Saila Kauppila

University of Helsinki — Finland

Biochemistry, Genetics and Molecular Biology · Life Sciences

39h-index8.5kcitations81works0.02yr avg
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Research Topics

BRCA gene mutations in cancer(13), Genetic Associations and Epidemiology(10), Cell Adhesion Molecules Research(9), DNA Repair Mechanisms(8), Protease and Inhibitor Mechanisms(6)

Publications58 total

Estrogen Metabolism Pathways in Pregnancy and Subsequent Breast Cancer Risk: A Prospective Follow-up Study
2025Open Access
Integrative single-cell and spatial mapping of oxidative stress response uncovers GCLC+ mesenchymal tumor cell state linked with favorable outcomes in triple negative breast cancer
2025Open Access
Corrigendum to Targeting collagen XVIII improves the efficiency of ErbB inhibitors in breast cancer models
Journal of Clinical Investigation·2025Open Access
Targeting collagen XVIII improves the efficiency of ErbB inhibitors in breast cancer models
Journal of Clinical Investigation·2023· 16 citedOpen Access
PB2271: GERMLINE LOSS OF RHOG IDENTIFIES ITS ROLE AS AN ESSENTIAL REGULATOR OF HUMAN LYMPHOCYTE CYTOTOXICITY
HemaSphere·2022· 1 citedOpen Access
Collagen XVIII promotes breast cancer through EGFR/ErbB signaling and its ablation improves the efficacy of ErbB-targeting inhibitors
2022· 2 citedOpen Access
Additional file 1 of Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Figshare·2022Open Access
Incidence and clinicopathological features of Follicular T-cell lymphoma in Finland: a population-based immunohistochemical study
Human Pathology·2021· 3 citedOpen Access
Common variants in breast cancer risk loci predispose to distinct tumor subtypes.
Apollo (University of Cambridge)·2021· 6 citedOpen Access
RhoG deficiency abrogates cytotoxicity of human lymphocytes and causes hemophagocytic lymphohistiocytosis
Blood·2021· 52 citedOpen Access
Exome sequencing identifies a recurrent variant in SERPINA3 associating with hereditary susceptibility to breast cancer
European Journal of Cancer·2020· 27 citedOpen Access
Impact of central nervous system (CNS) prophylaxis on the incidence of CNS relapse in patients with high-risk diffuse large B cell/follicular grade 3B lymphoma
Annals of Hematology·2020· 15 citedOpen Access
Tonsillar granuloma associated with hypogammaglobulinemia
Allergy Asthma and Clinical Immunology·2020· 2 citedOpen Access
Rare missense mutations in <i>RECQL</i> and <i>POLG</i> associate with inherited predisposition to breast cancer
International Journal of Cancer·2018· 17 cited
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility
Scientific Reports·2017· 34 citedOpen Access
Abstract P4-04-13: Comparison of tumor and stroma CD73 expression with TLR9 and survival in breast cancer
Cancer Research·2016
Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility
PLoS Genetics·2016· 25 citedOpen Access
Prebiopsy Multiparametric Magnetic Resonance Imaging for Prostate Cancer Diagnosis in Biopsy-naive Men with Suspected Prostate Cancer Based on Elevated Prostate-specific Antigen Values: Results from a Randomized Prospective Blinded Controlled Trial
European Urology·2015· 178 cited
Tumor infiltrating CD8<sup>+</sup>T lymphocyte count is independent of tumor TLR9 status in treatment naïve triple negative breast cancer and renal cell carcinoma
OncoImmunology·2015· 44 citedOpen Access
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade
Human Molecular Genetics·2014· 15 citedOpen Access
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Frequent Co-authors

Leila Risteli(13), Juha Risteli(13), Arja Jukkola‐Vuorinen(12), Peeter Karihtala(11), Robert Winqvist(9), Markku H. Vaarala(7), Katri Pylkäs(7), Jukka Melkko(6), Frej Stenbäck(6), Ylermi Soini(6), Graham J. Mann(6), Arja Jukkola‐Vuorinen(5), Ulla Puistola(5), Jaana M. Hartikainen(5), Pasi Hirvikoski(5), Päivi Auvinen(4), Kirsi‐Maria Haapasaari(4), Carl Blomqvist(4), Katri Vuopala(4), Hanna Ronkainen(4)