Markus J. Kemper
Asklepios Fachklinikum Brandenburg(DE)Asklepios Klinikum Harburg(DE)Asklepios(DE)Asklepios Kliniken Hamburg(DE)
Publications by Year
Research Areas
Renal Diseases and Glomerulopathies, Coagulation, Bradykinin, Polyphosphates, and Angioedema, Autoimmune Bullous Skin Diseases, Parathyroid Disorders and Treatments, Amyloidosis: Diagnosis, Treatment, Outcomes
Most-Cited Works
- → A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome(2014)640 cited
- → The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4(2006)572 cited
- → SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes(2004)417 cited
- → IPNA clinical practice recommendations for the diagnosis and management of children with steroid-sensitive nephrotic syndrome(2022)240 cited
- → Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome(2017)228 cited
- → Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome(2016)216 cited