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Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.
Free accessSchulte, Eva C / Kousi, Maria / Tan, Perciliz L et al. | BASE | 2017 -
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
National licenceWinkelmann, Juliane / Schormair, Barbara / Lichtner, Peter et al. | Nature Publishing Group | 2007 -
Fat Mass and Obesity-Associated Gene (FTO) in Eating Disorders: Evidence for Association of the rs9939609 Obesity Risk Allele with Bulimia nervosa and Anorexia nervosa
Müller, Timo D. / Greene, Brandon H. / Bellodi, Laura et al. | Karger Verlag | 2012 -
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
National licenceSchormair, Barbara / Kemlink, David / Roeske, Darina et al. | Nature Publishing Group | 2008 -
The NINJA-2 catalog of hybrid post-Newtonian/numerical-relativity waveforms for non-precessing black-hole binaries
Free accessAjith, P. / Boyle, Michael / Brown, Duncan A. et al. | ArXiv | 2012 -
Error-analysis and comparison to analytical models of numerical waveforms produced by the NRAR Collaboration
Free accessHinder, Ian / Buonanno, Alessandra / Boyle, Michael et al. | ArXiv | 2013 -
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
Free accessSchormair, Barbara / Zhao, Chen / Bell, Steven et al. | BASE | 2018 -
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
Free accessSchormair, Barbara / Zhao, Chen / Bell, Steven et al. | BASE | 2018 -
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Degenhardt, Frauke / Ellinghaus, David / Juzenas, Simonas et al. | DataCite | 2022 -
Large-scale association analysis identifies new risk loci for coronary artery disease.
Free accessCARDIoGRAMplusC4D Consortium / Deloukas, Panos / Kanoni, Stavroula et al. | BASE | 2017 -
The genetic architecture of type 2 diabetes
Free accessFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2016 -
The genetic architecture of type 2 diabetes
Free accessFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2016 -
The genetic architecture of type 2 diabetes
Free accessFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2016 -
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Free accessLango Allen, Hana / Estrada, Karol / Lettre, Guillaume et al. | BASE | 2010 -
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Free accessJason, Flannick / Fuchsberger, Christian / Mahajan, Anubha et al. | BASE | 2017 -
Data Descriptor:Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Free accessFlannick, Jason / Fuchsberger, Christian / Mahajan, Anubha et al. | BASE | 2017 -
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls:Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Free accessFlannick, Jason / Fuchsberger, Christian / Mahajan, Anubha et al. | BASE | 2017 -
Data Descriptor : Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Free accessFlannick, Jason / Fuchsberger, Christian / Mahajan, Anubha et al. | BASE | 2017 -
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Free accessFlannick, Jason / Fuchsberger, Christian / Mahajan, Anubha et al. | BASE | 2018 -
The genetic architecture of type 2 diabetes.
Free accessFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2018 -
Data Descriptor : Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Free accessFlannick, Jason / Fuchsberger, Christian / Mahajan, Anubha et al. | BASE | 2017
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