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Alexander Teumer (1976-)

Name	Alexander Teumer
Zeit	1976- (Lebensdaten)
Ort	Zwickau (Geburtsort) Greifswald (Wirkungsort) Deutschland
Akademischer Grad bzw. Titel	Dr. rer. nat. Dr. rer. med. habil.
Beziehung	Ernst-Moritz-Arndt-Universität Greifswald (Promotion) (2010)
Weitere Angaben	Stand 2019: Mitarbeiter am Institut für Community Medicine, Abt. SHIP KEF, Universitätsmedizin Greifswald
Datensatztyp	Person
GND-Nummer	1196553432
Datensatz-ID	1196553432
Beteiligt an alle anzeigen A meta-analysis of genome-wide studies of resilience in the German population Distinct genetic liability profiles define clinically relevant patient strata across common diseases Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements Methylation Patterns of the FKBP5 Gene in Association with Childhood Maltreatment and Depressive Disorders Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease OTTERS: a powerful TWAS framework leveraging summary-level reference data High Thyroid-Stimulating Hormone and Low Free Triiodothyronine Levels Are Associated with Chronic Kidney Disease in Three Population-Based Studies from Germany Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus Meta-analyses identify DNA methylation associated with kidney function and damage Cerebral small vessel disease genomics and its implications across the lifespan Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution Methylation of the FKBP5 gene in association with FKBP5 genotypes, childhood maltreatment and depression Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity Multi-ethnic genome-wide association study for atrial fibrillation Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function Genome-wide association and functional follow-up reveals new Loci for kidney function Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function Microarray-based Genome-Wide Association Studies (GWAS) using data generated by Allelotyping and by individual Genotyping Replication of the association of chromosomal region 9p21.3with generalized aggressive periodontitis (gAgP) using an independent case-control cohort Microarray-based genome-wide association studies (GWAS) using data generated by allelotyping and by individual genotyping

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Katalog der Deutschen Nationalbibliothek

Alexander Teumer (1976-)

A meta-analysis of genome-wide studies of resilience in the German population

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

Methylation Patterns of the FKBP5 Gene in Association with Childhood Maltreatment and Depressive Disorders

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

OTTERS: a powerful TWAS framework leveraging summary-level reference data

High Thyroid-Stimulating Hormone and Low Free Triiodothyronine Levels Are Associated with Chronic Kidney Disease in Three Population-Based Studies from Germany

Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning

Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women

Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus

Meta-analyses identify DNA methylation associated with kidney function and damage

Cerebral small vessel disease genomics and its implications across the lifespan

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

Methylation of the FKBP5 gene in association with FKBP5 genotypes, childhood maltreatment and depression

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels

Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci

Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus

PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

Multi-ethnic genome-wide association study for atrial fibrillation

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Genome-wide association and functional follow-up reveals new Loci for kidney function

Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function

Microarray-based Genome-Wide Association Studies (GWAS) using data generated by Allelotyping and by individual Genotyping

Replication of the association of chromosomal region 9p21.3with generalized aggressive periodontitis (gAgP) using an independent case-control cohort

Microarray-based genome-wide association studies (GWAS) using data generated by allelotyping and by individual genotyping