Heli Nevanlinna


Ontology type: schema:Person     


Person Info

NAME

Heli

SURNAME

Nevanlinna

Publications in SciGraph latest 50 shown

  • 2018-12 E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium in SCIENTIFIC REPORTS
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2018-07 Family history influences the tumor characteristics and prognosis of breast cancers developing during postmenopausal hormone therapy in FAMILIAL CANCER
  • 2017-12 CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population in BMC CANCER
  • 2017-12 Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study in BREAST CANCER RESEARCH
  • 2017-12 Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility in SCIENTIFIC REPORTS
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-12 Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women in NATURE COMMUNICATIONS
  • 2017-11 FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-05 Genetic modifiers of CHEK2*1100delC-associated breast cancer risk in GENETICS IN MEDICINE
  • 2017-02 Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci in BRITISH JOURNAL OF CANCER
  • 2017-01 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 in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-12 Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women in BREAST CANCER RESEARCH
  • 2016-12 Patient survival and tumor characteristics associated with CHEK2:p.I157T – findings from the Breast Cancer Association Consortium in BREAST CANCER RESEARCH
  • 2016-12 Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 in BREAST CANCER RESEARCH
  • 2016-12 Genetic predisposition to ductal carcinoma in situ of the breast in BREAST CANCER RESEARCH
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-10 Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) in SCIENTIFIC REPORTS
  • 2016-08 Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-07 Assessing the genetic architecture of epithelial ovarian cancer histological subtypes in HUMAN GENETICS
  • 2016-05 Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-05 Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry in CANCER CAUSES & CONTROL
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-04 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2016-02 Heterogeneity of luminal breast cancer characterised by immunohistochemical expression of basal markers in BRITISH JOURNAL OF CANCER
  • 2016-01 Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium in HUMAN GENETICS
  • 2016-01 Screening of HELQ in breast and ovarian cancer families in FAMILIAL CANCER
  • 2015-12 A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients in BMC CANCER
  • 2015-12 RAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer families in SPRINGERPLUS
  • 2015-12 Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer in NATURE COMMUNICATIONS
  • 2015-12 Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy in BREAST CANCER RESEARCH
  • 2015-12 An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2015-12 Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis in BMC MEDICINE
  • 2015-12 Common germline polymorphisms associated with breast cancer-specific survival in BREAST CANCER RESEARCH
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-08 Genome-wide significant risk associations for mucinous ovarian carcinoma in NATURE GENETICS
  • 2015-04 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer in NATURE GENETICS
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2015-01 INPP4B and RAD50 have an interactive effect on survival after breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-12 Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2014-12 Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia in BREAST CANCER RESEARCH
  • 2014-12 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy in NATURE COMMUNICATIONS
  • 2014-12 Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
  • 2014-10 Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche in NATURE
  • 2014-06 Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study in BREAST CANCER RESEARCH
  • 2014-05 Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA in HUMAN GENETICS
  • 2014-04 Evaluation of the RHINO gene for breast cancer predisposition in Finnish breast cancer families in BREAST CANCER RESEARCH AND TREATMENT
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