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Kommentteja Outi Vuorenrinteelle
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Pirjo Tuomen kommentteja Outi Vuorenrinteelle koskien Vuorenrinteen väitöskirjaa.
Title: Kommentteja Outi Vuorenrinteelle
Description:
Pirjo Tuomen kommentteja Outi Vuorenrinteelle koskien Vuorenrinteen väitöskirjaa.
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Keppulointia ja rehjustusta Rööperin kulmilla: Paikannimistö sosiaalisen maantieteen rakentajana Outi Pakkasen ja Matti Yrjänä Joensuun rikosromaaneissa
Keppulointia ja rehjustusta Rööperin kulmilla: Paikannimistö sosiaalisen maantieteen rakentajana Outi Pakkasen ja Matti Yrjänä Joensuun rikosromaaneissa
Artikkeli tarkastelee Outi Pakkasen Maanantaihin on paljon matkaa (1975) ja Matti Yrjänä Joensuun Väkivallan virkamies (1976) -rikosromaaneissa esiintyvää paikannimistöä. Tutkimuks...
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Murrebuumin myötä monenlaiset murretta käyttävät sarjakuvasankarit ja sketsihahmot ovat muodostuneet lehtien ja television vakiokasvoiksi. Tällaisilla hahmoilla on suuri vaikutus i...
Opponentindlæg: Outi Turpeinen - Recombining ideas from art and cultural history museums in theory and practice
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Outi Turpeinen M.A. defended her doctoral dissertation, entitled “A Meaningful Museum Object. Critical visuality in cultural history museum exhibitions”, in public at the Universit...
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
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Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty
Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty
Abstract
Frailty is a clinically relevant phenotype with notable gaps in our understanding of its etiology. Using the Hospital Frailty Risk Score (HFRS) to define frailty...
NTHL1 is a recessive cancer susceptibility gene
NTHL1 is a recessive cancer susceptibility gene
AbstractIn search of novel breast cancer (BC) risk variants, we performed a whole-exome sequencing and variant analysis of 69 Finnish BC patients as well as analysed loss-of-functi...
A FinnGen pilot clinical recall study for Alzheimer’s disease
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AbstractSuccessful development of novel therapies requires that clinical trials are conducted in patient cohorts with the highest benefit-to-risk ratio. Population-based biobanks w...
Monoallelic TYROBP deletion is a novel risk factor for Alzheimer’s disease
Monoallelic TYROBP deletion is a novel risk factor for Alzheimer’s disease
Abstract
Biallelic loss-of-function variants in TYROBP and TREM2 cause autosomal recessive presenile dementia with bone cysts known as Nasu-Hakola disease (NHD, alternati...