Hannah Hugo

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.

Thomas M. Kitzler, S. Mane, R. Lifton, 2019, Journal of the American Society of Nephrology : JASN.

A Pilot Study: Observations of Patients Participating in Heart Failure Shared Medical Appointments while Receiveing Nutrition Education

Hannah Hugo, hugoh, 2020 .

Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent Approaches

Thomas M. Kitzler, S. Mane, H. Rehm, 2020, Kidney international reports.

Treatment with 2,4-Dihydroxybenzoic Acid Prevents FSGS Progression and Renal Fibrosis in Podocyte-Specific Coq6 Knockout Mice.

F. Hildebrandt, M. Schueler, C. Clarke, 2019, Journal of the American Society of Nephrology : JASN.

ADCK4 deficiency destabilizes the coenzyme Q complex, which is rescued by 2,4-dihydroxybenzoic acid treatment

Min Goo Lee, F. Hildebrandt, J. Ryu, 2019, bioRxiv.

Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome

S. Mane, R. Lifton, F. Hildebrandt, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

Kristen M. Laricchia, Thomas M. Kitzler, Richard S. Lee, 2018, Journal of the American Society of Nephrology : JASN.

Mutations in WDR4 as a new cause of Galloway–Mowat syndrome

Kristen M. Laricchia, M. Lek, A. Sinha, 2018, American journal of medical genetics. Part A.

Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome

Thomas M. Kitzler, S. Mane, F. Alkuraya, 2018, The Journal of clinical investigation.

Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome.

S. Mane, F. Hildebrandt, C. Bergmann, 2019, Kidney international.

DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes

Emily K. Mis, S. Ellard, J. Baptista, 2020, Journal of Medical Genetics.

ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment.

Min Goo Lee, F. Hildebrandt, J. Ryu, 2020, Journal of the American Society of Nephrology : JASN.