Detlef Böckenhauer

Also affiliated with Universitair Ziekenhuis Leuven, Great Ormond Street Hospital for Children NHS Foundation Trust, University College London, KU Leuven

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 7 papers. Top paper: “The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis”.

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

Nature Communications(2020)10.1038/s41467-020-15383-w

N/A

4.6DataRank · unranked

223 citations

Lili Liu, Nikol Mladkova, Yifu Li, Hong Ren, Weiming Wang +95 more

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Kidney International(2022)10.1016/j.kint.2022.03.019

N/A

4.5DataRank · unranked

193 citations

Émilie Cornec-Le Gall, Jan Halbritter, Krzysztof Kiryluk, Andrew Mallett, Rulan S. Parekh +57 more

Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference

Kidney International(2020)10.1016/j.kint.2020.02.010

N/A

0.982DataRank · unranked

694 citations

Kai‐Uwe Eckardt, Nijsje Dorman, Stacy Christiansen, Ewout J. Hoorn, Julie R. Ingelfinger +36 more

Rare disease gene association discovery in the 100,000 GenomesProject

Nature(2025)10.1038/s41586-025-08623-w

N/A

0.515DataRank · unranked

18 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness

Journal of the American Society of Nephrology(2021)10.1681/asn.2020111587

N/A

0DataRank · unranked

73 citations

Aparna Renigunta, Ewout J. Hoorn, A. W. Forst, Vijay Renigunta, Velko Atanasov +26 more

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

medRxiv(2023)10.1101/2023.12.20.23300294

N/A

0DataRank · unranked

3 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries

Kidney International(2025)10.1016/j.kint.2025.02.026

N/A

0DataRank · unranked

7 citations

Steffen Fieuws, Jonas Hofstetter, David Pitcher, Lotte Vanmeerbeek, Stefanie Haeberle +95 more