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List of works by Jaana M Hartikainen

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

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

scientific article
RAD51B in Familial Breast Cancer

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

scientific article published on 21 February 2019
Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls

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

scientific article
The UGT1A6_19_GG genotype is a breast cancer risk factor

scientific article published on 11 June 2013
E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium

scientific article published on 26 April 2018
Type II transmembrane serine protease gene variants associate with breast cancer

scientific article
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

scientific article published on 30 November 2015
Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

scientific article published on 27 October 2011
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

scientific article published on 07 January 2020
Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer

scientific article published on 17 January 2018
Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

scientific article published in PLoS ONE
Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk

scholarly article published in Nature Genetics
Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

scientific article published on 10 April 2018
A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients

scientific article published on 16 December 2015
High mutation burden of circulating cell-free DNA in early-stage breast cancer patients is associated with a poor relapse-free survival

scientific article published on 29 June 2020
CD44s Assembles Hyaluronan Coat on Filopodia and Extracellular Vesicles and Induces Tumorigenicity of MKN74 Gastric Carcinoma Cells

scientific article published on 22 March 2019
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

scientific article published on 18 August 2021
DPYSL5 is highly expressed in treatment-induced neuroendocrine prostate cancer and promotes lineage plasticity via EZH2/PRC2

scientific article published on 18 January 2024
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival

scientific article published on 3 July 2023
Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

scientific article published on 17 March 2022
Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

article

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