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Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts
Schwantes-An, Tae-Hwi / Zhang, Juan / Chen, Li-Shiun et al. | Online Contents | 2015 -
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 -
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 -
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 -
Developmental Dyslexia – Recurrence Risk Estimates from a German Bi-Center Study Using the Single Proband Sib Pair Design
Ziegler, Andreas / König, Inke R. / Deimel, Wolfgang et al. | Karger Verlag | 2005 -
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 -
Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder
Mühleisen, Thomas W. / Reinbold, Céline S. / Forstner, Andreas J. et al. | British Library Online Contents | 2018 -
Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder
Mühleisen, Thomas W. / Reinbold, Céline S. / Forstner, Andreas J. et al. | British Library Online Contents | 2018 -
Genetic architecture of subcortical brain structures in 38,851 individuals
Freier ZugriffSatizabal, Claudia L / Adams, Hieab H H / Hibar, Derrek P et al. | BASE | 2019 -
Genetic architecture of subcortical brain structures in 38,851 individuals
Freier ZugriffSatizabal, Claudia L / Adams, Hieab H H / Hibar, Derrek P et al. | BASE | 2019 -
Genetic architecture of subcortical brain structures in 38,851 individuals
Freier ZugriffSatizabal, Claudia L. / Adams, Hieab H.H. / Hibar, Derrek P. et al. | BASE | 2019 -
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
NationallizenzWinkelmann, Juliane / Schormair, Barbara / Lichtner, Peter et al. | Nature Publishing Group | 2007 -
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Freier ZugriffLango Allen, Hana / Estrada, Karol / Lettre, Guillaume et al. | BASE | 2010 -
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk.
Freier ZugriffFischer, Annegret / Ellinghaus, David / Nutsua, Marcel 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 -
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 -
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 shared risk loci and pathways for bipolar disorder and schizophrenia
Freier ZugriffForstner, Andreas J. / Hecker, Julian / Mattheisen, Manuel et al. | BASE | 2017 -
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Freier ZugriffTrubetskoy, Vassily / Pardiñas, Antonio F / Qi, Ting et al. | BASE | 2022 -
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality
Freier ZugriffBöger, Carsten A. / Gorski, Mathias / McMahon, Gearoid M. et al. | BASE | 2017 -
Novel genetic loci associated with hippocampal volume
Freier ZugriffHibar, Derrek P. / Adams, Hieab H.H. / Jahanshad, Neda et al. | BASE | 2017 -
Novel genetic loci associated with hippocampal volume
Freier ZugriffHibar, Derrek P / Adams, Hieab H H / Jahanshad, Neda et al. | BASE | 2017 -
Novel genetic loci associated with hippocampal volume
Freier ZugriffHibar, Derrek / Adams, Hieab H.H. / Jahanshad, Neda et al. | BASE | 2017 -
Novel genetic loci associated with hippocampal volume
Freier ZugriffHibar, Derrek P. / Hieab, H.H. Adams / Chauhan, Ganesh et al. | BASE | 2017 -
Novel genetic loci associated with hippocampal volume
Freier ZugriffHibar, Derrek P / Adams, Hieab H H / Jahanshad, Neda et al. | BASE | 2017 -
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
NationallizenzSchormair, Barbara / Kemlink, David / Roeske, Darina et al. | Nature Publishing Group | 2008 -
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 | 2014 -
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 -
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 -
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 -
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 -
Shared genetic etiology between alcohol dependence and major depressive disorder
Foo, Jerome C. / Streit, Fabian / Treutlein, Jens et al. | British Library Online Contents | 2018 -
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease
Shadrin, Alexey A. / Mucha, Sören / Ellinghaus, David et al. | Wiley | 2021 -
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 | 2014 -
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 -
The genetic architecture of the human cerebral cortex
Grasby, Katrina L. / Jahanshad, Neda / Painter, Jodie N. et al. | AAAS | 2020 -
The genetic architecture of type 2 diabetes
Freier ZugriffFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2016 -
The genetic architecture of type 2 diabetes
Freier ZugriffFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2016 -
The genetic architecture of type 2 diabetes
Freier ZugriffFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2016 -
The genetic architecture of type 2 diabetes.
Freier ZugriffFuchsberger, Christian / Flannick, Jason / Teslovich, Tanya M et al. | BASE | 2018
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