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Adrienne Tin

Name	Adrienne Tin
Ort	USA
Beziehung	Johns Hopkins Bloomberg School of Public Health Epidemiologie (Thema)
Datensatztyp	Person
GND-Nummer	1204518203
Datensatz-ID	1204518203
Beteiligt an alle anzeigen 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 Large scale plasma proteomics identifies novel proteins and protein networks associated with heart failure development Identification of circulating proteins associated with general cognitive function among middle-aged and older adults Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies Association between Circulating Protein C Levels and Incident Dementia: The Atherosclerosis Risk in Communities Study 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 Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline Urine 6-bromotryptophan: associations with genetic variants and incident end-stage kidney disease Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans Rare variants in SLC5A10 are associated with serum 1,5-anhydroglucitol (1,5-AG) in the Atherosclerosis Risk in Communities (ARIC) Study Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria Rare variants in SLC5A10 are associated with serum 1,5-anhydroglucitol (1,5-AG) in the Atherosclerosis Risk in Communities (ARIC) Study Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes Serum metabolomic profile of incident diabetes Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels Epigenome-wide association studies identify DNA methylation associated with kidney function 1000 genomes-based meta-analysis identifies 10 novel loci for kidney function Epigenome-wide association studies identify DNA methylation associated with kidney function Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function

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Adrienne Tin

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

Large scale plasma proteomics identifies novel proteins and protein networks associated with heart failure development

Identification of circulating proteins associated with general cognitive function among middle-aged and older adults

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

Association between Circulating Protein C Levels and Incident Dementia: The Atherosclerosis Risk in Communities Study

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

Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

Urine 6-bromotryptophan: associations with genetic variants and incident end-stage kidney disease

Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans

Rare variants in SLC5A10 are associated with serum 1,5-anhydroglucitol (1,5-AG) in the Atherosclerosis Risk in Communities (ARIC) Study

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

Rare variants in SLC5A10 are associated with serum 1,5-anhydroglucitol (1,5-AG) in the Atherosclerosis Risk in Communities (ARIC) Study

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

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

Serum metabolomic profile of incident diabetes

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

Epigenome-wide association studies identify DNA methylation associated with kidney function

1000 genomes-based meta-analysis identifies 10 novel loci for kidney function

Epigenome-wide association studies identify DNA methylation associated with kidney function

Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations

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