Search engine for discovering works of Art, research articles, and books related to Art and Culture
Javascript must be enabled to continue!
In Memoriam Gunnar Kulldorff (1927 –2015) by Risto Lehtonen and Imbi Traat
View through CrossRef
Gunnar Kulldorff, an influential scientist and leading person in several scientific and professional organizations, passed away on 25 June 2015 in Umeå, Sweden.
Title: In Memoriam Gunnar Kulldorff (1927 –2015) by Risto Lehtonen and Imbi Traat
Description:
Gunnar Kulldorff, an influential scientist and leading person in several scientific and professional organizations, passed away on 25 June 2015 in Umeå, Sweden.
Related Results
Nomenclatural Studies Toward a World List of Diptera Genus-Group Names. Part IV: Charles Henry Tyler Townsend
Nomenclatural Studies Toward a World List of Diptera Genus-Group Names. Part IV: Charles Henry Tyler Townsend
The Diptera genus-group names of Charles Henry Tyler Townsend are reviewed and annotated. A total of 1506 available genus-group names in 12 families of Diptera are listed alphabeti...
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
AbstractAutosomal genetic analyses of blood lipids have yielded key insights for coronary heart disease (CHD). However, X chromosome genetic variation is understudied for blood lip...
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
AbstractUterine leiomyomata (UL) are the most common tumours of the female genital tract and the primary cause of surgical removal of the uterus. Genetic factors contribute to UL s...
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
A FinnGen pilot clinical recall study for Alzheimer’s disease
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...
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
ImportanceA genetic contribution to preeclampsia susceptibility has been established but is still incompletely understood.ObjectiveTo disentangle the underlying genetic architectur...