Timo J. Wagner

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Journal: medRxiv : the preprint server for health sciences

Published: April 16, 2025

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Journal: American journal of human genetics

Published: April 01, 2025

Real-Time Detection and Control of Correlated Charge Tunneling in a Quantum Dot.

Journal: Physical review letters

Published: August 15, 2024

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

Journal: The Journal of clinical investigation

Published: June 01, 2022

Correction to: The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 24, 2021

Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.

Journal: Kidney international

Published: February 24, 2021

Collagen IVα345 dysfunction in glomerular basement membrane diseases. I. Discovery of a COL4A3 variant in familial Goodpasture's and Alport diseases.

Journal: The Journal of biological chemistry

Published: December 29, 2020

Loss of the collagen IV modifier prolyl 3-hydroxylase 2 causes thin basement membrane nephropathy.

Journal: The Journal of clinical investigation

Published: December 29, 2020

The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 12, 2020

Controlled emission time statistics of a dynamic single-electron transistor.

Journal: Science advances

Published: August 03, 2020

Spectral Properties of Stochastic Resonance in Quantum Transport.

Journal: Physical review letters

Published: June 24, 2020

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

Journal: The Journal of clinical investigation

Published: April 29, 2019

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Real-Time Detection and Control of Correlated Charge Tunneling in a Quantum Dot.

Real-Time Detection and Control of Correlated Charge Tunneling in a Quantum Dot.

Human C-terminal CUBN﻿﻿ variants associate with chronic proteinuria and normal renal function.

Human C-terminal CUBN﻿﻿ variants associate with chronic proteinuria and normal renal function.

Correction to: The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation.

Correction to: The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation.

Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.

Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.

Collagen IVα345 dysfunction in glomerular basement membrane diseases. I. Discovery of a COL4A3 variant in familial Goodpasture's and Alport diseases.

Collagen IVα345 dysfunction in glomerular basement membrane diseases. I. Discovery of a COL4A3 variant in familial Goodpasture's and Alport diseases.

Loss of the collagen IV modifier prolyl 3-hydroxylase 2 causes thin basement membrane nephropathy.

Loss of the collagen IV modifier prolyl 3-hydroxylase 2 causes thin basement membrane nephropathy.

The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation.

The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation.

Controlled emission time statistics of a dynamic single-electron transistor.

Controlled emission time statistics of a dynamic single-electron transistor.

Spectral Properties of Stochastic Resonance in Quantum Transport.

Spectral Properties of Stochastic Resonance in Quantum Transport.

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.