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Diminishing benefits of urban living for children and adolescents’ growth and development
Freier ZugriffMishra, Anu / Zhou, Bin / Rodriguez-Martinez, Andrea et al. | BASE | 2023 -
Diminishing benefits of urban living for children and adolescents’ growth and development
Freier ZugriffMishra, Anu / Zhou, Bin / Rodriguez-Martinez, Andrea et al. | BASE | 2023 -
Diminishing benefits of urban living for children and adolescents’ growth and development
Freier ZugriffMishra, Anu / Zhou, Bin / Rodriguez-Martinez, Andrea et al. | BASE | 2023 -
Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study
Bauer, Alina / Zierer, Astrid / Gieger, Christian et al. | Wiley | 2021 -
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease
Shadrin, Alexey A. / Mucha, Sören / Ellinghaus, David et al. | Wiley | 2021 -
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis
Tilch, Erik / Schormair, Barbara / Zhao, Chen et al. | Wiley | 2020 -
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis
Freier ZugriffTilch, Erik / Schormair, Barbara / Zhao, Chen et al. | BASE | 2019 -
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
Freier ZugriffSchormair, 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.
Freier ZugriffSchormair, Barbara / Zhao, Chen / Bell, Steven et al. | BASE | 2018 -
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Freier ZugriffFlannick, Jason / Fuchsberger, Christian / Mahajan, Anubha et al. | BASE | 2018 -
The genetic architecture of type 2 diabetes.
Freier ZugriffFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2018 -
Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.
Freier ZugriffSchulte, Eva C / Kousi, Maria / Tan, Perciliz L et al. | BASE | 2017 -
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk.
Freier ZugriffFischer, Annegret / Ellinghaus, David / Nutsua, Marcel et al. | BASE | 2017 -
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon.
Freier ZugriffSpieler, Derek / Kaffe, Maria / Knauf, Franziska et al. | BASE | 2017 -
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
Freier ZugriffSchormair, Barbara / Zhao, Chen / Bell, Steven et al. | BASE | 2017 -
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality
Freier ZugriffBöger, Carsten A. / Gorski, Mathias / McMahon, Gearoid M. et al. | BASE | 2017 -
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Freier ZugriffJason, 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
Freier ZugriffFlannick, 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
Freier ZugriffFlannick, 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
Freier ZugriffFlannick, Jason / Fuchsberger, Christian / Mahajan, Anubha et al. | BASE | 2017