Author details

Full Name

Matthias Wuttke

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36993625	Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).	medRxiv	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36719378	SLC26A1 is a major determinant of sulfate homeostasis in humans.	J Clin Invest	2023
37277652	Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine.	Nat Genet	2023
36890159	Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank.	Nat Commun	2023
36481179	A polygenic score for reduced kidney function and adverse outcomes in a cohort with chronic kidney disease.	Kidney Int	2023
37126668	Genetic Association Analysis of Chronic Kidney Disease Progression in a Small Korean Cohort Study.		2023
34999880	Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease.	Int J Epidemiol	2022
35446786	Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases.	JCI Insight	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35985372	Including APOL1 alleles and ancestry adjustments improve a genome-wide polygenic CKD score.	Kidney International	2022
35228297	Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.	J Am Soc Nephrol	2022
33137338	Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.	Kidney Int	2021
34272381	Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals.	Nat Commun	2021
34140400	Self-Reported Medication Use and Urinary Drug Metabolites in the German Chronic Kidney Disease (GCKD) Study.	J Am Soc Nephrol	2021
33978749	Assessment of significance of conditionally independent GWAS signals.	Bioinformatics	2021
34337522	<i>CDH12</i> as a Candidate Gene for Kidney Injury in Posterior Urethral Valve Cases: A Genome-wide Association Study Among Patients with Obstructive Uropathies.	Eur Urol Open Sci	2021
32764137	Integration of GWAS Summary Statistics and Gene Expression Reveals Target Cell Types Underlying Kidney Function Traits.	J Am Soc Nephrol	2020
31959995	Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans.	Nat Genet	2020
31734095	Corrigendum to "Preeclampsia postpartum: Impairment of cerebral autoregulation and reversible cerebral hyperperfusion" [Pregnancy Hypertens. 17 (2019) 121-126].	Pregnancy Hypertension	2020
32231244	The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.	Nat Commun	2020
31152163	A catalog of genetic loci associated with kidney function from analyses of a million individuals.	Nat Genet	2019
30140068	Genetic associations of hemoglobin in children with chronic kidney disease in the PediGFR Consortium.	Pediatr Res	2019
31494641	Maternal blood pressure levels prepartum correlate with neonatal birth weight in preeclampsia.	Journal of Perinatal Medicine	2019
31487628	Preeclampsia postpartum: Impairment of cerebral autoregulation and reversible cerebral hyperperfusion.	Pregnancy Hypertension	2019
31451708	Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.	Nat Commun	2019
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018
30297969	Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.	Nat Genet	2018
29198386	X-Linked Glomerulopathy Due to COL4A5 FounderÂ Variant.	Am J Kidney Dis	2018
29545352	Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.	J Am Soc Nephrol	2018
27333618	Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies.	Nephrol Dial Transplant	2017
29066732	Associations between genetic risk variants for kidney diseases and kidney disease etiology.	Sci Rep	2017
26490952	Genome-wide association studies in pediatric chronic kidney disease.	Pediatr Nephrol	2016
27313313	Genetic, Environmental, and Disease-Associated Correlates of Vitamin D Status in Children with CKD.	Clin J Am Soc Nephrol	2016
27477491	Insights into kidney diseases from genome-wide association studies.	Nat Rev Nephrol	2016
26420894	Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium.	Nephrol Dial Transplant	2016
26613025	A COL4A5 mutation with glomerular disease and signs of chronic thrombotic microangiopathy.	Clin Kidney J	2015
25465167	Genome-wide association studies in nephrology: using known associations for data checks.	Am J Kidney Dis	2015
25893603	Genomic imbalances in pediatric patients with chronic kidney disease.	J Clin Invest	2015
21246027	Correspondence (letter to the editor): Computerized Physician Order System (CPOE).	Deutsches A&#x0308;rzteblatt international	2010