Anja Buescher

Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants

Kathrin Burgmaier, Leonie Violetta Brinker, Florian Erger et al. · Kidney International · 2021 · 87 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies

Bodo B. Beck, Anne Baasner, Anja Buescher et al. · European Journal of Human Genetics · 2012 · 81 citations · Full text

Medicine, Internal Medicine, Molecular Medicine +6

The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results

Giulia Bassanese, Tanja Wlodkowski, Aude Servais et al. · Orphanet Journal of Rare Diseases · 2021 · 68 citations · Full text

Medicine, Biomedical Informatics, Nephrology +15

Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

Kathrin Burgmaier, Kevin Kunzmann, Gema Ariceta et al. · The Journal of Pediatrics · 2018 · 61 citations · Full text

Medicine, Nephrology, Dialysis +13

Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)

Kathrin Burgmaier, Gema Ariceta, Martin Bald et al. · Scientific Reports · 2020 · 28 citations · Full text

Medicine, Nephrology, Pediatrics +14