to Neoadjuvant Chemotherapy with and without Bevacizumab in Breast Cancer

artículo científico publicado en 2017

The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers

scientific article published on 28 January 2020

The novel p21 polymorphism p21G251A is associated with locally advanced breast cancer.

artículo científico publicado en 2006

Time series analysis of neoadjuvant chemotherapy and bevacizumab-treated breast carcinomas reveals a systemic shift in genomic aberrations

scholarly article by Elen Kristine Höglander published in November 2018

Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing

artículo científico publicado en 2016

Transcriptional networks inferred from molecular signatures of breast cancer

artículo científico publicado en 2008

Lista de obras de Silje H Nordgard

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

A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients

ABCB1 and GST polymorphisms associated with TP53 status in breast cancer

ABI3 mediates expression of the peroxiredoxin antioxidant AtPER1 gene and induction by oxidative stress

Allele-specific copy number analysis of tumors

Analyzing cancer samples with SNP arrays

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

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

Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors

Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors

Basal-like Breast cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival

Basal-like breast cancer engages tumor-supportive macrophages via secreted factors induced by extracellular S100A4

Breast cancer quantitative proteome and proteogenomic landscape

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

Canine Mammary Tumours Are Affected by Frequent Copy Number Aberrations, including Amplification of MYC and Loss of PTEN

Deregulation of cancer-related miRNAs is a common event in both benign and malignant human breast tumors

Differential in vivo tumorigenicity of distinct subpopulations from a luminal-like breast cancer xenograft

ESR1 gene amplification in breast cancer: a common phenomenon?

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

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-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk

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

Genes harbouring susceptibility SNPs are differentially expressed in the breast cancer subtypes

Genetic variation in putative regulatory loci controlling gene expression in breast cancer

Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients.

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

Glycan-related gene expression signatures in breast cancer subtypes; relation to survival

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

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

Identification of novel genetic markers of breast cancer survival

Integrated molecular profiles of invasive breast tumors and ductal carcinoma in situ (DCIS) reveal differential vascular and interleukin signaling

Integrated study of copy number states and genotype calls using high-density SNP arrays

Integrative clustering reveals a novel split in the luminal A subtype of breast cancer with impact on outcome

Intrinsic subtypes and benefit from postmastectomy radiotherapy in node-positive premenopausal breast cancer patients who received adjuvant chemotherapy - results from two independent randomized trials

Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size

Methylation profiling with a panel of cancer related genes: association with estrogen receptor, TP53 mutation status and expression subtypes in sporadic breast cancer

Next-generation sequencing of disseminated tumor cells

Overrepresentation of transcription factor families in the genesets underlying breast cancer subtypes

Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors.

Pathway based analysis of SNPs with relevance to 5-FU therapy: relation to intratumoral mRNA expression and survival.

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

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.

Relationship between the prognostic and predictive value of the intrinsic subtypes and a validated gene profile predictive of loco-regional control and benefit from post-mastectomy radiotherapy in patients with high-risk breast cancer.

Seed 1-cysteine peroxiredoxin antioxidants are not involved in dormancy, but contribute to inhibition of germination during stress

Single nucleotide polymorphisms in the multidrug resistance gene 1 (ABCB1): effects on its expression and clinicopathological characteristics in breast cancer patients.

The 5p12 breast cancer susceptibility locus affects MRPS30 expression in estrogen-receptor positive tumors

The Genomic Landscape of Pancreatic and Periampullary Adenocarcinoma

The Longitudinal Transcriptional Response to Neoadjuvant Chemotherapy with and without Bevacizumab in Breast Cancer

The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers

The novel p21 polymorphism p21G251A is associated with locally advanced breast cancer.

Time series analysis of neoadjuvant chemotherapy and bevacizumab-treated breast carcinomas reveals a systemic shift in genomic aberrations

Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing

Transcriptional networks inferred from molecular signatures of breast cancer