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1.. MANSCH GÂNGLÁT 2. PCIKA Po],KETTE GA],OPP J. SCHOTTTs nn¡¡¡jiNDER PAS DE QUATTRE 4. ANGIAIS ENGEI,Sr¡, snÄ}¡NvINSPOISKA 5. MAZURKA NUMPEDA.RRA HA¡I.BO 6. VATS 7" MARKERAD POISKA SVINGEDANS BUGADANS RUNî¡¡IOU TONEPOISKA g¡ SLÄNCPOLSKA POI,ONAIS SEXTONDELSPOLSKA 9. l,ll¡cD¡,¡gs. 10. MeNUEttn 1 1. ovRroA r,Ãr.nn 12. ÖVRIGT MATEI{IAL .i 6 vAlS 5ot\4 kÁLIÅ0ES "kur'IGENS vÁe5" S?ËlÄ¡ 4V PrR o¡.gsoN

https://www.folklivsarkivet.lu.se/fileadmin/user_upload/folklivsarkivet/Musiksamlingarna_webb/Dokument/Parm_4_B.pdf - 2026-05-28

K Nilsson LTHs 8:e Pedagogiska Inspirationskonferens, 17 december 2014 Abstract — Examination genom akademiskt artikelskrivande inom en grundkurs på LTH, tidigt i studenternas utbildning, beskrivs och diskuteras mot bakgrund av de senaste årens uppmärksammade krav på hög kvalitet på skrivna texter. Olika aspekter av den valda examinationsformen skildras, så som vilka typer av återkoppling som anvä

https://www.lth.se/fileadmin/lth/genombrottet/konferens2014/21c_Nilsson.pdf - 2026-05-29

Flextidsark Grunddata Lunds universitet Flextidsredovisning för år 2023 Startsida Fyll i dina personuppgifter i den inramade rutan nedan - fyll i alla färgade fält, tack (och ändra sådana förifyllda uppgifter, även tjänsteomfattning och start-/slutdatum, som inte stämmer för dig)! Uppgifterna överförs till månadsbladen och hamnar ovanför kolumnrubrikerna – de syns först när du skriver ut eller när

https://www.lusem.lu.se/internal/sites/lusem.lu.se.internal/files/2024-02/flex2023_avancerad_korr-3.xlsx - 2026-05-30

1 Inconvenient Human Rights: A report of the Raoul Wallenberg Institute for Human Rights and Humanitarian Law, Södertörn University, and the NuLawLab of Northeastern University School of Law, April 2016. Access to Water and Sanitation in Sweden’s Informal Roma Settlements 2 3 Acknowledgements The primary authors of this report are Martha Davis (Raoul Wallenberg Institute), and Na- tasha Ryan (Söde

https://rwi.lu.se/app/uploads/2016/06/Inconvenient-Human-Rights.pdf - 2026-05-28

Microsoft Word - HemsideinfoPressreleaseNov2015_sv_2015117 ICOS Sweden    20151117  1    Europeisk satsning kartlägger kolbalansen – några exempel från ICOS  Swedens mätstationer  ICOS har byggts upp för att kartlägga växthusgasflödena i Europa och ICOS Sweden är det svenska  bidraget till denna europeiska forskningsinfrastruktur. Hur kan då dessa flöden kartläggas? Nedan har vi  samlat några exem

https://www.hallbarhet.lu.se/sites/hallbarhet.lu.se/files/icos_info_sve_pressreleasenov2015.pdf - 2026-05-30

rapport.dvi Department of Construction Sciences Solid Mechanics ISRN LUTFD2/TFHF–07/5128-SE(1-60) AN IMPLEMENTATION OF MESH FREE METHODS FOR MECHANICAL PROBLEMS AT LARGE STRAINS Master Thesis by VIKTOR PETERSSON SUPERVISOR PH. D. PAUL HÅKANSSON EXAMINER PROF. MATTI RISTINMAA Copyright c© 2007 by Div. of Solid Mechanics, Viktor Petersson Printed by Media-Tryck, Lund ,Sweden For information, addres

https://www.solid.lth.se/fileadmin/hallfasthetslara/utbildning/examensarbete/TFHF5128.pdf - 2026-05-28

Reduced glomerular filtration rate defines chronic kidney disease and is associated with cardiovascular and all-cause mortality. We conducted a meta-analysis of genome-wide association studies for estimated glomerular filtration rate (eGFR), combining data across 133,413 individuals with replication in up to 42,166 individuals. We identify 24 new and confirm 29 previously identified loci. Of these

Sjögren's disease is a complex autoimmune disease with twelve established susceptibility loci. This genome-wide association study (GWAS) identifies ten novel genome-wide significant (GWS) regions in Sjögren's cases of European ancestry: CD247, NAB1, PTTG1-MIR146A, PRDM1-ATG5, TNFAIP3, XKR6, MAPT-CRHR1, RPTOR-CHMP6-BAIAP6, TYK2, SYNGR1. Polygenic risk scores yield predictability (AUROC = 0.71) and

Two single nucleotide polymorphisms (SNPs) at 6q25.1, near the ESR1 gene, have been implicated in the susceptibility to breast cancer for Asian (rs2046210) and European women (rs9397435). A genome-wide association study in Europeans identified two further breast cancer susceptibility variants: rs11249433 at 1p11.2 and rs999737 in RAD51L1 at 14q24.1. Although previously identified breast cancer sus

Numerous obesity loci have been identified using genome-wide association studies. A UK study indicated that physical activity may attenuate the cumulative effect of 12 of these loci, but replication studies are lacking. Therefore, we tested whether the aggregate effect of these loci is diminished in adults of European ancestry reporting high levels of physical activity. Twelve obesity-susceptibili

A recent genome-wide association study reported five loci for which there was strong, but sub-genome-wide significant evidence for association with multiple sclerosis risk. The aim of this study was to evaluate the role of these potential risk loci in a large and independent data set of ≈ 20,000 subjects. We tested five single nucleotide polymorphisms rs228614 (MANBA), rs630923 (CXCR5), rs2744148

Atrial fibrillation (AF) is a prevalent and morbid abnormality of the heart rhythm with a strong genetic component. Here, we meta-analyzed genome and exome sequencing data from 36 studies that included 52,416 AF cases and 277,762 controls. In burden tests of rare coding variation, we identified novel associations between AF and the genes MYBPC3, LMNA, PKP2, FAM189A2 and KDM5B. We further identifie

Genome-wide association studies (GWASs) have revealed numerous loci for areal bone mineral density (aBMD). We completed the first GWAS meta-analysis (n=15,275) of lumbar spine volumetric BMD (vBMD) measured by quantitative computed tomography (QCT), allowing for examination of the trabecular bone compartment. SNPs that were significantly associated with vBMD were also examined in two GWAS meta-ana

Germline mutations in BRCA1 and BRCA2 are associated with increased risks of breast and ovarian cancer. A genome-wide association study (GWAS) identified six alleles associated with risk of ovarian cancer for women in the general population. We evaluated four of these loci as potential modifiers of ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. Four single-nucleotide polymorphisms (SNP

BACKGROUND: Breast cancer (BC) patients with a germline CHEK2 c.1100delC variant have an increased risk of contralateral BC (CBC) and worse BC-specific survival (BCSS) compared to non-carriers.AIM: To assessed the associations of CHEK2 c.1100delC, radiotherapy, and systemic treatment with CBC risk and BCSS.METHODS: Analyses were based on 82,701 women diagnosed with a first primary invasive BC incl

BACKGROUND: Genome-wide studies of gene-environment interactions (G×E) may identify variants associated with disease risk in conjunction with lifestyle/environmental exposures. We conducted a genome-wide G×E analysis of ~ 7.6 million common variants and seven lifestyle/environmental risk factors for breast cancer risk overall and for estrogen receptor positive (ER +) breast cancer.METHODS: Analyse

Background: Low-frequency variants play an important role in breast cancer (BC) susceptibility. Gene-based methods can increase power by combining multiple variants in the same gene and help identify target genes. Methods: We evaluated the potential of gene-based aggregation in the Breast Cancer Association Consortium cohorts including 83,471 cases and 59,199 controls. Low-frequency variants were

OBJECTIVE: In observational epidemiologic studies, higher plasma high-density lipoprotein cholesterol (HDL-C) has been associated with increased risk of intracerebral hemorrhage (ICH). DNA sequence variants that decrease cholesteryl ester transfer protein (CETP) gene activity increase plasma HDL-C; as such, medicines that inhibit CETP and raise HDL-C are in clinical development. Here, we test the

High-profile studies have provided conflicting results regarding the involvement of the Omi/HtrA2 gene in Parkinson's disease (PD) susceptibility. Therefore, we performed a large-scale analysis of the association of common Omi/HtrA2 variants in the Genetic Epidemiology of Parkinson's disease (GEO-PD) consortium. GEO-PD sites provided clinical and genetic data including affection status, gender, et

OBJECTIVE: Eleven genetic loci have reached genome-wide significance in a recent meta-analysis of genome-wide association studies in Parkinson disease (PD) based on populations of Caucasian descent. The extent to which these genetic effects are consistent across different populations is unknown.METHODS: Investigators from the Genetic Epidemiology of Parkinson's Disease Consortium were invited to p