Articles with public access mandates - Stefan CoassinLearn more
Not available anywhere: 4
Association of mitochondrial iron deficiency and dysfunction with idiopathic restless legs syndrome
D Haschka, C Volani, A Stefani, P Tymoszuk, T Mitterling, E Holzknecht, ...
Movement Disorders 34 (1), 114-123, 2019
Mandates: Austrian Science Fund
No association of two functional polymorphisms in human ALOX15 with myocardial infarction
M Hersberger, M Müller, J Marti-Jaun, IM Heid, S Coassin, TF Young, ...
Atherosclerosis 205 (1), 192-196, 2009
Mandates: Swiss National Science Foundation, US National Institutes of Health
Update of the effect estimates for common variants associated with carotid intima media thickness within four independent samples: The Bonn IMT Family Study, the Heinz Nixdorf …
MH Geisel, S Coassin, N Heßler, M Bauer, L Eisele, R Erbel, M Haun, ...
Atherosclerosis 249, 83-87, 2016
Mandates: German Research Foundation
Mechanistic insights into lipoprotein (a): from infamous to ‘inflammous’
S Coassin, F Kronenberg
European Heart Journal 41 (24), 2272-2274, 2020
Mandates: Austrian Science Fund
Available somewhere: 60
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
Z Dastani, MF Hivert, N Timpson, JRB Perry, X Yuan, RA Scott, ...
PLoS genetics 8 (3), e1002607, 2012
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
C Pattaro, A Teumer, M Gorski, AY Chu, M Li, V Mijatovic, M Garnaas, ...
Nature communications 7 (1), 10023, 2016
Mandates: US National Institutes of Health, British Heart Foundation, UK Economic and …
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
AF Schmidt, DI Swerdlow, MV Holmes, RS Patel, Z Fairhurst-Hunter, ...
The lancet Diabetes & endocrinology 5 (2), 97-105, 2017
Mandates: US National Institutes of Health, British Heart Foundation, UK Economic and …
CUBN is a gene locus for albuminuria
CA Böger, MH Chen, A Tin, M Olden, A Köttgen, IH de Boer, ...
Journal of the American Society of Nephrology 22 (3), 555-570, 2011
Mandates: US National Institutes of Health, Austrian Science Fund, Swedish Research …
Association of eGFR-related loci identified by GWAS with incident CKD and ESRD
CA Böger, M Gorski, M Li, MM Hoffmann, C Huang, Q Yang, A Teumer, ...
PLoS genetics 7 (9), e1002292, 2011
Mandates: Swiss National Science Foundation, US National Institutes of Health, German …
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals
IM Heid, P Henneman, A Hicks, S Coassin, T Winkler, YS Aulchenko, ...
Atherosclerosis 208 (2), 412-420, 2010
Mandates: US National Institutes of Health
Genome-wide association studies identify genetic loci associated with albuminuria in diabetes
A Teumer, A Tin, R Sorice, M Gorski, NC Yeo, AY Chu, M Li, Y Li, ...
Diabetes 65 (3), 803-817, 2016
Mandates: Swiss National Science Foundation, US National Institutes of Health, US …
Genome-wide association study of kidney function decline in individuals of European descent
M Gorski, A Tin, M Garnaas, GM McMahon, AY Chu, BO Tayo, C Pattaro, ...
Kidney international 87 (5), 1017-1029, 2015
Mandates: Swiss National Science Foundation, US National Institutes of Health, US …
Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review
E Boes, S Coassin, B Kollerits, IM Heid, F Kronenberg
Experimental gerontology 44 (3), 136-160, 2009
Mandates: US National Institutes of Health
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms [S]
S Mack, S Coassin, R Rueedi, NA Yousri, I Seppälä, C Gieger, ...
Journal of lipid research 58 (9), 1834-1844, 2017
Mandates: Swiss National Science Foundation, US National Institutes of Health …
Sex-Specific Association of the Putative Fructose Transporter SLC2A9 Variants With Uric Acid Levels Is Modified by BMI
A BRANDSTatter, S Kiechl, B Kollerits, SC Hunt, IM Heid, S Coassin, ...
Diabetes care 31 (8), 1662-1667, 2008
Mandates: US National Institutes of Health
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies
JM Murabito, CC White, M Kavousi, YV Sun, MF Feitosa, V Nambi, ...
Circulation: Cardiovascular Genetics 5 (1), 100-112, 2012
Mandates: US National Institutes of Health, Dunhill Medical Trust, UK
Lipoprotein (a) beyond the kringle IV repeat polymorphism: the complexity of genetic variation in the LPA gene
S Coassin, F Kronenberg
Atherosclerosis 349, 17-35, 2022
Mandates: US National Institutes of Health, Austrian Science Fund
The TMEM189 gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogens
ER Werner, MA Keller, S Sailer, K Lackner, J Koch, M Hermann, ...
Proceedings of the National Academy of Sciences 117 (14), 7792-7798, 2020
Mandates: Austrian Science Fund, Wellcome Trust
A novel but frequent variant in LPA KIV-2 is associated with a pronounced Lp(a) and cardiovascular risk reduction
S Coassin, G Erhart, H Weissensteiner, M Eca Guimarães de Araújo, ...
European heart journal 38 (23), 1823-1831, 2017
Mandates: Austrian Science Fund, Helmholtz Association, Federal Ministry of Education …
A common variant in the adiponutrin gene influences liver enzyme values
B Kollerits, S Coassin, S Kiechl, SC Hunt, B Paulweber, J Willeit, ...
Journal of medical genetics 47 (2), 116-119, 2010
Mandates: US National Institutes of Health
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