(Q34185066)

31 July 2017

title

A genome-wide association study of metabolic traits in human urine (English)

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genome-wide association study

31 July 2017

main subject

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11

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22

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14

Henry Völzke

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Alexander Teumer

16

Alexander Teumer

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Thomas Illig

20

Thomas Illig

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Henri Wallaschofski

2

Henri Wallaschofski

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Werner Römisch-Margl

23

Werner Römisch-Margl

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Robin Haring

Robin Haring

5

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Florian Kronenberg

Florian Kronenberg

9

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Karsten Suhre

Karsten Suhre

1

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Johannes Raffler

Johannes Raffler

3

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Uwe Völker

Uwe Völker

15

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Heinz Erich Wichmann

12

H-Erich Wichmann

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19

Stephan B Felix

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4

Nele Friedrich

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17

Reiner Biffar

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24

Matthias Nauck

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21

Heyo K Kroemer

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Kathrin Michael

6

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Christina Wasner

7

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Alexander Krebs

8

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David Chang

10

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Wolfgang Hoffmann

13

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Thomas Kocher

18

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31 July 2017

language of work or name

English

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publication date

15 May 2011

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31 July 2017

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31 July 2017

volume

43

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31 July 2017

issue

6

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31 July 2017

page(s)

565-569

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describes a project that uses

31 July 2017

genome-wide association study

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.837

inferred from title

exact match

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cites work

Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum

1 reference

A genome-wide perspective of genetic variation in human metabolism

21 January 2018

1 reference

Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study

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Genetic determinants of circulating sphingolipid concentrations in European populations

21 January 2018

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Targeted profiling: quantitative analysis of 1H NMR metabolomics data

21 January 2018

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Bioinformatics analysis of targeted metabolomics--uncovering old and new tales of diabetic mice under medication

21 January 2018

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Metabolic footprint of diabetes: a multiplatform metabolomics study in an epidemiological setting

21 January 2018

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beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities

21 January 2018

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Human alanine-glyoxylate aminotransferase 2 lowers asymmetric dimethylarginine and protects from inhibition of nitric oxide production

21 January 2018

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Association between exaggerated blood pressure response to exercise and serum asymmetric dimethylarginine levels

21 January 2018

1 reference

Differential effects of arginine methylation on diastolic dysfunction and disease progression in patients with chronic systolic heart failure

21 January 2018

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Accumulation of an endogenous inhibitor of nitric oxide synthesis in chronic renal failure

21 January 2018

1 reference

Asymmetric dimethylarginine and progression of chronic kidney disease: the mild to moderate kidney disease study

21 January 2018

1 reference

Asymmetrical dimethylarginine predicts progression to dialysis and death in patients with chronic kidney disease: a competing risks modeling approach

21 January 2018

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Disruption of methylarginine metabolism impairs vascular homeostasis

21 January 2018

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Joint effects of the N-acetyltransferase 1 and 2 (NAT1 and NAT2) genes and smoking on bladder carcinogenesis: a literature-based systematic HuGE review and evidence synthesis

21 January 2018

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A pharmacogenetic study of docetaxel and thalidomide in patients with castration-resistant prostate cancer using the DMET genotyping platform.

21 January 2018

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Biological, clinical and population relevance of 95 loci for blood lipids

21 January 2018

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Drug-induced liver injury: past, present and future.

21 January 2018

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A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

21 January 2018

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The genetic tyrosinemias

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Renal crystal deposits and histopathology in patients with cystine stones.

21 January 2018

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New loci associated with kidney function and chronic kidney disease

21 January 2018

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Genetic loci influencing kidney function and chronic kidney disease

21 January 2018

1 reference

Identification of mammalian proline transporter SIT1 (SLC6A20) with characteristics of classical system imino

21 January 2018

1 reference

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

21 January 2018

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Cohort Profile: The Study of Health in Pomerania

21 January 2018

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Study of Health In Pomerania (SHIP): a health examination survey in an east German region: objectives and design

21 January 2018

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21 January 2018

1 reference

β-Aminoisobutyric Acid (α-Methyl-β-Alanine): A New Amino-Acid Obtained from Human Urine

21 January 2018

1 reference

D-β-Aminoisobutyrate:pyruvate Aminotransferase in Mammalian Liver and Excretion of β-Aminoisobutyrate by Man

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21572414

12 December 2020

inferred from PubMed ID database lookup

Family studies on the urinary excretion of beta-aminoisobutyric acid

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21572414

12 December 2020

inferred from PubMed ID database lookup

Genetic study of beta-aminoisobutyric acid excretion by Japanese

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21572414

12 December 2020

inferred from PubMed ID database lookup

Urinary amino-acids in mice of different genotypes

1 reference

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.837

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31 July 2017

1 reference