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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 -
The genetic architecture of type 2 diabetes.
Free accessFuchsberger, 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.
Free accessSchulte, Eva C. / Kousi, Maria / Tan, Perciliz L. et al. | BASE | 2014 -
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 -
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 -
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 -
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 -
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon
Free accessSpieler, Derek / Kaffe, Maria / Knauf, Franziska et al. | BASE | 2014 -
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon.
Free accessSpieler, Derek / Kaffe, Maria / Knauf, Franziska et al. | BASE | 2017 -
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality
Free accessBöger, Carsten A. / Gorski, Mathias / McMahon, Gearoid M. et al. | BASE | 2017 -
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis
Free accessTilch, 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.
Free accessSchormair, Barbara / Zhao, Chen / Bell, Steven 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.
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 -
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk.
Free accessFischer, Annegret / Ellinghaus, David / Nutsua, Marcel et al. | BASE | 2017 -
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 -
Diminishing benefits of urban living for children and adolescents’ growth and development
Free accessMishra, Anu / Zhou, Bin / Rodriguez-Martinez, Andrea et al. | BASE | 2023 -
Diminishing benefits of urban living for children and adolescents’ growth and development
Free accessMishra, Anu / Zhou, Bin / Rodriguez-Martinez, Andrea et al. | BASE | 2023
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