[BOOK][B] The drosophilidae (Diptera) of fennoscandia and Denmark

G Bächli, F Viljoen, SA Escher, A Saura - 2005 - books.google.com
Many species of Drosophila are very important laboratory animals in almost all fields of
biological research, because of the ease of culturing on artificial media as well as of their rapid …

Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease

…, C Meisinger, T Esko, E Mihailov, SA Escher… - Journal of the American …, 2017 - jacc.org
Background : Genome-wide association studies have so far identified 56 loci associated with
risk of coronary artery disease (CAD). Many CAD loci show pleiotropy; that is, they are also …

[HTML][HTML] Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

…, A Dehghan, GB Ehret, G Eiriksdottir, SA Escher… - Nature …, 2015 - nature.com
Fasting glucose and insulin are intermediate traits for type 2 diabetes. Here we explore the
role of coding variation on these traits by analysis of variants on the HumanExome BeadChip …

A comprehensive evaluation of the genetic architecture of sudden cardiac arrest

…, C Glinge, V Tragante, SA Escher… - European heart …, 2018 - academic.oup.com
Aims Sudden cardiac arrest (SCA) accounts for 10% of adult mortality in Western populations.
We aim to identify potential loci associated with SCA and to identify risk factors causally …

The Drosophila Glucose Transporter Gene: cDNA Sequence, Phylogenetic Comparisons, Analysis of Functional Sites and Secondary Structures

SA Escher, Å Rasmuson‐Lestander - Hereditas, 1999 - Wiley Online Library
Facilitative glucose transport is mediated by members of the glucose transporter (GLUT)
protein family that belong to the large superfamily of twelve transmembrane segment …

A novel mutation in the LIM homeobox 3 gene is responsible for combined pituitary hormone deficiency, hearing impairment, and vertebral malformations

…, H Jonsson, P Sehlin, SA Escher - The Journal of …, 2009 - academic.oup.com
Context: The LIM homeobox 3 (LHX3) LIM-homeodomain transcription factor gene, found in
both man and mouse, is required for development of the pituitary and motor neurons, and is …

Linkage of Ischemic Stroke to the PDE4D Region on 5q in a Swedish Population

…, P Lindgren, AK Nilsson, T Janunger, SA Escher… - Stroke, 2005 - Am Heart Assoc
Background and Purpose— Recent Icelandic studies have demonstrated linkage for common
forms of stroke to chromosome 5q12 and association between phosphodiesterase4D (…

[HTML][HTML] Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study

…, D Shungin, RW Koivula, G Hallmans, SA Escher… - PLoS …, 2014 - journals.plos.org
Recent genome-wide meta-analyses identified 157 loci associated with cross-sectional lipid
traits. Here we tested whether these loci associate (singly and in trait-specific genetic risk …

[HTML][HTML] CELSR2 is a candidate susceptibility gene in idiopathic scoliosis

E Einarsdottir, A Grauers, J Wang, H Jiao, SA Escher… - PLoS …, 2017 - journals.plos.org
A Swedish pedigree with an autosomal dominant inheritance of idiopathic scoliosis was initially
studied by genetic linkage analysis, prioritising genomic regions for further analysis. This …

Diabetes mellitus, high BMI and low education level predict sudden cardiac death within 24 hours of incident myocardial infarction

…, P Wennberg, D Lundblad, SA Escher… - European Journal of …, 2016 - academic.oup.com
Background More than half of cardiovascular mortality occurs outside the hospital, mainly
due to consistently low survival rates from out-of-hospital cardiac arrest. Methods This is a …